ࡱ> 0'` 0bjbj{P{P _::=  & T@d4d4d448@PA`E(EEEV2V,W$hZҞyZ@V@V"ZZҞ((EEXKnKKKZ0O(*EEKZKKF ?R:yEDA #шd4ѩhVT HrXD!Y9YyyNY WXKXfY;WWWҞҞKWWWZZZZ@@@$d4@@@d4@@@(((((( SAQs_ Elbow ossification centre- CRITOL Capitellum 6/12 - 2yrs Radial head 4yrs Internal (medial) epicondyle 6yrs Trochlea 8yrs Olecranon 10yrs Lateral epicondyle 12yrs Osteosarcoma: M:F 1.5:1 Most commonly affects adolescents peak incidence during period of maximum growth velocity 2nd peak in >50yrs due to malignant change in Pagets Primary is most often found at epiphysis or metaphysis of fastest growing sites usually around knee Patients with hereditary retinoblastoma have a 500X ( risk of osteosarcoma ? related to deletions in long arm of chromosome 13 Can also occur post radiotherapy Clinically 43% femur, 19% tibia, 10% humerus pain or swelling initially noted Diagnosis plain XR/CXR/MRI/bone scan/biopsy CT thorax - 10-15% metastasize to the chest 80-90% have micrometastases at presentation Poor prognostic factors age<10y large tumour >15cm osteoblastic cell type axial skeleton or humeral involvement ( serum LDH symptoms < 2/12 metastases NAI: XR features suggestive of NAI >1 #, especially if evolution of #s are different Subperiosteal bone formation never present on the day of the injury XR features pathognomic of NAI Metaphyseal long bone # - bucket handle (corner) Posterior rib # # pelvis/sternum/vertebral transverse processes Unicameral Bone Cyst or Juvenile Bone Cysts: Benign lesion which occurs during growth 20% of benign bone lesions Age 5-15 years Not found in adults Sex male to female is 3:1 The most common location is the proximal humerus (67%) followed by the proximal femur (15%) JBCs may be found in unusual sites (e.g. calcaneum, pelvis) in patients >17 years Cysts may be Active or Latent: Active cysts are located near the growth plate, but they move further away as the child grows and become inactive (latent) Presentation Asymptomatic Usually presents as a pathological fracture (~ 65%) Radiographic features Well defined, central osteolytic area with a thin sclerotic margin Metaphyseal in young - moves towards diaphysis with growth It fills and slightly expands the juxta- epiphyseal metaphysis CT not helpful unless the JBC is in the pelvis Treatment Treatment goal is to minimise fracture risk until the cyst heals (but this can take years) Steroid injection 1-3 percutaneous injections repeated at 2 monthly intervals 60-80% success rate Curettage and bone graft - 50% recurrence rate and possibility of damage to the growth plate Spontaneous healing after fracture occurs only in minority of cases Epiphyseal injuries: Risks: risk of premature fusion of the growth plate ( limb shortening( gait disturbance unequal growth may occur if only one part of the plate is injured Ewing Sarcoma: X-ray features of Ewings sarcoma: Periosteal elevation, onion-skin appearance, patchy lysis of marrow cavity, usually present in diaphysis of long bones highly malignant Rare Arises from vascular endothelium in marrow Lower extremity > upper extremity Any long bone affected commonest metaphysis + diaphysis of femur, then humerus Occurs most commonly between 10 and 20yrs Whites >> blacks/asians M:F 3>2 Clinically pain/ swelling/ erythema/wt loss/fatigue/fever Usual to have (WCC, (ESR,(Hb at presn Radiologically: bone destruction with overlying onion skin layers of periosteal new bone Usually lytic but can be sclerotic Investigations Biospy CT/MRI Bone scan Genetic screen Treatment pre-op chemotherapy vincristine/dactinomycin/cyclophosphamide Local resection Adjuvant chemo post-op - ( recurrence Metastases - lungs/LN Poor prognosis associated with; (Age, (ESR, Leucocytosis, (Serum LDH Prognosis if initial chemo/surgery unsuccessful - further chemo/radiotherapy gives 80-90% local control without metastases at presentation: 40-70% long-term survival Septic Arthritis: 4 powerful predictors of septic arthritis WBC >12 ESR >40 Fever Non weight-bearing Combined sensitivity 99.6% Organisms identified: Staph. 58%, Pneumococcus 16%, Haem.Infl. 13%, Meningococcus. 8%, Strep. 5% Koehlers disease Flattening, ! density and irregular shape of navicular of the foot Osteochondrosis of navicular bone Mean age 4-5, boys:girls 6:1 15% bilateral Aetiology: ?vasculitis / ? x-linked Treatment: ? POP , recovery 3-15 months Nutritional Rickets: x-ray Splayed, irregular epiphyses Cupped metaphyses Hazy growth plates Blounts deformity = tibia vara Varus knee, tibial bowing/proximal angulation Disturbed enchondral ossification of medial tibial plateau More common in black/Hispanic population Corrective surgery possible Associated with obesity Scheuermanns disease (adolescent kyphosis): 4-8% incidence on routine x-rays Disorder of endplate growth Document neurological/respiratory symptoms Cobbs angle > 40 degrees = brace > 70 degrees = surgery Basal cell carcinoma Features: rolled edge / pearly nodules/ keratin plug treatment options : Excision Topical 5 fluorouracil ?DXT Keratoacanthoma Umbilicated violaceous hyperkeratinous scaly treatment : Observe, Biopsy , Excise Currette/Cauterise A 10-year-old boy is brought to the department with bilateral parotid swelling. He has been diagnosed as having mumps by his GP the previous day. He is otherwise well. Give 3 complications of this condition (3) Orchitis Encephalitis Pancreatitis Give 2 other causes of parotid swelling (2) Stone Cancer Alcohol abuse HIV What 4 things are you going to do for this patient in A&E? (4) Notifiable disease Analgesia Feeding advice non-acid foods Mouth care advice Vaccination advice List 4 complications of an elbow fracture in any patient (4) Restricted movement Volkmanns contracture Malunion Myositis ossificans Diarrhoea in children: List 4 things that you would ask for in the history. (4) Wet nappies Episodes of vomiting Frequency & description of stools and vomitus Affected contacts Food & Fluid intake (food poisoning- notifiable) Drugs taken Travel Other symptoms - abdominal pain, fever Weight loss- very important to assess degree of dehydration What is the classification of dehydration according to APLS with percentages Mild 5% Moderate 5-10% Severe >10% Mild dehydration: 5% Decreased urine output (<4 wet nappies/24 hrs) Dry mouth Thirst Moderate dehydration: 5 10% Sunken frontenelle in infants Sunken eyes Tachypnoea due to metabolic acidosis Tachycardia Severe dehydration: >10% Decreased skin turgor Drowsiness or irritability Give 4 indications for admission in a child with gastroenteritis Moderate or severe dehydration (>10% dehydration needs i.v. fluid) Parents unable to cope at home High fever unresponsive to anti-pyretics Baby <3 months old NB: severe illness with bloody diarrhoea, haemolysis and renal failure may result from infection with vero-cytotoxin producing E. coli (E. coli VTEC O157) CO poisoning may cause malaise and vomiting in several members of a family and be misdiagnosed as food poisoning. ABG in a patient with confusion and low blood glucose- pH 7.3, pO2 >13kPa, pCO2 3kP, Base excess -6.0, Na 129, K 6.2, HCO3 12 What 2 urgent treatments- Glucose i.v. hydrocortisone Causes for hypoglycaemia: (ExPLAIN MAD) Exogenous- overdose of insulin or hypoglycaemic drugs Pituitary insufficiency & Post-gastric surgery Liver failure Adisonian crisis Insulinoma Non-pancreatic neoplasms Malaria Alcohol overdose Drugs What are the criteria for ITU admission in asthma: Life threatening features Silent chest Poor respiratory effort Agitation Altered consciousness Cyanosis Poor response to treatment Erythema nodosum Causes: i) sarcoidosis ii) infections: streptococci, TB, infectious mononucleosis, chlamydia, viral iii) drugs: sulphonamides, OCP, salicylates iv) inflammatory bowel disease v) idiopathic Management: Advise NSAID, bed rest, elevate legs. Remove underlying cause OCP. Most attacks settle within 2-12 weeks. Systemic steroids may be used for severe cases. Hyperkalaemia notes Mild (5.5-6.0) Moderate (6.1-6.9) Severe (>7.0) Causes i) Factitious e.g. haemolysed sample. ii) Reduced renal excretion ARF, CRF, K+ sparing diuretics e.g. spironolactone. iii) Cell injury e.g. burns, rhabdomyolysis. iv) Hyperaldosteronism Addisons disease, drug induced (NSAID, ACE inhibitors). v) K+ cellular shifts acidosis from any cause (DKA), drugs (suxamethonium). Clinical features include muscle weakness/ cramps, paraesthesiae, hypotonia. Treatment i) 10ml 10% calcium gluconate. ii) 10u Actrapid with 50ml of 50% dextrose IV helps cellular uptake of K+. iii) Nebulised salbutamol. iv) Careful fluid balance, correct acidosis with sodium bicarbonate. v) ? calcium resonium. vi) Correct underlying cause. Pulmonary embolism. ECG: Sinus tachycardia is the most common ECG finding. RBBB and right axis deviation are usually only present in large PE. There may be non-specific T wave changes in the anterior and inferior leads. Investigations: Doppler USS of legs CTPA Inherited procoagulant screen (protein C, S, antithrombin III, Factor V Leiden) Autoimmune screen (anticardiolipin antibodies, ANA) USS or CT of abdomen and pelvis to look for occult masses If a patient with suspected PE has arrested or is deteriorating, or in a stable patient with confirmed PE, thrombolysis with alteplase 50mg IV is appropriate The Wells score: clinically suspected  HYPERLINK "http://en.wikipedia.org/wiki/DVT" \o "DVT" DVT - 3.0 points alternative diagnosis is less likely than PE - 3.0 points  HYPERLINK "http://en.wikipedia.org/wiki/Tachycardia" \o "Tachycardia" tachycardia - 1.5 points immobilization/surgery in previous four weeks - 1.5 points history of  HYPERLINK "http://en.wikipedia.org/wiki/DVT" \o "DVT" DVT or PE - 1.5 points  HYPERLINK "http://en.wikipedia.org/wiki/Hemoptysis" \o "Hemoptysis" hemoptysis - 1.0 points malignancy (treatment for within 6 months, palliative) - 1.0 points Traditional interpretation Score >6.0 - High (probability 59% based on pooled data HYPERLINK "http://en.wikipedia.org/wiki/Pulmonary_embolism" \l "cite_note-pmid17185658-9" [10]) Score 2.0 to 6.0 - Moderate (probability 29% based on pooled data HYPERLINK "http://en.wikipedia.org/wiki/Pulmonary_embolism" \l "cite_note-pmid17185658-9" [10]) Score <2.0 - Low (probability 15% based on pooled data HYPERLINK "http://en.wikipedia.org/wiki/Pulmonary_embolism" \l "cite_note-pmid17185658-9" [10]) Alternate interpretation (used practically) Score > 4 - PE likely. Consider diagnostic imaging. Score 4 or less - PE unlikely. Consider  HYPERLINK "http://en.wikipedia.org/wiki/D-dimer" \o "D-dimer" D-dimer to rule out PE. Simplified Geneva Score Age 65 years or over (1 point) Previous DVT or PE (1 point) General anesthesia or fracture within 1 month (1 point) Active malignant condition or malignant condition that has been cured within 1 year (1 point) Unilateral lower limb pain (1 point) Hemoptysis (1 points) Pain on deep palpation of lower limb and unilateral edema (1 point) Heart rate of: 75 to 94 (1 point) Heart rate of: Greater than 94 (1 point) Patients with a score of 2 or less are considered unlikely to have a current PE. Authors suggest that the likelihood of patients having a PE with a simplified Geneva score less than 2 and a normal D-Dimer is 3 percent. HYPERLINK "http://en.wikipedia.org/wiki/Geneva_score" \l "cite_note-Geneva_Scoring_for_Pulmonary_Embolism_Simplified_Further-5" [6] If signs of severe haemodynamic compromise, arrange for urgent CTPA or echocardiogram Collapse Hypotension A-a gradient more > x2 normal when CXR is normal and no other explanation Compromised peripheral perfusion Request for CTPA / VQ scan should include Wells score D-dimer level Previous lung disease (asthma, COPD) for which patient required admission or under care of respiratory clinic Oesophageal F.B. Objects that stick in the oesophagus do so at sites of anatomical narrowing; i) Cricopharyngeus ii) Aortic indentation iii) Diaphragm Neglected objects may result in oesophageal perforation and mediastinitis. May require removal with rigid endoscopy. Foley catheters and magnets have also been used but without much success. TIMI score= Thrombolysis in Myocardial Infarction trials. (AMERICA) i) Age e"65 years ii) e"3 CAD risk factors iii) Prior CAD (stenosis >50%) iv) Aspirin in last 7 days v) e"2 anginal events in d"24 hours vi) ST deviation vii) Elevated cardiac markers The score (0-7) gives the risk of cardiac events (death, MI or urgent revascularisation) within 14 days in TIMI IIB. Typhoid: Organism responsible Salmonella typhi. Spread by faecal/ oral route. Along with malaria, first disease to consider if fever develops after visit to affected areas. Incubation period 8-14 days. Symptoms 1st phase - fever, headache, sweating, dry cough, myalgia, arthralgia, abdominal discomfort, anorexia, constipation. Children are prone to diarrhoea. There may be splenomegaly. Rose spots are pink macular spots on the lower chest or upper abdomen which blanch on pressure 2nd phase - fever, severe diarrhoea (may be bloody), unwell++, confusion. Pneumonia and intestinal perforation are possible complications. Treatment Isolate and barrier nurse. Ciprofloxacin. Careful fluid balance. Notify communicable disease control. 3rd nerve palsy: ptosis. divergent strabismus and pupil is dilated. Differential diagnosis Space occupying lesions, after surgery (e.g. for pituitary lesions), aneurysms of the posterior communicating artery, Infections e.g. meningitis, encephalitis, herpes, syphilis. Worthwhile mentioning; Isolated 4th nerve palsy (superior oblique moves eye downward) ! diplopia on downward gaze. Isolated 6th nerve palsy (lateral rectus moves eye laterally) ! failure of lateral movement with diplopia on looking at the affected side. Fascial spaces of the hand. i) Superficial pulp spaces of fingers ii) Synovial tendon sheaths of the flexor tendons ~ that of the 2nd, 3rd and 4th fingers are closed off proximally at the metacarpal head but the synovial sheaths of the thumb and little finger extend into the palm (see diagram). iii) Midpalmar space iv) Thenar space  Hand tendon injuries Flexor tendon injuries are often associated with neurovascular damage Extensor tendon injuries often associated with articular damage Anatomy Flexor tendons Flexor tendons run a fibro-osseous canals Synovial sheath for index to ring finger begins at neck of metacarpals Synovial sheath of little finger is continuous with ulna bursa Sheath thickened to form pulleys (A1 to A5) Extensor tendons Extensor tendons are extra-synovial, except at the wrist Surrounded by extensive paratenon with segmental arterial input Extensor retinaculum prevents bowstringing of the extensors Main action is extension of the MCP joints Zone of injury  Zone II is the No Mans Land where the flexor tendons are located in a narrow fibro-osseous tunnel; injuries to the flexors in this region have a worse prognosis as the finger tends to become stiff as adhesions form. Flexor tendons Flexor tendons are divided into 5 zones Zone 1 is distal and Zone 5 is proximal The five zones are 1 - contains flexor digitorum profundus only distal to the insertion of flexor digitorum superficialis 2 - from insertion of flexor digitorum superficialis to the proximal edge of the A1 pulley 3 - from the proximal edge if the A1 pulley to the distal edge of the carpal tunnel 4 - within the carpal tunnel 5 - proximal to the carpal tunnel Extensor tendons Extensor tendons are divided into 8 zones Zones 1,3 and 5 lie over the DIP, PIP and MCP joints Assessment Accurate history required Important to know handedness and patients occupation Observing hand at rest my indicated tendons involved Level of tendon injury may corresponds to site of any laceration - but not always If both flexor tendons divided the finger will be extended If profundus tendon alone divided then only the DIP will be extended Further assessment should involve testing of individual tendons Flexor digitorum superficialis Flexor digitorum profundus Neurovascular assessment also required Flexor tendon injuries Early exploration and repair is required Ideally surgery should be performed within 24 hours Primary repair is the gold standard Primary repair may not be possible id delayed presentation or tendons retracted Antibiotic prophylaxis required if delayed presentation or would contamination The ideal tendon repair requires Sutures easily placed in the tendon Secure suture knots Smooth junction if the tendon ends Minimal gapping at repair site Minimal interference with tendon vascularity Sufficient repair strength Many techniques of tendon repair have been described They invariably involve Core suture Epitendinous suture Zone 1 injuries Direct repair usually possible Periosteal flap raised and tendon anchored with a core suture Zone 2 to 5 injuries Wounds should be excised and irrigated May need to be extended to retrieve and repair tendons Avoid incisions that cross skin creases Careful planning required to prevent skin necrosis or contracture Incision may be required in tendon sheaths between the main pulleys Neurovascular bundles should be identified and repaired is necessary Tendons should be repaired using a standard technique Post-operative management After repair the hand should be placed in a back-slab with Wrist at 0 - 30 degrees MCP joints at 60 - 90 degrees PIP and DIP joints in full extension Hand should be elevated to reduce swelling Early mobilisation required to Reduce adhesion formation Improve tendon healing Improve final outcome Requires close supervision by hand physiotherapist Mobilisation can begin as early as first postoperative day Passive extension should be avoided Extensor tendon injuries Open exploration and repair is required Can often be performed under local anaesthetic Management depends on the zone of the injury Proximal injuries require immobilisation with the wrist extended and the MCP joint flexed Active movement can begin after 3 weeks Distal injuries require longer period of immobilisation Anatomic Zones of the neck. (peneterating injuries) Serving as the line of demarcation, the sternocleidomastoid separates the neck into anterior and posterior triangles. The majority of the important vascular and visceral organs lie within the anterior triangle bounded by the sternocleidomastoid posteriorly, the midline anteriorly, and the mandible superiorly. Except for individual nerves to specific muscles, few vital structures cross the posterior triangle, which is delineated by the sternocleidomastoid, the trapezius, and the clavicle (with the exception of the region just superior to the clavicle). [  HYPERLINK "javascript:showcontent('inactive','hiddenlayerd26e1502');" CLOSE WINDOW ]  INCLUDEPICTURE "http://img.medscape.com/pi/emed/ckb/emergency_medicine/756148-827223-976.jpg" \* MERGEFORMATINET  Neck trauma. Zones of the neck. For clinical purposes, the neck is partitioned into 3 Zone I, the base of the neck, is demarcated by the thoracic inlet inferiorly and the cricoid cartilage superiorly. Structures at greatest risk in this zone are the great vessels (subclavian vessels, brachiocephalic veins, common carotid arteries, aortic arch, and jugular veins, trachea, esophagus, lung apices, cervical spine, spinal cord, and cervical nerve roots. Signs of a significant injury in the zone I region may be hidden from inspection of the chest or the mediastinum. [  HYPERLINK "javascript:showcontent('inactive','hiddenlayerd26e1517');" CLOSE WINDOW ] INCLUDEPICTURE "http://img.medscape.com/pi/emed/ckb/emergency_medicine/756148-827223-973.jpg" \* MERGEFORMATINET Neck trauma. Zone I injury. Zone II encompasses the midportion of the neck and the region from the cricoid cartilage to the angle of the mandible. Important structures in this region include the carotid and vertebral arteries, jugular veins, pharynx, larynx, trachea, esophagus, and cervical spine and spinal cord. Zone II injuries are likely to be the most apparent on inspection and tend not to be occult. Additionally, most carotid artery injuries are associated with zone II injuries. [  HYPERLINK "javascript:showcontent('inactive','hiddenlayerd26e1532');" CLOSE WINDOW ]  INCLUDEPICTURE "http://img.medscape.com/pi/emed/ckb/emergency_medicine/756148-827223-974.jpg" \* MERGEFORMATINET  Neck trauma. Zone II injury. Zone III characterizes the superior aspect of the neck and is bounded by the angle of the mandible and the base of the skull. Diverse structures, such as the salivary and parotid glands, esophagus, trachea, vertebral bodies, carotid arteries, jugular veins, and major nerves (including cranial nerves IX-XII), traverse this zone. Injuries in zone III can prove difficult to access surgically. torsades de pointes Also known as polymorphous ventricular tachycardia. May present as recurrent syncope or dizziness. Potentially reversible causes, hypokalaemia, hypocalcaemia, hypomagnesaemia, CHB, congenital long QT interval or drug related e.g. sotalol, tricyclics, antihistamines. Torsades may be self-limiting but may progress to VF. Treat by: i) Correcting underlying cause if possible. ii) IV magnesium sulphate 2g over 10 min. iii) May require temporary overdrive pacing. subdural haematoma. What groups of patients are prone to this? Alcoholics, the elderly, patients on anticoagulants. List 5 features which may be present. i) Headache ii) Fluctuating GCS iii) Confusion iv) Memory loss v) Focal neurological deficit Ulnar nerve palsy Look for: Wasting of interossei: Wasting of the first dorsal interossei (ulnar n. supplies all interossei but 1st is almost always the first to become noticeably affected) ulnar claw appearance of hand. The claw hand appearance is due to paralysis of the intrinsic hand muscles (lumbricals) which normally flex the MCPJs and extend the PIPJs. Unopposed action of the long extensors pulls the MCPJs into hyperextension and the long flexors pull the PIPJs into flexion. hypothenar wasting Scars/ deformity around elbow, wrist and hand. Trophic changes. Motor: Test flexor carpi ulnaris. Test FDP in little finger. Interossei: hold sheet of paper between ring and little fingers and withdraw. First interosseus: attempt to adduct index against resistance, look and feel for contraction in 1st webspace. Froments test (adductor pollicis). State 2 causes of this condition. At wrist lacerations, ganglia. At elbow occupational secondary to excessive leaning. median nerve Supplies: Muscles in forearm (through anterior interosseous branch) FPL of FDP FDS FCR Palmaris longus Pronator quadratus and teres Muscles in hand L lumbricals (lateral two) O opponens pollicis A abductor pollicis brevis F flexor pollicis brevis Look for: Index finger held in extension (Benediction attitude). Wasting of thenar muscles, deformity/ scars around wrist and elbow. Trophic changes. Motor: Test APB by asking patient to lift thumb off flat surface against resistance. Test FCR. Test FPL and FDP in the index by flexing joint against resistance. Test pronator quadratus by asking patient to pronate arm against resistance with elbow extended. Parkinsons disease. Name 3 features of this condition. Tremor, rigidity, bradykinesia. Other features: Stooped posture/ shuffling gait, fixed facial expression, speech problems, poor balance, dementia List 3 drugs used as treatment. Levodopa, dopamine agonists (e.g. bromocriptine), selegiline Causes for delirium: H hypoxia I infection D drugs D dural haemorrhage E endocrine (hypoglycaemia) N neoplasis / neurological M metabolic (hypercalcaemia) A alcohol (overdose, withdrawal, DT) P psychosis Causes for increased anion gap M methanol U uraemia D DKA P I INH L lactic acidosis E ethylene glycol A 45 year old man is referred to the ED by his GP. He had a two day history of progressive right-sided facial weakness and lower limb weakness. He had been previously fit apart from a mild URTI one week previously. Examination revealed a right-sided LMN CN VII palsy, generalised weakness of the legs with reflexes diminished in the upper limbs and absent in the lower limbs. No other findings of note. What is the diagnosis? Guillan-Barr syndrome What are the diagnostic features? i) Ascending, usually symmetrical, progressive LMN weakness. ii) Sensory loss is not usually profound but paraesthesiae may precede weakness. If there is a sensory level then spinal cord compression should be the diagnosis until proved otherwise. iii) Reflexes are diminished. iv) Autonomic dysfunction is common. v) Ventilatory failure as disease progresses. vi) Often involves the cranial nerves (7th commonest). How would you investigate this patient? GBS is a diagnosis of exclusion with an extensive differential (see below). The management of the patient with GBS is that of any patient with neuromuscular failure but specific measures include; i) Autonomic instability is a common feature so pulse/BP/ECG monitoring is essential. ii) Check spirometry and ABGs; early ventilatory support may be required iii) CT head if diagnosis unclear. iv) CSF analysis may be required CSF protein characteristically rises and peaks at 4-6 weeks but may be normal initially. v) Specific treatment with immunoglobulin. What is the mortality of this condition? Associated mortality is 10%. Poor prognostic features on presentation: rapid onset, requirement for ventilation, age>40. Grading system from I (able to run) to V (ventilated). GBS probably represents an immune-mediated attack on peripheral nerves. Differential diagnosis of acute generalized weakness: Myasthenia gravis Tetanus Multiple sclerosis Spinal cord compression Alcoholic myopathy Botulism Poisoning (lead, organophosphates) Hypokalaemia Trifascicular block This may show: 1 heart block+RBBB+left anterior hemiblock 1 heart block and LBBB Block of the right bundle branch and either fascicle is bifascicular block. If this is combined with 1st degree AV block then it is called trifascicular block. If the patient is in CHB and bradyarrhythmia is causing severe haemodynamic compromise then Temporary pacing is the best option. Atropine 1mg IV bolus repeated if necessary up to 3mg. Isoprenaline 0.2mg IV if there is a delay in pacing and the patient remains unstable. A 22 year old Caucasian woman presents acutely unwell. She has been previously fit and well and there is no history of IV drug abuse. On examination she is pale, dyspnoeic and tachycardic rate 130, no organomegaly. Blood results show: Hb 5.2 Bilirubin 74 WCC 3.9 ALT 25 Plt 195 AST 29 MCV 94 Alk phos 235 U+Es and clotting were normal. What is the diagnosis? Haemolytic anaemia (normal MCV, elevated bilirubin). Causes may be congenital (e.g. G-6-PD deficiency, sickle cell disease, hereditary spherocytosis) or acquired. In this patient it is likely to be an acquired cause as hereditary disorders usually present early in life. Splenomegaly would have suggested an underlying systemic disorder such as CLL or SLE. Give 3 further investigations you would like to perform. Coombs test (detects circulating antibodies against RBCs presence may indicate autoimmune or drug-induced haemolytic anaemia). Blood film CXR Give 2 further features in the history that you would like to know. Foreign travel Drug history Give some possible causes. i) Drugs e.g. penicillin, methyldopa. ii) Infections; viral, bacterial (mycoplasma) or protozoal (malaria). iii) Fava beans may precipitate haemolysis in patients with G-6PD deficiency. iv) Idiopathic autoimmune disorder. v) Underlying systemic disorder e.g. CLL, SLE. A 72 year old lady is brought into the ED by concerned relatives. She has recently become increasingly confused and agitated and today is very unwell. The only medication that she is taking is thyroxine. You are concerned that she may be suffering a thyroid storm. thyroid storm: Look for evidence of thyroid disease e.g. goitre, exopthalmos. It may be precipitated by Inappropriate cessation of anti-thyroid therapy, Infection, Trauma, DKA, Iodine administration, Recent surgery or Thyroid hormone overdose. What other clinical signs would help confirm your diagnosis? CVS Tachycardia, palpitations AF Cardiac failure CNS Agitation, anxiety Tremor Delirium, coma Other Fever Sweating Abdominal pain Vomiting What would be your first investigation? ? TFTs TFTs do not discriminate between simple thyrotoxicosis and thyroid crisis but an urgent TSH or free T4 may be useful if diagnosis is unclear. What 3 medications would you use as first-line treatment? 1) Steroids  hydrocortisone 200mg IV 2) Propranolol 1mg IV inhibits peripheral T4!T3 conversion. Remember that a history of cardiac failure (rate-dependent failure not included) or asthma may be CI for -blockade; guanethidine may also be used. 3) Antithyroid drug; propylthiouracil is more effective than carbimazole. Treat the precipitating factor if possible. Fluid balance is important and CVP monitoring is usually necessary. Monitor BM. Sedation should be given if necessary. Broad spectrum antibiotics are indicated if infection is suspected. Do not give aspirin as this may displace thyroxine from thyroid binding globulin. Treat fever with paracetamol. Iodine will be given on the ITU once antithyroid medication has commenced effect. Differential diagnosis neuroleptic malignant syndrome, septic shock, anticholinergic or sympathomimetic overdose, withdrawal states. Another thyroid storm question was given: A 35 year old woman is admitted confused, pyrexial and vomiting. Her flat-mate reports that she has been unwell for the last three months and has lost weight. Three days previously she was bed-bound with a severe cold. Her brother is diabetic. On examination she is disorientated, pyrexial and tachycardic with an irregular pulse. There is no neck stiffness and no focal neurological signs, no obvious focus of infection Blood results were unremarkable, BM 5.2. Clues in this question; History Weight loss Recent viral illness Family history of autoimmune disease (presumably she has Graves disease) Examination AF Confusion Pyrexial A 35 year old male solicitor attends with a headache. He was diagnosed as being hypertensive a year ago and despite drug treatment including -blockers, calcium antagonists and an ACE inhibitor his blood pressure remains elevated. He drinks 4 pints of beer/day and smokes 2 cigars every evening. In the department, supine blood pressure is 210/110mmHg. Fundal examination shows grade 3 retinopathy (flame haemorrhages and cotton wool exudates). The rest of the examination is normal. Investigations: Sodium 148, Potassium 3.0, Bicarbonate 32, Urea 4, Glucose 4 Urinalysis NAD What is the likely diagnosis? Conns syndrome (primary hyperaldosteronism). High aldosterone levels increase renal excretion of potassium, but this is not diagnostic for this disease. Essential hypertension which is being treated with diuretics may mimic this. High blood pressure is the main, and often only, symptom. Excess secretion of aldosterone may be caused by an adrenal adenoma or adrenal hyperplasia. What further investigations are indicated? CT abdomen. Serum aldosterone (elevated) and renin (low or undetectable). However these are specialist investigations as they need to be done under controlled conditions. Refer to an endocrinologist for appropriate treatment surgical adrenalectomy (adenoma) or spironolactone (hyperplasia). Other conditions that may present with severe hypertension CVA, renal artery stenosis, CREST syndrome, renal failure, phaeochromocytoma, Cushings syndrome. Malignant hypertension Phaeochromocytomas Phaeochromocytomas are catecholamine-producing tumours of the adrenal glands. They may present with hypertension, hypertensive crises, cardiac arrhythmias, anxiety attacks, tremor, sweating and cold extremities. Careful rehydration is necessary before -blockade and referral. Send urinary and plasma catecholamines. Malignant hypertension may presents with hypertensive encephalopathy (headache, nausea, vomiting, visual symptoms, confusion, fits) and needs careful blood pressure management after consultation with physicians. Cautious reduction of the BP is necessary to avoid complication such as CVA and AMI Avoid sublingual nifedipine. A 64 year old Somali woman has a 6 month history of significant weight loss and episodic colicky abdominal pain not associated with meals or posture and no change in bowel habit. Investigations: Sodium 125, Potassium 6.0, Urea 14, Calcium 2.76 (2.2-2.6), Glucose 3.3 What is the diagnosis? Addisons disease. This frequently has an insidious onset with weakness, apathy and anorexia in addition to the other symptoms described. 80% of cases in the UK are idiopathic (autoimmune); Other causes include TB, metastatic disease, drugs (e.g. rifampicin, phenytoin), adrenal haemorrhage 2 anticoagulation and sepsis. The biochemical picture is typical. Treatment consists of identifying the underlying cause and steroid replacement therapy. Chronic features of Addisons disease include areas of vitiligo and hyperpigmentation in the palmar creases, buccal mucosae and axillae. Addisonian crisis (acute adrenal cortical insufficiency) is rare and usually precipitated by sudden steroid withdrawal. Other causes include trauma, infection or stress. Main features are shock, confusion and hypoglycaemia. Treatment of crisis involves i) Fluid resuscitation ii) Check BM and treat if hypoglycaemic iii) Take blood for cortisol and ACTH iv) Hydrocortisone 100mg IV v) Infection screen and IVAB if suspected infection Q. A 45 year old smoker complains of tiredness and weakness. Investigations: Blood pressure 180/110mmHg Sodium 140, Potassium 2.8, Bicarbonate 32, Urea 5, Glucose 12 What is the probable diagnosis? ACTH-producing oat cell lung carcinoma Cushings syndrome, caused by excess glucocorticoids. The commonest cause is the use of steroid medications e.g. for asthma. Classical signs and symptoms; Moon face Central obesity Abdominal striae & Thinning skin Weight gain Osteoporosis Diabetes Hypertension Infections esp. skin What investigations would you perform to confirm your diagnosis? CXR Serum and urine cortisol Dexamethasone suppression test Pretibial myxoedema. Can be present in either Graves disease or hypothyroidism. It is an infiltrative dermopathy that most frequently appears symmetrically over the anterior tibia and dorsum of feet. Can present in nodular or diffuse forms. It is likely that thyroid hormones affect the synthesis and catabolism of mucopolysaccharides and collagen by dermal fibroblasts. Treatment with steroids and/or immunoglobulins may give some relief. This patient presented with a rash following an URTI.  What is the likely diagnosis? Henoch-Schonlein purpura. Aetiology IgA-mediated vasculitis of small blood vessels. The exact causative mechanism is unknown but it usually follows bacterial (particularly strep.) or viral infection. What is the likely sex and age of the patient? M:F 2:1 4-11 years What is the prognosis? Generally good but need follow up because of the possibility of delayed renal involvement and development of nephrotic syndrome which indicates severe disease. What other symptoms may the patient present with? i) Malaise, low grade fever ii) Hepatosplenomegaly iii) Lymphadenopathy iv) Colicky abdominal pain (may develop bloody diarrhoea, intussusception). v) Arthritis/ arthralgia vi) Testicular pain and/ or swelling Causes of purpuric rashes in children: i) meningococcaemia ii) HSP iii) thrombocytopenia 2 ITP, leukaemia, aplastic anaemia iv) trauma, coughing or retching Erythema multiforme: Typical target lesions. It can occur at any age This is a localised form of vasculitis. Causes: idiopathic, drugs (e.g. sulphonamides, phenytoin, barbiturates), infection (viral (esp. Herpes simplex) or Mycoplasma pneumonia), or related to malignancy. What is the eponymous name for the severe form of this condition? Stevens-Johnson syndrome. There may be oral, ocular and genital lesions. This form carries a significant morbidity and mortality; complications may include renal and respiratory involvement. Management is symptomatic. Steroids may reduce the severity of the attack. The underlying cause should be treated where possible. SLE. This is a chronic autoimmune disorder characterised by the production of a range of autoantibodies, most commonly ANA. Commoner in young women. Patients may present as a new diagnosis or with a flare up of the disease. Clinical features (in descending order of frequency); Constitutional fever, malaise, weight loss Musculoskeletal athralgia, myalgia Cutaneous butterfly rash, photosensitive rash, discoid lupus, Raynauds Haematological thrombocytopenia, anaemia, leucopenia Neuropsychiatric depression, psychosis, fits, CN lesions, ataxia Renal glomerulonephritis, nephritic syndrome CVS or RS pleurisy, pericarditis, pericardial/ pleural effusions Apthous ulcers What 4 important emergency investigations would you now consider? FBC, U&E, CRP, CXR, urinalysis, ECG Other investigations include ANA, DNA, ENA, ACA, complement levels, viral serology, 24hr urine collection. 80% of patients are ANA +ve. Pneumococcal and meningococcal infections are more common in patients with SLE as a consequence of deficiencies of the complement pathway. Treatment is with steroids, immunosuppresants e.g. azathioprine, antibiotics if infection suspected. Lung abscess and Empyema: The most common cause of lung abscess, or empyema (pus in the pleural cavity), is aspiration. Patients at risk include the elderly, alcoholics, those with poor dentition or primary lung disease. Other causes of empyema include penetrating chest trauma (including chest drains) and oesophageal rupture. The patient is usually elderly and the abscess is most commonly located in the dependent part of the lung on the right side. Organisms are usually polymicrobial oral flora e.g. Bacteroides and Fusobacterium. Increasingly in the paediatric population S. aureus has become the predominant organism because of the use of the pneumococcal conjugate vaccine. Treatment is with broad-spectrum antibiotics and drainage by tube thoracostomy. Primary chancre of syphilis. What is the offending organism and how is it transmitted? Treponema pallidum, a spirochaete. It is almost always transmitted by sexual contact with infectious lesions Can be transmitted in utero and by blood transfusion. List 4 other causes of genital ulceration. i) Other infections e.g. herpes simplex, gonorrhoea. ii) Neoplasms e.g. carcinoma of penis iii) Behets disease. iv) Trauma (may be self-inflicted). What investigations could confirm the diagnosis? Direct visualisation by darkfield microscopy. VDRL serology. What is the treatment of choice? Primary and secondary syphilis are highly responsive to penicillin and cure is likely. How may secondary syphilis present? localised or diffuse mucocutaneous rash and generalised lymphadenopathy. Constitutional symptoms include malaise, sore throat, headache, fever, arthralgia and myalgia. Other less common manifestations include hepatitis, nephropathy, optic neuritis, proctitis. Necrobiosis lipoidica. Commonly affects the shins, seen more often in women. More than fifty percent of sufferers have DM. It is a chronic condition; ulceration may occur. Flare-ups may respond to cortisone cream or UV light. Aspirin may also help. Pancreatitis Aetiologies (GET SMASHED) Gall stone, Ethanol, trauma & post-surgery (ERCP), steroid, mumps, autoimmune (SLE), hyperlipidaemia/hypercalcaemia, scorpion bite, drugs (salicylate) USG should be organized within 24 hours to find out the cause. CT scan is indicated To confirm the diagnosis of acute necotising pancreatitis If patient deteriorates - to confirm the diagnosis of necrosis and CT guided aspiration of the infected secretion. Antibiotics is required in Pancreatic necrosis Biliary tract obstruction Cephalosporine or carbapenum Complications Local Necrosis infection. Fluid collections. Pseudocysts. GI haemorrhage. Systemic Shock. Coagulopathy & DIC Renal failure. Respiratory failure & ARDS Hyperglycaemia. Hypocalcaemia. Glasgow criteria Glasgow's criteria[: The original system used 9 data elements. This was subsequently modified to 8 data elements, with removal of assessment for transaminase levels (either AST (SGOT) or ALT (SGPT) greater than 100 U/L). On Admission Age >55 yrs WBC Count >16 x109/L Blood Glucose >10 mmol/L (No Diabetic History) Serum Urea >16mmol/L ( No response to IV fluids) Arterial Oxygen Saturation <7.9 kPa Within 48 hours Serum Calcium <2mmol/L Serum Albumin <32 g/L LDH >600 units/L AST/ALT >100 units/L All patients with Glasgow score 3 or more should be referred to ITU / HDU. Orbital Cellulitis: Name 2 possible causative organisms. Since invasive H. influenza infection has been all but eradicated by immunisation, S. aureus and Strep. pneumoniae are the commonest pathogens. What is the likely source of infection? It is usually caused by spread from the sinuses (ethmoidal or para-nasal) but may arise from local trauma (e.g. bites, foreign body) or haematological spread. List 3 complications. i) Cavernous sinus thrombosis. ii) Cerebral abscess. iii) Optic nerve compression leading to loss of vision. Patients should be admitted under joint care of paeds./ ENT/ eyes. Antibiotics IV flucloxacillin and metronidazole. Essential investigation is CT scan of orbit and sinuses. Community Acquired Pneumonia: Investigations: All patients admitted to hospital: FBC, U&E, CRP, ABG, blood cultures, sputum cultures. For patients with severe CAP: pneumococcal antigen, legionella urine antigen, chlamydial antigen and mycoplasma CFT are appropriate. What features may indicate an adverse prognosis? Core clinical adverse features (CURB 65) Confusion: new confusion or defined as an AMT score of 8 or less. Urea: raised >7mmol/l. Respiratory rate: raised e"30/min. Blood pressure: low BP systolic <90 and or diastolic d"60. Age: >65 years. A score of 2 or greater on CURB 65 means hospital treatment is usually necessary. Pre-existing Age >50 years. Presence of co-existing disease. Additional adverse features Hypoxaemia: SaO2 <92% or PaO2 <8kPa regardless of FiO2. Bilateral or multilobe involvement on the CXR. What antibiotic therapy is recommended? For hospital-treated, not severe CAP: amoxicillin 500mg tds plus clarithromycin 500mg bd. For severe CAP: co-amoxiclav 1.2g tds IV plus clarithromycin 500mg bd. BTS guideline recommends macrolide antibiotics In children above the age of 5 years, but macrolide antibiotics smay be preferred preferred in children because it is effective against pneumococci as well as pertusis and mycoplasma, whereas amoxicillin is not effective against pertusis and mycoplasma. Infectious endocarditis. Mitral valve is most commonly affected. Presentation: malaise, night sweats and weight loss What signs will you look for on further examination? i) Splenomegaly. ii) Roth spots (retinal haemorrhages with central clearing). iii) Splinter haemorrhages. iv) Anaemia. v) Janeway lesions (red skin spots on the palms and soles). vi) Oslers nodes (red, painful intradermal pads in the fingers and toes). vii) Urine- microscopic Haematuria. Viii Changing murmur What investigations are appropriate? ECG, CXR, FBC, blood cultures X 3, ECHO, ASO test. Organisms: Commonest organism is S. viridans (found in the mouth, 40%) others S. aureus (which presents with heart failure), enterococci and fungal e.g. candida, aspergillus. Complications valve destruction, heart block, LVF, embolic events, lung abscesses (right-sided disease). Which patients are at risk from this condition? May develop on previously normal valves as well as diseased valves or prosthetic valves. IV drug abusers are prone to staphyloccal infection of the tricuspid valve (i.e. right-sided), with fever and pneumonia from septic PE. What antibiotics would be appropriate for initial management? Benzylpenicillin and gentamicin IV. Hypertrophic Pyloric stenosis. Hypochloraemic, hypokalaemic alkalosis. Congenital pyloric stenosis is the most common cause of intestinal obstruction in infancy. It is more prevalent in males, usually a first-born aged 3-6 months. Vomiting is projectile and bile-free. Test feed may reveal a palpable tumour. USS may also be used in diagnosis. Vomiting leads to the characteristic metabolic picture as the metabolic alkalosis leads to K+ loss in the urine. The child should be kept NBM and an NG tube passed. If rehydration is necessary use Normal saline with dextrose. Refer for surgery Ramstedts pyloromyotomy. Pyloric stenosis in adults results from scarring, usually secondary to a chronic DU. It presents with vomiting, dehydration, weight loss and malnutrition. There may be an audible succession splash. HIV . RNA retrovirus. Binds to CD4 receptors on T-lymphocytes, monocytes and macrophages. These CD4 cells normally play a crucial role in co-ordinating the immune response. CD4 cell counts provide an indication of disease progression. Presentations to the ED: i) Respiratory: PCP pneumonia, pulmonary TB, Aspergillus, Cryptococcus. ii) Neurological: Cryptococcus meningitis, cerebral toxoplasmosis, cerebral lymphoma, CMV encephalitis. iii) Eye: CMV retinitis. iv) GI problems: Nausea, vomiting, weight loss are common and may be drug effects. Oesophageal candida or herpes simplex infection. CMV colitis and other causes of infectious diarrhoea e.g. cryptosporidium, Giardia, Salmonella. v) Mucocutaneous: Oral candidiasis, seborrheic dermatisis. Oral hairy leukoplakia, herpes infections, molluscum contagiosum, Kaposis sarcoma. Explain the mechanism for these deformities. Mallet: avulsion fracture at dorsal aspect of base of terminal phalanx or avulsion of terminal portion of extensor tendon. Boutonniere: rupture or laceration of central slip of extensor tendon, remaining lateral parts of extensor tendon slip along side of finger producing characteristic deformity. Swan neck: damage to volar plate of the PIP joint either by trauma or degeneration as in RA. Inability to extend thumb: Rupture of EPL may occur a few weeks after (usually undisplaced) fracture of the distal radius. Tendon ruptures are also associated with RA, OA, CRF and SLE. i) Ankylosing spondylitis. Usually presents as chronic low back pain in men aged 15-30. There is progressive spinal fusion and immobility. Other features include iritis, apical lung fibrosis and plantar fasciitis. There may be a normochromic anaemia and ! ESR. X-ray shows bamboo spine, obliterated SI joints. ii) Reiter s syndrome. Triad of urethritis, conjunctivitis and seronegative arthritis. May cause monoarthritis, typically of larger lower limb joint. Other features include psoriaform skin lesions (keratoderma blenorrhagicum), circinate balanitis and plantar fasciitis. May progress to give aortic incompetence, heart block, pericarditis. iii) Behcets syndrome. Polyarthritis ( erythema nodosum) with painful orogenital ulceration and iritis. iv) Feltys syndrome. A variant of RA characterised by RA, splenomegaly, leucopenia and recurrent infections. Splenectomy may improve the WCC. Necrotising fasciitis Group A haemolytic Strep. pyogenes, may also be Staph. aureus and anaerobes. Gas gangrene Clostridium perfringens (anaerobic Gram +ve bacillus, produces exotoxins). Treatment involves analgesia, resuscitation, IV antibiotics (penicillin with metronidazole), surgical debridement of affected tissues. Sometimes hyperbaric oxygen is used and gas gangrene antitoxin may be useful if Clostridium is suspected. Q A 45 year old woman with a long-standing history of RA presents with a 6-month history of worsening dyspnoea. She does not experience orthopnea. No raised JVP, heart sounds normal. ECG is normal. Blood gases on air show type 1 respiratory failure, no acidosis. What is the probable diagnosis? Pulmonary fibrosis 2 to RA. Other extra-articular features may include SC nodules, vasculitis, splenomegaly, neuropathy, anaemia, pleurisy, pericarditis and eye problems. What other physical signs would you look for? RA is a symmetrical polyarthritis typically affecting the hands and feet of young women. Remember cervical-spine involvement. X-rays show soft tissue swelling, peri-articular erosions and joint space narrowing, deformities She should undergo CXR, ? CT chest and spirometry. 5) A 65 year old woman presents c/o severe headaches for several weeks and of now having lost vision in one eye. The eye is not red or painful. Investigations show FBC normal, ESR 90. What is the probable diagnosis? Temporal arteritis. Beware in any patient >50yrs who presents with new headache or change in headache, weight loss, night sweats and jaw claudication. There is an association with polymyalgia. What features would be important in the physical examination? i) Tenderness over temporal artery or loss of pulsation. ii) fundoscopy papilloedema may occur late in the disease. iii) if the patient is in AF or has a carotid bruit then need to consider other causes of painless monocular visual loss, e.g. central retinal artery occlusion, stroke. What diagnostic test will confirm this diagnosis and what treatment is indicated in the ED? Temporal artery biopsy. Hydrocortisone 200mg IV. What may be the Side Effects of steroids in the elderly? Loss of diabetic control, peptic ulceration, hypertension, thinning of skin (bruise easily), osteoporosis. rness over temporal artery or loss of pulsation. Causes of a prolonged QT interval. i) Hereditary Lange-Nielsen (high-tone deafness) and Romano-Ward syndromes). Both carry risk of ventricular arrhythmias and are associated with torsades de pointes and sudden cardiac death. ii) Hypocalcaemia: clinical features include paraesthesiae, tetany, fits and psychiatric disturbance. Look for Trousseaus sign (carpal spasm when brachial artery occluded with BP cuff) and Chvosteks sign (twitching of facial muscles when tapping facial nerve) and papilloedema. iii) Drugs: anti-arrhythmics (quinidine, amiodarone, sotalol), antihistamines, antimalarials, organophosphates. iv) Hypomagnesaemia v) Hypokalaemia vi) Intrinsic heart disease (IHD, myocarditis). vii) SAH viii) Hypothermia Congenital long QT syndromes may be treated with long-term propranolol or an ICD. Other family members should be screened for disease. infectious diseases of childhood. Pertussis Bordetella pertussis. Notifiable disease. Incubation 5-14 days. Features ~ coryza wirth worsening cough, may persist for weeks. Risk of apnoeic episodes in infants. Treat with erythromycin. Measles Viral infection, droplet spread. Incubation 10-14 days. Features ~ fever, malaise, coryza, conjunctivitis, cough. Kopliks spots. Spreading maculopapular rash. Treatment is symptomatic unless complications ensue e.g. otitis media, bacterial pneumonia, encephalitis. Mortality low in UK. Mumps Viral infection, saliva and droplet spread. Incubation 14-18 days. Features ~ fever, pain and swelling of parotids, orchitis (10%). Aseptic meningitis may occur. Treament is with analgesia and possibly steroids for orchitis. Rubella Viral infection, airborne spread. Incubation 2-3 weeks. Usually a mild disease with rash, mild fever, occipital lymphadenopathy and arthralgia. Infection during pregnancy may cause severe congenital disorders. If any concern take blood for viral antibody levels. TORCH agents Toxoplasmosis may cause periventricular microglial nodules, thrombosis and necrosis; obstruction of cerebral foramina causes hydrocephalus; with prolonged survival, there is intracranial calcification, hepatocellular, adrenal, pulmonary, cardiac necrosis and extramedullary hematopoiesis Rubellamay cause LBW, hepatosplenomegaly, petechiae and purpura, congenital heart disease, cataracts, microophthalmia and microcephaly; CNS symptoms include lethargy, irritability, dystonia, bulging fontanelles and seizures.. Cytomegalovirus may cause hepatosplenomegaly, hyperbilirubinemia, neonatal thrombocytopenia, microcephaly and a mortality of 20-30%; later manifestations include mental retardation, deafness, psychomotor delays, dysodontogenesis, chorioretinitis, learning disabilities; 33 000 congenital cases/yearUS, of which 10% are symptomatic Herpes simplex may cause prematurity, and becomes symptomatic after the first week of life; CNS symptoms include irritability, seizures, chorioretinitis, hydrocephalus, flaccid or spastic paralysis, opisthotonos, decerebrate rigidity and coma; in neonatal HSV infection, no deaths occur in those with localized disease, 15% die if encephalitis is present and 57% die if HSV is disseminated, potentially evoking DIC NEJM 1991; 324:450 Syphilis an optional 'TORCH' Congenital syphilis has ! to epidemic rates in the urban US since the mid-1980s; the clinical findings are nonspecific and include fever, lethargy, failure to thrive, and irritability TORCH panel TORCH antibody panel Pediatrics A serologic screen for diagnosing prenatal infection; the finding of ! IgM in the neonate implies in utero infection by one of the TORCH agents toxoplasma, rubella, CMV, herpes simplex, which is then characterized by measuring specific IgM levels. A 25 year old man attends after returning from a diving holiday that day. He complains of mild headache, lower back pain and painful (non- tender) knees. Give 4 important points in the history. i) Time of onset of Sx related to the dive. ii) Dive profile (depth, duration, activity, speed of ascent, water temp. etc). iii) Previous medical history. iv) Did he fly back? (decompression illness may be precipitated if insufficient time is left between diving and flying). If suspected, discuss with Duty Diving Doctor. Treatment is recompression, pending this give high-flow O2, IV fluids and aspirin (to prevent sludging). Meningitis: What organisms are responsible and what is appropriate initial management? Meningitis may be bacterial, viral or rarely, fungal. Usual bacteria are Neisseria meningitidis or pneumococcus. Other bacteria (e.g. TB, Listeria) may cause meningitis in the elderly, the immunosuppressed and neonates. Initial management consists of A/B/C and: i) cefotaxime or ceftriaxone 80mg/kg. ii) look for signs of shock or raised ICP (decreasing or fluctuating level of consciousness, unequal or poorly reacting pupils, focal neurological signs, abnormal posturing or seizures). iii) if shocked give colloid bolus (20ml/kg 4.5% HAS) and repeat if necessary; observe closely, may require inotropes, intubation etc. on PICU. iv) if evidence of ! ICP, give mannitol (0.25g/kg bolus) followed by frusemide (1mg/kg) and steroids (dexamethasone 0.4mg/kg bd). Treat seizures as usual. Will require intubation and PICU. What risks are there to healthcare workers? Minimal; prophylaxis is unnecessary unless mouth-to-mouth resuscitation has occurred. Household contacts should be given rifampicin (warn about orange discoloration of urine and interaction with OCP). Remember to inform the Public Health Department. Hydrofluoric acid. HF acid rapidly crosses lipid membranes and penetrates tissues deeply where it releases the highly toxic fluoride ion. These ions may gain access to the circulation producing a variety of systemic problems, notably hypocalcaemia. What is the immediate management? i) Analgesia. ii) Copious lavage. iii) Calcium gluconate gel may be applied to the burn. iv) Check serum Ca2+, U&E and Mg2+. v) Record ECG and monitor. vi) Treat hypocalcaemia. Swallowed button battery What is the appropriate course of action? NPIS advice: i) Batteries lodged in the oesophagus require immediate retrieval by endoscopy. ii) Batteries in the stomach require review at 48 hours to ensure that they have passed through the pylorus; if not then they require endoscopic removal. ii) If the battery has passed through the pylorus and remains asymptomatic then stools should be monitored for up to one week and the patient reviewed if the battery has not passed. iv) If at any time the patient develops symptoms or signs of GI bleeding or obstruction then the battery should be retrieved. Human bite- treatment: i) Analgesia. ii) History regarding tetanus status. iii) X-ray. iv) Wound irrigation/ exploration. v) Augmentin. vi) Counsel regarding HIV and hep. B transmission: if thought to be high- risk then give prophylaxis. DVT: Wells score 1) active cancer (treatment ongoing or within 6 months of palliative) 1 2) paralysis, paresis or immobilisation of lower limb 1 3) recently bedridden >3 days or major surgery within 4 weeks 1 4) localised tenderness along the deep veins 1 5) entire leg swollen 1 6) calf swelling 3cm more than asymptomatic side 1 7) pitting oedema confined to affected leg 1 8) dilated superficial veins 1 9) alternative diagnosis as likely or greater than DVT -2 Wells categorized patients into; Low risk (score d"0) Moderate risk (score 1 or 2) High risk (score e"3) The use of the Wells score is as a  rule out test in combination with D-dimer testing; i.e. those patients who have a low risk and a -ve D-dimer do not require further investigation for DVT. Anyone with a moderate risk should undergo duplex USS. Amaurosis fugax Artery involved: left internal carotid. Other features of carotid TIA may be hemiparesis or dysphasia. Most TIAs result from thrombo-embolic disease involving either the heart or extra-cranial vessels. Differential diagnosis includes cerebral tumour, focal migraine, Todds paresis, hypoglycaemic episode and other causes of monocular visual loss e.g. retinal vessel occlusion, temporal arteritis, vitreous haemorrhage etc. Ask about risk factors e.g. hypertension, polycythaemia, anaemia, vascultits, sickle cell disease. Look for AF, heart murmurs (mitral stenosis, artificial valves), carotid bruit, evidence of AMI. Check BM, send bloods and get ECG and CXR. Acute uveitis. The pupil is irregular due to previous adhesions. Give 5 associated diseases. Ankylosing spondylitis, ulcerative colitis, sarcoid, AIDS, Behcets syndrome. Outline your management plan. Give analgesia. Check VA. Pain on accommodation as pupils react is called Talbots test. Fundoscopy, Slit lamp examination. Refer to ophthalmology for steroid eye drops. Antidiuretic Hormone (ADH) is produced in response to serious illness, pain, dehydration, in response to surgery (see Box B) ADH leads to reduced urine output, concentrated urine and retention of water and can result in hyponatraemia. Maintenance fluid requirements in illness are therefore LESS than maintenance fluid requirements in health. Maintenance fluids in illness should be restricted to 2/3rds (66%) of calculated requirements Child at risk of hyponatraemia Na+ <135mmol/L Peri or post-operative CNS infection Head injury Excess gastric or GI losses Bronchiolitis Severe sepsis Hypotension Intravascular volume depletion Gastroenteritis with dehydration Salt-wasting syndromes Estimate deficit in Dehydration: mL = %dehydration x weight (kg) x 10 Give 0.9% sodium chloride (+/- glucose +/- potassium) Replace over 24 hours (or 48 hours if Na+ <135mmol/L or >145mmol/L) Fluid volumes in dehydration Calculate deficit to be replaced over 24hours (or 48 hrs if hypo/hypernatraemia) Add to this maintenance fluid requirement in 24 hours (full / 100% maintenance) Add to this ongoing losses Losses should be replaced mL for mL with a solution roughly comparable to this loss e.g. NG loss with 0.9% sodium chloride with 10mmol KCl per 500mL. Fluid volumes without dehydration The majority of children requiring IV fluids are sick and will be fluid retaining under the influence of ADH (Box B). In this case, fluids should be restricted to 2/3rds (66%) of maintenance volumes. In a well child (eg. pre-op and NBM) full maintenance can be given. Fluid Type In those at risk of ADH secretion (Box B): Sodium chloride 0.9% (with glucose 5% in infants under 1 year and consider glucose requirement in older children) OR Compound sodium lactate (Hartmanns solution) with / without 1% glucose In other patients, or in response to U&E results: Sodium Chloride 0.45% with 2.5% or 5% glucose Potassium replacement Potassium requirements are approx 2mmol/kg/day. Once the plasma potassium is known, and child has passed urine, 500mL bags with 10mmol KCl pre-added should be used. If potassium is low, 20mmol/500mL is used. Higher concentrations may be used at the discretion of the consultant (consider cardiac monitoring/ central line insertion). Pharmacy stock sodium chloride 0.9% with 60mmol/litre, 80mmol/litre or 40mmol/500mL. Hypoglycaemia - Glucose <3mmol/L. Medical emergency - Give 5mL/kg of glucose 10%. Recheck level after 15 mins. Review maintenance fluids. Monitor. Symptomatic hyponatraemia in children: Check U&E (Ca and Mg) if symptoms of nausea, vomiting, headache, irritability, altered consciousness, seizures or apnoea. If Na <130mmol/L get senior advice immediately. If child is seizing, commence infusion of sodium chloride 3% solution. One mL/Kg of sodium chloride 3% will normally raise the serum sodium by 1mmol/L. Serum Na should be raised quickly until the child has regained consciousness and has stopped fitting or the serum Na is above 125mmol/L. The amount of Na required can be calculated according to the following formula: mmol of Na required = (130-present serum Na) x 0.6 x Weight (kg) sodium chloride 3% is made by withdrawing 5mL of sodium chloride 30% (available on NICU) and making it up to 50mL with water for injections.immediately prior to administration Asymptomatic hyponatraemia with normovolaemia Fluid restrict to 50% maintenance If dehydrated use sodium chloride 0.9% as rehydration fluids Hypernatraemic dehydration (Na>160mmol/L) Give sodium chloride 0.9% (or compound sodium lactate (Hartmanns solution)) and correct deficit slowly (over 48 hours) to reduce the risk of neurological injury associated with a rapid fall in plasma sodium. The correction rate should be by no more than 12mmol/24hr. Sodium chloride 0.45% can also be used. HONK. This usually occurs in elderly patients with NIDDM and can develop over days or weeks; glucose levels are often >30mmol/l. It often occurs with intercurrent illness, especially infection. Patients are usually severely dehydrated and there is impairment of consciousness. Diagnosis is made by: i) hyperglycaemia with osmolality >350mmol/l (normal 280-305) ii) no acidosis ii) <++ ketones on urinalysis There may be a coexistent lactic acidosis (which implies a poor prognosis). Suggest 4 essential investigations. ABG, blood glucose, septic screen, ECG ~ look for evidence of infection and AMI or myocardial ischaemia. Apart from ABC, what should the initial treatment be? Mainstays of treatment are fluid resuscitation and insulin. IV fluids: 1l in 1hr 1l in 2hrs 1l in 2 hrs then continue with 1l every 4hrs. if Na+ <160mmol/l use normal saline if Na+ >160mmol/l use normal saline K+ is usually normal; no K+ in first litre of fluid, subsequent replacement depends on K+ level. Insulin infusion commenced (50U Actrapid in 50ml N/saline start at 3U/hr) to maintain fall of about 3-6mmol/hr. Full anticoagulation with heparin. May need catheter and CVP line. NG tube if consciousness impaired. Treat underlying cause if found e.g. UTI. ICU/ HDU admission. Current guidelines for tetanus prophylaxis Standard active immunisation involves an initial course of 3 doses of tetanus toxoid at 2, 3 and 4 months of age followed by booster doses at 4yrs and 14yrs. A full course of 5 doses is considered to give lifelong immunity. Inadequate immunity against tetanus is likely in immigrants, the elderly, patients who are immune-suppressed and those who have refused vaccination. The following wounds are regarded as tetanus prone: i) heavy contamination (esp. soil or faeces) ii) devitalised tissue iii) infected or wounds >6hrs old iv) puncture wounds and animal bites For fully immunised patients, a dose of human anti-tetanus immunoglobulin (HATI, 250U IM) is only necessary for very high-risk wounds. For other patients, continue/ begin the standard schedule and give HATI for tetanus-prone wounds. Standard immunisation schedule: 2 months D, T, P, polio, Hib, meningitis C 3 months D, T, P, polio, Hib, meningitis C 4 months D, T, P, polio, Hib, meningitis C 12-15 months MMR 3-5yrs D, T, P, polio, MMR 10-14yrs BCG 13-18yrs D, T, polio WPW question. Impulses are conducted from the atria via the AV node and an accessory pathway (bundle of Kent). The accessory pathway conducts more quickly than the AV node so the PR interval is short. The region of ventricle activated by the accessory pathway slowly depolarises giving rise to a delta wave. Shortly afterwards the rest of the ventricular muscle is depolarised by the arrival of the impulse from the AV node. It is one of the commonest causes of tachyarrhythmias in children (may be accompanied by palpitations, dizziness, faints, chest pain) but can be asymptomatic. In infancy 80% are idiopathic but other causes include ASD and cardiomyopathy. It can present with AF associated with WPW ~ consult cardiology as this a potentially dangerous rhythm. Patients with WPW should not be given drugs that block the AV node (digoxin, calcium channel blockers) as this can result in acceleration of conduction through the accessory pathway leading to VF. Cure may be achieved by radiofrequency ablation. Adenosine acts by slowing conduction through the AV node. Maximum dose is 12mg. It has a very short half-life. CI include 2nd or 3rd degree heart block, sick sinus syndrome, AF and atrial flutter. Caution in patients with asthma as it may induce bronchoconstriction. Burn: What are the fluid requirements? 4ml X (burn surface area) X (body weight (kg)) 50% given in first 8 hours, 50% over next 16 hours. Object is to obtain urine output of 1ml/kg/hr. Children receive maintenance requirements in addition to above amount. Q) A 3 year old child presents after 4 days of D&V. He is afebrile with a dry mouth and a pulse rate of 150. What is his maintenance fluid requirement? Need to calculate percentage dehydration: Mild (<5%) Thirst Dry mouth Concentrated urine Moderate (5-10%) Sunken fontanelle/ sunken eyes !urinary output (<4 wet nappies/24hrs in a baby) Tachypnoea Tachycardia Severe (>10%) Hypotension (very late) Skin turgor Drowsiness/ irritability Maintenance requirements are: 100ml/kg/day for first 10kg 50ml/kg/day for next 10kg 20ml/kg/day for each subsequent kg So his maintenance requirements are: Estimated weight (age+4) X 2 = 14kg (10 X 100) + (4 X 50) = 1200ml Assume deficit of 10%: 10 X 10(%) X 14 = 1400ml So total daily requirement is 2,600ml. Use 0.45% saline/ 5% dextrose if not able to tolerate oral rehydration or is deteriorating. APGAR scores: APGAR scores are done at 1 and 5 minutes post delivery. 210Heart rate>100<100AbsentRespirationsGood, cryingSlow, irregularAbsentMuscle toneActive motionSome flexionLimpReflex irritability (catheter in nares)Cough or sneezegrimaceNo responseColourCompletely pinkPink body, blue limbsBlue or pale Remember if you need to cannulate the umbilical vein (fastest method of venous access in newborn) it is the single large dilated vessel adjacent to the 2 constricted arteries. Insert a 5F catheter 5cm into the vein and secure with a tie. . chickenpox pneumonia in a child ~ remember this is usually staphylococcal in children. Dendritic Ulcer of cornea: Give 3 features of management. i) Analgesia ii) Topical acyclovir 3% X5/d iii) Refer ophthalmology Pre-eclampsia: List 6 symptoms/signs of pre-eclampsia. i) Headache ii) Visual disturbance iii) Hyperreflexia iv) Abdominal pain v) Tremor vi) Reduced urine output List 4 risk factors for pre-eclampsia. i) Primiparity. ii) Maternal systemic disease DM, renal disease, hypertension. iii) Low socioeconomic status. iv) Maternal age <20 or >35 years. Give 3 immediate treatments. i) beta-blocker / Hydralazine 5mg IV over 20mins to max. 20mg. ii) Careful fluid balance; preload of 500ml colloid prior to hydralazine may reduce risk of hypotension and fetal distress. ii) Magnesium sulphate 4g IV over 5-10 minutes followed by maintenance of 1g/hr for 24hrs. What are the signs of magnesium toxicity? Loss of deep tendon reflexes and respiratory depression. What strategies can be used to facilitate suturing of the wound with minimal distress to the child? i) Distraction/ play techniques. ii) Suitable environment. iii) Reassurance by good interaction with carers/ parents. iv) Oral analgesia. Ramsay-Hunt syndrome. Facial nerve palsy caused by herpes zoster infection of the geniculate ganglion. There may also be loss of taste on the anterior part of the tongue, tinnitus, hearing loss and vertigo. Give analgesia and refer to ENT for IV acyclovir and eye care. Sickle cell crisis: Outline your initial treatment. i) Keep patient warm, rested and give O2. ii) Opioid analgesia is usually required for pain. ii) Careful rehydration with fluids crystalloid. iv) Empirical antibiotic therapy e.g. cefuroxime 750mg IV tds. v) Exchange transfusion may be required; aim for Hb between 7-9g/dl as any higher can increase blood viscosity and precipitate further sickling. List the most useful investigations i) FBC ii) Infection screen blood culture, CXR, MSU iii) U&E, ABG, ECG Patients with sickle cell trait usually have no disability except at times of severe hypoxia. Patients with sickle cell anaemia have chronic anaemia (8-10g/dl) and a small percentage have recurrent crises. Later in life, chronic ill-health supervenes with renal failure, bone necrosis, osteomyelitis (Salmonella), there is an increased susceptibility to infection, leg ulcers. Sickle cell crises can occur spontaneously or follow infection, cold, dehydration or any situation where tissue hypoxia exists. Acute medical and surgical emergencies may be mimicked. i) Acute painful crises are the most common presentation; severe pain at one or more sites associated with pyrexia, tenderness and local warmth and swelling. Haemolysis may be increased there is a fall in Hb and reticulocyte count is increased. There are no reliable markers to indicate severity. ii) Chest crisis is the most common cause of mortality. There is vaso- occlusion of the pulmonary microvasculature resulting in local infarction. May be precipitated by infection. iii) Cerebral infarction: usually children <5yrs, rare in adults. Presents as acute stroke. iv) Splenic/ hepatic sequestration: usually children <5yrs, RBCs become trapped in spleen and liver, causes severe anaemia and circulatory collapse. v) Aplastic crisis: usually in children and young adults, mainly caused by parvovirus infection. Reduced reticulocyte count. vi) Priapism: Local vaso-occlusion causes prolonged, painful erections. Urological emergency. Q. 25 year old man admits to regular use of crack cocaine. He has presented with SOB and pleuritic chest pain. Clinical examination is unremarkable. What is the diagnosis? Crack pneumonitis. Give 3 differential diagnoses. i) Atypical pneumonia. ii) Sarcoidosis. iii) Extrinsic allergic alveolitis. Respiratory complications of crack use can include pneumonitis, infections, pulmonary oedema, pulmonary fibrosis and ARDS. A 5 month old boy presents with fever, irritability and vomiting. His temperature at home was 38.0. He has vomited 5 times since yesterday. Past medical history is unremarkable. On examination he does not focus or interact well. Anterior fontanelle is full but he is crying. PEARL. Normal muscle tone. No other abnormalities. What is the differential diagnosis? Meningitis. Septicaemia. Encephalitis. Shaken baby syndrome. Cerebello-pontine angle lesions: Acoustic neuroma. other lesions that occur in this area. cholesteatoma meningioma neuromas of CN V, VII, X basilar artery aneurysm medulloblastoma What cranial nerves may be affected by such lesions? V-XI Vth nerve symptoms most common; depression of the corneal reflex occurs early. Facial pain, paraesthesiae and numbness may develop. Large tumours may compress cerebellum, pons and 4th ventricle. Retinopathy and malignant hypertension. Early signs of retinopathy correlate less well with mortality and morbidity than used to be thought, but signs of accelerated or "malignant" hypertension indicate severe illness. Symptoms Most patients with hypertensive retinopathy present without visual symptoms, however, some may report decreased  HYPERLINK "http://en.wikipedia.org/wiki/Visual_perception" \o "Visual perception" vision or  HYPERLINK "http://en.wikipedia.org/wiki/Headache" \o "Headache" headaches.  HYPERLINK "http://en.wikipedia.org/wiki/Sign_(medicine)" \o "Sign (medicine)" Signs of damage to the retina caused by hypertension include:  HYPERLINK "http://en.wikipedia.org/wiki/Arteriosclerosis" \o "Arteriosclerosis" Arteriosclerotic changes Arteriolar narrowing that is almost always bilateral Grade I - 3/4 normal caliber Grade II - 1/2 normal caliber Grade III - 1/3 normal caliber Grade IV - thread-like or invisible Arterio-venous crossing changes (aka " HYPERLINK "http://en.wikipedia.org/wiki/AV_nicking" \o "AV nicking" AV nicking") with venous constriction and banking Arteriolar color changes Copper wire arterioles are those  HYPERLINK "http://en.wikipedia.org/wiki/Arteriole" \o "Arteriole" arterioles in which the central light reflex occupies most of the width. Silver wire arterioles are those in which the central light reflex occupies all of the width of the arteriole. Vessel  HYPERLINK "http://en.wikipedia.org/wiki/Sclerosis" \o "Sclerosis" sclerosis  HYPERLINK "http://en.wikipedia.org/wiki/Ischemia" \o "Ischemia" Ischemic changes (e.g. " HYPERLINK "http://en.wikipedia.org/wiki/Cotton_wool_spots" \o "Cotton wool spots" cotton wool spots")  HYPERLINK "http://en.wikipedia.org/wiki/Hemorrhage" \o "Hemorrhage" Hemorrhages, often flame shaped.  HYPERLINK "http://en.wikipedia.org/wiki/Edema" \o "Edema" Edema Ring of  HYPERLINK "http://en.wikipedia.org/wiki/Exudate" \o "Exudate" exudates around the retina called a " HYPERLINK "http://en.wikipedia.org/wiki/Macula" \o "Macula" macular star"  HYPERLINK "http://en.wikipedia.org/wiki/Papilledema" \o "Papilledema" Papilledema, or  HYPERLINK "http://en.wikipedia.org/wiki/Optic_disc" \o "Optic disc" optic disc  HYPERLINK "http://en.wikipedia.org/wiki/Edema" \o "Edema" edema, in patients with  HYPERLINK "http://en.wikipedia.org/wiki/Malignant_hypertension" \o "Malignant hypertension" malignant hypertension  HYPERLINK "http://en.wikipedia.org/wiki/Visual_acuity" \o "Visual acuity" Visual acuity loss, typically due to macular involvement Exams and Tests  HYPERLINK "http://www.nlm.nih.gov/medlineplus/ency/article/003398.htm" Blood pressure  HYPERLINK "http://www.nlm.nih.gov/medlineplus/ency/article/003846.htm" Fluorescein angiography  HYPERLINK "http://www.nlm.nih.gov/medlineplus/ency/article/003881.htm" Ophthalmoscopic examination, which can show changes even if you have no symptoms Retinal changes mirror the systemic circulation and their severity correlates well with the development of systemic complications and survival Grade 1 consists of mild generalized retinal arteriolar narrowing; grade 2 consists of more severe generalized narrowing, focal areas of arteriolar narrowing, and AV nicking; grade 3 consists of grade 1 and 2 signs plus the presence of retinal hemorrhages, microaneurysms, hard exudates and cotton wool spots; and grade 4, sometimes referred to as accelerated (malignant) hypertensive retinopathy, consists of signs from the three previous grades with the addition of optic disc swelling and macular edema. One of the major limitations of this classification system is the difficulty in distinguishing early hypertensive retinopathy grades (e.g., grade 1 from grade 2); . Patients with mild hypertensive retinopathy signs will likely require routine care and blood pressure control should be based on established guidelines. Patients with moderate hypertensive retinopathy signs may benefit from further assessment of cardiovascular risk (e.g., cholesterol levels) and, if clinically indicated, appropriate risk-reduction therapy (e.g., cholesterol-lowering agents). Patients with severe hypertensive retinopathy will continue to need urgent, immediate, anti-hypertensive management Diabetic retinopathy is the most frequent cause of new cases of blindness amongst adults aged 20-74 years. Diabetic retinopathy is classified as: Background dot and blot haemorrhages, microaneurysms, exudates Maculopathy macular oedema Pre-proliferative ! cotton wool spots, dot and blot haemorrhages Proliferative new vessel formation Remember there may be evidence of laser therapy. Grade 1 (US) Haemorrhages & microaneurysms only Mild non-proliferative (mild pre-proliferative)  INCLUDEPICTURE "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/Dstd1l.JPG" \* MERGEFORMATINET  Grade 2 (US) Extensive Microaneurysm, intraretinal haemorrhage, and hard exudates. Moderate non-proliferative, moderate pre-proliferative  INCLUDEPICTURE "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/Dstd2Ar.JPG" \* MERGEFORMATINET  Grade 3 (US) Previously termed severe pre-proliferative. Venous abnormalities, large blot haemorrhages, cotton wool spots (small infarcts), venous beading, venous loop, venous reduplication,  INCLUDEPICTURE "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/Dstd2Br.JPG" \* MERGEFORMATINET  Grade 4a (US) Proliferative retinopathy. New vessel formation either at the disc (NVD) or elsewhere (NVE). Cl/f- Floaters, sudden visual loss  INCLUDEPICTURE "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/Dstd6Bl.JPG" \* MERGEFORMATINET  Grade 4b (US). Extensive fibrovascular proliferation, retinal detachment,  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd13.htm" \t "_blank" pre-retinal or vitreous haemorrhage, glaucoma, Traction. Subhyaloid haemorrhage Pre-retinal fibrosis+/- tractional retinal detachment  INCLUDEPICTURE "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/Dstd15l.JPG" \* MERGEFORMATINET   INCLUDEPICTURE "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/Dstd13l.JPG" \* MERGEFORMATINET  National Screening Committee The  HYPERLINK "http://www.nscretinopathy.org.uk/" \t "_blank" National Screening Committee (NSC) propose the following classification. Some centres use a more detailed classification, based onthe NSC system proposal. The condition is graded by examination of digital retinal photographs. Abreviations: DR = diabetic retinopathy NPDR = non-proliferative retinopathy NVE = new vessels elsewhere IRMAs = intraretinal microvascular abnormalities (part of severe pre-proliferative retinopathy, vessels will not leak with angiogram, otherwise they would be 'new vessels' making the condition 'proliferative') NSC International Term Symptoms Features  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds.htm" \t "_blank" (see)ActionR0 No DR None Normal retina. Grade 0 (US)annual rescreenRIMild non-proliferative (mild pre-proliferative) NoneHaemorrhages & microaneurysms only only  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd1.htm" \t "_blank" see photo Grade 1 (US)Inform diabetes teamR2 Moderate non-proliferative, moderate pre-proliferative None Previously termed mild pre-proliferative. Extensive Microaneurysm, intraretinal haemorrhage, and hard exudates.  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd2A.htm" \t "_blank" See photo   HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd8a.htm" \t "_blank" and photo Grade 2 (US) refer HESR2Severe non-proliferative severe pre-proliferativeNone Previously termed severe pre-proliferative. Venous abnormalities, large blot haemorrhages, cotton wool spots (small infarcts), venous beading, venous loop, venous reduplication,  HYPERLINK "http://medweb.bham.ac.uk/easdec/gradingretinopathy.htm" \l "irma" IRMA,  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd2b.htm" \t "_blank" See photo and  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd6a.htm" \t "_blank" photo. Grade 3 (US) urgent refer HESR3Proliferative retinopathyFloaters, sudden visual loss New vessel formation either at the disc (NVD) or elsewhere (NVE). Photos:  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd6b.htm" \t "_blank" flat new vessels,  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd5.htm" \t "_blank" raised,  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd7.htm" \t "_blank" florid Grade 4a (US) urgent refer HESR3 Pre-retinal fibrosis+/- tractional retinal detachment Floaters, central loss of vision Extensive fibrovascular proliferation, retinal detachment,  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd13.htm" \t "_blank" pre-retinal or vitreous haemorrhage, glaucoma. Grade 4b (US). Traction  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd15.htm" \t "_blank" photo and  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd12.htm" \t "_blank" photo. Subhyaloid haemorrhage  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd13.htm" \t "_blank" photourgent refer HESM 0no maculopathy annual rescreenM 1Diabetic maculopathy Blurred central vision The macula is defined as a circle centred on the fovea, with a radius of the distance to the disc margin. If the leakage involves or is near the fovea the condition is termed clinically significant macular oedema (CSME). Exudative maculopathy presents with leakage , retinal thickening, microaneurysms, hard exudates at the macula. Ischaemic form can have a featureless macular with NVE and poor vision. Photos:  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd3.htm" \t "_blank" moderate,  HYPERLINK "http://eyephoto.ophth.wisc.edu/ResearchAreas/Diabetes/DiabStds/DStd4.htm" \t "_blank" severe Milder forms: exudate < or = 1DD of centre of fovea circinate or group of exudates within macula any microaneurysm or haemorrhage < or = 1DD of centre of fovea only is associated with a best VA of < or = 6/12 retinal thickening < or = 1DD of centre of fovea (if stereos available) refer HESP Photocoagulation Reduced night vision, glare Small retinal scars through out the peripheral retina. Grade 4b (US)OL/ UG Other lesion / Un-gradableUn-gradable is usually due to cataract, other lesions usually referred for assessmentClinical Examination Examination can also be carried out using an ophthalmoscope. This should include use of the green filter (red free) as It shows haemorrhages and new vessels much more easily,  HYPERLINK "http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=15889546&query_hl=3" \t "_blank" see . The slit lamp is very useful clinically. Q. This patient has recently started lamotrigine.  What is this rash? Toxic epidermal necrolysis. This is an immunological disease most often caused by adverse drug reactions (antibiotics, NSAIDs, anticonvulsants). Non-drug causes include viral and bacterial infections, idiopathic and malignancy. Thought to be related to Stevens-Johnson syndrome. Needs to be distinguished from staphyloccocal scalded skin syndrome (skin biopsy). It is a potentially life-threatening emergency as the patient may develop dehydration, eye problems, renal involvement leading to ARF, systemic infections, shock and MOF. Management consists of treating cause, supportive care, prevent complication angioneurotic oedema (C1-esterase inhibitor deficiency). Autosomal dominant inheritance, usually presents in 2nd decade. May also be acquired as paraneoplastic syndrome. Clinical features; S/C oedema affecting face, limbs, buttocks, genitals (91%). laryngeal oedema (48% of attacks). abdominal symptoms. Precipitating factors include stress, infection, OCP, ACE inhibitors Management of severe attacks may require; chlorpheniramine 10mg IV hydrocortisone 200mg IV adrenaline 0.5ml of 1:1000 S/C FFP or C1-esterase inhibitor plasma concentrate Diagnosis made by low complement C4 levels. A-a gradient (Alveolar-arterial oxygen gradient). In the EM setting the A-a gradient is usually used to evaluate patients with a suspected pulmonary embolus. It is a fairly reliable measure of oxygen exchange. Unfortunately there appear to be lots of different formulae, using different units, calculating at sea level etc My formula, using kPa as units is: FiO2-(PaO2+(PaCO2/0.8)) Where 0.8 is the respiratory quotient. A normal A-a gradient is less than 2kPa when breathing air; it may reach 4kPa in the elderly. An increased A-a gradient identifies decreased oxygen in the arterial blood compared to the oxygen in the alveolus. This suggests a process that interferes with gas transfer, or in general terms, suggests ventilation-perfusion mismatch. A normal A-a gradient in the face of hypoxemia suggests the hypoxemia is due to hypoventilation and not due to underlying lung disorders. However neither measured PaO2 (18% normal) nor the A-a gradient (6% normal) are reliably sensitive in predicting PE. What in a chronic alcoholic predisposes them to fitting? (4 marks) Hypoglycaemia/Excess Alcohol or Alcohol Withdrawal Hyponatraemia Falls & ICH Poor compliance to anticonvulsants Hepatic Encephalopathy Overdose of TCAs Community acquired pneumonia in children PCR and other investigations suggest commonest organisms are- viruses, mycoplasma, pneumococci and pertusis. Types Lobar pneumonia- toxic and ill child with fever, classical signs of consolidation. Usually due to pneumococci, and associated with effusion. Atypical or patchy pneumonia more common than lobar pneumonia, usually caused by mycoplasma, also chlamydial, viral or legionella. Oral treatment- clarithromycin or amoxicillin i.v. treatment- Penicillin 25 mg/kg qds (or cefuroxime 20 mg/kg tds in resistant case) and oral clarithomycin 7.5 mg/kg bd If child remain unwell and pyrexial after 48 hrs- treatment failure due to antibiotics resistant underlying condition such as empyema, cystic fibrosis, ciliary dyskinesia, broncheictasis, trachea-oesphageal fistula, immune-deficiency poor compliance Pertusis can cause severe illness and even death during the first year of life. X-ray showing abscess may be secondary to staph aureus, klebsiella or TB. Hospital acquired pneumonias have different organisms, contact microbiologists. Children with special need (eg paraplegia, scoliosis, muscular dystrophy) have different pathophysiology- aspiration, reflux and poor lung function. Management is very difficult. Chest physiotherapy, suctioning and good general care is very important. Immunocompromised children (neutropenia, on chemotherapy, risk of HIV) risk of PCP, patient may have respiratory distress with few or no chest signs, chest x-rays may be non-specific . a firm diagnosis require broncho-alveolar lavage or sputum induction after saline nebulizer. Microbiologist should be contacted. Treatment- co-trimoxazole 120 mg/kg in two divided doses. Recurrent chest infection- think of asthma Palivizumab is a monoclonal antibody developed for the prevention of serious lower respiratory tract infections caused by RSV. Palivizumab immunisation will be offered to: All infants under 2 years of age with chronic lung disease of prematurity who are on home oxygen at the start of the RSV season (RSV season is from beginning of October until March). All preterm infants on the NICU with chronic lung disease (requiring continuous supplementary oxygen at 36 weeks corrected gestational age and likely to be discharged on supplementary home O2 during the RSV season. Children under 2 years of age with severe congenital immuno-deficiency e.g. Severe combined immunodeficiency, or Di George syndrome with T-cell abnormality. Infants with severe (haemodynamically significant) congenital cardiac disease who are aged 12 months or younger at the start of the RSV season. 5. Palivizumab immunisation may be considered on an individual basis for rare conditions such: Severe multiple congenital abnormalities Tracheomalacia Recurrent aspiration Neuromuscular disorders Diarrhoea: The following features may be indicative of diagnoses other than acute viral gastroenteritis; Abdominal pain with tenderness/guarding and/or bilious vomiting (?surgical) Pallor, jaundice, oligoanuria, bloody stool (?HUS) Systemically unwell, out of proportion to the level of dehydration (other infections, surgical, CAH etc) Shock Category ExamplesInfectionsEnteral: viral (commonest cause), bacterial, parasitic Non enteral infections (UTI, pneumonia, Otitis media)- vomiting predominates Surgical Appendicitis, Intussusception, Obstruction, Short bowel syndrome Systemic illnessEndocrinopathy (Diabetes, Hyperthyroidism, Congenital Adrenal Hyperplasia, Addisons disease, hypoparathyroidism), Immunodeficiency. Antibiotic associatedWhilst taking antibiotics and rarely Pseudo-membranous colitis MiscellaneousConstipation with overflow, Toxins, Haemolytic-uraemic syndrome (HUS), Toddler diarrhoea, Child Abuse (Munchausen by proxy, sexual) Dietary disturbanceFood allergy/ intolerance (Lactose, Cows milk protein), starvation stools. Malabsorption Cystic fibrosis, Coeliac disease, InflammationUlcerative colitis/ Crohns, Hirschsprungs enterocolitis Idiopathic/ PsychogenicIrritable bowel syndrome  Calculation of Oral Rehydration Solution (ORS) requirements in dehydration. Mild to Moderate (3% - 8%) dehydration.30 to 80mls per Kg in 4 hoursSevere dehydration (>9%) 100mls per Kg in 4 hoursPractical Points: Children who are dehydrated are thirsty and do not normally refuse ORS. Give fluid little and often. If the child is vomiting decrease volumes and increase frequency (every 5-10 minutes). Where carers are not willing/able to do this under supervision (or child is asleep) then rehydrate by NGT. Suitable ORS are Dioralyte, Diocalm Junior or Electrolade. Ongoing losses: These requirements should be supplemented if the child has frequent or substantial watery stools or vomits, by an additional 10ml/Kg per stool/vomit. Table 5: When to send a stool to the lab for microscopy, culture, sensitivity and virology. A history of blood +/- mucous in the stool Systemically unwell, severe or prolonged diarrhoea If the child is admitted to hospital A history suggestive of food poisoning (Notify public health) Recent travel abroad Management of feeding during gastroenteritis. Breast fed Continue breastfeeding throughout rehydration and maintenance phasesFormula fed Restart feed at full strength as soon as rehydration complete (ideally 4 hours)Weaned childrenChilds normal fluids and solids following rehydration. Avoid fatty foods or foods high in simple sugars. Guide to drug treatment. Antidiarrhoeals Infants and Children should not be treated with antidiarrhoeal agents.Antibiotics Patients with invasive Salmonella typhi, Shigella, amoebiasis and Giardiasis should be treated with antibiotics. Consider in infants<6months with other salmonellas, those who are systemically unwell and the immunocompromised. (Notify public health where necessary) Clostridium difficile associated diarrhoea Clostridium difficile diarrhoea is a common side effect of antibiotic use. Key steps in the prevention and management of C.difficile include: Prudent use of antibiotics Narrow spectrum preferably Short courses recommended Wherever possible, avoid use of high risk ( lactams (amoxicillin, co-amoxy-clav), clindamycin, cefalosporins and/or quinolones. Isolation of confirmed/suspected cases Ensure affected patients are nursed in single rooms, with Enteric precautions (see page 25) When dealing with clusters of cases, follow the guidance of the Infection Prevention & Control Team re: cohort nursing. Ensure Bristol stool chart is used to guide management. Patients should be isolated on suspicion of Clostridium difficile associated diarrhoea (CDAD), and not more than 2 hours after a result is confirmed. Hand Hygiene In all infective gastrointestinal cases, hand hygiene with hot soapy water is recommended. Specific treatment recommendations See section 3.2 p.9 Review cases daily, and escalate treatment if patient not responding as per above. The diarrhoea and colitis occur as consequences of toxins secreted by C.difficile. The clinical picture in C.difficile infection may vary from mild diarrhoea through to the fulminant life-threatening pseudomembranous colitis. Diagnosis of Clostridium difficile diarrhoea Microbiological Examination of C.difficile Toxin (CDT) The toxin biodegrades at room temperature (increasing the possibility of false negatives results), stool samples should therefore be placed in a refrigerator if there is to be any delay in transportation. If the first stool sample is negative for CDT, another sample should be sent for examination before the patient is considered to be CDT negative. Sigmoidoscopy (excludes haematology and neutropenic patients) Flexible sigmoidoscopy may detect pseudomembranous colitis in patients with a negative Clostridium difficile toxin test, and may need to be considered, in patients with moderate/severe diarrhoea (>4 x day) not responding to supportive measures and one stool sample negative for Clostridium difficile cytotoxin Management of Clostridium difficile associated diarrhoea General Measures Discontinue precipitating antibiotics if possible If not possible to stop antibiotics, alter the regimen to use antibiotics with a lower risk of exacerbating Clostridium difficile associated diarrhoea Discontinue antiperistaltic agents (opioids, anti-diarrhoeal agents etc.) Discontinue promotility/prokinetic agents (laxatives, stool bulking agents etc.) Review use of proton pump inhibitors and discontinue if possible No additional treatment is necessary if the stools have become formed or semi-formed and the patient is well. Antimicrobial Treatment Treatment of mild to moderately severe Clostridium difficile diarrhoea and colitis First line: Metronidazole 400mg tds po (500mg tds IV) for 10 days Second line: Vancomycin 125mg qds po for 10 days Vancomycin therapy should be used in patients: Who have failed to respond to 3-5days of oral metronidazole therapy Critically ill patients Severe pseudomembranous colitis Unable to tolerate metronidazole Pregnant Where the infecting organism proved to be metronidazole resistant Treatment of severe disease and/or pseudomembranous colitis Severe Clostridium difficile diarrhoea and colitis Critically ill WBC > 15 x 109 cells/L Temperature > 38.3C Albumin < 25g/L Impending ileus Colonic dilation Fulminant pseudomembranous colitis (endoscopic evidence) First line: Vancomycin 250-500mg qds po for 10 to 14 days Additional information Oral antibiotics are preferred as they act directly on the gut, (IV Vancomycin has no useful penetration into the gut). If a patient cannot swallow, the PR route (for metronidazole) or syrup via a PEG are equally effective. Clinical progress must be reviewed daily. If condition worsens, or there is no evidence of diarrhoea settling after 3 days, change from Metronidazole/low dose Vancomycin treatment to Vancomycin 250mg po qds for 10-14 days*. Consult duty Medical Microbiologist if any of the above and/or persistent failure to respond. Treatment of recurrences Initial recurrence: Treat with the same antibiotic that was effective for the treatment of the first Clostridium difficile positive stool, either Metronidazole 400mg tds po or Vancomycin 125mg qds po for 10 days (250-500mg qds po for 10 to 14 days for severe colitis) There may be a role for IV immunoglobulin (400 mg/kg, as a single infusion), under the guidance and advice of a Consultant Gastroenterologist. Surgical Treatment Patients with clinical features indicative of likely 027 type infection and/or evidence of pseudomembranous colitis will need urgent surgical referral. Colectomy must be considered, as it may be life saving, and advantages vs. disadvantages assessed based on a surgical opinion. Infection Control Aspects Prevention of spread Isolation/Cohort nursing: These spores are resistant to alcohol and acids in the stomach. They can also survive in patients and the surrounding environments for long periods of time. Isolate symptomatic patients at the onset of symptoms in a single room, preferably with en-suite toilet facilities. An Enteric Isolation poster should be clearly displayed, If a single room is not available, or if there are several infected patients, then it may be more appropriate to cohort affected patients together. Affected patients should be nursed in a bay area with doors, away from immunocompromised patients and not on the main route for ward and near to hand hygiene facilities. Duration of isolation. Isolation may be discontinued when the patient has been symptom free (formed stools) for at least 72 hrs as the main infection source is faeces. There is no requirement to submit further faeces samples for toxin detection, as toxin may be present in the gut for a time after the patient has become asymptomatic. When patients have been symptom free for 72 hours, they should be moved to a clean bed in a clean environment (single room or bedspace), taking with them only their personal belongings. Hand Hygiene: Visitors + Staff + patients hands Movement of patients: Discharges and ward transfers. Patients with explosive C. difficile diarrhoea should not be transferred to other wards in the hospital, except for purposes of isolation or cohort nursing. Visits to other departments should be kept to a minimum. These patients should be seen at the end of the session and should only be sent for when the department is ready to see them; they should not be left in a waiting area with other patients. Stool Chart Information leaflet Staff should wear disposable aprons, gloves and visors when dealing with faecal material. Meticulous infection control procedures should be employed when dealing with faecal material. All discharge summaries MUST clarify if the patient is now or has during this recent admission suffered from diarrhoea. Room cleaning (clinical clean) Following discharge/ transfer of the patient, the room and its contents should be cleaned thoroughly. Outbreaks of C.difficile Clostridium difficile outbreaks are expensive, disruptive to the delivery of healthcare services and often result in prolonged in-patient care. Wards and services are likely to be closed temporarily with consequent difficulties admitting urgent and waiting list patients. Prompt and vigorous control measures taken as soon as a problem of Clostridium difficile infection is recognised are the best way of ensuring the safety of patients and continued hospital activity. 5.1 Definition of an Outbreak C difficile figures for the Trust are reviewed daily and weekly by the Infection Control Team. A risk assessment is carried out when the number of C difficile cases on a ward exceeds the average base line, or when the cases of C. difficile are not obviously related to antimicrobial therapy. The Infection Control Team will normally consider: What is normal background level of Clostridium difficile in the clinical area? Is the diarrhoea attributable to any other cause i.e. medication or surgery? Is there any time/special relationship between the cases? If an outbreak situation is considered likely, the Infection Prevention and Control Team will advise further action and implement necessary Infection Control measures. A decision will be made by the Director of Infection Prevention & Control and the Team will contact the Health Protection Unit and the Primary Care Trust (Commissioning) regarding any closures. A Serious Untoward Incident (SUI) report will be sent to the Strategic Health Authority. This will be completed by the Saving Lives Lead, under the direction of the Risk Manager with support from the Infection Prevention and Control Team. Management of an Outbreak Patients should be cohort nursed and staff allocated for their care. Enteric precautions should be employed, as previously described. The ward may be closed to admissions and transfers. Clearance and Repeat specimens a) Symptoms resolve no further C difficile toxin test required. b) Symptoms persist despite treatment further Clostridium difficile testing only justified at least 4 weeks after the previous test. c) Symptoms resolve then recur repeat Clostridium difficile testing is justified to diagnose relapse of the condition. There is a risk of relapse of symptoms in 20 30% of patients. d) Initial negative test, but symptoms persist only in exceptional circumstances and with particular clinical suspicion (i.e. diagnosis of pseudomembranous colitis). Liaison with the Consultant Microbiologist is recommended by senior clinician. Ciprofloxacin and cephalosporins are currently considered to be high risk of precipitating Clostridium difficile infection Prescribing in Penicillin allergy: Patients with a history of anaphylaxis or urticaria occurring immediately after penicillin therapy are at increased risk of immediate hypersensitivity to penicillins and should not receive treatment with a beta- lactam antibiotic (this includes cephalosporins) or carbapenem, unless they have previously received a beta-lactam and had no adverse effects Patients with a history of rash occurring more than 72 hours after administration of penicillins are probably not allergic to penicillins, (SIGN, 2000) and many patients with a history of rash after penicillins will have received cephalosporins with no ill effect. For patients who do NOT report an anaphylactic or urticarial response to penicillin a cephalosporin or carbapenem (e.g. meropenem) may be administered with caution. Please note that penicillins include amoxicillin, co-amoxiclav (Augmentin), flucloxacillin, Tazocin. Patients who are prescribed ciprofloxacin, clindamycin or a cephalosporin should be counselled what to do if diarrhoea develops. Biliary tract infection(including cholangitis and cholecystitis) and Abdominal infection e.g. perforation, peritonitis ,diverticulitis (excludingCAPD peritonitis) (including if due to appendicitis) If gentamicin contraindicated and a cephalosporin tolerated Cefuroxime 1.5g tds IV + Metronidazole 500mg tds IV In truly penicillin allergic patients use Metronidazole 500mg tds IV + Gentamicin# 5mg/kg IV (single daily dose regimen) Max 480mg Amoxicillin 1g tds IV and Metronidazole 500mg tds IV and Gentamicin 5mg/kg IV (single daily dose regimen) Max 480mg If Gentamicin contraindicated use Co-amoxiclav 1.2g tds IV (or in serious sepsis Tazocin 4.5g tds IV) in place of above regimen. Review after 48 hours. Suitable oral regimens include co-amoxiclav 625 mg po tds OR Ciprofloxacin 500mg bd po (in truly penicillin allergic patients) plus Metronidazole po 400mg tds. Co-amoxiclav has good anaerobic activity, therefore the addition of metronidazole is not usually indicated. Meningitis Treatment If meningococcal disease suspected: Benzylpenicillin 1.8g 2-hourly IV or 2.4g 4-hourly IV for 12-24 hours followed by 2.4g 4-hourly IV for 7 to 10 days If causative organism unknown: Cefotaxime 2g tds IV for 7 days If causative organism unknown and/or Cephalosporins (penicillin allergy) are also contraindicated: Chloramphenicol 500mg qds IV (consult microbiology for advice) Meningitis Prophylaxis for H.influenza and N.meningitis (not normally required for Strep pneumoniae) Rifampicin 600mg bd po for 2 days or Ciprofloxacin 500mg po single dose (unlicensed indication) Meningitis associated with operative interventions or intracranial device will require consideration of other pathogens. Discuss with Consultant Medical Microbiologist. Severe cellulitis (gastrointestinal/biliary tract NOT entered, i.e non-surgical) Benzylpenicillin 1.2-2.4g qds IV and Flucloxacillin 1-2g qds IV for 5-10 days depending on progress, OR Once daily Ceftriaxone 2g IM if treated as outpatient In penicillin allergy: Clarithromycin 500mg bd IV for 5-10 days depending on progress, OR Teicoplanin IM if treated as outpatient Severe cellulitis (gastrointestinal / biliary tract entered i.e. post surgery) or necrotising fasciitis Tazocin 4.5g tds IV. Review after 48 hours and step down to oral therapy: Co-amoxiclav 625 mg tds po In Penicillin allergy, If carbapenems tolerated and if gentamicin contra-indicated (see below) use Meropenem 500mg-1g tds IV In truly penicillin allergic patients use Gentamicin 5mg/kg IV (single daily dose regimen) and Clarithromycin 500mg bd IV and Metronidazole 500mg tds IV Review after 48 hours and step down to oral therapy: Clarithromycin 500mg bd po and Metronidazole 400mg tds po Respiratory tract infection by MRSA Doxycycline (PO 200mg stat then 100mg od 1/52) OR 2nd LINE Clindamycin following medical microbiologist approval only (PO 300mg qds 1/52) + Rifampicin (PO 300mg qds 1/52) Osteomyelitis (Therapy 4-6 weeks) / Septic arthritis (Therapy usually 2-4 weeks) Staph aureus identified or, no other suggested sources Flucloxacillin 1 2 g qds IV and Sodium fusidate 500mg tds po, or Vancomycin* 1g bd IV and Sodium fusidate 500mg tds po, OR Vancomycin* 1g bd IV and Rifampicin 600mg bd po Neutropenia/Immunocompromised patients- Prophylaxis Prophylaxis for patients in whom prolonged (>7 days) neutropenia anticipated (e.g. acute leukaemia treatment) Ciprofloxacin 250mg bd po, and Fluconazole 100mg stat po and 50mg od po Monday, Wednesday and Friday If strong history of significant/recurrent cold sores or mouth ulcers add in: Aciclovir 200mg tds po Prophylaxis in patients received chemotherapy where only a short period of neutropenia is expected. Antimicrobial prophylaxis is NOT usually required, but in cases where it is indicated use: Ciprofloxacin 250mg bd po Pneumocystitis prophylaxis Co-trimoxazole 960mg od Treatment of pyrexia episodes in neutropenic patients (Refer to Trust Policy for the Care of Neutropenic/ Immunocompromised Patients) Temperature >39O C on one occasion OR Temperature > 38O C on 2 occasions OR Rigor OR Hypotension +37.5 OC OR Other signs of sepsis. Treatment: Tazocin 4.5g tds IV and Gentamicin# 5mg/kg IV (single daily dose regimen) Max 480mg If MRSA colonised or suspected consider: Vancomycin *1g od IV (or Teicoplanin 400mg bd IV for 3 doses then 400mg od thereafter) Line-associate septicaemia (peripheral and central cannulae, Hickman line) Vancomycin* 1g bd IV Peripheral cannulaassociated soft tissue infections without sepsis Flucloxacillin 500mg qds po for 7 days Helicobacter pylori eradication Lansoprazole 30mg bd po and Amoxicillin 1g bd po (in penicillin allergy, Metronidazole 400 mg bd and Clarithromycin 500mg bd po for 7 days Catheter associated bacteriuria Urine dipsticks are unreliable for catheter urine. Antibiotics are NOT required unless the patient is systemically unwell. Send CSU if patient systemically unwell. Treat according to culture and consider remove/change catheter. Moderately severe UTI Co-amoxiclav 1.2g tds IV for 5 days (3 days in women) unless MSU indicates otherwise or if infection not resolving.or Gentamicin# 5mg/kg IV (single daily dose regimen) Max 480mg in penicillin allergy Severe UTI and/or acute pyelonephritis (acute pyelonephritis will require 7-10 days treatment in total) Gentamicin# 5mg/kg IV (single daily dose regimen) Max 480mg. Review after 48 hours and step down to oral therapy as for mild uncomplicated UTI Tazocin 4.5g tds IV (if Gentamicin contraindicated) Review after 48 hours and step down to oral therapy as for mild uncomplicated UTI If Gentamicin contraindicated in penicillin allergic patients and carbapenems tolerated use Meropenem 500mg tds -1g tds IV. If neither gentamicin or meropenem appropriate consider Ciprofloxacin 500mg bd po Periorbital cellulitis Organisms other than staphs and streps, such as Haemophilus can cause this serious infection hence the need to consider Cephalosporins and for quinolones if benefit is felt to outweigh risk Benzylpenicillin 1.2-2.4g qds IV AND Flucloxacillin 1-2g qds IV OR Ceftriaxone 2g od and Metronidazole 500mg IV tds (400 mg po tds) if severe and spreading. Review after 48 hours and modify according to progress + organisms isolated In penicillin allergic patients- Vancomycin* 1g IV twice daily plus Ciprofloxacin 200mg bd IV and metronidazole 500mg tds IV if severe and spreading Review after 48 hours and modify according to progress + organisms isolated, and consider oral therapy: Clarithromycin 500mg bd po for 7 days then review Diabetes Related Foot Infection: criteria for admission Severe Borderline admission Cellulitis >2cm around the ulcer associated with; Lymphangitis Foot failing to respond to oral antibiotics alone Severe Admission Cellulits as well as features of systemic toxicity: Fever Hypotension, Leukocytosis Hypotension Fever Or Abscess formation Lymphangitis Wet gangrene Failure of antibiotics Alcohol withdrawal Signs and symptoms of alcohol withdrawal can appear any time between 6 and 72 hours after last alcohol use. Delirium tremens (DTs) occurs usually 2-5 days after alcohol cessation or decreased intake. DTs is fatal in 15-20% of inappropriately managed patients, It is characterised by: Increasing confusion and disorientation Severe tremor and autonomic disturbance Visual and auditory hallucinations Delusional beliefs Wernickes Encephalopathy (WE) may develop rapidly or in a couple of days. WE is initially reversible with parenteral Vitamin B. It carries a mortality rate of 15% and can result in permanent brain damage The classical triad of signs (acute confusion, ataxia and ophthalmoplegia) occurs in only 10% of patients. Therefore, the triad cannot be used as the basis of diagnosis. The presence of only one of the signs should be sufficient to assign a diagnosis and commence treatment. In general longer acting benzodiazepines (such as Chlordiazepoxide) are more effective in reducing seizures, and allow a smoother withdrawal with less rebound 0.5 mg lorazepam = 5 mg diazepam = 10-15 mg Chlordiazepoxide Acute Compartment Syndrome in adults The end result of unchecked ACS includes neurological deficit, muscle necrosis, ischaemic contracture, infection and delayed fracture healing. Irreversible damage can also lead to amputation, renal failure and even loss of life (Appendix 3). The diagnosis of ACS has been based on The detection of clinical signs and symptoms and routine monitoring of the extremities for neurovascular status EXTREME PAIN (on passive stretch/out of proportion to injury) Continuous compartment pressure monitoring. All patients who have sustained diaphyseal tibial fractures or who are deemed at risk of developing ACS, are to have compartment pressure monitoring via continuous compartment pressure monitoring. Causes: A Fracture or contusion Most common cause Soft tissue trauma Not to be excluded Constriction and external compression Unconscious patients following anaesthesia or alcohol/substance misuse leading to entrapment of the limb Entrapment of the limb under a heavy load Prolonged inflation of air splints Incorrect application of circumferential casts (POP, Scotchcast"!) Revascularisation Post-ischaemic swelling after circulation restored following vascular reconstruction - particularly if restoration of the circulation is delayed > 6hours Surgical procedures with elevation of the lower limbs e.g. Lloyd Davies/Lithotomy position for > 4 hours Thermal Injuries Circumferential burns Electrical burns (raised interstitial pressure resulting from associated oedema) Intravenous extravasation Occlusion or spasm of a major vessel with an inadequate collateral circulation can also cause swelling of the contents to a muscle group Patients taking anticoagulants or with bleeding disorders are at greater risk Signs and Symptoms The 6 Ps Pain Out of proportion to the injury Unrelieved by narcotics Excessive use of analgesic devices (PCA) Increases with elevation of the extremity May not be present if central/peripheral sensory deficits are present Parasthesia Subtle first symptom Best elicited by direct stimulation Patient complains of tingling or burning sensation Can lead to hypoesthesia (numbness) Pressure Involved compartment or limb will feel tense and warm on palpation Skin will be tight and shiny Skin occasionally appears cellulitic Pallor Prolonged capillary refill - > 3 seconds Cool feel to skin due to lack of capillary reperfusion Paralysis Pulselessness ACS - Important Points to Remember Parasthesia/hyperparasthesia (Sensory changes in the nerve) Develop within 30 minutes of the onset of ischemia Irreversible functional changes Start in the muscle after 4 hours Irreversible nerve damage Begins after 12/24 hours of total ischaemia Fracture blisters Represent areas of necrosis of the epidermis and separation of the skin layers Often occur in areas of swollen skin over a fracture site. When the intracompartmental pressure is too high to be relieved by normal physiological means, blisters occur as the body attempts to relieve the pressure Associated swelling must be noted as a sign of significant interstitial pressure Elevation Too high - can contribute to the risk Should not be above the level of the heart Renal Failure All patients are at risk of renal failure Monitor renal function and urine output regularly Patient Information Sheet Enables patient to recognise early symptoms Enables patient to alert nursing staff of any symptoms Recordings: The diastolic blood pressure and the compartment pressures are recorded HOURLY on the compartment pressure monitoring form. Differential Pressure ((P). should be above 30mmHg to be considered within normal range. If the (P falls below 30mmHg for two consecutive readings, the SHO/SPR should be informed. A falling trend signifies the onset of ACS and early return to theatre for Fasciotomy is desirable. The monitor remains in situ for 48 hours post fixation/pre POP if non-operative treatment. Adult Patients requiring Anticoagulation with Warfarin VTE (DVT and/or PE) - based on BCSH recommendations (2005 update of guidelines on oral anticoagulation (3rd edition)IndicationTarget INRMinimum duration Calf irrespective of risk factor2.56/52 proximal DVT or PE temporary risk factor2.53/12 proximal DVT or PE - idiopathic or permanent risk factor2.5at least 6/12VTE associated with Antiphospholipid syndrome2.5while disease active ? lifelongRecurrence of VTE while on Warfarin in therapeutic range3.5lifelongRecurrence of VTE after cessation of warfarin2.5review for permanent risk factors ? lifelongCancer with VTE2.5 consideration for therapeutic LMWH as an alternativewhile cancer activeCardiac Indications for valve replacementsIndicationTarget INRMinimum duration Atrial Fibrillation 2.5Lifelong unless for cardioversionCardioversion2.5Should be in therapeutic range (2-3) for at least 4 wks before and 4 weeks after cardioversionMural thrombus2.53/12Mechanical Mitral valve3.0lifelongMechanical Aortic valve2.5lifelongBioprosthetic (tissue) valveNone unless specifiedNone unless specifiedOtherIndicationTarget INRMinimum duration Arterial thrombosis associated with anti-phospholipid syndrome2.5 3.5while disease active ? lifelongPeripheral arterial thrombosis and graftsantiplatelet drugs first line if given 2.5long termParoxysmal Nocturnal Haemoglobinuria If clones >50% blood mononuclear cells and platelets >100 x109/L target 2.5. Consider for smaller clones and lower platelet counts if other risk factors and risks of thrombosis > bleeding.long term Patient overanticoagulated INR too high but <8, NOT bleeding (if major bleeding intracranial, intraocular, compartment syndrome, haemorrhage with hypovolaemic shock, pericardial INRomit Warfarin daysRepeat INRSuggested % dose reduction once Warfarin restarted*3.1-3.50at 2 days unless clinically indicated e.g. active bleeding or medically unstable153.6-4.00at 2 days unless clinically indicated e.g. active bleeding or medically unstable204.1-5.01 day at 2 days unless clinically indicated e.g. active bleeding or medically unstable255.1-6.0at least 1daily restart Warfarin once INR <5256.1-7.9at least 2daily restart Warfarin once INR <533 INR >8 or major bleeding INRActionINR >8.0, no bleeding or minor bleeding stop Warfarin give 2mg of phytomenadione orally (use iv Konakion MM preparation orally) recheck INR daily try to identify precipitating cause - is it temporary e.g. drug or permanent e.g. liver failure? if INR still >8 at 24 hours consider repeating dose of phytomenadione when INR <5, review need for anticoagulation restart Warfarin if appropriate at reduced dose - 50% of previous doseMajor bleeding - defined as haemorrhage with hypovolaemic shock or bleeding into a confined space - intracranial intraocular compartment syndrome pericardial irrespective of INR Contact consultant haematologist (tel 6744 9-5, Mon to Fri; via switchboard otherwise) Contact consultant cardiologist if patient has a mechanical prosthetic heart valve stop Warfarin urgent clinical assessment urgent clotting screen give 5mg phytomenadione iv give Beriplex 30IU/kg by slow iv injection max rate 210 IU/min generally over 10 mins (obtained from Blood bank) check clotting screen 1 hr after administration inadequate correction consider other causes e.g. DIC; discuss with consultant haematologist consider second dose of Beriplex 20 IU/Kg recheck INR within 24 hours and daily thereafter a source of bleeding should be looked for both Beriplex and phytomenadione may need to be repeated if bleeding continues/INR rises/complete reversal of Warfarin is required when INR <5, review need for anticoagulation restart Warfarin if appropriate at reduced dose - 50% of previous dose Notes patients with mechanical prosthetic heart valves should be discussed with a consultant cardiologist some patients who require interruption of anticoagulation may require insertion of temporary filter (see Trust guideline on VC filters) e.g. with very recent PE who require emergency surgery all patients should have their indications for anticoagulation reviewed prior to restarting warfarin and the risks of thrombosis versus further bleeding assessed incident forms should be completed for patients who develop INRs > 8 while hospital in-patients or who are admitted to hospital as a result of overanticoagulation Beriplex must be discussed with consultant haematologist before use is NOT a substitute for FFP in situations of massive haemorrhage where all coagulation factors may be reduced is a Prothrombin complex concentrate (PCC) derived from human plasma which has been virally inactivated contains coagulation factors II, VII, IX and X but no other coagulation factors is kept in Blood Bank as a freeze-dried powder which is reconstituted with a small volume of water just prior to use is given by slow iv injection maximum rate 210 IU/min generally over 10 mins it is NOT useful in patients whose INRs are prolonged for reasons other than warfarin/ coumarin treatment e.g. liver disease doses given are based on the dose of administered factor IX vial contains 500IU factor IX Indications patients to be considered: recent abrupt intracranial haemorrhage, preferably demonstrated on CT scan; patient expected to survive 24hr haemorrhage with hypovolaemic shock (remember all coagulation factors may eventually decline and FFP may be required) intraocular bleeding muscle bleed with compartment syndrome patients requiring emergency surgery who are anticoagulated with warfarin Contraindication relatively contraindicated in patients with venous thromboembolism within last month as Beriplex is thrombogenic. You may need to consider placement of inferior venal caval filter in these patients (see Trust guideline CA2101 Insertion of Vena Cava Filters) contraindicated in patients known to be allergic to Beriplex Possible side effects may cause thrombosis allergic reactions plasma derived product so risk of infection must be borne in mind Surgical patients on Warfarin emergency surgery requiring reversal within 1hr give Prothrombin Complex Concentrate Beriplex 30IU/kg (see Beriplex section E) check INR pre operatively emergency surgery requiring reversal in 4 to 48 hr give phytomenadione 5 mg by slow iv injection; check INR d" 6 hours pre operatively On discharge all patients should have counselling regarding the risks and benefits of anticoagulation with Warfarin the DoH yellow anticoagulant therapy record with patient details completed and the contents explained to patient arrangements must be made for subsequent monitoring of the INR Control of Chemotherapy and Radiotherapy Induced Nausea and Vomiting in Adults Ondansetron 8mg po bd 3/7 Dexamethasone 4mg po bd 3/7 Domperidone 10-20mg po qds prn Extra pyramidal reactions - may occur (rarely) with metoclopramide, levomepromazine and prochlorperazine; consider stopping causing drug or switching metoclopramide to domperidone (which causes fewer side effects). Treatment - Procyclidine 5 mg iv (usually effective within 5 mins) Long Lines Long lines are small gauge silastic or polyurethane catheters, which are inserted into a peripheral vein and advanced to a central position, ideally in the inferior or superior vena cava, lying outside the heart. Indications ۃ Administration of parenteral nutrition. ۃ Long term administration of intravenous medication. ۃ Administration of inotropes. ۃ Administration of hyperosmolar fluids or irritant drugs ۃ Limited intravenous access Notes In cases of recent sepsis wait at least 24 hours after removal of previously infected lines if possible. Consider the infants comfort during the procedure - analgesia, anaesthetic creams or comfort measures The catheter tip position must be verified with an x-ray (plus contrast if PACS does not confirm position tip) The ideal position is the superior vena cava atrial junction or in the inferior vena cava at the level of the diaphragm1 Looped catheters must be withdrawn as there is a risk of migration In any infant who collapses with a long line in situ, it is critical to urgently exclude cardiac tamponade as a cause of the collapse. Insertion sites1 Antecubital veins- basilic and cephalic veins Saphenous veins Scalp veins - temporal and posterior auricular veins Occasionally: Axillary vein External jugular vein Femoral vein Complications Malposition from outset This is identified by the x-ray taken after insertion. Infection Catheter migration ۃ The catheter may have looped during dwell time or on insertion. ۃ May migrate to the cardiac chambers, internal jugular vein, subclavian vein, ascending lumbar vein. ۃ Can cause pericardial effusion, pleural effusion, cardiac arrhythmias , tamponade, or cardiac perforation and tissue extravasation Consider pericardial effusion/cardiac tamponade in any neonate who collapses with a long line/central venous catheter Catheter Dysfunction ۃ Indicated by a rise in the pressures or inability to infuse fluid ۃ Due to malposition, fibrin clot, precipitate from infusate with high mineral content, drugs or lipid deposits. ۃ Flexion of an extremity may also lead to temporary occlusion14 Catheter Breakage Tethered Catheter Difficulty in removing the catheter due to the formation of a fibrin clot especially when multiple attempts are made at insertion Other Complications: ۃ Thrombosis (renal, intracardiac, deep vein) ۃ Pulmonary embolism ۃ Air embolism Damage to other vessels: ۃ Pneumothorax ۃ Puncture of the subclavian artery ۃ Pneumomediastinum CHICKENPOX AND PREGNANCY It may cause maternal mortality or serious morbidity. It may also cause fetal varicella syndrome. The incubation period is 10-21 days and the disease is infectious 48 hours before the rash appears and until the last vesicles have crusted over. Immunity is checked by sero-positivity for VZV immunoglobulin G (Ig G) antibody Complications: Pneumonia, Hepatitis and encephalitis MANAGEMENT OF SUSPECTED VARICELLA CONTACT IN PREGNANCY Three aspects of exposure should be ascertained:- The type of VZV infection in the index case the risk of acquiring infection from an immune-competent person with non-exposed chickenpox or zoster lesions (ie. all lesions covered by clothing), is remote. Exposure to uncovered chickenpox lesions, disseminated zoster or localised zoster on any part of the body of an immunocompromised patient is a significant risk to a pregnant woman or neonate. Timing of exposure in relation to onset of the rash in the index case In chickenpox or disseminated zoster the risk is significant between 48 hours prior to rash onset until crusting of the lesions. In localised zoster, the index case is infective from the day of onset until crusting of the lesions. Closeness and duration of contact - face-to-face contact during a conversation and contact within the same room for more than 15 minutes would constitute a significant exposure (risk of infection is remote if lesions covered). If there is a definite history of chickenpox in the pregnant woman, it is reasonable to assume immunity. If there is any doubt about the immune status, serum should be tested for VZV IgG. Contact Microbiology department, NNUH (telephone number 01603 611816 or N.N.U.H. extension 4588) who may be able to use the serum stored from the booking antenatal bloods. At least 80-90% of women tested will have VZV IgG and can be reassured. If a pregnant woman is susceptible to VZV and she has had a significant exposure to chickenpox, she should receive VZIG regardless of the stage of pregnancy (available from Microbiology Department) within 10 days of contact. VZIG may not prevent but may attenuate the infection if given up to 10 days after exposure. There is no benefit in administering VZIG >10 days after contact but prophylactic aciclovir may be considered, after discussion with a consultant. MANAGEMENT OF THE PREGNANT WOMAN WHO DEVELOPS CHICKENPOX General They should avoid contact with other pregnant women and neonates until at least five days after the onset of the rash or until all the lesions have crusted over. Oral aciclovir, given within 24 hours of onset, reduces the duration of fever and symptomatology of varicella infection but is not licensed for use in pregnancy. The UK Advisory Group on Chickenpox recommends that oral aciclovir should be considered, after discussion with a consultant, for women with chickenpox if they present within 24 hours of developing the rash. The dose is 800mg five times a day for 7 days. Indications for referral to hospital include: development of chest symptoms neurological symptoms haemorrhagic rash or bleeding a dense rash with or without mucosal lesions Delivery during the viraemic period may be very hazardous. The maternal risks include bleeding, thrombocytopenia, D.I.C. and hepatitis. There is also a high risk of varicella of the newborn with significant morbidity and mortality. Admission under a physician may be more appropriate with close liason with the obstetric team. RISK TO NEONATE IF A SIBLING HAS CHICKENPOX If there is contact with chickenpox in the first 7 days of life and the mother is immune, the risk to a neonate born at term is minimal because it is protected by passively acquired maternal antibodies. No intervention is required. However, in the following circumstances the infant should receive VZIG: if the mother is not immune to VZV if the neonate delivered before 28 weeks, regardless of maternal history. Sero-testing of the premature infant should be attempted if there is a maternal history of VZV. If the infant weighs less than 1kg If the infant is known or suspected to be immuno-compromised by disease or treatment eg. steroid therapy . Major differential diagnoses of the child with a limp and typical features ConditionTypical featuresSeptic arthritis (hip or other joint)Any age. Most common <2yrs. Very painful (pseudo-paralysis). Often non-weight bearing. Fever and unwellOsteomyelitisAs septic arthritis but often more indolent presentation. Partial treatment with antibiotics commonIrritable hip syndrome4-10 years. Post viral. Pain and limpFracture non-accidental injury or unrecognised traumaTake history carefully. Be alert to late presentations, inconsistencies. Special consideration to fractured fibulaInflammatory arthritis (reactive, JIA, lyme disease, HSP)Definite joint swelling (not detectable in hip but seen in other joints). Decreased ROM but not as painful as septic arthritis. Longer history. Morning stiffness / pain after period of restLate presentation of Developmental DysplasiaDelayed walking, always walked with limp. Asymmetrical skin creases, shortened leg, limitation of abduction in flexion.Perthes disease4-10 years, boys>girls. Limp, groin, thigh or knee pain. Internal rotation of hip often reduced first.Slipped upper femoral epiphysis8-15yrs boys>girls. Longer history limp, sudden minor trauma often worsens pain and leads to presentation, knee painNeoplasia (leukaemia, osteosarcoma etc.)Night pain. General malaise. Weight loss, hepato-spleno megally / pallor/ bruising HSP- Henoch Schnlein purpura, JIA Juvenile idiopathic arthritis, ROM range of movement Assessment Initial assessment and documentation: Pain - assess on pain scales according to age. Give appropriate analgesia Temp, pulse, resps. Weight (height if able) Medical assessment: B. Key points of history A history of preceding viral symptoms is often found in irritable hip. Preceding streptococcal sore throat / diarrhoeal illness in reactive arthritis Fever height, duration, frequency Recent antibiotic use may mask or partially treat a septic arthritis / osteomyelitis Is the child generally well or unwell? Is s/he eating and drinking normally C. Examination key points Is the child generally well or ill? Gait and are they able to weight bear? Observe, palpate and move all bones and joints (erythema, swelling, restriction, pain) Severity of pain? Temperature? In Septic arthritis or osteomyelitis please try to obtain synovial fluid or tissue biopsy before commencing antibiotics to ensure organism and sensitivities known. All children < 2 years This age group are difficult to assess. Sudden onset of non- weight bearing or limp is highly unlikely to be irritable hip and may include all the above differential diagnoses (except Perthes or SUFE). Careful and full examination is imperative if clues concerning non-accidental injury, osteomyelitis and septic arthritis at any site or inflammatory arthritis are to be detected. Fully expose, palpate and move all bones / joints. Ensure full general examination is done including ENT and urine dip if febrile. Consider haemarthroses in child with excessive bruising. Developmental dysplasia of hip may present late with limp in first walking toddler. X-Ray affected bones / joints (or whole of lower limb if very difficult to localise problem). If a fracture is present consider mechanism and any child protection issues. Refer to orthopaedics for fracture management. If no fracture, consider differential diagnosis and request blood tests accordingly (FBC, ESR, CRP, Blood culture as a minimum). Request ASOtitre, anti-DNAse B and viral serology if reactive arthritis likely. ANA, autoantibody screen, immunoglobulins and rheumatoid factor are indicated if arthritis is likely but are not required urgently, or at first presentation. Children 2-9 years This is the commonest age group for irritable hip. The key is not to miss children with a septic hip joint since severe destruction of the joint can occur within 24 hours if not treated. If any doubt, investigate with blood tests and consider USS and aspiration / observation / admission / orthopaedic opinion. If Perthes is seen on X-ray refer to Mr Tucker. All children > 9 years Request AP and frog leg lateral hip X-ray to look for SUFE or Perthes Child with non-blanching rash No single clinical feature is discriminating. High risk clinical features: Listlessness and lethargy Irritability Shock, prolonged capillary refill time &/or hypotension Purpura (non-blanching leasion) >2mm diameter Neck rigidity Distribution of the rash: In the absence of high risk clinical features, the distribution of the rash is helpful. If the lesions are largely confined to limbs (particularly lower limbs and buttocks), urticarial at onset and progression to purpura then a diagnosis of HSP should be considered. If the lesions are petechial and restricted to the distribution of the SVC, sepsis is extremely unlikely. If no high risk features are present, patient can be discharged. Parents ahould be given information on the symptoms and signs of sepsis and instructed to return if such features develop. Investigations: FBC CRP Clotting studies Blood culture If the results (WBC, neutrophil, CRP, and INR) are within normal limits, the patient may be discharged. Patients with abnormal values for any of these should be managed as meningococcal disease. Diabetic Keto-acidosis: DIAGNOSIS CharacteristicDKAHHS / HONKKnown to have diabetes?Usually yesNot as oftenDuration of symptomsHours or daysOften daysBlood glucose (mmol/L)>14>33Ketones in urine or blood?YesUsually nopH<7.3Usually normalBicarbonate (mmol/L)<15Usually normal 1. DKA usually presents in someone who is known to have type 1 diabetes. HONK may be the first presentation of type 2 diabetes 2. Vomiting is common in DKA, but abdominal pain is sometime present always perform a blood glucose on someone presenting with abdominal pain or unexplained vomiting. Operating on a patient with untreated DKA is almost always fatal. Call HDU / ITU if the patient is seriously ill pH<7.2, Base Excess >-12, GCS d" 9 oliguria, renal cardiac failure or other significant co-morbidity) If GCS d" 8 then patient should be intubated and ventilated FIRST STEPS  1. Airway - 35% oxygen via mask. If GCS d" 8 then patient should be intubated and ventilated. 2. Establish 14 or 16 gauge peripheral intravenous access. If this is not possible due to the clinical state of the patient, central venous access may be necessary. Call HDU. A CVP LINE IS ADVISABLE IF THE PATIENT HAS A HISTORY OF CARDIAC FAILURE OR RENAL IMPAIRMENT (CREATININE >150 mol/L), OR IS NOT CLINICALLY IMPROVING AFTER INITIAL FLUID RESUSITATION 3. Measure arterial blood gases on admission 4. Obtain venous blood for U&E s, LFT s, glucose, FBC, osmolality, blood ketones, and blood cultures 5. Give 1 litre of 0.9% Sodium Chloride stat 6. Give 10 IU of human Actrapid insulin intravenously (or IM if there is a delay in setting up the IV infusion) then set up an insulin infusion 7. Start intravenous Actrapid insulin at a constant rate of 6 IU/hr. SECOND STEPS 1. Naso-gastric tube if conscious level is depressed or the patient is vomiting. If no gag reflex refer to HDU 2. Insert a urinary catheter if conscious level is depressed or the patient is oliguric 3. Subcutaneous Low Molecular Weight heparin. This should be therapeutic dose in HONK, and prophylactic dose in DKA 4. ECG and continuous cardiac monitoring is essential in all patients where there is a potential for significant electrolyte swings, and where a cardiac precipitant is possible. 5. Look for a precipitant e.g. MI, CVA, chest or urinary infection, the acute abdomen 6. Chest X-Ray 7. Intravenous broad spectrum antibiotics if the patient is pyrexial and / or severely ill Fluids: Normal saline or Hartmanns if Sodium<155 mmol/l. If the sodium level is >155 mmol/l they should be considered for HDU - 1st Litre stat, 2nd Litre over 60 minutes, 3rd Litre over 2 hours Potassium: Aim for levels between 4 and 5 mmol/Lby adjusting the KCL concentration in each bag of fluid. Initially use normal saline with 20 mmol/L KCL. However: If K+ < 4.0 mmol/L, then use 40 mmol/L in each litre of 0.9% sodium chloride or glucose If K+ >5.0 mmol/L, use 0.9% sodium chloride only or glucose only, without K+ Bicarbonate Highly controversial. It should be considered if the pH is < 7.0, remembering that it can cause a precipitous drop in the potassium level. If bicarbonate is being considered, the patient MUST be on HDU / ITU for monitoring. Lesser degrees of acidosis can be adequately treated with fluids and insulin alone. PROBLEMS 1. If conscious level deteriorates with treatment, consider cerebral oedema or an intracranial event. Acute cerebral oedema is rare in people over 20 years old, and is associated with the use of artificial ventilation and bicarbonate infusion. Refer to ITU / HDU. 2. As mentioned above, DKA can cause abdominal pain. However, if the patient has a bicarbonate level of > 15 mmol/L and still has abdominal pain, ask for a surgical opinion. 3. DKA is associated with leukocytosis (without sepsis), increased creatinine levels (ketones interfere with the assay) and increased amylase (of salivary origin NOT pancreatitis) 4. Remember: overdoses of aspirin, alcohol or ethylene glycol can mimic DKA and should be born in mind if the presentation is atypical. Diabetic Keto-acidosis in children DKA is characterised by: Unwell child with clinical features of dehydration Hyperglycaemia (Glucose >11.0mmol/l) Elevated blood ketones (>3.0mmol/l on ward test) or Heavy ketonuria (3+ or 4+) Acidosis (pH <7.35, HCO3 <15mmol/l) Why important Diabetic Ketoacidosis is an emergency. Scrupulous attention to fluid and insulin management is essential Cerebral oedema is the principal cause of death and disability. Other causes include aspiration and cardiac arrhythmias. Children requiring large volumes of fluid resuscitation (greater than 40ml/kg) usually require transfer to a paediatric intensive care unit. These measures have been shown to improve outcome. Immediate Management steps It is essential to monitor Airways, Breathing & Circulation, and to frequently reassess the child. Initial assessment and diagnosis Shock management Fluid & Insulin administration Monitoring Recommendations for transfer to a Paediatric Intensive Care Unit. Children with Decompensated Shock, or who are very young (<3y), or who require greater than 40ml/kg of fluid resuscitation usually require Paediatric Intensive Care Risk factors for cerebral oedema include young age (<5y), severe acidosis, hypocapnia, elevated urea at presentation, large amounts of fluid resuscitation (>40ml/kg), use of bicarbonate and overly rapid fall in blood glucose. Fluid replacement is based on maintenance + correction for dehydration. Shock is corrected by the boluses of 20 ml/kg of normal saline. Maintenance fluid rate is calculated from body weight (Kg) 100ml/kg/day or 4ml/kg/hr for first 10kg body weight 50ml/kg/day or 2ml/kg/hour for each kg between 10 and 20kg 20ml/kg/day or 1ml/kg/hour for each kg above 20kg Example: Child of 23kg admitted with DKA:Maintenance calculation [10x100] +[10x50] + [3x20] = 1560ml/day = 65ml/hr Percentage dehydration is based on clinical estimate or a recent clinic weight. It is easy to over-estimate % dehydration in DKA, therefore NEVER assume dehydration exceeds 10%. The correction for dehydration is administered over 48 hours. Example: Child of 23kg admitted with DKA Estimated % dehydration is 5%, therefore deficit = 0.05 x 23 = 1.15 litres (1150ml), given over 48 hours ie 575ml/day + maintenance. Administer insulin at 0.1u/kg/hour. Adjust iv fluids to maintain glucose at adequate levels. Insulin may be reduced to 0.05u/kg/hr if: a rapid reduction in glucose occurs (>5mmol/hr), particularly in young children. Or Blood glucose is persistently below 7.0mmol/l, despite using 10% glucose Fluids Used: If glucose >13mmol/l, use 0.9% (Normal) Sodium chloride If glucose between 7.0 and 12.9mmol/l, use 0.45% Sodium chloride with 5% glucose unless hyponatraemic (Na <132mmol/l) If glucose between 7.0 and 12.9mmol/l with hyponatraemia, use 0.9% Sodium chloride with 5% Glucose. All children require - hourly neurological observations until stable when the frequency may be reduced. These may be discontinued when the child is completely alert and stable. Children with a depressed level of consciousness require a nasogastric tube. Children with DKA are at high risk of aspiration, particularly if there is significant depression of consciousness Cerebral oedema is a rare and serious complication of treatment of DKA. Morbidity and mortality is high. If suspected, remember ABC and give Mannitol 0.5g/kg [2.5ml/kg 20% Mannitol] immediately Call ICU anaesthetic registrar and notify paediatric consultant Reduce fluid replacement to 2/3 maintenance only with no correction for dehydration Children with cerebral oedema require intubation, ventilation and urgent transfer to a paediatric intensive care unit DKA is associated with a potassium deficit, irrespective of the initial plasma potassium. Once urine has been passed, commence potassium replacement: Potassium Chloride (KCl) 40mmol/l (20mmol in 500ml bag) Use of sodium bicarbonate is potentially extremely hazardous, and increases the risk of cerebral oedema. Use may be justified by severe acidosis with shock, (arterial pH < 7.0, HCO3 < 5mmol/l), to improve myocardial function. When bicarbonate therapy is under consideration, an arterial blood gas sample is essential to confirm pH. When bicarbonate is required, use 1-2mmol/kg over 1-2 hours [1-2ml/kg 8.4% NaHCO3 diluted with an equal volume of normal sodium chloride Nephrotic syndrome Diagnosis: Heavy proteinuria, hypoproteinaemia and oedema. Oedema, which may be peri-orbital (often thought to be allergic initially) or generalised. Decreased urine output. Abdominal pain. Ascites, pleural effusions and genital oedema may occur. Some children may present with hypotension and dyspnoea. 2-6 years of age most commonly. Investigations Urinalysis and culture Heavy proteinuria (3-4+ on albustix). Early morning urine protein / creatinine ratio. >200 mg/mmol in patients with nephrotic syndrome. Blood tests U&Es, LFTs, FBC, varicella zoster titres. ASO titre, C3 and C4 components of complement, and antinuclear factor should be measured in selected cases especially when there is a mixed nephritic/nephrotic picture. Consider Hepatitis B serology if any risk factors. Management During the initial attack attention is focused on management of the oedematous state and any arising complications until hopefully steroids induce remission. a) Volume replacement Rapid correction of shock or hypovolaemia is essential as per standard resuscitation guidelines. 20ml/kg of normal saline is the usual recommendation, but an alternative is 4.5% human albumin solution (HAS) Hypovolaemia can be associated with sepsis, diarrhoea or the injudicious use of diuretics. Hypovolaemia may cause acute tubular necrosis, be complicated by thromboses (arterial or venous) or lead to sudden death. Initial treatment with corticosteroids At presentation a high dose of prednisolone 60 mg/m2/day, (maximum 80mg/day) is accepted practice. Children with Hydrocephalus and Ventriculo-peritoneal Shunts Shunt malfunction may be the result of obstruction, infection, disconnection at the junction or break, hardware erosion through the skin and over shunting. Shunt evaluation includes ascertaining the reason for initial shunt insertion (e.g. meningitis, tumour, myelomeningocele)  SHAPE \* MERGEFORMAT  Indications for red cell transfusion acute blood loss (ie>=150mL min-1 or 1 blood volume/24hrs or 50% blood volume in 3 hours, blood volume is 70mL kg-1 adult, 80mL kg-1 child) Acute anaemia, fit patient, Hb<7g/dL Acute anaemia, patient with cardiovascular risks, Hb<9g/dL Critical care patients, Hb<7g/dL Post-chemotherapy, Hb<9g/dL Radiotherapy, Hb<10g/dL Chronic anaemia, Hb<8g/dL Indications for the use of fresh frozen plasma Replacement of some single coagulation factor deficiencies Non-urgent reversal of warfarin effect Acute disseminated intravascular coagulation As plasma exchange in thrombotic thrombocytopenic purpura Massive transfusion and PT >1.5 x control Liver disease if PT>1.5 x control Indications for cryoprecipitate in acute disseminated intravascular coagulation with bleeding and fibrinogen <1g/L in advanced liver disease to correct or prevent bleeding with fibrinogen <1g/L to correct bleeding in association with fibrinolytic therapy causing hypofibrinogenaemia in massive transfusion associated with hypofibrinogenaemia to treat abnormal bleeding in renal or liver failure where desmopressin is ineffective/unsuitable Indications for platelet transfusion (refer to full guidance for platelet counts) In bone marrow failure: to prevent bleeding, platelet count<10 x109/L to prevent bleeding in patients at increased risk of haemorrhage, platelet count <20 x109/L to prevent bleeding in association with invasive procedures, platelet count <80 x 109/L In critical care/surgery: in massive blood transfusion, platelet count <75 x 109/L in bleeding in association with acquired platelet dysfunction, irrespective of platelet count in DIC with bleeding, platelet count <75 x 109/L in inherited platelet dysfunction In immune thrombocytopenia: in immune ITP if major significant bleeding in post-transfusion purpura only if actively bleeding in neonatal alloimmune thrombocytopenia (NAITP) to treat bleeding or to maintain platelet count >30x109/L Do not Resuscitate order: DNACPR status means that in the event of an arrest or collapse the crash team is not called. Neither advanced nor basic cardiopulmonary resuscitation are given. This means oxygen and suction may be given, but assisted ventilation using bag and mask or mouth-to-mouth are not indicated. This DNACPR order in itself has no other implication for the patients management. Indications for DNACPR order : 1 The child has such severe disease that cardiopulmonary resuscitation would simply delay death without significant alleviation of suffering. 2 Although the patient may be able to survive with treatment the degree of physical or mental impairment would be so great that it is unreasonable to expect them to bear it. 3 The child and/or family feel that in the face of progressive and irreversible illness further treatment or resuscitation is more than can be borne by the child. Neonates with murmur Consider each of these signs Is the lower limb SaO2 <96%? Central cyanosis present? Are there signs of heart failure? Symptoms & signs of heart failure Poor feeding, tired and breathless whilst feeding, takes a long time to complete feeds Tachypnoea, respiratory distress Clammy skin, poor perfusion, pallor, cyanosis Tachycardia, hyperactive praecordium, gallop rhythm Oedema, hepatomegaly Clinical features suggestive of Congenital Heart Disease Symptoms of heart failure Cyanosis, SaO2 <96% (pre and/or post-ductal) Abnormally strong or weak pulses (Check femoral pulses) Praecordial hyperactivity Abnormal intensity and character of heart sounds Murmur >grade 2/6, harsh Diastolic, pansystolic or continuous Associated with an ejection click Henoch Schnlein Purpura (HSP) in Children HSP is the commonest vasculitis of childhood. It is characterised by inflammation of small vessels leading to non-thrombocytopenic purpura, arthritis/ arthralgia, GI haemorrhage and glomerulonephritis. Clinical features The commonest age group is 2 - 8 years. There may be a recent history of an upper respiratory tract infection. Abdominal pain or arthralgias sometimes precede the rash. Purpura: On the extensor surfaces of limbs (mainly lower), or dependent and pressure bearing areas (ankles / buttocks). Also consult guideline on non-blanching purpuric rash Joint Pain: Knees and ankles commonly affected. In most situations this pain resolves spontaneously within 24-48 hours. Abdominal pain: Uncomplicated abdominal pain often resolves spontaneously within 72 hours. Complications include GI haemorrhage (haematemesis, bloody stools), intussusception, perforation, and pancreatitis. Renal disease: Haematuria is present in 90% of cases, and in up to 40% may recur. Less common renal manifestations include proteinuria, nephritic/nephrotic syndrome, isolated hypertension, and renal failure (<1%). Renal involvement may only become apparent during the convalescent period. Subcutaneous oedema (scrotum, hands, feet, and sacrum): seen especially in children <3yrs, can be painful, also resolves spontaneously in 24 - 48hrs. Investigations BP in all children Urine dipstick in all children U & E only if renal involvement other than isolated haematuria is suspected. Include LFT and Albumin if phlebotomy undertaken Consider prednisolone for: severe GI haemorrhage, severe joint manifestation, and testicular pain. If there are features of abdominal complications or painful scrotal swelling seek a surgical opinion (testicular haemorrhage is difficult to differentiate from testicular torsion). Indications for admission: Abdominal complications Renal complications (other than isolated hematuria and/or 2+ proteinuria): Nephritis (persistently elevated BP even after adequate analgesia, oliguria) Nephrotic syndrome (oedema, proteinuria, hypoalbuminaemia) Discuss with consultant. Consider further discussions with Dr Upton if available or Nottingham renal team (0115 9691169 bleep paediatric renal registrar) Also consider admission for symptomatic treatment of: Severe joint pain Severe abdominal pain Exposure Prone Procedures (EPPs) EPPs are those procedures where there is a risk that injury to the worker may result in exposure of the patients open tissues to the blood of the worker. These procedures include those where the workers gloved hands may be in contact with sharp instruments, needle tips or sharp tissues (spicules of bone or teeth) inside a patients open body cavity, wound or confined anatomical space where the hands or fingertips may not be completely visible at all times. Any HCW who is involved in EPPs and has reason to believe that they have been infected with Hepatitis C must inform the COH. They will be tested for antibodies to HCV and, if positive, two specimens of blood for Hepatitis C virus ribonucleic acid (HCV RNA) will be required two months apart. If positive for HCV RNA, HCWs will be restricted from performing EPPs. HCV infected HCWs who respond successfully to treatment with anti viral therapy, i.e. remain HCV RNA negative 6 months after cessation of treatment, may resume EPPs following advice from the COH. These HCWs will be tested at 6 monthly intervals. Any HCW who refuses to be tested will not be allowed to continue undertaking EPPs and may be subject to disciplinary action if such refusal could adversely affect patient safety. HCWs that are aware, or have reason to believe that a HCV infected colleague is practising in a way, which places patients at risk, must report this in confidence to the COH. All HCWs must comply with the Trust policy and report all blood/body fluid exposure incidents to the COH. Prophylaxis with immunoglobulin or anti-viral agents is not indicated following exposure to Hepatitis C, as there is no scientific evidence of any benefit. Where the source patient/individual of an exposure is found to be anti-HCV antibody positive, the recipient HCW will be offered blood tests to detect seroconversion to HCV. The COH will provide information and advice on Hepatitis C and its potential impact on work and lifestyle. It will not normally be necessary to exclude the HCW from performing EPPs during the period before the results of blood tests are known. ITP Take a history of onset of bruising, presence / absence of mucosal bleeding and family history of bleeding disorder. They are well at presentation. They may have had a viral infection in preceding 2-3 weeks (50%) On exam- record purpura, petechiae and echymoses, anaemia, lymphadenopathy, organomegaly and signs of sepsis. Occasionally nose bleed, melaena or rarely microscopic haematuria. Investigations: FBC and Film. No other investigation unless atypical features All children who receive specific treatment for ITP (steroid or i.v. Ig) should have evidence of life-threatening heamorrhage. Patients with Latex allergy : Natural rubber latex (NRL) There are 5 possible ways for patients to come into contact with NRL. These are: - Cutaneous - touching the skin via gloves or other latex products Mucous membranes - via products used in dental treatment, intubation and internal examinations and catheterisation. Intravascular - via latex products used in intravascular devices e.g. IV cannulae or devices used to deliver IV fluids and injectables (medicine bungs). Internal tissue - during surgical procedures Inhalation of glove protein (rare) Broad Recommendations The use of latex should be minimised where possible. Staff is required to follow the Trust guideline regarding the choice of gloves staff education The history of any patients, who are known or suspected to have a latex allergy, must be passed on as part of their clinical care. This involves liaison within and outside the Trust. each area to develop and maintain latex free box/trolley containing items relevant to the department. Patients should be nursed in a side room which is clearly labelled Natural Rubber Latex Free Identification of patients with Latex allergy Patient admission assessment must involve a careful history to detect known or possible occurrence of latex allergy. Risk Factors Patients who have a history of any of the following may have an increased risk of developing a latex allergy: - Spina bifida or other neural tube defects who have required frequent surgery. Atopic individuals especially those with eczema and/or asthma. Genito urinary tract abnormalities that have required frequent catheterisation or surgical intervention. Multiple surgical procedures. Food allergy in particular bananas, avocados, tomato, kiwi, melon and mango. Those individuals who have occupational exposure to latex, e.g. health care workers. A Complete full screening questionnaire with the patient, if they have a documented positive test or history of allergy/sensitivity or where a latex allergy is suspected following history taking When feasible, patients with a suspected latex allergy will be referred by the medical staff to the Dermatology Department for allergy investigations. Procedures on all patients with a suspected or positive history of latex allergy should be performed in a latex free environment. This is defined as an area where latex gloves are not used by any personnel, and no latex products of any kind come into direct contact with the patient. Emergency or elective procedures and Investigations At the first point of hospital contact for the patient, it is important to identify latex sensitive patients. To aid in this:- A screening questionnaire is used. Latex allergy leaflets Blood samples may be required for IgE and RAST for latex at the discretion of the medical staff. Medical staff should ascertain if the patient is sensitive to latex at the out patient appointment when the decision is made to proceed with surgery. When feasible, patients with suspected allergy should be investigated by referral to the Dermatology Department, especially before medical or surgical procedures that will entail latex exposure. When urgent treatment is required this will be undertaken in a latex free environment. The patients G.P. should be contacted with any results or recommendations. These should be recorded on PAS and in the patients notes. Patients identified as allergic to latex should receive education in latex avoidance by the nurse responsible for the patients care and should also be advised to obtain a medical alert bracelet or similar. It may also be appropriate to advise them to carry a supply of non-latex gloves and to seek advice from their GP about the necessity of carrying auto -injectable adrenaline (Epi-pens). Ward Preparation and Management of Patients with known or suspected latex allergy All should be familiar with:- The preparation of latex free environment The use of latex free equipment The management of acute anaphylactic shock The patient should be allocated a well-ventilated side room, which has been clinically cleaned by staff wearing latex-free gloves. The need for a side/single room needs to be balanced with the clinical need of patients currently occupying a single/side room. All items containing latex should be removed from the room at least two hours before admission, but preferably the night before. Aprons and latex free gloves should be available by the door. Warning signs should be placed at the door (Appendix 4). The patient should wear a clearly marked patient ID bracelet indicating LATEX ALLERGIC. All documentation i.e. medical notes, prescription charts and observation chart will clearly annotated latex allergic. Ensure there are no elastic bands around health records. Ensure that PAS has been updated with the ALERT status. The number of clinical staff involved with the patients care should be restricted to a minimum. All personnel must wash their hands before entering the room, or having contact with patients to ensure that they are free of NRL particles. Intravenous solutions or drugs must not be stored with other NRL products. Drugs with NRL seals should not be used. Syringes should have NRL diaphragms. Two component syringes, mini-jet system and epi-pens are all NRL free. Giving sets without NRL ports should be used (or ports removed and replaced by stopcocks and taped up). Advice should be sought in hours from the ward Pharmacist or Medicines Information regarding appropriate medications and their preparation e.g. latex stoppers on IV drug containers which they are concerned, may contain NRL (e.g. rubber bungs). Emergency drugs must always be available to manage anaphylactic shock i.e. epinephrine, hydrocortisone, chlorphenanime. Diagnosis of Legionella Infection Patients at risk: Patients with severe pneumonia, nosocomially-acquired pneumonia, or significant immunosuppression Patients admitted to hospital with radiologically confirmed, community-acquired, pneumonia and any of the following risk factors: Recent travel history Middle-age male heavy smoker Organ transplant recipient Associated with other cases (e.g. place of work) Suggested testing protocol On admission Culture of respiratory specimens for legionellae, preferably on invasive respiratory specimens.e.g.obtained at bronchoscopy. Urine (for antigen detection Serum to be stored for comparison with later sera. At one week after admission Test serum in parallel with admission serum. Repeat at weekly intervals until 4 weeks after onset or until an alternative diagnosis is established. N.B. Urinary antigen - antigen may disappear rapidly >5 days after onset, therefore important to store admission specimen as routine. Do not collect in boric acid container. Causes of scrotal pain: infection, (epididymitis, orchitis and epididymorchitis) trauma, twisting or torsion of the testis, torsion of an appendage of the testis, idiopathic scrotal oedema, incarcerated inguinal hernia and Henoch-Schonlein purpura Urgent scrotal exploration should take place within one hour of a provisional diagnosis of acute testicular torsion being made Signs The child may be in obvious discomfort, have an unusual gait or be reluctant to move. The scrotal region is usually very tender and may be red and swollen. There may also be a high riding testicle, absence of cremasteric reflex, a focal blue-dot at the upper pole of the testis, diffuse blue discoloration of the hemiscrotum or a reactive hydrocele. A high temperature may also be observed Investigations A urine sample should be obtained as soon as possible and a dipstix test performed. Management Every boy with acute scrotal pain should be reviewed urgently by a paediatric registrar or Consultant. A history of previous transient scrotal pain is significant. Testicular loss from infarction can occur after as little as 2 hours of onset of symptoms A delay in treatment can result in orchiectomy, and has been associated with reduced fertility Thus surgical intervention should ideally take within one hour and acute scrotal pain should be treated as torsion of the testis until proven otherwise. Radioisotope scans and Doppler ultrasonography are not part of the initial management of acute scrotal pain in many centres. This is because it may contribute to delay in treatment with unacceptable consequences. Moreover, in obese boys and when the testicular volume is about 2 ml, the diagnostic accuracy of these tests is low resulting in limited clinical benefit. Special Situations a. Where the duration of symptoms is 48 hours or more, the emergency surgery need not follow the 1 hour rule. b. When on examination, the patient has become symptom free and there are no signs of an acute episode of torsion of testis. If a diagnosis of a spontaneous detortion / intermittent detortion is made, the testis should be explored as soon as possible but need not be within 1 hour. Necrotizing enterocolitis Clinical features Temperature instability GI bleeding Apnoea Lethargy Pallor CVS or resp compromise Abdominal distension Discolouration / tenderness or abdominal wall oedema Absent bowel sound Abdominal mass Investigations FBC, Biochemistry, blood gas Group and save, cross match Blood and stool culture AXR to check perforation, distended bowels, pneumonatosis intestinalis Risk factores Prematurity Any cause for compromised splanchnic blood flow in the infant, eg maternal cocaine use,PDA High osmolarity of formula feed, Organisms- Klebsiella, staph, E.coli Treatment Stop enteral feeding, NBM NG tube and hourly aspiration Antibiotics- penicillin, gentamicin, metronidazole i.v. fluid- N saline 10 ml/kg, repat correct abnormal U&E and glucose and abnormal coagulation analgesia- i.v. morphine paed surgery referral Differential diagnoses Intestinal perforation vovulus Umbilical sepsis UTI/sepsis Ascites Insertion of umbilical venous catheter (UVC) 1. Goal To ensure the safe insertion of an umbilical venous catheter 2. Indications Venous access for low birth weight infants to avoid multiple peripheral cannulation Emergency vascular access for resuscitation of infants at birth Exchange transfusion 3. Contraindications ۃ Abnormalities of the abdominal wall ۃ Necrotising enterocolitis ۃ Peritonitis 4. Complications " Sepsis2,3 " Embolism " Venous thrombosis4 " Pericardial effusion5 " Pleural effusion6 " Portal hypertension " Displacement leading to blood loss Breakage of catheter on removal 4.1 Malpositioned catheters Catheters placed in the heart can cause pericardial effusion, cardiac tamponade, endocarditis, arrhythmias. Catheters placed in the portal system are associated with necrotising enterocolitis, perforation of colon and hepatic necrosis 5. Key notes ۃ The catheter tip should ideally lie in the inferior vena cava. ۃ The catheter position should always be checked prior to use with an x-ray ۃ Once secured in place the catheter ideally should not be advanced into the vein ۃ Do not use hypertonic solutions if the catheter is not in the inferior vena cava ۃ UVC s placed during newborn resuscitation should be placed where there is adequate blood sampling. Position of the catheter " Determine the desired length of catheter by calculating 2 x weight in kg + 5cm + stump length in cms13,14,15. i.e. if infant weighs 1.5kg (1.5 x 2) + 5 = 8cm + stump This should place the tip of the catheter above the diaphragm and outside the chambers of the heart. CSP - Nexus criteria (National Emergency X-Radiography Utilization Study Group) GCS 15 and appropriate responses Absence of alcohol, opiates, intoxicants No significant distracting injury No midline tenderness, steps or neurological injury or impairment to full range of movement of neck. Recombinant factor VIIa (rFVIIa; Novoseven, Novo Nordisk) It is an analogue of the naturally occurring coagulation factor, which is manufactured by recombinant technology from a cell line and autoactivated during the purification procedure1. It was developed for use in patients with haemophilia A and B who have developed inhibitors (antibodies) against FVIII or FIX, respectively. rFVIIa aims to bypass the missing coagulation factor: supraphysiological doses of rVIIa seem to enhance thrombin generation on the surface of activated platelets, allowing the formation of a stable fibrin clot. Role of recombinant factor VIIa Haemophilia care Uncontrolled massive bleeding, particularly trauma and obstetric haemorrhage Peri-operative settings Intracranial haemorrhage If rFVIIa is considered, every effort should be made to achieve the following parameters to ensure maximal effectiveness: Platelets >50x109/L Fibrinogen >0.5 g/L (ideally >1.0g/L) pH >7.2 Haematocrit >24% Appropriate blood product replacement: FFP 10-15mL/kg: aim INR and APTTr <1.5 Cryoprecipitate 1-1.5 packs/10kg: aim fibrinogen >0.5g/L, ideally >1.0g/L Platelets 1-2 adult doses: aim platelets >50x109/L Correct acidosis, hypothermia, hypocalcaemia Contraindication Thromboembolic events are the main potential concern with the use of rFVIIa, because of the possibility of systemic activation of coagulation rFVIIa should not be used in patients who are considered to be unsalvageable by the clinical team. A history of thromboembolic events, coronary artery disease or disseminated intravascular coagulation should not be considered an absolute contraindication to the use of rFVIIa, but the clinical team should be aware of the potential for increased risk of thromboembolic events. Patients who have received rFVIIa should be monitored clinically for evidence of thromboembolic events, and should be assessed regularly for appropriate thromboprophylaxis (compression stockings, and/or low molecular weight heparin once bleeding has stopped). Safeguarding Children All health service professionals, whether they work within adult services or child care services, have a responsibility to refer to childrens social care services any child who they believe is suffering or may be at risk of suffering significant harm. Section 11 of the Children Act 2004 places a statutory duty on key people and bodies to make arrangements to safeguard and promote the welfare of children The Trust has a nominated Safeguarding Children team whom staff can consult if they have concerns or wish to seek general advice. A paediatrician, with some exceptions, should be involved if there are concerns about an immediate risk to a child. Although professionals have a duty of confidentiality, in certain circumstances, the law permits the disclosure of confidential information necessary to safeguard a child. It is the responsibility of the professional identifying the concern to ensure that a referral to childrens social care services has been made if appropriate and to access the proper support. Parents permission should be sought before a referral is made unless permission seeking may in itself place a child at risk of significant harm. All staff have a responsibility to ensure they keep up to date with relevant training. Members of staff should also be aware that they should not write reports for case conferences, court or strategy meetings without first contacting a member of the Safeguarding Children team, nor should they attend such a conference or court without the support of the team. . If any members of the Trust identifies a concern that a child may be at risk there should be discussion and, if necessary, referral. The initial discussion should involve the line manager and, if necessary, a member of the Trust Safeguarding Children team. Further advice can be obtained from the on-call community paediatrician via switchboard. If, in the light of initial discussions, concerns are confirmed then the child should be referred. Referrals can be passed to the on-call paediatric team Staff are reminded of the importance of keeping safe and avoiding conflict. The parents or carers should not be confronted. No attempt should be made to physically restrain families who are acting against advice and are seeking to leave. If families leave under these circumstances police and childrens social care services should be involved as a matter of urgency. If families or carers become threatening or abusive call security or the police. GMC guidance The safety of the child is paramount and overrides the usual duties of confidentiality. Guidance from the General Medical Council states, If you believe a patient to be a victim of neglect or physical or sexual abuse and unable to give or withhold consent to disclosure you should usually give this information to an appropriate responsible person or statutory agency in order to prevent further harm to the patient. In these and similar circumstances you may release information without the patients consent, but only if you consider that the patient is unable to give consent and that disclosure is in the patients best interests. Scabies in Adults/Children Scabies mites, Sarcoptes scabiei, burrow in human epidermis digesting it as they go. They burrow primarily at night and rest to lay eggs during the day. Although, at standard room conditions, infectious mites can survive for up to 36 hours off the host, there is little risk of transfer of the infestation via clothing, bedding, towels or upholstery used by patients with typical symptoms of scabies. However, such transfer is a risk in patients presenting with the less common variant, crusted scabies (formerly called Norwegian scabies), characterised by heavy infestation of mites. Diagnosis of Case A Consultant Dermatologist or Consultant Paediatrician should confirm the diagnosis Finding adult mites, eggs or faecal particles (scybala) may all confirm the diagnosis. General measures Latex gloves and plastic aprons must be worn when attending to the patient before and during treatment. Scabies cannot be transmitted 24 hours after treatment with an effective scabicide. Isolation is unnecessary for common scabies, but patients with crusted scabies should be isolated until infection is clear. Management of single case of ordinary scabies (=index case) Treat index case and some contacts. A contact is defined as: All household (i.e. someone who lives in the same house) and sexual contacts of the index case. The patients visitors during the in-patient stay (where there has been a likelihood of prolonged (at least 10 minutes) skin-to-skin contact e.g. hand holding). The patients carer (nurse, OT, etc) where there has been a likelihood of prolonged (as above) skin-to-skin contact. Staff will be advised to attend the Occupational Health Department; other contacts (e.g. visitors, relatives) should be referred to their own GP promptly for treatment, even if they have no symptoms. Management of 2 or more linked cases of scabies (i.e. when an outbreak is defined). Treat all cases and contacts. The Hospital Infection Control Doctor (HICD) working with the dermatologist and the Consultant in Communicable Disease Control (CCDC), should decide which contacts (e.g. patients, staff in hospital, household or other relevant persons) require prophylactic treatment. This will amount to those suspected to have had prolonged (at least 10 minutes) skin-to-skin contact with the cases in question. Failure to do so may lead to persistence of infection. Management of crusted scabies Treat all known and suspected cases and contacts. Index case(s) need to be treated. Patients should be isolated until infection is clear. This may take days or even weeks. Gloves and long sleeved gowns should be worn when coming into close (skin-to-skin) contact. Staff and other contacts must be treated as described above. CCDC should be informed if patient comes from nursing home or similar institution. Secondary contacts of staff and patient(s) should be advised to see their GP to discuss treatment. Contacts of confirmed secondary cases should be treated without delay. Recently used underclothes, bed linen and towels should be machine washed at temperatures above 50(C, or kept in plastic bags for at least 72 hours to contain mites until they die Recommended Drugs Table Drug Available as Strength/form Application  Permethrin  Lyclear Dermal Cream 5% cream Apply to whole body except head and face, wash off 8-12 hours later. Repeat once after 7 days if necessary.  Malathion (<2 yrs old) Derbac-M Quellada-M liquid 0.5% aqueous liquid 0.5% liquid emulsion  Apply to whole body except head and face, wash off after 24 hours. Repeat after 7 days if necessary.  Vaccination and antimicrobial prophylaxis for patients undergoing elective or emergency splenectomy or those who are asplenic or have a dysfunctional spleen Overwhelming infection is a major risk in patients with an absent or dysfunctional spleen and although uncommon, is associated with a high mortality. These infections are often due to encapsulated bacteria such as Streptococcus pneumoniae, Haemophilus influenzae type b and Neisseria meningitidis and more than half of those infected die. Other serious infections include malaria, babesiosis (caused by tick bite) and Capnocytophagia canimorsus (caused by dog bites) and secondary infections following Adults vaccination summary Elective Splenectomy Immunise at least TWO (ideally four to six) weeks prior to surgery. Prophylactic antibiotics to start post surgery. Emergency Splenectomy Immunise ideally at least TWO weeks post surgery, or immediately before discharge from hospital. Prophylactic antibiotics to be started immediately. VaccineDosage/regimen Re-immunisationPneumococcal vaccine polyvalent (Pneumovax II() Pneumovax II(, single dose of (0.5mL im) Adults and Children > 10 years: Reimmunise every 5 years or sooner if high risk patient (sickle cell anaemia or lymphoproliferative disorders)Hib and Meninogococcal Conjugate Group C (Menitorix()Previously unimmunised: Two doses 0.5mL im of Hib/MenC (menitorix) two months apart. Previously fully immunised: Offer reinforcing dose of 0.5mL im of Hib/MenC (Menitorix()Not currently recommendedInfluenzaAdults should receive yearly immunisation via their G.P. (September to April)Yearly (September to April)Meningococcal ACWY (ACWY Vax() Only if travelling to high risk areas (see main guidance)Single dose 0.5mL deep sc of ACWY Vax(Reimmunise after 5 years if still at high riskLifelong Adult antibiotic prophylaxis summary Prophylaxis DurationFirst linePenicillin V 500mg bd Minimum 2 year prophylactic course but preferably lifelongIf penicillin allergyErythromycin 500mg bd   Indications for Percutaneous Coronary Intervention (PCI)Single or two vessel coronary diseasePrevious CABG (sometimes - see below)Triple vessel disease where CABG high risk Indications for CABGSymptomatic but unsuitable for PCILeft main stem stenosis (50%Proximal triple vessel diseaseTwo vessel disease including proximal left anterior descending stenosis Indications for referral to Cardiologist Prognostic Assessment. The National Service Framework for Coronary Heart Disease recommends that all patients thought to have new onset angina should, unless thought unsuitable for revascularisation because of frailty, intercurrent illness etc., be referred for prognostic assessment by means of treadmill or other testing. Diagnostic Uncertainty. Refractory Symptoms despite full pharmacological treatment as outlined below. Suddenly Worsening or Unstable Symptoms may require urgent or emergency referral. Angina with a murmur needs investigating further (e.g. with Echocardiography) to exclude haemodynamically significant valve disease. 4. Indications for Exercise Testing Diagnostic - if the aetiology of chest pain (or dyspnoea) is in doubt (except in the presence of Left Bundle Branch Block). Positive predictive accuracy depends on the prevalence of the disease in the population being tested (e.g. is very low in younger women with few risk factors and atypical symptoms). Prognostic - to identify those patients who may need revascularisation on prognostic grounds. Exercise testing for this reason may not be necessary in the elderly in whom symptom control is more important than long-term prognosis.  Therapeutic - to reassure some patients that they can exercise safely (e.g. post AMI). Alternatives to Exercise Testing Isotope perfusion (MIBI) scanning / Stress Echocardiography These techniques may be used instead of ECG based stress testing, in the presence of Left Bundle Branch Block or other pre-existing ECG abnormalities (such as LVH) or where the ECG changes on exercise testing are equivocal It is the investigations of choice in young/middle aged women with chest pain if clinically indicated. Exercise Testing in RBBB, especially if QRS duration is prolonged, may lead to difficulties of interpretation. Stress Echo is the recommended non-invasive test for reversible ischaemia in end-stage CRF. They can be used to determine whether a particular angiographically demonstrated stenosis is causing reversible ischaemia. Pharmacological stress (eg Dipyridamole, Dobutamine or Adenosine) may be used in patients who are unable to exercise for non-cardiac reasons. Treatment to relieve symptoms (-Blockers : All angina patients should be on a (-blocker unless contraindicated. Impaired left ventricular function is an indication for, rather than a contraindication to, (-blockade. Bisoprolol and Carvedilol are particularly indicated for patients with impaired left ventricular function Potassium Channel Openers Nicorandil (10mg bd increasing after 2 weeks to 20mg bd) may be useful in providing symptomatic relief. Calcium Channel Blockers Rate limiting calcium blockers (such as Diltiazem or Verapamil) may be used as an alternative when (-blockers are contraindicated (e.g. in the presence of asthma or severe PVD) but should be used with caution in the presence of (-blockade because of the possibility of excessive bradycardia. Once daily preparations are preferred. Dihydropyridine calcium antagonists (such as Amlodipine or Nifedipine) may be used in addition to (-blockers if symptom control is inadequate. All calcium antagonists (especially Verapamil) are negatively inotropic and should be used with caution where contractility is already impaired. Short acting Nifedipine has been shown to increase mortality in CHD patients. Nitrates GTN sub-lingual tablets or spray are useful for immediate prophylaxis of angina and in producing relief of symptoms. Long acting nitrate tablets, transdermal patches or buccal preparations can provide useful symptomatic relief but should be prescribed with at least a six hour nitrate-free period every 24hrs. Ivabradine (Procorolan) This new selective sinus node inhibitor specifically slows the sinus rate and can be used in stable angina where  blockers are contraindicated (other than because of sinus bradycardia). (Dose 5mg bd increasing to 7.5mg bd if necessary) 7. Indications for Coronary Angiography Elective: Limiting stable angina despite optimal medical therapy where patients may benefit symptomatically from coronary revascularisation. Where clinical characteristics or non-invasive investigations suggest that the patient has an adverse prognosis and may benefit prognostically from coronary revascularisation. To define coronary anatomy prior to valve surgery. Where non-invasive tests have been inconclusive or negative, but the patient continues to have symptoms, which are troublesome, severe or result in recurrent admission to hospital, in order to define a management strategy. Emergency: In unstable angina (acute coronary syndromes without ST elevation) where ischaemic chest pain continues despite optimal medical treatment or there is evidence of high risk (from ECG, Troponins, CRP etc). See separate guidelines, serial number CA2008 For continuing ischaemic chest pain despite optimal medical treatment in the immediate period following acute myocardial infarction. 8. Indications for Percutaneous Coronary Intervention Limiting or unstable angina despite optimal medical treatment where the coronary anatomy is considered suitable: Single or two vessel coronary disease. Previous CABG with native coronary anatomy suitable for PCI or with bypass graft disease particularly when repeat CABG is regarded as an inappropriate revascularisation strategy. Triple vessel disease where the coronary anatomy is considered suitable for PCI particularly when CABG is regarded as high risk because of poor left ventricular function or disease co morbidity. Indications for Coronary Artery Bypass Grafting Symptomatic Limiting or unstable angina despite optimal medical treatment where the coronary anatomy is considered unsuitable for PCI (see above). Prognostic Left main stem stenosis of 50% or greater. Proximal triple vessel disease. Two vessel disease including significant proximal Left Anterior Descending stenosis particularly if left ventricular function is impaired Thromboprophylaxis. Risk Factors Previous DVT / PE Cancer, particularly metastatic / pelvic Hemiparetic stroke Myocardial infarction Thrombophilia Varicose veins Heart failure COPD Severe infection / dehydration Inflammatory bowel disease Rheumatic diseases Polycythaemia Nephrotic syndrome Diabetic coma Pregnancy / oestrogen therapy Age > 70 years Obesity (BMI >30) Lower limb paralysis Enoxaparin Consider thromboprophylaxis with Enoxaparin 40 mg od in any immobilised medical patient with one or more of the above risk factors. Encourage mobilisation & ensure adequate hydration in all patients. Thromboprophylaxis may be inappropriate in patients who are terminally ill. Avoid Enoxaparin in stroke patients, unless very high risk for DVT / PE and cerebral haemorrhage has been excluded (consultant decision). Use anti-embolism stockings and aspirin (aspirin only if haemorrhagic stroke excluded) instead. In pregnancy use Tinzaparin 4500 IU once daily for prophylaxis in preference to enoxaparin Contraindications to prophylactic Enoxaparin include: Bleeding disorders, already receiving therapeutic anticoagulation, known hypersensitivity to heparin, previous heparin induced thrombocytopaenia or thrombosis, haemorrhagic stroke, active gastro-intestinal bleeding, acute MI or acute coronary syndrome receiving high dose LMWH. Caution in renal failure, reduce dose to Enoxaparin 20 mg od if eGFR < 30 mL/min/1.73m2). If performing epidural or spinal anaesthesia, lumbar puncture or epidural catheter removal, more than 12 hours should have lapsed since the last dose of enoxaparin. Enoxaparin can be administered 4 hours AFTER the above procedures have been performed (see Trust guideline CA2031). Anti-embolism stockings Anti-embolism stockings should be considered for use as an alternative to Enoxaparin where contra-indications exist, such as in acute stroke. They should be properly fitted and worn until the patient is fully mobile or the risk of thromboembolism is considered to be minimal. Contraindications to anti embolism stockings include: Dermatitis, ulceration, gangrene, peripheral vascular disease, leg deformity preventing proper application, recent skin graft and severe leg oedema. Varicella - Zoster Virus (VZV). (VZV) is a herpes virus which causes 2 distinct clinical syndromes - chickenpox and shingles. Chickenpox. Chickenpox is the primary infection and is predominantly an infection of childhood. It may begin with a flu-like illness for 1-2 days before onset of the rash. Skin lesions develop in crops and progress from macules through papules and vesicles to scabs over several days. Virus can be isolated from vesicle fluid and the base of fresh lesions. The incubation period is 10 - 21 days, usually about 14 days, but may be prolonged in immunocompromised patients. Infectivity commences for 1-2 days, but may be as long as 4 days before onset of rash, and persists until crusts have formed, usually about 5 days after rash appears. Shingles Shingles is due to the reactivation of latent VZV. It can occur at any age but most patients are over 50 years. The disease often begins with paraesthesiae in the involved segment for 2-3 days. Erythematous maculopapular lesions develop which rapidly evolve into vesicles and may coalesce to form bullae. Infectivity persists for 5-7 days after onset of rash although immuno-compromised patients may be infectious for longer. Varicella (Chickenpox) is an acute, highly infectious disease caused by the Varicella Zoster Virus (VZV). In hospitals Varicella infected persons have transmitted the illness to susceptible persons through airborne routes and without having direct contact. Groups most at risk of serious illness if infected include: patients with leukaemia and other haematological and non- haematological malignancies. transplant recipients patients with AIDS patients on high dose steroids neonates pregnant women. The Department of Health PL CMO (2003)8: Chickenpox (Varicella) immunisation for Health Care Workers (HCWs).recommended that Health Care Workers with a negative or uncertain history of chicken pox should be serologically tested and vaccine offered to those without Varicella zoster antibody HCWs who develop a rash after having the vaccine should report to Occupational Health before having patient contact. Responsibility of Managers To ensure all staff within their environments attend immunisation updates when commencing employment within the trust. To inform infection control and occupational health if a member of staff or patient is diagnosed / exposed to VZV. Immunocompromised patients with no/equivocal history of VZV infection and all bone marrow transplant recipients. Take clotted blood for VZV serology. Include on request form whether patient has been given VZIG or blood transfusion recently. Booking bloods from pregnant women may be stored in the microbiology laboratory thus negating the need for venepuncture Seek advice from the Duty Virologist in the microbiology department about the use of VZIG (see later) Isolate the patient immediately until 21 days after last exposure. 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9!]gd^* ]^gd/. & F]gd^* If the patient is susceptible take a second serum 2-3 weeks after exposure. On the request form indicate if VZIG was given. b. Immunocompromised patients with a positive history of VZV infection (with the exception of bone marrow transplant recipients - see above) No further action. Immunocompetent patients with no/equivocal history of VZV infection (who are in a location where they may become a source of infection to immunosuppressed individuals) Take clotted blood for VZV serology. Include on request form whether patient has been given VZIG or blood transfusion recently. If the patient cannot be discharged, he/she must be isolated from 8 days after first contact until 21 days after last contact. If VZV serology shows immunity, isolation can be discontinued. If the patient is susceptible, take a second serum 2-3 weeks after exposure. d. Immunocompetent patients with a positive history VZV infection No further action. II. STAFF - RELATED INVESTIGATION A history of VZV infection or serological status must be sought from all exposed staff if not already available. 2. a. Staff with a positive history of VZV infection or serological evidence of immunity No further action. b. Staff with no/equivocal history of VZV infection and significant exposure Take clotted blood for VZV serology. Include on request form whether individual has been given VZIG or blood transfusion recently. Pending results, staff should go off duty from 8 days after first contact until 21 days after last contact or be redeployed in a non-sensitive area if possible. If they are found to be immune - no further action. A second serum should be taken from susceptible staff 2-3 weeks after exposure. Staff without VZ antibodies will be offered VZ vaccination. Pregnancy- do not immunize, but give immunoglobulin The Role of the Consultant in Emergency Medicine "On Call" To provide senior clinical leadership to the ED. This will consist of providing direct clinical care to individual patients, the supervision and support of doctors in training in EM and other specialties and a close working relationshipwith Departmental and Trust management teams to ensure safe systems and processes are in place for all patients attending with emergent and urgent conditions It is also expected that the consultant should be kept informed of any significant departmental events that may represent clinical risk to individual or multiple patients, including excessive attendance numbers, unusual case mix or staffing issues. Communications of this nature will normally be dealt with by telephone advice and support. The on-call EM consultant will also provide required clinical leadership in the event of Major Incident activation. When on-call, an EM consultant should not be recalled to hospital solely to deal with a build up of less serious cases, because of excessive waiting times for first assessment or because of potential breaches in the DH operational emergency access standard ("4 hour target"). Chest Drain insertion: Clinical governance leads in local organisations should audit current practice and develop local policies to ensure: Chest drains are only inserted by staff with relevant competencies and adequate supervision Ultrasound guidance is strongly advised when inserting a drain for fluid Clinical guidelines are followed and staff made aware of the risks, reflecting the questions above Identify a lead for training of all staff involved in chest drain insertion Written evidence of consent is obtained from patients before the procedure, wherever possible Local incident data relating to chest drains is reviewed and staff encouraged to report further incidents Minimising risks of suprapubic catheter insertion (adults only) Risks include injury to the intestine and haemorrhage due to perforation of vascular structures in the pelvis. Indications for intubation (CATS) Reduced LOC (GCS 8, AVPU P) Respiratory failure Worsening tachypnoea >40mls/kg fluid resus (likely pulm oed) Impending cardioresp collapse Mental Capacity Act Underlying principles A person must be assumed to have capacity unless it is established that they lack capacity. A person is not to be treated as unable to make a decision unless all practicable steps to help them to do so have been taken without success. A person is not to be treated as unable to make a decision merely because he or she makes an unwise decision. An act done or decision on behalf of a person who lacks capacity must be done in their best interests. The decision should be less restrictive of the persons rights and freedom of action. Assessment of capacity involves 2 stage test Do they have an impairment or disturbance that affects the way their mind or brain works (either temporary or permanent) Does the impairment or disturbance mean that they cannot make a specific decision at the time it needs to be made......... Can they make a decision? They are provided with and understand the relevant information They are able to retain that information in their mind They can use that information to make a decision (weigh it in the balance) They believe the information given They can communicate that decision. Usual approach to assessment of capacity NICE Guidance If a person appears to be calm but refuses potentially life-saving treatment, or expresses the wish to die by suicide, the assumption of capacity could be rebutted by evidence that the person does not truly comprehend the consequences of his or her decision, that the person is acting under the undue influence of another, that the persons emotional distress associated with the stated reason for wishing to be dead is impairing his or her judgement, or that the persons behaviour shows that he or she is deeply ambivalent about the decision (for example if the person initially sought help for the effects of the self-harm). The fact that a person has a mental disorder is not sufficient to override the assumption of mental capacity. However, a mentally capable person who suffers from a mental disorder could be detained under the Mental Health Act if the relevant criteria under that Act are satisfied. The Court of Appeal has held that the compulsory treatment for the mental disorder of a person who has been detained under Section 2 or 3 of the Act can involve treatment for the consequences of the mental disorder and for the symptoms of the disorder (B. v. Croydon Health Authority [1995] 1 All ER 683). In this case, one of the judges ruled that it would seem strange to me if a hospital could, without the patients consent, give him treatment directed at alleviating a disorder showing itself in suicidal tendencies, but not without such consent be able to treat the consequences of a suicide attempt. In my judgment the term medical treatment for mental disorder in s.63 includes such ancillary acts (ibid., pp. 6867). Therefore, although it is not a common occurrence, compulsory treatment can include medical and surgical treatment for the physical effects of self-harm if the self-harm can be categorised as either the consequence of or a symptom of the patients mental disorder. If, in a particular case, staff are in doubt about the extent of treatment permissible under the Mental Health Act, they should consider seeking legal advice and, when necessary, a court ruling. Relevance of AD in OD cant really cover suicide! What is needed for AD covering life threatening illness (written, signed, witnessed, specify life threatening illness) Cant refuse basic comfort (note this means the offer of food and water. AD can refuse ANH as is medical treatment) Clinicians must be satisfied of validity Assessment of validity capacity at time of AD? Any thing done since to suggest change of heart? AD and MHA cant refuse MHA in advance    Admission of patients with syncope in ED: ADMIT Hx of CCF or Dysrhythmia - Chest pain - Evidence of CCF or VHD - ECG with ischaemia/dysrhythmia/BBB/long QTc CONSIDER - >60 years - Hx of IHD - FHx of sudden death - Younger patients with exertional syncope       Page  PAGE 75 of  NUMPAGES 113 PAGE \# "'Page: '#' '"  Assess the Clinical status of the child ABC Life threatening symptoms present? Unconsciousness Intractable seizures Unstable vital signs Dilated pupils Arrange intubation and ventilation by Anaesthetic team. Consider controlling intracranial hypertension with mannitol (0.5 gram/Kg iv). For initial advice liaise with Neurosurgeon and PICU at Addenbrookes hospital.(#6100) Needle the reservoir to relieve pressure if valve will not depress.* (send CSF to Microbiology and Biochemistry). CT scanning in Norwich is usually inadvisable as it may delay treatment. Arrange for transfer once stabilised with CATS Team (0800 085 0003) Discuss with and consider transfer to Neurosurgical Unit at Addenbrookes Perform CT scan, in Norwich or at the Neurosurgical centre depending on availability and consultant advice. DO NOT GIVE SEDATION for CT scan if any Impairment of conscious level: transfer to Neurosurgical centre if sedation / anaesthetic thought necessary for scanning Needle the reservoir if present to relieve pressure if valve will not depress.* (send CSF to Microbiology and Biochemistry Are subacute symptoms and signs present? Fever Irritability Intermittent Drowsiness drowsiness Consider CT scan in Norwich if previous scans are available for comparison Observe carefully (2 hourly Neuro observations) Consider discussion with the Neurosurgical Unit If symptoms are mild or resolving consider discharge home *Consider needling the reservoir only as an emergency. Aspirate 10mL/kg/min, please note that you may not be able to aspirate with ventricular shunt blockage. Remember: A shunt that pumps normally can still be blocked. A normal scan does not exclude shunt malfunction. If in doubt seek Neurosurgical advice Are acute symptoms & signs present? 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