Propofol dosing body weight

• [DOC File]Pharmacy Benefits Management Services Home

  https://info.5y1.org/propofol-dosing-body-weight_1_8d4e48.html

  Recommended dosing: Weight ≥ 50 kg: 650 mg every 4 hours or 1000 mg every 6 hours. ... Mean Body weight = 79.9 kg. Race = Caucasian (75%), African American (21.7%) ... Pretreatments were given prior to propofol injection to compare their ability to prevent propofol-induced pain during induction of anesthesia Parameters.

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• [DOC File]National PBM Monograph Template Rev20091005

  https://info.5y1.org/propofol-dosing-body-weight_1_b0e803.html

  -Propofol from GPI 15715 showed a different disposition function and larger volumes of distribution, compared with propofol emulsion-The propofol effect site concentration for half maximum effect was lower for GPI 15715 than for propofol emulsion (2.0±0.5 mcg/mL and 3.0±0.7 mcg/mL, respectively)

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• [DOC File]Propofol Dosing Guidelines

  https://info.5y1.org/propofol-dosing-body-weight_1_930dbb.html

  D. Titrate the propofol infusion rate, not the ketamine infusion rate. If the patient seems to require a lot of propofol, give 25-50 µg fentanyl boluses. F. As with propofol, the ketamine infusion rate was designed for adults of average weight (60-80 kg). Adjust upward or downward for larger or smaller patients.

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• [DOCX File]ACCRAC Podcast – Anesthesia and Critical Care Reviews and ...

  https://info.5y1.org/propofol-dosing-body-weight_1_68ce92.html

  Propofol: one 50ml vial divided into 2x20cc syringes and 1x10cc syringe (1-3 mg lean body weight) Lidocaine 2%: One 5cc syringe (1-1.5mg/kg lean body weight usually 100mg) Fentanyl: one 250mcg (5cc) vial (1-3mcg/kg lean body weight usually 100-150mcg) Neuromuscular blockade:

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• [DOCX File]Appendix - Lippincott Williams & Wilkins

  https://info.5y1.org/propofol-dosing-body-weight_1_cf61a1.html

  Total body clearance and volume at steady state correlated linearly with body weight in obese and controls, but distribution clearance did not. Context-sensitive half time (time required for the central compartment drug concentration at the end of infusion to decrease by 50%) was much faster than elimination half-life.

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