What are the appropriate total intravenous anesthesia (TIVA) doses of propofol, fentanyl, and remifentanil for a 110‑kg adult undergoing a spine procedure?

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TIVA Dosing for 110 kg Patient Undergoing Spine Surgery

For a 110 kg adult undergoing spine surgery, use propofol target-controlled infusion (effect-site concentration 0.5-1 mcg/mL), remifentanil infusion (0.05-0.3 mcg/kg/min), and maintain BIS monitoring at 40-60 throughout the procedure. 1, 2

Pre-Induction Preparation

  • Establish invasive arterial blood pressure monitoring before induction with transducer at tragus level 1, 2
  • Have vasopressors immediately available (ephedrine or metaraminol) to treat propofol-induced hypotension 1, 2
  • Ensure quantitative neuromuscular monitoring equipment is ready 1, 2

Induction Protocol

Opioid Selection and Dosing

Choose either fentanyl OR remifentanil for induction:

Fentanyl option:

  • Administer fentanyl 5 mcg/kg IV (550 mcg for 110 kg patient) over 2-3 minutes 1
  • Give 3-5 minutes before propofol to allow peak effect during laryngoscopy 3

Remifentanil option (preferred for spine surgery):

  • Start remifentanil infusion at 0.5 mcg/kg/min (55 mcg/min for 110 kg patient) for 5 minutes before propofol 2, 4
  • This reduces propofol requirements by approximately 29% and provides faster induction 4

Hypnotic Induction

  • Administer propofol 2 mg/kg IV bolus (220 mg for 110 kg patient) for rapid onset 1
  • Avoid excessive bolus dosing to prevent hemodynamic instability 5, 1
  • Critical caveat: Expect mean arterial pressure to decrease by 26% with propofol-remifentanil combination 4

Muscle Relaxation

  • Administer rocuronium 0.9-1.2 mg/kg (99-132 mg for 110 kg patient) for intubation 5, 2
  • Alternative: succinylcholine 1-2 mg/kg (110-220 mg) if rocuronium unavailable 5
  • Give neuromuscular blocking agent immediately after loss of consciousness to prevent fentanyl-induced rigidity 3

Maintenance Protocol

Propofol Maintenance

  • Use propofol target-controlled infusion with effect-site concentration of 0.5-1 mcg/mL 1, 2
  • Never exceed 1.5 mcg/mL as this significantly increases risk of over-sedation and hypoventilation 5, 1
  • Avoid bolus dosing during maintenance 5, 1
  • Expected infusion rate: approximately 81 mcg/kg/min (8,910 mcg/min or 534 mg/hour for 110 kg patient) 6

Opioid Maintenance

Remifentanil maintenance (preferred for spine surgery):

  • Reduce remifentanil to 0.05-0.3 mcg/kg/min (5.5-33 mcg/min for 110 kg patient) after intubation 2, 7
  • Titrate within this range to control intraoperative responses while allowing rapid emergence 7
  • Key advantage: Context-sensitive half-time of 3 minutes allows rapid recovery regardless of infusion duration 7

Fentanyl maintenance (if used for induction):

  • Give supplemental boluses of 2 mcg/kg (220 mcg for 110 kg patient) as needed for inadequate analgesia 1
  • Important limitation: Fentanyl has longer duration requiring careful timing before emergence 3

Optional Adjuncts for Enhanced Recovery

  • Consider ketamine 0.5 mg/kg bolus (55 mg) followed by 0.1-0.2 mg/kg/h infusion (11-22 mg/hour) to reduce opioid requirements 1, 2
  • Consider dexmedetomidine 0.5-1 mcg/kg bolus (55-110 mcg) then 0.2-0.7 mcg/kg/h (22-77 mcg/hour) to minimize postoperative pain 2

Intraoperative Monitoring Requirements

  • Use BIS monitoring targeting 40-60 throughout procedure 1, 2
  • Avoid BIS values below 35 in patients over 60 years to reduce postoperative delirium risk 5, 1, 2
  • Use quantitative neuromuscular monitoring when muscle relaxants administered 1, 2
  • Monitor standard ASA parameters including pulse oximetry, capnography, ECG, invasive arterial blood pressure 1
  • Monitor core temperature routinely 1

Emergence Protocol

  • Discontinue propofol and opioid infusions 5-10 minutes before anticipated end of surgery 1, 2
  • With remifentanil: Expect recovery within 3-7 minutes regardless of case duration 7
  • With fentanyl: Recovery may be delayed; respiratory depression may persist postoperatively in approximately 10% of patients 3
  • Document train-of-four ratio ≥0.90 with quantitative monitoring before extubation 1, 2
  • Ensure return of airway reflexes and adequate tidal volumes before extubation 1, 2

Critical Dosing Considerations for 110 kg Patient

Weight-based calculations:

  • Consider using lean body weight for propofol dosing in obese patients to avoid overdosing 5, 1
  • For 110 kg patient, if BMI >30, calculate lean body weight and adjust propofol accordingly 5
  • Opioid dosing typically uses total body weight 3

Hemodynamic management:

  • Propofol increases vasopressor requirements, especially in hemodynamically challenged patients 5
  • Remifentanil causes greater blood pressure reduction than fentanyl during induction (mean arterial pressure decrease of 26% vs 18% with thiopental) 4
  • Have vasopressors drawn up and ready before induction 1, 2

Common Pitfalls to Avoid

  • Do not use bolus dosing of propofol during maintenance - this causes hemodynamic instability 5, 1
  • Do not exceed propofol effect-site concentration of 1.5 mcg/mL - significantly increases over-sedation risk 5, 1
  • Do not give fentanyl immediately before propofol - allow 3-5 minutes for peak effect 3
  • Do not forget neuromuscular monitoring - mandatory when using muscle relaxants 1, 2
  • Do not allow BIS <35 in elderly patients - increases postoperative delirium risk 5, 1, 2

References

Guideline

Anesthesia Protocol for Endoscopic Spine Surgery

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Effective TIVA Protocol for Prolonged Endoscopic Spine Surgery

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Fentanyl Dosing for Induction of Anesthesia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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