PONV Management
Based on the Fourth Consensus Guidelines for the Management of Postoperative Nausea and Vomiting (PONV)
Risk Assessment
Risk Factors
Patient-specific factors (evidence B1):
Female gender
History of PONV or motion sickness
Non-smoking status
Young age
Surgery-specific factors (evidence B1):
Laparoscopic procedures
Bariatric surgery
Gynecological surgery
Cholecystectomy
Anesthetic risk factors:
Volatile anesthetics (dose-dependent, especially first 2-6 hours) (evidence A1)
Nitrous oxide (duration-dependent, significant if >1 hour) (evidence A1)
Postoperative opioids (dose-dependent) (evidence A1)
Risk Scoring Systems for Adults
Apfel Score: 0, 1, 2, 3, or 4 risk factors correspond to PONV risks of approximately 10%, 20%, 40%, 60%, and 80%, respectively
Female gender
History of PONV/motion sickness
Non-smoking status
Postoperative opioid use
Risk Categories:
Low risk: 0-1 risk factors
Medium risk: 2 risk factors
High risk: 3+ risk factors
PDNV Risk Score (Post-Discharge Nausea and Vomiting):
Female gender
Age <50 years
History of PONV
Opioid use in PACU
Nausea in PACU
Prevention Strategies
General strategies
Use regional anesthesia instead of general anesthesia when possible
Propofol for induction and maintenance (TIVA)
Avoid nitrous oxide in surgeries lasting >1 hour
Avoid volatile anesthetics
Minimise intraoperative and postoperative opioids
Ensure adequate hydration (10-30 mL/kg crystalloids)
Consider using sugammadex instead of neostigmine for neuromuscular blockade reversal
Multimodal Analgesia to Reduce PONV
IV acetaminophen (given before onset of pain) (evidence A1)
NSAIDs (evidence A1)
COX-2 inhibitors (evidence A1)
Dexmedetomidine (evidence A1)
Esmolol (evidence A3)
Prophylactic Antiemetics for Adults
Major change in 2020 guidelines: Recommend multimodal prophylaxis (at least 2 antiemetics) for patients with 1 or more risk factors
5-HT3 Receptor Antagonists:
Ondansetron: 4 mg IV or 8 mg PO/ODT (evidence A1)
Granisetron: 0.35-3 mg IV (evidence A1)
Palonosetron: 0.075 mg IV (evidence A1)
Ramosetron: 0.3 mg IV (evidence A1)
NK1 Receptor Antagonists:
Aprepitant: 40 mg PO (evidence A1)
Fosaprepitant: 150 mg IV (evidence A1)
Corticosteroids:
Dexamethasone: 4-8 mg IV at induction (evidence A1)
Methylprednisolone: 40 mg IV (evidence A2)
Antidopaminergics:
Amisulpride: 5 mg IV (evidence A2)
Droperidol: 0.625 mg IV (evidence A1)
Haloperidol: 0.5-2 mg IM/IV (evidence A1)
Metoclopramide: 10 mg (evidence A1)
Other Agents:
Scopolamine: transdermal patch (evidence A1)
Dimenhydrinate: 1 mg/kg IV (evidence A1)
Gabapentin: 600-800 mg PO (evidence A1)
Midazolam: at induction (evidence A1)
Prophylactic Antiemetics for Children
Recommended agents:
Ondansetron: 50-100 μg/kg up to 4 mg (evidence A1)
Dexamethasone: 150 μg/kg up to 5 mg (evidence A1)
Combination of ondansetron + dexamethasone (evidence A1)
Treatment Approaches
Treatment of Established PONV
Key principle: Use antiemetic from a different pharmacological class than those used for prophylaxis
Do not repeat same class of antiemetic within 6 hours (evidence A2)
First-line options:
5-HT3 antagonists: ondansetron 4 mg IV, ramosetron 0.3 mg IV
Amisulpride 5-10 mg IV
Promethazine 6.25 mg IV
Droperidol 0.625 mg IV
For rescue after failed prophylaxis:
Consider NK1 receptor antagonists
Consider combination therapy with multiple antiemetics
Treatment of PDNV
Multimodal antiemetics are more effective than monotherapy
Consider extended-release formulations or longer-acting agents
Implementation strategies
Institutional Protocol Development
Implement PONV management protocols
Consider general multimodal prophylaxis for all at-risk patients
Ensure timely treatment of established PONV
Regular compliance and outcome measurements
Enhanced Recovery Pathways (ERPs)
PONV management is a vital component of ERPs
Multimodal prophylaxis recommended for all surgical patients with any risk factors
Baseline risk reduction strategies should be incorporated into ERPs
Key messages
Risk assessment should be performed for all patients
Multimodal prophylaxis (≥2 agents) is now recommended for patients with ≥1 risk factor
Use antiemetics from different classes for combination therapy
For treatment of established PONV, use an agent from a different class than prophylaxis
Consider both pharmacological and non-pharmacological approaches
Implement institutional protocols with regular monitoring and evaluation
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