What is the recommended dose of Zofran (ondansetron) for a 20-month-old child weighing 13.5 kilograms?

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Ondansetron Dosing for a 20-Month-Old Weighing 13.5 kg

For a 20-month-old child weighing 13.5 kg, the recommended ondansetron dose is 0.15 mg/kg, which equals approximately 2 mg per dose. 1

Weight-Based Dosing Calculation

  • At 13.5 kg, this child falls below the 15 kg threshold used in most pediatric dosing guidelines 1
  • Using the standard 0.15 mg/kg/dose recommendation: 13.5 kg × 0.15 mg/kg = 2.025 mg (round to 2 mg) 1
  • The maximum single dose should not exceed 16 mg 1

Age-Specific Safety Considerations

  • Ondansetron is recommended for infants ≥6 months of age, and at 20 months, this child is well within the safe age range 1
  • For infants <6 months, ondansetron should only be used if the situation is judged critical due to limited safety and efficacy data 1

Clinical Context and Indications

  • Ondansetron is most commonly used in pediatrics for:
    • Chemotherapy-induced nausea and vomiting: Multiple 0.15 mg/kg IV doses have shown efficacy, with 70-72% of children experiencing ≤2 emetic episodes 2
    • Postoperative nausea and vomiting: 0.1-0.15 mg/kg IV has proven significantly superior to placebo and other antiemetics 2
    • Acute gastroenteritis with vomiting: Reduces emesis during oral rehydration and lowers rates of IV fluid administration and hospital admission 3
    • Food Protein-Induced Enterocolitis Syndrome (FPIES): 0.15 mg/kg/dose for moderate to severe reactions 1

Route of Administration

  • Oral route: Bioavailability is approximately 60%, with peak plasma concentrations at 1 hour after administration 4, 5
  • Intravenous route: Preferred when IV access is already established, particularly in severe presentations requiring fluid resuscitation 1
  • Intramuscular route: Preferred when IV access is difficult or delayed 1
  • Ondansetron should be administered at least 30 minutes before chemotherapy when used prophylactically 6

Dosing Frequency

  • Standard dosing: 0.15 mg/kg per dose, which can be repeated every 8 hours as needed 4, 2
  • For chemotherapy-induced emesis, the typical regimen is three doses on the day of chemotherapy (30 minutes before, then 4 and 8 hours afterward) 4
  • For gastroenteritis, additional doses every 8 hours may be given after discharge 3

Important Safety Points and Monitoring

  • Common adverse effects include headache (most frequent), constipation, and diarrhea 2, 5
  • Ondansetron is notably free of extrapyramidal side effects, unlike metoclopramide or prochlorperazine 5
  • In gastroenteritis patients, ondansetron may increase episodes of diarrhea during the 48-hour follow-up period 3
  • Monitor for response over 4-6 hours from onset of treatment 1
  • Ondansetron is generally well tolerated and rarely necessitates treatment withdrawal 2

Pharmacokinetic Considerations

  • Elimination half-life: Approximately 3.5 hours in healthy volunteers, but shorter in pediatric patients due to increased clearance 4, 5
  • Hepatic metabolism accounts for 95% of clearance; <5% is excreted unchanged in urine 5
  • No dosage adjustment needed based on age alone in children ≥6 months 1

Common Pitfalls to Avoid

  • Do not underdose: The 0.15 mg/kg dose has been validated in multiple studies and should not be reduced arbitrarily 1, 2
  • Avoid use in infants <6 months unless the clinical situation is critical 1
  • Do not rely on ondansetron alone for delayed chemotherapy-induced emesis, as efficacy for delayed symptoms has not been well established 4
  • Consider combination with dexamethasone in chemotherapy settings, as this significantly improves antiemetic efficacy 2

References

Guideline

Ondansetron Dosing Guidelines for Infants

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Ondansetron: a novel antiemetic agent.

Southern medical journal, 1993

Research

Ondansetron clinical pharmacokinetics.

Clinical pharmacokinetics, 1995

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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