What is the recommended IV dose of metoclopramide (Metoclopramide) for a patient with Chronic Kidney Disease (CKD) grade 5?

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Metoclopramide IV Dosing in CKD Grade 5

For patients with CKD grade 5 (creatinine clearance <15 mL/min), initiate metoclopramide IV at approximately 5 mg (half the standard 10 mg dose) administered slowly over 1-2 minutes, with subsequent doses adjusted based on clinical efficacy and safety. 1

Dose Reduction Rationale

  • Metoclopramide is principally excreted through the kidneys, making dose reduction essential in severe renal impairment to prevent drug accumulation and toxicity 1
  • The FDA label explicitly states that therapy should be initiated at approximately one-half the recommended dosage when creatinine clearance is below 40 mL/min 1
  • CKD grade 5 represents creatinine clearance <15 mL/min, which falls well below this 40 mL/min threshold and necessitates the 50% dose reduction 1

Specific Dosing Recommendations by Indication

For Diabetic Gastroparesis

  • Start with 5 mg IV (half of the standard 10 mg dose) administered slowly over 1-2 minutes 1
  • May administer intramuscularly or intravenously depending on symptom severity 1
  • Treatment may continue up to 10 days before transitioning to oral therapy if symptoms improve 1

For Chemotherapy-Induced Nausea/Vomiting

  • Reduce the standard dose by 50%: use 1 mg/kg (instead of 2 mg/kg) for highly emetogenic regimens, or 0.5 mg/kg (instead of 1 mg/kg) for less emetogenic regimens 1
  • Administer as slow IV infusion over at least 15 minutes 1
  • Dilute doses exceeding 5 mg in 50 mL of parenteral solution 1

For Postoperative Nausea/Vomiting

  • Use 5 mg IM or IV (half of the standard 10 mg dose) near the end of surgery 1
  • The standard 20 mg dose option should be reduced to 10 mg in CKD grade 5 1

For Small Bowel Intubation or Radiological Examination

  • Administer 5 mg IV (half of the standard 10 mg dose) as a single dose over 1-2 minutes 1

Critical Safety Considerations

  • Monitor for extrapyramidal reactions and sedation, which may be more pronounced with reduced drug clearance in severe CKD 1
  • The elimination half-life of metoclopramide increases from 5-6 hours in normal renal function to significantly longer durations as creatinine clearance decreases 1
  • Metoclopramide undergoes minimal hepatic metabolism, so dose adjustment is primarily driven by renal function rather than liver disease 1

Dose Titration Strategy

  • Begin with the 50% reduced dose as outlined above 1
  • Adjust upward or downward based on clinical efficacy and safety considerations, but maintain caution given the reduced clearance 1
  • The linear kinetics of metoclopramide remain intact even in renal impairment, though clearance is substantially reduced 1

Comparative Efficacy in Uremia

  • Research demonstrates that ondansetron (8 mg IV) is approximately twice as effective as metoclopramide (10 mg IV) for uremia-induced nausea and vomiting 2
  • If metoclopramide proves inadequate at the reduced dose, consider switching to ondansetron rather than escalating metoclopramide dose in CKD grade 5 patients 2, 3

Dialysis Considerations

  • Metoclopramide is dialyzable, though the FDA label provides limited specific guidance on post-dialysis dosing 1
  • Standard doses of metoclopramide (≤0.2 mg/kg) do not antagonize renal effects of low-dose dopamine in critically ill patients, should concurrent therapy be necessary 4

Common Pitfalls to Avoid

  • Do not use standard 10 mg doses without dose reduction in CKD grade 5, as this leads to drug accumulation 1
  • Avoid assuming hepatic metabolism compensates for reduced renal clearance—metoclopramide relies primarily on renal elimination 1
  • Do not extend dosing intervals as the primary adjustment strategy; the FDA recommends reducing individual doses while maintaining standard intervals 1

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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