What is the recommended dose of Meropenem (generic name) for a 42-year-old female patient with severe impaired renal function (creatinine level of 5.5)?

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Meropenem Dosing in Severe Renal Impairment

For a 42-year-old female with a serum creatinine of 5.5 mg/dL (indicating severe renal impairment with estimated creatinine clearance <30 mL/min), meropenem should be dosed at 500 mg every 24 hours, or 1000 mg every 24 hours for severe infections, unless the patient is receiving renal replacement therapy. 1, 2

Estimating Renal Function

  • With a serum creatinine of 5.5 mg/dL in a 42-year-old female, the estimated creatinine clearance is likely <10-15 mL/min, placing her in the severe renal impairment or end-stage renal disease category 2
  • Standard dosing of meropenem (1000 mg every 8 hours) would result in drug accumulation and potential toxicity in this patient 1

Recommended Dosing Regimen

For creatinine clearance <30 mL/min (not on dialysis):

  • Standard infections: 500 mg every 24 hours 1, 2
  • Severe infections or pathogens with MIC ≥2 mg/L: 1000 mg every 24 hours 1
  • The terminal half-life of meropenem is prolonged from 1 hour in healthy individuals to 10-13.7 hours in anuric patients 1, 2

If Patient is on Hemodialysis

  • Administer 500 mg after each hemodialysis session 1, 2
  • Approximately 50% of meropenem is removed during a hemodialysis session 1
  • The dialysis clearance is approximately 81 mL/min 2
  • Do not give supplemental doses between dialysis sessions unless treating severe infections 2

If Patient is on Continuous Renal Replacement Therapy (CRRT)

For continuous venovenous hemofiltration (CVVHF):

  • 500 mg every 8-12 hours is appropriate for most infections 3, 4
  • For severe infections or pathogens with MIC ≥4 mg/L: consider 1000 mg every 8 hours or continuous infusion 4
  • CVVHF removes 25-50% of meropenem, with hemofiltration clearance of approximately 22 mL/min 1, 3
  • The terminal half-life during CVVHF is approximately 8.7 hours 3

For continuous venovenous hemodiafiltration (CVVHDF):

  • Similar dosing to CVVHF, though CVVHDF may remove 13-53% of the drug depending on treatment parameters 1

Critical Considerations for Severe Infections

  • For infections caused by pathogens with MIC ≥8 mg/L, standard dosing may be insufficient even with dose adjustments 4
  • Consider continuous infusion (1000-2000 mg over 24 hours) for critically ill patients with severe infections and preserved residual renal function 4
  • Target attainment of 100% time above MIC is only achieved in 48.4% of critically ill patients with standard dosing when MIC is 2 mg/L 5

Monitoring Parameters

  • Check renal function (serum creatinine and estimated creatinine clearance) at baseline and monitor during therapy 2
  • For patients with fluctuating renal function, reassess dosing every 2-3 days 5
  • Monitor for signs of drug accumulation, particularly neurological symptoms (seizures can occur with excessive meropenem levels) 1

Common Pitfalls to Avoid

  • Do not use standard dosing (1000 mg every 8 hours) in patients with creatinine clearance <30 mL/min, as this will lead to drug accumulation 1, 2
  • Do not rely solely on serum creatinine without calculating creatinine clearance, especially in patients with low muscle mass 6
  • Do not underdose in patients on CRRT—the recommended dose should be increased by up to 100% compared to anuric patients not receiving renal replacement therapy 3
  • Recognize that meropenem and its metabolite are effectively removed by hemodialysis, requiring post-dialysis dosing 2

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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