What is the recommended dose of Augmentin (amoxicillin/clavulanic acid) for a patient with moderate renal impairment (eGFR 49.5)?

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Augmentin Dosing for eGFR 49.5 mL/min/1.73 m²

For a patient with eGFR 49.5 mL/min/1.73 m² (CKD Stage 3a), standard Augmentin dosing can be used without dose adjustment, as renal dose modifications are only required when eGFR falls below 30 mL/min/1.73 m². 1

Rationale for Standard Dosing

  • No dose adjustment is necessary for eGFR >30 mL/min/1.73 m² because both amoxicillin and clavulanic acid maintain adequate clearance at this level of renal function 1

  • The pharmacokinetic study in patients with varying degrees of renal impairment demonstrated that total body clearance of both amoxicillin and clavulanic acid remains sufficient until GFR drops below 35 mL/min/1.73 m² 1

  • At eGFR 49.5 mL/min/1.73 m², the patient falls into the GFR range of 35-75 mL/min, where the ratio of amoxicillin to clavulanic acid exposure (5.3 ± 2.4) remains close to normal (4.9 ± 1.2 at GFR 75 mL/min), indicating balanced drug disposition 1

Recommended Dosing Regimens

Standard adult dosing options include:

  • 875 mg/125 mg orally twice daily for most infections 2
  • 500 mg/125 mg orally three times daily as an alternative for less severe infections 2
  • 1000 mg/200 mg intravenously every 8 hours for severe infections requiring parenteral therapy 3, 4

Important Clinical Considerations

  • Monitor renal function periodically during treatment, as acute changes in kidney function could necessitate dose adjustment if eGFR drops below 30 mL/min/1.73 m² 5

  • Dose reduction becomes necessary only when eGFR <30 mL/min/1.73 m², at which point the dosing interval should be extended or the dose reduced to prevent amoxicillin accumulation while maintaining adequate clavulanic acid levels 1

  • The most pronounced accumulation occurs with amoxicillin rather than clavulanic acid in renal impairment, as clavulanic acid maintains relatively preserved non-renal clearance 1, 3

Common Pitfalls to Avoid

  • Do not unnecessarily reduce the dose in patients with eGFR >30 mL/min/1.73 m², as this may lead to subtherapeutic levels and treatment failure 1

  • Avoid confusing CKD stage with dosing requirements: CKD Stage 3a (eGFR 45-59) and 3b (eGFR 30-44) both allow standard dosing, while dose adjustment is reserved for Stage 4 and beyond (eGFR <30) 5

  • Be aware that gastrointestinal side effects (nausea, vomiting, diarrhea) occur with similar frequency regardless of renal function and are not an indication for dose reduction 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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