Gabapentin Dosing in Patients with Renal Impairment (eGFR 57)
For a patient with an eGFR of 57 mL/min, gabapentin should be initiated at a lower dose of 100-300 mg at bedtime or 100-300 mg three times daily, with slower titration by increasing the dose by 100-300 mg every 1-7 days as tolerated, due to reduced renal clearance. 1, 2
Pharmacokinetics and Renal Considerations
- Gabapentin is primarily eliminated unchanged by renal excretion, with clearance directly proportional to creatinine clearance 3
- In patients with normal renal function (creatinine clearance >60 mL/min), gabapentin's half-life is approximately 6.5 hours 3
- As renal function declines, gabapentin's half-life increases significantly - up to 52 hours in patients with creatinine clearance <30 mL/min 3
- Mean plasma clearance (CL/F) decreases from approximately 190 mL/min in normal renal function to 20 mL/min in severe renal impairment 3
Dosing Recommendations for eGFR 57
- For patients with moderate renal impairment (eGFR 30-59 mL/min), dosage reduction is necessary 1, 2
- Start with a lower dose of 100-300 mg at bedtime or 100-300 mg three times daily 1, 2
- Titrate more slowly than in patients with normal renal function, increasing by 100-300 mg every 1-7 days as tolerated 1
- Monitor closely for adverse effects during titration, particularly dizziness and sedation 1, 2
Monitoring and Adverse Effects
- Common dose-dependent adverse effects include dizziness and sedation, which can be minimized by starting with lower doses and titrating cautiously 1, 2
- In patients with renal impairment, gabapentin toxicity can manifest as altered consciousness, myoclonus, confusion, and even hearing loss 4, 5
- Regular monitoring of renal function is recommended, as further decline in renal function would necessitate additional dose adjustments 6
- Patients should be educated about potential adverse effects and instructed to report any new or worsening symptoms 4
Special Considerations
- Hemodialysis significantly reduces gabapentin levels - during dialysis, the half-life decreases to approximately 3.8 hours from 132 hours on non-dialysis days 3, 7
- For patients who progress to end-stage renal disease requiring hemodialysis, supplemental doses may be needed after dialysis sessions 7
- Gabapentin has minimal drug interactions as it is not metabolized by the liver and has negligible protein binding 3
- Avoid concurrent use of CNS depressants when possible, as they may potentiate sedative effects 1
Practical Approach to Dosing
- Start with 100-300 mg at bedtime or 100-300 mg three times daily 1, 2
- Increase dose by 100-300 mg every 1-7 days as tolerated 1
- Monitor for adverse effects (dizziness, sedation, confusion) 1, 4
- Target effective dose based on clinical response and tolerability 1
- Maximum daily dose should be lower than the 3600 mg/day used in patients with normal renal function 1, 2
- Reassess dosing if renal function changes 6, 8
Remember that gabapentin accumulation due to reduced renal clearance can lead to serious adverse effects, so a conservative approach to dosing is warranted in patients with renal impairment 4, 5, 8.