Division of Nephrology, Department of Medicine, Duke University Medical Center, Durham, NC.
Division of Nephrology, Department of Medicine, Duke University Medical Center, Durham, NC; Renal Section, Durham VA Medical Center, Durham, NC.
Am J Kidney Dis. 2018 Feb;71(2):275-280. doi: 10.1053/j.ajkd.2017.07.005. Epub 2017 Sep 9.
Baclofen, a commonly prescribed muscle relaxant, is primarily excreted via the kidneys; toxicity is a potentially serious adverse outcome in patients with decreased kidney function. We describe a patient with end-stage kidney disease receiving hemodialysis who developed neurotoxicity and hemodynamic instability after receiving baclofen for muscle spasms. In this case, prompt recognition of baclofen toxicity and urgent hemodialysis were effective in reversing this toxicity. This case is used to examine the pharmacokinetics and pathophysiology of baclofen toxicity and discuss appropriate diagnosis and management of baclofen toxicity. We recommend reducing the baclofen dose in patients who have moderately reduced kidney function (estimated glomerular filtration rate, 30-60mL/min/1.73m) and avoiding use in patients with severely reduced kidney function (estimated glomerular filtration rate < 30mL/min/1.73m) or on renal replacement therapy.
巴氯芬是一种常用的肌肉松弛剂,主要通过肾脏排泄;对于肾功能下降的患者,毒性是一种潜在的严重不良后果。我们描述了一位接受血液透析的终末期肾病患者,在接受巴氯芬治疗肌肉痉挛后出现神经毒性和血流动力学不稳定。在这种情况下,及时识别巴氯芬毒性并紧急进行血液透析可有效逆转这种毒性。本病例用于检查巴氯芬毒性的药代动力学和病理生理学,并讨论巴氯芬毒性的适当诊断和管理。我们建议减少中度肾功能下降(估计肾小球滤过率 30-60mL/min/1.73m)患者的巴氯芬剂量,并避免在严重肾功能下降(估计肾小球滤过率 < 30mL/min/1.73m)或接受肾脏替代治疗的患者中使用。