Research Center, CIUSSS du Nord-de-l'île-de-Montréal, Hôpital du Sacré-Coeur de Montréal, University of Montreal, Montreal, Quebec, Canada.
Emergency Department and Clinical Toxicology Unit, Hospital Universitari Son Espases, SAMU 061, Balears, Spain; IdISBa Clinical Toxicology Workgroup, Palma de Mallorca, Spain.
Am J Kidney Dis. 2022 Jan;79(1):88-104. doi: 10.1053/j.ajkd.2021.06.027. Epub 2021 Nov 17.
Toxicity from gabapentin and pregabalin overdose is commonly encountered. Treatment is supportive, and the use of extracorporeal treatments (ECTRs) is controversial. The EXTRIP workgroup conducted systematic reviews of the literature and summarized findings following published methods. Thirty-three articles (30 patient reports and 3 pharmacokinetic studies) met the inclusion criteria. High gabapentinoid extracorporeal clearance (>150mL/min) and short elimination half-life (<5 hours) were reported with hemodialysis. The workgroup assessed gabapentin and pregabalin as "dialyzable" for patients with decreased kidney function (quality of the evidence grade as A and B, respectively). Limited clinical data were available (24 patients with gabapentin toxicity and 7 with pregabalin toxicity received ECTR). Severe toxicity, mortality, and sequelae were rare in cases receiving ECTR and in historical controls receiving standard care alone. No clear clinical benefit from ECTR could be identified although major knowledge gaps were acknowledged, as well as costs and harms of ECTR. The EXTRIP workgroup suggests against performing ECTR in addition to standard care rather than standard care alone (weak recommendation, very low quality of evidence) for gabapentinoid poisoning in patients with normal kidney function. If decreased kidney function and coma requiring mechanical ventilation are present, the workgroup suggests performing ECTR in addition to standard care (weak recommendation, very low quality of evidence).
加巴喷丁和普瑞巴林过量中毒较为常见。治疗方法为支持性治疗,而体外治疗(ECTR)的应用存在争议。EXTRIP 工作组对文献进行了系统评价,并按照已发表的方法总结了研究结果。符合纳入标准的文章共有 33 篇(30 篇患者报告和 3 项药代动力学研究)。血液透析可实现较高的加巴喷丁类药物体外清除率(>150ml/min)和较短的消除半衰期(<5 小时)。工作组评估认为对于肾功能降低的患者,加巴喷丁和普瑞巴林具有“可透析性”(证据质量等级分别为 A 和 B)。虽然有 24 例加巴喷丁中毒和 7 例普瑞巴林中毒患者接受了 ECTR,但可获得的临床数据有限,仅接受标准治疗的患者也有严重毒性、死亡率和后遗症。尽管存在主要知识空白、成本和 ECTR 危害,但在接受 ECTR 治疗的患者和接受标准治疗的历史对照患者中,均未发现 ECTR 有明确的临床获益。EXTRIP 工作组建议,对于肾功能正常的加巴喷丁类药物中毒患者,不建议在标准治疗的基础上联合 ECTR 治疗(弱推荐,极低质量证据)。如果存在肾功能降低和需要机械通气的昏迷,工作组建议在标准治疗的基础上联合 ECTR 治疗(弱推荐,极低质量证据)。