Kuriyama Akira, Jackson Jeffrey L, Doi Asako, Kamiya Toru
Department of General Internal Medicine, Rakuwakai Otowa Hospital, Kyoto, Japan.
Clin Neuropharmacol. 2011 Nov-Dec;34(6):241-7. doi: 10.1097/WNF.0b013e3182334b35.
To assess patient and medication factors that contribute to metronidazole toxicity.
We searched PUBMED from 1965 through April 7, 2011, and performed a hand search of bibliographies.
Case reports or case series reporting metronidazole-induced central nervous toxicity.
Two authors independently abstracted demographics, metronidazole indication, dose and duration, neurological manifestations, and outcomes as well as brain imaging findings.
Among 64 patients, 48 (77%) had cerebellar dysfunction, 21 (33%) had altered mental status, and 8 (15%) had seizures. Patients' ages averaged 53.3 years (range, 12-87 years), and 64% were male. The median duration of metronidazole was 54 days, although 26% had taken it less than a week and 11% had taken it less than 72 hours. Among cases with outcome data, most patients either improved (n = 18 [29%]) or had complete resolution of their symptoms with discontinuation of metronidazole (n = 41 [65%]). There was no difference in resolution of symptom by age (P = 0.71) or sex (P = 0.34). The patients with cerebellar dysfunction were less likely to experience complete resolution than those with mental status changes or seizures (relative risk, 0.67; 95% confidence interval (CI), 0.49-0.92). Nearly all patients (n = 55 [86%]) underwent imaging of the brain: 44 (69%) underwent magnetic resonance imaging (MRI) and 12 (19%) underwent computed tomographic studies. All patients with cerebellar dysfunction had abnormalities on imaging: 93% (n = 39) had a cerebellar lesion, although numerous areas in the brain were affected. On follow-up MRIs, 25 patients (83%) had complete resolution of abnormalities.
Metronidazole can rarely cause central nervous system toxicity; it does not seem to be a dose- or duration-related phenomenon. Most patients will have MRI abnormalities. Prognosis is excellent with metronidazole cessation.
评估导致甲硝唑毒性的患者因素和药物因素。
我们检索了1965年至2011年4月7日的PubMed,并对手头文献进行了检索。
报告甲硝唑诱发中枢神经毒性的病例报告或病例系列。
两名作者独立提取了人口统计学信息、甲硝唑适应证、剂量和疗程、神经学表现、结局以及脑成像结果。
64例患者中,48例(77%)有小脑功能障碍,21例(33%)有精神状态改变,8例(15%)有癫痫发作。患者平均年龄为53.3岁(范围12 - 87岁),64%为男性。甲硝唑的中位疗程为54天,尽管26%的患者用药时间不到一周,11%的患者用药时间不到72小时。在有结局数据的病例中,大多数患者症状改善(n = 18 [29%])或停用甲硝唑后症状完全缓解(n = 41 [65%])。症状缓解情况在年龄(P = 0.71)或性别(P = 0.34)方面无差异。与有精神状态改变或癫痫发作的患者相比,有小脑功能障碍的患者症状完全缓解的可能性较小(相对风险,0.67;95%置信区间[CI],0.49 - 0.92)。几乎所有患者(n = 55 [86%])都进行了脑部成像:44例(69%)进行了磁共振成像(MRI),12例(19%)进行了计算机断层扫描研究。所有有小脑功能障碍的患者成像均有异常:93%(n = 39)有小脑病变,尽管脑部多个区域均受影响。在随访MRI中,25例患者(83%)异常完全消失。
甲硝唑很少引起中枢神经系统毒性;这似乎不是剂量或疗程相关现象。大多数患者MRI会有异常。停用甲硝唑后预后良好。