Department of Pharmacy, Kaetsu Hospital.
Department of Internal Medicine, Kaetsu Hospital.
Biol Pharm Bull. 2020;43(8):1275-1278. doi: 10.1248/bpb.b20-00216.
Although distigmine is known to sometimes cause severe adverse drug reactions (ADRs), such as cholinergic crisis, there are limited data on the risk factors for these ADRs. In this study, we defined a serum cholinesterase (sChE) cutoff level for early detection of ADRs to distigmine and sought to identify risk factors for these ADRs based on this value. This retrospective cohort study included all patients who were prescribed distigmine and underwent measurement of sChE over a period of 8 years at Kaetsu Hospital. Ninety-three patients were included. The sChE cutoff level below which there was an increase in risk of ADRs was defined as 129 U/L based on the levels in patients who had ADRs by receiver operating characteristic analysis. The percentage of ADRs tended to increase with advancing chronic kidney disease (CKD) stage. Multivariate logistic regression analyses showed that a distigmine dose >0.1 mg/kg/d (odds ratio 3.19, 95% confidence interval 1.24-8.19) and age >85 years (odds ratio 3.04, 95% confidence interval 1.18-7.82) were positively associated with an sChE level ≤129 U/L. An sChE cutoff level of 129 U/L is a useful predictor of the risk of an ADR to distigmine, and dose per body weight, age, and CKD progression may pose potential risk of an ADR to distigmine. Therefore, for patients taking distigmine who have these risk factors, the risk of a severe ADR to distigmine can be reduced by decreasing the dose of distigmine and close monitoring of the sChE level.
虽然已知地美溴铵有时会引起严重的药物不良反应(ADR),如胆碱能危象,但关于这些 ADR 的危险因素的数据有限。在本研究中,我们定义了一个血清胆碱酯酶(sChE)的截止值,用于早期检测地美溴铵的 ADR,并试图根据该值确定这些 ADR 的危险因素。这项回顾性队列研究包括了在 8 年内,在桂由医院接受地美溴铵治疗并检测 sChE 的所有患者。共纳入 93 例患者。根据 ADR 患者的 sChE 水平,通过受试者工作特征分析,我们将 ADR 风险增加的 sChE 截止值定义为 129U/L。随着慢性肾脏病(CKD)分期的进展,ADR 的比例有增加的趋势。多变量逻辑回归分析显示,地美溴铵剂量>0.1mg/kg/d(比值比 3.19,95%置信区间 1.24-8.19)和年龄>85 岁(比值比 3.04,95%置信区间 1.18-7.82)与 sChE 水平≤129U/L 呈正相关。sChE 截止值为 129U/L 对地美溴铵 ADR 风险具有预测价值,而剂量与体重、年龄和 CKD 进展可能对地美溴铵的 ADR 风险构成潜在威胁。因此,对于服用地美溴铵且具有这些危险因素的患者,通过减少地美溴铵的剂量和密切监测 sChE 水平,可以降低地美溴铵严重 ADR 的风险。