Department of Public Health and Institute of Public Health, Chung Shan Medical University, Taichung City, Taiwan.
Department of Neurology, Lu-Tung Christian Hospital, Changhua, Taiwan.
Sci Rep. 2019 Feb 8;9(1):1705. doi: 10.1038/s41598-018-37901-z.
Flunarizine (fz) causes side effects such as movement disorders (MDs). We investigated risk factors associated with fz-related MDs. Participants were recruited from the longitudinal health insurance databases and included patients who took fz for more than 1 month. Patients with one of the underlying diseases, or with concomitant drug use (antipsychotics, metoclopramide or reserpine), and those diagnosed with MDs before fz use were excluded. Fz-related MD was defined as a new diagnosis of parkinsonism or hyperkinetic syndrome including dyskinesia or secondary dystonia during fz use or within 3 months after drug discontinuation. After exposure, 288 individuals had fz-related MDs (parkinsonism, n = 240; hyperkinesia, n = 48). Risk factors associated with these disorders were higher-dose exposure (cumulative defined daily dose [cDDD] ≥87.75, odds ratio [OR]: 3.80; 95% CI: 2.61-5.52), older age (OR: 1.07; 95% CI: 1.06-1.09), history of essential tremor (OR: 6.39; 95% CI: 2.29-17.78) and cardiovascular disease (CVD) (OR: 1.47; 95% CI: 1.14-1.9). The optimal value of cDDD to predict MDs was 58.5 (sensitivity: 0.67, specificity: 0.60), indicating an overall exposure of 585 mg. Higher exposure dose and duration, older age, history of essential tremor, and CVD were associated with fz-associated MDs. Clinicians ought to watch for extrapyramidal side effects when prescribing fz.
氟桂利嗪(fz)会引起运动障碍(MDs)等副作用。我们研究了与 fz 相关 MDs 相关的危险因素。参与者从纵向健康保险数据库中招募,包括服用 fz 超过 1 个月的患者。排除患有潜在疾病之一或同时使用药物(抗精神病药、甲氧氯普胺或利血平)的患者,以及在使用 fz 之前被诊断为 MDs 的患者。fz 相关 MDs 定义为在使用 fz 期间或停药后 3 个月内新诊断为帕金森病或多动综合征,包括运动障碍或继发性肌张力障碍。暴露后,288 人出现 fz 相关 MDs(帕金森病,n=240;多动,n=48)。与这些疾病相关的危险因素包括更高剂量的暴露(累积定义日剂量[cDDD]≥87.75,比值比[OR]:3.80;95%CI:2.61-5.52)、年龄较大(OR:1.07;95%CI:1.06-1.09)、特发性震颤史(OR:6.39;95%CI:2.29-17.78)和心血管疾病(CVD)(OR:1.47;95%CI:1.14-1.9)。预测 MDs 的最佳 cDDD 值为 58.5(灵敏度:0.67,特异性:0.60),表明总体暴露量为 585mg。更高的暴露剂量和持续时间、年龄较大、特发性震颤史和 CVD 与 fz 相关 MDs 相关。临床医生在开处方时应注意锥体外系副作用。