Department of Pharmacotherapy, College of Pharmacy, University of North Texas Health Sciences Center, Fort Worth, TX, USA.
Wise Regional Health System Emergency Department, Decatur, TX, USA.
Ann Pharmacother. 2024 May;58(5):523-532. doi: 10.1177/10600280231193080. Epub 2023 Aug 17.
This review highlights adverse effects of baclofen and tizanidine in older community-dwelling adults.
A literature search was conducted, including search terms of "adverse effect," "baclofen," "elderly," "falls," "fractures," and "tizanidine." Studies were included if they described community-dwelling adults aged 50 years and older who received oral baclofen or tizanidine. The Federal Drug Administration Adverse Event Reporting System (FAERS) data were compiled for adverse effect incidence.
The literature search was completed in July 2019 and updated in June 2023. Reviews performed by 2 independent reviewers yielded 15 records. FAERS identified 486 (baclofen) and 305 (tizanidine) adverse effects of interest.
Two retrospective cohort studies evaluating baclofen use in older adults showed increased hospitalizations for encephalopathy in chronic kidney disease (7.2% vs 0.1%) and end-stage renal disease (daily dose 20 mg or more; relative risk [RR] 19.8, 95% CI = [14.0-28.0]). Other articles were case reports; 10 articles reported dyskinesias, encephalopathy or disorientation, and drowsiness associated with baclofen, and 5 articles reported bradycardia and/or hypotension with tizanidine. The FAERS Public Dashboard revealed 12.1% and 28.7% overall incidence of adverse effects of interest, with a 27.8% and 29.2% incidence of falls for baclofen and tizanidine, respectively. Baclofen and tizanidine are associated with concerning adverse effects in older adults. Alternative agents should be considered, but, if necessary, providers should start at lower doses and increase slowly.
This review highlights the importance of using baclofen and tizanidine with caution in older adults.
本综述强调了巴氯芬和替扎尼丁在老年社区居民中的不良影响。
进行了文献检索,包括使用“不良影响”、“巴氯芬”、“老年人”、“跌倒”、“骨折”和“替扎尼丁”等术语。如果研究描述了年龄在 50 岁及以上、接受口服巴氯芬或替扎尼丁治疗的社区居民,则将其纳入研究。联邦药物管理局不良事件报告系统(FAERS)数据被汇编用于不良影响发生率。
文献检索于 2019 年 7 月完成,并于 2023 年 6 月更新。两名独立评审员进行的综述产生了 15 条记录。FAERS 确定了 486 例(巴氯芬)和 305 例(替扎尼丁)感兴趣的不良影响。
两项评估老年人群中使用巴氯芬的回顾性队列研究表明,慢性肾脏病(发生率为 0.1%)和终末期肾病(每日剂量 20 毫克或更高)患者的脑病住院率增加(发生率为 7.2%;相对风险 [RR],19.8;95%置信区间 [14.0-28.0])。其他文章是病例报告;10 篇文章报告了巴氯芬引起的运动障碍、脑病或定向障碍和嗜睡,5 篇文章报告了替扎尼丁引起的心动过缓和/低血压。FAERS 公共仪表板显示,感兴趣的不良影响总发生率分别为 12.1%和 28.7%,巴氯芬和替扎尼丁的跌倒发生率分别为 27.8%和 29.2%。巴氯芬和替扎尼丁与老年患者的不良影响有关。应考虑替代药物,但如果需要,应从较低剂量开始并缓慢增加。
本综述强调了在老年人群中谨慎使用巴氯芬和替扎尼丁的重要性。