Risk of Cardiovascular Events in Schizophrenic Patients Treated with Paliperidone Palmitate Once-Monthly Injection (PP1M): A Population-Based Retrospective Cohort Study in Taiwan

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY Clinical Drug Investigation Pub Date : 2024-04-15 DOI:10.1007/s40261-024-01358-y
Shih-Pei Shen, Li Yan, Tao Wu, Min-Wei Huang, Kuan-Chih Huang, Hong Qiu, Yongjing Zhang, Chao-Hsiun Tang
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Abstract

Background

Schizophrenia is one of the leading causes of disability. Paliperidone palmitate once-monthly injection (PP1M) was developed to provide consistent drug delivery and improve medication adherence for maintenance treatment. It is well known that patients with schizophrenia have higher cardiovascular risks, however little is known about the cardiovascular risks of patients with schizophrenia treated with PP1M in Asia.

Objective

This study aimed to estimate the incidence of cardiovascular events after initiating PP1M treatment and evaluate the cardiovascular risk associations compared with oral second-generation antipsychotics (SGAs).

Methods

Data from Taiwan’s National Health Insurance Research Database were used to identify a cohort of adult patients with schizophrenia who received any SGAs from 1 March 2012 to 31 December 2018. Patients who initiated PP1M treatment were enrolled for descriptive analysis of incidence rates. PP1M patients were propensity matched 1:1 to patients initiating a new oral SGA, for comparative analysis based on demographics, clinical characteristics and treatment history at baseline, in three-step matching procedures, following the prevalent new-user design to enhance comparability. Follow-up ended at the end of the treatment episode of index drug, death, last record available, or end of the study (31 December 2019). Study endpoints included serious cardiovascular events (including severe ventricular arrhythmia and sudden death), expanded serious cardiovascular events (which further included acute myocardial infarction and ischemic stroke), and cardiovascular hospitalizations. Risks of study endpoints between matched cohorts were compared using Cox regression.

Results

Overall, 11,023 patients initiating PP1M treatment were identified (49.5% were females; mean age of 43.2 [12.2] years). Overall incidences for serious cardiovascular events, expanded serious cardiovascular events, and cardiovascular hospitalizations were 3.92, 7.88 and 51.96 per 1000 person-years, respectively. In matched cohort analysis (N = 10,115), the hazard ratios (HRs) between initiating PP1M and a new oral SGA for serious cardiovascular events, expanded serious cardiovascular events, and cardiovascular hospitalizations were 0.86 (95% confidence interval [CI] 0.55–1.36), 0.88 (95% CI 0.63–1.21), and 0.78 (95% CI 0.69–0.89), respectively.

Conclusion

This study reported the population-based incidence of cardiovascular events in schizophrenic patients initiating PP1M treatment. PP1M was not associated with increased risks of serious cardiovascular events but was potentially associated with lower risks of cardiovascular hospitalizations compared with oral SGAs.

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帕潘立酮棕榈酸酯每月一次注射液(PP1M)治疗精神分裂症患者发生心血管事件的风险:台湾一项基于人群的回顾性队列研究
背景精神分裂症是导致残疾的主要原因之一。帕潘立酮棕榈酸酯每月一次注射液(PP1M)的开发旨在为维持治疗提供稳定的给药方式并提高用药依从性。众所周知,精神分裂症患者的心血管风险较高,但在亚洲,人们对接受帕利哌酮棕榈酸酯注射液治疗的精神分裂症患者的心血管风险知之甚少。本研究旨在估算开始接受帕利哌酮棕榈酸酯注射液治疗后心血管事件的发生率,并评估与口服第二代抗精神病药物(SGAs)相比的心血管风险关联。方法利用台湾国民健康保险研究数据库的数据,对2012年3月1日至2018年12月31日期间接受过任何SGAs治疗的成年精神分裂症患者进行队列识别。开始接受 PP1M 治疗的患者被纳入其中,用于对发病率进行描述性分析。根据基线时的人口统计学特征、临床特征和治疗史,将 PP1M 患者与新开始口服 SGA 的患者进行 1:1 的倾向性匹配,通过三步匹配程序进行比较分析,采用普遍的新用户设计以提高可比性。随访结束于指数药物治疗疗程结束、死亡、有最后记录或研究结束(2019 年 12 月 31 日)。研究终点包括严重心血管事件(包括严重室性心律失常和猝死)、扩大严重心血管事件(进一步包括急性心肌梗死和缺血性中风)和心血管住院治疗。采用 Cox 回归法比较了匹配队列间研究终点的风险。结果共发现 11,023 名开始接受 PP1M 治疗的患者(49.5% 为女性;平均年龄为 43.2 [12.2] 岁)。严重心血管事件、扩大严重心血管事件和心血管住院治疗的总发生率分别为每千人年 3.92 例、7.88 例和 51.96 例。在配对队列分析中(N = 10,115),开始使用 PP1M 和新的口服 SGA 对严重心血管事件、扩大的严重心血管事件和心血管住院治疗的危险比(HRs)分别为 0.结论本研究报告了开始接受 PP1M 治疗的精神分裂症患者心血管事件的人群发生率。与口服 SGAs 相比,PP1M 与严重心血管事件风险增加无关,但与心血管住院风险降低可能有关。
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来源期刊
CiteScore
5.90
自引率
3.10%
发文量
108
审稿时长
6-12 weeks
期刊介绍: Clinical Drug Investigation provides rapid publication of original research covering all phases of clinical drug development and therapeutic use of drugs. The Journal includes: -Clinical trials, outcomes research, clinical pharmacoeconomic studies and pharmacoepidemiology studies with a strong link to optimum prescribing practice for a drug or group of drugs. -Clinical pharmacodynamic and clinical pharmacokinetic studies with a strong link to clinical practice. -Pharmacodynamic and pharmacokinetic studies in healthy volunteers in which significant implications for clinical prescribing are discussed. -Studies focusing on the application of drug delivery technology in healthcare. -Short communications and case study reports that meet the above criteria will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Clinical Drug Investigation may be accompanied by plain language summaries to assist readers who have some knowledge, but non in-depth expertise in, the area to understand important medical advances.
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