Decuypere Flore, Sermon Jan, Geerts Paul, Denee Tom R, De Vos Cedric, Malfait Bart, Lamotte Mark, Mulder Cornelis L
Commercial Services, QuintilesIMS, Zaventem, Belgium.
Health Economics, Market Access, Reimbursement, Janssen-Cilag NV, Beerse, Belgium.
PLoS One. 2017 Jun 14;12(6):e0179049. doi: 10.1371/journal.pone.0179049. eCollection 2017.
Achieving greater continuation of treatment is a key element to improve treatment outcomes in schizophrenia patients. However, reported treatment continuation can differ markedly depending on the study design. In a retrospective setting, treatment continuation remains overall poor among patients using antipsychotics. This study aimed to document the difference in treatment continuation between four long-acting injectable antipsychotics based on the QuintilesIMS LRx databases, national, longitudinal, panel based prescription databases of retail pharmacies, in the Netherlands and Belgium. Paliperidone palmitate once monthly, risperidone microspheres, haloperidol decanoate, and olanzapine pamoate were studied. This study demonstrated significantly higher treatment continuation of paliperidone palmitate once monthly compared to risperidone microspheres (p-value<0,01) and haloperidol decanoate (p-value<0,01) in both countries, a significantly higher treatment continuation of paliperidone palmitate once monthly compared to olanzapine pamoate in the Netherlands (p-value<0,01), and a general trend towards better treatment continuation versus olanzapine pamoate in Belgium. Analysing the subgroup of patients without previous exposure to long-acting antipsychotic treatment revealed the positive impact of previous exposure on treatment continuation with a subsequent long acting treatment. Additionally, the probability of restarting the index therapy was higher among patients treated with paliperidone palmitate once monthly compared to patients treated with risperidone microspheres and haloperidol decanoate. The data source used and the methodology defined ensured for the first time a comparison of treatment continuation in a non-interventional study design for the four long-acting injectable antipsychotics studied.
实现更高的治疗持续性是改善精神分裂症患者治疗效果的关键因素。然而,报告的治疗持续性可能因研究设计的不同而有显著差异。在回顾性研究中,使用抗精神病药物的患者总体治疗持续性仍然较差。本研究旨在根据昆泰IMS LRx数据库(荷兰和比利时零售药店基于全国纵向面板的处方数据库)记录四种长效注射用抗精神病药物在治疗持续性方面的差异。研究了棕榈酸帕利哌酮每月一次、利培酮微球、癸酸氟哌啶醇和奥氮平棕榈酸酯。本研究表明,在两个国家,棕榈酸帕利哌酮每月一次的治疗持续性显著高于利培酮微球(p值<0.01)和癸酸氟哌啶醇(p值<0.01);在荷兰,棕榈酸帕利哌酮每月一次的治疗持续性显著高于奥氮平棕榈酸酯(p值<0.01),在比利时,与奥氮平棕榈酸酯相比,总体上有更好的治疗持续性趋势。对既往未接触过长效抗精神病药物治疗的患者亚组进行分析发现,既往接触对后续长效治疗的持续性有积极影响。此外,与接受利培酮微球和癸酸氟哌啶醇治疗的患者相比,接受棕榈酸帕利哌酮每月一次治疗的患者重新开始索引治疗的概率更高。所使用的数据源和定义的方法首次确保了在非干预性研究设计中对所研究的四种长效注射用抗精神病药物的治疗持续性进行比较。