Janssen Global Commercial Strategy Organization, Budapest, Hungary.
Department of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary.
PLoS One. 2019 Jun 13;14(6):e0218071. doi: 10.1371/journal.pone.0218071. eCollection 2019.
Schizophrenia is a severe condition that affects approximately 1% of the population. Certain elements of antipsychotic treatment can only be examined in large population, thus the need for population-based real-world analyses has been increasing.
Hungarian National Health Fund database includes all healthcare data of the population of Hungary. All patients diagnosed with schizophrenia between 01.01.2006 and 31.12.2015 were included in the study. We analyzed all patients with newly initiated second-generation antipsychotic during the inclusion period (01.01.2012-31.12.2013). Patients were followed for 2 years. All-cause treatment discontinuation served as the primary outcome of the study. Patients with newly initiated long-acting injectable treatments were further investigated in stratified analyses based on their previous treatment.
106,624 patients had schizophrenia diagnosis during the study period. 12,232 patients met the inclusion criteria for newly initiating second-generation antipsychotic during the inclusion period. The proportion of patients still on treatment after 1 year for oral treatments varied between 17% (oral risperidone) and 31% (oral olanzapine) while the analogous data for long acting injectables were between 32% (risperidone long acting) and 64% (paliperidone long acting one monthly). The 2-year data were similarly in favor of long-actings. Median time to discontinuation in the oral group varied between 57 days (clozapine) and 121 days (olanzapine). The median time to discontinuation for long-actings was significantly longer: between 176 and 287 days; in case of paliperidone long acting, median was not reached during the observation period. Patients receiving long-acting treatment switched from another long-acting remained on the newly initiated treatment significantly longer than those switched from orals.
Our results indicate the superiority of second generation long-acting antipsychotics with regard to rates of treatment discontinuation and periods of persistence to the assigned medication.
精神分裂症是一种严重的疾病,影响大约 1%的人口。某些抗精神病药物治疗的元素只能在大人群中进行检查,因此对基于人群的真实世界分析的需求不断增加。
匈牙利国家健康基金数据库包含匈牙利人口的所有医疗保健数据。所有在 2006 年 1 月 1 日至 2015 年 12 月 31 日期间被诊断患有精神分裂症的患者均被纳入本研究。我们分析了在纳入期间(2012 年 1 月 1 日至 2013 年 12 月 31 日)新开始第二代抗精神病药物治疗的所有患者。全因治疗停药是本研究的主要结局。在基于他们之前治疗的分层分析中,进一步调查了新开始长效注射治疗的患者。
在研究期间,有 106624 名患者患有精神分裂症诊断。在纳入期间,有 12232 名患者符合新开始第二代抗精神病药物治疗的纳入标准。口服治疗 1 年后仍在治疗的患者比例在 17%(口服利培酮)至 31%(口服奥氮平)之间,而长效注射剂的类似数据在 32%(利培酮长效)至 64%(帕利哌酮长效每月)之间。2 年的数据也同样有利于长效药物。口服组停药的中位时间在 57 天(氯氮平)至 121 天(奥氮平)之间。长效药物的停药中位时间明显更长:在 176 天至 287 天之间;在帕利哌酮长效的情况下,在观察期间未达到中位时间。接受长效治疗的患者从另一种长效药物转换而来,与从口服药物转换而来的患者相比,继续接受新开始治疗的时间明显更长。
我们的结果表明,第二代长效抗精神病药物在停药率和持续用药时间方面具有优势。