Department of Psychiatry, The Zucker Hillside Hospital, Northwell Health, Glen Oaks, NY, USA.
Department of Psychiatry and Molecular Medicine, Zucker School of Medicine at Hofstra/Northwell, Hempstead, NY, USA.
Schizophr Bull. 2021 Oct 21;47(6):1611-1620. doi: 10.1093/schbul/sbab063.
Schizophrenia often requires long-term treatment with antipsychotic medication. This study aims to measure the continuity of antipsychotic treatment over the course of illness in schizophrenia, as well as factors involved in the interruption of treatment. For this, we followed up a national cohort of first-episode psychosis patients in Finland for up to 18 years. Stratified Cox proportional hazards regressions were conducted for "within-participant" risk of discontinuation of subsequent treatments compared to the first, and by specific antipsychotic compared to oral olanzapine, the most prescribed antipsychotic in this cohort. Adjusted hazard ratios (aHRs) and 95% confidence intervals (95% CIs) were calculated. Among 3343 participants followed up for a mean of 8 years (SD = 4.93), the median number of continuous treatment episodes was 6 (interquartile range [IQR] = 3-11) with a median duration of 11.4 months (IQR = 5.3-25.6). In the first year after diagnosis, the incidence rate of treatment discontinuation was 30.12 (95% CI = 29.89-30.35) events per 100 participant-years, decreasing to 8.90 (95% CI = 8.75-9.05) in the 10th year. The risk of discontinuation progressively decreased over successive treatment episodes (aHR = 0.30; 95% CI = 0.20-0.46 for episodes after the 15th compared to the first). Individuals were 67% less likely to interrupt treatment with long-acting injectable than oral antipsychotics (aHR = 0.33; 95% CI = 0.27-0.41). Treatment for schizophrenia over the long term is often characterized by recurrent cycles of interruptions and reintroductions of antipsychotic medication, which is typically not recommended by management guidelines. Greater utilization of long-acting injectable formulations earlier in the course of illness may facilitate the continuity of antipsychotic treatment in schizophrenia.
精神分裂症通常需要长期使用抗精神病药物治疗。本研究旨在测量精神分裂症患者在发病过程中抗精神病治疗的连续性,以及治疗中断的相关因素。为此,我们对芬兰的首发精神病患者进行了一项全国性队列研究,随访时间长达 18 年。采用分层 Cox 比例风险回归分析,比较了与首次治疗相比,随后治疗的参与者停药风险,以及与本队列中最常开的口服奥氮平相比,特定抗精神病药物的停药风险。计算了调整后的危险比 (aHR) 和 95%置信区间 (95%CI)。在 3343 名平均随访 8 年(SD=4.93)的参与者中,连续治疗发作的中位数为 6 次(四分位距 [IQR]=3-11),中位持续时间为 11.4 个月(IQR=5.3-25.6)。在诊断后的第一年,治疗中断的发生率为 30.12(95%CI=29.89-30.35)/100 人年,在第 10 年降至 8.90(95%CI=8.75-9.05)。随着连续治疗发作次数的增加,停药风险逐渐降低(第 15 次发作后与首次发作相比,aHR=0.30;95%CI=0.20-0.46)。长效注射制剂与口服抗精神病药物相比,中断治疗的可能性降低 67%(aHR=0.33;95%CI=0.27-0.41)。长期使用抗精神病药物治疗精神分裂症通常会出现反复中断和重新引入药物的循环,这通常不符合管理指南的建议。在疾病早期更广泛地使用长效注射制剂可能会促进精神分裂症抗精神病治疗的连续性。