Department of Psychiatry, Psychotherapy and Psychosomatics, Hospital of Psychiatry, University of Zurich, Zurich, Switzerland.
Department of Psychiatry, Northwell Health, The Zucker Hillside Hospital, Glen Oaks, NY, USA.
Schizophr Bull. 2022 Mar 1;48(2):296-306. doi: 10.1093/schbul/sbab091.
To quantify the risk and predictors of relapse among individuals with schizophrenia randomly withdrawn from antipsychotic maintenance treatment.
We re-analyzed time-to-event and baseline predictors from placebo arms in five placebo-controlled randomized trials of antipsychotics (n = 688 individuals; 173 stabilized on oral antipsychotic [OAP] and 515 on long-acting injectables [LAI]) for relapse-prevention available in the Yale Open Data Access repository. Using a survival and Cox-proportional hazards regression analyses, we estimated survival rates of "relapse-free" individuals by the end of follow-up (median = 118 days, IQR = 52.0-208.0), the rate of study-confirmed relapse, and adjusted hazard ratios (aHR, 95% confidence intervals [CI]) associated with baseline predictors. We also estimated these parameters for individuals followed for >5 half-lives of the stabilizing antipsychotic, and studied predictors of "rebound psychosis" in OAP-stabilized participants, defined as occurring within 30 days of antipsychotic withdrawal.
29.9% (95%CI = 23.2-38.5) remained relapse-free by the end of follow-up, 11.1% (95%CI = 5.65-21.9) among those OAP-stabilized, 36.4% (95%CI = 28.4-46.7) among those LAI-stabilized. The study-confirmed relapse rate was 45.2%, 62.4% among those OAP-stabilized and 39.4% among those LAI-stabilized. Predictors of relapse included smoking (aHR = 1.54, 95%CI = 1.19-2.00), female sex (aHR = 1.37, 95%CI = 1.08-1.79), and having been stabilized on OAPs vs LAIs (aHR = 3.56, 95%CI = 2.68-4.72). Greater risk of relapse on OAP persisted even after sufficient time had elapsed to clear antipsychotic plasma level among LAI-stabilized (aHR = 5.0, 95%CI = 3.5-7.1). "Rebound psychosis" did not show predictors.
Our results corroborate the high relapse risk following antipsychotic withdrawal after symptom stabilization with limited patient-related predictors of safe treatment discontinuation. Stabilization with LAIs reduces the short-/medium-term relapse risk.
定量评估精神分裂症个体在停止抗精神病维持治疗后复发的风险和预测因素。
我们重新分析了耶鲁大学开放数据访问库中可用的五项抗精神病药物安慰剂对照随机试验(n=688 人;173 人稳定服用口服抗精神病药[OAP],515 人稳定服用长效注射剂[LAI])的安慰剂臂中的时间事件和基线预测因素,这些试验旨在预防复发。使用生存和 Cox 比例风险回归分析,我们根据随访结束时(中位数=118 天,IQR=52.0-208.0)“无复发”个体的生存率、研究确认的复发率以及与基线预测因素相关的调整后危险比(aHR,95%置信区间[CI])进行了估计。我们还估计了在稳定使用抗精神病药物的半衰期超过 5 倍的个体中这些参数,并研究了 OAP 稳定参与者中“反弹精神病”的预测因素,定义为在抗精神病药物停药后 30 天内发生。
29.9%(95%CI=23.2-38.5)在随访结束时无复发,OAP 稳定者为 11.1%(95%CI=5.65-21.9),LAI 稳定者为 36.4%(95%CI=28.4-46.7)。研究确认的复发率为 45.2%,OAP 稳定者为 62.4%,LAI 稳定者为 39.4%。复发的预测因素包括吸烟(aHR=1.54,95%CI=1.19-2.00)、女性(aHR=1.37,95%CI=1.08-1.79)以及从 OAP 稳定转为 LAI 稳定(aHR=3.56,95%CI=2.68-4.72)。即使在 LAI 稳定者中清除抗精神病药物血浆水平所需的时间足够长,OAP 稳定者的复发风险仍然较高(aHR=5.0,95%CI=3.5-7.1)。“反弹精神病”没有表现出预测因素。
我们的结果证实了精神分裂症个体在症状稳定后停止抗精神病药物治疗后的高复发风险,且与安全停药相关的患者相关预测因素有限。使用 LAI 稳定可降低短期/中期复发风险。