Hui Christy L M, Honer William G, Lee Edwin H M, Chang Wing Chung, Chan Sherry K W, Chen Emily S M, Pang Edwin P F, Lui Simon S Y, Chung Dicky W S, Yeung Wai Song, Ng Roger M K, Lo William T L, Jones Peter B, Sham Pak, Chen Eric Y H
Department of Psychiatry, University of Hong Kong, Hong Kong Special Administrative Region, China.
Department of Psychiatry, University of British Columbia, Canada.
Lancet Psychiatry. 2018 May;5(5):432-442. doi: 10.1016/S2215-0366(18)30090-7. Epub 2018 Mar 15.
The long-term consequences of discontinuing antipsychotic medication after successful treatment of first-episode psychosis are not well studied. We assess the relation between early maintenance therapy decisions in first-episode psychosis and the subsequent clinical outcome at 10 years.
This is a 10 year follow-up study, spanning Sept 5, 2003, to Dec 30, 2014, of a randomised, double-blind trial in seven centres in Hong Kong in which 178 patients with first-episode psychosis with full positive symptom resolution after at least 1 year of antipsychotic treatment were given maintenance treatment (n=89; oral quetiapine 400 mg daily) or early treatment discontinuation (n=89; placebo) for 12 months. After the trial, patients received naturalistic treatment. Overall this cohort of patients will have received about 3 years of treatment before entering the follow-up phase of the study: about 2 years of maintenance treatment before study entry and 1 year of treatment in the trial. The primary outcome of this follow-up was the proportion of patients in each group (including those for whom direct follow-up was not available) with good or poor long-term clinical outcomes at 10 years, with poor outcome defined as a composite of persistent psychotic symptoms, a requirement for clozapine treatment, or death by suicide. The randomised trial was registered with ClinicalTrials.gov, number NCT00334035, and the follow-up study was registered with ClinicalTrials.gov, number NCT01926340.
Poor 10 year clinical outcome occurred in 35 (39%) of 89 patients in the discontinuation group and 19 (21%) of 89 patients in the maintenance treatment group (risk ratio 1·84, 95% CI 1·15-2·96; p=0·012). Suicide was the only serious adverse event that occurred in the follow-up phase (four [4%] patients in the early discontinuation group vs two [2%] in the maintenance group).
In patients with first-episode psychosis with a full initial response to treatment, medication continuation for at least the first 3 years after starting treatment decreases the risk of relapse and poor long-term clinical outcome.
Food and Health Bureau, Research Grants Council of Hong Kong, and AstraZeneca.
首次发作精神病成功治疗后停用抗精神病药物的长期后果尚未得到充分研究。我们评估首次发作精神病的早期维持治疗决策与10年后的后续临床结局之间的关系。
这是一项为期10年的随访研究,时间跨度为2003年9月5日至2014年12月30日,是在香港7个中心进行的一项随机双盲试验。在该试验中,178例首次发作精神病患者在接受至少1年抗精神病药物治疗且阳性症状完全缓解后,被给予维持治疗(n = 89;口服喹硫平每日400 mg)或早期停药(n = 89;安慰剂)12个月。试验结束后,患者接受自然治疗。总体而言,这组患者在进入研究随访阶段之前将接受约3年的治疗:研究入组前约2年的维持治疗和试验中1年的治疗。本次随访的主要结局是每组患者(包括那些无法直接随访的患者)在10年时具有良好或不良长期临床结局的比例,不良结局定义为持续性精神病性症状、需要氯氮平治疗或自杀死亡的综合情况。该随机试验已在ClinicalTrials.gov注册,编号为NCT00334035,随访研究已在ClinicalTrials.gov注册,编号为NCT01926340。
停药组89例患者中有35例(39%)出现10年不良临床结局,维持治疗组89例患者中有19例(21%)出现不良临床结局(风险比1.84,95%置信区间1.15 - 2.96;p = 0.012)。自杀是随访阶段唯一发生的严重不良事件(早期停药组4例[4%]患者,维持组2例[2%]患者)。
对于首次发作精神病且初始治疗有完全反应的患者,治疗开始后至少前3年持续用药可降低复发风险和不良长期临床结局的风险。
香港食物及卫生局、香港研究资助局和阿斯利康公司。