• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

精神分裂症的抗精神病药物维持治疗。

Maintenance treatment with antipsychotic drugs for schizophrenia.

作者信息

Ceraso Anna, Lin Jessie Jingxia, Schneider-Thoma Johannes, Siafis Spyridon, Tardy Magdolna, Komossa Katja, Heres Stephan, Kissling Werner, Davis John M, Leucht Stefan

机构信息

Department of Clinical and Experimental Sciences, Section of Psychiatry, University of Brescia, Brescia, Italy.

School of Nursing, The University of Hong Kong, Hong Kong SAR, Hong Kong.

出版信息

Cochrane Database Syst Rev. 2020 Aug 11;8(8):CD008016. doi: 10.1002/14651858.CD008016.pub3.

DOI:10.1002/14651858.CD008016.pub3
PMID:32840872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9702459/
Abstract

BACKGROUND

The symptoms and signs of schizophrenia have been linked to high levels of dopamine in specific areas of the brain (limbic system). Antipsychotic drugs block the transmission of dopamine in the brain and reduce the acute symptoms of the disorder. An original version of the current review, published in 2012, examined whether antipsychotic drugs are also effective for relapse prevention. This is the updated version of the aforesaid review.

OBJECTIVES

To review the effects of maintaining antipsychotic drugs for people with schizophrenia compared to withdrawing these agents.

SEARCH METHODS

We searched the Cochrane Schizophrenia Group's Study-Based Register of Trials including the registries of clinical trials (12 November 2008, 10 October 2017, 3 July 2018, 11 September 2019).

SELECTION CRITERIA

We included all randomised trials comparing maintenance treatment with antipsychotic drugs and placebo for people with schizophrenia or schizophrenia-like psychoses.

DATA COLLECTION AND ANALYSIS

We extracted data independently. For dichotomous data we calculated risk ratios (RR) and their 95% confidence intervals (CIs) on an intention-to-treat basis based on a random-effects model. For continuous data, we calculated mean differences (MD) or standardised mean differences (SMD), again based on a random-effects model.

MAIN RESULTS

The review currently includes 75 randomised controlled trials (RCTs) involving 9145 participants comparing antipsychotic medication with placebo. The trials were published from 1959 to 2017 and their size ranged between 14 and 420 participants. In many studies the methods of randomisation, allocation and blinding were poorly reported. However, restricting the analysis to studies at low risk of bias gave similar results. Although this and other potential sources of bias limited the overall quality, the efficacy of antipsychotic drugs for maintenance treatment in schizophrenia was clear. Antipsychotic drugs were more effective than placebo in preventing relapse at seven to 12 months (primary outcome; drug 24% versus placebo 61%, 30 RCTs, n = 4249, RR 0.38, 95% CI 0.32 to 0.45, number needed to treat for an additional beneficial outcome (NNTB) 3, 95% CI 2 to 3; high-certainty evidence). Hospitalisation was also reduced, however, the baseline risk was lower (drug 7% versus placebo 18%, 21 RCTs, n = 3558, RR 0.43, 95% CI 0.32 to 0.57, NNTB 8, 95% CI 6 to 14; high-certainty evidence). More participants in the placebo group than in the antipsychotic drug group left the studies early due to any reason (at seven to 12 months: drug 36% versus placebo 62%, 24 RCTs, n = 3951, RR 0.56, 95% CI 0.48 to 0.65, NNTB 4, 95% CI 3 to 5; high-certainty evidence) and due to inefficacy of treatment (at seven to 12 months: drug 18% versus placebo 46%, 24 RCTs, n = 3951, RR 0.37, 95% CI 0.31 to 0.44, NNTB 3, 95% CI 3 to 4). Quality of life might be better in drug-treated participants (7 RCTs, n = 1573 SMD -0.32, 95% CI to -0.57 to -0.07; low-certainty evidence); probably the same for social functioning (15 RCTs, n = 3588, SMD -0.43, 95% CI -0.53 to -0.34; moderate-certainty evidence). Underpowered data revealed no evidence of a difference between groups for the outcome 'Death due to suicide' (drug 0.04% versus placebo 0.1%, 19 RCTs, n = 4634, RR 0.60, 95% CI 0.12 to 2.97,low-certainty evidence) and for the number of participants in employment (at 9 to 15 months, drug 39% versus placebo 34%, 3 RCTs, n = 593, RR 1.08, 95% CI 0.82 to 1.41, low certainty evidence). Antipsychotic drugs (as a group and irrespective of duration) were associated with more participants experiencing movement disorders (e.g. at least one movement disorder: drug 14% versus placebo 8%, 29 RCTs, n = 5276, RR 1.52, 95% CI 1.25 to 1.85, number needed to treat for an additional harmful outcome (NNTH) 20, 95% CI 14 to 50), sedation (drug 8% versus placebo 5%, 18 RCTs, n = 4078, RR 1.52, 95% CI 1.24 to 1.86, NNTH 50, 95% CI not significant), and weight gain (drug 9% versus placebo 6%, 19 RCTs, n = 4767, RR 1.69, 95% CI 1.21 to 2.35, NNTH 25, 95% CI 20 to 50).

AUTHORS' CONCLUSIONS: For people with schizophrenia, the evidence suggests that maintenance on antipsychotic drugs prevents relapse to a much greater extent than placebo for approximately up to two years of follow-up. This effect must be weighed against the adverse effects of antipsychotic drugs. Future studies should better clarify the long-term morbidity and mortality associated with these drugs.

摘要

背景

精神分裂症的症状和体征与大脑特定区域(边缘系统)中高水平的多巴胺有关。抗精神病药物可阻断大脑中多巴胺的传递,并减轻该疾病的急性症状。本综述的原始版本于2012年发表,探讨了抗精神病药物对预防复发是否也有效。这是上述综述的更新版本。

目的

比较维持使用抗精神病药物与停用这些药物对精神分裂症患者的影响。

检索方法

我们检索了Cochrane精神分裂症研究组基于研究的试验注册库,包括临床试验注册库(2008年11月12日、2017年10月10日、2018年7月3日、2019年9月11日)。

选择标准

我们纳入了所有比较抗精神病药物维持治疗与安慰剂对精神分裂症或精神分裂症样精神病患者疗效的随机试验。

数据收集与分析

我们独立提取数据。对于二分法数据,我们基于随机效应模型,在意向性分析的基础上计算风险比(RR)及其95%置信区间(CI)。对于连续数据,我们同样基于随机效应模型计算平均差(MD)或标准化平均差(SMD)。

主要结果

本综述目前纳入了75项随机对照试验(RCT),涉及9145名参与者,比较了抗精神病药物与安慰剂。这些试验发表于1959年至2017年,样本量在14至420名参与者之间。在许多研究中,随机化、分配和盲法的方法报告不佳。然而,将分析限制在低偏倚风险的研究中得到了类似的结果。尽管这以及其他潜在的偏倚来源限制了总体质量,但抗精神病药物在精神分裂症维持治疗中的疗效是明确的。抗精神病药物在预防7至12个月复发方面比安慰剂更有效(主要结局;药物组24% 对比安慰剂组61%,30项RCT,n = 4249,RR 0.38,95% CI 0.32至0.45,额外有益结局的需治疗人数(NNTB)为3,95% CI 2至3;高确定性证据)。住院率也有所降低,然而基线风险较低(药物组7% 对比安慰剂组18%,21项RCT,n = 3558,RR 0.43,95% CI 0.32至0.57,NNTB 8,95% CI 6至14;高确定性证据)。由于任何原因,安慰剂组比抗精神病药物组有更多参与者提前退出研究(7至12个月时:药物组36% 对比安慰剂组62%,24项RCT,n = 3951,RR 0.56,95% CI 0.48至0.65,NNTB 4,95% CI 3至5;高确定性证据),以及由于治疗无效(7至12个月时:药物组18% 对比安慰剂组46%,24项RCT,n = 3951,RR 0.37,95% CI 0.31至0.44,NNTB 3,95% CI 3至4)。接受药物治疗的参与者的生活质量可能更好(7项RCT,n = 1573,SMD -0.32,95% CI -0.57至 -0.07;低确定性证据);社交功能可能相同(15项RCT,n = 3588,SMD -0.43,95% CI -0.53至 -0.34;中度确定性证据)。样本量不足的数据显示,在“自杀死亡”结局上两组之间没有差异的证据(药物组0.04% 对比安慰剂组0.1%,19项RCT,n = 4634,RR 0.60,95% CI 0.12至2.97,低确定性证据),以及就业参与者数量方面(9至15个月时,药物组39% 对比安慰剂组34%,3项RCT,n = 593,RR 1.08,95% CI 0.82至1.41,低确定性证据)。抗精神病药物(作为一个整体且不考虑疗程)与更多参与者出现运动障碍相关(例如至少一种运动障碍:药物组14% 对比安慰剂组8%,29项RCT,n = 5276,RR 1.52,95% CI 1.25至1.85,额外有害结局的需治疗人数(NNTH)为20,95% CI 14至50)、镇静作用(药物组8% 对比安慰剂组5%,18项RCT,n = 4078,RR 1.52,95% CI 1.24至1.86,NNTH 50,95% CI不显著)和体重增加(药物组9% 对比安慰剂组6%,19项RCT,n = 4767,RR 1.69,95% CI 1.21至2.35,NNTH 25,95% CI 20至50)。

作者结论

对于精神分裂症患者,证据表明在长达约两年的随访中,维持使用抗精神病药物比安慰剂能更大程度地预防复发。这种效果必须与抗精神病药物的不良反应相权衡。未来的研究应更好地阐明与这些药物相关的长期发病率和死亡率。

相似文献

1
Maintenance treatment with antipsychotic drugs for schizophrenia.精神分裂症的抗精神病药物维持治疗。
Cochrane Database Syst Rev. 2020 Aug 11;8(8):CD008016. doi: 10.1002/14651858.CD008016.pub3.
2
Maintenance treatment with antipsychotic drugs for schizophrenia.使用抗精神病药物对精神分裂症进行维持治疗。
Cochrane Database Syst Rev. 2012 May 16(5):CD008016. doi: 10.1002/14651858.CD008016.pub2.
3
Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.在流行地区,服用抗叶酸抗疟药物的人群中,叶酸补充剂与疟疾易感性和严重程度的关系。
Cochrane Database Syst Rev. 2022 Feb 1;2(2022):CD014217. doi: 10.1002/14651858.CD014217.
4
Antipsychotic dose reduction compared to dose continuation for people with schizophrenia.抗精神病药剂量减少与继续用药治疗精神分裂症患者的比较。
Cochrane Database Syst Rev. 2022 Nov 24;11(11):CD014384. doi: 10.1002/14651858.CD014384.pub2.
5
Haloperidol (oral) versus olanzapine (oral) for people with schizophrenia and schizophrenia-spectrum disorders.氟哌啶醇(口服)与奥氮平(口服)治疗精神分裂症及精神分裂症谱系障碍患者。
Cochrane Database Syst Rev. 2024 Jul 3;7(7):CD013425. doi: 10.1002/14651858.CD013425.pub2.
6
Lithium for schizophrenia.用于治疗精神分裂症的锂盐。
Cochrane Database Syst Rev. 2015 Oct 28;2015(10):CD003834. doi: 10.1002/14651858.CD003834.pub3.
7
Haloperidol versus low-potency first-generation antipsychotic drugs for schizophrenia.用于治疗精神分裂症的氟哌啶醇与低效价第一代抗精神病药物的对比
Cochrane Database Syst Rev. 2014 Jul 9;2014(7):CD009268. doi: 10.1002/14651858.CD009268.pub2.
8
Risperidone (depot) for schizophrenia.用于治疗精神分裂症的长效利培酮
Cochrane Database Syst Rev. 2016 Apr 14;4(4):CD004161. doi: 10.1002/14651858.CD004161.pub2.
9
Sertindole for schizophrenia.用于治疗精神分裂症的舍吲哚。
Cochrane Database Syst Rev. 2005 Jul 20;2005(3):CD001715. doi: 10.1002/14651858.CD001715.pub2.
10
Maintenance Treatment With Antipsychotic Drugs in Schizophrenia: A Cochrane Systematic Review and Meta-analysis.精神分裂症的抗精神病药物维持治疗:一项 Cochrane 系统评价和荟萃分析。
Schizophr Bull. 2022 Jun 21;48(4):738-740. doi: 10.1093/schbul/sbac041.

引用本文的文献

1
Use of long-acting injectable antipsychotics in an acute inpatient psychiatric unit and 90-day re-hospitalization rates: results of an observational prospective study.长效注射用抗精神病药物在急性住院精神科病房的使用情况及90天再住院率:一项前瞻性观察研究的结果
Ther Adv Psychopharmacol. 2025 Sep 9;15:20451253251367591. doi: 10.1177/20451253251367591. eCollection 2025.
2
The ILIA study: protocol for a randomized-controlled multicenter clinical trial on smartphone- and web-based relapse monitoring for patients with schizophrenia or schizoaffective disorder.ILIA研究:一项针对精神分裂症或精神分裂情感性障碍患者基于智能手机和网络的复发监测的随机对照多中心临床试验方案。
Eur Arch Psychiatry Clin Neurosci. 2025 Aug 19. doi: 10.1007/s00406-025-02089-7.
3
Antipsychotic Potential of Opioids: Rethinking Substance-Induced Psychosis and Treatment Stratification.阿片类药物的抗精神病潜力:重新思考物质所致精神病及治疗分层
J Clin Med. 2025 Aug 7;14(15):5596. doi: 10.3390/jcm14155596.
4
Pomgulated methionil (LY2140023) in schizophrenia patients: a systematic review and meta-analysis.精神分裂症患者中聚谷氨酸化甲硫氨酸(LY2140023):一项系统评价与荟萃分析。
BMC Psychiatry. 2025 Aug 8;25(1):775. doi: 10.1186/s12888-025-07199-z.
5
A Review of Pharmacokinetic and Pharmacodynamic Properties of Quetiapine IR and XR: Insights and Clinical Practice Implications.喹硫平即释片和缓释片的药代动力学和药效学特性综述:见解与临床实践意义
Cureus. 2025 Jun 18;17(6):e86258. doi: 10.7759/cureus.86258. eCollection 2025 Jun.
6
Placebo and nocebo phenomena in schizophrenia spectrum disorders: a narrative review on current knowledge and potential future directions.精神分裂症谱系障碍中的安慰剂和反安慰剂现象:关于当前知识及潜在未来方向的叙述性综述
Psychol Med. 2025 Jul 18;55:e199. doi: 10.1017/S0033291725100901.
7
Efficacy and Safety of TV-46000 and Second-Generation Long-Acting Injectable Antipsychotics for Schizophrenia: A Systematic Literature Review and Network Meta-Analysis of Randomized Controlled Trials.TV-46000与第二代长效注射用抗精神病药物治疗精神分裂症的疗效与安全性:一项随机对照试验的系统文献综述与网状Meta分析
Adv Ther. 2025 Jul 16. doi: 10.1007/s12325-025-03274-9.
8
Safety and Tolerability of Brexpiprazole in Adolescents With Schizophrenia: A Long-Term, Open-Label Study.布雷哌嗪治疗青少年精神分裂症的安全性和耐受性:一项长期开放标签研究。
JAACAP Open. 2024 May 27;3(2):313-322. doi: 10.1016/j.jaacop.2024.04.005. eCollection 2025 Jun.
9
Auditory efferent suppression during alternate auditory attention in schizophrenia patients with auditory hallucinations.伴有幻听的精神分裂症患者在交替听觉注意过程中的听觉传出抑制。
Sci Rep. 2025 Mar 20;15(1):9662. doi: 10.1038/s41598-025-94412-4.
10
Risperidone In Situ Microparticles: A Review in Schizophrenia.利培酮原位微粒:精神分裂症研究综述
Drugs. 2025 Mar;85(3):425-435. doi: 10.1007/s40265-024-02140-2. Epub 2025 Feb 11.

本文引用的文献

1
Rates and predictors of one-year antipsychotic treatment discontinuation in first-episode schizophrenia: Results from an open-label, randomized, "real world" clinical trial.首发精神分裂症患者一年抗精神病药物治疗中断的发生率和预测因素:一项开放标签、随机、“真实世界”临床试验的结果。
Psychiatry Res. 2019 Mar;273:631-640. doi: 10.1016/j.psychres.2019.01.068. Epub 2019 Jan 24.
2
Long-Term Remission With Cariprazine Treatment in Patients With Schizophrenia: A Post Hoc Analysis of a Randomized, Double-Blind, Placebo-Controlled, Relapse Prevention Trial.卡利拉嗪治疗精神分裂症患者的长期缓解:一项随机、双盲、安慰剂对照、预防复发试验的事后分析。
J Clin Psychiatry. 2019 Jan 8;80(2):18m12495. doi: 10.4088/JCP.18m12495.
3
Factors Associated With Successful Medication Discontinuation After a Randomized Clinical Trial of Relapse Prevention in First-Episode Psychosis: A 10-Year Follow-up.首发精神病患者复发预防的随机临床试验后成功停药的相关因素:10 年随访。
JAMA Psychiatry. 2019 Feb 1;76(2):217-219. doi: 10.1001/jamapsychiatry.2018.3120.
4
Can antipsychotic dose reduction lead to better functional recovery in first-episode psychosis? A randomized controlled-trial of antipsychotic dose reduction. The reduce trial: Study protocol.抗精神病药剂量减少能否促进首发精神病患者更好的功能恢复?一项抗精神病药剂量减少的随机对照试验。减少试验:研究方案。
Early Interv Psychiatry. 2019 Dec;13(6):1345-1356. doi: 10.1111/eip.12769. Epub 2018 Nov 29.
5
Efficacy of cariprazine across symptom domains in patients with acute exacerbation of schizophrenia: Pooled analyses from 3 phase II/III studies.卡利拉嗪在精神分裂症急性加重期患者多个症状领域的疗效:来自 3 项 2/3 期研究的汇总分析。
Eur Neuropsychopharmacol. 2019 Jan;29(1):127-136. doi: 10.1016/j.euroneuro.2018.10.008. Epub 2018 Nov 20.
6
Predicting first-episode psychosis patients who will never relapse over 10 years.预测 10 年内不会复发的首发精神病患者。
Psychol Med. 2019 Oct;49(13):2206-2214. doi: 10.1017/S0033291718003070. Epub 2018 Oct 30.
7
Successful switching of patients with acute schizophrenia from another antipsychotic to brexpiprazole: comparison of clinicians' choice of cross-titration schedules in a post hoc analysis of a randomized, double-blind, maintenance treatment study.成功将急性精神分裂症患者从其他抗精神病药物切换为布瑞哌唑:一项随机、双盲、维持治疗研究的事后分析中比较临床医生对交叉滴定方案的选择。
CNS Spectr. 2019 Oct;24(5):507-517. doi: 10.1017/S1092852918001086.
8
Implementation and fidelity assessment of the NAVIGATE treatment program for first episode psychosis in a multi-site study.在一项多中心研究中,实施 NAVIGATE 治疗方案治疗首发精神病的效果和忠实度评估。
Schizophr Res. 2019 Feb;204:271-281. doi: 10.1016/j.schres.2018.08.015. Epub 2018 Aug 20.
9
Impact of comprehensive treatment for first episode psychosis on substance use outcomes: A randomized controlled trial.首发精神病的综合治疗对物质使用结果的影响:一项随机对照试验。
Psychiatry Res. 2018 Oct;268:303-311. doi: 10.1016/j.psychres.2018.06.055. Epub 2018 Jul 24.
10
Staged treatment and acceptability guidelines in early psychosis study (STAGES): A randomized placebo controlled trial of intensive psychosocial treatment plus or minus antipsychotic medication for first-episode psychosis with low-risk of self-harm or aggression. Study protocol and baseline characteristics of participants.分期治疗和早期精神病研究中的可接受性指南 (STAGES):一项针对首发精神病且自我伤害或攻击风险低的患者的随机安慰剂对照试验,比较强化心理社会治疗加或不加抗精神病药物治疗的效果。研究方案和参与者的基线特征。
Early Interv Psychiatry. 2019 Aug;13(4):953-960. doi: 10.1111/eip.12716. Epub 2018 Jul 19.