Ceraso Anna, Lin Jessie Jingxia, Schneider-Thoma Johannes, Siafis Spyridon, Tardy Magdolna, Komossa Katja, Heres Stephan, Kissling Werner, Davis John M, Leucht Stefan
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.
Cochrane Database Syst Rev. 2020 Aug 11;8(8):CD008016. doi: 10.1002/14651858.CD008016.pub3.
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.
To review the effects of maintaining antipsychotic drugs for people with schizophrenia compared to withdrawing these agents.
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).
We included all randomised trials comparing maintenance treatment with antipsychotic drugs and placebo for people with schizophrenia or schizophrenia-like psychoses.
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.
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.
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。
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。
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)。
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。
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)。
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)。
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。