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精神分裂症的非药物认知行为疗法。

Cognitive behavioural therapy without medication for schizophrenia.

机构信息

Section for Evidence-Based Medicine in Psychiatry and Psychotherapy, School of Medicine and Health, Technical University of Munich, Munich, Germany.

German Center for Mental Health (DZPG), Munich, Germany.

出版信息

Cochrane Database Syst Rev. 2024 Feb 7;2(2):CD015332. doi: 10.1002/14651858.CD015332.pub2.

Abstract

BACKGROUND

Cognitive behavioural therapy (CBT) can be effective in people with schizophrenia when provided in combination with antipsychotic medication. It remains unclear whether CBT could be safely and effectively offered in the absence of concomitant antipsychotic therapy.

OBJECTIVES

To investigate the effects of CBT for schizophrenia when administered without concomitant pharmacological treatment with antipsychotics.

SEARCH METHODS

We conducted a systematic search on 6 March 2022 in the Cochrane Schizophrenia Group's Study-Based Register of Trials, which is based on CENTRAL, MEDLINE, Embase, CINAHL, PsycINFO, PubMed, ClinicalTrials.gov, and WHO ICTRP.

SELECTION CRITERIA

We included randomised controlled trials (RCTs) in people with schizophrenia comparing CBT without antipsychotics to standard care, standard care without antipsychotics, or the combination of CBT and antipsychotics.

DATA COLLECTION AND ANALYSIS

Two review authors independently screened references for inclusion, extracted data from eligible studies, and assessed risk of bias using Cochrane's RoB 2 tool. We contacted study authors for missing data and additional information. Our primary outcome was general mental state measured with a validated rating scale. Key secondary outcomes were specific symptoms of schizophrenia, relapse, service use, number of participants leaving the study early, functioning, quality of life, and number of participants actually receiving antipsychotics during the trial. We also assessed behaviour, adverse effects, and mortality.

MAIN RESULTS

We included 4 studies providing data for 300 participants (average age 21.94 years). The mean sample size was 75 participants (range 61 to 90 participants). Study duration was between 26 and 39 weeks for the intervention period and 26 to 104 weeks for the follow-up period. Three studies employed a blind rater, while one study was triple-blind. All analyses included data from a maximum of three studies. The certainty of the evidence was low or very low for all outcomes. For the primary outcome overall symptoms of schizophrenia, results showed a difference favouring CBT without antipsychotics when compared to no specific treatment at long term (> 1 year mean difference measured with the Positive and Negative Syndrome Scale (PANSS MD) -14.77, 95% confidence interval (CI) -27.75 to -1.79, 1 RCT, n = 34). There was no difference between CBT without antipsychotics compared with antipsychotics (up to 12 months PANSS MD 3.38, 95% CI -2.38 to 9.14, 2 RCTs, n = 63) (very low-certainty evidence) or compared with CBT in combination with antipsychotics (up to 12 months standardised mean difference (SMD) 0.30, 95% CI -0.06 to 0.65, 3 RCTs, n = 125). Compared with no specific treatment, CBT without antipsychotics was associated with a reduction in overall symptoms (as described above) and negative symptoms (PANSS negative MD -4.06, 95% CI -7.50 to -0.62, 1 RCT, n = 34) at longer than 12 months. It was also associated with a lower duration of hospital stay (number of days in hospital MD -22.45, 95% CI -28.82 to -16.08, 1 RCT, n = 74) and better functioning (Personal and Social Performance Scale MD -12.42, 95% CI -22.75 to -2.09, 1 RCT, n = 40, low-certainty evidence) at up to 12 months. We did not find a difference between CBT and antipsychotics in any of the investigated outcomes, with the exception of adverse events measured with the Antipsychotic Non-Neurological Side-Effects Rating Scale (ANNSERS) at both 6 and 12 months (MD -4.94, 95% CI -8.60 to -1.28, 2 RCTs, n = 48; MD -6.96, 95% CI -11.55 to -2.37, 2 RCTs, n = 42). CBT without antipsychotics was less effective than CBT combined with antipsychotics in reducing positive symptoms at up to 12 months (SMD 0.40, 95% CI 0.05 to 0.76, 3 RCTs, n = 126). CBT without antipsychotics was associated with a lower number of participants experiencing at least one adverse event in comparison with CBT combined with antipsychotics at up to 12 months (risk ratio 0.36, 95% CI 0.17 to 0.80, 1 RCT, n = 39, low-certainty evidence).

AUTHORS' CONCLUSIONS: This review is the first attempt to systematically synthesise the evidence about CBT delivered without medication to people with schizophrenia. The limited number of studies and low to very low certainty of the evidence prevented any strong conclusions. An important limitation in the available studies was that participants in the CBT without medication group (about 35% on average) received antipsychotic treatment, highlighting the challenges of this approach. Further high-quality RCTs are needed to provide additional data on the feasibility and efficacy of CBT without antipsychotics.

摘要

背景

认知行为疗法(CBT)在精神分裂症患者中联合使用抗精神病药物时可能有效。目前尚不清楚在没有伴随抗精神病药物治疗的情况下,CBT 是否可以安全有效地提供。

目的

研究在没有抗精神病药物药理学治疗的情况下提供 CBT 对精神分裂症的影响。

检索方法

我们于 2022 年 3 月 6 日在 Cochrane 精神分裂症组的试验登记册中进行了系统检索,该登记册基于 CENTRAL、MEDLINE、Embase、CINAHL、PsycINFO、PubMed、ClinicalTrials.gov 和 WHO ICTRP。

纳入标准

我们纳入了比较无抗精神病药物的 CBT 与标准护理、无抗精神病药物的标准护理或 CBT 和抗精神病药物联合治疗的精神分裂症患者的随机对照试验(RCT)。

数据收集和分析

两位综述作者独立筛选参考文献的纳入情况,从合格研究中提取数据,并使用 Cochrane 的 RoB 2 工具评估偏倚风险。我们联系研究作者以获取缺失数据和其他信息。我们的主要结局是使用经过验证的评定量表测量的一般心理状态。关键次要结局是精神分裂症的特定症状、复发、服务使用、提前退出研究的参与者人数、功能、生活质量以及参与者在试验期间实际接受抗精神病药物的数量。我们还评估了行为、不良反应和死亡率。

主要结果

我们纳入了 4 项研究,共 300 名参与者(平均年龄 21.94 岁)。平均样本量为 75 名参与者(范围为 61 至 90 名参与者)。干预期的研究持续时间为 26 至 39 周,随访期的研究持续时间为 26 至 104 周。三项研究采用了盲法评估者,而一项研究为三重盲法。所有分析均包含最多三项研究的数据。对于所有结局,证据的确定性均为低或极低。对于整体精神分裂症症状这一主要结局,与无特定治疗相比,结果表明在长期(>1 年)时,无抗精神病药物的 CBT 更有利(使用阳性和阴性综合征量表(PANSS)的差值-14.77,95%置信区间(CI)-27.75 至-1.79,1 项 RCT,n=34)。与抗精神病药物(长达 12 个月的 PANSS 差值 3.38,95%CI-2.38 至 9.14,2 项 RCT,n=63)或与 CBT 联合抗精神病药物(长达 12 个月的标准化均数差值(SMD)0.30,95%CI-0.06 至 0.65,3 项 RCT,n=125)相比,无抗精神病药物的 CBT 之间没有差异。与无特定治疗相比,无抗精神病药物的 CBT 与整体症状(如前所述)和阴性症状(PANSS 阴性差值-4.06,95%CI-7.50 至-0.62,1 项 RCT,n=34)的改善相关,持续时间超过 12 个月。它还与较短的住院时间(住院天数差值-22.45,95%CI-28.82 至-16.08,1 项 RCT,n=74)和更好的功能(个人和社会表现量表差值-12.42,95%CI-22.75 至-2.09,1 项 RCT,n=40,低确定性证据)相关,持续时间长达 12 个月。我们没有发现 CBT 与抗精神病药物在任何调查结局上的差异,除了使用抗精神病药物非神经副作用评定量表(ANNSERS)在 6 个月和 12 个月时测量的不良反应(差值-4.94,95%CI-8.60 至-1.28,2 项 RCT,n=48;差值-6.96,95%CI-11.55 至-2.37,2 项 RCT,n=42)。无抗精神病药物的 CBT 在减少阳性症状方面不如 CBT 联合抗精神病药物有效,持续时间长达 12 个月(SMD 0.40,95%CI 0.05 至 0.76,3 项 RCT,n=126)。与 CBT 联合抗精神病药物相比,无抗精神病药物的 CBT 导致至少发生一次不良反应的参与者人数较少,持续时间长达 12 个月(风险比 0.36,95%CI 0.17 至 0.80,1 项 RCT,n=39,低确定性证据)。

作者结论

这是首次系统综合关于在没有药物治疗的情况下向精神分裂症患者提供 CBT 的证据。研究数量有限,证据的确定性低至极低,这使得无法得出任何强有力的结论。在现有研究中一个重要的局限性是,无药物治疗组的参与者(平均约 35%)接受了抗精神病药物治疗,这突出了这种方法的挑战。需要进一步开展高质量的 RCT,以提供更多关于无抗精神病药物的 CBT 的可行性和疗效的数据。

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