Shanghai Key Laboratory of Psychotic Disorders, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
CAS Center for Excellence in Brain Science and Intelligence Technology (CEBSIT), Chinese Academy of Science, Shanghai, China.
Schizophr Bull. 2022 Jan 21;48(1):8-19. doi: 10.1093/schbul/sbab044.
This study aimed to provide insight into the efficacy of cognitive-behavioral therapy for psychosis (CBTp) in patients with "clinical high risk of psychosis (CHR-P)".
Major scientific databases were searched up to April 17, 2020. Randomized controlled trials in CHR-P individuals, comparing CBTp with needs-based interventions (NBI, including treatment as usual or nonspecific control treatment) were included, following PRISMA guidelines. The primary outcome (efficacy) was transition to psychosis by 6 months, 12 months, 24 months, and over 24 months. Secondary outcomes were change in attenuated psychotic symptoms, depression, distress, improvements in functioning, and quality of life.
Ten randomized controlled studies met inclusion criteria. The comparisons included 1128 participants. CBTp was significantly more efficacious in reducing rate of transition to psychosis by 6 months (after post-hoc sensitivity analysis) (relative risk [RR] = 0.44, 95% confidence interval [CI]: 0.26, 0.73), 12 months (RR = 0.44, 95% CI: 0.30, 0.64), 12 months (RR = 0.46, 95%CI: 0.30, 0.69), and over 24 months (RR = 0.58, 95% CI: 0.35, 0.95) after treatment, compared with those receiving NBI. CBTp was also associated with more reduced attenuated psychotic symptoms by 12 months (SMD = -0.17, 95% CI: -0.33, -0.02) and by 24 months (SMD = -0.24, 95% CI: -0.43, -0.06). No beneficial effects on functioning, depression, quality of life, or distress were observed favoring CBTp.
CBTp is effective in reducing both psychosis transition rates and attenuated psychotic symptoms for the prodromal stage of psychosis. It is a promising intervention at the preventative stage.
本研究旨在深入了解认知行为疗法(CBTp)对“临床精神病高危人群(CHR-P)”的疗效。
截至 2020 年 4 月 17 日,我们在主要科学数据库中进行了检索。纳入了 CHR-P 个体的随机对照试验,比较了 CBTp 与基于需求的干预(NBI,包括常规治疗或非特异性对照治疗),并遵循 PRISMA 指南。主要结局(疗效)为 6 个月、12 个月、24 个月和 24 个月以上的精神病转化率。次要结局包括减轻的精神病症状、抑郁、痛苦、功能改善和生活质量的变化。
符合纳入标准的有 10 项随机对照研究。这些比较共纳入了 1128 名参与者。CBTp 在降低精神病转化率方面更为有效,6 个月时(经事后敏感性分析)(相对风险[RR] = 0.44,95%置信区间[CI]:0.26,0.73),12 个月时(RR = 0.44,95%CI:0.30,0.64),12 个月时(RR = 0.46,95%CI:0.30,0.69)和 24 个月以上时(RR = 0.58,95%CI:0.35,0.95),与接受 NBI 的患者相比。CBTp 还与 12 个月时(SMD = -0.17,95%CI:-0.33,-0.02)和 24 个月时(SMD = -0.24,95%CI:-0.43,-0.06)减轻精神病前症状有关。未观察到 CBTp 有利于功能、抑郁、生活质量或痛苦的有益影响。
CBTp 可有效降低精神病前驱期的精神病转化率和精神病前症状。它是预防阶段很有前途的干预措施。