Lewis Catrin, Roberts Neil P, Bethell Andrew, Robertson Lindsay, Bisson Jonathan I
Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Hadyn Ellis Building, Maindy Road, Cardiff, UK, CF24 4HQ.
Cochrane Database Syst Rev. 2018 Dec 14;12(12):CD011710. doi: 10.1002/14651858.CD011710.pub2.
Therapist-delivered trauma-focused psychological therapies are an effective treatment for post-traumatic stress disorder (PTSD). These have become the accepted first-line treatments for the disorder. Despite the established evidence-base for these therapies, they are not always widely available or accessible. Many barriers limit treatment uptake, such as the limited number of qualified therapists to deliver the interventions, cost, and compliance issues, such as time off work, childcare, and transportation, associated with the need to attend weekly appointments. Delivering cognitive behavioural therapy (CBT) on the Internet is an effective and acceptable alternative to therapist-delivered treatments for anxiety and depression. However, fewer Internet-based therapies have been developed and evaluated for PTSD, and uncertainty surrounds the efficacy of Internet-based cognitive and behavioural therapy (I-C/BT) for PTSD.
To assess the effects of I-C/BT for PTSD in adults.
We searched the Cochrane Common Mental Disorders Group's Specialised Register (CCMDCTR) to June 2016 and identified four studies meeting the inclusion criteria. The CCMDCTR includes relevant randomised controlled trials (RCT) from MEDLINE, Embase, and PsycINFO. We also searched online clinical trial registries and reference lists of included studies, and contacted researchers in the field to identify additional and ongoing studies. We ran an update search on 1 March 2018, and identified four additional completed studies, which we added to the analyses along with two that were previously awaiting classification.
We searched for RCTs of I-C/BT compared to face-to-face or Internet-based psychological treatment, psychoeducation, wait list or care as usual. We included studies of adults (aged over 16 years or over), in which at least 70% of the participants met the diagnostic criteria for PTSD, according to the Diagnostic and Statistical Manual (DSM) or the International Classification of Diseases (ICD).
We entered data into Review Manager 5 software. We analysed categorical outcomes as risk ratios (RRs), and continuous outcomes as mean differences (MD) or standardised mean differences (SMDs), with 95% confidence intervals (CI). We pooled data with a fixed-effect meta-analysis, except where heterogeneity was present, in which case we used a random-effects model. Two review authors independently assessed the included studies for risk of bias; any conflicts were discussed with a third author, with the aim of reaching a unanimous decision.
We included 10 studies with 720 participants in the review. Eight of the studies compared I-C/BT delivered with therapist guidance to a wait list control. Two studies compared guided I-C/BT with I-non-C/BT. There was considerable heterogeneity among the included studies.Very low-quality evidence showed that, compared with wait list, I-C/BT may be associated with a clinically important reduction in PTSD post-treatment (SMD -0.60, 95% CI -0.97 to -0.24; studies = 8, participants = 560). However, there was no evidence of a difference in PTSD symptoms when follow-up was less than six months (SMD -0.43, 95% CI -1.41 to 0.56; studies = 3, participants = 146). There may be little or no difference in dropout rates between the I-C/BT and wait list groups (RR 1.39, 95% CI 1.03 to 1.88; studies = 8, participants = 585; low-quality evidence). I-C/BT was no more effective than wait list at reducing the risk of a diagnosis of PTSD after treatment (RR 0.53, 95% CI 0.28 to 1.00; studies = 1, participants = 62; very low-quality evidence). I-C/BT may be associated with a clinically important reduction in symptoms of depression both post-treatment (SMD -0.61, 95% CI -1.17 to -0.05; studies = 5, participants = 425; very low-quality evidence). Very low-quality evidence also suggested that I-C/BT may be associated with a clinically important reduction in symptoms of anxiety post-treatment (SMD -0.67, 95% CI -0.98 to -0.36; studies = 4, participants = 305), and at follow-up less than six months (MD -12.59, 95% CI -20.74 to -4.44; studies = 1, participants = 42; very low-quality evidence). The effects of I-C/BT on quality of life were uncertain (SMD 0.60, 95% CI 0.08 to 1.12; studies = 2, participants = 221; very low-quality evidence).Two studies found no difference in PTSD symptoms between the I-C/BT and I-non-C/BT groups when measured post-treatment (SMD -0.08, 95% CI -0.52 to 0.35; studies = 2, participants = 82; very low-quality evidence), or when follow-up was less than six months (SMD 0.08, 95% CI -0.41 to 0.57; studies = 2, participants = 65; very low-quality evidence). However, those who received I-C/BT reported their PTSD symptoms were better at six- to 12-month follow-up (MD -8.83, 95% CI -17.32 to -0.34; studies = 1, participants = 18; very low-quality evidence). Two studies found no difference in depressive symptoms between the I-C/BT and I-non-C/BT groups when measured post-treatment (SMD -0.12, 95% CI -0.78 to 0.54; studies = 2, participants = 84; very low-quality evidence) or when follow-up was less than six months (SMD 0.20, 95% CI -0.31 to 0.71; studies = 2, participants = 61; very low-quality evidence). However, those who received I-C/BT reported their depressive symptoms were better at six- to 12-month follow-up (MD -8.34, 95% CI -15.83 to -0.85; studies = 1, participants = 18; very low-quality evidence). Two studies found no difference in symptoms of anxiety between the I-C/BT and I-non-C/BT groups when measured post-treatment (SMD 0.08, 95% CI -0.78 to 0.95; studies = 2, participants = 74; very low-quality evidence) or when follow-up was less than six months (SMD -0.16, 95% CI -0.67 to 0.35; studies = 2, participants = 60; very low-quality evidence). However, those who received I-C/BT reported their symptoms of anxiety were better at six- to 12-month follow-up (MD -8.05, 95% CI -15.20 to -0.90; studies = 1, participants = 18; very low-quality evidence).None of the included studies reported on cost-effectiveness or adverse events.
AUTHORS' CONCLUSIONS: While the review found some beneficial effects of I-C/BT for PTSD, the quality of the evidence was very low due to the small number of included trials. Further work is required to: establish non-inferiority to current first-line interventions, explore mechanisms of change, establish optimal levels of guidance, explore cost-effectiveness, measure adverse events, and determine predictors of efficacy and dropout.
由治疗师提供的针对创伤的心理疗法是治疗创伤后应激障碍(PTSD)的有效方法。这些疗法已成为该疾病公认的一线治疗方法。尽管这些疗法有既定的证据基础,但它们并非总是广泛可得或易于获得。许多障碍限制了治疗的采用,例如能够提供干预措施的合格治疗师数量有限、成本以及与每周就诊相关的依从性问题,如请假、 childcare和交通等。在互联网上提供认知行为疗法(CBT)是治疗师提供的焦虑和抑郁治疗的一种有效且可接受的替代方法。然而,针对PTSD开发和评估的基于互联网的疗法较少,基于互联网的认知行为疗法(I-C/BT)对PTSD的疗效存在不确定性。
评估I-C/BT对成人PTSD的影响。
我们检索了Cochrane常见精神障碍小组的专业注册库(CCMDCTR)至2016年6月,并确定了四项符合纳入标准的研究。CCMDCTR包括来自MEDLINE、Embase和PsycINFO的相关随机对照试验(RCT)。我们还搜索了在线临床试验注册库和纳入研究的参考文献列表,并联系了该领域的研究人员以识别其他和正在进行的研究。我们于2018年3月1日进行了更新搜索,并确定了另外四项已完成的研究,我们将其与之前等待分类分析的两项研究一起纳入分析。
我们搜索了I-C/BT与面对面或基于互联网的心理治疗、心理教育、等待列表或常规护理相比的RCT。我们纳入了成人(16岁及以上)的研究,其中至少70%的参与者根据《诊断和统计手册》(DSM)或《国际疾病分类》(ICD)符合PTSD的诊断标准。
我们将数据录入Review Manager 5软件。我们将分类结果分析为风险比(RRs),将连续结果分析为平均差(MD)或标准化平均差(SMD),并带有95%置信区间(CI)。我们采用固定效应荟萃分析合并数据,除非存在异质性,在这种情况下我们使用随机效应模型。两位综述作者独立评估纳入研究的偏倚风险;任何冲突都与第三位作者讨论,旨在达成一致决定。
我们在综述中纳入了10项研究,共720名参与者。其中八项研究将在治疗师指导下提供的I-C/BT与等待列表对照进行了比较。两项研究将有指导的I-C/BT与I-非C/BT进行了比较。纳入研究之间存在相当大的异质性。极低质量的证据表明,与等待列表相比,I-C/BT可能与治疗后PTSD的临床显著降低相关(SMD -0.60,95% CI -0.97至-0.24;研究 = 8,参与者 = 560)。然而,当随访少于六个月时,没有证据表明PTSD症状存在差异(SMD -0.43,95% CI -1.41至0.56;研究 = 3,参与者 = 146)。I-C/BT组和等待列表组之间的脱落率可能几乎没有差异(RR 1.39,95% CI 1.03至1.88;研究 = 8,参与者 = 585;低质量证据)。I-C/BT在降低治疗后PTSD诊断风险方面并不比等待列表更有效(RR 0.53,95% CI 0.28至1.00;研究 = 1,参与者 = 62;极低质量证据)。I-C/BT可能与治疗后抑郁症状的临床显著降低相关(SMD -0.61,95% CI -1.17至-0.05;研究 = 5,参与者 = 425;极低质量证据)。极低质量的证据还表明,I-C/BT可能与治疗后焦虑症状的临床显著降低相关(SMD -0.67,95% CI -0.98至-0.36;研究 = 4,参与者 = 305),以及在随访少于六个月时(MD -12.59,95% CI -20.74至-4.44;研究 = 1,参与者 = 42;极低质量证据)。I-C/BT对生活质量的影响尚不确定(SMD 0.60,95% CI 0.08至1.12;研究 = 2,参与者 = 221;极低质量证据)。两项研究发现,治疗后测量时I-C/BT组和I-非C/BT组之间的PTSD症状没有差异(SMD -0.08,95% CI -0.52至0.35;研究 = 2,参与者 = 82;极低质量证据),或者随访少于六个月时(SMD 0.08,95% CI -0.41至0.57;研究 = 2,参与者 = 65;极低质量证据)。然而,接受I-C/BT的人在6至12个月的随访中报告他们的PTSD症状有所改善(MD -8.83,95% CI -17.32至-0.34;研究 = 1,参与者 = 18;极低质量证据)。两项研究发现,治疗后测量时I-C/BT组和I-非C/BT组之间的抑郁症状没有差异(SMD -0.12,95% CI -0.78至0.54;研究 = 2,参与者 = 84;极低质量证据),或者随访少于六个月时(SMD 0.20,95% CI -0.31至0.71;研究 = 2,参与者 = 61;极低质量证据)。然而,接受I-C/BT的人在6至12个月的随访中报告他们的抑郁症状有所改善(MD -8.34,95% CI -15.83至-0.85;研究 = 1,参与者 = 18;极低质量证据)。两项研究发现,治疗后测量时I-C/BT组和I-非C/BT组之间的焦虑症状没有差异(SMD 0.08,95% CI -0.78至0.95;研究 = 2,参与者 = 74;极低质量证据),或者随访少于六个月时(SMD -0.16,95% CI -0.67至0.35;研究 = 2,参与者 = 60;极低质量证据)。然而,接受I-C/BT的人在6至12个月的随访中报告他们的焦虑症状有所改善(MD -8.05,95% CI -15.20至-0.90;研究 = 1,参与者 = 18;极低质量证据)。纳入的研究均未报告成本效益或不良事件。
虽然综述发现I-C/BT对PTSD有一些有益影响,但由于纳入试验数量较少,证据质量非常低。需要进一步开展工作以:确定与当前一线干预措施的非劣效性、探索变化机制、确定最佳指导水平、探索成本效益、测量不良事件以及确定疗效和脱落的预测因素。