Department of Counseling Psychology, University of Wisconsin, Madison, WI, USA.
Lyssn.io, Seattle, WA, USA.
Cochrane Database Syst Rev. 2021 Oct 20;10(10):CD011723. doi: 10.1002/14651858.CD011723.pub2.
Substance use disorders (SUDs) are highly prevalent and associated with a substantial public health burden. Although evidence-based interventions exist for treating SUDs, many individuals remain symptomatic despite treatment, and relapse is common.Mindfulness-based interventions (MBIs) have been examined for the treatment of SUDs, but available evidence is mixed.
To determine the effects of MBIs for SUDs in terms of substance use outcomes, craving and adverse events compared to standard care, further psychotherapeutic, psychosocial or pharmacological interventions, or instructions, waiting list and no treatment.
We searched the following databases up to April 2021: Cochrane Drugs and Alcohol Specialised Register, CENTRAL, PubMed, Embase, Web of Science, CINAHL and PsycINFO. We searched two trial registries and checked the reference lists of included studies for relevant randomized controlled trials (RCTs).
RCTs testing a MBI versus no treatment or another treatment in individuals with SUDs. SUDs included alcohol and/or drug use disorders but excluded tobacco use disorders. MBIs were defined as interventions including training in mindfulness meditation with repeated meditation practice. Studies in which SUDs were formally diagnosed as well as those merely demonstrating elevated SUD risk were eligible.
We used standard methodological procedures expected by Cochrane.
Forty RCTs met our inclusion criteria, with 35 RCTs involving 2825 participants eligible for meta-analysis. All studies were at high risk of performance bias and most were at high risk of detection bias. Mindfulness-based interventions (MBIs) versus no treatment Twenty-four RCTs included a comparison between MBI and no treatment. The evidence was uncertain about the effects of MBIs relative to no treatment on all primary outcomes: continuous abstinence rate (post: risk ratio (RR) = 0.96, 95% CI 0.44 to 2.14, 1 RCT, 112 participants; follow-up: RR = 1.04, 95% CI 0.54 to 2.01, 1 RCT, 112 participants); percentage of days with substance use (post-treatment: standardized mean difference (SMD) = 0.05, 95% CI -0.37 to 0.47, 4 RCTs, 248 participants; follow-up: SMD = 0.21, 95% CI -0.12 to 0.54, 3 RCTs, 167 participants); and consumed amount (post-treatment: SMD = 0.10, 95% CI -0.31 to 0.52, 3 RCTs, 221 participants; follow-up: SMD = 0.33, 95% CI 0.00 to 0.66, 2 RCTs, 142 participants). Evidence was uncertain for craving intensity and serious adverse events. Analysis of treatment acceptability indicated MBIs result in little to no increase in study attrition relative to no treatment (RR = 1.04, 95% CI 0.77 to 1.40, 21 RCTs, 1087 participants). Certainty of evidence for all other outcomes was very low due to imprecision, risk of bias, and/or inconsistency. Data were unavailable to evaluate adverse events. Mindfulness-based interventions (MBIs) versus other treatments (standard of care, cognitive behavioral therapy, psychoeducation, support group, physical exercise, medication) Nineteen RCTs included a comparison between MBI and another treatment. The evidence was very uncertain about the effects of MBIs relative to other treatments on continuous abstinence rate at post-treatment (RR = 0.80, 95% CI 0.45 to 1.44, 1 RCT, 286 participants) and follow-up (RR = 0.57, 95% CI 0.28 to 1.16, 1 RCT, 286 participants), and on consumed amount at post-treatment (SMD = -0.42, 95% CI -1.23 to 0.39, 1 RCT, 25 participants) due to imprecision and risk of bias. The evidence suggests that MBIs reduce percentage of days with substance use slightly relative to other treatments at post-treatment (SMD = -0.21, 95% CI -0.45 to 0.03, 5 RCTs, 523 participants) and follow-up (SMD = -0.39, 95% CI -0.96 to 0.17, 3 RCTs, 409 participants). The evidence was very uncertain about the effects of MBIs relative to other treatments on craving intensity due to imprecision and inconsistency. Analysis of treatment acceptability indicated MBIs result in little to no increase in attrition relative to other treatments (RR = 1.06, 95% CI 0.89 to 1.26, 14 RCTs, 1531 participants). Data were unavailable to evaluate adverse events.
AUTHORS' CONCLUSIONS: In comparison with no treatment, the evidence is uncertain regarding the impact of MBIs on SUD-related outcomes. MBIs result in little to no higher attrition than no treatment. In comparison with other treatments, MBIs may slightly reduce days with substance use at post-treatment and follow-up (4 to 10 months). The evidence is uncertain regarding the impact of MBIs relative to other treatments on abstinence, consumed substance amount, or craving. MBIs result in little to no higher attrition than other treatments. Few studies reported adverse events.
物质使用障碍(SUDs)非常普遍,与大量的公共卫生负担有关。尽管存在针对 SUDs 的循证干预措施,但许多人在治疗后仍有症状,且复发很常见。正念干预(MBIs)已被用于治疗 SUDs,但现有证据存在差异。
确定 MBIs 对 SUD 患者的物质使用结果、渴望和不良反应的影响,与标准护理、进一步的心理治疗、心理社会或药物干预或指导、等待名单和无治疗相比。
我们检索了以下数据库,截至 2021 年 4 月:Cochrane 药物和酒精专业注册库、CENTRAL、PubMed、Embase、Web of Science、CINAHL 和 PsycINFO。我们检索了两个试验注册库,并检查了纳入研究的参考文献,以查找相关的随机对照试验(RCTs)。
RCTs 测试 MBI 与无治疗或其他治疗在 SUD 患者中的比较。SUDs 包括酒精和/或药物使用障碍,但不包括烟草使用障碍。MBIs 被定义为包括正念冥想训练和重复冥想练习的干预措施。正式诊断为 SUDs 的研究以及仅表现出升高的 SUD 风险的研究都符合纳入标准。
我们使用了 Cochrane 预期的标准方法学程序。
40 项 RCT 符合我们的纳入标准,其中 35 项 RCT 涉及 2825 名符合荟萃分析条件的参与者。所有研究均存在高度的偏倚风险,且大多数研究存在高度的检测偏倚。MBIs 与无治疗:24 项 RCT 比较了 MBI 与无治疗。关于 MBIs 相对于无治疗对所有主要结局的影响,证据不确定:连续戒断率(治疗后:风险比(RR)=0.96,95%CI 0.44 至 2.14,1 项 RCT,112 名参与者;随访:RR=1.04,95%CI 0.54 至 2.01,1 项 RCT,112 名参与者);物质使用天数(治疗后:标准化均数差(SMD)=0.05,95%CI-0.37 至 0.47,4 项 RCT,248 名参与者;随访:SMD=0.21,95%CI-0.12 至 0.54,3 项 RCT,167 名参与者);和消耗量(治疗后:SMD=0.10,95%CI-0.31 至 0.52,3 项 RCT,221 名参与者;随访:SMD=0.33,95%CI 0.00 至 0.66,2 项 RCT,142 名参与者)。渴望强度和严重不良事件的证据不确定。治疗可接受性分析表明,与无治疗相比,MBIs 导致研究脱落率略有增加(RR=1.04,95%CI 0.77 至 1.40,21 项 RCT,1087 名参与者)。由于不精确、偏倚风险和/或不一致性,所有其他结局的证据确定性非常低。数据不可用,无法评估不良反应。MBIs 与其他治疗(标准护理、认知行为疗法、心理教育、支持小组、体育锻炼、药物治疗):19 项 RCT 比较了 MBI 与其他治疗。关于 MBIs 相对于其他治疗对治疗后(RR=0.80,95%CI 0.45 至 1.44,1 项 RCT,286 名参与者)和随访(RR=0.57,95%CI 0.28 至 1.16,1 项 RCT,286 名参与者)的连续戒断率,以及治疗后(SMD=-0.42,95%CI-1.23 至 0.39,1 项 RCT,25 名参与者)的消耗量的影响,证据非常不确定,原因是不精确和偏倚风险。证据表明,与其他治疗相比,MBIs 略微减少治疗后物质使用天数(SMD=-0.21,95%CI-0.45 至 0.03,5 项 RCT,523 名参与者)和随访(SMD=-0.39,95%CI-0.96 至 0.17,3 项 RCT,409 名参与者)。由于不精确和不一致性,关于 MBIs 相对于其他治疗对渴望强度的影响,证据不确定。治疗可接受性分析表明,与其他治疗相比,MBIs 导致脱落率略有增加(RR=1.06,95%CI 0.89 至 1.26,14 项 RCT,1531 名参与者)。数据不可用,无法评估不良反应。
与无治疗相比,MBIs 对 SUD 相关结局的影响证据不确定。MBIs 导致的脱落率略高于无治疗。与其他治疗相比,MBIs 可能会在治疗后和随访时(4 至 10 个月)减少物质使用天数。关于 MBIs 相对于其他治疗对戒断、消耗物质量或渴望的影响,证据不确定。MBIs 导致的脱落率略高于其他治疗。少数研究报告了不良反应。