Department of Epidemiology, Lazio Regional Health Service, Rome, Italy.
Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, Pavia, Italy.
Cochrane Database Syst Rev. 2024 Apr 29;4(4):CD015042. doi: 10.1002/14651858.CD015042.pub2.
Despite the known harms, alcohol consumption is common in pregnancy. Rates vary between countries, and are estimated to be 10% globally, with up to 25% in Europe.
To assess the efficacy of psychosocial interventions and medications to reduce or stop alcohol consumption during pregnancy.
We searched the Cochrane Drugs and Alcohol Group Specialised Register (via CRSLive), Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, Embase, CINAHL, Web of Science, and PsycINFO, from inception to 8 January 2024. We also searched for ongoing and unpublished studies via ClinicalTrials.gov and the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP). All searches included non-English language literature. We handsearched references of topic-related systematic reviews and included studies.
We included randomised controlled trials that compared medications or psychosocial interventions, or both, to placebo, no intervention, usual care, or other medications or psychosocial interventions used to reduce or stop alcohol use during pregnancy. Our primary outcomes of interest were abstinence from alcohol, reduction in alcohol consumption, retention in treatment, and women with any adverse event.
We used standard Cochrane methodological procedures.
We included eight studies (1369 participants) in which pregnant women received an intervention to stop or reduce alcohol use during pregnancy. In one study, almost half of participants had a current diagnosis of alcohol use disorder (AUD); in another study, 40% of participants had a lifetime diagnosis of AUD. Six studies took place in the USA, one in Spain, and one in the Netherlands. All included studies evaluated the efficacy of psychosocial interventions; we did not find any study that evaluated the efficacy of medications for the treatment of AUD during pregnancy. Psychosocial interventions were mainly brief interventions ranging from a single session of 10 to 60 minutes to five sessions of 10 minutes each. Pregnant women received the psychosocial intervention approximately at the end of the first trimester of pregnancy, and the outcome of alcohol use was reassessed 8 to 24 weeks after the psychosocial intervention. Women in the control group received treatment as usual (TAU) or similar treatments such as comprehensive assessment of alcohol use and advice to stop drinking during pregnancy. Globally, we found that, compared to TAU, psychosocial interventions may increase the rate of continuously abstinent participants (risk ratio (RR) 1.34, 95% confidence interval (CI) 1.14 to 1.57; I =0%; 3 studies; 378 women; low certainty evidence). Psychosocial interventions may have little to no effect on the number of drinks per day, but the evidence is very uncertain (mean difference -0.42, 95% CI -1.13 to 0.28; I = 86%; 2 studies; 157 women; very low certainty evidence). Psychosocial interventions probably have little to no effect on the number of women who completed treatment (RR 0.98, 95% CI 0.94 to 1.02; I = 0%; 7 studies; 1283 women; moderate certainty evidence). None of the included studies assessed adverse events of treatments. We downgraded the certainty of the evidence due to risk of bias and imprecision of the estimates.
AUTHORS' CONCLUSIONS: Brief psychosocial interventions may increase the rate of continuous abstinence among pregnant women who report alcohol use during pregnancy. Further studies should be conducted to investigate the efficacy and safety of psychosocial interventions and other treatments (e.g. medications) for women with AUD. These studies should provide detailed information on alcohol use before and during pregnancy using consistent measures such as the number of drinks per drinking day. When heterogeneous populations are recruited, more detailed information on alcohol use during pregnancy should be provided to allow future systematic reviews to be conducted. Other important information that would enhance the usefulness of these studies would be the presence of other comorbid conditions such as anxiety, mood disorders, and the use of other psychoactive substances.
尽管已知饮酒对胎儿有危害,但怀孕期间饮酒仍很常见。各国的饮酒率不同,全球估计为 10%,欧洲高达 25%。
评估心理社会干预和药物治疗减少或停止孕妇饮酒的效果。
我们检索了 Cochrane 药物和酒精组专业注册库(通过 CRSLive)、Cochrane 对照试验中心注册库(CENTRAL)、MEDLINE、Embase、CINAHL、Web of Science 和 PsycINFO,检索时间截至 2024 年 1 月 8 日。我们还通过 ClinicalTrials.gov 和世界卫生组织(WHO)国际临床试验注册平台(ICTRP)检索了正在进行和未发表的研究。所有检索均包括非英语文献。我们还手工检索了与专题相关的系统评价和纳入研究的参考文献。
我们纳入了比较药物或心理社会干预,或两者联合与安慰剂、无干预、常规护理或用于减少或停止孕妇饮酒的其他药物或心理社会干预的随机对照试验。我们主要关注的结局是酒精戒断、饮酒量减少、治疗保留率和任何不良事件发生的女性。
我们使用了标准的 Cochrane 方法学程序。
我们纳入了八项研究(1369 名参与者),这些孕妇接受了一项干预措施以停止或减少怀孕期间的饮酒。在一项研究中,近一半的参与者目前被诊断为酒精使用障碍(AUD);在另一项研究中,40%的参与者有终生 AUD 诊断。六项研究在美国进行,一项在西班牙进行,一项在荷兰进行。所有纳入的研究均评估了心理社会干预的效果;我们没有发现任何评估药物治疗 AUD 的研究。心理社会干预主要是简短干预,范围从 10 到 60 分钟的单次干预到每次 10 分钟的五次干预。孕妇在妊娠第一 trimester 末接受心理社会干预,在心理社会干预后 8 至 24 周重新评估饮酒情况。对照组的女性接受常规治疗(TAU)或类似的治疗,如酒精使用综合评估和建议在怀孕期间戒酒。总的来说,与 TAU 相比,心理社会干预可能会增加持续戒酒的参与者比例(风险比(RR)1.34,95%置信区间(CI)1.14 至 1.57;I = 0%;3 项研究;378 名女性;低确定性证据)。心理社会干预可能对每天的饮酒量影响不大,但证据极不确定(平均差异-0.42,95%CI-1.13 至 0.28;I = 86%;2 项研究;157 名女性;极低确定性证据)。心理社会干预可能对完成治疗的女性数量影响不大(RR 0.98,95%CI 0.94 至 1.02;I = 0%;7 项研究;1283 名女性;中等确定性证据)。纳入的研究均未评估治疗的不良事件。由于偏倚风险和估计值的不精确性,我们降低了证据的确定性。
简短的心理社会干预可能会增加报告怀孕期间饮酒的孕妇的持续戒酒率。需要进一步研究以评估心理社会干预和其他治疗(例如药物)对 AUD 女性的疗效和安全性。这些研究应使用一致的措施(如每天饮酒量)提供怀孕前后酒精使用的详细信息。当招募异质人群时,应提供更详细的怀孕期间饮酒信息,以便未来的系统评价能够进行。其他增强这些研究有用性的重要信息将是其他合并症的存在,如焦虑、情绪障碍和其他精神活性物质的使用。