在综合医院环境中对危险饮酒进行 1 分钟超简短干预的有效性:准随机试点试验。

PCN reports : psychiatry and clinical neurosciences Pub Date : 2024-06-18 eCollection Date: 2024-06-01 DOI:10.1002/pcn5.216
Yukio Tezuka, Ryuhei So, Takahiro Fukuda
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引用次数: 0

摘要

目的我们研究了超短期干预(Ultra-BI)对综合医院住院的危险饮酒行为患者的效果:在日本一家综合医院进行的准随机对照试验中,我们根据患者身份证的最后一位数字(奇数为干预组,偶数为对照组)将参与者分配到干预组或对照组。研究对象包括男性酒精使用障碍识别测试-消费(AUDIT-C)得分≥5 分,女性得分≥4 分的住院患者。干预措施包括在 1 分钟内提供建议和反馈,并随附酒精相关问题的宣传单(Ultra-BI)。对照组不接受任何干预。主要结果是干预后 3 个月的平均每周饮酒量:研究包括 68 名参与者。与对照组相比,干预组的每周平均饮酒量减少了-69.7克(95%置信区间[CI] -145.7至6.3克/周,P = 0.07)。调整基线值后进行的事后分析表明,组间差异为-78.7克/周(95% 置信区间为-135.2至-22.2克/周,P = 0.007):这项试点试验表明,Ultra-BI 在综合医院病房中具有潜在的有效性。需要进一步开展大规模研究来证实这些发现。
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The effectiveness of an ultra-brief intervention in 1 min for hazardous drinking in a general hospital setting: A quasi-randomized pilot trial.

Objective: We investigated the effectiveness of an ultra-brief intervention (Ultra-BI) for patients with hazardous drinking behaviors admitted to a general hospital.

Method: In a quasi-randomized controlled trial at a general hospital in Japan, we assigned participants to intervention or control groups based on the last digit of their patient ID (odd for intervention, even for control). The study included inpatients with Alcohol Use Disorder Identification Test-Consumption (AUDIT-C) scores of ≥5 for men and ≥4 for women. The intervention involved providing advice and feedback within 1 min, accompanied by a leaflet on alcohol-related issues (Ultra-BI). The control group did not receive any intervention. The primary outcome was average weekly alcohol consumption at 3 months postintervention.

Results: The study included 68 participants. The intervention group showed a reduction in average weekly alcohol consumption by -69.7 g/week compared to the control group (95% confidence interval [CI] -145.7 to 6.3 g/week, p = 0.07). Post-hoc analysis, adjusting for baseline values, indicated a between-group difference of -78.7 g/week (95% CI -135.2 to -22.2 g/week, p = 0.007).

Conclusion: This pilot trial suggests the potential effectiveness of the Ultra-BI in general hospital wards. Further large-scale studies are required to confirm these findings.

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