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苯巴比妥用于酒精戒断的全院实施情况、临床结局及安全性

Hospital-Wide Implementation, Clinical Outcomes, and Safety of Phenobarbital for Alcohol Withdrawal.

作者信息

Wolpaw Benjamin J, Oren Hannah, Quinnan-Hostein Laura, Bradley Katharine A, Johnson Nicholas J, Hallgren Kevin A, Gupta Ayushi, Kim H Nina, Granich Marion A, Steel Tessa L

机构信息

Division of General Internal Medicine, Department of Medicine, University of Washington, Seattle.

Kaiser Permanente Washington Health Research Institute, Seattle.

出版信息

JAMA Netw Open. 2025 Aug 1;8(8):e2528694. doi: 10.1001/jamanetworkopen.2025.28694.

Abstract

IMPORTANCE

Phenobarbital monotherapy is increasingly used to treat alcohol withdrawal syndrome (AWS) in hospitalized patients, but its implementation outside academic emergency departments (EDs) and intensive care units (ICUs) remains understudied.

OBJECTIVE

To evaluate the implementation, clinical outcomes, and safety of an electronic health record (EHR) order set for intravenous weight-based phenobarbital loading (10 or 15 mg/kg) across all care locations (ED, acute care, and ICU) of a community hospital.

DESIGN, SETTING, AND PARTICIPANTS: This retrospective quality improvement study was conducted at a 281-bed community hospital in Seattle, Washington, including all hospitalized adults treated for AWS 11 months before and 12 months after implementation of the phenobarbital EHR order set (April 1, 2021, to March 31, 2023). Data analysis occurred in May 2024.

EXPOSURE

Initiation of AWS treatment before vs on or after March 24, 2022.

MAIN OUTCOMES AND MEASURES

Implementation was assessed by order set use and cumulative phenobarbital and benzodiazepine exposure. Clinical outcomes included daily maximum Clinical Institute Withdrawal Assessment of Alcohol Scale Revised (CIWA-Ar) scores, AWS treatment duration (time from first to last medication), and time from AWS treatment initiation to hospital discharge. Safety outcomes included prolonged use of physical restraints (>1 day), intubation, and in-hospital mortality. Logistic and negative binomial regression models were used to estimate differences in each outcome, before vs after implementation, adjusting for baseline group differences.

RESULTS

Among 254 patients, the preimplementation (154 patients) and postimplementation (100 patients) groups were similar in terms of baseline characteristics; most were middle-aged (mean [SD] age, 53.0 [14.9] years), male (177 men [66.9%]), and publicly insured (186 patients [73.2%]). After implementation, the phenobarbital order set was used for 67 patients (67.0%), predominantly in ED and acute care locations. AWS symptoms resolved more rapidly after implementation, with a 4.2- to 5.0-point reduction in daily maximum CIWA-Ar scores at 24 to 96 hours from hospital presentation, 30.1-hour reduction in AWS treatment duration (95% CI, 16.7-43.5 hours), and 2.2-day reduction in time to hospital discharge (95% CI, 0.7-3.7 days). Safety outcomes did not significantly differ before and after implementation.

CONCLUSIONS AND RELEVANCE

In this quality improvement study, implementation of a weight-based phenobarbital order set for AWS in all care locations of a community hospital was associated with faster symptom resolution, shorter length of stay, and no differences in safety outcomes. These findings support the broader adoption of phenobarbital-based AWS treatment across diverse hospital settings.

摘要

重要性

苯巴比妥单药疗法越来越多地用于治疗住院患者的酒精戒断综合征(AWS),但其在学术急诊部门(ED)和重症监护病房(ICU)之外的实施情况仍研究不足。

目的

评估社区医院所有护理地点(ED、急性护理和ICU)基于体重的静脉注射苯巴比妥负荷剂量(10或15mg/kg)的电子健康记录(EHR)医嘱集的实施情况、临床结局和安全性。

设计、设置和参与者:这项回顾性质量改进研究在华盛顿州西雅图市一家拥有281张床位的社区医院进行,纳入了在苯巴比妥EHR医嘱集实施前11个月和实施后12个月(2021年4月1日至2023年3月31日)接受AWS治疗的所有成年住院患者。数据分析于2024年5月进行。

暴露因素

2022年3月24日之前与之后开始AWS治疗。

主要结局和测量指标

通过医嘱集使用情况以及苯巴比妥和苯二氮䓬的累积暴露量评估实施情况。临床结局包括每日最大酒精戒断临床研究所修订评估量表(CIWA-Ar)评分、AWS治疗持续时间(从首次用药到最后一次用药的时间)以及从AWS治疗开始到出院的时间。安全结局包括长期使用身体约束(>1天)、插管和院内死亡率。使用逻辑回归和负二项回归模型估计实施前后各结局的差异,并对基线组差异进行调整。

结果

在254例患者中,实施前组(154例患者)和实施后组(100例患者)在基线特征方面相似;大多数为中年患者(平均[标准差]年龄,53.0[14.9]岁),男性(177例男性[66.9%]),且有公共保险(186例患者[73.2%])。实施后,67例患者(67.0%)使用了苯巴比妥医嘱集,主要在ED和急性护理地点。实施后AWS症状缓解更快,从入院后24至96小时每日最大CIWA-Ar评分降低4.2至5.0分,AWS治疗持续时间缩短30.1小时(95%CI,16.7 - 43.5小时),出院时间缩短2.2天(95%CI,0.7 - 3.7天)。实施前后安全结局无显著差异。

结论和相关性

在这项质量改进研究中,社区医院所有护理地点实施基于体重的苯巴比妥AWS医嘱集与症状缓解更快、住院时间缩短以及安全结局无差异相关。这些发现支持在不同医院环境中更广泛地采用基于苯巴比妥的AWS治疗。

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