Cowan Ethan, O'Brien-Lambert Clare, Eiting Erick, Bull Edward, Ryder Jacqueline, Calderon Yvette, Salsitz Edwin
Department of Emergency Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Department of Emergency Medicine, Rutgers New Jersey Medical School, Newark, New Jersey, USA.
Acad Emerg Med. 2025 May;32(5):488-497. doi: 10.1111/acem.15059. Epub 2025 Jan 8.
Alcohol use disorder (AUD) is the most common substance use disorder in the United States. Despite availability of four FDA-approved medications, fewer than 10% of patients are prescribed medication. This study aimed to evaluate the impact and feasibility of emergency department (ED)-initiated oral naltrexone in patients with moderate to severe AUD.
This was a prospective, single-arm, open-label, nonrandomized clinical trial conducted a single ED. Consenting participants were adults with moderate to severe AUD who were provided a single 50-mg dose of oral naltrexone, a 14-day starter pack of naltrexone, and referral for treatment. Follow-up was conducted at 14 and 30 days post-ED visit. The primary outcome was engagement in formal addiction treatment. Secondary outcomes included alcohol consumption, craving, quality-of-life measures, satisfaction, and safety.
Of 761 patients screened, 21 enrolled and received at least one dose of naltrexone. At 14 days, 29% were engaged in treatment, increasing to 33% at 30 days. There was a decrease in the mean (±SD) number of drinks per day from 5.20 (±4.67) at baseline to 2.23 (±4.35) during the follow-up period (p = 0.078). There was a decrease in alcohol craving scores, with median scores dropping from 19 at baseline to 8.27 during the follow-up period (p < 0.001). Quality-of-life measures improved, with a statistically significant increase in the reported number of healthy days (p = 0.006) and decrease in depressive symptoms (p < 0.001). Reported side effects were mild and satisfaction with the screening process was high.
ED-initiated oral naltrexone is feasible and acceptable for patients with moderate to severe AUD. While engagement in treatment was moderate, significant reductions in alcohol craving and improvements in quality of life suggest potential benefits. Further research is warranted to confirm these findings.
酒精使用障碍(AUD)是美国最常见的物质使用障碍。尽管有四种经美国食品药品监督管理局(FDA)批准的药物,但接受药物治疗的患者不到10%。本研究旨在评估急诊科(ED)启动口服纳曲酮对中重度AUD患者的影响和可行性。
这是一项在单一急诊科进行的前瞻性、单臂、开放标签、非随机临床试验。同意参与的受试者为中重度AUD的成年人,他们接受了一剂50毫克的口服纳曲酮、一个为期14天的纳曲酮起始装,并被转介接受治疗。在急诊科就诊后14天和30天进行随访。主要结局是参与正式的成瘾治疗。次要结局包括酒精消费、渴望、生活质量指标、满意度和安全性。
在761名接受筛查的患者中,21名入组并接受了至少一剂纳曲酮。在14天时,29%的患者参与了治疗,在30天时增至33%。每天饮酒的平均(±标准差)数量从基线时的5.20(±4.67)降至随访期间的2.23(±4.35)(p = 0.078)。酒精渴望评分降低,中位数评分从基线时的19降至随访期间的8.27(p < 0.001)。生活质量指标有所改善,报告的健康天数有统计学意义的增加(p = 0.006),抑郁症状有所减轻(p < 0.001)。报告的副作用较轻,对筛查过程的满意度较高。
急诊科启动口服纳曲酮对中重度AUD患者是可行且可接受的。虽然参与治疗的程度一般,但酒精渴望的显著降低和生活质量的改善表明有潜在益处。有必要进行进一步研究以证实这些发现。