Risk of mortality among patients with alcohol-associated hepatitis in the US from 2007 to 2021

IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Alcohol Pub Date : 2024-06-20 DOI:10.1016/j.alcohol.2024.06.006
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Abstract

Background/Aims

Alcohol-associated hepatitis (AH) mortality and risk factors have not been carefully studied in real-world settings. We examined the rate, temporal trend, and risk factors of mortality in AH.

Methods

We conducted a cohort study of individuals with AH diagnoses using medical claims data from Optum's Clinformatics® Data Mart (CDM). Participants were individuals covered by Medicare Advantage and commercial insurance policies. Cases were identified using diagnostic codes. Cox regressions were used to estimate 90 and 180-day mortality rates by hospitalization status.

Results

The cohort included 32,001 patients (72% men) who had at least one year of continuous insurance coverage prior to AH diagnoses. Of these, 20,912 were hospitalized within seven days of diagnosis. Ninety and 180-day mortality rates were 12.0% (95% CI [11.6%, 12.5%]) and 16.0% (95% CI [15.4%, 16.5%]), respectively, for the hospitalized patients and 3.1% (95% CI [2.8%, 3.4%]) and 5.1% (95% CI [4.6%, 5.5%]) for the non-hospitalized patients. Pre-existing liver disease, even in a mild form, was associated with an increased risk of death. In hospitalized patients, a history of mild liver disease was associated with a 24% increase in 180-day mortality risk (HR = 1.24, 95% CI: [1.14, 1.36]). Moderate-to-severe liver disease was associated with a more than doubled risk (HR = 2.33, 95% CI: [2.12, 2.56]).

Conclusions

History of liver disease was associated with significantly increased AH mortality. The finding highlights the chronic disease context of AH and suggests that prior diagnosis of liver disease should be considered for prognosis and targeted prevention.

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2007 年至 2021 年美国酒精相关肝炎患者的死亡风险。
背景:/Aims: 酒精相关性肝炎(AH)的死亡率和风险因素尚未在真实世界环境中得到仔细研究。我们研究了酒精相关性肝炎的死亡率、时间趋势和风险因素:我们使用 Optum 的 Clinformatics® Data Mart (CDM) 中的医疗索赔数据,对确诊为 AH 的患者进行了一项队列研究。研究对象为医疗保险优势计划和商业保险的受保人。病例通过诊断代码确定。采用 Cox 回归估算住院状态下的 90 天和 180 天死亡率:该队列包括 32,001 名患者(72% 为男性),他们在确诊急性呼吸系统综合症之前至少已连续投保一年。其中 20,912 人在确诊后七天内住院治疗。住院患者的 90 天和 180 天死亡率分别为 12.0% (95% CI [11.6%, 12.5%]) 和 16.0% (95% CI [15.4%, 16.5%]) ,非住院患者的 90 天和 180 天死亡率分别为 3.1% (95% CI [2.8%, 3.4%]) 和 5.1% (95% CI [4.6%, 5.5%]) 。既往肝病,即使是轻度肝病,也会增加死亡风险。在住院患者中,轻度肝病史与 180 天死亡风险增加 24% 相关(HR= 1.24,95% CI:[1.14, 1.36])。中度至重度肝病的风险增加了一倍多(HR= 2.33,95% CI:[2.12,2.56]):结论:肝脏疾病史与甲型肝炎死亡率的显著增加有关。这一发现强调了急性呼吸系统综合症的慢性疾病背景,并建议在进行预后判断和有针对性的预防时应考虑肝脏疾病的既往诊断。
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来源期刊
Alcohol
Alcohol 医学-毒理学
CiteScore
4.60
自引率
4.30%
发文量
74
审稿时长
15.6 weeks
期刊介绍: Alcohol is an international, peer-reviewed journal that is devoted to publishing multi-disciplinary biomedical research on all aspects of the actions or effects of alcohol on the nervous system or on other organ systems. Emphasis is given to studies into the causes and consequences of alcohol abuse and alcoholism, and biomedical aspects of diagnosis, etiology, treatment or prevention of alcohol-related health effects. Intended for both research scientists and practicing clinicians, the journal publishes original research on the neurobiological, neurobehavioral, and pathophysiological processes associated with alcohol drinking, alcohol abuse, alcohol-seeking behavior, tolerance, dependence, withdrawal, protracted abstinence, and relapse. In addition, the journal reports studies on the effects alcohol on brain mechanisms of neuroplasticity over the life span, biological factors associated with adolescent alcohol abuse, pharmacotherapeutic strategies in the treatment of alcoholism, biological and biochemical markers of alcohol abuse and alcoholism, pathological effects of uncontrolled drinking, biomedical and molecular factors in the effects on liver, immune system, and other organ systems, and biomedical aspects of fetal alcohol spectrum disorder including mechanisms of damage, diagnosis and early detection, treatment, and prevention. Articles are published from all levels of biomedical inquiry, including the following: molecular and cellular studies of alcohol''s actions in vitro and in vivo; animal model studies of genetic, pharmacological, behavioral, developmental or pathophysiological aspects of alcohol; human studies of genetic, behavioral, cognitive, neuroimaging, or pathological aspects of alcohol drinking; clinical studies of diagnosis (including dual diagnosis), treatment, prevention, and epidemiology. The journal will publish 9 issues per year; the accepted abbreviation for Alcohol for bibliographic citation is Alcohol.
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