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1
Improving Estimates of Alcohol-Attributable Deaths in the United States: Impact of Adjusting for the Underreporting of Alcohol Consumption.改进美国酒精所致死亡人数的估计:调整酒精消费漏报情况的影响
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2
Global Epidemiology of Chronic Liver Disease.慢性肝病的全球流行病学
Clin Liver Dis (Hoboken). 2021 Jun 4;17(5):365-370. doi: 10.1002/cld.1061. eCollection 2021 May.
3
The role of alcohol use in the aetiology and progression of liver disease: A narrative review and a quantification.酒精使用在肝脏疾病病因学和进展中的作用:叙述性综述和定量评估。
Drug Alcohol Rev. 2021 Nov;40(7):1377-1386. doi: 10.1111/dar.13286. Epub 2021 Mar 30.
4
Alcohol Policies and Alcohol-related Liver Disease Mortality.酒精政策与酒精性肝病死亡率
Gastroenterology. 2021 Jul;161(1):350-352. doi: 10.1053/j.gastro.2021.03.031. Epub 2021 Mar 19.
5
The International Model of Alcohol Harms and Policies: A New Method for Estimating Alcohol Health Harms With Application to Alcohol-Attributable Mortality in Canada.国际酒精危害与政策模型:一种新的酒精健康危害估计方法及其在加拿大归因于酒精的死亡率中的应用。
J Stud Alcohol Drugs. 2020 May;81(3):339-351.
6
Projected prevalence and mortality associated with alcohol-related liver disease in the USA, 2019-40: a modelling study.预计 2019-2040 年美国与酒精性肝病相关的患病率和死亡率:一项建模研究。
Lancet Public Health. 2020 Jun;5(6):e316-e323. doi: 10.1016/S2468-2667(20)30062-1.
7
Global Burden of Alcohol Use Disorders and Alcohol Liver Disease.酒精使用障碍和酒精性肝病的全球负担
Biomedicines. 2019 Dec 13;7(4):99. doi: 10.3390/biomedicines7040099.
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Alcohol Use Is Associated With Hepatic Steatosis Among Persons With Presumed Nonalcoholic Fatty Liver Disease.酒精使用与疑似非酒精性脂肪性肝病患者的肝脂肪变性有关。
Clin Gastroenterol Hepatol. 2020 Jul;18(8):1831-1841.e5. doi: 10.1016/j.cgh.2019.11.022. Epub 2019 Nov 14.
9
Consistency of Drinker Status Over Time: Drinking Patterns of Ex-Drinkers Who Describe Themselves as Lifetime Abstainers.随着时间推移,饮酒者身份的一致性:描述自己为终身戒酒者的前饮酒者的饮酒模式。
J Stud Alcohol Drugs. 2019 Sep;80(5):552-556.
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Alcohol Consumption and Risk of Liver Cirrhosis: A Systematic Review and Meta-Analysis.饮酒与肝硬化风险:系统评价和荟萃分析。
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估算酒精性肝病死亡率:方法比较。

Estimating alcohol-attributable liver disease mortality: A comparison of methods.

机构信息

Canadian Institute for Substance Use Research, Victoria, Canada.

National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, USA.

出版信息

Drug Alcohol Rev. 2022 Jul;41(5):1245-1253. doi: 10.1111/dar.13470. Epub 2022 Apr 1.

DOI:10.1111/dar.13470
PMID:35363378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9253033/
Abstract

INTRODUCTION

Alcohol is a leading contributor to liver disease, however, estimating the proportion of liver disease deaths attributable to alcohol use can be methodologically challenging.

METHODS

We compared three approaches for estimating alcohol-attributable liver disease deaths (AALDD), using the USA as an example. One involved summing deaths from alcoholic liver disease and a proportion from unspecified cirrhosis (direct method); two used population attributable fraction (PAF) methodology, including one that adjusted for per capita alcohol sales. For PAFs, the 2011-2015 Behavioral Risk Factor Surveillance System and per capita sales from the Alcohol Epidemiologic Data System were used to derive alcohol consumption prevalence estimates at various levels (excessive alcohol use was defined by medium and high consumption levels). Prevalence estimates were used with relative risks from two meta-analyses, and PAFs were applied to the 2011-2015 average annual number of deaths from alcoholic cirrhosis and unspecified cirrhosis (using National Vital Statistics System data) to estimate AALDD.

RESULTS

The number of AALDD was higher using the direct method (28 345 annually) than the PAF methods, but similar when alcohol prevalence was adjusted using per capita sales and all alcohol consumption levels were considered (e.g. 25 145 AALDD). Using the PAF method, disaggregating non-drinkers into lifetime abstainers and former drinkers to incorporate relative risks for former drinkers yielded higher AALDD estimates (e.g. 27 686) than methods with all non-drinkers combined.

DISCUSSION AND CONCLUSIONS

Using PAF methods that adjust for per capita sales and model risks for former drinkers yield more complete and possibly more valid AALDD estimates.

摘要

简介

酒精是导致肝病的主要原因之一,然而,估计与饮酒相关的肝病死亡比例在方法学上具有挑战性。

方法

我们以美国为例,比较了三种估计酒精性肝病死亡归因(AALDD)的方法。一种方法是将酒精性肝病死亡和一部分未指明的肝硬化死亡相加(直接法);两种方法使用人群归因分数(PAF)方法,包括一种调整人均酒精销售的方法。对于 PAF,使用 2011-2015 年行为风险因素监测系统和酒精流行病学数据系统的人均销售额来推导不同水平的酒精消费流行率估计值(过量饮酒定义为中高消费水平)。使用两项荟萃分析的相对风险来估计流行率,将 PAF 应用于 2011-2015 年每年死于酒精性肝硬化和未指明肝硬化的平均人数(使用国家生命统计系统数据),以估计 AALDD。

结果

直接法(每年 28345 人)估计的 AALDD 数量高于 PAF 方法,但当使用人均销售额调整酒精流行率并考虑所有酒精消费水平时,结果相似(例如,每年 25145 人归因于酒精性肝病死亡)。使用 PAF 方法,将非饮酒者细分为终身戒酒者和曾经饮酒者,以纳入曾经饮酒者的相对风险,得出的 AALDD 估计值高于将所有非饮酒者合并的方法(例如,每年 27686 人归因于酒精性肝病死亡)。

讨论和结论

使用调整人均销售额和模型风险的 PAF 方法可以得出更完整和可能更有效的 AALDD 估计值。