Assessing an ICD-10 code approach for estimating xylazine-involved overdose deaths in the United States

IF 3.6 2区 医学 Q1 PSYCHIATRY
Joseph R. Friedman
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引用次数: 0

Abstract

Introduction

The prevalence of the veterinary sedative xylazine in US overdose deaths rose between 2018 and 2021. More updated estimates are limited, partially due to the lack of a dedicated ICD-10 code—a primary mechanism used to specify drugs implicated in overdose deaths in the US, including in the CDC WONDER system, which provides public data for download with a 6-month lag. For other emerging substances lacking dedicated codes, over time umbrella codes have come to de facto represent them, yet it has not been demonstrated if this has occurred for xylazine.

Methods

Overdose deaths in CDC WONDER involving T42.7 (“Antiepileptic and sedative-hypnotic drugs, unspecified”) or T46.5 (“Other antihypertensive drugs, not elsewhere classified”) were compared to two more specific, albeit delayed, sources: NVSS describing national trends in 2018–2021 and SUDORS describing state-level trends in 2020–2022. This CDC WONDER approach was also used to estimate trends in xylazine-involved deaths through 2024 Q1 by geography, race/ethnicity, substance co-involvement, and demographic categories.

Results

At the national level, concordance between CDC WONDER records and previous NVSS estimates improved after 2019 and became highly similar in 2021 (3480 vs 3468 deaths). Concordance was also high for estimates stratified by race, age, and region. At the state-level, across 49 state-year pairs, correlation between CDC WONDER and SUDORS was 0.97. Estimated xylazine-involved deaths doubled between 2021 and 2024 Q1, and estimated racial inequalities widened.

Discussion

T42.7 or T46.5, together, may have become the de facto coding scheme representing xylazine-involved deaths. This approach provides more up-to-date estimates, showing increasing prevalence and worsening racial inequalities in xylazine-involved deaths into 2024.
评估ICD-10代码方法用于估计美国与氯胺嘧啶有关的过量死亡
在2018年至2021年期间,美国兽医镇静剂噻嗪在过量死亡中的患病率有所上升。更多的最新估计是有限的,部分原因是缺乏专门的ICD-10代码,这是美国用于指定与过量死亡有关的药物的主要机制,包括CDC WONDER系统,该系统提供公共数据供下载,有6个月的滞后。对于其他缺乏专用代码的新兴物质,随着时间的推移,保护伞代码实际上代表了它们,但尚未证明这种情况是否发生在噻嗪上。方法将CDC WONDER中涉及T42.7(“抗癫痫和镇静催眠药物,未指明”)或T46.5(“其他抗高血压药物,未在其他地方分类”)的过量死亡与两个更具体(尽管延迟)的来源进行比较:描述2018-2021年全国趋势的NVSS和描述2020-2022年州级趋势的SUDORS。CDC WONDER方法还用于估计到2024年第一季度,按地理、种族/民族、物质共涉和人口类别划分的与噻嗪有关的死亡趋势。在国家层面,CDC WONDER记录与之前的NVSS估计之间的一致性在2019年之后有所改善,并在2021年变得非常相似(3480对3468)。按种族、年龄和地区分层估计的一致性也很高。在州一级,在49个州-年份对中,CDC WONDER和SUDORS之间的相关性为0.97。估计的与木嗪有关的死亡人数在2021年至2024年期间翻了一番,估计的种族不平等现象也扩大了。讨论t42.7或T46.5可能已经成为代表与木嗪有关的死亡人数的事实上的编码方案。这种方法提供了更多最新的估计,显示到2024年,与氯嗪有关的死亡人数将增加,种族不平等现象将加剧。
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来源期刊
Drug and alcohol dependence
Drug and alcohol dependence 医学-精神病学
CiteScore
7.40
自引率
7.10%
发文量
409
审稿时长
41 days
期刊介绍: Drug and Alcohol Dependence is an international journal devoted to publishing original research, scholarly reviews, commentaries, and policy analyses in the area of drug, alcohol and tobacco use and dependence. Articles range from studies of the chemistry of substances of abuse, their actions at molecular and cellular sites, in vitro and in vivo investigations of their biochemical, pharmacological and behavioural actions, laboratory-based and clinical research in humans, substance abuse treatment and prevention research, and studies employing methods from epidemiology, sociology, and economics.
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