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建模康涅狄格州致命苯甲二氮卓类药物过量涉及的时间变化。

Modeling Changes of Fatal Xylazine-Involved Drug Overdoses in Connecticut Across Time.

机构信息

Department of Public Health, University of Connecticut Health Center, Farmington, Connecticut, USA.

The Cato T. Laurencin Institute for Regenerative Engineering, University of Connecticut, Farmington, Connecticut, USA.

出版信息

Subst Use Misuse. 2024;59(14):2103-2111. doi: 10.1080/10826084.2024.2393220. Epub 2024 Sep 16.

Abstract

BACKGROUND

Fatal drug overdoses have involved both xylazine and fentanyl. Xylazine is a non-opioid substance used in veterinary medicine. This study aimed to model changes in fatal xylazine-involved drug overdose deaths from 2019 to 2023 in Connecticut using overdose death data from the Office of the Chief Medical Examiner.

METHODS

Xylazine-involved drug overdose fatality rates were calculated by number of deaths per year per 100,000 population from 2019 to 2023. We used joinpoint regression modeling to evaluate quarterly overdose rates across age, number of drugs, and drug types with a significance level of  < 0.05.

RESULTS

From 2019 to 2023, there were 1116 xylazine-involved fatal overdoses with a cumulative rate of 31.3 deaths per 100,000. Xylazine-involved overdose death rates were significantly higher in Hispanic populations compared to both non-Hispanic White and Black populations ( < 0.05). The joinpoint analyses showed that xylazine-fentanyl mortality rates significantly increased by 0.18 per 100,000 per quarter from 2019 to 2022. Xylazine-fentanyl overdoses involving at least 4 or 5 substances significantly increased. Windham, Hartford, New London, and New Haven counties had the highest xylazine-involved death rates.

CONCLUSION

Xylazine-fentanyl deaths increased from 2019 to 2023, and often involved multiple substances (e.g., cocaine, ethanol, benzodiazepines, and oxycodone). Results show Hispanic populations, those aged 35-49, and 50+ experienced high rates of xylazine-fentanyl overdose deaths. Vulnerable populations in Connecticut for special consideration for future intervention and local resource allocation are recommended.

摘要

背景

致命的药物过量涉及到唑来膦酸和芬太尼。唑来膦酸是一种用于兽医的非阿片类物质。本研究旨在利用首席法医办公室的过量死亡数据,对康涅狄格州 2019 年至 2023 年涉及唑来膦酸的致命药物过量死亡病例进行建模。

方法

通过每年每 10 万人的死亡人数计算唑来膦酸涉及的药物过量死亡率,从 2019 年至 2023 年。我们使用 Joinpoint 回归模型评估了不同年龄、药物数量和药物类型的季度药物过量率,显著性水平为 <0.05。

结果

从 2019 年至 2023 年,有 1116 例唑来膦酸涉及的致命过量,累积死亡率为每 10 万人 31.3 人。与非西班牙裔白人和黑人群体相比,西班牙裔人群的唑来膦酸涉及的过量死亡发生率明显更高(<0.05)。Joinpoint 分析表明,从 2019 年到 2022 年,唑来膦酸-芬太尼的死亡率每季度以 0.18 每 10 万人的速度显著增加。涉及至少 4 种或 5 种物质的唑来膦酸-芬太尼过量明显增加。温德姆、哈特福德、新伦敦和纽黑文县的唑来膦酸涉及的死亡人数最高。

结论

唑来膦酸-芬太尼的死亡人数从 2019 年到 2023 年有所增加,并且经常涉及多种物质(例如可卡因、乙醇、苯二氮䓬类和羟考酮)。结果表明,西班牙裔人群、35-49 岁和 50 岁以上人群的唑来膦酸-芬太尼过量死亡发生率较高。建议对康涅狄格州的弱势群体进行特别考虑,以便为他们提供未来的干预和当地资源配置。

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