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Impact of comprehensive tobacco control policies on stroke and acute myocardial infarction among patients with hypertension and type 2 diabetes in Beijing, China: An interrupted time-series analysis. 综合控烟政策对中国北京高血压和2型糖尿病患者脑卒中和急性心肌梗死的影响:一项中断时间序列分析
IF 5.3 1区 医学 Q1 PSYCHIATRY Pub Date : 2025-08-31 DOI: 10.1111/add.70178
Ruotong Yang, Yunting Zheng, Huan Yu, Junhui Wu, Siyue Wang, Hongbo Chen, Mengying Wang, Xueying Qin, Tao Wu, Chun Chang, Yiqun Wu, Yonghua Hu

Background and aims: Tobacco control policies enhance cardiovascular health at the population level, but their effects on high-risk individuals, such as those with type 2 diabetes mellitus (T2DM) or hypertension, remain unclear. This study evaluated the association between a tobacco control policy and hospital admissions for stroke and acute myocardial infarction (AMI) in hypertensive and T2DM individuals.

Design: Interrupted time series study.

Setting: Beijing, China.

Participants: 2 144 133 hypertensive and 1 446 750 T2DM patients residing in Beijing from January 2013 to June 2017.

Intervention: A comprehensive tobacco control policy package, incorporating all MPOWER components, was implemented in June 2015.

Measurements: Changes in admission rates and admissions for stroke and AMI.

Findings: Patients with T2DM showed immediate decreases in stroke [-9.4% (95% confidence interval = -13.3% to -5.3%)] and AMI [-24.3% (-31.2% to -16.7%)] admission rates after the policy. Similarly, the immediate post-policy change in stroke and AMI admission rates for hypertensive patients was -7.5% (-10.9% to -3.9%) and -23.0% (-29.2% to -16.3%), respectively. However, these reductions did not differ from those without either condition (P-interaction >0.05). For long-term trends, significant decreases were only seen for stroke [T2DM: -32.9% (-39.9% to -25.1%); hypertension: -33.3% (-39.3% to -26.7%)], but not AMI admissions, and again did not differ from those without either disease (P-interaction >0.05). Compared with healthy controls without T2DM or hypertension, patients with both conditions showed greater long-term reductions in stroke admission rates [-29.2% (-37.0% to -20.5%) vs. -14.4% (-26.3% to -0.5%), P-interaction = 0.05), whereas the opposite trend was observed for AMI admissions [7.9% (-15.9% to 38.4%) vs. -29.9% (-46.9% to -7.3%), P-interaction = 0.02].

Conclusions: Beijing's 2015 comprehensive tobacco control policy appears to be associated with reduced acute myocardial infarction and stroke admissions among high-risk groups (individuals with type 2 diabetes mellitus and hypertension), although admission rates showed no statistically significant difference between high-risk and non-high-risk populations.

背景和目的:烟草控制政策在人群水平上促进心血管健康,但其对高危人群,如2型糖尿病(T2DM)或高血压患者的影响尚不清楚。本研究评估了烟草控制政策与高血压和2型糖尿病患者中风和急性心肌梗死(AMI)住院之间的关系。设计:中断时间序列研究。地点:中国北京。参与者:2013年1月至2017年6月在北京居住的高血压患者2 144 133例,T2DM患者1 446 750例。干预措施:2015年6月实施了一套综合烟草控制政策,其中包括MPOWER的所有组成部分。测量:卒中和AMI的入院率和入院率的变化。结果:T2DM患者在政策实施后卒中[-9.4%(95%可信区间= -13.3%至-5.3%)]和AMI[-24.3%(-31.2%至-16.7%)]住院率立即下降。同样,高血压患者的卒中和AMI入院率在政策后立即变化分别为-7.5%(-10.9%至-3.9%)和-23.0%(-29.2%至-16.3%)。然而,这些减少与没有任何条件的人没有差异(p -相互作用0.05)。从长期趋势来看,只有中风患者出现显著下降[2型糖尿病:-32.9%(-39.9%至-25.1%);高血压:-33.3%(-39.3%至-26.7%)],但AMI入院率不存在差异,并且与没有这两种疾病的患者没有差异(p -相互作用>.05)。与无2型糖尿病或高血压的健康对照者相比,两种情况的患者卒中入院率的长期降低幅度更大[-29.2%(-37.0%至-20.5%)对-14.4%(-26.3%至-0.5%),p相互作用= 0.05],而AMI入院率的趋势相反[7.9%(-15.9%至38.4%)对-29.9%(-46.9%至-7.3%),p相互作用= 0.02]。结论:北京市2015年全面控烟政策似乎与高危人群(2型糖尿病和高血压患者)急性心肌梗死和卒中住院率降低有关,尽管高危人群和非高危人群的住院率无统计学差异。
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引用次数: 0
Comparative effectiveness of urine drug testing schedules alongside opioid agonist treatment: Emulation of a population-based target trial in British Columbia, Canada 尿药检测时间表与阿片类激动剂治疗的比较有效性:加拿大不列颠哥伦比亚省一项基于人群的目标试验的模拟。
IF 5.3 1区 医学 Q1 PSYCHIATRY Pub Date : 2025-08-31 DOI: 10.1111/add.70171
Megan Kurz, Brenda Carolina Guerra-Alejos, Jeong Eun Min, Shaun R. Seaman, Micah Piske, Paxton Bach, Julie Bruneau, Sander Greenland, Paul Gustafson, Kyle Kampman, Mohammad Ehsanul Karim, P. Todd Korthuis, Robert W. Platt, Uwe Siebert, M. Eugenia Socías, Evan Wood, Bohdan Nosyk
<div> <section> <h3> Background and aim</h3> <p>Urine drug testing is often utilized alongside opioid agonist treatment to assess client progress by validating self-reported substance use, monitoring for diversion and supporting clinical decisions for take-home dosing. However, there is a paucity of evidence to support the practice of urine drug testing. We aimed to determine the association of alternative urine drug testing frequencies with opioid agonist treatment discontinuation, compared with no monitoring, among individuals receiving methadone or buprenorphine/naloxone treatment.</p> </section> <section> <h3> Design</h3> <p>Population-based retrospective cohort study and target trial emulation based on nine-linked administrative databases.</p> </section> <section> <h3> Setting</h3> <p>British Columbia, Canada, between 1 January 2010 and 17 March 2020.</p> </section> <section> <h3> Participants</h3> <p>Individuals with no history of cancer or palliative care, aged 18 or older and no indication of pregnancy who initiated methadone or buprenorphine/naloxone. A total of 18 988 methadone and 11 910 buprenorphine/naloxone recipients were included in the incident user design (individuals with no past opioid agonist treatment experience).</p> </section> <section> <h3> Measurements</h3> <p>We used a clone-censor-weight approach to estimate hazard ratios with 95% compatibility (“confidence”) intervals for treatment discontinuation (lasting at least 5 and 6 days for methadone and buprenorphine, respectively) and all-cause mortality on treatment within 12 months for static urine drug testing strategies.</p> </section> <section> <h3> Findings</h3> <p>Under static monitoring strategies, weekly urine drug testing was associated with a slightly reduced risk of discontinuation in the first year of continuous retention in treatment [methadone: adjusted hazard ratio (aHR) = 0.96, 95% compatibility interval (CI) = (0.95–0.98); buprenorphine/naloxone: aHR = 0.95 (0.94–0.97)] compared with no monitoring. The estimated associations of weekly urine drug testing with all-cause mortality were similar in size but extremely imprecise [methadone: aHR = 0.95 (0.78–1.15), buprenorphine/naloxone: aHR = 0.99 (0.62–1.58)]. Less frequent testing demonstrated no observed difference on treatment discontinuation or all-cause mortality compared with no monitoring.</p>
背景和目的:尿检通常与阿片类激动剂治疗一起使用,通过验证自我报告的药物使用,监测转移和支持临床决定带回家给药来评估患者的进展。然而,缺乏证据支持尿液药物检测的做法。我们的目的是确定在接受美沙酮或丁丙诺啡/纳洛酮治疗的个体中,与不进行监测的个体相比,替代尿检频率与阿片类激动剂治疗中断的关系。设计:以人群为基础的回顾性队列研究和基于9个关联的行政数据库的目标试验模拟。地点:加拿大不列颠哥伦比亚省,2010年1月1日至2020年3月17日。参与者:没有癌症或姑息治疗史的个体,18岁或以上,没有怀孕迹象,开始使用美沙酮或丁丙诺啡/纳洛酮。共有18988名美沙酮接受者和11010名丁丙诺啡/纳洛酮接受者被纳入事件使用者设计(过去没有阿片类激动剂治疗经历的个体)。测量方法:我们使用克隆-审查器-权重方法,以95%的相容性(“置信度”)区间估计停药(美沙酮和丁丙诺啡分别持续至少5天和6天)和12个月内治疗的全因死亡率,采用静态尿液药物检测策略。结果:在静态监测策略下,每周尿检与持续治疗第一年停药风险略有降低相关[美沙酮:调整风险比(aHR) = 0.96, 95%相容区间(CI) = (0.95-0.98);丁丙诺啡/纳洛酮:aHR = 0.95(0.94-0.97)]。每周尿检与全因死亡率的估计相关性在大小上相似,但极不精确[美沙酮:aHR = 0.95(0.78-1.15),丁丙诺啡/纳洛酮:aHR = 0.99(0.62-1.58)]。较不频繁的检测表明,与不进行监测相比,在停药或全因死亡率方面没有观察到差异。结论:与不尿检相比,每周尿检可能与阿片受体激动剂治疗效果的改善有关;然而,由于频繁检测而造成的高成本可能不符合成本效益,需要进一步评估。与没有监测相比,较少的检测频率没有改善。
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引用次数: 0
The relationship between 3,4-methylenedioxymethamphetamine (MDMA) use in young adulthood and anxiety or depressive disorders in the mid-30s: Findings from the Victorian Adolescent Health Cohort Study 青年期使用3,4-亚甲基二氧基甲基苯丙胺(MDMA)与35岁左右的焦虑或抑郁障碍之间的关系:来自维多利亚青少年健康队列研究的发现
IF 5.3 1区 医学 Q1 PSYCHIATRY Pub Date : 2025-08-28 DOI: 10.1111/add.70173
Zachary Bryant, Kirsten Morley, Jessica A. Kerr, Craig A. Olsson, Tim Slade
<div> <section> <h3> Background and aims</h3> <p>MDMA (3,4-methylenedioxymethamphetamine or “Ecstasy”) is the fourth-most used illicit substance globally. While previous research found links between MDMA use and mental health outcomes, the direction and nature of this relationship remain unclear. This study assessed whether MDMA use in early adulthood increases the risk of anxiety or depression in mid-30s.</p> </section> <section> <h3> Design</h3> <p>A longitudinal, population-based study using doubly robust inverse probability treatment weighted regression analysis, a contemporary confounder adjustment technique, to examine the relationship between MDMA use in early adulthood (age 20–29) and subsequent anxiety or depression at age 35.</p> </section> <section> <h3> Setting</h3> <p>Victoria, Australia.</p> </section> <section> <h3> Participants</h3> <p>Data were drawn from the Victorian Adolescent Health Cohort Study (VAHCS), which began in 1992 with a statewide representative sample of 1943 Year 9 students (aged 14–15) from 44 Victorian schools. This paper uses data collected from wave 2 to wave 10 (ages 15–35).</p> </section> <section> <h3> Measurements</h3> <p>Across waves 7–9 (ages 20–29), MDMA use was categorised as any use, persistent use (none, one wave, two or more waves) and frequent use (none, infrequent, frequent). Wave 10 (age 35) outcomes were 12-month diagnoses of major depressive disorder and anxiety disorders assessed using the Composite International Diagnostic Interview (CIDI).</p> </section> <section> <h3> Findings</h3> <p>There was little evidence linking any pattern of MDMA use in early adulthood with depressive disorders by the mid-30s; however, compared with non-MDMA users, the adjusted odds of an anxiety disorder were higher in those who reported past 12-month MDMA use [odds ratio (OR) = 1.73, 95% confidence interval (CI) = 1.12–2.68), persistent MDMA use at two or more waves (OR = 2.05, 95% CI = 1.07–3.94), as well as infrequent (OR = 2.11, 95% CI = 1.14–3.92) and frequent MDMA use (OR = 2.56, 95% CI = 1.15–5.71).</p> </section> <section> <h3> Conclusions</h3> <p>MDMA use (3,4-methylenedioxymethamphetamine or “Ecstasy”) in early adulthood appears to be associated with increased odds of anxiety disorders but not depressive di
背景和目的:MDMA(3,4-亚甲基二氧基甲基苯丙胺或“摇头丸”)是全球第四大使用的非法物质。虽然之前的研究发现了MDMA使用与心理健康结果之间的联系,但这种关系的方向和性质仍不清楚。这项研究评估了在成年早期使用MDMA是否会增加35岁左右焦虑或抑郁的风险。设计:一项以人群为基础的纵向研究,采用双稳健反概率处理加权回归分析,一种当代混杂校正技术,研究成年早期(20-29岁)使用MDMA与35岁时随后的焦虑或抑郁之间的关系。背景:澳大利亚维多利亚。参与者:数据来自维多利亚青少年健康队列研究(VAHCS),该研究于1992年开始,从44所维多利亚学校中选取了1943名9年级学生(14-15岁)作为全州代表性样本。本文使用的数据是从第2波到第10波(15-35岁)收集的。测量:在7-9波(20-29岁)中,MDMA使用分为任意使用、持续使用(无、一波、两波或更多波)和频繁使用(无、不频繁、频繁)。第10波(35岁)的结果是12个月的重度抑郁症和焦虑症的诊断,使用综合国际诊断访谈(CIDI)进行评估。研究发现:几乎没有证据表明成年早期使用MDMA与35岁左右的抑郁症有任何关系;然而,与非MDMA使用者相比,报告过去12个月使用MDMA的人患焦虑症的调整后几率更高[比值比(OR) = 1.73, 95%可信区间(CI) = 1.12-2.68),持续使用MDMA两次或两次以上(OR = 2.05, 95% CI = 1.07-3.94),以及不频繁(OR = 2.11, 95% CI = 1.14-3.92)和频繁使用MDMA (OR = 2.56, 95% CI = 1.15-5.71)。结论:在成年早期使用MDMA(3,4-亚甲基二氧基甲基苯丙胺或“摇头丸”)似乎与30岁左右患焦虑症的几率增加有关,但与抑郁症的几率无关。
{"title":"The relationship between 3,4-methylenedioxymethamphetamine (MDMA) use in young adulthood and anxiety or depressive disorders in the mid-30s: Findings from the Victorian Adolescent Health Cohort Study","authors":"Zachary Bryant,&nbsp;Kirsten Morley,&nbsp;Jessica A. Kerr,&nbsp;Craig A. Olsson,&nbsp;Tim Slade","doi":"10.1111/add.70173","DOIUrl":"10.1111/add.70173","url":null,"abstract":"&lt;div&gt;\u0000 \u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Background and aims&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;MDMA (3,4-methylenedioxymethamphetamine or “Ecstasy”) is the fourth-most used illicit substance globally. While previous research found links between MDMA use and mental health outcomes, the direction and nature of this relationship remain unclear. This study assessed whether MDMA use in early adulthood increases the risk of anxiety or depression in mid-30s.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Design&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;A longitudinal, population-based study using doubly robust inverse probability treatment weighted regression analysis, a contemporary confounder adjustment technique, to examine the relationship between MDMA use in early adulthood (age 20–29) and subsequent anxiety or depression at age 35.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Setting&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;Victoria, Australia.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Participants&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;Data were drawn from the Victorian Adolescent Health Cohort Study (VAHCS), which began in 1992 with a statewide representative sample of 1943 Year 9 students (aged 14–15) from 44 Victorian schools. This paper uses data collected from wave 2 to wave 10 (ages 15–35).&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Measurements&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;Across waves 7–9 (ages 20–29), MDMA use was categorised as any use, persistent use (none, one wave, two or more waves) and frequent use (none, infrequent, frequent). Wave 10 (age 35) outcomes were 12-month diagnoses of major depressive disorder and anxiety disorders assessed using the Composite International Diagnostic Interview (CIDI).&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Findings&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;There was little evidence linking any pattern of MDMA use in early adulthood with depressive disorders by the mid-30s; however, compared with non-MDMA users, the adjusted odds of an anxiety disorder were higher in those who reported past 12-month MDMA use [odds ratio (OR) = 1.73, 95% confidence interval (CI) = 1.12–2.68), persistent MDMA use at two or more waves (OR = 2.05, 95% CI = 1.07–3.94), as well as infrequent (OR = 2.11, 95% CI = 1.14–3.92) and frequent MDMA use (OR = 2.56, 95% CI = 1.15–5.71).&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Conclusions&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;MDMA use (3,4-methylenedioxymethamphetamine or “Ecstasy”) in early adulthood appears to be associated with increased odds of anxiety disorders but not depressive di","PeriodicalId":109,"journal":{"name":"Addiction","volume":"120 12","pages":"2448-2464"},"PeriodicalIF":5.3,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/add.70173","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144936761","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Removing arbitrary limitations on buprenorphine for opioid use disorder 消除对丁丙诺啡治疗阿片类药物使用障碍的任意限制。
IF 5.3 1区 医学 Q1 PSYCHIATRY Pub Date : 2025-08-27 DOI: 10.1111/add.70127
Nicole Gastala, Brianna Hudak, Mai T. Pho, Harold A. Pollack, Katharine Wilcox
<p>The opioid crisis has sharply evolved over the past two decades, shifting first from prescription opioids to heroin and now to fentanyl and other synthetic opioids far more potent than their predecessors. Buprenorphine, a partial opioid agonist, has long been a cornerstone of opioid use disorder (OUD) treatment, demonstrating significant reductions in morbidity and mortality when prescribed appropriately. However, legacy dosing recommendations from an era preceding fentanyl's dominance have resulted in restrictive state and insurance policies that limit patient access to clinically necessary dosages. In the United States (US), recent US Food and Drug Administration (FDA) updates seek to mitigate this issue [<span>1</span>], but broader structural and international policy shifts are needed to align buprenorphine treatment with the contemporary realities of opioid pharmacology and patient need.</p><p>The US FDA initially approved buprenorphine-based medications for OUD treatment in 2002, establishing a recommended target dose of 16 mg per day, with 24 mg per day cited as the upper limit beyond which no additional clinical benefit was believed to occur. These recommendations were based on studies conducted in the pre-fentanyl landscape. Today, fentanyl's high potency, low street price per morphine milligram equivalent (MME), and long half-life complicate withdrawal management, often necessitating higher doses of buprenorphine to suppress cravings and stabilize patients effectively [<span>2</span>]. The growing body of evidence supporting higher doses has not yet translated into widespread policy reform. Instead, outdated dosage limits have been used by US states and insurers to justify restrictive prescribing practices that hinder effective treatment [<span>3</span>].</p><p>Local policies on buprenorphine dosing vary considerably, often in ways that can undermine patient care [<span>4</span>]. Some US states, such as Kentucky, impose arbitrary dosage caps, while others, such as Tennessee and West Virginia, enforce dosage restrictions with cumbersome exceptions, such as chart documentation or required referral to an addiction specialist. Additional bureaucratic barriers—such as prior authorizations or excessive documentation requirements—further delay or prevent treatment escalation, disproportionately affecting Medicaid beneficiaries and uninsured individuals [<span>5</span>].</p><p>Additionally, insurance coverage for extended-release injectable buprenorphine (Sublocade), presents another significant hurdle. Originally approved for monthly administration, new data suggest that an accelerated induction phase—including a second 300 mg dose as early as day 8—may improve stabilization outcomes. Insurance coverage has not kept pace with these findings, leaving patients with inadequate options for stabilization and relapse prevention [<span>6</span>]. Although barriers such as quantity limits and prior authorization are in place to ensure appropriate
阿片类药物危机在过去二十年里急剧演变,先是从处方阿片类药物转向海洛因,现在又转向芬太尼和其他合成阿片类药物,其效力远远超过它们的前身。丁丙诺啡是一种部分阿片类药物激动剂,长期以来一直是阿片类药物使用障碍(OUD)治疗的基石,在适当的处方下,发病率和死亡率显著降低。然而,在芬太尼占主导地位之前,遗留的剂量建议导致了限制性的州和保险政策,限制了患者获得临床必要的剂量。在美国,最近美国食品和药物管理局(FDA)的更新寻求缓解这一问题,但需要更广泛的结构性和国际政策转变,以使丁丙诺啡治疗与阿片类药物的当代现实和患者需求保持一致。2002年,美国食品和药物管理局最初批准丁丙诺啡类药物用于OUD治疗,建议目标剂量为每天16毫克,每天24毫克被认为是上限,超过这个上限不会产生额外的临床益处。这些建议是基于在芬太尼出现之前进行的研究。如今,芬太尼的高效、每吗啡毫克当量(MME)的低街头价格和较长的半衰期使戒断管理复杂化,通常需要更高剂量的丁丙诺啡来抑制渴望并有效地稳定患者的病情。越来越多的证据支持提高剂量,但尚未转化为广泛的政策改革。相反,过时的剂量限制被美国各州和保险公司用来证明限制性处方做法的合理性,这些做法阻碍了有效的治疗。各地对丁丙诺啡剂量的政策差异很大,往往会损害病人的护理。美国的一些州,如肯塔基州,强制实施任意剂量上限,而其他州,如田纳西州和西弗吉尼亚州,强制实施剂量限制,但有繁琐的例外,如图表文件或要求转诊给成瘾专家。额外的官僚障碍——如事先授权或过多的文件要求——进一步延迟或阻止治疗升级,不成比例地影响医疗补助受益人和未参保个人。此外,延长释放注射丁丙诺啡(Sublocade)的保险覆盖范围是另一个重大障碍。最初批准每月给药,新的数据表明,加速诱导阶段(包括第8天第二次300 mg剂量)可能改善稳定结果。保险覆盖率没有跟上这些发现的步伐,使患者没有足够的选择来稳定和预防复发。虽然设置了数量限制和事先授权等障碍,以确保适当使用药物,但阿片类药物流行的现实是,治疗情况变化很快。护理标准可能没有大规模的随机对照试验。相反,为了转移和挽救生命,有效的OUD管理必须依靠专家意见,这一做法广泛应用于医学指南的制定,以解决已发表文献中的证据差距[10]。这对公共和私营保险公司构成了明显的挑战。为了响应越来越多的临床医生和患者的倡导,FDA于2024年12月27日修订了丁丙诺啡的标签,澄清可能需要更高的剂量,并劝阻使用先前的剂量语言作为拒绝治疗的理由。尽管这一更新是有价值的一步,但各州和保险公司是否会迅速调整他们的政策仍有待观察。历史先例表明,除非通过诉讼、政策倡导和专业指南更新施加额外压力,否则监管惰性可能会推迟有意义的变革。限制给药的问题并不是美国独有的。在世界各地,人们越来越认识到个性化给药策略的必要性。加拿大、澳大利亚和其他国家已开始针对芬太尼调整OUD治疗战略,允许灵活给药和快速诱导方案。一项关于美沙酮的研究发现,一些患者需要的剂量明显高于传统的建议指南,以达到最佳效果。来自加拿大的新数据表明,高剂量丁丙诺啡可以改善芬太尼暴露个体的滞留并减少非法阿片类药物的使用[10]。此外,欧洲国家已经建立了海洛因辅助治疗方案,为管理可能在标准丁丙诺啡方案下不稳定的严重OUD患者提供了另一种框架。 不列颠哥伦比亚省OUD临床管理指南承认,Suboxone产品专论中引用的每日最大剂量早于芬太尼时代,并且最近的数据支持每日剂量高达32mg[12]。英国药物滥用咨询委员会承认“有充分的证据表明,大剂量的美沙酮和丁丙诺啡可以减少阿片类药物的使用,减少危险行为。””[13]。波拉克:概念化(平等);获得资金(牵头);写作-原稿(同等);写作—评审与编辑(同等)。Nicole Gastala:概念化(平等);写作-原稿(同等);写作—评审与编辑(同等)。Brianna Hudak:概念化(平等);写作-原稿(同等);写作—评审与编辑(同等)。Mai T. Pho:概念化(平等);写作—评审与编辑(同等)。凯瑟琳·威尔科克斯:概念化(平等);写作-原稿(同等);写作—评审与编辑(同等)。本社论由美国国家药物滥用研究所(NIDA)提供经费。任何观点都是作者的观点,不代表NIDA或任何雇主或组织的观点。
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引用次数: 0
Exploratory analysis of United States-based cannabis product health benefit claims on online marketplaces 对在线市场上美国大麻产品健康益处声明的探索性分析。
IF 5.3 1区 医学 Q1 PSYCHIATRY Pub Date : 2025-08-27 DOI: 10.1111/add.70177
Matthew C. Nali, Meng Zhen Larsen, Zhuoran Li, Jiawei Li, Douglas R. Roehler, Vanessa Mallory, Tim K. Mackey
<div> <section> <h3> Background and aims</h3> <p>Cannabis-derived products (CDPs), including cannabidiol (CBD) and tetrahydrocannabinol (THC) products, are widely diverse and readily available through physical and online retail channels in the United States (US) marketplace and may also include claims of treating or providing benefit for health issues. This study aimed to systematically classify the various types of health benefit claim(s) present on CDP listings based on publicly available online marketplace data.</p> </section> <section> <h3> Design</h3> <p>Exploratory analysis to identify health benefit claims.</p> </section> <section> <h3> Setting and cases</h3> <p>A total of 624 805 unique CDPs sold in the US on Leafly and Weedmaps, cannabis online marketplace service platforms.</p> </section> <section> <h3> Measurements</h3> <p>This exploratory study was conducted in four phases: (1) data mining of cannabis e-commerce websites Weedmaps and Leafly for product listings in the US; (2) data filtering, text matching and content coding to identify types of advertised health benefit(s) made; (3) analysis on consumer-generated product reviews for sentiment toward advertised health benefit(s); and (4) ANOVA was used to test differences in mean number of health benefit claims based on product characteristic of route-of-administration (RoA).</p> </section> <section> <h3> Findings</h3> <p>A total of 624 805 unique US CDP sales listings from Leafly (<i>n</i> = 50 951) and Weedmaps (<i>n </i>= 573 854) were analyzed. CDP listings with a specific health benefit claim(s) were detected in 998 (1.9%) Leafly and 25 671 (4.47%) Weedmaps CDP listings. The top 5 advertised health benefits were treatment of mood disorders, general discomfort, general wellness, sleep disorders and chronic conditions. Among consumer reviews, 295 (4.6% of consumer reviews from products that advertised health benefit(s)) expressed sentiment toward CDP addressing their health issue with 82.4% being positive, 14.6% negative and 3.1% neutral. We also observed statistically significant differences between RoA and frequency of health benefit claims among those with at least one health benefit claim, with multisystem products (>1RoA) generally having a higher number of average health benefit claims compared with other RoAs.</p> </section> <section> <h3> Conclusions</h3> <p>Over 26 000 cannabis-derived products listed on two popular US cannabis online marketplaces have at least one health benefit claim.</p>
背景和目的:大麻衍生产品(CDPs),包括大麻二酚(CBD)和四氢大麻酚(THC)产品,种类繁多,很容易通过美国市场的实体和在线零售渠道获得,还可能包括声称治疗或提供健康问题益处的产品。本研究旨在基于公开的在线市场数据,系统地对CDP清单上出现的各种类型的健康福利索赔进行分类。设计:探索性分析以确定健康益处声明。背景和案例:大麻在线市场服务平台Leafly和Weedmaps在美国共销售了624805个独特的cd。测量方法:本探索性研究分为四个阶段:(1)对大麻电子商务网站Weedmaps和Leafly进行数据挖掘,获取美国的产品列表;(2)数据过滤、文本匹配和内容编码,以识别所宣传的健康益处的类型;(3)分析消费者生成的产品评论对广告健康益处的看法;(4)采用方差分析(ANOVA)检验基于给药途径(RoA)的产品特征的健康益处索赔平均数量的差异。研究结果:共分析了来自Leafly (n = 50 951)和Weedmaps (n = 573 854)的624 805个独特的美国CDP销售列表。在998份(1.9%)Leafly和25671份(4.47%)Weedmaps CDP清单中检测到具有特定健康益处声明的CDP清单。广告中排名前五的健康益处是治疗情绪障碍、一般不适、一般健康、睡眠障碍和慢性疾病。在消费者评论中,295条(4.6%的消费者评论来自宣传健康益处的产品)表达了对CDP解决其健康问题的看法,其中82.4%是正面的,14.6%是负面的,3.1%是中性的。我们还观察到,在至少有一项健康益处索赔的人群中,RoA和健康益处索赔频率之间存在统计学上的显著差异,与其他RoA相比,多系统产品(bbb1roa)通常具有更高的平均健康益处索赔数量。结论:在美国两个流行的大麻在线市场上列出的26000多种大麻衍生产品至少有一种健康益处声明。
{"title":"Exploratory analysis of United States-based cannabis product health benefit claims on online marketplaces","authors":"Matthew C. Nali,&nbsp;Meng Zhen Larsen,&nbsp;Zhuoran Li,&nbsp;Jiawei Li,&nbsp;Douglas R. Roehler,&nbsp;Vanessa Mallory,&nbsp;Tim K. Mackey","doi":"10.1111/add.70177","DOIUrl":"10.1111/add.70177","url":null,"abstract":"&lt;div&gt;\u0000 \u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Background and aims&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;Cannabis-derived products (CDPs), including cannabidiol (CBD) and tetrahydrocannabinol (THC) products, are widely diverse and readily available through physical and online retail channels in the United States (US) marketplace and may also include claims of treating or providing benefit for health issues. This study aimed to systematically classify the various types of health benefit claim(s) present on CDP listings based on publicly available online marketplace data.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Design&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;Exploratory analysis to identify health benefit claims.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Setting and cases&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;A total of 624 805 unique CDPs sold in the US on Leafly and Weedmaps, cannabis online marketplace service platforms.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Measurements&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;This exploratory study was conducted in four phases: (1) data mining of cannabis e-commerce websites Weedmaps and Leafly for product listings in the US; (2) data filtering, text matching and content coding to identify types of advertised health benefit(s) made; (3) analysis on consumer-generated product reviews for sentiment toward advertised health benefit(s); and (4) ANOVA was used to test differences in mean number of health benefit claims based on product characteristic of route-of-administration (RoA).&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Findings&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;A total of 624 805 unique US CDP sales listings from Leafly (&lt;i&gt;n&lt;/i&gt; = 50 951) and Weedmaps (&lt;i&gt;n &lt;/i&gt;= 573 854) were analyzed. CDP listings with a specific health benefit claim(s) were detected in 998 (1.9%) Leafly and 25 671 (4.47%) Weedmaps CDP listings. The top 5 advertised health benefits were treatment of mood disorders, general discomfort, general wellness, sleep disorders and chronic conditions. Among consumer reviews, 295 (4.6% of consumer reviews from products that advertised health benefit(s)) expressed sentiment toward CDP addressing their health issue with 82.4% being positive, 14.6% negative and 3.1% neutral. We also observed statistically significant differences between RoA and frequency of health benefit claims among those with at least one health benefit claim, with multisystem products (&gt;1RoA) generally having a higher number of average health benefit claims compared with other RoAs.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Conclusions&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;Over 26 000 cannabis-derived products listed on two popular US cannabis online marketplaces have at least one health benefit claim.&lt;/p&gt;\u0000 ","PeriodicalId":109,"journal":{"name":"Addiction","volume":"120 12","pages":"2489-2499"},"PeriodicalIF":5.3,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144936672","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Commentary on Harding et al.: Responding to ketamine use disorder—Integrating practice, research, and whole-system approaches to harm reduction 对哈丁等人的评论:对氯胺酮使用障碍的反应——减少危害的综合实践、研究和全系统方法。
IF 5.3 1区 医学 Q1 PSYCHIATRY Pub Date : 2025-08-27 DOI: 10.1111/add.70181
Rob Ralphs, Janine Day, Jonathan Dewhurst

Harding and colleagues [1] recent study contributes to an established body of international evidence [2-6] on the physical harms associated with ketamine use disorder (KUD), including bladder dysfunction, abdominal pain (‘K-cramps’), nasal complications from insufflation and abstinence symptoms such as cravings, low mood, anxiety and irritability. More significantly, the study offers valuable insights into attitudes toward treatment services, revealing widespread reluctance to engage and dissatisfaction among those who did. These findings underscore the need to improve awareness, accessibility and responsiveness of treatment services for individuals with KUD, ensuring they are better aligned with users' needs and expectations.

Rob Ralphs: Writing—review and editing (lead). Janine Day: Writing—review and editing (supporting). Jonathan Dewhurst: Writing—review and editing (supporting).

None.

Harding和他的同事最近的研究为氯胺酮使用障碍(KUD)相关的身体危害提供了国际证据[2-6],包括膀胱功能障碍、腹痛(“k -痉挛”)、由充气引起的鼻腔并发症和戒断症状(如渴望、情绪低落、焦虑和易怒)。更重要的是,这项研究为人们对治疗服务的态度提供了有价值的见解,揭示了那些接受治疗的人普遍不愿意接受治疗,也不满意。这些发现强调需要提高对KUD患者治疗服务的认识、可及性和响应性,确保它们更好地符合用户的需求和期望。罗布·拉尔夫斯:写作、评论和编辑(主笔)。珍妮·戴:写作、评论和编辑(辅助)。乔纳森·杜赫斯特:写作-评论和编辑(辅助)。无。
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引用次数: 0
Recurrent care proceedings and use of services for substance use disorder: A retrospective linked data cohort study of mothers in South London. 药物使用障碍的经常性护理程序和服务的使用:伦敦南部母亲的回顾性关联数据队列研究。
IF 5.3 1区 医学 Q1 PSYCHIATRY Pub Date : 2025-08-27 DOI: 10.1111/add.70179
Martha Canfield, Gail Gilchrist, Johnny Downs, Sam Norton

Background and aims: In public family law cases ('care proceedings'), many mothers return to proceedings after having a child removed. Substance use disorder (SUD) is a common feature in these cases. We used a linked dataset between SUD treatment services and family court to identify: i) the prevalence and estimated time for returning to care proceedings, ii) the characteristics of mothers who returned, and iii) differences in SUD treatment service use between mothers who returned to care proceedings and those who did not.

Design: Retrospective study.

Setting: South London and Maudsley NHS Mental Health Trust (SLaM) catchment area, UK.

Participants: 480 mothers involved in care proceedings with SUD between 2007 and 2019.

Measurements: Substance use treatment records were linked to family court records. Kaplan Meier's time-to-event analysis was used to estimate the probability of returning to court and the recurrence rate. Hazard ratios (95% confidence intervals) were estimated to identify factors using Cox proportional regression analysis.

Findings: Following the completion of the first care proceeding case, one-quarter of the cohort returned to proceedings (n = 119). Of returning mothers, 58.0% returned with a new baby and 52.0% had not received SUD treatment during the first proceedings. The risk of returning was highest within five years and was positively associated with younger maternal age [adjusted hazard ratio (aHR) 0.26, 95% confidence interval (CI) = 0.11-0.61], multiple children in initial proceedings (aHR 2.07, 95% CI = 1.36-3.18) and not receiving SUD treatment during initial proceedings (aHR 0.42, 95% CI = 0.29-0.61). The number of contact events with SUD treatment was not statistically significantly associated with returning to proceedings.

Conclusion: Among mothers receiving treatment for substance use disorder and involved in care proceedings in England, nearly one in four were likely to appear in a subsequent care proceeding case.

背景和目的:在公开的家庭法案件(“照料诉讼”)中,许多母亲在将孩子带走后再次提起诉讼。物质使用障碍(SUD)是这些病例的共同特征。我们使用SUD治疗服务和家庭法院之间的关联数据集来确定:i)返回护理程序的患病率和估计时间,ii)返回的母亲的特征,以及iii)返回护理程序的母亲与未返回护理程序的母亲之间使用SUD治疗服务的差异。设计:回顾性研究。环境:南伦敦和莫兹利NHS心理健康信托(SLaM)集水区,英国。参与者:2007年至2019年期间参与SUD护理程序的480名母亲。测量方法:药物使用治疗记录与家庭法庭记录相关联。Kaplan Meier的事件时间分析法用于估计重返法庭的概率和复发率。使用Cox比例回归分析估计风险比(95%置信区间)以确定因素。结果:在完成第一个护理程序病例后,四分之一的队列返回程序(n = 119)。在返回的母亲中,58.0%带着新生儿返回,52.0%在第一次程序中未接受SUD治疗。复发风险在5年内最高,并与较年轻的母亲年龄呈正相关[调整风险比(aHR) 0.26, 95%可信区间(CI) = 0.11-0.61],初始程序中的多个孩子(aHR 2.07, 95% CI = 1.36-3.18)以及初始程序中未接受SUD治疗(aHR 0.42, 95% CI = 0.29-0.61)。与SUD治疗的接触事件数量与复诊无统计学意义相关。结论:在英国接受药物使用障碍治疗并参与护理程序的母亲中,近四分之一的母亲可能出现在随后的护理程序中。
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引用次数: 0
Counterfeit ‘Xanax®’ tablets: A comparative study of clinical and seizure data in Victoria, Australia 假冒“Xanax®”片剂:澳大利亚维多利亚州临床和缉获数据的比较研究。
IF 5.3 1区 医学 Q1 PSYCHIATRY Pub Date : 2025-08-26 DOI: 10.1111/add.70174
Rebekka Syrjanen, Shaun L. Greene, Sarah E. Hodgson, Rachelle Abouchedid, Dimitri Gerostamoulos, Christie Magee, Melissa Bremner, Jennifer L. Schumann, Emerging Drugs Network of Australia – Victoria (EDNAV) research group

Background and aim

There is growing evidence of counterfeit benzodiazepine products containing other substances, including non-regulated benzodiazepine-type new psychoactive substances (NPSs). This study sought to compare detections of seized suspect counterfeit alprazolam products with clinical cases that reported use of an alprazolam-containing product to better characterise community use.

Design and setting

Observational study set in Victoria, Australia, using data from the Victoria Police Drug Sciences Group (which compiles information about seized drugs submitted for evidential analysis and intelligence purposes) and the Emerging Drugs Network of Australia – Victoria (EDNAV) project (a prospective, observational study collecting clinical and analytical data for illicit drug-related presentations across a network of hospitals in Victoria, Australia).

Cases

Police seizures expected to contain alprazolam (March 2020 and August 2022) and EDNAV cases with a reported exposure to an alprazolam-containing product (September 2020 and August 2022).

Measurements

Descriptive study outlining drug detections in seized tablets and blood samples from EDNAV cases, comparing patterns of detection and changes over time.

Findings

A total of 623 police seizures were analysed, most commonly products labelled as ‘Xanax®’ (n = 266), ‘Kalma®’ (n = 196) or ‘Mylan®’ (n = 124). Thirty percent of seizures contained alprazolam only. A benzodiazepine-type NPS was detected in 375 seizures (60.2%). Exposure to non-prescribed alprazolam was reported in 11.2% (n = 125/1112) of EDNAV cases, with 68.8% identifying as male and a median age of 26 years (range 16–68 years). Eighty-seven cases reported the use of ‘Xanax®’. Alprazolam was detected in 19 EDNAV cases. A benzodiazepine-type NPS was detected in 78.4% of EDNAV cases. Both datasets saw a shift in detections from etizolam (2020) to clonazolam (2021) and then clobromazolam (2022).

Conclusions

Suspect counterfeit alprazolam products seized by police in Victoria, Australia, in 2020 and 2022 commonly contained other drugs and/or new psychoactive substances, with an apparent limited cons

背景和目的:越来越多的证据表明假冒苯二氮卓类产品含有其他物质,包括不受管制的苯二氮卓类新型精神活性物质(nps)。这项研究试图将查获的疑似假冒阿普唑仑产品的检测结果与报告使用含阿普唑仑产品的临床病例进行比较,以更好地描述社区使用情况。设计和环境:在澳大利亚维多利亚州进行观察性研究,使用来自维多利亚州警察药物科学小组(该小组汇编了为证据分析和情报目的提交的有关缉获药物的信息)和澳大利亚-维多利亚州新兴药物网络(EDNAV)项目(一项前瞻性观察性研究,收集了澳大利亚维多利亚州医院网络中与非法药物有关的临床和分析数据)的数据。案件:警方缉获的含有阿普唑仑的案件(2020年3月和2022年8月)和据报告接触含有阿普唑仑产品的EDNAV案件(2020年9月和2022年8月)。测量:描述性研究概述了从EDNAV病例中缉获的片剂和血液样本中检测到的药物,比较了检测模式和随时间的变化。调查结果:共分析了623例警方缉获的药物,最常见的产品标记为“Xanax®”(n = 266),“Kalma®”(n = 196)或“Mylan®”(n = 124)。30%的癫痫发作只含有阿普唑仑。375例癫痫发作中检出苯二氮卓类NPS(60.2%)。11.2% (n = 125/1112)的EDNAV病例报告有非处方阿普唑仑暴露,其中68.8%为男性,中位年龄为26岁(16-68岁)。87例报告使用“Xanax®”。19例EDNAV检出阿普唑仑。78.4%的EDNAV病例检出苯二氮卓类NPS。这两个数据集的检测结果都从依替唑仑(2020年)转变为氯硝唑仑(2021年),然后是氯丙唑仑(2022年)。结论:澳大利亚维多利亚州警方在2020年和2022年查获的涉嫌假冒阿普唑仑产品通常含有其他药物和/或新的精神活性物质,消费者对片剂成分的认识显然有限。
{"title":"Counterfeit ‘Xanax®’ tablets: A comparative study of clinical and seizure data in Victoria, Australia","authors":"Rebekka Syrjanen,&nbsp;Shaun L. Greene,&nbsp;Sarah E. Hodgson,&nbsp;Rachelle Abouchedid,&nbsp;Dimitri Gerostamoulos,&nbsp;Christie Magee,&nbsp;Melissa Bremner,&nbsp;Jennifer L. Schumann,&nbsp;Emerging Drugs Network of Australia – Victoria (EDNAV) research group","doi":"10.1111/add.70174","DOIUrl":"10.1111/add.70174","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background and aim</h3>\u0000 \u0000 <p>There is growing evidence of counterfeit benzodiazepine products containing other substances, including non-regulated benzodiazepine-type new psychoactive substances (NPSs). This study sought to compare detections of seized suspect counterfeit alprazolam products with clinical cases that reported use of an alprazolam-containing product to better characterise community use.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Design and setting</h3>\u0000 \u0000 <p>Observational study set in Victoria, Australia, using data from the Victoria Police Drug Sciences Group (which compiles information about seized drugs submitted for evidential analysis and intelligence purposes) and the Emerging Drugs Network of Australia – Victoria (EDNAV) project (a prospective, observational study collecting clinical and analytical data for illicit drug-related presentations across a network of hospitals in Victoria, Australia).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Cases</h3>\u0000 \u0000 <p>Police seizures expected to contain alprazolam (March 2020 and August 2022) and EDNAV cases with a reported exposure to an alprazolam-containing product (September 2020 and August 2022).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Measurements</h3>\u0000 \u0000 <p>Descriptive study outlining drug detections in seized tablets and blood samples from EDNAV cases, comparing patterns of detection and changes over time.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Findings</h3>\u0000 \u0000 <p>A total of 623 police seizures were analysed, most commonly products labelled as ‘Xanax®’ (<i>n</i> = 266), ‘Kalma®’ (<i>n</i> = 196) or ‘Mylan®’ (<i>n</i> = 124). Thirty percent of seizures contained alprazolam only. A benzodiazepine-type NPS was detected in 375 seizures (60.2%). Exposure to non-prescribed alprazolam was reported in 11.2% (<i>n</i> = 125/1112) of EDNAV cases, with 68.8% identifying as male and a median age of 26 years (range 16–68 years). Eighty-seven cases reported the use of ‘Xanax®’. Alprazolam was detected in 19 EDNAV cases. A benzodiazepine-type NPS was detected in 78.4% of EDNAV cases. Both datasets saw a shift in detections from etizolam (2020) to clonazolam (2021) and then clobromazolam (2022).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Suspect counterfeit alprazolam products seized by police in Victoria, Australia, in 2020 and 2022 commonly contained other drugs and/or new psychoactive substances, with an apparent limited cons","PeriodicalId":109,"journal":{"name":"Addiction","volume":"120 12","pages":"2465-2475"},"PeriodicalIF":5.3,"publicationDate":"2025-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/add.70174","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144936656","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Can alcohol use explain the increase in educational inequalities in all-cause mortality after 2010 in the USA? A three-way interaction analysis. 饮酒能解释2010年后美国全因死亡率中教育不平等的增加吗?三方互动分析。
IF 5.3 1区 医学 Q1 PSYCHIATRY Pub Date : 2025-08-26 DOI: 10.1111/add.70168
Yachen Zhu, Carolin Kilian, Charlotte Probst, William C Kerr, Jürgen Rehm

Background and aims: In the United States, the educational gap in all-cause mortality and life expectancy has dramatically increased since 2010. This study investigated whether alcohol use has contributed to the increasing educational gap in mortality by testing the three-way interaction of alcohol use, education and period on all-cause mortality.

Design: Cohort study with 9 years' follow-up on average.

Setting: United States.

Participants: 207 223 males and 255 833 females aged 25 years and older from the 2000-2018 National Health Interview Survey.

Measurements: The outcome was time to all-cause death or last presumed alive by 12/31/2019 based on the National Death Index. Three-way interaction effects between educational attainment (bachelor degree or more vs. high school degree or less), alcohol use (drinking >60 g/day in males and >40 g/day in females vs. lifetime abstinence) and period (after vs. before 2010) were investigated on the multiplicative and additive scales using Cox proportional hazards and Aalen's additive hazards models, respectively, with age as the time scale. Analyses were stratified by sex and adjusted for marital status, race and ethnicity, smoking status, body mass index, physical activity and self-rated health status.

Findings: During the follow-up period, 30 467 and 34 618 deaths occurred in males and females, respectively, with a pronounced educational gradient. In males, the differential vulnerability to high-level alcohol use by educational attainment substantially increased after 2010 than before 2010 on both multiplicative and additive scales. Specifically, the relative all-cause mortality risk associated with drinking above 60 g per day (vs. lifetime abstinence) in males with low vs. high education increased by 89% after 2010 compared with before 2010 [three-way interaction term: hazard ratio (HR) = 1.89, 95% confidence interval (CI) = 1.03-3.47, P = 0.04 from the Cox model]. This result was further supported by the Aalen's model, indicating that the educational difference in mortality risk linked to drinking above 60 g per day increased by 8.85 additional deaths per 1000 person-years (95% CI = 0.90-16.79, P = 0.029) after 2010. No change of differential vulnerability to alcohol use was found in females.

Conclusions: Alcohol use appears to be a key element in the widening educational gap in all-cause mortality risk in males after 2010 in the United States.

背景和目的:在美国,自2010年以来,全因死亡率和预期寿命的教育差距急剧增加。本研究通过测试酒精使用、教育和时期对全因死亡率的三向相互作用,调查了酒精使用是否导致了死亡率教育差距的扩大。设计:队列研究,平均随访9年。背景:美国。参与者:来自2000-2018年全国健康访谈调查的年龄在25岁及以上的男性207 223名,女性255 833名。测量方法:根据国家死亡指数,结果是到2019年12月31日的全因死亡时间或最后推定存活时间。以年龄为时间尺度,分别采用Cox比例风险模型和Aalen加性风险模型,在乘法和加性尺度上研究受教育程度(本科以上vs高中以下)、饮酒(男性饮酒60 g/d,女性饮酒40 g/d vs终身戒酒)和月经(2010年后vs 2010年前)之间的三向交互效应。分析按性别分层,并根据婚姻状况、种族和民族、吸烟状况、体重指数、体力活动和自评健康状况进行调整。研究结果:在随访期间,男性和女性分别有30467例和34618例死亡,教育程度有明显的差异。在男性中,受教育程度的差异在2010年之后比2010年之前在乘数和相加尺度上都显著增加。具体而言,与2010年之前相比,2010年后,低学历男性与高学历男性中,每天饮酒超过60克(与终生戒酒相比)相关的相对全因死亡风险增加了89%[三因素相互作用项:风险比(HR) = 1.89, 95%可信区间(CI) = 1.03-3.47, Cox模型P = 0.04]。Aalen的模型进一步支持了这一结果,表明2010年后,与每天饮酒超过60克相关的死亡风险的教育差异每1000人年增加8.85例额外死亡(95% CI = 0.90-16.79, P = 0.029)。女性对酒精使用的差异易感性没有变化。结论:饮酒似乎是2010年后美国男性全因死亡风险教育差距扩大的一个关键因素。
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引用次数: 0
Qualitative analysis of barriers and facilitators to healthcare engagement for people with injecting-related invasive infections using a social ecological framework 使用社会生态框架对注射相关侵袭性感染患者医疗保健参与的障碍和促进因素进行定性分析。
IF 5.3 1区 医学 Q1 PSYCHIATRY Pub Date : 2025-08-15 DOI: 10.1111/add.70175
Lucy O. Attwood, Sophia E. Schroeder, Olga Vujovic, Andrew J. Stewardson, Joseph S. Doyle, Paul Dietze, Peter Higgs, Samantha Colledge-Frisby

Background and aims

Injecting-related bacterial infections are increasing in many countries. Systemic infections often require prolonged treatment. Evidence suggests that people who inject drugs who have invasive infections are less likely to complete antimicrobial treatment and have poorer outcomes than patients without a history of injecting drug use. We used a social ecological model to identify critical barriers and facilitators that impact healthcare service access for people who inject drugs with an invasive infection.

Design

A qualitative study using semi-structured interviews.

Setting

Melbourne, Victoria, Australia in 2023.

Participants

Twenty participants were recruited from SuperMIX, a longitudinal cohort of people who inject drugs.

Measurements

Thematic analysis used inductive coding to chart themes onto the core domains of the social ecological model.

Findings

Participant experiences informed five key themes. (1) Health literacy influenced how participants responded to the physical and experiential embodiment of symptoms. (2) The intersection between drug use and marginalisation created compounding barriers to care. (3) Familial and social embeddedness of participants could both enable or restrict their healthcare access. (4) The use of patient-centred care to respond to intersecting needs directly contributed to healthcare engagement outcomes. Finally, (5) trust was a critical dimension that influenced participants' experiences of healthcare access. While its presence or absence was felt at intrapersonal and interpersonal levels, cultivating or discouraging trust had its roots at the societal and institutional level.

Conclusions

Among people who inject drugs, facilitators and barriers to seeking healthcare for invasive infections appear to be influenced by factors at all levels of the social ecological model (intrapersonal, interpersonal, institutional and societal).

背景和目的:在许多国家,与注射有关的细菌感染正在增加。全身性感染通常需要长期治疗。有证据表明,与没有注射吸毒史的患者相比,有侵袭性感染的注射吸毒者完成抗菌治疗的可能性较小,预后也较差。我们使用社会生态模型来确定影响侵入性感染注射吸毒者获得医疗保健服务的关键障碍和促进因素。设计:采用半结构化访谈的定性研究。背景:2023年,澳大利亚维多利亚州墨尔本。参与者:20名参与者从SuperMIX中招募,SuperMIX是一个注射吸毒者的纵向队列。测量:主题分析使用归纳编码将主题绘制到社会生态模型的核心领域。调查结果:参与者的经历为五个关键主题提供了信息。(1)健康素养影响参与者对症状的身体体现和体验体现的反应。(2)药物使用和边缘化之间的交叉造成了护理的复合障碍。(3)参与者的家庭嵌入性和社会嵌入性对其获得医疗服务既有促进作用,也有限制作用。(4)使用以患者为中心的护理来应对相互交叉的需求,直接促进了医疗保健参与的结果。最后,(5)信任是影响参与者医疗保健获取体验的关键维度。虽然它的存在或不存在是在个人和人际层面感受到的,但培养或阻碍信任的根源在于社会和体制层面。结论:在注射吸毒者中,侵入性感染寻求医疗保健的便利因素和障碍因素似乎受到社会生态模型各个层面因素(个人、人际、制度和社会)的影响。
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引用次数: 0
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Addiction
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