Kevin B Laupland, Adam G Stewart, Felicity Edwards, Patrick N A Harris, Sonali Coulter
{"title":"Community-onset bloodstream infection among people with opioid use disorders: a twenty-year population-based cohort study in Queensland, Australia.","authors":"Kevin B Laupland, Adam G Stewart, Felicity Edwards, Patrick N A Harris, Sonali Coulter","doi":"10.1080/23744235.2025.2471823","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Few studies have examined infection risk related to opioid misuse in non-selected populations.</p><p><strong>Objectives: </strong>We sought to identify clinical factors and outcomes among adults with opioid use disorder-associated bloodstream infections (BSI)in Queensland, Australia.</p><p><strong>Methods: </strong>All Queensland residents aged ≥20 years with incident community-onset BSI hospitalised within the public healthcare system during 2000-2019 were included. Patients with opioid use disorders were identified and clinical and outcome information obtained using state-wide databases.</p><p><strong>Results: </strong>77,392 community-onset BSIs occurred among 66,424 individuals of which 828 (1.3%) patients were diagnosed with an opioid use disorder. Subjects with opioid use disorders were younger and less likely to have healthcare-associated infections. While the prevalence of nearly all co-morbidities evaluated was higher among subjects without opioid use disorders, patients with opioid use disorders were six times more likely to have liver disease. Endocarditis was eight times more likely among subjects with opioid use disorders, and these patients were more likely to be infected with <i>Staphylococcus aureus</i> and/or yeasts, and less likely <i>Escherichia coli</i> as compared to those without opioid use disorders. The median hospital stays were 18 and 8 days and crude all cause 30-day case-fatality was 5.1% versus 11.4% for those with and without opioid use disorders, respectively (<i>p</i> < 0.001 for each). After adjusting for confounding variables, an opioid use disorder was not associated with increased risk for death (adjusted odds ratio; 1.0; 95% confidence interval, 0.7-1.4; <i>p</i> = 0.9).</p><p><strong>Conclusion: </strong>Opioid use disorders are potentially modifiable conditions that are associated with a major burden of BSI-related disease.</p>","PeriodicalId":73372,"journal":{"name":"Infectious diseases (London, England)","volume":" ","pages":"669-675"},"PeriodicalIF":0.0000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infectious diseases (London, England)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/23744235.2025.2471823","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/5 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Few studies have examined infection risk related to opioid misuse in non-selected populations.
Objectives: We sought to identify clinical factors and outcomes among adults with opioid use disorder-associated bloodstream infections (BSI)in Queensland, Australia.
Methods: All Queensland residents aged ≥20 years with incident community-onset BSI hospitalised within the public healthcare system during 2000-2019 were included. Patients with opioid use disorders were identified and clinical and outcome information obtained using state-wide databases.
Results: 77,392 community-onset BSIs occurred among 66,424 individuals of which 828 (1.3%) patients were diagnosed with an opioid use disorder. Subjects with opioid use disorders were younger and less likely to have healthcare-associated infections. While the prevalence of nearly all co-morbidities evaluated was higher among subjects without opioid use disorders, patients with opioid use disorders were six times more likely to have liver disease. Endocarditis was eight times more likely among subjects with opioid use disorders, and these patients were more likely to be infected with Staphylococcus aureus and/or yeasts, and less likely Escherichia coli as compared to those without opioid use disorders. The median hospital stays were 18 and 8 days and crude all cause 30-day case-fatality was 5.1% versus 11.4% for those with and without opioid use disorders, respectively (p < 0.001 for each). After adjusting for confounding variables, an opioid use disorder was not associated with increased risk for death (adjusted odds ratio; 1.0; 95% confidence interval, 0.7-1.4; p = 0.9).
Conclusion: Opioid use disorders are potentially modifiable conditions that are associated with a major burden of BSI-related disease.
背景:很少有研究在非选定人群中检查与阿片类药物滥用相关的感染风险。目的:我们试图确定澳大利亚昆士兰州成人阿片类药物使用障碍相关血流感染(BSI)的临床因素和结果。方法:纳入2000-2019年期间在公共医疗保健系统住院的所有年龄≥20岁的突发社区发病BSI昆士兰居民。确定阿片类药物使用障碍患者,并使用全州数据库获得临床和结果信息。结果:66,424名患者中发生了77,392例社区发病的bsi,其中828例(1.3%)患者被诊断为阿片类药物使用障碍。阿片类药物使用障碍的受试者更年轻,更不容易发生与医疗保健相关的感染。虽然在没有阿片类药物使用障碍的受试者中,评估的几乎所有合并症的患病率较高,但阿片类药物使用障碍患者患肝脏疾病的可能性是其他受试者的6倍。阿片类药物使用障碍患者发生心内膜炎的可能性是无阿片类药物使用障碍患者的8倍,与无阿片类药物使用障碍患者相比,这些患者感染金黄色葡萄球菌和/或酵母菌的可能性更大,感染大肠杆菌的可能性更小。中位住院时间为18天和8天,有阿片类药物使用障碍和无阿片类药物使用障碍患者的30天粗全因病死率分别为5.1%和11.4% (p p = 0.9)。结论:阿片类药物使用障碍是潜在的可改变的条件,与bsi相关疾病的主要负担相关。