Risk of myocardial infarction and stroke following bloodstream infection: a population-based self-controlled case series.

IF 2.8 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Open Heart Pub Date : 2025-03-25 DOI:10.1136/openhrt-2025-003241
Jonathan Underwood, Nicola Reeve, Victoria Best, Ashley Akbari, Haroon Ahmed
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Abstract

Background: Cardiovascular disease (CVD) events triggered by inflammation are an underappreciated and poorly quantified cause of morbidity and mortality in patients with bloodstream infections (BSIs). We aimed to determine the risk of myocardial infarction (MI) and stroke after BSI.

Methods: This self-controlled case series study was conducted within the Secure Anonymised Information Linkage Databank, containing anonymised population-scale electronic health record data for Wales, UK. We included adults with community-acquired BSI between 2010 and 2020. MI and stroke were determined from International Classification of Disease Version 10 coded admissions. Predefined risk periods after BSI were compared with the baseline period using pseudo-Poisson regression adjusted for age. Maximum C-reactive protein (CRP), a proxy for the magnitude of the inflammatory response, was determined within the first 7 days after BSI.

Results: We identified 50 450 individuals with MI and 56 890 with stroke, of whom 1000 and 1290, respectively, also had at least one community-associated BSI. The risk of MI was most elevated in the first 1-7 days after BSI (adjusted incidence rate ratio (IRR) (95% CI): 9.67 (6.54 to 14.3)) and returned to baseline after 28 days. The risk was similarly elevated for stroke.The largest magnitude of risk was observed for those with a maximal CRP>300 mg/L (MI IRR: 21.54 (9.57 to 48.52); stroke IRR: 6.94 (3.14 to 15.32)).

Conclusion: BSI is associated with an increased risk of CVD events in the first 2 weeks after infection. Greater systemic inflammation was associated with a higher risk of CVD events and suggests targeting the inflammatory response caused by BSI warrants further study.

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血流感染后心肌梗死和中风的风险:基于人群的自我控制病例系列
背景:炎症引发的心血管疾病(CVD)事件是血流感染(bsi)患者发病率和死亡率的一个未被充分认识和量化的原因。我们的目的是确定BSI后心肌梗死(MI)和中风的风险。方法:这项自我控制的病例系列研究是在安全匿名信息链接数据库中进行的,该数据库包含英国威尔士的匿名人口规模电子健康记录数据。我们纳入了2010年至2020年间患有社区获得性BSI的成年人。心肌梗死和中风由国际疾病分类第10版编码入院确定。使用年龄调整后的伪泊松回归将BSI后的预定义风险期与基线期进行比较。最大c反应蛋白(CRP)是炎症反应程度的代表,在BSI后的前7天内测定。结果:我们确定了50450例心肌梗死患者和56890例脑卒中患者,其中分别有1000例和1290例至少有一种社区相关BSI。心肌梗死的风险在BSI后的前1-7天最高(校正发病率比(IRR) (95% CI): 9.67(6.54至14.3)),并在28天后恢复到基线水平。中风的风险也同样升高。最高CRP值为300 mg/L的患者的风险最大(MI IRR: 21.54 (9.57 ~ 48.52);冲程IRR: 6.94(3.14至15.32))。结论:BSI与感染后2周CVD事件风险增加有关。更大的全身炎症与更高的CVD事件风险相关,这表明针对BSI引起的炎症反应值得进一步研究。
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来源期刊
Open Heart
Open Heart CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
4.60
自引率
3.70%
发文量
145
审稿时长
20 weeks
期刊介绍: Open Heart is an online-only, open access cardiology journal that aims to be “open” in many ways: open access (free access for all readers), open peer review (unblinded peer review) and open data (data sharing is encouraged). The goal is to ensure maximum transparency and maximum impact on research progress and patient care. The journal is dedicated to publishing high quality, peer reviewed medical research in all disciplines and therapeutic areas of cardiovascular medicine. Research is published across all study phases and designs, from study protocols to phase I trials to meta-analyses, including small or specialist studies. Opinionated discussions on controversial topics are welcomed. Open Heart aims to operate a fast submission and review process with continuous publication online, to ensure timely, up-to-date research is available worldwide. The journal adheres to a rigorous and transparent peer review process, and all articles go through a statistical assessment to ensure robustness of the analyses. Open Heart is an official journal of the British Cardiovascular Society.
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