E ach year, >1 000 000 Americans experience acute myocardial infarction (AMI) or acute ischemic stroke (AIS). 1 Any role of acute infection in triggering acute cardiovascular events is of major clinical and public health interest. [2][3][4][5] Infections may increase the risk of AMI and AIS 6-14 by inducing demand ischemia, decreasing myocardial contractility, or causing endothelial dysfunction, coagulation disturbance, or direct platelet activation. [2][3][4][15][16][17][18] The magnitude and duration of the increased cardiovascular risk is debatable. Cohort studies have reported short-term risks of AMI and stroke varying from 0.2% to >10% after patients have been hospitalized with pneumonia, sepsis, endocarditis, or meningitis. [7][8][9][10][11][19][20][21]
Editorial see p 1375 Clinical Perspective on p 1396Case-only studies suggest a 10-to 50-fold increased risk for AMI or stroke shortly after patients have been hospitalized with infection, 6,9,12 and a 2-to 5-fold increased risk shortly after infection diagnosed by general practitioners. 13,14 Only 1 cohort study of 206 patients with pneumonia included a comparison group, 9 and we are aware of only 3 studies that included microbiological test results. 6,9,10 The lack of laboratory confirmation of infection may have falsely inflated the effect estimates if cardiovascular events were initially misdiagnosed as infections. Community-acquired bacteremia (CAB) is a well-defined clinical entity that embraces a wide range of mechanisms whereby infection may trigger cardiovascular events. We conducted a 20-year population-based cohort study in Denmark to assess the short-and longer-term risks of AMI and AIS among medical patients with CAB in Background-Infections may trigger acute cardiovascular events, but the risk after community-acquired bacteremia is unknown. We assessed the risk for acute myocardial infarction and ischemic stroke within 1 year of community-acquired bacteremia. Methods and Results-Thispopulation-based cohort study was conducted in Northern Denmark. We included 4389 hospitalized medical patients with positive blood cultures obtained on the day of admission. Patients hospitalized with bacteremia were matched with up to 10 general population controls and up to 5 acutely admitted nonbacteremic controls, matched on age, sex, and calendar time. All incident events of myocardial infarction and stroke during the following 365 days were ascertained from population-based healthcare databases. Multivariable regression analyses were used to assess relative risks with 95% confidence intervals (CIs) for myocardial infarction and stroke among bacteremia patients and their controls. The risk for myocardial infarction or stroke was greatly increased within 30 days of community-acquired bacteremia: 3.6% versus 0.2% among population controls (adjusted relative risk, 20.86; 95% CI,) and 1.7% among hospitalized controls (adjusted relative risk, 2.18; 95% CI, 1.80-2.65). The risks for myocardial infarction or stroke remained modestly increased from 31 to 180 days aft...