Risk of Acute Myocardial Infarction Among Patients With Laboratory-Confirmed Invasive Pneumococcal Disease: A Self-Controlled Case Series Study

Author:

Wiese Andrew D1ORCID,Mitchel Ed1,Ndi Danielle1,Markus Tiffanie M1,Talbot H Keipp12,Schaffner William12,Grijalva Carlos G134

Affiliation:

1. Department of Health Policy, Vanderbilt University Medical Center , Nashville, Tennessee , USA

2. Department of Medicine, Vanderbilt University Medical Center , Nashville, Tennessee , USA

3. Department of Biomedical Informatics, Vanderbilt University Medical Center , Nashville, Tennessee , USA

4. Veteran Affairs TN Valley Health Care System , Nashville, TN , USA

Abstract

Abstract Background Acute myocardial infarction (AMI) events have been reported among patients with certain viral and bacterial infections. Whether invasive pneumococcal disease (IPD) increases the risk of AMI remains unclear. We examined whether laboratory-confirmed IPD was associated with the risk of AMI. Methods We conducted a self-controlled case series analysis among adult Tennessee residents with evidence of an AMI hospitalization (2003–2019). Patient follow-up started 1 year before the earliest AMI and continued through the date of death, 1 year after AMI, or study end (December 2019). Periods for AMI assessment included the 7 to 1 days before IPD specimen collection (pre-IPD detection), day 0 through day 7 after IPD specimen collection (current IPD), day 8 to 28 after IPD specimen collection (post-IPD), and a control period (all other follow-up). We used conditional Poisson regression to calculate incidence rate ratios (IRRs) and 95% confidence intervals (CIs) for each risk period compared with control periods using within-person comparisons. Results We studied 324 patients hospitalized for AMI with laboratory-confirmed IPD within 1 year before or after the AMI hospitalization. The incidence of AMI was significantly higher during the pre-IPD detection (IRR, 10.29; 95% CI: 6.33–16.73) and the current IPD (IRR, 92.95; 95% CI: 72.17–119.71) periods but nonsignificantly elevated in the post-IPD risk period (IRR, 1.83; 95% CI: .86–3.91) compared with control periods. The AMI incidence was higher in the post-IPD control period (29 to 365 days after IPD; IRR, 2.95; 95% CI: 2.01–4.32). Conclusions Hospitalizations with AMI were strongly associated with laboratory-confirmed IPD.

Funder

National Institute on Drug Abuse

National Institutes of Health

(NIH)

National Institute on Aging

Centers for Disease Control and Prevention

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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