Department of Health Policy, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Clin Infect Dis. 2023 Jun 16;76(12):2171-2177. doi: 10.1093/cid/ciad065.
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.
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.
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).
Hospitalizations with AMI were strongly associated with laboratory-confirmed IPD.
已有研究报告称,某些病毒和细菌感染可引发急性心肌梗死(AMI)事件。但侵袭性肺炎球菌病(IPD)是否会增加 AMI 风险尚不清楚。本研究旨在探讨实验室确诊的 IPD 是否与 AMI 风险相关。
本研究采用病例对照研究方法,纳入了田纳西州符合 AMI 住院标准的成年居民(2003-2019 年)。患者随访从最早的 AMI 前 1 年开始,持续至死亡、AMI 后 1 年或研究结束(2019 年 12 月)。AMI 评估期包括 IPD 标本采集前 7-1 天(IPD 检测前)、IPD 标本采集后 0-7 天(当前 IPD)、IPD 标本采集后 8-28 天(IPD 后)和对照期(其余所有随访期)。采用条件泊松回归模型计算每个风险期与对照期相比的发病率比值(IRR)及其 95%置信区间(CI),并采用个体内比较进行分析。
本研究共纳入了 324 例 AMI 住院患者,其中 1 年内有实验室确诊的 IPD。与对照期相比,IPD 检测前(IRR,10.29;95%CI:6.33-16.73)和当前 IPD 期(IRR,92.95;95%CI:72.17-119.71)的 AMI 发病率显著升高,而 IPD 后风险期(IRR,1.83;95%CI:.86-3.91)的 AMI 发病率虽略有升高,但无统计学意义。与 IPD 后对照期(IPD 后 29-365 天)相比,所有其他对照期(IRR,2.95;95%CI:2.01-4.32)的 AMI 发病率也较高。
实验室确诊的 IPD 与 AMI 住院密切相关。