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Meta-Analysis
. 2011 Jun;8(6):e1001048.
doi: 10.1371/journal.pmed.1001048. Epub 2011 Jun 28.

Cardiac complications in patients with community-acquired pneumonia: a systematic review and meta-analysis of observational studies

Affiliations
Meta-Analysis

Cardiac complications in patients with community-acquired pneumonia: a systematic review and meta-analysis of observational studies

Vicente F Corrales-Medina et al. PLoS Med. 2011 Jun.

Abstract

Background: Community-acquired pneumonia (CAP) is a leading cause of morbidity and mortality. CAP can trigger acute cardiac events. We sought to determine the incidence of major cardiac complications in CAP patients to characterize the magnitude of this problem.

Methods and findings: Two investigators searched MEDLINE, Scopus, and EMBASE for observational studies of immunocompetent adults with clinical and radiological evidence of CAP that reported any of the following: overall cardiac complications, incident heart failure, acute coronary syndromes (ACS), or incident cardiac arrhythmias occurring within 30 days of CAP diagnosis. At a minimum, studies had to establish enrolment procedures and inclusion and exclusion criteria, enroll their patients sequentially, and report the incidence of cardiac complications as a function of their entire cohorts. Studies with focus on nosocomial or health care-associated pneumonia were not included. Review of 2,176 citations yielded 25 articles that met eligibility and minimum quality criteria. Seventeen articles (68%) reported cohorts of CAP inpatients. In this group, the pooled incidence rates for overall cardiac complications (six cohorts, 2,119 patients), incident heart failure (eight cohorts, 4,215 patients), acute coronary syndromes (six cohorts, 2,657 patients), and incident cardiac arrhythmias (six cohorts, 2,596 patients), were 17.7% (confidence interval [CI] 13.9-22.2), 14.1% (9.3-20.6), 5.3% (3.2-8.6), and 4.7% (2.4-8.9), respectively. One article reported cardiac complications in CAP outpatients, four in low-risk (not severely ill) inpatients, and three in high-risk inpatients. The incidences for all outcomes except overall cardiac complications were lower in the two former groups and higher in the latter. One additional study reported on CAP outpatients and low-risk inpatients without discriminating between these groups. Twelve studies (48%) asserted the evaluation of cardiac complications in their methods but only six (24%) provided a definition for them. Only three studies, all examining ACS, carried out risk factor analysis for these events. No study analyzed the association between cardiac complications and other medical complications or their impact on other CAP outcomes.

Conclusions: Major cardiac complications occur in a substantial proportion of patients with CAP. Physicians and patients need to appreciate the significance of this association for timely recognition and management of these events. Strategies aimed at preventing pneumonia (i.e., influenza and pneumococcal vaccination) in high-risk populations need to be optimized. Further research is needed to understand the mechanisms underlying this association, measure the impact of cardiac complications on other CAP outcomes, identify those patients with CAP at high risk of developing cardiac complications, and design strategies to prevent their occurrence in this population.

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Conflict of interest statement

VFCM has provided consulting services to CEMPRA pharmaceuticals. GR is involved in a research study sponsored by CEMPRA pharmaceuticals.

Figures

Figure 1
Figure 1. PRISMA flow diagram: selection process.
Figure 2
Figure 2. Pooled rates of the incidence of cardiac complications in patients with CAP.
One study reporting the incidence of ACS and incident cardiac arrhythmias on outpatients and low-risk inpatients without making distinction between them was not included in the calculations of pooled rates . aFor definitions refer to Table 1. bLow-risk inpatients included studies of inpatients with no indication for hospital admission, pneumonia severity index (PSI) risk-classes I–II, not initially admitted to intensive care units or who survived the first 48 h of hospitalization. High-risk inpatients included patients admitted to intensive care units. cWhen only one study was available, the reported rate represents the study event rate.

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