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Relationship between pneumonia and cardiovascular diseases: A retrospective cohort study of the general population

  • Jun-Jun Yeh
    Affiliations
    Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chiayi, Taiwan

    Chia Nan University of Pharmacy and Science, Tainan, Taiwan

    Meiho University, Pingtung, Taiwan
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  • Cheng-Li Lin
    Affiliations
    Management Office for Health Data, China Medical University Hospital, Taichung, Taiwan

    College of Medicine, China Medical University, Taichung, Taiwan
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  • Chia-Hung Kao
    Correspondence
    Corresponding author at: Graduate Institute of Biomedical Sciences, College of Medicine, China Medical University, No. 2, Yuh-Der Road, Taichung 40447, Taiwan.
    Affiliations
    Grdaduate Institute of Biomedical Sciences and School of Medicine, College of Medicine, China Medical University, Taichung, Taiwan

    Department of Nuclear Medicine and PET Center, China Medical University Hospital, Taichung, Taiwan

    Department of Bioinformatics and Medical Engineering, Asia University, Taichung, Taiwan
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Published:August 09, 2018DOI:https://doi.org/10.1016/j.ejim.2018.08.003

      Highlights

      • Pneumonia risk was associated with CVDs, especially for the heart failure and elderly male patients.
      • Patients with CVDs had a higher risk of CAP and HAP.
      • Patients with CVDs had higher frequency of ICU admission but shorter admission lengths.

      Abstract

      Aims

      To evaluate the relationship between cardiovascular diseases (CVDs) and pneumonia in the general population.

      Methods

      This retrospective observational study included two cohorts, namely CVD (n = 28,363) and non-CVD (n = 28,363) cohorts, which were matched by propensity score and examined for cases of pneumonia. Data were obtained from 2000 to 2011. In both cohorts, pneumonia risk was measured using multivariable Cox proportional hazard models.

      Results

      With the non-CVD cohort as reference, the corresponding adjusted hazard ratios (aHRs) [95% confidence intervals (CIs)] of pneumonia were 2.03 [1.77–2.31] for coronary artery disease, 4.11 [3.15–5.36] for heart failure, 3.21 [2.70–3.81] for cerebrovascular disease, 1.46 [1.07–1.98] for peripheral vascular disease, and 2.27 [2.01–2.56] for the CVD cohort. The cohort with comorbidities had a higher risk (all p < .05) of pneumonia compared with that without comorbidities, except for patients with the comorbidities of hypertension, hyperlipidemia, obesity, and liver disease. The aHR (95% CI) of pneumonia for antibiotic use was 1.26 (1.09–1.47). The aHRs of community-acquired pneumonia (CAP) and hospital-acquired pneumonia (HAP) were 3.25 (95% CI = 1.04–10.1) and 2.95 (95% CI = 2.25–3.88), respectively. The aHRs (95% CI) were 1.78 (1.05–3.03) for intensive care unit (ICU) risk and 0.98 (0.96–0.99) for length of admission.

      Conclusion

      Pneumonia risk was associated with CVDs, especially heart failure, regardless of age, gender, comorbidities, and antibiotic use, particularly in elderly male patients. In addition, Patients with CVDs had a higher risk of CAP and HAP. The CVD cohort had a higher frequency of ICU admissions, but shorter admission lengths.

      Keywords

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