Journal of Clinical Medicine (Jul 2020)

Prevalence, Determinants, and Prognostic Significance of Hospital Acquired Pneumonia in Patients with Acute Heart Failure

  • Atsushi Tada,
  • Kazunori Omote,
  • Toshiyuki Nagai,
  • Yasuyuki Honda,
  • Hiroki Nakano,
  • Satoshi Honda,
  • Naotsugu Iwakami,
  • Yasuhiro Hamatani,
  • Michikazu Nakai,
  • Kunihiro Nishimura,
  • Yasuhide Asaumi,
  • Takeshi Aiba,
  • Teruo Noguchi,
  • Kengo Kusano,
  • Hiroyuki Yokoyama,
  • Satoshi Yasuda,
  • Hisao Ogawa,
  • Toshihisa Anzai

DOI
https://doi.org/10.3390/jcm9072219
Journal volume & issue
Vol. 9, no. 7
p. 2219

Abstract

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The prognostic impact of hospital-acquired pneumonia (HAP) in acute heart failure (AHF) patients have not been fully elucidated. We evaluated 776 consecutive hospitalized AHF patients. The primary in-hospital outcomes were all-cause death and worsening heart failure (WHF), while the outcome following discharge was all-cause death. The clinical diagnosis of HAP was based on clinical practice guidelines by the Infectious Diseases Society of America and the American Thoracic Society. Patients with HAP had a significantly higher incidence of in-hospital death (12% vs. 1%, p p p = 0.003) than those without. Among patients who survived at discharge, during a median follow-up period of 741 (interquartile range 422–1000) days, the incidence of all-cause death was significantly higher in patients with HAP than in those without (p < 0.001). In the multivariable Cox regression, HAP development was independently associated with all-cause death after discharge (HR [hazard ratio] 1.86, 95%CI [confidence interval] 1.08–3.19). Furthermore, older age (OR [odds ratio] 1.04, 95%CI 1.01–1.08), male sex (OR 2.21, 95%CI 1.14–4.28), and higher serum white blood cell count (OR 1.18, 95%CI 1.09–1.29) and serum C-reactive protein (OR 1.08, 95%CI 1.01–1.06) were independently associated with HAP development. In hospitalized patients with AHF, HAP development was associated with worse clinical outcomes, suggesting the importance of prevention and early screening for HAP.

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