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Is elevated red cell distribution width a prognostic predictor in adult patients with community acquired pneumonia?

Eyal Braun1, Jad Kheir, Tanya Mashiach

  • 1Departments of Medicine H and B, Rambam Health Care Campus, P,O, Box 9602, 31096 Haifa, Israel. e_braun@rambam.health.gov.il.

Insights

Elevated red blood cell distribution width (RDW) predicts worse outcomes in community-acquired pneumonia (CAP). Higher RDW levels correlate with increased mortality and severe complications in adult CAP patients.

Area of Science:

  • Internal Medicine
  • Pulmonology
  • Critical Care Medicine

Background:

  • Community-acquired pneumonia (CAP) is a significant cause of illness and death.
  • Previous research indicated elevated red blood cell distribution width (RDW) is linked to higher mortality in younger CAP patients.
  • This study examines RDW's prognostic value in a broader adult CAP population.

Purpose of the Study:

  • To assess the predictive value of red blood cell distribution width (RDW) for mortality and severe morbidity in adult patients with community-acquired pneumonia (CAP).

Main Methods:

  • Retrospective analysis of 3815 adult patients diagnosed with CAP between 2005 and 2010.
  • Primary endpoint: 90-day mortality. Secondary endpoint: complicated hospitalization (in-hospital mortality, prolonged stay, or ICU admission).
  • Binary logistic regression used to identify risk factors and associations with RDW levels.

Main Results:

  • Elevated RDW (>15%) was independently associated with increased 90-day mortality and complicated hospitalization.
  • Other mortality predictors included advanced age, high comorbidity index, low hemoglobin, low sodium, high BUN, and low systolic blood pressure.
  • RDW's prognostic value was independent of hemoglobin levels, white blood cell count, age, or Charlson score.

Conclusions:

  • Elevated RDW on admission is a significant predictor of mortality and severe morbidity in adult CAP patients.
  • RDW serves as a valuable prognostic marker in CAP, irrespective of other common clinical indicators.
Abstract

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