Abstract

Patients with influenza infection may develop acute respiratory distress syndrome (ARDS), which is associated with high mortality. Some patients with ARDS receiving extracorporeal membrane oxygenation (ECMO) support die of infectious complications. We aimed to investigate the risk factors affecting the clinical outcomes in critically ill patients with influenza. We retrospectively reviewed the medical records of influenza patients between January 2006 and May 2016 at the Kaohsiung Veterans General Hospital in Taiwan. Patients aged below 20 years or without laboratory-confirmed influenza were excluded. Critically ill patients who presented with ARDS (P = 0.004, odds ratio (OR): 8.054, 95% confidence interval (CI): 1.975–32.855), a higher Acute Physiology and Chronic Health Evaluation (APACHE) II score (P = 0.008, OR: 1.102, 95% CI: 1.025–1.184), or higher positive end-expiratory pressure (P = 0.008, OR: 1.259, 95% CI: 1.061–1.493) may have a higher risk of receiving ECMO. Influenza A (P = 0.037, OR: 0.105, 95% CI: 0.013–0.876) and multiple organ failure (P = 0.007, OR: 0.056, 95% CI: 0.007–0.457) were significantly associated with higher mortality rates. In conclusion, our study showed critically ill influenza patients with ARDS, higher APACHE II scores, and higher positive end-expiratory pressure have a higher risk of receiving ECMO support. Influenza A and multiple organ failure are predictors of mortality.

Highlights

  • Influenza viruses have segmented genomes to enable virus reassortments and display antigenic variation [1]

  • This study aimed to investigate the clinical characteristics and risk factors affecting the clinical outcomes of critically ill patients with influenza

  • In the multivariable logistic regression analysis of the predictors of extracorporeal membrane oxygenation (ECMO) use, critically ill patients with influenza who presented with acute respiratory distress syndrome (ARDS) (P = 0.004, odds ratio (OR): 8.054, 95% confidence interval (CI): 1.975–32.855), a higher Acute Physiology and Chronic Health Evaluation (APACHE) II score (P = 0.008, OR: 1.102, 95% CI: 1.025–1.184), or higher positive end-expiratory pressure (PEEP) (P = 0.008, OR: 1.259, 95% CI: 1.061–1.493)

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Summary

Introduction

Influenza viruses have segmented genomes to enable virus reassortments and display antigenic variation [1]. There are three types of influenza viruses: A, B, and C [1]. The H1N1 pandemic from 1918 to 1919 caused 40–50 million deaths globally [1]. Over 60.8 million cases, 274,304 hospitalizations, and 12,469 deaths were reported in the entire United States due to the 2009 influenza A virus (pH1N1) pandemic from 12 April 2009 to 10 April 2010 [2]. Influenza infections are mostly self-limiting, but some patients may develop severe complications, such as pneumonia or acute respiratory distress syndrome (ARDS) [4]. The use of corticosteroids has been associated with poor prognosis in patients with influenza pneumonia [8]

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