Abstract

Early identification of severe viral pneumonia in influenza virus A (H1N1pdm09) patients is extremely important for prompt admission to the ICU. The objective is to evaluate the usefulness of MR-proadrenomedullin (MR-proADM) compared to C reactive protein (CRP), procalcitonin (PCT), and ferritin in the prognosis of influenza A pneumonia. This prospective, observational, multicenter study included one hundred thirteen patients with confirmed influenza virus A (H1N1pdm09) admitted to an Emergency Department and ICUs of six hospitals in Spain. Measurements and Main Results: one-hundred thirteen patients with confirmed influenza virus A (H1N1pdm09) were enrolled. Seventy-five subjects (mortality 29.3%) with severe pneumonia caused by influenza A H1N1pdm09 virus (H1N1vIPN) were compared with 38 controls (CG).The median MR-proADM levels at hospital admission were 1.2 nmol/L (IQR (0.8–2.6) vs. 0.5 nmol/L (IQR 0.2–0.9) in the CG (p = 0.01), and PCT levels were 0.43 μg/L (IQR 0.2–1.2) in the H1N1vIPN group and 0.1 μg/L (IQR 0.1–0.2) in the CG (p < 0.01). CRP levels at admission were 15.5 mg/dL(IQR 9.2–24.9) in H1N1vIPN and 8.6 mg/dL(IQR 3–17.3) in the CG (p < 0.01). Ferritin levels at admission were 558.1 ng/mL(IQR 180–1880) in H1N1vIPN and 167.7 ng/mL(IQR 34.8–292.9) in the CG (p < 0.01). A breakpoint for hospital admission of MR-proADM of 1.1 nmol/L showed a sensitivity of 55% and a specificity of 90% (AUC-ROC0.822). Non-survivors showed higher MR-proADM levels: median of 2.5 nmol/L vs. 0.9 nmol/L among survivors (p < 0.01). PCT, CRP, and ferritin levels also showed significant differences in predicting mortality. The MR-proADM AUC-ROC for mortality was 0.853 (p < 0.01). In a Cox proportional hazards model, MR-proADM levels > 1.2 nmol/L at hospital admission were significant predictive factors for ICU and 90-day mortality (HR: 1.3). Conclusions: the initial MR-proADM, ferritin, CRP, and PCT levels effectively determine adverse outcomes and risk of ICU admission and mortality in patients with influenza virus pneumonia. MR-proADM has the highest potency for survival prediction.

Highlights

  • Compared to other types of pneumonia, patients with severe pneumonia caused by influenza A H1N1pdm09 virus (H1N1vIPN) have particular features of their own

  • We included patients admitted to the ICUs of six hospitals in Spain diagnosed with sepsis due to confirmed influenza virus A (H1N1) pneumonia over five years, from February 2013 to March 2018

  • One hundred thirteen patients with confirmed influenza virus A (H1N1pdm09) were enrolled: 75 with severe pneumonia caused by influenza A H1N1pdm09 virus (H1N1vIPN)

Read more

Summary

Introduction

Compared to other types of pneumonia, patients with severe pneumonia caused by influenza A H1N1pdm virus (H1N1vIPN) have particular features of their own. The flu pandemic of 1918 [1] was characterized by increased mortality in young adults, obese patients, and pregnant women [2,3], a phenomenon that remains unexplained but was repeated in the pandemic of 2009. H1N1 influenza affects young patients and others with important comorbidities and is the main cause of viral community-acquired pneumonia. 13–45% are admitted to the ICU; despite advances in treatment, mortality remains around 30% [4,5]. Identification of severe viral pneumonia is critical because mortality is high, and predicting the severity is vital in order to allow prompt admission to the ICU. Communityacquired pneumonia-specific scores (PSI, CURB 65, or PIRO-CAP) have not proved helpful in these patients [6,7]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call