1. Adjuvant Corticosteroid Treatment in Adults With Influenza A (H7N9) Viral Pneumonia*
- Author
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Jingyuan Liu, Zenghui Pu, Chaosheng Deng, Ling Chen, Carol Dukes Hamilton, Baoxia Sun, Hainv Gao, Chengping Hu, Yida Yang, Yuping Li, Hongzhou Lu, Bin Cao, Boping Zhou, Jianhe Gan, Wei Zhao, Lanjuan Li, Qin Gu, Qiang Fang, Xi Liu, Hui Li, Xilong Deng, Xian-Mei Zhou, Yinzhong Shen, and Yao Zhang
- Subjects
Adult ,Male ,China ,medicine.medical_specialty ,Time Factors ,Adolescent ,medicine.drug_class ,Pneumonia, Viral ,Influenza A Virus, H7N9 Subtype ,Critical Care and Intensive Care Medicine ,medicine.disease_cause ,Antiviral Agents ,Young Adult ,03 medical and health sciences ,0302 clinical medicine ,Adrenal Cortex Hormones ,Interquartile range ,Internal medicine ,Influenza, Human ,medicine ,Influenza A virus ,Humans ,030212 general & internal medicine ,Viral shedding ,Propensity Score ,Aged ,Proportional Hazards Models ,Aged, 80 and over ,business.industry ,Hazard ratio ,Middle Aged ,medicine.disease ,Virus Shedding ,Pneumonia ,030228 respiratory system ,Methylprednisolone ,Case-Control Studies ,Viral pneumonia ,Immunology ,Corticosteroid ,Drug Therapy, Combination ,Female ,business ,medicine.drug - Abstract
Objective To determine the impact of adjuvant corticosteroids administered to patients hospitalized with influenza A (H7N9) viral pneumonia. Design The effects of adjuvant corticosteroids on mortality were assessed using multivariate Cox regression and a propensity score-matched case-control study. Nosocomial infections and viral shedding were also compared. Setting Hospitals with influenza A (H7N9) viral pneumonia patient admission in 84 cities and 16 provinces of Mainland China. Patients Adolescent and Adult patients aged >14 yr with severe laboratory-confirmed influenza A (H7N9) virus infections were screened from April 2013 to March 2015. Interventions None. Measurements and main results The study population comprised 288 cases who were hospitalized with influenza A (H7N9) viral pneumonia. The median age of the study population was 58 years, 69.8% of the cohort comprised male patients, and 51.4% had at least one type of underlying diseases. The in-hospital mortality was 31.9%. Two hundred and four patients (70.8%) received adjuvant corticosteroids; among them, 193 had hypoxemia and lung infiltrates, 11 had chronic obstructive pulmonary disease, and 11 had pneumonia only. Corticosteroids were initiated within 7 days (interquartile range, 5.0-9.4 d) of the onset of illness and the maximum dose administered was equivalent to 80-mg methylprednisolone (interquartile range, 40-120 mg). The patients were treated with corticosteroids for a median duration of 7 days (interquartile range, 4.0-11.3 d). Cox regression analysis showed that compared with the patients who did not receive corticosteroid, those who received corticosteroid had a significantly higher 60-day mortality (adjusted hazards ratio, 1.98; 95% CI, 1.03-3.79; p = 0.04). Subgroup analysis showed that high-dose corticosteroid therapy (> 150 mg/d methylprednisolone or equivalent) significantly increased both 30-day and 60-day mortality, whereas no significant impact was observed for low-to-moderate doses of corticosteroids (25-150 mg/d methylprednisolone or equivalent). The propensity score-matched case-control analysis showed that the median viral shedding time was much longer in the group that received high-dose corticosteroids (15 d), compared with patients who did not receive corticosteroids (13 d; p = 0.039). Conclusions High-dose corticosteroids were associated with increased mortality and longer viral shedding in patients with influenza A (H7N9) viral pneumonia.
- Published
- 2016
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