• Wen-Qing Yu, Ning-Fei Ji, Ming-Dong Ding, Cheng-Jing Gu, Yuan Ma, Zhen-Zhen Wu, Yan-Li Wang, Chao-Jie Wu, Gui-Hong Dai, Yan Chen, Rong-Rong Jin, Yi-Bin Tan, Zhu Yang, Da-Ming Zhou, Jian-Chun Xian, Hong-Tao Xu, and Mao Huang.
• Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
• Intern Med J. 2020 Sep 1; 50 (9): 1115-1123.

BackgroundH7N9 avian influenza is an infection of public health concern, in part because of its high mortality rate and pandemic potential.AimsTo describe the clinical features of H7N9 avian influenza and the response to treatment.MethodsClinical, radiological and histopathological data, and treatment-related of H7N9-infected patients hospitalised during 2014-2017 were extracted and analysed.ResultsA total of 17 H7N9 patients (three females; mean age, 58.4 ± 13.7 years) was identified; of these six died. All patients presented with fever and productive cough; four patients had haemoptysis and 13 had chest distress and/or shortness of breath. Early subnormal white blood cell count and elevation of serum liver enzymes were common. Multilobar patchy shadows, rapid progression to ground-glass opacities, air bronchograms and consolidation were the most common imaging findings. Histopathological examination of lung tissue of three patients who died showed severe alveolar epithelial cell damage, with inflammatory exudation into the alveolar space and hyaline membrane formation; widened alveolar septae, prominent inflammatory cell infiltration; and hyperplasia of pneumocytes. Viral inclusions were found in the lung tissue of two patients. All patients received antiviral drugs (oseltamivir ± peramivir). Four patients carried the rs12252-C/C interferon-induced transmembrane protein-3 (IFITM3) genotype, while the others had the C/T genotype.ConclusionsH7N9 virus infection causes human influenza-like symptoms, but may rapidly progress to severe pneumonia and even death. Clinicians should be alert to the possibility of H7N9 infection in high-risk patients. The presence of the IFITM3 rs12252-C genotype may predict severe illness.© 2019 Royal Australasian College of Physicians.

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