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Article: Influenza A-associated severe pneumonia in hospitalized patients: Risk factors and NAI treatments
Title | Influenza A-associated severe pneumonia in hospitalized patients: Risk factors and NAI treatments |
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Authors | |
Keywords | Double dose Severe pneumonia Influenza Oseltamivir |
Issue Date | 2020 |
Citation | International Journal of Infectious Diseases, 2020, v. 92, p. 208-213 How to Cite? |
Abstract | © 2020 The Authors Objective: The risk factors and the impact of NAI treatments in patients with severe influenza A-associated pneumonia remain unclear. Methods: A multicenter, retrospective, observational study was conducted in Zhejiang, China during a severe influenza epidemic in August 2017–May 2018. Clinical records of patients (>14 y) hospitalized with laboratory-confirmed influenza A virus infection and who developed severe pneumonia were compared to those with mild-to-moderate pneumonia. Risk factors related to pneumonia severity and effects of NAI treatments (monotherapy and combination of peramivir and oseltamivir) were analyzed. Results: 202 patients with influenza A-associated severe pneumonia were enrolled, of whom 84 (41.6%) had died. Male gender (OR = 1.782; 95% CI: 1.089–2.917; P = 0.022), chronic pulmonary disease (OR = 2.581; 95% CI: 1.447–4.603; P = 0.001) and diabetes mellitus (OR = 2.042; 95% CI: 1.135–3.673; P = 0.017) were risk factors related to influenza A pneumonia severity. In cox proportional hazards model, severe pneumonia patients treated with double dose oseltamivir (300mg/d) had a better survival rate compared to those receiving a single dose (150 mg/d) (HR = 0.475; 95%CI: 0.254–0.887; P = 0.019). However, different doses of peramivir (300 mg/d vs. 600 mg/d) and combination therapy (oseltamivir-peramivir vs. monotherapy) showed no differences in 60-day mortality (P = 0.392 and P = 0.658, respectively). Conclusions: Patients with male gender, chronic pulmonary disease, or diabetes mellitus were at high risk of developing severe pneumonia after influenza A infection. Double dose oseltamivir might be considered in treating influenza A-associated severe pneumonia. |
Persistent Identifier | http://hdl.handle.net/10722/288790 |
ISSN | 2023 Impact Factor: 4.8 2023 SCImago Journal Rankings: 1.435 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Zou, Qianda | - |
dc.contributor.author | Zheng, Shufa | - |
dc.contributor.author | Wang, Xiaochen | - |
dc.contributor.author | Liu, Sijia | - |
dc.contributor.author | Bao, Jiaqi | - |
dc.contributor.author | Yu, Fei | - |
dc.contributor.author | Wu, Wei | - |
dc.contributor.author | Wang, Xianjun | - |
dc.contributor.author | Shen, Bo | - |
dc.contributor.author | Zhou, Tieli | - |
dc.contributor.author | Zhao, Zhigang | - |
dc.contributor.author | Wang, Yiping | - |
dc.contributor.author | Chen, Ruchang | - |
dc.contributor.author | Wang, Wei | - |
dc.contributor.author | Ma, Jianbo | - |
dc.contributor.author | Li, Yongcheng | - |
dc.contributor.author | Wu, Xiaoyan | - |
dc.contributor.author | Shen, Weifeng | - |
dc.contributor.author | Xie, Fuyi | - |
dc.contributor.author | Vijaykrishna, Dhanasekaran | - |
dc.contributor.author | Chen, Yu | - |
dc.date.accessioned | 2020-10-12T08:05:52Z | - |
dc.date.available | 2020-10-12T08:05:52Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | International Journal of Infectious Diseases, 2020, v. 92, p. 208-213 | - |
dc.identifier.issn | 1201-9712 | - |
dc.identifier.uri | http://hdl.handle.net/10722/288790 | - |
dc.description.abstract | © 2020 The Authors Objective: The risk factors and the impact of NAI treatments in patients with severe influenza A-associated pneumonia remain unclear. Methods: A multicenter, retrospective, observational study was conducted in Zhejiang, China during a severe influenza epidemic in August 2017–May 2018. Clinical records of patients (>14 y) hospitalized with laboratory-confirmed influenza A virus infection and who developed severe pneumonia were compared to those with mild-to-moderate pneumonia. Risk factors related to pneumonia severity and effects of NAI treatments (monotherapy and combination of peramivir and oseltamivir) were analyzed. Results: 202 patients with influenza A-associated severe pneumonia were enrolled, of whom 84 (41.6%) had died. Male gender (OR = 1.782; 95% CI: 1.089–2.917; P = 0.022), chronic pulmonary disease (OR = 2.581; 95% CI: 1.447–4.603; P = 0.001) and diabetes mellitus (OR = 2.042; 95% CI: 1.135–3.673; P = 0.017) were risk factors related to influenza A pneumonia severity. In cox proportional hazards model, severe pneumonia patients treated with double dose oseltamivir (300mg/d) had a better survival rate compared to those receiving a single dose (150 mg/d) (HR = 0.475; 95%CI: 0.254–0.887; P = 0.019). However, different doses of peramivir (300 mg/d vs. 600 mg/d) and combination therapy (oseltamivir-peramivir vs. monotherapy) showed no differences in 60-day mortality (P = 0.392 and P = 0.658, respectively). Conclusions: Patients with male gender, chronic pulmonary disease, or diabetes mellitus were at high risk of developing severe pneumonia after influenza A infection. Double dose oseltamivir might be considered in treating influenza A-associated severe pneumonia. | - |
dc.language | eng | - |
dc.relation.ispartof | International Journal of Infectious Diseases | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Double dose | - |
dc.subject | Severe pneumonia | - |
dc.subject | Influenza | - |
dc.subject | Oseltamivir | - |
dc.title | Influenza A-associated severe pneumonia in hospitalized patients: Risk factors and NAI treatments | - |
dc.type | Article | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1016/j.ijid.2020.01.017 | - |
dc.identifier.pmid | 31978583 | - |
dc.identifier.scopus | eid_2-s2.0-85079281122 | - |
dc.identifier.hkuros | 317459 | - |
dc.identifier.volume | 92 | - |
dc.identifier.spage | 208 | - |
dc.identifier.epage | 213 | - |
dc.identifier.eissn | 1878-3511 | - |
dc.identifier.isi | WOS:000519191900033 | - |
dc.identifier.issnl | 1201-9712 | - |