401
Views
61
Downloads
0
Crossref
N/A
WoS
N/A
Scopus
N/A
CSCD
The infection of the coronavirus disease 2019 (COVID‐19) is often accompanied by pneumonia with both high incidence and mortality. Paxlovid is commonly prescribed in patients with mild and normal pneumonia within 5 days from the symptom onset. Herein, we report a practically effective use of Paxlovid compensatively in patients with COVID‐19 and severe pneumonia after 5 days of infection in a typical case in China. In this case, a 75‐year‐old man was diagnosed with severe COVID‐19 complicated with a pulmonary bacterial infection. After treatment with oxygen inhalation, Cefoperazone‐sulbactam and ambroxol, fever and upper respiratory symptoms were alleviated, except for the Oxygenation index (OI) remaining worse, Coronavirus was detected as positive, and levels of interleukin‐6 remained high. Paxlovid was prescribed for 5 days subsequently though it was 14 days since symptom onset. Thereafter, the nucleic acid of the patient turned negative in 7 days and the symptoms resolved. This case showed that Paxlovid can be considered in patients with COVID‐19 and severe pneumonia even in the later course of infection in clinical practice in China.
The infection of the coronavirus disease 2019 (COVID‐19) is often accompanied by pneumonia with both high incidence and mortality. Paxlovid is commonly prescribed in patients with mild and normal pneumonia within 5 days from the symptom onset. Herein, we report a practically effective use of Paxlovid compensatively in patients with COVID‐19 and severe pneumonia after 5 days of infection in a typical case in China. In this case, a 75‐year‐old man was diagnosed with severe COVID‐19 complicated with a pulmonary bacterial infection. After treatment with oxygen inhalation, Cefoperazone‐sulbactam and ambroxol, fever and upper respiratory symptoms were alleviated, except for the Oxygenation index (OI) remaining worse, Coronavirus was detected as positive, and levels of interleukin‐6 remained high. Paxlovid was prescribed for 5 days subsequently though it was 14 days since symptom onset. Thereafter, the nucleic acid of the patient turned negative in 7 days and the symptoms resolved. This case showed that Paxlovid can be considered in patients with COVID‐19 and severe pneumonia even in the later course of infection in clinical practice in China.
Dong E, Ratcliff J, Goyea TD, Katz A, Lau R, Ng TK, et al. The Johns Hopkins University Center for Systems Science and Engineering COVID‐19 dashboard: data collection process, challenges faced, and lessons learned. Lancet Infect Dis. 2022;22(12): e370–6. https://doi.org/10.1016/s1473-3099(22)00434-0
Hammond J, Leister‐Tebbe H, Gardner A, Abreu P, Bao W, Wisemandle W, et al. Oral Nirmatrelvir for high‐risk, nonhospitalized adults with Covid‐19. N Engl J Med. 2022; 386(15): 1397–408. https://doi.org/10.1056/NEJMoa2118542
Chinese Thoracic Society, Chinese Association of Chest Physicians Critical Care Group. Expert consensus on treatment of severe COVID‐19 caused by Omicron variants. Chin J Tuberc Respir Dis. 2023;46(2):101–10. https://doi.org/10.3760/cma.j.cn112147-20221230-00994
Owen DR, Allerton CMN, Anderson AS, Aschenbrenner L, Avery M, Berritt S, et al. An oral SARS‐CoV‐2 M(pro) inhibitor clinical candidate for the treatment of COVID‐19. Science. 2021;374(6575):1586–93. https://doi.org/10.1126/science.abl4784
Stein SR, Ramelli SC, Grazioli A, Chung JY, Singh M, Yinda CK, et al. SARS‐CoV‐2 infection and persistence in the human body and brain at autopsy. Nature. 2022;612(7941):758–63. https://doi.org/10.1038/s41586-022-05542-y
Liu J, Pan X, Zhang S, Li M, Ma K, Fan C, et al. Efficacy and safety of Paxlovid in severe adult patients with SARS‐Cov‐2 infection: a multicenter randomized controlled study. Lancet Reg Health West Pac. 2023:100694. https://doi.org/10.1016/j.lanwpc.2023.100694
This study was funded by the Beijing Lisheng Cardiovascular Health Foundation (LHJJ20141751) and Guangdong Provincial Key Laboratory of Coronary Heart Disease Prevention (No. Y0120220151). The funders were not involved in study design, data collection, analysis, interpretation, or reporting.
This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.