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本文引用的文献

1
Efficacy and safety of nintedanib for pulmonary fibrosis in severe pneumonia induced by COVID-19: An interventional study.尼达尼布治疗 COVID-19 重症肺炎所致肺纤维化的疗效和安全性:一项干预性研究。
Int J Infect Dis. 2021 Jul;108:454-460. doi: 10.1016/j.ijid.2021.05.055. Epub 2021 May 25.
2
Role of pirfenidone in TGF-β pathways and other inflammatory pathways in acute respiratory syndrome coronavirus 2 (SARS-Cov-2) infection: a theoretical perspective.吡非尼酮在转化生长因子-β(TGF-β)途径和急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染其他炎症途径中的作用:理论观点。
Pharmacol Rep. 2021 Jun;73(3):712-727. doi: 10.1007/s43440-021-00255-x. Epub 2021 Apr 21.
3
Post-COVID lung fibrosis: The tsunami that will follow the earthquake.新冠后肺纤维化:地震之后的海啸。
Lung India. 2021 Mar;38(Supplement):S41-S47. doi: 10.4103/lungindia.lungindia_818_20.
4
Post COVID-19 fibrosis, an emerging complicationof SARS-CoV-2 infection.新冠后纤维化,一种新型冠状病毒感染后出现的并发症。
IDCases. 2020 Dec 31;23:e01041. doi: 10.1016/j.idcr.2020.e01041. eCollection 2021.
5
Pulmonary function and radiological features 4 months after COVID-19: first results from the national prospective observational Swiss COVID-19 lung study.新冠病毒病感染4个月后的肺功能和放射学特征:瑞士全国前瞻性观察性新冠病毒病肺部研究的初步结果
Eur Respir J. 2021 Apr 29;57(4). doi: 10.1183/13993003.03690-2020. Print 2021 Apr.
6
Converging pathways in pulmonary fibrosis and Covid-19 - The fibrotic link to disease severity.肺纤维化与新冠疫情中的汇聚通路——纤维化与疾病严重程度的关联。
Respir Med X. 2020 Nov;2:100023. doi: 10.1016/j.yrmex.2020.100023. Epub 2020 Oct 9.
7
Antifibrotics in COVID-19 Lung Disease: Let Us Stay Focused.新冠肺病中的抗纤维化药物:让我们专注于此。
Front Med (Lausanne). 2020 Sep 9;7:539. doi: 10.3389/fmed.2020.00539. eCollection 2020.
8
Pulmonary fibrosis in critical ill patients recovered from COVID-19 pneumonia: Preliminary experience.COVID-19 肺炎治愈后危重症患者的肺纤维化:初步经验。
Am J Emerg Med. 2020 Oct;38(10):2134-2138. doi: 10.1016/j.ajem.2020.05.120. Epub 2020 Jul 19.
9
The potential indicators for pulmonary fibrosis in survivors of severe COVID-19.重症 COVID-19 幸存者中肺纤维化的潜在指标。
J Infect. 2021 Feb;82(2):e5-e7. doi: 10.1016/j.jinf.2020.09.027. Epub 2020 Sep 28.
10
Pulmonary fibrosis in the aftermath of the COVID-19 era (Review).新冠疫情时代后的肺纤维化(综述)
Exp Ther Med. 2020 Sep;20(3):2557-2560. doi: 10.3892/etm.2020.8980. Epub 2020 Jul 9.

人工智能支持下的胸部计算机断层扫描指导下 COVID-19 肺炎中吡非尼酮和皮质类固醇治疗的比较。

Comparison of pirfenidone and corticosteroid treatments at the COVID-19 pneumonia with the guide of artificial intelligence supported thoracic computed tomography.

机构信息

Department of Pulmonary Diseases, Karabuk University, Karabuk Training and Research Hospital, Karabuk, Turkey.

Department of Chest Diseases, Duzce University Faculty of Medicine, Duzce, Turkey.

出版信息

Int J Clin Pract. 2021 Dec;75(12):e14961. doi: 10.1111/ijcp.14961. Epub 2021 Oct 17.

DOI:10.1111/ijcp.14961
PMID:34624155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8646554/
Abstract

AIM

We aimed to investigate the effect of short-term pirfenidone treatment on prolonged COVID-19 pneumonia.

METHOD

Hospital files of patients hospitalised with a diagnosis of critical COVID-19 pneumonia from November 2020 to March 2021 were retrospectively reviewed. Chest computed tomography images taken both before treatment and 2 months after treatment, demographic characteristics and laboratory parameters of patients receiving pirfenidone + methylprednisolone (n = 13) and only methylprednisolones (n = 9) were recorded. Pulmonary function tests were performed after the second month of the treatment. CT involvement rates were determined by machine learning.

RESULTS

A total of 22 patients, 13 of whom (59.1%) were using methylprednisolone + pirfenidone and 9 of whom (40.9%) were using only methylprednisolone were included. When the blood gas parameters and pulmonary function tests of the patients were compared at the end of the second month, it was found that the FEV1, FEV1%, FVC and FVC% values were statistically significantly higher in the methylprednisolone + pirfenidone group compared with the methylprednisolone group (P = .025, P = .012, P = .026 and P = .017, respectively). When the rates of change in CT scans at diagnosis and second month of treatment were examined, it was found that the involvement rates in the methylprednisolone + pirfenidone group were statistically significantly decreased (P < .001).

CONCLUSION

Antifibrotic agents can reduce fibrosis that may develop in the future. These can also help dose reduction and/or non-use strategy for methylprednisolone therapy, which has many side effects. Further large series and randomised controlled studies are needed on this subject.

摘要

目的

我们旨在研究短期吡非尼酮治疗对新冠长期肺炎的影响。

方法

回顾性分析 2020 年 11 月至 2021 年 3 月因危重症 COVID-19 肺炎住院的患者的住院病历。记录接受吡非尼酮+甲泼尼龙(n=13)和仅接受甲泼尼龙(n=9)治疗的患者的治疗前和治疗后 2 个月的胸部计算机断层扫描(CT)图像、人口统计学特征和实验室参数。治疗后第 2 个月进行肺功能检查。通过机器学习确定 CT 受累率。

结果

共纳入 22 例患者,其中 13 例(59.1%)接受甲泼尼龙+吡非尼酮治疗,9 例(40.9%)仅接受甲泼尼龙治疗。在第 2 个月结束时比较患者的血气参数和肺功能检查结果时,发现与仅接受甲泼尼龙组相比,甲泼尼龙+吡非尼酮组的 FEV1、FEV1%、FVC 和 FVC% 值显著更高(P=0.025、P=0.012、P=0.026 和 P=0.017)。检查诊断时和治疗后第 2 个月的 CT 扫描变化率时,发现甲泼尼龙+吡非尼酮组的受累率显著降低(P<0.001)。

结论

抗纤维化药物可减少可能发生的未来纤维化。这也有助于减少甲基强的松龙治疗的剂量和/或不使用该药物,因为它有许多副作用。需要进一步进行该主题的大型系列和随机对照研究。