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新冠病毒肺炎与特发性肺纤维化:一种新的组合。

COVID-19 Pneumonia and Idiopathic Pulmonary Fibrosis: A Novel Combination.

作者信息

Uzel Fatma Işıl, İliaz Sinem, Karataş Ferhan, Çağlayan Benan

机构信息

Department of Pulmonology, Koç University Hospital, İstanbul, Turkey.

出版信息

Turk Thorac J. 2020 Nov;21(6):451-453. doi: 10.5152/TurkThoracJ.2020.20123. Epub 2020 Nov 1.

DOI:10.5152/TurkThoracJ.2020.20123
PMID:33352102
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7752110/
Abstract

Coronavirus disease 2019 (COVID-19) has become a game changer in many aspects of clinical practice. Acute exacerbations of idiopathic pulmonary fibrosis (IPF) are known as serious events, which can reach a mortality rate of 50%, where viral infections may play a role. We describe the case of a 64-year-old male patient with a diagnosis of IPF under antifibrotic treatment for 1 year; the patient tested positive for COVID-19 with polymerase chain reaction test of the nasopharyngeal swab, and his chest computed tomography results were compatible with COVID-19 pneumonia described in the literature as well as the findings compatible with interstitial lung disease. The patient was successfully treated in the pulmonology ward according to official guidelines about COVID-19 along with antifibrotic treatment and required only a short course of oxygen therapy. We experienced no drug interactions, serious side effects, or complications during treatment. The patient was discharged after 1 week, and he is still in a good condition after 3 weeks. COVID-19 pneumonia in a patient with IPF who survived under antifibrotic treatment without serious deterioration is a new experience. Such cases will probably change our perspective in treating patients with IPF.

摘要

2019冠状病毒病(COVID-19)已成为临床实践诸多方面的变革因素。特发性肺纤维化(IPF)急性加重是严重事件,死亡率可达50%,病毒感染可能在其中起作用。我们描述了一例64岁男性患者,诊断为IPF,接受抗纤维化治疗1年;该患者鼻咽拭子聚合酶链反应检测COVID-19呈阳性,其胸部计算机断层扫描结果与文献中描述的COVID-19肺炎相符,也与间质性肺疾病的表现相符。根据关于COVID-19的官方指南,该患者在呼吸内科病房接受了成功治疗,同时进行了抗纤维化治疗,仅需短期吸氧治疗。治疗期间未出现药物相互作用、严重副作用或并发症。患者1周后出院,3周后仍状况良好。在接受抗纤维化治疗且未出现严重病情恶化的情况下存活的IPF患者发生COVID-19肺炎是一种新情况。此类病例可能会改变我们治疗IPF患者的观点。

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本文引用的文献

1
A Fatal Case of Coronavirus Disease 2019 (COVID-19) in a Patient With Idiopathic Pulmonary Fibrosis.一例特发性肺纤维化患者的新型冠状病毒肺炎(COVID-19)致死病例
Cureus. 2020 Jun 3;12(6):e8432. doi: 10.7759/cureus.8432.
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Radiology Perspective of Coronavirus Disease 2019 (COVID-19): Lessons From Severe Acute Respiratory Syndrome and Middle East Respiratory Syndrome.2019 年冠状病毒病(COVID-19)的放射学视角:严重急性呼吸综合征和中东呼吸综合征的教训。
AJR Am J Roentgenol. 2020 May;214(5):1078-1082. doi: 10.2214/AJR.20.22969. Epub 2020 Feb 28.
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Idiopathic Pulmonary Fibrosis: Best Practice in Monitoring and Managing a Relentless Fibrotic Disease.特发性肺纤维化:监测和管理无情纤维化疾病的最佳实践。
Respiration. 2020;99(1):73-82. doi: 10.1159/000504763. Epub 2019 Dec 12.
4
Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline.特发性肺纤维化诊断。美国胸科学会/欧洲呼吸学会/日本呼吸学会/拉丁美洲胸科学会临床实践指南。
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