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The interstitial lung disease spectrum under a uniform diagnostic algorithm: a retrospective study of 1,945 individuals

BACKGROUND: Reported data on the disease spectrum of interstitial lung diseases (ILDs) of China are sparse and varied. We aimed to investigate the spectrum of ILDs and the distribution of diagnostic methods under a uniform diagnosis. METHODS: This retrospective study enrolled ILDs cases from Guangzh...

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Autores principales: Guo, Bingpeng, Wang, Lulin, Xia, Shu, Mao, Mengmeng, Qian, Weiping, Peng, Xiaomin, Zheng, Zexuan, Chen, Rongchang, Han, Qian, Luo, Qun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399396/
https://www.ncbi.nlm.nih.gov/pubmed/32802448
http://dx.doi.org/10.21037/jtd-19-4021
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author Guo, Bingpeng
Wang, Lulin
Xia, Shu
Mao, Mengmeng
Qian, Weiping
Peng, Xiaomin
Zheng, Zexuan
Chen, Rongchang
Han, Qian
Luo, Qun
author_facet Guo, Bingpeng
Wang, Lulin
Xia, Shu
Mao, Mengmeng
Qian, Weiping
Peng, Xiaomin
Zheng, Zexuan
Chen, Rongchang
Han, Qian
Luo, Qun
author_sort Guo, Bingpeng
collection PubMed
description BACKGROUND: Reported data on the disease spectrum of interstitial lung diseases (ILDs) of China are sparse and varied. We aimed to investigate the spectrum of ILDs and the distribution of diagnostic methods under a uniform diagnosis. METHODS: This retrospective study enrolled ILDs cases from Guangzhou Institute of Respiratory Health (GIRH). All cases were classified into specific subgroups of ILDs according to updated guidelines. RESULTS: A total of 1,945 subjects were enrolled from January 2012 to December 2017. The mean age was 57.9 years, and 1,080 (55.5%) patients were male. The most common subtype of ILDs was idiopathic pulmonary fibrosis (IPF, 20.3%), followed by interstitial pneumonia with autoimmune features (IPAF, 17.9%), connective tissue disease associated ILD (CTD-ILD, 18.3%) and unclassifiable idiopathic interstitial pneumonia (UIIP, 14.7%). A total of 818 (42.1%) patients underwent lung biopsy in order to obtain a histological diagnose. TBLB was performed in 565 (29.0%) patients, eleven of whom underwent SLB because TBLB failed to obtain lung samples. SLB was performed in 213 (11.0%) patients and TBCB was performed in 51 (2.6%) patients. Among them, histological results were considered clinically helpful in 722 (88.3%) cases, and provided definitive histopathological diagnoses in 368 cases. Surgical lung biopsy (SLB) was performed in 213 (10.9%) subjects, while 115 (54.0%) cases were performed among the idiopathic interstitial pneumonia (IIP). Among SLB cases in IIP, the highest rate of SLB was desquamative interstitial pneumonia/respiratory bronchiolitis-interstitial lung disease (DIP/RB-ILD, 10/10), lymphoid interstitial pneumonia (LIP, 9/9), followed by cryptogenic organizing (COP, 18/26), nonspecific interstitial pneumonia (NSIP, 22/53), IPF (43/395), UIIP (13/285). CONCLUSIONS: IPF was the most common ILDs in our ILD center, followed by IPAF, CTD-ILD and UIIP. Histological information may help to establish diagnostic algorithm in ILD.
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spelling pubmed-73993962020-08-13 The interstitial lung disease spectrum under a uniform diagnostic algorithm: a retrospective study of 1,945 individuals Guo, Bingpeng Wang, Lulin Xia, Shu Mao, Mengmeng Qian, Weiping Peng, Xiaomin Zheng, Zexuan Chen, Rongchang Han, Qian Luo, Qun J Thorac Dis Original Article BACKGROUND: Reported data on the disease spectrum of interstitial lung diseases (ILDs) of China are sparse and varied. We aimed to investigate the spectrum of ILDs and the distribution of diagnostic methods under a uniform diagnosis. METHODS: This retrospective study enrolled ILDs cases from Guangzhou Institute of Respiratory Health (GIRH). All cases were classified into specific subgroups of ILDs according to updated guidelines. RESULTS: A total of 1,945 subjects were enrolled from January 2012 to December 2017. The mean age was 57.9 years, and 1,080 (55.5%) patients were male. The most common subtype of ILDs was idiopathic pulmonary fibrosis (IPF, 20.3%), followed by interstitial pneumonia with autoimmune features (IPAF, 17.9%), connective tissue disease associated ILD (CTD-ILD, 18.3%) and unclassifiable idiopathic interstitial pneumonia (UIIP, 14.7%). A total of 818 (42.1%) patients underwent lung biopsy in order to obtain a histological diagnose. TBLB was performed in 565 (29.0%) patients, eleven of whom underwent SLB because TBLB failed to obtain lung samples. SLB was performed in 213 (11.0%) patients and TBCB was performed in 51 (2.6%) patients. Among them, histological results were considered clinically helpful in 722 (88.3%) cases, and provided definitive histopathological diagnoses in 368 cases. Surgical lung biopsy (SLB) was performed in 213 (10.9%) subjects, while 115 (54.0%) cases were performed among the idiopathic interstitial pneumonia (IIP). Among SLB cases in IIP, the highest rate of SLB was desquamative interstitial pneumonia/respiratory bronchiolitis-interstitial lung disease (DIP/RB-ILD, 10/10), lymphoid interstitial pneumonia (LIP, 9/9), followed by cryptogenic organizing (COP, 18/26), nonspecific interstitial pneumonia (NSIP, 22/53), IPF (43/395), UIIP (13/285). CONCLUSIONS: IPF was the most common ILDs in our ILD center, followed by IPAF, CTD-ILD and UIIP. Histological information may help to establish diagnostic algorithm in ILD. AME Publishing Company 2020-07 /pmc/articles/PMC7399396/ /pubmed/32802448 http://dx.doi.org/10.21037/jtd-19-4021 Text en 2020 Journal of Thoracic Disease. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Guo, Bingpeng
Wang, Lulin
Xia, Shu
Mao, Mengmeng
Qian, Weiping
Peng, Xiaomin
Zheng, Zexuan
Chen, Rongchang
Han, Qian
Luo, Qun
The interstitial lung disease spectrum under a uniform diagnostic algorithm: a retrospective study of 1,945 individuals
title The interstitial lung disease spectrum under a uniform diagnostic algorithm: a retrospective study of 1,945 individuals
title_full The interstitial lung disease spectrum under a uniform diagnostic algorithm: a retrospective study of 1,945 individuals
title_fullStr The interstitial lung disease spectrum under a uniform diagnostic algorithm: a retrospective study of 1,945 individuals
title_full_unstemmed The interstitial lung disease spectrum under a uniform diagnostic algorithm: a retrospective study of 1,945 individuals
title_short The interstitial lung disease spectrum under a uniform diagnostic algorithm: a retrospective study of 1,945 individuals
title_sort interstitial lung disease spectrum under a uniform diagnostic algorithm: a retrospective study of 1,945 individuals
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399396/
https://www.ncbi.nlm.nih.gov/pubmed/32802448
http://dx.doi.org/10.21037/jtd-19-4021
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