Pulmonary rehabilitation for adults with chronic respiratory disease: an official American Thoracic Society clinical practice guideline

CL Rochester, JA Alison, B Carlin… - American journal of …, 2023 - atsjournals.org
Background: Despite the known benefits of pulmonary rehabilitation (PR) for patients with
chronic respiratory disease, this treatment is underused. Evidence-based guidelines should …

Interstitial lung fibrosis imaging reporting and data system: what radiologist wants to know?

AAKA Razek, MK El Badrawy… - Journal of Computer …, 2020 - journals.lww.com
The aim of this work is to review interstitial lung fibrosis Imaging Reporting and Data System
(ILF-RADS) that was designed for reporting of interstitial lung fibrosis (ILF). Findings include …

Guidelines of the polish respiratory society on the diagnosis and treatment of progressive fibrosing interstitial lung diseases other than idiopathic pulmonary fibrosis

WJ Piotrowski, MM Martusewicz-Boros… - … in Respiratory Medicine, 2022 - mdpi.com
Highlights The working group of the Polish Respiratory Society (PTChP) developed
guidelines for diagnosis and treatment of PF-ILD. What are the main findings? A …

Serial measurements of circulating KL-6, SP-D, MMP-7, CA19-9, CA-125, CCL18, and periostin in patients with idiopathic pulmonary fibrosis receiving antifibrotic …

S Majewski, K Szewczyk, A Żal, AJ Białas… - Journal of Clinical …, 2021 - mdpi.com
Idiopathic pulmonary fibrosis (IPF) is a progressive and inevitably fatal disease with a
heterogeneous clinical course. This study aimed to evaluate the usefulness of circulating …

IPF Respiratory Symptoms Management—Current Evidence

P Janowiak, A Szymanowska-Narloch… - Frontiers in …, 2022 - frontiersin.org
Idiopathic pulmonary fibrosis (IPF) is a progressive, chronic disease of the lungs which is
characterized by heavy symptom burden, especially in the last year of life. Despite recently …

Bronchoalveolar lavage cell count and lymphocytosis are the important discriminators between fibrotic hypersensitivity pneumonitis and idiopathic pulmonary fibrosis

M Sobiecka, M Szturmowicz, KB Lewandowska… - Diagnostics, 2023 - mdpi.com
Background: Fibrotic hypersensitivity pneumonitis (fHP) shares many features with other
fibrotic interstitial lung diseases (ILD), and as a result it can be misdiagnosed as idiopathic …

[PDF][PDF] T 细胞亚群在肺纤维化过程中的研究进展

千孟丹, 马宁怡, 王炎, 李亚 - 中国医药导报, 2023 - yiyaodaobao.com.cn
肺纤维化是1 种以肺组织结构改变为主要特征的慢性间质性疾病, 特发性肺纤维化是其中最为
严重的1 种, 特发性肺纤维化病因不明, 发病机制复杂, 以T 淋巴细胞为主导的免疫炎症在肺纤维 …

[HTML][HTML] Critical appraisal of the quality of clinical practice guidelines for idiopathic pulmonary fibrosis

X Li, X Yu, Y Xie, Z Feng, Y Ma, Y Chen… - Annals of Translational …, 2020 - ncbi.nlm.nih.gov
Background Clinical practice guidelines (CPGs) have long served as an essential tool for
clinicians to rationalize their treatment in practice. However, the quality of guidelines varies …

Clinical evidence for improving exercise tolerance and quality of life with pulmonary rehabilitation in patients with idiopathic pulmonary fibrosis: A systematic review …

S Lei, X Li, Y Xie, J Li - Clinical Rehabilitation, 2022 - journals.sagepub.com
Objective To evaluate the efficacy and safety of pulmonary rehabilitation for exercise
tolerance and quality of life improvement in idiopathic pulmonary fibrosis. Methods We …

[HTML][HTML] Therapeutic utility of human umbilical cord-derived mesenchymal stem cells-based approaches in pulmonary diseases: Recent advancements and prospects

M Meng, WW Zhang, SF Chen, DR Wang… - World Journal of Stem …, 2024 - ncbi.nlm.nih.gov
Pulmonary diseases across all ages threaten millions of people and have emerged as one
of the major public health issues worldwide. For diverse disease conditions, the currently …