Exercise-Induced Oxygen Desaturation and Outcomes After Nintedanib Therapy for Fibrosing Interstitial Lung Disease in Patients Without Dyspnea

<b>Background:</b> The degree of exercise-induced oxygen desaturation and outcomes following antifibrotic drug therapy in asymptomatic patients with fibrosing interstitial lung disease (FILD) remain unclear. <b>Methods:</b> We compared clinical data, incidence of annual FILD progression, overall survival, and tolerability after initiating nintedanib between 58 patients with dyspnea and 18 patients without. Annual FILD progression was defined as >10% decrease in forced vital capacity (FVC), >15% decrease in diffusing capacity of the lungs for carbon monoxide (D<sub>LCO</sub>), developing acute exacerbations, or FILD-related death within 1 year of starting nintedanib. Outcomes between the two groups were adjusted for covariates, including age, gender, FVC, D<sub>LCO</sub>, and diagnosis of idiopathic pulmonary fibrosis, all known prognostic factors for FILD. <b>Results:</b> In 6-min walk test, incidence of decrease to <90% of SpO<sub>2</sub> was significantly lower in non-dyspnea group than in dyspnea group (24% vs. 55%, <i>p</i> = 0.028), but incidence of >4% decreases showed no significant difference (71% vs. 89%, <i>p</i> = 0.11) The incidence of annual progression was significantly lower in non-dyspnea than in dyspnea group (17% vs. 53%, adjusted <i>p</i> = 0.026). The relative change in D<sub>LCO</sub> was significantly slower in non-dyspnea group (adjusted <i>p</i> = 0.036), but FVC was not (adjusted <i>p</i> = 0.067). Overall survival was longer in non-dyspnea group (adjusted <i>p</i> = 0.0089). The discontinuation rate and therapeutic period of nintedanib were not significantly different between the groups. <b>Conclusions:</b> Asymptomatic patients with FILD have severe exercise-induced oxygen desaturation and better outcomes after nintedanib therapy than symptomatic patients. Antifibrotic drug therapy should not be avoided solely because of a lack of symptoms.

Authors

Institutions

Publication Details

Journal
Journal of Clinical Medicine
Published
2024-12-23
DOI
https://doi.org/10.3390/jcm13247865
Citations
1
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
0.42
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Exercise-Induced Oxygen Desaturation and Outcomes After Nintedanib Therapy for Fibrosing Interstitial Lung Disease in Patients Without Dyspnea

Yoshiaki Zaizen, Toyoshi Yanagihara, Takashi Nouno, Tomonori Chikasue et al.
1 citations
Journal of Clinical Medicine
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
0.42
article

Exercise-Induced Oxygen Desaturation and Outcomes After Nintedanib Therapy for Fibrosing Interstitial Lung Disease in Patients Without Dyspnea

Yoshiaki Zaizen, Toyoshi Yanagihara, Takashi Nouno, Tomonori Chikasue, Kiminori Fujimoto, Tomoaki Hoshino, Kazuhiro Tabata, Masaki Tominaga, Akiko Sumi, Shuji Matsuura, Yuuya Nishii, Masaki Okamoto, Atsushi Kawaguchi, Norikazu Matsuo
article en
1 citations

Abstract

<b>Background:</b> The degree of exercise-induced oxygen desaturation and outcomes following antifibrotic drug therapy in asymptomatic patients with fibrosing interstitial lung disease (FILD) remain unclear. <b>Methods:</b> We compared clinical data, incidence of annual FILD progression, overall survival, and tolerability after initiating nintedanib between 58 patients with dyspnea and 18 patients without. Annual FILD progression was defined as >10% decrease in forced vital capacity (FVC), >15% decrease in diffusing capacity of the lungs for carbon monoxide (D<sub>LCO</sub>), developing acute exacerbations, or FILD-related death within 1 year of starting nintedanib. Outcomes between the two groups were adjusted for covariates, including age, gender, FVC, D<sub>LCO</sub>, and diagnosis of idiopathic pulmonary fibrosis, all known prognostic factors for FILD. <b>Results:</b> In 6-min walk test, incidence of decrease to <90% of SpO<sub>2</sub> was significantly lower in non-dyspnea group than in dyspnea group (24% vs. 55%, <i>p</i> = 0.028), but incidence of >4% decreases showed no significant difference (71% vs. 89%, <i>p</i> = 0.11) The incidence of annual progression was significantly lower in non-dyspnea than in dyspnea group (17% vs. 53%, adjusted <i>p</i> = 0.026). The relative change in D<sub>LCO</sub> was significantly slower in non-dyspnea group (adjusted <i>p</i> = 0.036), but FVC was not (adjusted <i>p</i> = 0.067). Overall survival was longer in non-dyspnea group (adjusted <i>p</i> = 0.0089). The discontinuation rate and therapeutic period of nintedanib were not significantly different between the groups. <b>Conclusions:</b> Asymptomatic patients with FILD have severe exercise-induced oxygen desaturation and better outcomes after nintedanib therapy than symptomatic patients. Antifibrotic drug therapy should not be avoided solely because of a lack of symptoms.

Journal of Clinical MedicineVol. 13(24)
Kurume University (JP), Kagoshima University (JP), National Kyushu Medical Center (JP), Fukuoka University Hospital (JP)
Good health and well-being
Openalex Percentile: Top 29%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
0.42
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.