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Patient Selection for Bronchoscopic Lung Volume Reduction

Authors Welling JBA, Hartman JE, Augustijn SWS, Kerstjens HAM, Vanfleteren LEGW, Klooster K, Slebos DJ

Received 2 December 2019

Accepted for publication 10 March 2020

Published 23 April 2020 Volume 2020:15 Pages 871—881

DOI https://doi.org/10.2147/COPD.S240848

Checked for plagiarism Yes

Review by Single-blind

Peer reviewer comments 3

Editor who approved publication: Dr Richard Russell


Jorrit BA Welling, 1, 2 Jorine E Hartman, 1, 2 Sonja WS Augustijn, 1 Huib AM Kerstjens, 1, 2 Lowie EGW Vanfleteren, 3 Karin Klooster, 1, 2 Dirk-Jan Slebos 1, 2

1University of Groningen, University Medical Center Groningen, Department of Pulmonary Diseases, Groningen, the Netherlands; 2Groningen Research Institute for Asthma and COPD, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands; 3COPD Center, Sahlgrenska University Medical Hospital and Institute of Medicine, Gothenburg University, Gothenburg, Sweden

Correspondence: Jorrit BA Welling
Department of Pulmonary Diseases, University Medical Center Groningen, Groningen, the Netherlands
Email j.b.a.welling@umcg.nl

Purpose: Bronchoscopic lung volume reduction (BLVR) is a valuable treatment option for carefully selected patients with severe COPD. There is limited knowledge about the characteristics and outcomes of patients referred to a specialized center for BLVR. The study objectives were to investigate the selection rate for BLVR treatment in patients referred for this treatment and to investigate the differences between patients that were selected for BLVR and patients that were not.
Patients and Methods: We performed a retrospective analysis of patients with severe COPD who were referred to our hospital to assess eligibility for BLVR treatment. Our parameters included demographics, comorbidity, chest computed tomography characteristics, reasons for rejection from BLVR treatment and patient survival.
Results: In total, 1500 patients were included (mean age 62 years, 50% female and forced expiratory volume in 1 s 33% of predicted). Out of this group, 282 (19%) patients were selected for BLVR treatment. The absence of a suitable target lobe for treatment, an unsuitable disease phenotype and insufficient lung hyperinflation were the most important factors for not being selected. Patients that were selected for any BLVR option lived significantly longer than the group of patients that were not selected for BLVR (median 3060 versus 2079 days, P< 0.001).
Conclusion: We found that only a small proportion of patients that are referred for BLVR treatment is eligible for a BLVR treatment, indicating a need for both better referral tools and for the development of new therapies for this group of patients. Furthermore, our data suggest that selection for BLVR is associated with a significant survival benefit.

Keywords: bronchoscopic lung volume reduction, patient selection, endobronchial valves, lung volume reduction coils

Corrigendum for this paper has been published

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