Lung transplant airway complications treated with biodegradable airway stents: The Dutch multi‐center experience

Author:

van Pel Roel123ORCID,Gan Tji1,Daniels Johannes M. A.4,Ruigrok Dieuwertje5,Hellemons Merel E.23,Klooster Karin1,Slebos Dirk‐Jan1

Affiliation:

1. Department of Pulmonary medicine University medical center Groningen Groningen The Netherlands

2. Department of Respiratory Medicine Erasmus University Medical Center Rotterdam Rotterdam The Netherlands

3. Erasmus MC Transplant Institute, Erasmus University Medical Center Rotterdam Rotterdam The Netherlands

4. Department of Pulmonary medicine Amsterdam university medical center Amsterdam The Netherlands

5. Department of Pulmonary medicine University medical center Utrecht Utrecht The Netherlands

Abstract

AbstractIntroductionTreatment of post lung‐transplant airway complications is challenging, and treatment with conventional airway stents is associated with adverse events. More recently, biodegradable airway stents (BDS) have been introduced and may be used to reduce these adverse events. In this study we explore the feasibility of treatment with BDS post lung transplant.MethodsAll patients treated with BDS in The Netherlands were included in this retrospective multicenter study. Feasibility, life span of the stent, occurrence of adverse events, and evolution of lung function were evaluated.ResultsTwelve patients (six malacia and six stenosis) received a total of 57 BDS, ranging from 1 to 10 BDS per patient. Six patients had been pretreated with conventional airway stents. Median stent life span was 112 days (range 66–202). No adverse events occurred during stent placement. In 5 out of 57 stent placements, a single additional bronchoscopy was necessary because of mucus accumulation (n = 4) or excessive granulation tissue (n = 1). All stent naïve patients became airway stent independent after treatment; all patients pretreated with conventional airway stents were still airway stent dependent at the end of follow up.ConclusionTreatment with BDS is safe and feasible. Adverse events were mild and easily treatable. All patients with initial treatment with BDS were airway stent independent at the end of follow up with a median treatment of 4 BDS.

Publisher

Wiley

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