4.5 Article

Hyperbaric oxygen therapy to prevent central airway stenosis after lung transplantation

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JOURNAL OF HEART AND LUNG TRANSPLANTATION
卷 40, 期 4, 页码 269-278

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.healun.2021.01.008

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lung transplantation; hyperbaric oxygenation; cell hypoxia/genetics; gene expression; post-operative complications

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A study comparing hyperbaric oxygen therapy (HBOT) and usual care in patients with extensive airway necrosis after lung transplantation found that HBOT did not reduce the incidence of central airway stenosis (CAS). However, elevated expression of HIF genes in donor tissues and increased levels of HMOX1 and VEGFA were associated with the development of CAS or the need for stenting.
BACKGROUND: Central airway stenosis (CAS) is a severe airway complication after lung transplantation associated with bronchial ischemia and necrosis. We sought to determine whether hyperbaric oxygen therapy (HBOT), an established treatment for tissue ischemia, attenuates post-transplant bronchial injury. METHODS: We performed a randomized, controlled trial comparing usual care with HBOT (2 atm absolute for 2 hours x 20 sessions) in subjects with extensive airway necrosis 4 weeks after transplantation. Endobronchial biopsies were collected at 4, 7, and 10 weeks after transplantation for a quantitative polymerase chain reaction. Coprimary outcomes were incidence of airway stenting and acute cellular rejection (ACR) at 1 year. RESULTS: The trial was stopped after enrolling 20 subjects (n = 10 per group) after a pre-planned interim analysis showed no difference between usual care and HBOT groups in stenting (both 40%), ACR (70% and 40%, respectively), or CAS (40% and 60%, respectively). Time to first stent placement (median [interquartile range]) was significantly shorter in the HBOT group (150 [73-150] vs 186 [167-206] days, p < 0.05). HIF gene expression was significantly increased in donor tissues at 4, 7, and 10 weeks after transplantation but was not altered by HBOT. Subjects who developed CAS or required stenting had significantly higher HMOX1 and VEGFA expression at 4 weeks (both p < 0.05). Subjects who developed ACR had significant FLT1, TIE2, and KDR expression at 4 weeks (all p < 0.05). CONCLUSIONS: Incidence of CAS is high after severe, established airway necrosis after transplantation. HBOT does not reduce CAS severity or stenting. Elevated HMOX1 and VEGFA expressions appear to associate with airway complications. (C) Published by Elsevier Inc.

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