Hyperbaric oxygen therapy to prevent central airway stenosis after lung transplantation

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. We per...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of heart and lung transplantation 2021-04, Vol.40 (4), p.269-278
Hauptverfasser: Kraft, Bryan D., Mahmood, Kamran, Harlan, Nicole P., Hartwig, Matthew G., Snyder, Laurie D., Suliman, Hagir B., Shofer, Scott L.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 278
container_issue 4
container_start_page 269
container_title The Journal of heart and lung transplantation
container_volume 40
creator Kraft, Bryan D.
Mahmood, Kamran
Harlan, Nicole P.
Hartwig, Matthew G.
Snyder, Laurie D.
Suliman, Hagir B.
Shofer, Scott L.
description 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. We performed a randomized, controlled trial comparing usual care with HBOT (2 atm absolute for 2 hours × 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. 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). 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.
doi_str_mv 10.1016/j.healun.2021.01.008
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8026673</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1053249821000206</els_id><sourcerecordid>2484240369</sourcerecordid><originalsourceid>FETCH-LOGICAL-c463t-c45a60b1d1f6df3852da232853424baf9f54b798b46f8268d8774e655292f57b3</originalsourceid><addsrcrecordid>eNp9UUuLGzEMNqWl-2j_QVl87CVZv8dzKSxL9wELvbT0aDwzcuIwsae2k3b-fb0k3celICSBpE-f9CH0iZIlJVRdbpZrsOMuLBlhdEmqEf0GnVIpmwWntHlbcyL5golWn6CznDeEEMYle49OOJdUC8lO0c-7eYLU2eR7HP_MKwi4rCHZacYl4inBHkLBfXXJjtj69NvOOBcIMfuMrSuQcCWxwrUe8jTaUGzxMXxA75wdM3w8xnP04-br9-u7xcO32_vrq4dFLxQv1UurSEcH6tTguJZssIwzLblgorOudVJ0Tas7oZxmSg-6aQQoKVnLnGw6fo6-HHCnXbeF4UjUTMlvbZpNtN68rgS_Nqu4N5owpRpeAT4fAVL8tYNczNbnHsZ6CcRdNkzoSoVw1dZWcWjtU8w5gXtaQ4l51MRszEET86iJIdWIrmMXLyk-Df0T4fkGqI_ae0gm9x5CD4NP0BczRP__DX8B4R6hqQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2484240369</pqid></control><display><type>article</type><title>Hyperbaric oxygen therapy to prevent central airway stenosis after lung transplantation</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Kraft, Bryan D. ; Mahmood, Kamran ; Harlan, Nicole P. ; Hartwig, Matthew G. ; Snyder, Laurie D. ; Suliman, Hagir B. ; Shofer, Scott L.</creator><creatorcontrib>Kraft, Bryan D. ; Mahmood, Kamran ; Harlan, Nicole P. ; Hartwig, Matthew G. ; Snyder, Laurie D. ; Suliman, Hagir B. ; Shofer, Scott L.</creatorcontrib><description>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. We performed a randomized, controlled trial comparing usual care with HBOT (2 atm absolute for 2 hours × 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. 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 &lt; 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 &lt; 0.05). Subjects who developed ACR had significant FLT1, TIE2, and KDR expression at 4 weeks (all p &lt; 0.05). 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.</description><identifier>ISSN: 1053-2498</identifier><identifier>EISSN: 1557-3117</identifier><identifier>DOI: 10.1016/j.healun.2021.01.008</identifier><identifier>PMID: 33518452</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Airway Obstruction - diagnosis ; Airway Obstruction - etiology ; Airway Obstruction - prevention &amp; control ; Biopsy - methods ; Bronchi - pathology ; Bronchoscopy ; cell hypoxia/genetics ; Female ; Follow-Up Studies ; gene expression ; Graft Rejection - complications ; Graft Rejection - diagnosis ; Humans ; hyperbaric oxygenation ; Hyperbaric Oxygenation - methods ; lung transplantation ; Lung Transplantation - adverse effects ; Male ; Middle Aged ; post-operative complications ; Postoperative Complications - diagnosis ; Postoperative Complications - etiology ; Postoperative Complications - prevention &amp; control ; Treatment Outcome ; Young Adult</subject><ispartof>The Journal of heart and lung transplantation, 2021-04, Vol.40 (4), p.269-278</ispartof><rights>2021</rights><rights>Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-c45a60b1d1f6df3852da232853424baf9f54b798b46f8268d8774e655292f57b3</citedby><cites>FETCH-LOGICAL-c463t-c45a60b1d1f6df3852da232853424baf9f54b798b46f8268d8774e655292f57b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1053249821000206$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33518452$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kraft, Bryan D.</creatorcontrib><creatorcontrib>Mahmood, Kamran</creatorcontrib><creatorcontrib>Harlan, Nicole P.</creatorcontrib><creatorcontrib>Hartwig, Matthew G.</creatorcontrib><creatorcontrib>Snyder, Laurie D.</creatorcontrib><creatorcontrib>Suliman, Hagir B.</creatorcontrib><creatorcontrib>Shofer, Scott L.</creatorcontrib><title>Hyperbaric oxygen therapy to prevent central airway stenosis after lung transplantation</title><title>The Journal of heart and lung transplantation</title><addtitle>J Heart Lung Transplant</addtitle><description>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. We performed a randomized, controlled trial comparing usual care with HBOT (2 atm absolute for 2 hours × 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. 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 &lt; 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 &lt; 0.05). Subjects who developed ACR had significant FLT1, TIE2, and KDR expression at 4 weeks (all p &lt; 0.05). 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.</description><subject>Adult</subject><subject>Aged</subject><subject>Airway Obstruction - diagnosis</subject><subject>Airway Obstruction - etiology</subject><subject>Airway Obstruction - prevention &amp; control</subject><subject>Biopsy - methods</subject><subject>Bronchi - pathology</subject><subject>Bronchoscopy</subject><subject>cell hypoxia/genetics</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>gene expression</subject><subject>Graft Rejection - complications</subject><subject>Graft Rejection - diagnosis</subject><subject>Humans</subject><subject>hyperbaric oxygenation</subject><subject>Hyperbaric Oxygenation - methods</subject><subject>lung transplantation</subject><subject>Lung Transplantation - adverse effects</subject><subject>Male</subject><subject>Middle Aged</subject><subject>post-operative complications</subject><subject>Postoperative Complications - diagnosis</subject><subject>Postoperative Complications - etiology</subject><subject>Postoperative Complications - prevention &amp; control</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>1053-2498</issn><issn>1557-3117</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UUuLGzEMNqWl-2j_QVl87CVZv8dzKSxL9wELvbT0aDwzcuIwsae2k3b-fb0k3celICSBpE-f9CH0iZIlJVRdbpZrsOMuLBlhdEmqEf0GnVIpmwWntHlbcyL5golWn6CznDeEEMYle49OOJdUC8lO0c-7eYLU2eR7HP_MKwi4rCHZacYl4inBHkLBfXXJjtj69NvOOBcIMfuMrSuQcCWxwrUe8jTaUGzxMXxA75wdM3w8xnP04-br9-u7xcO32_vrq4dFLxQv1UurSEcH6tTguJZssIwzLblgorOudVJ0Tas7oZxmSg-6aQQoKVnLnGw6fo6-HHCnXbeF4UjUTMlvbZpNtN68rgS_Nqu4N5owpRpeAT4fAVL8tYNczNbnHsZ6CcRdNkzoSoVw1dZWcWjtU8w5gXtaQ4l51MRszEET86iJIdWIrmMXLyk-Df0T4fkGqI_ae0gm9x5CD4NP0BczRP__DX8B4R6hqQ</recordid><startdate>20210401</startdate><enddate>20210401</enddate><creator>Kraft, Bryan D.</creator><creator>Mahmood, Kamran</creator><creator>Harlan, Nicole P.</creator><creator>Hartwig, Matthew G.</creator><creator>Snyder, Laurie D.</creator><creator>Suliman, Hagir B.</creator><creator>Shofer, Scott L.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20210401</creationdate><title>Hyperbaric oxygen therapy to prevent central airway stenosis after lung transplantation</title><author>Kraft, Bryan D. ; Mahmood, Kamran ; Harlan, Nicole P. ; Hartwig, Matthew G. ; Snyder, Laurie D. ; Suliman, Hagir B. ; Shofer, Scott L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-c45a60b1d1f6df3852da232853424baf9f54b798b46f8268d8774e655292f57b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Airway Obstruction - diagnosis</topic><topic>Airway Obstruction - etiology</topic><topic>Airway Obstruction - prevention &amp; control</topic><topic>Biopsy - methods</topic><topic>Bronchi - pathology</topic><topic>Bronchoscopy</topic><topic>cell hypoxia/genetics</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>gene expression</topic><topic>Graft Rejection - complications</topic><topic>Graft Rejection - diagnosis</topic><topic>Humans</topic><topic>hyperbaric oxygenation</topic><topic>Hyperbaric Oxygenation - methods</topic><topic>lung transplantation</topic><topic>Lung Transplantation - adverse effects</topic><topic>Male</topic><topic>Middle Aged</topic><topic>post-operative complications</topic><topic>Postoperative Complications - diagnosis</topic><topic>Postoperative Complications - etiology</topic><topic>Postoperative Complications - prevention &amp; control</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kraft, Bryan D.</creatorcontrib><creatorcontrib>Mahmood, Kamran</creatorcontrib><creatorcontrib>Harlan, Nicole P.</creatorcontrib><creatorcontrib>Hartwig, Matthew G.</creatorcontrib><creatorcontrib>Snyder, Laurie D.</creatorcontrib><creatorcontrib>Suliman, Hagir B.</creatorcontrib><creatorcontrib>Shofer, Scott L.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of heart and lung transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kraft, Bryan D.</au><au>Mahmood, Kamran</au><au>Harlan, Nicole P.</au><au>Hartwig, Matthew G.</au><au>Snyder, Laurie D.</au><au>Suliman, Hagir B.</au><au>Shofer, Scott L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hyperbaric oxygen therapy to prevent central airway stenosis after lung transplantation</atitle><jtitle>The Journal of heart and lung transplantation</jtitle><addtitle>J Heart Lung Transplant</addtitle><date>2021-04-01</date><risdate>2021</risdate><volume>40</volume><issue>4</issue><spage>269</spage><epage>278</epage><pages>269-278</pages><issn>1053-2498</issn><eissn>1557-3117</eissn><abstract>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. We performed a randomized, controlled trial comparing usual care with HBOT (2 atm absolute for 2 hours × 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. 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 &lt; 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 &lt; 0.05). Subjects who developed ACR had significant FLT1, TIE2, and KDR expression at 4 weeks (all p &lt; 0.05). 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.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>33518452</pmid><doi>10.1016/j.healun.2021.01.008</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1053-2498
ispartof The Journal of heart and lung transplantation, 2021-04, Vol.40 (4), p.269-278
issn 1053-2498
1557-3117
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8026673
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Adult
Aged
Airway Obstruction - diagnosis
Airway Obstruction - etiology
Airway Obstruction - prevention & control
Biopsy - methods
Bronchi - pathology
Bronchoscopy
cell hypoxia/genetics
Female
Follow-Up Studies
gene expression
Graft Rejection - complications
Graft Rejection - diagnosis
Humans
hyperbaric oxygenation
Hyperbaric Oxygenation - methods
lung transplantation
Lung Transplantation - adverse effects
Male
Middle Aged
post-operative complications
Postoperative Complications - diagnosis
Postoperative Complications - etiology
Postoperative Complications - prevention & control
Treatment Outcome
Young Adult
title Hyperbaric oxygen therapy to prevent central airway stenosis after lung transplantation
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-12T14%3A54%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Hyperbaric%20oxygen%20therapy%20to%20prevent%20central%20airway%20stenosis%20after%20lung%20transplantation&rft.jtitle=The%20Journal%20of%20heart%20and%20lung%20transplantation&rft.au=Kraft,%20Bryan%20D.&rft.date=2021-04-01&rft.volume=40&rft.issue=4&rft.spage=269&rft.epage=278&rft.pages=269-278&rft.issn=1053-2498&rft.eissn=1557-3117&rft_id=info:doi/10.1016/j.healun.2021.01.008&rft_dat=%3Cproquest_pubme%3E2484240369%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2484240369&rft_id=info:pmid/33518452&rft_els_id=S1053249821000206&rfr_iscdi=true