Primary graft dysfunction grade 3 following pediatric lung transplantation is associated with chronic lung allograft dysfunction
Severe primary graft dysfunction (PGD) is associated with the development of bronchiolitis obliterans syndrome (BOS), the most common form of chronic lung allograft dysfunction (CLAD), in adults. However, PGD associations with long-term outcomes following pediatric lung transplantation are unknown....
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Veröffentlicht in: | The Journal of heart and lung transplantation 2023-05, Vol.42 (5), p.669-678 |
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creator | Wong, Wai Johnson, Brandy Cheng, Pi Chun Josephson, Maureen B. Maeda, Katsuhide Berg, Robert A. Kawut, Steven M. Harhay, Michael O. Goldfarb, Samuel B. Yehya, Nadir Himebauch, Adam S. |
description | Severe primary graft dysfunction (PGD) is associated with the development of bronchiolitis obliterans syndrome (BOS), the most common form of chronic lung allograft dysfunction (CLAD), in adults. However, PGD associations with long-term outcomes following pediatric lung transplantation are unknown. We hypothesized that PGD grade 3 (PGD 3) at 48- or 72-hours would be associated with shorter CLAD-free survival following pediatric lung transplantation.
This was a single center retrospective cohort study of patients ≤ 21 years of age who underwent bilateral lung transplantation between 2005 and 2019 with ≥ 1 year of follow-up. PGD and CLAD were defined by published criteria. We evaluated the association of PGD 3 at 48- or 72-hours with CLAD-free survival by using time-to-event analyses.
Fifty-one patients were included (median age 12.7 years; 51% female). The most common transplant indications were cystic fibrosis (29%) and pulmonary hypertension (20%). Seventeen patients (33%) had PGD 3 at either 48- or 72-hours. In unadjusted analysis, PGD 3 was associated with an increased risk of CLAD or mortality (HR 2.10, 95% CI 1.01-4.37, p=0.047). This association remained when adjusting individually for multiple potential confounders. There was evidence of effect modification by sex (interaction p = 0.055) with the association of PGD 3 and shorter CLAD-free survival driven predominantly by males (HR 4.73, 95% CI 1.44-15.6) rather than females (HR 1.23, 95% CI 0.47-3.20).
PGD 3 at 48- or 72-hours following pediatric lung transplantation was associated with shorter CLAD-free survival. Sex may be a modifier of this association. |
doi_str_mv | 10.1016/j.healun.2022.12.014 |
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This was a single center retrospective cohort study of patients ≤ 21 years of age who underwent bilateral lung transplantation between 2005 and 2019 with ≥ 1 year of follow-up. PGD and CLAD were defined by published criteria. We evaluated the association of PGD 3 at 48- or 72-hours with CLAD-free survival by using time-to-event analyses.
Fifty-one patients were included (median age 12.7 years; 51% female). The most common transplant indications were cystic fibrosis (29%) and pulmonary hypertension (20%). Seventeen patients (33%) had PGD 3 at either 48- or 72-hours. In unadjusted analysis, PGD 3 was associated with an increased risk of CLAD or mortality (HR 2.10, 95% CI 1.01-4.37, p=0.047). This association remained when adjusting individually for multiple potential confounders. There was evidence of effect modification by sex (interaction p = 0.055) with the association of PGD 3 and shorter CLAD-free survival driven predominantly by males (HR 4.73, 95% CI 1.44-15.6) rather than females (HR 1.23, 95% CI 0.47-3.20).
PGD 3 at 48- or 72-hours following pediatric lung transplantation was associated with shorter CLAD-free survival. Sex may be a modifier of this association.</description><identifier>ISSN: 1053-2498</identifier><identifier>ISSN: 1557-3117</identifier><identifier>EISSN: 1557-3117</identifier><identifier>DOI: 10.1016/j.healun.2022.12.014</identifier><identifier>PMID: 36639317</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Allografts ; Bronchiolitis Obliterans - etiology ; Bronchiolitis Obliterans - surgery ; bronchiolitis obliterans syndrome ; Child ; chronic lung allograft dysfunction ; Female ; Humans ; Lung ; Lung Transplantation - adverse effects ; Male ; pediatric ; primary graft dysfunction ; Primary Graft Dysfunction - epidemiology ; Primary Graft Dysfunction - etiology ; rejection ; Retrospective Studies ; transplant</subject><ispartof>The Journal of heart and lung transplantation, 2023-05, Vol.42 (5), p.669-678</ispartof><rights>2022 International Society for Heart and Lung Transplantation</rights><rights>Copyright © 2022 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-d354a3d1c136fb2ca06a957f5432258dcc57567e1b2db7eda701eeced36dc6b13</citedby><cites>FETCH-LOGICAL-c362t-d354a3d1c136fb2ca06a957f5432258dcc57567e1b2db7eda701eeced36dc6b13</cites><orcidid>0000-0002-2996-217X ; 0000-0001-8363-9309 ; 0000-0002-0553-674X ; 0000-0002-2809-5799 ; 0000-0003-1848-2477</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1053249822022628$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36639317$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wong, Wai</creatorcontrib><creatorcontrib>Johnson, Brandy</creatorcontrib><creatorcontrib>Cheng, Pi Chun</creatorcontrib><creatorcontrib>Josephson, Maureen B.</creatorcontrib><creatorcontrib>Maeda, Katsuhide</creatorcontrib><creatorcontrib>Berg, Robert A.</creatorcontrib><creatorcontrib>Kawut, Steven M.</creatorcontrib><creatorcontrib>Harhay, Michael O.</creatorcontrib><creatorcontrib>Goldfarb, Samuel B.</creatorcontrib><creatorcontrib>Yehya, Nadir</creatorcontrib><creatorcontrib>Himebauch, Adam S.</creatorcontrib><title>Primary graft dysfunction grade 3 following pediatric lung transplantation is associated with chronic lung allograft dysfunction</title><title>The Journal of heart and lung transplantation</title><addtitle>J Heart Lung Transplant</addtitle><description>Severe primary graft dysfunction (PGD) is associated with the development of bronchiolitis obliterans syndrome (BOS), the most common form of chronic lung allograft dysfunction (CLAD), in adults. However, PGD associations with long-term outcomes following pediatric lung transplantation are unknown. We hypothesized that PGD grade 3 (PGD 3) at 48- or 72-hours would be associated with shorter CLAD-free survival following pediatric lung transplantation.
This was a single center retrospective cohort study of patients ≤ 21 years of age who underwent bilateral lung transplantation between 2005 and 2019 with ≥ 1 year of follow-up. PGD and CLAD were defined by published criteria. We evaluated the association of PGD 3 at 48- or 72-hours with CLAD-free survival by using time-to-event analyses.
Fifty-one patients were included (median age 12.7 years; 51% female). The most common transplant indications were cystic fibrosis (29%) and pulmonary hypertension (20%). Seventeen patients (33%) had PGD 3 at either 48- or 72-hours. In unadjusted analysis, PGD 3 was associated with an increased risk of CLAD or mortality (HR 2.10, 95% CI 1.01-4.37, p=0.047). This association remained when adjusting individually for multiple potential confounders. There was evidence of effect modification by sex (interaction p = 0.055) with the association of PGD 3 and shorter CLAD-free survival driven predominantly by males (HR 4.73, 95% CI 1.44-15.6) rather than females (HR 1.23, 95% CI 0.47-3.20).
PGD 3 at 48- or 72-hours following pediatric lung transplantation was associated with shorter CLAD-free survival. Sex may be a modifier of this association.</description><subject>Adult</subject><subject>Allografts</subject><subject>Bronchiolitis Obliterans - etiology</subject><subject>Bronchiolitis Obliterans - surgery</subject><subject>bronchiolitis obliterans syndrome</subject><subject>Child</subject><subject>chronic lung allograft dysfunction</subject><subject>Female</subject><subject>Humans</subject><subject>Lung</subject><subject>Lung Transplantation - adverse effects</subject><subject>Male</subject><subject>pediatric</subject><subject>primary graft dysfunction</subject><subject>Primary Graft Dysfunction - epidemiology</subject><subject>Primary Graft Dysfunction - etiology</subject><subject>rejection</subject><subject>Retrospective Studies</subject><subject>transplant</subject><issn>1053-2498</issn><issn>1557-3117</issn><issn>1557-3117</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1uGyEUhVGVqnHcvkEVscxmpvwMYG8qVVb-JEvtol0jBu7YWOPBAaZWdnn04EzSTaSuQOg791w-hL5SUlNC5bddvQXTj0PNCGM1ZTWhzQc0o0KoilOqzsqdCF6xZrk4Rxcp7QghjAv2CZ1zKfmSUzVDT7-i35v4iDfRdBm7x9SNg80-DKcXB5jjLvR9OPphgw_gvMnRW1x6NzhHM6RDb4ZsXgI-YZNSsIUBh48-b7HdxjC88abMeVfzGX3sTJ_gy-s5R39urn-v7qr1z9v71Y91ZblkuXJcNIY7aimXXcusIdIshepEwxkTC2etUEIqoC1zrQJnFKEAFhyXzsqW8jm6muYeYngYIWW998lCX9aHMCbNlBRKcSkWBW0m1MaQUoROHyZJmhJ9cq93enKvT-41Zbq4L7HL14ax3YP7F3qTXYDvEwDln389RJ2sh6Es6SPYrF3w_294BveNmzU</recordid><startdate>202305</startdate><enddate>202305</enddate><creator>Wong, Wai</creator><creator>Johnson, Brandy</creator><creator>Cheng, Pi Chun</creator><creator>Josephson, Maureen B.</creator><creator>Maeda, Katsuhide</creator><creator>Berg, Robert A.</creator><creator>Kawut, Steven M.</creator><creator>Harhay, Michael O.</creator><creator>Goldfarb, Samuel B.</creator><creator>Yehya, Nadir</creator><creator>Himebauch, Adam S.</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><orcidid>https://orcid.org/0000-0002-2996-217X</orcidid><orcidid>https://orcid.org/0000-0001-8363-9309</orcidid><orcidid>https://orcid.org/0000-0002-0553-674X</orcidid><orcidid>https://orcid.org/0000-0002-2809-5799</orcidid><orcidid>https://orcid.org/0000-0003-1848-2477</orcidid></search><sort><creationdate>202305</creationdate><title>Primary graft dysfunction grade 3 following pediatric lung transplantation is associated with chronic lung allograft dysfunction</title><author>Wong, Wai ; Johnson, Brandy ; Cheng, Pi Chun ; Josephson, Maureen B. ; Maeda, Katsuhide ; Berg, Robert A. ; Kawut, Steven M. ; Harhay, Michael O. ; Goldfarb, Samuel B. ; Yehya, Nadir ; Himebauch, Adam S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-d354a3d1c136fb2ca06a957f5432258dcc57567e1b2db7eda701eeced36dc6b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adult</topic><topic>Allografts</topic><topic>Bronchiolitis Obliterans - etiology</topic><topic>Bronchiolitis Obliterans - surgery</topic><topic>bronchiolitis obliterans syndrome</topic><topic>Child</topic><topic>chronic lung allograft dysfunction</topic><topic>Female</topic><topic>Humans</topic><topic>Lung</topic><topic>Lung Transplantation - adverse effects</topic><topic>Male</topic><topic>pediatric</topic><topic>primary graft dysfunction</topic><topic>Primary Graft Dysfunction - epidemiology</topic><topic>Primary Graft Dysfunction - etiology</topic><topic>rejection</topic><topic>Retrospective Studies</topic><topic>transplant</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wong, Wai</creatorcontrib><creatorcontrib>Johnson, Brandy</creatorcontrib><creatorcontrib>Cheng, Pi Chun</creatorcontrib><creatorcontrib>Josephson, Maureen B.</creatorcontrib><creatorcontrib>Maeda, Katsuhide</creatorcontrib><creatorcontrib>Berg, Robert A.</creatorcontrib><creatorcontrib>Kawut, Steven M.</creatorcontrib><creatorcontrib>Harhay, Michael O.</creatorcontrib><creatorcontrib>Goldfarb, Samuel B.</creatorcontrib><creatorcontrib>Yehya, Nadir</creatorcontrib><creatorcontrib>Himebauch, Adam S.</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><jtitle>The Journal of heart and lung transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wong, Wai</au><au>Johnson, Brandy</au><au>Cheng, Pi Chun</au><au>Josephson, Maureen B.</au><au>Maeda, Katsuhide</au><au>Berg, Robert A.</au><au>Kawut, Steven M.</au><au>Harhay, Michael O.</au><au>Goldfarb, Samuel B.</au><au>Yehya, Nadir</au><au>Himebauch, Adam S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Primary graft dysfunction grade 3 following pediatric lung transplantation is associated with chronic lung allograft dysfunction</atitle><jtitle>The Journal of heart and lung transplantation</jtitle><addtitle>J Heart Lung Transplant</addtitle><date>2023-05</date><risdate>2023</risdate><volume>42</volume><issue>5</issue><spage>669</spage><epage>678</epage><pages>669-678</pages><issn>1053-2498</issn><issn>1557-3117</issn><eissn>1557-3117</eissn><abstract>Severe primary graft dysfunction (PGD) is associated with the development of bronchiolitis obliterans syndrome (BOS), the most common form of chronic lung allograft dysfunction (CLAD), in adults. However, PGD associations with long-term outcomes following pediatric lung transplantation are unknown. We hypothesized that PGD grade 3 (PGD 3) at 48- or 72-hours would be associated with shorter CLAD-free survival following pediatric lung transplantation.
This was a single center retrospective cohort study of patients ≤ 21 years of age who underwent bilateral lung transplantation between 2005 and 2019 with ≥ 1 year of follow-up. PGD and CLAD were defined by published criteria. We evaluated the association of PGD 3 at 48- or 72-hours with CLAD-free survival by using time-to-event analyses.
Fifty-one patients were included (median age 12.7 years; 51% female). The most common transplant indications were cystic fibrosis (29%) and pulmonary hypertension (20%). Seventeen patients (33%) had PGD 3 at either 48- or 72-hours. In unadjusted analysis, PGD 3 was associated with an increased risk of CLAD or mortality (HR 2.10, 95% CI 1.01-4.37, p=0.047). This association remained when adjusting individually for multiple potential confounders. There was evidence of effect modification by sex (interaction p = 0.055) with the association of PGD 3 and shorter CLAD-free survival driven predominantly by males (HR 4.73, 95% CI 1.44-15.6) rather than females (HR 1.23, 95% CI 0.47-3.20).
PGD 3 at 48- or 72-hours following pediatric lung transplantation was associated with shorter CLAD-free survival. Sex may be a modifier of this association.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>36639317</pmid><doi>10.1016/j.healun.2022.12.014</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-2996-217X</orcidid><orcidid>https://orcid.org/0000-0001-8363-9309</orcidid><orcidid>https://orcid.org/0000-0002-0553-674X</orcidid><orcidid>https://orcid.org/0000-0002-2809-5799</orcidid><orcidid>https://orcid.org/0000-0003-1848-2477</orcidid></addata></record> |
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subjects | Adult Allografts Bronchiolitis Obliterans - etiology Bronchiolitis Obliterans - surgery bronchiolitis obliterans syndrome Child chronic lung allograft dysfunction Female Humans Lung Lung Transplantation - adverse effects Male pediatric primary graft dysfunction Primary Graft Dysfunction - epidemiology Primary Graft Dysfunction - etiology rejection Retrospective Studies transplant |
title | Primary graft dysfunction grade 3 following pediatric lung transplantation is associated with chronic lung allograft dysfunction |
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