Favorable outcome of children and adolescents undergoing lung transplantation at a European adult center in the new era

Summary Lung transplantation (LTx) is an accepted therapy in children with end‐stage lung diseases. Pediatric‐specific experience is considered important in pediatric LTx. We present our institutional experience and its outcome since the year 2000, asking whether different treatment strategies produ...

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Veröffentlicht in:Pediatric pulmonology 2016-11, Vol.51 (11), p.1222-1228
Hauptverfasser: Schmid, Florian A., Inci, Ilhan, Bürgi, Urs, Hillinger, Sven, Schneiter, Didier, Opitz, Isabelle, Huber, Lars C., Isenring, Bruno D., Jungraithmayr, Wolfgang, Schuurmans, Macé M., Weder, Walter, Benden, Christian
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container_end_page 1228
container_issue 11
container_start_page 1222
container_title Pediatric pulmonology
container_volume 51
creator Schmid, Florian A.
Inci, Ilhan
Bürgi, Urs
Hillinger, Sven
Schneiter, Didier
Opitz, Isabelle
Huber, Lars C.
Isenring, Bruno D.
Jungraithmayr, Wolfgang
Schuurmans, Macé M.
Weder, Walter
Benden, Christian
description Summary Lung transplantation (LTx) is an accepted therapy in children with end‐stage lung diseases. Pediatric‐specific experience is considered important in pediatric LTx. We present our institutional experience and its outcome since the year 2000, asking whether different treatment strategies produce comparable outcomes in pediatric lung transplant recipients at our predominantly adult center. This is a retrospective analysis of children and adolescents aged ≤20 years, undergoing LTx between January 2001 and December 2013. Minimum follow‐up was 12 months. Primary endpoints were re‐transplantation or death. We performed 33 lung transplant procedures in 29 patients. Survival 1 month post‐operatively was 96.6%, at 3 months 93.1% and at 12 months 82.8%, respectively. At the end of our follow up, 72.4% of our pediatric cohort was still alive — median post‐transplant survival was 59 months (range 0–159). 72.4% of the children were transplanted with support of extracorporeal membrane oxygenation (ECMO), size‐reduced donor grafts were used in 69.0%. The differences between post‐transplant survival of the “non‐ECMO‐group” versus the “ECMO‐group” (137 vs. 28 months, P=0.7) and “full size” versus “size‐reduced bilateral transplants” (61 vs. 28 months, P = 0.7) were not significant, though. There were no anastomotic complications, also not in size‐reduced lungs. Our results are well comparable to the international data and show excellent short‐ and mid‐term outcomes. We advocate ECMO‐bridge to be considered as a valuable treatment option to prolong time on the waiting list in highly selected patients, as well as size reduction and lobar transplants as a strong strategy to increase the donor pool and reduce donor‐recipient size‐mismatches. Pediatr Pulmonol. 2016;51:1222–1228. © 2016 Wiley Periodicals, Inc.
doi_str_mv 10.1002/ppul.23383
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Pediatric‐specific experience is considered important in pediatric LTx. We present our institutional experience and its outcome since the year 2000, asking whether different treatment strategies produce comparable outcomes in pediatric lung transplant recipients at our predominantly adult center. This is a retrospective analysis of children and adolescents aged ≤20 years, undergoing LTx between January 2001 and December 2013. Minimum follow‐up was 12 months. Primary endpoints were re‐transplantation or death. We performed 33 lung transplant procedures in 29 patients. Survival 1 month post‐operatively was 96.6%, at 3 months 93.1% and at 12 months 82.8%, respectively. At the end of our follow up, 72.4% of our pediatric cohort was still alive — median post‐transplant survival was 59 months (range 0–159). 72.4% of the children were transplanted with support of extracorporeal membrane oxygenation (ECMO), size‐reduced donor grafts were used in 69.0%. The differences between post‐transplant survival of the “non‐ECMO‐group” versus the “ECMO‐group” (137 vs. 28 months, P=0.7) and “full size” versus “size‐reduced bilateral transplants” (61 vs. 28 months, P = 0.7) were not significant, though. There were no anastomotic complications, also not in size‐reduced lungs. Our results are well comparable to the international data and show excellent short‐ and mid‐term outcomes. We advocate ECMO‐bridge to be considered as a valuable treatment option to prolong time on the waiting list in highly selected patients, as well as size reduction and lobar transplants as a strong strategy to increase the donor pool and reduce donor‐recipient size‐mismatches. 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The differences between post‐transplant survival of the “non‐ECMO‐group” versus the “ECMO‐group” (137 vs. 28 months, P=0.7) and “full size” versus “size‐reduced bilateral transplants” (61 vs. 28 months, P = 0.7) were not significant, though. There were no anastomotic complications, also not in size‐reduced lungs. Our results are well comparable to the international data and show excellent short‐ and mid‐term outcomes. We advocate ECMO‐bridge to be considered as a valuable treatment option to prolong time on the waiting list in highly selected patients, as well as size reduction and lobar transplants as a strong strategy to increase the donor pool and reduce donor‐recipient size‐mismatches. 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Pediatric‐specific experience is considered important in pediatric LTx. We present our institutional experience and its outcome since the year 2000, asking whether different treatment strategies produce comparable outcomes in pediatric lung transplant recipients at our predominantly adult center. This is a retrospective analysis of children and adolescents aged ≤20 years, undergoing LTx between January 2001 and December 2013. Minimum follow‐up was 12 months. Primary endpoints were re‐transplantation or death. We performed 33 lung transplant procedures in 29 patients. Survival 1 month post‐operatively was 96.6%, at 3 months 93.1% and at 12 months 82.8%, respectively. At the end of our follow up, 72.4% of our pediatric cohort was still alive — median post‐transplant survival was 59 months (range 0–159). 72.4% of the children were transplanted with support of extracorporeal membrane oxygenation (ECMO), size‐reduced donor grafts were used in 69.0%. 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subjects Adolescent
Child
children
Extracorporeal Membrane Oxygenation
Female
Humans
Lung Diseases - surgery
Lung Transplantation
Male
pediatric
Pediatrics
Respiratory therapy
Retrospective Studies
Tissue Donors
Transplants & implants
Treatment Outcome
Waiting Lists
Young Adult
title Favorable outcome of children and adolescents undergoing lung transplantation at a European adult center in the new era
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