A shifting landscape: Practice patterns and outcomes of cystic fibrosis and non‐cystic fibrosis pediatric lung transplantation

A shifting landscape: Practice patterns and outcomes of cystic fibrosis and non‐cystic fibrosis pediatric lung transplantation

Background New drugs may further decrease the need for lung transplant (LTx) in pediatric patients with cystic fibrosis (CF), but few studies highlight pediatric non‐CF LTx characteristics and outcomes. Methods The ISHLT registry was used to report morbidity, graft failure, and survival for primary...

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Veröffentlicht in:Pediatric transplantation 2021-11, Vol.25 (7), p.e14086-n/a
Hauptverfasser: Nelson, Jennifer S., Maul, Timothy M., Aughtman, Shelby L., Hurtado, Christopher G., Wearden, Peter D.
Format: Artikel
Sprache:eng
Schlagworte:
Adolescent
Child
Child, Preschool
Cystic fibrosis
Cystic Fibrosis - mortality
Cystic Fibrosis - surgery
Female
Graft Rejection
Graft Survival
Grafts
Humans
Hypertension
Immunosuppressive agents
Infant
infant lung transplantation
Lung transplantation
Lung Transplantation - mortality
Male
Morbidity
Mortality
outcomes
Oxygenation
Patients
pediatric lung transplantation
Pediatrics
Practice Patterns, Physicians' - statistics & numerical data
Pulmonary hypertension
Registries
Retrospective Studies
Risk factors
Survival
Survival Analysis
Transplants & implants
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Zusammenfassung:Background New drugs may further decrease the need for lung transplant (LTx) in pediatric patients with cystic fibrosis (CF), but few studies highlight pediatric non‐CF LTx characteristics and outcomes. Methods The ISHLT registry was used to report morbidity, graft failure, and survival for primary pediatric (
ISSN:1397-3142
1399-3046
DOI:10.1111/petr.14086