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Contemporary outcomes of pediatric cardiac transplantation with a positive retrospective crossmatch.
Lytrivi, Irene D; Koehl, Devin; Esteso, Paul; Frandsen, Erik L; Gibbons, Meredith K; Kirklin, James K; Cantor, Ryan; Lamour, Jacqueline M; Putschoegl, Adam; Shugh, Svetlana; Williams, Ryan J; Pearce, F Bennett.
Afiliación
  • Lytrivi ID; Columbia University Irving Medical Center, New York, New York, USA.
  • Koehl D; Kirklin Institute for Research in Surgical Outcomes, Birmingham, Alabama, USA.
  • Esteso P; Boston Children's Hospital, Boston, Massachusetts, USA.
  • Frandsen EL; Loma Linda University Children's Hospital, Loma Linda, California, USA.
  • Gibbons MK; Columbia University Irving Medical Center, New York, New York, USA.
  • Kirklin JK; Kirklin Institute for Research in Surgical Outcomes, Birmingham, Alabama, USA.
  • Cantor R; Division of Cardiothoracic Surgery, Department of Surgery, University of Alabama, Birmingham, Alabama, USA.
  • Lamour JM; Kirklin Institute for Research in Surgical Outcomes, Birmingham, Alabama, USA.
  • Putschoegl A; Mount Sinai Medical Center, Kravis Children's Hospital, New York, New York, USA.
  • Shugh S; Children's Hospital of Minnesota, Minneapolis, Minnesota, USA.
  • Williams RJ; Joe DiMaggio Children's Hospital, Hollywood, Florida, USA.
  • Pearce FB; Boston Children's Hospital, Boston, Massachusetts, USA.
Pediatr Transplant ; 27(7): e14593, 2023 Nov.
Article en En | MEDLINE | ID: mdl-37602972
ABSTRACT

BACKGROUND:

A positive crossmatch (+ XM) has traditionally been associated with adverse outcomes following pediatric heart transplantation. However, more recent studies suggest that favorable intermediate-term outcomes may be achieved despite a + XM. This study's hypothesis is that children with a + XM have similar long-term survival, but higher rate of complications such as rejection, coronary allograft vasculopathy (CAV), and infection, compared to patients with a negative (-) XM.

METHODS:

The Pediatric Heart Transplant Society Registry (PHTS) database was queried from 2010-2021 for all patients <18 years of age with a known XM. Baseline demographics were compared between + XM and - XM groups using appropriate parametric and non-parametric group comparisons. Cox Proportional Hazards Modeling was used to identify risk factors for post-transplant graft loss, rejection, and CAV.

RESULTS:

Of 4599 pediatric heart transplants during the study period, XM results were available for 3914 (85%), of which 373 (9.5%) had a + XM. Univariate analysis showed lower 10-year survival for patients with + XM (HR = 1.3, p = .04). Multivariate analyses revealed no significant difference in 10-year survival in the 2 groups; however, time to first rejection (p = .0001) remained significantly shorter in the + XM group.

CONCLUSIONS:

Pediatric patients transplanted across a + XM experience earlier rejection; however, after multivariate adjustment, + XM is not independently associated with intermediate-term graft loss. The risk of heart transplantation against a + XM must be balanced with the ongoing risk of waitlist mortality.
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Pediatr Transplant Asunto de la revista: PEDIATRIA / TRANSPLANTE Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Pediatr Transplant Asunto de la revista: PEDIATRIA / TRANSPLANTE Año: 2023 Tipo del documento: Article