Heart Transplantation for Pediatric and Congenital Cardiac Disease: A Comparison of Two Eras over 23 Years and 188 Transplants at a Single Institution.


Journal

World journal for pediatric & congenital heart surgery
ISSN: 2150-136X
Titre abrégé: World J Pediatr Congenit Heart Surg
Pays: United States
ID NLM: 101518415

Informations de publication

Date de publication:
Jan 2021
Historique:
entrez: 7 1 2021
pubmed: 8 1 2021
medline: 23 3 2021
Statut: ppublish

Résumé

To assess changes in patterns of practice and outcomes over time, we reviewed all patients who underwent heart transplantation (HTx) at our institution and compared two consecutive eras with significantly different immunosuppressive protocols (cohort 1 [80 HTx, June 1995-June 2006]; cohort 2 [108 HTx, July 2006-September 2018]). Retrospective study of 180 patients undergoing 188 HTx (June 1995-September 2018; 176 first time HTx, 10 second HTx, and 2 third HTx). In 2006, we commenced pre-HTx desensitization for highly sensitized patients and started using tacrolimus as our primary postoperative immunosuppressive agent. The primary outcome was mortality. Survival was modeled by the Kaplan-Meier method. Univariable and multivariable Cox proportional hazard models were created to identify prognostic factors for survival. Our 188 HTx included 18 neonates, 85 infants, 83 children, and 2 adults (>18 years). Median age was 260.0 days (range: 5 days-23.8 years). Median weight was 7.5 kg (range: 2.2-113 kg). Patients in cohort 1 were less likely to have been immunosensitized preoperatively (12.5% vs 28.7%, Our analysis of 23 years of pediatric and congenital HTx reveals superior survival in the most recent 12-year era, despite the higher proportion of patients with elevated panel reactive antibody in the most recent era. This improvement was temporally associated with changes in our immunosuppressive strategy.

Sections du résumé

BACKGROUND BACKGROUND
To assess changes in patterns of practice and outcomes over time, we reviewed all patients who underwent heart transplantation (HTx) at our institution and compared two consecutive eras with significantly different immunosuppressive protocols (cohort 1 [80 HTx, June 1995-June 2006]; cohort 2 [108 HTx, July 2006-September 2018]).
METHODS METHODS
Retrospective study of 180 patients undergoing 188 HTx (June 1995-September 2018; 176 first time HTx, 10 second HTx, and 2 third HTx). In 2006, we commenced pre-HTx desensitization for highly sensitized patients and started using tacrolimus as our primary postoperative immunosuppressive agent. The primary outcome was mortality. Survival was modeled by the Kaplan-Meier method. Univariable and multivariable Cox proportional hazard models were created to identify prognostic factors for survival.
RESULTS RESULTS
Our 188 HTx included 18 neonates, 85 infants, 83 children, and 2 adults (>18 years). Median age was 260.0 days (range: 5 days-23.8 years). Median weight was 7.5 kg (range: 2.2-113 kg). Patients in cohort 1 were less likely to have been immunosensitized preoperatively (12.5% vs 28.7%,
CONCLUSIONS CONCLUSIONS
Our analysis of 23 years of pediatric and congenital HTx reveals superior survival in the most recent 12-year era, despite the higher proportion of patients with elevated panel reactive antibody in the most recent era. This improvement was temporally associated with changes in our immunosuppressive strategy.

Identifiants

pubmed: 33407028
doi: 10.1177/2150135120954149
doi:

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

17-26

Auteurs

Genevieve C Tuite (GC)

Johns Hopkins All Children's Heart Institute, Saint Petersburg, FL, USA.

James A Quintessenza (JA)

Johns Hopkins All Children's Heart Institute, Saint Petersburg, FL, USA.

Alfred Asante-Korang (A)

Johns Hopkins All Children's Heart Institute, Saint Petersburg, FL, USA.

Sharon R Ghazarian (SR)

Johns Hopkins All Children's Heart Institute, Saint Petersburg, FL, USA.

Bethany L Wisotzkey (BL)

Phoenix Children's Cardiology, Phoenix Children's Hospital, AZ, USA.

Shawn Shah (S)

Johns Hopkins All Children's Heart Institute, Saint Petersburg, FL, USA.

Gary E Stapleton (GE)

Pediatric Interventional Cardiology, Texas Children's Hospital, Houston, TX, USA.

Jamie A Decker (JA)

Johns Hopkins All Children's Heart Institute, Saint Petersburg, FL, USA.

Carrie E Herbert (CE)

Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Vyas Kartha (V)

Johns Hopkins All Children's Heart Institute, Saint Petersburg, FL, USA.

Plato Alexander (P)

Johns Hopkins All Children's Heart Institute, Saint Petersburg, FL, USA.

Jennifer Carapellucci (J)

Johns Hopkins All Children's Heart Institute, Saint Petersburg, FL, USA.

Diane Krasnopero (D)

Children's Heart Center, Children's Healthcare of Atlanta, Emory University, Atlanta, GA, USA.

Jade Hanson (J)

Johns Hopkins All Children's Heart Institute, Saint Petersburg, FL, USA.

Neil A Goldenberg (NA)

Johns Hopkins All Children's Heart Institute, Saint Petersburg, FL, USA.

Nhue L Do (NL)

Division of Pediatric Cardiac Surgery, Vanderbilt University, Nashville, TN, USA.

Constantine Mavroudis (C)

Johns Hopkins All Children's Heart Institute, Saint Petersburg, FL, USA.

Tom R Karl (TR)

Johns Hopkins All Children's Heart Institute, Saint Petersburg, FL, USA.

Robert J Boucek (RJ)

Seattle Children's Research Institute, Seattle, WA, USA.

Shelby Kutty (S)

Division of Pediatric Cardiology, 1466Johns Hopkins University, Baltimore, MD, USA.

Luca A Vricella (LA)

Division of Pediatric Cardiac Surgery, 2462University of Chicago, IL, USA.

Hugh M van Gelder (HM)

Cardiac Surgery, US Department of Veteran Affairs, Tampa, Florida, USA.

Jeffrey P Jacobs (JP)

Congenital Heart Center, Division of Thoracic and Cardiovascular Surgery, Department of Surgery, University of Florida, Gainesville, FL, USA.

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Classifications MeSH