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Long-term Outcomes After Surgical Intervention for Congenital Supravalvar Aortic Stenosis in Children.
Zinyandu, Tawanda; Knight, Jessica H; Thomas, Amanda S; Claxton, J'Neka; Montero, Alejandro; Shaw, Fawwaz R; Kochilas, Lazaros K.
Afiliação
  • Zinyandu T; Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia.
  • Knight JH; Department of Epidemiology and Biostatistics, University of Georgia College of Public Health, Athens, Georgia.
  • Thomas AS; Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia.
  • Claxton J; Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia.
  • Montero A; Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia.
  • Shaw FR; Department of Cardiothoracic Surgery, Children's Healthcare of Atlanta, Atlanta, Georgia.
  • Kochilas LK; Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia; Children's Healthcare of Atlanta Cardiology, Atlanta, Georgia. Electronic address: lazaros.kochilas@emory.edu.
Ann Thorac Surg ; 117(5): 965-972, 2024 May.
Article em En | MEDLINE | ID: mdl-38302053
ABSTRACT

BACKGROUND:

Primary supravalvar aortic stenosis (SVAS) is a rare congenital cardiovascular condition that can coexist with Williams-Beuren syndrome, coronary artery involvement, aortic coarctation, and pulmonary artery stenosis. SVAS repair can be achieved with low perioperative mortality, but long-term survival remains less well understood. We used the Pediatric Cardiac Care Consortium, a multicenter United States-based registry for pediatric cardiac operations, to assess long-term outcomes after SVAS repair.

METHODS:

We used Kaplan-Meier plots and Cox proportional hazards regression to examine factors associated with postdischarge deaths. These included sex, age-group, weight z-score, coexisting conditions (Williams-Beuren syndrome, coronary artery involvement, coarctation, and pulmonary artery stenosis), surgical techniques, and era, defined as early (1982-1995) or late (1996-2003). Survival was assessed by matching with the National Death Index through 2021.

RESULTS:

Of 333 patients who met inclusion criteria, 313 (94.0%) survived to discharge and 188 (60.1%) had identifiers for National Death Index matching. Over a median follow-up of 25.2 years (interquartile range, 21.1-29.4 years), 17 deaths occurred. The 30-year survival after discharge from SVAS repair was 88.7% (95% CI, 82.9%-94.8%). Infantile surgery and non-Williams-Beuren syndrome were associated with decreased 30-year survival. From the various repairs, the 2-sinus technique had better outcomes compared with all other types, except the 3-sinus technique (nonsignificant difference). Adjusted analysis revealed infantile age and type of repair as associated with postdischarge probability of death.

CONCLUSIONS:

These data demonstrate favorable long-term outcomes after SVAS repair, except for the infantile group that was associated with more diffuse arteriopathy. As techniques continue to evolve, future studies are warranted to investigate their long-term outcomes.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estenose Aórtica Supravalvular Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male / Newborn País/Região como assunto: America do norte Idioma: En Revista: Ann Thorac Surg Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Geórgia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estenose Aórtica Supravalvular Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male / Newborn País/Região como assunto: America do norte Idioma: En Revista: Ann Thorac Surg Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Geórgia