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Outcomes of Neonates Born with Symptomatic Tetralogy of Fallot and Absent Ductus Arteriosus.
Maskatia, Shiraz A; Glatz, Andrew C; Goldstein, Bryan H; Qureshi, Athar M; Zampi, Jeffrey D; McCracken, Courtney E; Nicholson, George T; Meadows, Jeffery J; Shahanavaz, Shabana; Law, Mark A; Batlivala, Sarosh P; Mascio, Christopher E; Chai, Paul J; Romano, Jennifer C; O'Byrne, Michael L; Ligon, Allen; Beshish, Asaad G; Petit, Christopher J.
Afiliación
  • Maskatia SA; Department of Pediatrics, Berry Irene Moore Heart Center, Lucile Packard Children's Hospital, Stanford University School of Medicine, Palo Alto, CA. Electronic address: shirazm@stanford.edu.
  • Glatz AC; The Heart Center, Washington University and St. Louis Children's Hospital, St. Louis, MO.
  • Goldstein BH; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA.
  • Qureshi AM; The Lillie Frank Abercrombie Section of Cardiology, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, TX.
  • Zampi JD; Division of Pediatric Cardiology, Department of Pediatrics, University of Michigan C.S. Mott Children's Hospital, Ann Arbor, MI.
  • McCracken CE; Center for Research and Evaluation, Kaiser Permanente Georgia, Atlanta, GA.
  • Nicholson GT; Pediatric Heart Institute, Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, TN.
  • Meadows JJ; Department of Pediatrics, University of California San Francisco, San Francisco, CA.
  • Shahanavaz S; The Heart Institute, Cincinnati Children's Hospital, Cincinnati, OH; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.
  • Law MA; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL.
  • Batlivala SP; The Heart Institute, Cincinnati Children's Hospital, Cincinnati, OH; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.
  • Mascio CE; Pediatric Cardiothoracic Surgery, Department of Cardiovascular and Thoracic Surgery, West Virginia University Medicine Children's, Morgantown, WV.
  • Chai PJ; Children's Heart Center, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA.
  • Romano JC; Division of Pediatric Cardiology, Department of Pediatrics, University of Michigan C.S. Mott Children's Hospital, Ann Arbor, MI.
  • O'Byrne ML; Cardiac Center at the Children's Hospital of Philadelphia, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
  • Ligon A; Children's Heart Center, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA.
  • Beshish AG; Children's Heart Center, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA.
  • Petit CJ; Department of Pediatrics, Columbia University Vagelos College of Physicians & Surgeons, New York, NY.
J Pediatr ; 272: 114122, 2024 Sep.
Article en En | MEDLINE | ID: mdl-38815742
ABSTRACT

OBJECTIVE:

To test the hypothesis that neonates with symptomatic tetralogy of Fallot (TOF) and absent ductus arteriosus (ADA) have worse clinical outcomes compared with those with a ductus arteriosus (DA), and that this difference is driven by those born with ADA and with critically deficient pulmonary blood flow (CDPBF). STUDY

DESIGN:

We performed a retrospective, multicenter cohort study of neonates who underwent intervention for symptomatic TOF comparing death and reintervention between subjects with and without a DA identified on fetal echocardiogram or on echocardiogram performed in the first postnatal day. Exclusion criteria were as follows inability to define DA status, collaterals supplying pulmonary blood flow, atrioventricular septal defect, and absent pulmonary valve. We defined CDPBF as undergoing a procedure to augment pulmonary blood flow on the date of birth or extracorporeal membrane oxygenation prior to such a procedure.

RESULTS:

The study cohort included 519 patients, among whom 11% had ADA. Patients with ADA were more likely to have a genetic syndrome and had smaller branch pulmonary artery size. In analyses adjusting for center, interventional treatment strategy, genetic syndrome, and minimum branch pulmonary artery size, ADA was associated with higher mortality risk (adjusted hazard ratio of 2.37 (95% CI 1.07,5.27; P = .034). Seven patients had CDPBF (1.3% of the entire cohort and 12% of patients with ADA).

CONCLUSIONS:

A minority of symptomatic TOF neonates have ADA, which is associated with higher adjusted mortality risk compared with those with a DA. CDPBF appears to be a rare but important entity in this population.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tetralogía de Fallot Límite: Female / Humans / Male / Newborn Idioma: En Revista: J Pediatr Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tetralogía de Fallot Límite: Female / Humans / Male / Newborn Idioma: En Revista: J Pediatr Año: 2024 Tipo del documento: Article
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