Evidence map›Paper›PMID 39305323›Full record

ArticlePediatric cardiology2025

Health-Related Quality of Life After Neonatal Treatment of Symptomatic Tetralogy of Fallot: Insights from the Congenital Cardiac Research Collaborative.

George T Nicholson, Jeffrey D Zampi, Andrew C Glatz, Bryan H Goldstein, Christopher J Petit, Yun Zhang, Courtney E McCracken, Athar M Qureshi, Caren S Goldberg, Jennifer C Romano and 12 more

Erratum issuedAbstract readMulticenter Study
In one paragraph

Article in Pediatric cardiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

George T NicholsonDivision of Cardiology, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN, USA. george.t.nicholson@vumc.org.
Jeffrey D ZampiDivision of Cardiology, Department of Pediatrics, C.S. Mott Children's Hospital, University of Michigan School of Medicine, Ann Arbor, MI, USA.
Andrew C GlatzDivision of Cardiology, Department of Pediatrics, Washington University School of Medicine, St. Louis, MA, USA.
Bryan H GoldsteinDepartment of Pediatrics, Heart Institute, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Christopher J PetitMorgan Stanley Children's Hospital, Columbia University Vagelos College of Physicians & Surgeons, New York, NY, USA.
Yun ZhangMorgan Stanley Children's Hospital, Columbia University Vagelos College of Physicians & Surgeons, New York, NY, USA.
Courtney E McCrackenCenter for Research and Evaluation, Kaiser Permanente Georgia, Atlanta, GA, USA.
Athar M QureshiLillie Frank Abercrombie Division of Cardiology, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
Caren S GoldbergDivision of Cardiology, Department of Pediatrics, C.S. Mott Children's Hospital, University of Michigan School of Medicine, Ann Arbor, MI, USA.
Jennifer C RomanoSection of Pediatric Cardiothoracic Surgery, Department of Cardiac Surgery, C.S. Mott Children's Hospital, University of Michigan School of Medicine, Ann Arbor, MI, USA.
Mark A LawDivision of Pediatric Cardiology, Department of Pediatrics, Children's of Alabama, University of Alabama Birmingham School of Medicine, Birmingham, AL, USA.
Jeffery J MeadowsDivision of Cardiology, Department of Pediatrics, University of California San Francisco School of Medicine, San Francisco, CA, USA.
Shabana ShahanavazThe Heart Institute, Cincinnati Children's Hospital Medical Center and Division of Pediatric Cardiology, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Sarosh P BatlivalaThe Heart Institute, Cincinnati Children's Hospital Medical Center and Division of Pediatric Cardiology, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Shiraz A MaskatiaDivision of Pediatric Cardiology, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.
Asaad BeshishChildren's Heart Center Cardiology, Department of Pediatrics, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA, USA.
Michael L O'ByrneThe Cardiac Center at the Children's Hospital of Philadelphia, Philadelphia, PA, USA.
R Allen LigonChildren's Heart Center Cardiology, Department of Pediatrics, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA, USA.
Kathryn O StackThe Cardiac Center at the Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Hala Q KhanLillie Frank Abercrombie Division of Cardiology, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
Shalin ParekhDivision of Cardiology, Department of Pediatrics, University of California San Francisco School of Medicine, San Francisco, CA, USA.
Dawn L IlardiPediatric Neurodevelopmental Center, Atlanta, GA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To evaluate the association between initial management strategy of neonatal symptomatic Tetralogy of Fallot (sTOF) and later health-related quality of life (HRQOL) outcomes. We performed a multicenter, cross-sectional evaluation of a previously assembled cohort of infants with sTOF who underwent initial intervention at ≤ 30 days of age, between 2005 and 2017. Eligible patients' parents/guardians completed an age-appropriate Pediatric Quality of Life Inventory, a Pediatric Quality of Life Inventory Cardiac Module Heart Disease Symptoms Scale, and a parental survey. The association between treatment strategy and HRQOL was evaluated, and the entire sTOF cohort was compared to published values for the healthy pediatric population and to children with complex congenital heart disease and other chronic illness. The study cohort included 143 sTOF subjects, of which 59 underwent a primary repair, and 84 had a staged repair approach. There was no association between initial management strategy and lower HRQOL. For the entire cohort, in general, individual domain scores decreased as age sequentially increased. Across domain measurements, mean scores for the sTOF cohort were significantly lower than the healthy pediatric population and comparable to those with other forms of complex CHD and other chronic health conditions. The presence of a genetic syndrome was significantly associated with a poor HRQOL (p = 0.003). Initial treatment strategy for sTOF was not associated with differences in late HRQOL outcomes, though the overall HRQOL in this sTOF cohort was significantly lower than the general population, and comparable to others with chronic illness.

Indexed as

Cardiac Surgical ProceduresQuality of LifeTetralogy of FallotCross-Sectional StudiesFemaleHumansInfantInfant, NewbornMaleCongenital heart diseaseQuality of lifeTetralogy of fallot

Identifiers

PMID39305323
PMCPMC12583293

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.