Evidence map›Paper›PMID 30566184›Full record

ArticleJAMA cardiology2019

Long-term Outcomes of Tetralogy of Fallot: A Study From the Pediatric Cardiac Care Consortium.

Clayton A Smith, Courtney McCracken, Amanda S Thomas, Logan G Spector, James D St Louis, Matthew E Oster, James H Moller, Lazaros Kochilas

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in JAMA cardiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
6.8field-weighted citation impact, top 2% of its field
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

79 citing papers in PubMed, 160 citations in OpenAlex.

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  19. Interventions for adult congenital heart disease.Nature reviews. Cardiology · 2025
    Review
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19 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Clayton A SmithDepartment of Pediatrics, Emory University School of Medicine.
Courtney McCrackenDepartment of Pediatrics, Emory University School of Medicine.
Amanda S ThomasDepartment of Pediatrics, Emory University School of Medicine.
Logan G SpectorDepartment of Pediatrics, University of Minnesota, Minneapolis.
James D St LouisDepartment of Pediatric Surgery, University of Missouri, Kansas City School of Medicine.
Matthew E OsterDepartment of Pediatrics, Emory University School of Medicine.
James H MollerDepartment of Internal Medicine, University of Minnesota, Minneapolis.
Lazaros KochilasDepartment of Pediatrics, Emory University School of Medicine.
Children's Healthcare of Atlanta · USEmory University · USUniversity of Minnesota · USUniversity of Missouri–Kansas City · US

Funding

Long-term Outcomes after Interventions for Congenital Heart DiseaseR01HL122392 · NHLBI · UNIVERSITY OF MINNESOTA · PI KOCHILAS, LAZAROS K. · 2014 to 2022
$5.2M
NHLBI NIH HHS R01 HL122392
6 · The paper itself

Abstract

Importance: Tetralogy of Fallot (TOF) is a surgically repairable form of cyanotic congenital heart disease. Multicenter data for long-term survival following repair are sparse. Objective: To evaluate the long-term transplant-free survival of TOF by surgical strategy adjusted for era and patient characteristics. Design, Setting, and Participants: Retrospective cohort study enriched with data from the National Death Index and the Organ Procurement and Transplantation Network through 2014. Multicenter cohort from the Pediatric Cardiac Care Consortium (PCCC), a large, US-based clinical registry for interventions for congenital heart disease. The cohort included patients with adequate identifiers for linkage with the National Death Index and the Organ Procurement and Transplantation Network who were enrolled in the PCCC registry between 1982 and 2003 and survived surgical repair of simple TOF. Data were analyzed between September 2015 and April 2018. Exposures: We examined patient-associated and surgery-associated risk factors affecting survival. Main Outcomes and Measures: We analyzed the transplant-free survival during early (<6 years) and late (≥6 years) phase after TOF surgical repair. Results: Of the 3283 patients who survived repair for simple TOF and met the study's inclusion criteria, 56.4% were male and 43.6% were female. Twenty-five-year survival following TOF repair was 94.5%. Multivariable analysis demonstrated increased risk of early mortality with staged repair (HR, 2.68; 95% CI, 1.59-4.49) and non-valve-sparing operation (HR, 3.76; 95% CI, 1.53-9.19). Presence of a genetic abnormality was associated with increased risk of death both in the early (HR, 3.64; 95% CI, 2.05-6.47) and late postoperative phase (HR, 4.41; 95% CI, 2.62-7.44). Conclusions and Relevance: Long-term survival after simple TOF repair is excellent. Staged repair and non-valve-sparing operations were negatively associated with survival in the early postrepair phase but not the late postrepair phase. These data are important for patients with repaired TOF and their caretakers and may guide surgical strategies for optimizing the long-term outcomes of this population.

Indexed as

AdolescentCardiac Care FacilitiesCause of DeathChildChild, PreschoolCohort StudiesFemaleHospital MortalityHumansInfantMalePediatricsRegistriesRetrospective StudiesRisk FactorsSurvival Analysis

Identifiers

PMID30566184
PMCPMC6439686
OpenAlexW2904473257

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.