Evidence map›Paper›PMID 27826129›Full record

ArticleHeart rhythm2017

Genotypic and phenotypic predictors of complete heart block and recovery of conduction after surgical repair of congenital heart disease.

Laura E Murray, Andrew H Smith, English C Flack, Kim Crum, Jill Owen, Prince J Kannankeril

Abstract read
In one paragraph

Article in Heart rhythm, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

12 citing papers in PubMed, 39 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Laura E MurrayVanderbilt University Medical Center, Nashville, Tennessee. Electronic address: laura.e.murray@vanderbilt.edu.
Andrew H SmithDepartment of Pediatrics, Thomas P. Graham Jr. Division of Cardiology, Nashville, Tennessee,; Division of Critical Care Medicine, Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee.
English C FlackDepartment of Pediatrics, Thomas P. Graham Jr. Division of Cardiology, Nashville, Tennessee.
Kim CrumDepartment of Pediatrics, Thomas P. Graham Jr. Division of Cardiology, Nashville, Tennessee.
Jill OwenDepartment of Pediatrics, Thomas P. Graham Jr. Division of Cardiology, Nashville, Tennessee.
Prince J KannankerilDepartment of Pediatrics, Thomas P. Graham Jr. Division of Cardiology, Nashville, Tennessee.
Monroe Carell Jr. Children's Hospital · USVanderbilt University Medical Center · US

Funding

VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Pharmacogenetics and Personalized Medicine after Cardiac Surgery in ChildrenR01HD084461 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI EDWARDS, TODD L, KANNANKERIL, PRINCE JOSEPH · 2016 to 2020
$3.1M
NCATS NIH HHS UL1 TR000445NCRR NIH HHS UL1 RR024975NICHD NIH HHS R01 HD084461
6 · The paper itself

Abstract

backgroundComplete heart block (CHB) is a major complication that occurs after congenital heart surgery. We hypothesized that genetic and clinical factors are associated with the development of postoperative CHB and recovery of atrioventricular (AV) conduction.

objectiveThe purpose of this study was to identify predictors of CHB and recovery after congenital heart surgery.

methodsPatients undergoing congenital heart surgery at our institution from September 2007 through June 2015 were prospectively enrolled in a parent study of postoperative arrhythmias. Patients with onset of CHB within 48 hours postoperatively were included in the study. Daily rhythm assessment was performed until demonstration of 1:1 conduction or pacemaker implantation.

resultsOf 1199 subjects enrolled, 56 (4.7%) developed postoperative CHB. In multivariate analysis, preoperative digoxin exposure (odds ratio [OR] 2.4, 95% confidence interval [CI] 1.3-4.4), aortic cross-clamp time (OR 1.08, 95% CI 1.04-1.11), ventricular septal defect closure (OR 2.2, 95% CI 1.2-4.1), and a common polymorphism in the gene encoding connexin-40 (GJA5 rs10465885 TT genotype; OR 2.1, 95% CI 1.2-3.8) were independently associated with postoperative CHB. Junctional acceleration (JA) (OR 4.0, 95% CI 1.1-15.1) and intermittent conduction noted during complete AV block (OR 9.1, 95% CI 1.0-80) were independently associated with 1:1 AV conduction recovery. Use of a multivariate model including both JA and intermittent conduction demonstrated good discrimination with a positive predictive value of 86% (95% CI 67%-96%) in predicting 1:1 conduction recovery.

conclusionPreoperative factors, including a missense polymorphism in GJA5, are independently associated with increased risk for CHB. JA and intermittent conduction may prove useful in predicting recovery of AV conduction among patients with CHB after congenital heart surgery.

Indexed as

Atrioventricular BlockCardiac Surgical ProceduresHeart Defects, CongenitalPostoperative ComplicationsChild, PreschoolConnexinsFemaleGap Junction alpha-5 ProteinHeart Conduction SystemHumansInfantMaleMutation, MissensePolymorphism, Single NucleotidePredictive Value of TestsPrognosisConnexinsGap Junction alpha-5 ProteinArrhythmiaCongenital heart defectGenotypeHeart blockJunctional accelerationPacemakerPediatrics

Identifiers

PMID27826129
PMCPMC5345747
OpenAlexW2547193202

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.