Evidence map›Paper›PMID 22300696›Full record

ArticleJournal of the American College of Cardiology2012

Incidence of and risk factors for sudden cardiac death in children with dilated cardiomyopathy: a report from the Pediatric Cardiomyopathy Registry.

Elfriede Pahl, Lynn A Sleeper, Charles E Canter, Daphne T Hsu, Minmin Lu, Steven A Webber, Steven D Colan, Paul F Kantor, Melanie D Everitt, Jeffrey A Towbin and 5 more

Abstract readComparative StudyMulticenter Study
In one paragraph

Article in Journal of the American College of Cardiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
9.3field-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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 168 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 11 institutions in 2 countries.

Elfriede PahlChildren's Memorial Hospital, Northwestern University, Chicago, IL 60614, USA. epahl@childrensmemorial.org
Lynn A Sleeper
Charles E Canter
Daphne T Hsu
Minmin Lu
Steven A Webber
Steven D Colan
Paul F Kantor
Melanie D Everitt
Jeffrey A Towbin
John L Jefferies
Beth D Kaufman
James D Wilkinson
Steven E Lipshultz
Pediatric Cardiomyopathy Registry Investigators
Cincinnati Children's Hospital Medical Center · USNew England Research Institutes · USUniversity of Miami · USBoston Children's Hospital · USChildren's Hospital at Montefiore · USHospital for Sick Children · CANorthwestern University · USPrimary Children's Hospital · USUniversity of Pennsylvania · USUniversity of Pittsburgh · USWashington University in St. Louis · US

Funding

PEDIATRIC CARDIOMYOPATHY REGISTRYR01HL053392 · NHLBI · UNIVERSITY OF ROCHESTER · PI LIPSHULTZ, STEVEN EDWARD · 1995 to 2009
$8.3M
NHLBI NIH HHS HL53392NHLBI NIH HHS R01 HL053392
6 · The paper itself

Abstract

objectivesThe purpose of this study was to establish the incidence of and risk factors for sudden cardiac death (SCD) in pediatric dilated cardiomyopathy (DCM).

backgroundThe incidence of SCD in children with DCM is unknown. The ability to predict patients at high risk of SCD will help to define who may benefit most from implantable cardioverter-defibrillators.

methodsThe cohort was 1,803 children in the PCMR (Pediatric Cardiomyopathy Registry) with a diagnosis of DCM from 1990 to 2009. Cumulative incidence competing-risks event rates were estimated. We achieved risk stratification using Classification and Regression Tree methodology.

resultsThe 5-year incidence rates were 29% for heart transplantation, 12.1% non-SCD, 4.0% death from unknown cause, and 2.4% for SCD. Of 280 deaths, 35 were SCD, and the cause was unknown for 56. The 5-year incidence rate for SCD incorporating a subset of the unknown deaths is 3%. Patients receiving antiarrhythmic medication were at higher risk of SCD (hazard ratio: 3.0, 95% confidence interval: 1.1 to 8.3, p = 0.025). A risk stratification model based on most recent echocardiographic values had 86% sensitivity and 57% specificity. Thirty of 35 SCDs occurred in patients who met all these criteria: left ventricular (LV) end-systolic dimension z-score >2.6, age at diagnosis younger than 14.3 years, and the LV posterior wall thickness to end-diastolic dimension ratio <0.14. Sex, ethnicity, cause of DCM, and family history were not associated with SCD.

conclusionsThe 5-year incidence rate of SCD in children with DCM is 3%. A risk stratification rule (86% sensitivity) included age at diagnosis younger than 14.3 years, LV dilation, and LV posterior wall thinning. Patients who consistently meet these criteria should be considered for implantable cardioverter-defibrillator placement.

Indexed as

RegistriesAdolescentCardiomyopathy, DilatedChildChild, PreschoolDeath, Sudden, CardiacEchocardiographyFemaleFollow-Up StudiesHumansIncidenceInfantMaleRetrospective StudiesRisk FactorsSurvival Rate

Identifiers

PMID22300696
PMCPMC3280885
OpenAlexW1507557275

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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.