Evidence map›Paper›PMID 42005013›Full record

ArticleInternational journal of cardiology. Congenital heart disease2026

Complications after percutaneous device closure of atrial septal defects in children: Prevalence, outcomes and associated factors.

Michael N Gritti, Olivia Carere, Brian W McCrindle, Rajiv R Chaturvedi, Lee N Benson

Abstract read
In one paragraph

Article in International journal of cardiology. Congenital heart disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

5 authors.

Michael N GrittiTemerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Olivia CarereTemerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Brian W McCrindleTemerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Rajiv R ChaturvediTemerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Lee N BensonTemerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Atrial septal defects (ASDs) represent 10% of congenital heart disease. Transcatheter closure is the standard of care for anatomically suitable defects, but pediatric long-term outcomes remain underreported. This study examined the prevalence, outcomes, and risk factors for complications following ASD device closure in children. Methods: We retrospectively reviewed children <18 years undergoing transcatheter ASD closure at a single tertiary center (1989-2016). Demographic, procedural, and follow-up data were analyzed. Kaplan-Meier methods assessed freedom from major complications and associations with device type, imaging technique, and concomitant congenital heart disease (CHD). Results: A total of 971 children (mean age 8.2 ± 4.2 years, 62% female) underwent closure, with median follow-up 2.2 years (maximum 20.7). Concomitant CHD was present in 33%. Major complications occurred in 1.6%, including device embolization (0.6%), erosion (0.4%), and urgent surgery (0.6%). Rates were highest with early-era devices (8%). Kaplan-Meier analysis showed freedom from major complications of 98.1% at 5 years and 97.6% at 10 years. No significant differences were observed by imaging modality (ICE vs. TEE) or presence of concomitant CHD. Conclusions: In this large pediatric cohort, transcatheter ASD closure was associated with low rates of major complications and excellent long-term outcomes. Neither concomitant CHD nor imaging technique significantly affected complication risk. These findings reinforce the long-term safety of ASD device closure in children.

Indexed as

Atrial septal defectComplicationsCongenital heart defectLong-term outcomesPediatricsTranscatheter closure

Identifiers

PMID42005013
PMCPMC13091151

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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.