Evidence map›Paper›PMID 42599515›Full record

ArticlePediatric cardiology2026

Survival Benefit and Persistent Hospitalization Burden After Ventricular Septal Defect Closure in Infants with Trisomy 18 Headings: Hospitalization After VSD Closure in Trisomy 18.

Hiroyuki Nagao, Takamichi Uchiyama, Shintaro Nemoto

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Article in Pediatric cardiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

3 authors.

Hiroyuki NagaoDepartment of Pediatrics, Takatsuki General Hospital, Osaka, Japan.
Takamichi UchiyamaUchiyma Kids Clinic, Osaka, Japan.
Shintaro NemotoDepartment of Thoracic and Cardiovascular Surgery, Osaka Medical and Pharmaceutical University, Osaka, Japan. snemoto@ompu.ac.jp.ORCID https://orcid.org/0000-0001-6995-9760

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This retrospective study evaluated the impact of ventricular septal defect (VSD) closure on long-term survival and hospitalization status in infants with trisomy 18. Thirty-three infants with trisomy 18 and VSD (2002-2025) were categorized into three groups: staged VSD closure following pulmonary artery banding (PAB) (n = 7), PAB alone (n = 3), or non-surgical management (n = 23). Median follow-up durations (interquartile range) were 124.6 (75.8-153.1), 17.8 (11.4-18.1), and 17.1 (2.7-59.3) months, respectively. Kaplan-Meier analysis demonstrated significantly better survival in the VSD closure group (log-rank p = 0.009). However, these survivors required frequent unexpected hospitalizations for non-cardiac comorbidities. In univariate negative binomial regression, respiratory and digestive complications were significantly associated with higher unexpected admission rates (incidence rate ratio [IRR] = 1.07, 95% confidence interval [CI]: 1.02-1.12; and IRR = 1.24, 95% CI: 1.08-1.41, respectively; p < 0.01). After multivariable adjustment, only digestive complications showed a notable, though non-significant, trend (IRR = 1.15, 95% CI: 0.98-1.36, p = 0.09). Notably, VSD closure was associated with a higher admission rate in univariate analysis (IRR = 1.95, 95% CI: 0.95-4.00, p = 0.07), but this association disappeared after multivariable adjustment. VSD closure was associated with improved survival in infants with trisomy 18, but a substantial hospitalization burden persisted due to non-cardiac comorbidities. These findings highlight the importance of lifelong multidisciplinary care and detailed parental counseling regarding the expected long-term medical burden following VSD closure.

Indexed as

Cardiac surgeryHospitalizationLong-term survivalRespite careTrisomy 18Ventricular septal defect

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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.