Evidence map›Paper›PMID 39854275›Full record

ArticleInterdisciplinary cardiovascular and thoracic surgery2025

Closure of ventricular septal defect in children with trisomy 18: perioperative events and long-term survival.

Shintaro Nemoto, Kanta Kishi, Hayato Konishi, Akiyo Suzuki, Takahiro Katsumata, Noriyasu Ozaki, Yutaka Odanaka, Atsuko Ashida, Takamichi Uchiyama, Kenji Mine

Abstract read
In one paragraph

Article in Interdisciplinary cardiovascular and thoracic surgery, 2025. 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

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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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Shintaro NemotoDepartment of Thoracic and Cardiovascular Surgery, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, Japan.ORCID 0000-0001-6995-9760
Kanta KishiDepartment of Pediatrics, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, Japan.
Hayato KonishiDepartment of Thoracic and Cardiovascular Surgery, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, Japan.
Akiyo SuzukiDepartment of Thoracic and Cardiovascular Surgery, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, Japan.ORCID 0000-0002-4963-3138
Takahiro KatsumataDepartment of Thoracic and Cardiovascular Surgery, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, Japan.
Noriyasu OzakiDepartment of Pediatrics, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, Japan.
Yutaka OdanakaDepartment of Pediatrics, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, Japan.
Atsuko AshidaDepartment of Pediatrics, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, Japan.
Takamichi UchiyamaUchiyama Kids Clinic, Takatsuki, Osaka, Japan.
Kenji MineDepartment of Pediatrics, Kansai Medical University, Hirakata, Osaka, Japan.

Funding

Miyata Foundation Bounty for Paediatric Cardiovascular Research 2021-8
6 · The paper itself

Abstract

objectivesThis retrospective study aimed to investigate the feasibility of surgical closure of ventricular septal defect in children with trisomy 18 by assessing perioperative events and long-term survival.

methodsFrom April 2008 to March 2024, 41 consecutive patients were referred to us for ventricular septal defect surgery. The defect was closed in 35 patients at the end (median age, 16 months; median body weight, 5.7 kg), 31 out of 37 patients after the preceding pulmonary artery banding according to our staged surgery policy and 4 patients without the banding. Sixty-five significant non-cardiac lesions existed concurrently, and 14 patients underwent tracheostomy before closure. The investigation was conducted by checking medical records and contacting the primary physician.

resultsFour patients died during the inter-stage after banding to closure (10.8%). Two of them were awaiting closure. Concomitant surgeries, 15 right ventricular muscle resections, or 1 arch repair, were performed along with closure. Arrhythmia was the most common adverse event (51.4%). Three patients required extracorporeal membrane oxygenation support. Transient but severe hepatic injury occurred in 11 patients (31.4%). There were two hospital death (5.7%) due to severe respiratory insufficiency or fulminant sepsis. Five patients died after discharge, three pneumonia and two sudden death, resulting in a 5-year estimated survival of 79.5%. Three hepatoblastoma and one hepatoangioma developed, but complete remission was achieved in all patients.

conclusionsAlthough further studies are mandatory, surgical closure of ventricular septal defect may be an effective treatment option even for children with trisomy 18.

Indexed as

long-term survivalpulmonary artery bandingtrisomy 18ventricular septal defect closure

Identifiers

PMID39854275
PMCPMC11802472

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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.