Evidence map›Paper›PMID 42036706›Full record

ArticleJournal of cardiothoracic surgery2026

Multiple ventricular septal defects and severe tricuspid regurgitation in an infant - a case report and surgical dilemma.

Neerod Kumar Jha, Aleksandr Omelchenko, Ashutosh Goyal, Juan Pablo Montiel, Naveen Raj Hosabettu

Abstract readCase Reports
In one paragraph

Article in Journal of cardiothoracic surgery, 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Neerod Kumar JhaDivision of Paediatric Cardiac Surgery, Sheikh Khalifa Medical City, Abu Dhabi, United Arab Emirates. nk_jha@hotmail.com.
Aleksandr OmelchenkoDivision of Paediatric Cardiac Surgery, Sheikh Khalifa Medical City, Abu Dhabi, United Arab Emirates.
Ashutosh GoyalDivision of Paediatric Cardiology, Sheikh Khalifa Medical City, Abu Dhabi, United Arab Emirates.
Juan Pablo MontielDivision of Paediatric Cardiac Surgery, Sheikh Khalifa Medical City, Abu Dhabi, United Arab Emirates.
Naveen Raj HosabettuCardiac Anaesthesiology, Sheikh Khalifa Medical City, Abu Dhabi, United Arab Emirates.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVentricular septal defect is the most prevalent form of congenital heart disease, occurring as isolated lesion in approximately 20% of cases and as part of more complex malformations in up to 40%. Multiple ventricular septal defects are usually associated with "Swiss Cheese" variant characterized by multiple perforations throughout the muscular septum, often involving the apical, mid-muscular, and anterior regions, which creates a complex network of left-to-right shunts that are technically difficult to identify and close individually. Presence of severe tricuspid regurgitation contributes to risks related to poor prognosis. An infant with congestive heart failure, severe tricuspid regurgitation, large left-to-right shunting and elevated right ventricular pressure requires a critical decision-making process for surgical management due to higher risks and poor outcome. CASE PRESENTATION: We are presenting herewith a six-month-old infant with Holt-Oram syndrome, who presented with classic signs of congestive heart failure, tachypnoea, poor weight gain and hepatomegaly, all indicative of systemic and pulmonary venous congestion. Chest x-ray and echocardiography confirmed the diagnosis. Despite aggressive medical management the patient's condition continued to deteriorate and required surgical intervention. The traditional management paradigm for such infants involves a choice between palliative pulmonary artery banding or surgical closure. In this case, both options presented significant risks and were deemed suboptimal. Therefore, to avoid risks, we opted a minimal invasive perventricular device closure of the defects with success.

conclusionsChildren with severe tricuspid regurgitation, right ventricular failure, Swiss cheese morphology, multiple ventricular septal defects, genetic disorders and low weight may be considered for minimal invasive approaches including perventricular device closure of the ventricular septal defects whenever feasible to avoid operative risks and offer better outcomes.

Indexed as

Cardiac Surgical ProceduresHeart Septal Defects, VentricularTricuspid Valve InsufficiencyEchocardiographyHumansInfantMaleCardiacCongestive heart failureDeviceEchocardiographyPerventricularSwiss cheeseTricuspid regurgitationVentricular septal defect

Identifiers

PMID42036706
PMCPMC13262371

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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.