Evidence map›Paper›PMID 40241091›Full record

ArticleBMC pediatrics2025

A case of complete atrioventricular septal defect in which extracorporeal membrane oxygenation could be removed after performing the bilateral Glenn procedure for severe cardiac dysfunction after tricuspid valve replacement: a case report.

Hiroki Ishii, Yu Matsumura, Yuji Hamamichi, Yuya Komori, Naoki Wada, Tadahiro Yoshikawa

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In one paragraph

Article in BMC pediatrics, 2025. 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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5 · Who and what money

Authors and funding

6 authors.

Hiroki IshiiDepartment of Pediatric Cardiology, Sakakibara Heart Institute, 3-16-1 Asahi-cho, Fuchu-shi, Tokyo, 183-0003, Japan. h.ishii19810814@gmail.com.
Yu MatsumuraDepartment of Pediatric Cardiology, Sakakibara Heart Institute, 3-16-1 Asahi-cho, Fuchu-shi, Tokyo, 183-0003, Japan.
Yuji HamamichiDepartment of Pediatric Cardiology, Sakakibara Heart Institute, 3-16-1 Asahi-cho, Fuchu-shi, Tokyo, 183-0003, Japan.
Yuya KomoriDepartment of Pediatric Cardiovascular Surgery, Sakakibara Heart Institute, 3-16-1 Asahi-cho, Tokyo, 183-0003, Japan. kkomori@shi.heart.or.jp.
Naoki WadaDepartment of Pediatric Cardiovascular Surgery, Sakakibara Heart Institute, 3-16-1 Asahi-cho, Tokyo, 183-0003, Japan. nwada@shi.heart.or.jp.
Tadahiro YoshikawaDepartment of Pediatric Cardiology, Sakakibara Heart Institute, 3-16-1 Asahi-cho, Fuchu-shi, Tokyo, 183-0003, Japan. tayoshi@shi.heart.or.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundComplete atrioventricular septal defect (AVSD) is a congenital heart disease (CHD) in which patients require surgery in early infancy. Tricuspid valve regurgitation (TR) is a complication that can occur a long time after intracardial repair for AVSD, and surgical intervention is occasionally necessary. However, to date, there have been no reports of TR occurring in the acute phase after surgery for AVSD in infancy. In addition, the mortality rate is high for patients with severe symptomatic TR who undergo surgical intervention to correct the tricuspid valve position. CASE PRESENTATION: The patient was a 17-year-old adolescent girl with severe scoliosis, who was diagnosed as having complete AVSD in the neonatal period owing to a heart murmur detected after birth. The 2-patch repair method was performed at 2-months old, but severe TR was presented from an early phase after the operation. In addition, myxomatous degeneration of the atrioventricular valve was observed as an intraoperative finding. Subsequently, the patient was admitted to our hospital owing to chest discomfort at 17-years old, and tricuspid valve replacement (TVR) was performed. As substantial deterioration of cardiac contraction was observed after the TVR, the patient was placed on extracorporeal membrane oxygenation (ECMO). However, because it was subsequently difficult to remove the patient from ECMO, the bilateral Glenn procedure was performed to increase right ventricular (RV) protection. After the bilateral Glenn procedure, the patient's cardiac contractile function improved, and she could be taken off ECMO. The patient began treatment with 2new types of therapeutic agents for heart failure, and was discharged from our hospital on the 305th hospital day.

conclusionsIf severe TR appears in a patient, it is important to intervene surgically at the asymptomatic phase with no dilatation of the RA. However, in cases of severe symptomatic TR in patients with CHD, the Glenn procedure might be a useful treatment strategy to increase RV protection. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Extracorporeal Membrane OxygenationFontan ProcedureHeart Septal DefectsHeart Valve Prosthesis ImplantationPostoperative ComplicationsTricuspid ValveTricuspid Valve InsufficiencyAdolescentFemaleHumansAtrial fibrillationBilateral Glenn procedureComplete atrioventricular septal defectExtracorporeal membrane oxygenationSevere scoliosisSevere tricuspid regurgitationTricuspid valve replacementValvular myxomatous degeneration

Identifiers

PMID40241091
PMCPMC12001506

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