# Biventricular reverse remodelling achieved through combined surgical and optimal medical therapy in an adolescent female post-Rastelli procedure: a case report

**Authors:** Natsumi Kashimura, Tomohiro Kaneko, Takao Kato, Sakiko Miyazaki, Tohru Minamino

PMC · DOI: 10.1093/ehjcr/ytaf215 · European Heart Journal. Case Reports · 2025-04-28

## TL;DR

A 19-year-old woman with complex heart disease and a viral infection showed significant heart improvement through surgery and optimized medication.

## Contribution

Demonstrates successful biventricular reverse remodelling using combined surgical and medical therapy in a complex ACHD case.

## Key findings

- Combined surgical and medical therapy improved biventricular function in a post-Rastelli patient.
- Ivabradine and newer drugs like vericiguat and SGLT-2 inhibitors contributed to cardiac recovery.
- Chronic Epstein-Barr virus infection was identified as a contributing factor to heart failure.

## Abstract

Advances in medical treatments have allowed many congenital heart disease patients to reach adulthood, resulting in an increase in adult congenital heart disease (ACHD) cases. Managing heart failure (HF) in ACHD patients is a significant concern, particularly due to limited understanding of optimal pharmacological therapies. Conduit dysfunction and right heart failure are common in the late phase after the Rastelli procedure, but right HF is not well understood, and standard medications for acquired HF are not particularly effective. Consequently, there is a knowledge gap regarding optimal treatment strategies.

We report the case of a 19-year-old woman with a history of Blalock–Taussig shunt, Rastelli procedure, and reoperation for conduit stenosis. She was diagnosed with chronic active Epstein–Barr virus infection and admitted due to exertional dyspnoea and orthopnoea. On admission, she exhibited signs of acute HF with severe left ventricular dysfunction and conduit stenosis. Initial management with diuretics was insufficient, requiring inotropic support. Right heart catheterization revealed conduit failure, necessitating surgical replacement. Postoperatively, optimized medical therapy, including beta-blockers, ivabradine, vericiguat, and SGLT-2 inhibitors, was administered. Over several months, her biventricular function improved significantly, and she underwent umbilical cord blood transplantation for EBV infection, with a favourable outcome.

This case highlights the importance of combining surgical and pharmacological strategies in managing complex ACHD with biventricular dysfunction. Identifying underlying causes, such as chronic myocarditis due to EBV infection, is crucial. Ivabradine allowed for beta-blocker increase, and with newer agents like vericiguat and SGLT-2 inhibitors, significantly improved cardiac function.

## Linked entities

- **Chemicals:** ivabradine (PubChem CID 132999), vericiguat (PubChem CID 54674461)
- **Diseases:** congenital heart disease (MONDO:0005453), heart failure (MONDO:0005252), Epstein-Barr virus infection (MONDO:0005111)

## Full-text entities

- **Genes:** SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, NR3C2 (nuclear receptor subfamily 3 group C member 2) [NCBI Gene 4306] {aka MCR, MLR, MR, NR3C2VIT}
- **Diseases:** dizziness (MESH:D004244), biventricular reverse remodelling (MESH:D020257), HF (MESH:D006333), LVD (MESH:D018487), Conduit dysfunction (MESH:D006331), tetralogy of Fallot (MESH:D013771), ACHD (MESH:D006330), cardiomyopathy (MESH:D009202), Tachycardia (MESH:D013610), ventricular septal defect (MESH:D006345), inflammatory (MESH:D007249), hypoplasia of the left pulmonary artery (MESH:D000071079), pulmonary valve stenosis (MESH:D011666), EBV infection (MESH:D020031), electrical dyssynchrony (MESH:D004556), fever (MESH:D005334), sinus tachycardia (MESH:D013616), myocardial necrosis (MESH:D009336), aortic regurgitation (MESH:D001022), interstitial (MESH:D065167), cyanosis (MESH:D003490), hypotension (MESH:D007022), oedema (MESH:C536897), hyponatremia (MESH:D007010), atrial septal defect (MESH:D006344), pleural effusion (MESH:D010996), right ventricular dysfunction (MESH:D018497), cardiomegaly (MESH:D006332), LGE (MESH:C564835), conduit failure (MESH:D051437), right bundle brunch block (MESH:D002037), biventricular dysfunction (MESH:D018754), chronic (MESH:D002908), conduit stenosis (MESH:D003251), malposition of (MESH:D017760), low cardiac output (MESH:D002303), myocarditis (MESH:D009205)
- **Chemicals:** carvedilol (MESH:D000077261), Furosemide (MESH:D005665), aldosterone (MESH:D000450), Gore-Tex (MESH:D011138), Bisoprolol (MESH:D017298), Ivabradine (MESH:D000077550), Vericiguat (MESH:C000603960), bilirubin (MESH:D001663), empagliflozin (MESH:C570240), spironolactone (MESH:D013148), oxygen (MESH:D010100), losartan (MESH:D019808), tolvaptan (MESH:D000077602), If-channel (-), dobutamine (MESH:D004280), lactate (MESH:D019344)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12076148/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12076148/full.md

## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12076148/full.md

---
Source: https://tomesphere.com/paper/PMC12076148