| Literature DB >> 29062383 |
Akbar Molaei1, Abbas Afrasiabi1, Eisa Bilejani1, Mahmud Samadi1.
Abstract
Ventricular septal defects (VSDs) are among the most common congenital cardiac lesions. Large defects at apicomuscular regions, especially in young patients, are far from accessible to surgeons for conventional surgery. Moreover, the transcatheter closure of VSDs in these patients is difficult and carries a high risk of complications because of the large sheath size relative to the patient's size. The periventricular approach simplifies VSD closure and, thus, eliminates the potential complications of cardiac catheterization and fluoroscopy as it is performed under echocardiographic guidance. A 3-year-old girl with a body weight of 11 kg (failure to thrive) was referred to us. She had multiple adjacent apicomuscular VSDs, the largest one being about 19 mm in diameter, and subsystemic pulmonary artery pressure (PAP). The patient underwent periventricular apicomuscular VSD closure with a Lifetech muscular VSD occluder (size 22 mm) under epicardial echocardiography guidance without cardiopulmonary bypass. Post procedure, the PAP was decreased to mild level. The residual shunt was mild across the adjacent small defects. She was discharged after 7 days without complications. At 2 years' follow-up, the patient was hemodynamically stable and had a normal PAP (PAP = about 16 mmHg) by transthoracic echocardiographic assessment.Entities:
Keywords: Echocardiography; Heart defects, congenital; Heart septal defects, ventricular
Year: 2017 PMID: 29062383 PMCID: PMC5643873
Source DB: PubMed Journal: J Tehran Heart Cent ISSN: 1735-5370
Figure 1Parasternal short-axis view of the heart by epicardial echocardiography shows the large apicomuscular VSD.
Figure 2Apical 4-chamber view by epicardial echocardiography shows the device at the position of apicomuscular defect after defect closure via the periventricular procedure.
Figure 3Continuous wave Doppler tracing of the pulmonary valve of the patient by transthoracic echocardiography at 2 years’ follow up shows mild pulmonary valve insufficiency with a 16 mmHg pressure gradient.