Key result
Transcatheter pulmonary valve implantation with the MyVal transcatheter heart valve achieved 100% procedural success in 7 patients, with no pulmonary regurgitation and acceptable gradients at a median follow-up of 16 months.
Why the study?
TPVI is an alternative to surgery for dysfunctional RVOT conduits, but the MyVal transcatheter heart valve designed for the aortic position had not yet been used for TPVI.
Does transcatheter pulmonary valve implantation with the MyVal transcatheter heart valve improve hemodynamics in patients with dysfunctional stenosed right ventricular outflow tract conduits?
Observational (n=7)
Yes
Does transcatheter pulmonary valve implantation with the MyVal transcatheter heart valve improve hemodynamics in patients with dysfunctional stenosed right ventricular outflow tract conduits?
The MyVal transcatheter heart valve, originally designed for the aortic position, demonstrates early safety and feasibility for transcatheter pulmonary valve implantation in prestented dysfunctional RVOT conduits.
Supports early feasibility of MyVal TPVI after prestenting; hypothesis-generating pending larger prospective data.
BACKGROUND: Transcatheter pulmonary valve implantation (TPVI) is a surgical alternative for correcting dysfunctional right ventricular outflow tract conduits in previously operated patients. MyVal transcatheter heart valve (THV) (Meril Life Sciences, India), a new transcatheter valve designed for aortic position has not been used for TPVI. METHODS: Patients with stenosed dysfunctional conduits from the right ventricle to pulmonary artery (RV-PA) were prestented after initial computed tomography and balloon interrogation before the implantation of MyVal. Size of MyVal was chosen based on the final diameter of the prestent. Procedural details and post-TPVI follow-up were analyzed. RESULTS: Seven patients aged 17-60 years (median 26 years) had stenosed RV-PA conduits implanted 5-17 years (median 9 years) ago for tetralogy of Fallot in three, following Ross procedure in two, repair of pulmonary stenosis, and following PA debanding in one patient each. Prestenting improved the conduit diameter from 9.3 ± 2.8 mm to 20.8 ± 1.1 mm and relieved the gradient from 87.3 ± 31.7 mmHg (50-137 mmHg) to 12.7 ± 6.4 mmHg (5-20 mmHg). A 23 mm MyVal was implanted in all the seven patients successfully; one patient needed an additional 24.5 mm MyVal valve in valve implantation for residual regurgitation. The mean fluoroscopic time and dose area product were 38.7 ± 25.3 min and 66.917 ± 39.211Gray. cm2, respectively. At a median follow-up duration of 16 months (10-22 months), all patients were asymptomatic receiving dual antiplatelet therapy with no PR and the gradient was 12.5 ± 5.8 mmHg on echocardiography. Although one patient needed an additional valve-in-valve implantation, there were no valve-related adverse events. CONCLUSIONS: Early experience of TPVI with MyVal THV in prestented conduits is encouraging with procedural success in all patients and acceptable mid-term outcomes.
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Sivaprakasam et al. (2021) conducted an observational in Dysfunctional stenosed right ventricular outflow tract conduits (n=7). MyVal transcatheter heart valve was evaluated on Procedural success. Transcatheter pulmonary valve implantation with the MyVal transcatheter heart valve achieved 100% procedural success in 7 patients, with no pulmonary regurgitation and acceptable gradients at a median follow-up of 16 months.
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