A Study to Evaluate Long-term Outcomes of Alcohol Septal Ablation for Hypertrophic Cardiomyopathy

Overview

Información sobre este estudio

The purpose of this study is to determine long term vital status, symptoms, and need for repeat procedure after alcohol septal ablation, to determine patient and procedural factors associated with successful alcohol septal ablation and need for repeat procedure, and to determine the impact of conduction abnormalities after alcohol septal ablation on long-term outcomes.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • All patients 18 years or older that were evaluated at the Mayo Cardiomyopathy Clinic and underwent septal ablation between 1998 – 02/28/2019 at Mayo Clinic.
  • Each patient met the following criteria to be considered for septal ablation:
    • severe, drug-refractory cardiovascular symptoms, which was defined New York Heart Association class III/IV dyspnea, Canadian Cardiac Society angina class III/IV, or disabling syncope; 
    • dynamic LVOT obstruction due to systolic anterior motion of the mitral valve, with an LVOT gradient ≥ 30 mm Hg at rest or ≥ 50 mm Hg with provocation (e.g., Valsalva strain, amyl nitrate inhalation, and postectopic beat analysis); 
    • ventricular septal thickness ≥ 15 mm; 
    • no significant intrinsic mitral valve disease; 
    • absence of need for concomitant cardiac surgical procedure (e.g., bypass grafting and valve replacement);
    • suitable coronary anatomy; and 
    • informed patient consent.
    • The choice of alcohol septal ablation or surgical myectomy was made through a shared decision-making process after discussion of the risks of benefits of each alternative.

Exclusion Criteria: 

  • Patients who underwent septal ablation for purposes other than relieving severe dynamic LVOT obstruction (e.g., in preparation of transcatheter mitral valve replacement).

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Mackram Eleid, M.D.

Comunícate con nosotros para obtener el estatus más reciente

Contact information:

Mackram Eleid M.D.

(507)293-6168

Eleid.Mackram@mayo.edu

More information

Publicaciones

Publications are currently not available