To examine patients with hypertrophic obstructive cardiomyopathy (HOCM) before and after septal alcohol ablation, to investigate the effect of the treatment in regards to changes in myocardial function, perfusion, invasive hemodynamics and exercise tolerance.
Patients with HOCM who develop symptoms of heart failure are treated initially with non-vasodilating ß-blockers or verapamil to decrease myocardial contractility and heart rate. A substantial part of patients remain symptomatic despite medical treatment. In these patients interventional or surgical treatments (septal reduction therapies (SRT)) to reduce left ventricular outflow tract obstruction (LVOTO) is considered in the presence of moderate to-severe symptoms (New York Heart Association - functional class (NYHA) III-IV) and/or recurrent exertional syncope and an LVOTO gradient ≥50 mm Hg. In some centers, invasive therapy is also considered in patients with mild symptoms (NYHA Class II) who have a resting or maximum provoked gradient of ≥50 mm Hg (with exercise or Valsalva's maneuver) and moderate-to-severe mitral valve regurgitation. Advanced treatment options are alcohol septal ablation (ASA) or surgical myectomy often combined with mitral valve reconstructive surgery. These treatments have similar outcomes in terms of gradient reduction, symptom improvement and exercise capacity No previous trials have examined the effect of ASA in HOCM with respect to changes in central hemodynamics and myocardial performance during exercise. 24 HOCM patients will be examined prior to ASA, and approximately six-nine months after ASA. The examination set-up consists of simultaneous 1) transthoracic echocardiography (TTE), 2) right heart catheterization (RHC) and 3) cardiopulmonary exercise test (CPX).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
24
injection of 1-4 mL of 96% ethanol into a septal perforator of the left anterior coronary artery to produce a myocardial infarction
Aarhus University Hospital, Department of Cardiology
Aarhus N, Danmark, Denmark
Pulmonary capillary wedge pressure (PCWP) during exercise
Change in PCWP at 75 watt (or maximum exercise, if this is \< 75 W)
Time frame: Changes will be evaluated after an expected average of 6-9 months after treatment
Pulmonary capillary wedge pressure (PCWP) at rest
Changes in PCWP at rest
Time frame: Changes will be evaluated after an expected average of 6-9 months after treatment
Peak oxygen uptake (VO2-max)
Changes in maximal oxygen consumption (L/min) measured during cardiopulmonary exercise test
Time frame: Changes will be evaluated after an expected average of 6-9 months after treatment
Work capacity
work capacity measured in watt during a cardiopulmonary exercise test
Time frame: Changes will be evaluated after an expected average of 6-9 months after treatment
LVOT gradient during maximum exercise
Changes of the LVOT gradient during maximum exercise, measured in mmHg during 2D echocardiography
Time frame: Changes will be evaluated after an expected average of 6-9 months after treatment
Coronary flow reserve
Changes in the ratio of maximum coronary blood flow (induced by infusion of adenosin) to resting coronary blood flow, estimated by 2D doppler echocardiography
Time frame: Changes will be evaluated after an expected average of 6-9 months after treatment
Changes in biomarkers
Changes in N-terminal pro-brain natriuretic peptide (NT-proBNP) ng/l and troponin T ng/l
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Time frame: Changes will be evaluated after an expected average of 6-9 months after treatment
Change in GLS (%) at peak exercise
Change in global longitudinal strain (GLS) in % at peak exercise
Time frame: Changes will be evaluated after an expected average of 6-9 months after treatment
Changes of symptoms and quality of life estimated by KCCQ
Changes of symptoms and quality of life with Kansas City Cardiomyopathy Questionnaire (KCCQ) assessed by clinical evaluation
Time frame: Changes will be evaluated after an expected average of 6-9 months after treatment