Enhanced External Counterpulsation in Patients With Fontan Circulation
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Details and patient eligibility
About
The purpose of the proposed study is to determine the safety of enhanced external counterpulsation (EECP), a system for compressing the blood vessels in the legs in synchrony with an individual's cardiac rhythm, in clinically well, adult Fontan patients, to document the acute hemodynamic and myocardial effects of EECP on the Fontan circulation, and to demonstrate acute changes in endothelial function after one hour of the procedure.
Full description
The investigators plan to study the effects of enhanced external counterpulsation (EECP), on patients who have had Fontan surgery for treatment of complex congenital heart disease. Eligible patient volunteers will undergo a series of biophysical measurements at rest including echocardiographic assessment of ventricular function, pulmonary blood flow/cardiac output measurement using an inert gas rebreathing method (Innocor), and measurements of biomarkers of endothelial function (ET-1, NOx). Patients will then undergo 1 hour of treatment with EECP, during which additional echocardiographic assessment of ventricular function and pulmonary blood flow/cardiac output measurements will be performed at multiple levels of leg compression. Subjects will be assessed periodically for adverse effects and discomfort during the EECP treatment. At the completion of treatment, patients will be allowed 30 minutes to rest before undergoing one more echocardiographic assessment of ventricular function, pulmonary blood flow/cardiac output measurement, and measurements of biomarkers of endothelial function (ET-1, NOx). Measurements made during and after treatment will be compared to baseline measurements.
Enrollment
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Ages
Volunteers
Inclusion criteria
- Individuals with Fontan physiology being seen in the Boston Children's Hospital cardiology clinic for outpatient care.
Exclusion criteria
- Current pregnancy
- Decompensated heart failure/pulmonary edema
- Severe aortic insufficiency
- Active tachyarrhythmias
- Frequent atrial or ventricular ectopy
- Symptomatic peripheral vascular disease
- Thrombophlebitis or history of deep vein thrombosis or stasis ulcer
- Aortic aneurysm
- Uncontrolled hypertension (systolic blood pressure >180 mmHg or diastolic blood pressure>110 mmHg)
- Systolic blood pressure <90 mmHg
- Active femoral site bleeding or hematoma
Trial design
Primary purpose
Allocation
Interventional model
Masking
23 participants in 1 patient group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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