Myocardial Perfusion and Scarring in Congenital Heart Disease

This is a study of the perfusion of the myocardium in adults with specific forms of repaired
congenital heart disease using established cardiac MRI techniques and correlating perfusion
with clinical outcomes. Our objectives are to examine myocardial perfusion both during stress
and at rest in adults with repaired or palliated congenital heart disease as well as quantify
ventricular function, regional myocardial strain and evidence of myocardial fibrosis with
quantitative measures of myocardial perfusion. The specific aim of this study is to
understand whether clinical subendocardial perfusion defects contribute to the late
decompensation of adult subjects that have single ventricle physiology and adult subjects
that have a systemic right ventricle.

- INCLUSION CRITERIA:

Inclusion Criteria for All Arms of the Protocol:

- Subjects 18 years of age or older

- All defects that have a right ventricle that supports the systemic circulation

- All defects with a functional single ventricle

- Written informed consent

EXCLUSION CRITERIA:

Exclusion Criteria for All Arms of the Protocol:

- Subjects with a contraindication to MRI scanning will be excluded. These
contraindications include subjects with the following devices:

- Central nervous system aneurysm clips

- Implanted neural stimulator

- Implanted cardiac pacemaker or defibrillator

- Cochlear implant

- Ocular foreign body (e.g. metal shavings)

- Implanted Insulin pump

- Metal shrapnel or bullet

- Severe heart damage that makes it difficult to breathe while lying flat

- Pregnant women (Women of childbearing potential who are uncertain as to whether they
are pregnant will be required to have a screening urine or blood pregnancy test)

- Subjects with active symptoms of myocardial ischemia occurring despite maximally
tolerated doses of oral antianginal therapy and intravenous nitroglycerin

Furthermore, the following subject groups will be excluded from studies involving the
administration of MRI contrast agents:

- lactating women unless they are willing to discard breast milk for 24 hours after
receiving gadolinium

- renal disease (estimated glomerular filtration rate [eGFR] < 30 ml/min/1.73 m2 body
surface area)

The eGFR will be used to estimate renal function if reported by the laboratory. Otherwise,
estimated glomerular filtration rate (eGFR) can be based on the Modification of Diet in
Renal Disease (MDRD) study equation (see below) in subjects with stable renal function.
This formula is not applicable to subjects with acute renal insufficiency:

eGFR (ml/min/1.73 m2) = 175 x (serum creatinine)-1.154 x (age)-0.203 x 0.742 (if the
subject is female) x 1.212 (if the subject is black)

Additional Exclusion Criteria for Vasodilator Stress MRI:

- Myocardial infarction within 24 hours

- Uncontrolled heart failure

- Uncontrolled asthma or emphysema

- Ventricular arrhythmia (sustained ventricular arrhythmia at the time of MR scan)

- Second degree heart block or higher