Myocardial Perfusion in Hypoplastic Left Heart Syndrome

Carsten Rickers1, Philip Wegner2, Michael Silberbach3

  • 1University Heart Center, Adult Congenital Heart Disease Unit, University Hospital Hamburg-Eppendorf, Hamburg, Germany (C.R.).

Insights

Hypoplastic left heart syndrome (HLHS) patients show impaired coronary microcirculation in their systemic ventricle compared to healthy controls. Early intervention may improve outcomes by addressing HLHS-specific risk factors for microvascular dysfunction.

Area of Science:

  • Cardiology
  • Pediatric Cardiology
  • Cardiovascular Imaging

Background:

  • The coronary microcirculation of the systemic right ventricle in hypoplastic left heart syndrome (HLHS) is poorly understood.
  • HLHS patients in Fontan circulation may have unique pathophysiological characteristics affecting the systemic right ventricle's coronary microcirculation.

Purpose of the Study:

  • To quantify myocardial blood flow (MBF) using cardiac magnetic resonance imaging (CMR) in HLHS patients.
  • To evaluate determinants of microvascular coronary dysfunction and myocardial ischemia in HLHS.

Main Methods:

  • 119 HLHS patients and 34 controls underwent CMR approximately 1.8 years post-total cavopulmonary connection (TCPC).
  • Assessed right ventricular volumes and function, myocardial perfusion, fibrosis, and late gadolinium enhancement (LGE) in four HLHS subtypes.
  • Quantified resting and hyperemic MBF; estimated coronary conductance from MBF and aortic pressure.

Main Results:

  • HLHS patients had lower hyperemic MBF than controls (1.89 vs. 2.70 mL/g/min; P<0.001).
  • Risk factors for reduced hyperemic MBF included specific HLHS subtypes, LGE, RV diastolic dysfunction, and older age at TCPC.
  • Coronary conductance correlated negatively with systemic oxygen saturation (r=-0.29; P=0.02); LGE frequency increased with age at TCPC.

Conclusions:

  • Young HLHS patients exhibit distinct coronary microcirculation differences compared to controls.
  • Identified HLHS-specific risk factors for microvascular dysfunction.
  • Early relief of cyanosis via TCPC may benefit HLHS patients.
Abstract