Author/Authors :
Wartak, Siddharth Department of Cardiology - Maimonides Medical Center, Brooklyn, USA , Akkad, Isaac Department of Medicine - Maimonides Medical Center, Brooklyn, USA , Sadiq, Adnan Department of Cardiology - Maimonides Medical Center, Brooklyn, USA , Crooke, Gregory Department of Interventional Cardiology - Maimonides Medical Center, Brooklyn, USA , Moskovits, Manfred Department of Cardiology - Maimonides Medical Center, Brooklyn, USA , Frankel, Robert Department of Interventional Cardiology - Maimonides Medical Center, Brooklyn, USA , Hollander, Gerald Department of Cardiology - Maimonides Medical Center, Brooklyn, USA , Shani, Jacob Department of Interventional Cardiology - Maimonides Medical Center, Brooklyn, USA
Abstract :
A 23-year-old African American woman with a past medical history of systemic lupus erythematous (SLE), secondary hypertension,
and end stage renal disease (ESRD) on hemodialysis for eight years was stable until she developed symptomatic severe mitral
regurgitation with preserved ejection fraction. She underwent a bioprosthetic mitral valve replacement (MVR) at outside hospital.
However, within a year of her surgery, she presented to our hospital with NYHA class IV symptoms. She was treated for heart failure
but in view of her persistent symptoms and low EF was considered for heart and kidney transplant. This was a challenge in view of
her history of lupus.We presumed that her stenosis of bioprosthetic valve was secondary to lupus and renal disease.We hypothesized
that her low ejection fraction was secondary to mitral stenosis and potentially reversible. We performed a dobutamine stress
echocardiogram, which revealed an improved ejection fraction to more than 50% and confirmed preserved inotropic contractile
reserve of her myocardium. Based on this finding, she underwent a metallic mitral valve and tricuspid valve replacement. Following
surgery, her symptoms completely resolved. This case highlights the pathophysiology of lupus causing stenosis of prosthetic valves
and low ejection cardiomyopathy.