Tb. Levine et al., IMPACT OF MEDICAL THERAPY ON PULMONARY-HYPERTENSION IN PATIENTS WITH CONGESTIVE-HEART-FAILURE AWAITING CARDIAC TRANSPLANTATION, The American journal of cardiology, 78(4), 1996, pp. 440-443
Pulmonary artery (PA) hypertension in transplant recipients increases
mortality from right heart failure following heart transplantation. We
examined the impact of long-term medical therapy on the severity of P
A hypertension in patients with end-stage congestive heart failure on
a transplant waiting list. The initial and final, quarterly right hear
t catheterization data on 60 patients (50 men, aged 50 +/- 9 years, Ne
w York Heart Association class III to IV) awaiting heart transplantati
on were analyzed and the patients divided into 2 groups: group A, thos
e with persistent elevated systolic PA pressures throughout the 10-mon
th follow-up (n = 31 of 60), and group B, those who had any decrease i
n systolic PA pressure during that period (n = 29 of 60). Group A had
no change in hemodynamics. Group B had a significant decrease (+/- SD)
in right atrial (11 +/- 7 to 5 +/- 4 mm Hg), PA (57 +/- 11 to 37 +/-
11 mm Hg), and PA wedge (25 +/- 9 to 14 +/- 7 mm Hg) pressures, with i
ncreases in cardiac output (3.8 +/- 0.9 to 4.7 +/- 1.1 L/min) and elec
tion fraction (18 +/- 6% to 27 +/- 11%) (p <0.05). The combined end po
int of transplant or death occurred in 28 of 31 patients (90%) in grou
p A versus 14 of 29 (50%) in group B (p = 0.0004). Ischemic etiology w
as present in 71% of patients in group A versus 68% with idiopathic di
lated cardiomyopathy in group B (p = 0.003). The reversibility of PA h
ypertension rather than its initial severity is predictive of patient
clinical outcome. Idiopathic, as opposed to ischemic, cardiomyopathy r
esponds better to medical therapy.