Le. Wagoner et al., IMMUNOSUPPRESSIVE THERAPY, MANAGEMENT, AND OUTCOME OF HEART-TRANSPLANT RECIPIENTS DURING PREGNANCY, The Journal of heart and lung transplantation, 12(6), 1993, pp. 993-1000
To evaluate challenges facing heart transplant recipients who become p
regnant, we surveyed 194 heart transplantation centers and reviewed th
e literature. Thirty-two known pregnancies in heart (n = 29) or heart-
lung (n = 3) allograft recipients have resulted in 29 children, includ
ing two sets of twins. The method of delivery was most often vaginal (
cesarean section rate was 33%), and premature delivery was common (41%
). The onset of pregnancy from the time of transplantation was 2.6 +/-
0.3 years, with the age at conception ranging from 19 to 35 years. Hy
pertension (44%), premature labor (30%), and preeclampsia (22%) were t
he most frequent maternal complications. Four patients experienced a w
orsening of ongoing chronic renal insufficiency; four patients experie
nced infections during pregnancy, and six patients (22%) were successf
ully treated for rejection episodes during pregnancy by adjustments in
standard immunosuppressive agents. No peripartum deaths were reported
; three late deaths occurred. Of the 29 children born of heart transpl
ant recipients who became pregnant, no fetal anomalies or neonatal dea
ths occurred. Prematurity (41%) and low birth weight (17%) were the mo
st common complications. All children are reported in good health at 3
.4 +/- 0.4 years of age. Most transplant recipients (59%) were being t
reated with triple-drug immunosuppression with azathioprine, corticost
eroids, and cyclosporine during pregnancy. The most common alteration
to immunosuppressive therapy during pregnancy (41%) involved increasin
g cyclosporine doses caused by decreasing cyclosporine levels during p
regnancy. Twenty-two percent of patients underwent empiric lowering of
cyclosporine doses during pregnancy; four patients continued with cor
ticosteroid tapering during pregnancy, and four patients increased cor
ticosteroid doses. Three patients discontinued azathioprine, two becau
se of drug-induced cholestatic jaundice and one for severe anemia. The
specific immunosuppressive regimen used during pregnancy did not appe
ar to affect the outcome of the pregnancy; however, the data suggest t
hat immunosuppressive therapy must be monitored closely because of the
metabolic and hemodynamic changes of pregnancy. Although these result
s show increased complications in a high risk population, pregnancy ap
pears to be fairly well tolerated in heart transplant recipients.