Objective: To evaluate the efficacy of low-dose intravenous immunoglobulin
(IVIG) treatment in older women with immunologic abnormalities and recurren
t spontaneous abortion (RSA), a condition referred to as immunologic aborti
on.
Design: Prospective clinical trial.
Setting: Outpatient referral practice.
Patient(s): Forty-seven women were enrolled in the study. The mean age of t
he women was 37 years (range, 28-45 years), and the mean number of prior mi
scarriages was 3.7. Immunologic abnormalities included antiphospholipid ant
ibodies (32%),antithyroid antibodies (53%), antinuclear antibodies (28%), a
ntiovarian antibodies (2%), increased natural killer cells (40%), increased
immunoglobulin (Ig)M level (28%), and increased CD4/CD8 T-cell ratio (15%)
. One patient had IgA deficiency, and three women had endometriosis. Thirty
-one of the 47 patients (66%) had more than one immunologic abnormality.
Intervention(s): Treatment with IVIG at a dose of 0.2 g/kg within 2 weeks o
f attempted conception. Once conception was achieved, IVIG treatment was co
ntinued on a monthly basis at, the same dose through 26-30: weeks of gestat
ion.
Main Outcome Measure(s): Successful pregnancy or recurrent abortion.
Result(s): OF the 47 women, 36 received initial IVIG treatment, and 24 subs
equently became pregnant. Of these women, 20 continued IVIG treatment throu
gh 26-30 weeks of gestation, and 19 (95%) had a successful term pregnancy.
Four women discontinued IVIG therapy after 10-12 weeks of gestation, and 3
(75%) had a successful pregnancy outcome. Of the 11 women who refused IVIG
therapy, 7 became pregnant, and all 7 miscarried. The difference in pregnan
cy success rate between the IVIG-treated and untreated groups was significa
nt (P=.001). Three women had adverse reactions during the low-dose IVIG inf
usion, and these reactions resolved when the IVIG brand was changed. Fetal
abnormalities were not observed.
Conclusion(s): Low-dose IVIG therapy is beneficial for older women with imm
unologic abortion. The optimum duration of IVIG treatment in these women re
quires further study. (C) 2000 by American Society for Reproductive Medicin
e.