Open AccessEvaluation of fetuses in a study of intravenous immunoglobulin as preventive therapy for congenital heart block: Results of a multicenter, prospective, open‐label clinical trial
Author(s) -
Friedman Deborah M.,
Llanos Carolina,
Izmirly Peter M.,
Brock Brigit,
Byron John,
Copel Joshua,
Cummiskey Karen,
Dooley Mary Anne,
Foley Jill,
Graves Cornelia,
Hendershott Colleen,
Kates Richard,
Komissarova Elena V.,
Miller Michelle,
Paré Emmanuelle,
Phoon Colin K. L.,
Prosen Tracy,
Reisner Dale,
Ruderman Eric,
Samuels Philip,
Yu Jerry K.,
Kim Mimi Y.,
Buyon Jill P.
Publication year - 2010
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.27308
Subject(s) - medicine , rash , intravenous immunoglobulin therapy , pediatrics , gestation , pregnancy , fetus , prednisone , prospective cohort study , heart block , adverse effect , antibody , obstetrics , immunology , electrocardiography , biology , genetics
Abstract Objective The recurrence rate of anti‐SSA/Ro–associated congenital heart block (CHB) is 17%. Sustained reversal of third‐degree block has never been achieved. Based on potential reduction of maternal autoantibody titers as well as fetal inflammatory responses, intravenous immunoglobulin (IVIG) was evaluated as preventive therapy for CHB. Methods A multicenter, prospective, open‐label study based on Simon's 2‐stage optimal design was initiated. Enrollment criteria included the presence of anti‐SSA/Ro antibodies in the mother, birth of a previous child with CHB/neonatal lupus rash, current treatment with ≤20 mg/day of prednisone, and <12 weeks pregnant. IVIG (400 mg/kg) was given every 3 weeks from week 12 to week 24 of gestation. The primary outcome was the development of second‐degree or third‐degree CHB. Results Twenty mothers completed the IVIG protocol before the predetermined stopping rule of 3 cases of advanced CHB in the study was reached. CHB was detected at 19, 20, and 25 weeks; none of the cases occurred following the finding of an abnormal PR interval on fetal Doppler monitoring. One of these mothers had 2 previous children with CHB. One child without CHB developed a transient rash consistent with neonatal lupus. Sixteen children had no manifestations of neonatal lupus at birth. No significant changes in maternal titers of antibody to SSA/Ro, SSB/La, or Ro 52 kd were detected over the course of therapy or at delivery. There were no safety issues. Conclusion This study establishes the safety of IVIG and the feasibility of recruiting pregnant women who have previously had a child with CHB. However, IVIG at low doses consistent with replacement does not prevent the recurrence of CHB or reduce maternal antibody titers.