Prospective Evaluation of Fetuses With Autoimmune-Associated Congenital Heart Block Followed in the PR Interval and Dexamethasone Evaluation (PRIDE) Study

被引:109
作者
Friedman, Deborah A. [2 ]
Kim, Mimi Y. [3 ]
Copel, Joshua A. [4 ]
Llanos, Carolina [1 ]
Davis, Claudine [1 ]
Buyon, Jill P. [1 ]
机构
[1] NYU, Sch Med, New York, NY 10003 USA
[2] New York Med Coll, Valhalla, NY 10595 USA
[3] Albert Einstein Coll Med, New York, NY USA
[4] Yale Univ, Sch Med, New Haven, CT USA
基金
美国国家卫生研究院;
关键词
ATRIOVENTRICULAR-BLOCK; ANTI-SSA/RO; CLASSIFICATION; AUTOANTIBODIES; VALIDATION; CRITERIA; LUPUS;
D O I
10.1016/j.amjcard.2008.12.027
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We evaluated the efficacy of dexamethasone (DEX) in anti-SSA/Ro-exposed fetuses newly diagnosed with congenital heart block. Previous use of DEX has been anecdotal with varying reports of therapeutic benefit. This was a multicenter, open-label, nonrandomized study involving 30 pregnancies treated with DEX (22 with third-degree block, 6 with second-degree block, 2 with first-degree block) and 10 untreated (9 with third-degree block, I with first-degree block). Initial median ventricular rates, age at diagnosis, and degree of cardiac dysfunction were similar between groups. Six deaths occurred in the DEX group. There was no reversal of third-degree block with therapy or spontaneously. In fetuses treated with DEX, 1/6 with second-degree block progressed to third-degree block and 3 remained in second-degree block (postnatally I paced, 2 progressed to third degree); 2 reverted to normal sinus rhythm (NSR; postnatally 1 progressed to second degree). DEX reversed the 2 fetuses with first-degree block to NSR by 7 days with no regression at discontinuation. Absent DEX, the 1 with first-degree block detected at 38 weeks had NSR at birth (overall stability or improvement in 4 of 8 in the DEX group vs I of 1 in the non-DEX group). Median gestational birth age was 37 weeks in the DEX group versus 38 weeks in the non-DEX group (p = 0.019). Prematurity and small size for gestational age were restricted to the DEX group. Pacemaker use and growth parameters at birth and I year were similar between groups. In conclusion, these data confirm the irreversibility of third-degree block and progression of second- to third-degree block despite DEX. A potential benefit of DEX in reversing first- or second-degree block was supported in rare cases but should be weighed against potential steroid side effects such as growth restriction. 0 2009 Elsevier Inc. (Am J Cardiol 2009;103:1102-1106)
引用
收藏
页码:1102 / 1106
页数:5
相关论文
共 21 条
[1]   Spectrum and progression of conduction abnormalities in infants born to mothers with anti-SSA/Ro-SSB/La antibodies [J].
Askanase, AD ;
Friedman, DM ;
Copel, J ;
Dische, MR ;
Dubin, A ;
Starc, TJ ;
Katholi, MC ;
Buyon, JP .
LUPUS, 2002, 11 (03) :145-151
[2]   INVITRO METABOLISM OF PREDNISOLONE, DEXAMETHASONE, BETAMETHASONE, AND CORTISOL BY HUMAN PLACENTA [J].
BLANFORD, AT ;
MURPHY, BEP .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1977, 127 (03) :264-267
[3]   Treatment of fetal heart block with maternal steroid therapy: case report and review of the literature [J].
Breur, JMPJ ;
Visser, GHA ;
Kruize, AA ;
Stoutenbeek, P ;
Meijboom, EJ .
ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2004, 24 (04) :467-472
[4]   Normal neuropsychological development in children with congenital complete heart block who may or may not be exposed to high-dose dexamethasone in utero [J].
Brucato, A. ;
Astori, M. G. ;
Cimaz, R. ;
Villa, P. ;
Destri, M. Li ;
Chimini, L. ;
Vaccari, R. ;
Muscara, M. ;
Motta, M. ;
Tincani, A. ;
Neri, F. ;
Martinelli, S. .
ANNALS OF THE RHEUMATIC DISEASES, 2006, 65 (11) :1422-1426
[5]  
Buyon J. P., 2006, DUBOIS LUPUS ERYTHEM, P1058
[6]   Cellular rejection of the conduction system after orthotopic heart transplantation for congenital atrioventricular block [J].
Chan, Jessica B. ;
Levi, Daniel S. ;
Lai, Chi K. ;
Alejos, Juan C. ;
Fishbein, Michael C. .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2006, 25 (11) :1371-1375
[7]   Maternal antibody responses to the 52-kd SSA/Ro p200 peptide and the development of fetal conduction defects [J].
Clancy, RM ;
Buyon, JP ;
Ikeda, K ;
Nozawa, K ;
Argyle, DA ;
Friedman, DM ;
Chan, EKL .
ARTHRITIS AND RHEUMATISM, 2005, 52 (10) :3079-3086
[8]   Immunohistologic evidence supports apoptosis, IgG deposition, and novel macrophage/fibroblast crosstalk in the pathologic cascade leading to congenital heart block [J].
Clancy, RM ;
Kapur, RP ;
Molad, Y ;
Askanase, AD ;
Buyon, JP .
ARTHRITIS AND RHEUMATISM, 2004, 50 (01) :173-182
[9]   Utility of cardiac monitoring in fetuses at risk for congenital heart block - The PR interval and dexamethasone evaluation (PRIDE) prospective study [J].
Friedman, Deborah M. ;
Kim, Mimi Y. ;
Copel, Joshua A. ;
Davis, Claudine ;
Phoon, Colin K. L. ;
Glickstein, Julie S. ;
Buyon, Jill P. .
CIRCULATION, 2008, 117 (04) :485-493
[10]   The fetal Doppler mechanical PR interval: A validation study [J].
Glickstein, J ;
Buyon, J ;
Kim, M ;
Friedman, D .
FETAL DIAGNOSIS AND THERAPY, 2004, 19 (01) :31-34