Long-term outcome of mothers of children with complete congenital heart block

被引:75
作者
Press, J
Uziel, Y
Laxer, RM
Luy, L
Hamilton, RM
Silverman, ED
机构
[1] UNIV TORONTO,HOSP SICK CHILDREN,DIV RHEUMATOL,TORONTO,ON M5G 1X8,CANADA
[2] UNIV TORONTO,HOSP SICK CHILDREN,DIV CARDIOL,TORONTO,ON M5G 1X8,CANADA
[3] UNIV TORONTO,HOSP SICK CHILDREN,DEPT PEDIAT,TORONTO,ON M5G 1X8,CANADA
[4] UNIV TORONTO,HOSP SICK CHILDREN,DEPT IMMUNOL,TORONTO,ON M5G 1X8,CANADA
[5] UNIV TORONTO,HOSP SICK CHILDREN,DEPT MED,TORONTO,ON M5G 1X8,CANADA
[6] UNIV TORONTO,HOSP SICK CHILDREN,DEPT NURSING,TORONTO,ON M5G 1X8,CANADA
基金
加拿大自然科学与工程研究理事会;
关键词
D O I
10.1016/S0002-9343(97)89492-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES:To determine the health of mothers of offspring with complete congenital heart block (CHB) both at the time of delivery of the affected child and in the long-term, and the percentage of mothers of children with CHB who had anti-SSA/Ro and/or SSB/La antibodies. PATIENTS AND METHODS: Sixty-four mothers of 64 children with CHB (seen between 1964 and 1993) were identified through the Cardiology database of The Hospital for Sick Children, Toronto, Canada. Medical information from these of children with CHB was evaluated. Data were obtained from the mothers by mailed questionnaire, telephone interview, and/or from the attending physicians. The presence of anti-Re antibodies and anti-La antibodies were evaluated by ELISA assay. RESULTS: The mean age at the time of delivery of the first child with CHB was 28 +/- 6 years. At the time of delivery 42 (66%) mothers were healthy, 2 (3%) had systemic lupus erythematosus (SLE), 2 (3%) had linear scleroderma, 2 (3%) had rheumatoid arthritis; 3 (5%) had a history of rheumatic fever (but were otherwise well), 1 (2%) had Sjogren's syndrome (SS), and 12 (19%) had an undifferentiated autoimmune syndrome (UAS) (arthralgia, myalgia, photosensitivity, skin vasculitis, Raynaud's phenomenon). The mean time to follow-up from delivery to study was 121 +/- 88 months. The mean maternal age at study was 38 +/- 9 years. Three of 12 mothers who initially had a UAS progressed to SLE (average follow-up time of 80 months, median 96), and 2 developed SS (with average follow-up time 140 months, median 132) and 1 went into remission. The mean follow-up time for the other mothers who did not develop an autoimmune disease was 150 +/- 102 months. Thirty-six of the 42 initially healthy mothers remained well. One mother developed SLE; 1 developed hyperthyroidism; 1 developed ankylosing spondylitis; and 3 developed an UAS. The mean follow-up time of the 36 mothers who remained healthy was similar (123 +/- 97 months) to the 6 initially healthy mothers who developed an autoimmune disease (121 +/- 36 months). Anti-Ro and/or anti-La antibodies were positive in 32 of 53 (60%) mothers tested. Fourteen of the 53 mothers were symptomatic at the time of delivery and 39 were asymptomatic. Anti-Ro and/or anti-La antibodies were positive in 12 of 13 mothers tested at the time of delivery. CONCLUSIONS: The long-term maternal outcome in our cohort was very good as most of the initially healthy mothers remained well at follow-up. Twenty-five percent of the mothers with a UAS and only 2% of the initially healthy mothers developed SLE. The development of an autoimmune disease in an asymptomatic mother identified by the birth of a child with CHB was less common in our study than in previous studies. However, close follow-up of mothers with UAS is warranted.
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收藏
页码:328 / 332
页数:5
相关论文
共 39 条
[1]   THE NEONATAL LUPUS SYNDROME, AUTOANTIBODIES, AND CONNECTIVE-TISSUE DISEASE [J].
ABRUZZO, JL .
ANNALS OF INTERNAL MEDICINE, 1983, 99 (05) :716-717
[2]  
Aylward RD, 1928, BRIT MED J, V1, P943
[3]   LONG-TERM OUTCOME FOR THE MOTHERS OF INFANTS WITH ISOLATED CONGENITAL COMPLETE HEART-BLOCK - COMMENT ON THE ARTICLE BY JULKUNEN ET-AL [J].
BRUCATO, A ;
FERRARO, G ;
GASPARINI, M ;
DEJULI, E ;
FRANCESCHINI, F .
ARTHRITIS AND RHEUMATISM, 1994, 37 (08) :1261-1261
[4]   CONGENITAL COMPLETE HEART-BLOCK - A HUMAN-MODEL OF PASSIVELY ACQUIRED AUTOIMMUNE INJURY [J].
BUYON, JP ;
WINCHESTER, R .
ARTHRITIS AND RHEUMATISM, 1990, 33 (05) :609-614
[5]   IDENTIFICATION OF MOTHERS AT RISK FOR CONGENITAL HEART-BLOCK AND OTHER NEONATAL LUPUS SYNDROMES IN THEIR CHILDREN - COMPARISON OF ENZYME-LINKED-IMMUNOSORBENT-ASSAY AND IMMUNOBLOT FOR MEASUREMENT OF ANTI-SS-A RO AND ANTI-SS-B LA ANTIBODIES [J].
BUYON, JP ;
WINCHESTER, RJ ;
SLADE, SG ;
ARNETT, F ;
COPEL, J ;
FRIEDMAN, D ;
LOCKSHIN, MD .
ARTHRITIS AND RHEUMATISM, 1993, 36 (09) :1263-1273
[6]   ASSOCIATION OF MATERNAL SYSTEMIC LUPUS-ERYTHEMATOSUS WITH CONGENITAL COMPLETE HEART-BLOCK [J].
CHAMEIDES, L ;
TRUEX, RC ;
VETTER, V ;
RASHKIND, WJ ;
GALIOTO, FM ;
NOONAN, JA .
NEW ENGLAND JOURNAL OF MEDICINE, 1977, 297 (22) :1204-1207
[7]   ANTI-RO/SS-A AND ANTI-LA/SS-B AUTOANTIBODY LEVELS IN RELATION TO SYSTEMIC LUPUS-ERYTHEMATOSUS DISEASE-ACTIVITY AND CONGENITAL HEART-BLOCK - A LONGITUDINAL-STUDY COMPRISING 2 CONSECUTIVE PREGNANCIES IN A PATIENT WITH SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
DERKSEN, RHWM ;
MEILOF, JF .
ARTHRITIS AND RHEUMATISM, 1992, 35 (08) :953-959
[8]   CONGENITAL COMPLETE HEART-BLOCK [J].
ESSCHER, E .
ACTA PAEDIATRICA SCANDINAVICA, 1981, 70 (01) :131-136
[9]  
GOCHBERG SH, 1969, AM J OBSTET GYNECOL, V88, P238
[10]   ISOLATED CONGENITAL COMPLETE HEART-BLOCK IN OFFSPRING OF MOTHERS WITH PRIMARY SJOGRENS SYNDROME [J].
HANSEN, BU ;
MANTHORPE, T ;
MANTHORPE, R ;
MARSAL, K .
SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, 1989, 18 (04) :227-230