Consequences for fetus and neonate of maternal red cell allo-immunisation

被引:55
作者
Howard, H [1 ]
Martlew, V
McFadyen, I
Clarke, C
Duguid, J
Bromilow, I
Eggington, J
机构
[1] Mersey & N Wales Ctr, Natl Blood Serv, Liverpool L7 8TW, Merseyside, England
[2] Womens Hosp, Dept Obstet & Gynaecol, Liverpool, Merseyside, England
[3] Univ Liverpool, Dept Sci Biol, Liverpool L69 3BX, Merseyside, England
来源
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION | 1998年 / 78卷 / 01期
关键词
allo-immunisation; pregnancy; red cell antibodies; haemolytic disease of the new born;
D O I
10.1136/fn.78.1.F62
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Aims-To study the distribution of clinically important red cell antibodies in pregnancy, and the associated fetal and neonatal morbidity and mortality. Methods The case notes of women with clinically important red cell antibodies identified in their serum during pregnancy were reviewed. Results-During a 12 month period 22 264 women were referred for antenatal screening. Clinically important red cell antibodies were detected in 244 (1%). Of these, 100 were anti-D and 144 were non-RhD antibodies. There were three intrauterine deaths, three fetuses required intrauterine transfusion, 10 neonates were transfused, 27 others had phototherapy, and 27 with a positive direct antiglobulin test received no treatment. Early fetal losses occurred in the presence of both high and low levels of anti-D. Conclusions-Anti-D remains the most common clinically important antibody in pregnancy, and accounts for the greatest fetal and neonatal morbidity and mortality. Of the other antibodies detected, anti-c was associated with most neonatal morbidity. The production of many of the non-D antibodies detected could be avoided by the use of selected red cells when transfusing pre-menopausal women.
引用
收藏
页码:F62 / F66
页数:5
相关论文
共 15 条
[1]   Hemolytic disease of the newborn [J].
Bowman, JM .
VOX SANGUINIS, 1996, 70 :62-67
[2]  
CLARKE C, 1994, J ROY COLL PHYS LOND, V28, P310
[3]   THE PREVALENCE OF RED-CELL ANTIBODIES IN PREGNANCY CORRELATED TO THE OUTCOME OF THE NEWBORN - A 12 YEAR STUDY IN CENTRAL SWEDEN [J].
FILBEY, D ;
HANSON, U ;
WESSTROM, G .
ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA, 1995, 74 (09) :687-692
[4]   Female alloimmunization with antibodies known to cause hemolytic disease [J].
GeifmanHoltzman, O ;
Wojtowycz, M ;
Kosmas, E ;
Artal, R .
OBSTETRICS AND GYNECOLOGY, 1997, 89 (02) :272-275
[5]   Haemolytic disease of the newborn due to anti-G [J].
Hadley, AG ;
Poole, GD ;
Poole, J ;
Anderson, NA ;
Robson, M .
VOX SANGUINIS, 1996, 71 (02) :108-112
[6]  
HOWARD HL, 1997, BRIT J OBSTET GYNAEC, V104, P34
[7]   CAUSES AND CLINICAL CONSEQUENCES OF RHESUS (D) HEMOLYTIC-DISEASE OF THE NEWBORN - A STUDY OF A SCOTTISH POPULATION, 1985-1990 [J].
HUGHES, RG ;
CRAIG, JIO ;
MURPHY, WG ;
GREER, IA .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1994, 101 (04) :297-300
[8]   LACK OF CLINICAL-SIGNIFICANCE OF ENZYME-ONLY RED-CELL ALLOANTIBODIES [J].
ISSITT, PD ;
COMBS, MR ;
BREDEHOEFT, SJ ;
CAMPBELL, ML ;
HEIMER, M ;
JOYNER, L ;
LORENTSEN, L ;
REMLEY, C ;
BULLOCK, S ;
BUMGARNER, J ;
ZAKERINIASAR, M ;
KIRKLAND, A ;
MELROY, H ;
MILLIKIN, D .
TRANSFUSION, 1993, 33 (04) :284-293
[9]  
MARSH W L, 1968, Journal of Medical Laboratory Technology, V25, P335
[10]  
*NBTS IMM WORK PAR, 1991, PRESCRIBERS J, V31, P137