Literature DB >> 8021795

Prevalence and lack of clinical significance of blood group incompatibility in mothers with blood type A or B.

J A Ozolek1, J F Watchko, F Mimouni.   

Abstract

PURPOSE: To examine the prevalence and clinical significance of blood group incompatibility in infants whose mothers have blood type A or B.
METHODS: We prospectively analyzed cord blood samples from 4996 consecutive love-born infants for blood type, hematocrit, and results of direct antiglobulin (Coombs) test (DAT) and indirect Coombs test (ICT). OUTCOME MEASURES: Erythrocyte sensitization was determined by positive DAT or ICT results. Significant hyperbilirubinemia (> or = 224 mumol/L (12.8 mg/dl) and mean cord hematocrits were compared between mother-infant pairs with ABO incompatibility and positive DAT or ICT results and those with negative Coombs test results.
RESULTS: Of all births, 6.9% (343/4996) were of infants who had ABO incompatibility and had been born to mothers with blood type B or A; 44 (13%) of 343 infants had a positive antiglobulin test result, of whom 43 had a positive ICT result only. Type A or B mothers were 5.5 times less likely to have sensitization than type O mothers; A-B, B-A, A-AB, and B-AB mother-infant pairs with a positive antiglobulin test result had mean cord hematocrits and rates of significant hyperbilirubinemia similar to those of corresponding pairs whose antiglobulin tests both showed negative results. Infants with a positive DAT result had lower mean cord hematocrits than infants with negative results on both antiglobulin tests or on a positive ICT result only. Significant hyperbilirubinemia was more frequent in infants with a positive DAT result than in infants with negative results on both antiglobulin tests or a positive ICT result only.
CONCLUSION: Sensitization is much rare when the mother has blood type A or B than when she has blood type O, as demonstrated by the antiglobulin test. The incidence of significant hyperbilirubinemia and lower cord hematocrit is not increased by sensitization when the mother has type A or B.

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Year:  1994        PMID: 8021795     DOI: 10.1016/s0022-3476(94)70131-8

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  8 in total

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Review 4.  Evidence for maternal-fetal genotype incompatibility as a risk factor for schizophrenia.

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6.  Comparison of the direct antiglobulin test and the eluate technique for diagnosing haemolytic disease of the newborn.

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7.  Predicting the Origins of Anti-Blood Group Antibody Specificity: A Case Study of the ABO A- and B-Antigens.

Authors:  Spandana Makeneni; Ye Ji; David C Watson; N Martin Young; Robert J Woods
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8.  The role of UGT1A1 (c.-3279 T > G) gene polymorphisms in neonatal hyperbilirubinemia susceptibility.

Authors:  Zijin Li; Li Song; Lihong Hao
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  8 in total

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