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[出生时免疫血液学检查的患病率及新生儿溶血病的发病率]

[Prevalence of immunohematologic tests at birth and the incidence of hemolytic disease in the newborn].

作者信息

Cianciarullo Marco Antonio, Ceccon Maria Esther Jurfest, Vaz Fl vio Adolfo Costa

机构信息

Instituto da Criança, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brasil.

出版信息

Rev Assoc Med Bras (1992). 2003 Jan-Mar;49(1):45-53. doi: 10.1590/s0104-42302003000100033. Epub 2003 Apr 28.

DOI:10.1590/s0104-42302003000100033
PMID:12724812
Abstract

UNLABELLED

The administration of anti-D globulin to the mothers has decreased the incidence of Rh hemolytic disease but the improvement of technologic assays has made it possible to identify several hemolytics diseases of the newborn.

BACKGROUND

To identify the prevalence of immunohematologic tests demonstrated by indirect (IC), direct (DC) and elution tests; to identify the incidence of hemolytic disease and its treatment (phototherapy and/or exchange transfusion) in neonates with hemolytic disease. This is a retrospective cohort-study performed from January 1st 1996 to July 1st 1998.

METHODS

This is a descriptive study of the immunohematologic profile of 1698 mothers and their offsprings, as risk factors for developing hemolytic disease. The inclusion criteria were the positivity of the indirect (IC) and direct (DC) Coombs tests and elution tests. Based on the inclusion criteria three group of infants were analyzed: Group I was composed of 149 offsprings of Coombs-positive mothers (IC+) with antibodies associated with neonatal hemolytic disease. This group was further divided into two groups: Group I-A (IC+DC+) was composed of 83 Coombs-positive offsprings (DC+) of Coombs-positive mothers (IC+) and Group I-B (IC+DC-) was composed of 66 Coombs-negative offsprings (DC-) of Coombs-positive mothers (IC+); Group D was composed of 736 Coombs-positive offspring's of Coombs-negative mothers (IC-); and Group E was composed of 807 Coombs-negative and elution-positive offspring's of Coombs-negative mothers.

RESULTS

This study shown that the overall prevalence of immunohematologic tests associated with hemolytic disease was 9.07% (3212/35429), 0.43% (154/35429) among offsprings of Coombs-positive mothers, 4.10% (1453/35429) among Coombs-positive infants, and 4.53% (1605/35429) among elution-positive infants. The overall incidence of hemolytic disease was 36.23% (613/1692), 33.56% (50/149) among offspring's of Coombs-positive mothers, 44.43% (327/736) among Coombs-positive infants, and 29.24% (236/807) among elution-positive infants. The overall incidence of phototherapy among infants with hemolytic disease was 36.23% (613/1692), 49.40% (41/83) in group I-A (IC+DC+), 13.64% (9/66) in group I-B(IC+DC-), 44.43% (327/736) in group D, and 29.24% (236/807) in group E. The overall incidence of exchange transfusion among infants with hemolytic disease was 0.88% (15/1692), 14.46% (12/83) in group I-A (IC+DC+), 0% (0/66) in group I-B (IC+DC-), 0.27% (2/736) in group D, and 0.12% (1/807) in group E.

CONCLUSIONS

The results of this study allowed us to conclude that the overall prevalence of immunohematologic tests associated with hemolytic disease was 9.07% (3212/35429) and the overall incidence of hemolytic disease was 36.23% (613/1692) in this study-group. The highest incidences of hemolytic disease and phototherapy were observed among Coombs-positive offsprings of Coombs-positive mothers.

摘要

未标注

给母亲注射抗D球蛋白降低了Rh溶血病的发病率,但技术检测方法的改进使得识别几种新生儿溶血病成为可能。

背景

确定通过间接试验(IC)、直接试验(DC)和洗脱试验显示的免疫血液学检测的患病率;确定溶血病新生儿中溶血病的发病率及其治疗(光疗和/或换血疗法)。这是一项从1996年1月1日至1998年7月1日进行的回顾性队列研究。

方法

这是一项对1698名母亲及其后代的免疫血液学特征进行的描述性研究,作为发生溶血病的危险因素。纳入标准为间接试验(IC)、直接抗人球蛋白试验(DC)和洗脱试验呈阳性。根据纳入标准,分析了三组婴儿:第一组由149名抗人球蛋白试验阳性母亲(IC+)的后代组成,其抗体与新生儿溶血病相关。该组进一步分为两组:第一-A组(IC+DC+)由83名抗人球蛋白试验阳性母亲(IC+)的抗人球蛋白试验阳性后代(DC+)组成,第一-B组(IC+DC-)由66名抗人球蛋白试验阳性母亲(IC+)的抗人球蛋白试验阴性后代(DC-)组成;D组由736名抗人球蛋白试验阴性母亲(IC-)的抗人球蛋白试验阳性后代组成;E组由807名抗人球蛋白试验阴性母亲的抗人球蛋白试验阴性但洗脱试验阳性的后代组成。

结果

本研究表明,与溶血病相关的免疫血液学检测的总体患病率为9.07%(3212/35429),抗人球蛋白试验阳性母亲的后代中为0.43%(154/35429),抗人球蛋白试验阳性婴儿中为4.10%(1453/35429),洗脱试验阳性婴儿中为4.53%(1605/35429)。溶血病的总体发病率为36.23%(613/1692),抗人球蛋白试验阳性母亲的后代中为33.56%(50/149),抗人球蛋白试验阳性婴儿中为44.43%(327/736),洗脱试验阳性婴儿中为29.24%(236/807)。溶血病婴儿中光疗的总体发病率为36.23%(613/1692),第一-A组(IC+DC+)中为49.40%(41/83),第一-B组(IC+DC-)中为13.64%(9/66),D组中为44.43%(327/736),E组中为29.24%(236/807)。溶血病婴儿中换血疗法的总体发病率为0.88%(15/1692),第一-A组(IC+DC+)中为14.46%(12/83),第一-B组(IC+DC-)中为0%(0/66),D组中为0.27%(2/736),E组中为0.12%(1/807)。

结论

本研究结果使我们得出结论,在该研究组中,与溶血病相关的免疫血液学检测的总体患病率为9.07%(3212/35429),溶血病的总体发病率为36.23%(613/1692)。在抗人球蛋白试验阳性母亲的抗人球蛋白试验阳性后代中观察到溶血病和光疗的发病率最高。

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