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遗传性溶血性贫血患者中乙型肝炎、丙型肝炎和人类免疫缺陷病毒标志物的患病率。

Prevalence of hepatitis B, hepatitis C and human immune deficiency virus markers among patients with hereditary haemolytic anaemias.

作者信息

al-Mahroos F T, Ebrahim A

机构信息

Sulmaniya Medical Center, Arabian Gulf University, Bahrain.

出版信息

Ann Trop Paediatr. 1995 Jun;15(2):121-8. doi: 10.1080/02724936.1995.11747759.

Abstract

To determine the prevalence of hepatitis B virus (HBV), hepatitis C virus (HCV) and human immunodeficiency virus (HIV) markers among Bahraini children with hereditary haemolytic anaemias, a cross-sectional study was conducted at the paediatric outpatient clinic of Sulimaniya Medical Center in the State of Bahrain. A total of 242 patients with hereditary haemolytic anaemias were enrolled in the study: 171 (71%) with sickle cell syndromes, 59 (24%) with beta thalassaemia major and 12 (5%) with alpha thalassaemia. Among the 191 multi-transfused patients, 39 (20.5%) had one or more markers for HBV, 78 (40%) were seropositive for HCV antibody, and three (1.6%) were seropositive for HIV antibody. In contrast, none of the 51 non-transfusion group was seropositive for HBV and HIV antibodies but one patient was seropositive for HCV antibody. HBV, HCV and HIV infections therefore remain a major hazard for children with hereditary haemolytic anaemias, despite blood donor screening. More refined and sensitive tests which would detect infection in all stages of the disease are required. Hepatitis B vaccine should be given to all children with hereditary haemolytic anaemias.

摘要

为了确定巴林患有遗传性溶血性贫血的儿童中乙型肝炎病毒(HBV)、丙型肝炎病毒(HCV)和人类免疫缺陷病毒(HIV)标志物的流行情况,在巴林国苏利马尼亚医疗中心的儿科门诊进行了一项横断面研究。共有242例遗传性溶血性贫血患者纳入研究:171例(71%)患有镰状细胞综合征,59例(24%)患有重型β地中海贫血,12例(5%)患有α地中海贫血。在191例多次输血的患者中,39例(20.5%)有一项或多项HBV标志物,78例(40%)HCV抗体血清学阳性,3例(1.6%)HIV抗体血清学阳性。相比之下,51例未输血组中无人HBV和HIV抗体血清学阳性,但有1例患者HCV抗体血清学阳性。因此,尽管对献血者进行了筛查,但HBV、HCV和HIV感染仍然是患有遗传性溶血性贫血儿童的主要危险因素。需要更精细、更敏感的检测方法来检测疾病各个阶段的感染情况。所有患有遗传性溶血性贫血的儿童都应接种乙肝疫苗。

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