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Serological hepatitis A virus infections and ratio of clinical to serological infections in a controlled trial of pre-exposure prophylaxis with immune serum globulin.

机译:在免疫血清球蛋白预防暴露前预防的对照试验中,血清型A型肝炎病毒感染和临床感染与血清感染的比率。

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摘要

Seroconversion to hepatitis A virus was studied in a sub sample of 802 Israeli military recruits (611 men and 191 women) who were taking part in a randomised controlled trial of pre-exposure immune serum globulin (ISG) for the prevention of viral hepatitis. On intake into the service 35% of the men and 47% of the women were negative to hepatitis. A virus antibody (anti-HAV). After three years 7 of 71 men (9.9%) who had not received pre-exposure ISG had become positive to anti-HAV compared to 2 of 83 (2.4%) who had received it; the statistical significance of this difference was p = 0.052. At two years 2 of 30 women (6.7%) who had not received ISG had converted compared to 1 of 43 (2.3%) who had received ISG (p = 0.37). Pooling the sexes gave conversion rates of 8.9% in those not immunised and 2.4% in those immunised (p = 0.029). The sex adjusted odds ratio was 4.0 (95% confidence limits 1.3-19.0). The morbidity rates for clinical non B hepatitis over the three year period among 12 835 men were 7.2 per 1000 in those not immunised and 3.6 per 1000 in those immunised (p = 0.004). Point estimates of the ratio of clinical hepatitis to seroconversion in men ranged from 0.25 to 0.30. It is concluded that pre-exposure administration of ISG effectively prevented clinical expression of viral hepatitis, apparently reduced seroconversion, and did not induce passive-active immunisation.
机译:在参加一次暴露前免疫血清球蛋白(ISG)预防病毒性肝炎的一项随机对照试验的802名以色列军事新兵的亚样本中,研究了血清转化为甲型肝炎病毒的情况。在服役时,35%的男性和47%的女性对肝炎呈阴性。病毒抗体(抗HAV)。三年后,未接受ISG的71名男性中有7名(9.9%)对抗HAV呈阳性反应,而接受过ISG的83名男性中有2名(2.4%)接受了抗HAV阳性。该差异的统计显着性为p = 0.052。在两年中,未接受ISG的30名女性中有2名(6.7%)发生了转变,而接受ISG的43名女性中有1名(2.3%)有所转变(p = 0.37)。汇总性别,未免疫者的转化率为8.9%,未免疫者的转化率为2.4%(p = 0.029)。性别调整后的优势比为4.0(95%置信区间1.3-19.0)。在12年中,在12 835名男性中,非免疫性乙型肝炎的发病率是每千人中7.2例,每千人中3.6例(p = 0.004)。男性临床肝炎与血清转化率之比的估计值为0.25至0.30。结论是,ISG的暴露前给药有效地预防了病毒性肝炎的临床表达,明显减少了血清转化,并且没有诱导被动主动免疫。

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