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Safety immunization coverage and determinants of a new kind of Hepatitis B vaccine firstly applied in Ningbo China

机译:新型乙型肝炎疫苗的安全性免疫范围和决定因素在中国宁波首次应用

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摘要

Evaluate safety and immunization coverage of a new kind of recombinant Hepatitis B vaccine (HepB) in Ningbo city, China. Two groups were carried out in 2 of 11 randomly selected countries in Ningbo in 2009. All of the infants born from July 1 to December 31, 2009 were enrolled as subjects and received 3 doses of HepB at 0, 1, 6 month. Control group (N = 3452) received current HepB derived from Saccharomyces Cerevisiae Yeast (HepB made by recombinant DNA techniques in Saccharomyces Cerevisiae Yeast, HepB-SCY; 5 μg/0.5 ml per dose) and experimental group (N = 5104) received the new kind of HepB derived from Hansenula polymorpha Yeast (HepB made by recombinant DNA techniques in Hansenula polymorpha Yeast, HepB-HPY; 10 μg/0.5 ml per dose). 3-dose and timely birth dose (TBD) coverage were available and compared between 2 groups. Standard structured questionnaires were applied to record information from parents and hospitals for selecting determinants of coverage. The data were analyzed using stepwise multiple logistic regression models. After each dose, HepB-related adverse events (AEs) and recta-temperature were recorded for 7 days. 3-dose coverage in control group (89.98%) was higher than that in experimental group (χ2 = 575.1173, P < 0.0001). TBD coverage in control and experimental group were 98.41% and 98.53%, respectively. No statistically significant difference in TBD coverage was found between 2 groups (χ2 = 0.0623, P = 0.8029). A total of 9 local AEs were reported, 4 for control group and 5 for experimental group. The percentages of subjects reporting AEs were similar across the 2 vaccination groups. No serious or immediate reactions were found in this study. From logistic models, receiving 10 μg vaccine (odds ratio [OR]:0.38; 95% confidence interval [95%CI]: 0.34–0.44) and mother migrating from other cities (OR: 0.45; 95%CI: 0.42–0.47) were the determinants for non-acceptance of 3 doses of HepB; infants born from low grade hospitals and native mothers contributed to administrate the TBD.
机译:在中国宁波市评估一种新型重组乙型肝炎疫苗(HepB)的安全性和免疫覆盖率。 2009年在11个随机选择的国家/地区中的2个国家/地区进行了两组研究。所有2009年7月1日至12月31日出生的婴儿均作为研究对象,分别在0、1、6个月接受3剂HepB。对照组(N = 3452)接受了当前来自酿酒酵母酵母的HepB(通过重组DNA技术在酿酒酵母酵母中制备的HepB,HepB-SCY;每剂量5μg/ 0.5 ml),而实验组(N = 5104)接受了新的一种来源于多形汉逊酵母的HepB(通过重组DNA技术在多形汉逊酵母中制备的HepB,HepB-HPY;每剂量10μg/ 0.5 ml)。可获得3剂量和及时的出生剂量(TBD)覆盖率,并在两组之间进行比较。应用标准结构问卷来记录父母和医院的信息,以选择覆盖范围的决定因素。使用逐步多元逻辑回归模型分析数据。每次给药后,记录7天与HepB相关的不良事件(AEs)和直肠温度。对照组三剂量覆盖率(89.98%)高于实验组(χ2= 575.1173,P <0.0001)。对照组和实验组的TBD覆盖率分别为98.41%和98.53%。两组之间的TBD覆盖率无统计学差异(χ2= 0.0623,P = 0.8029)。总共报告了9种局部AE,对照组4种,实验组5种。在两个疫苗接种组中,报告不良事件的受试者百分比相似。在这项研究中没有发现严重或立即的反应。从逻辑模型中,接受10μg疫苗(比值[OR]:0.38; 95%置信区间[95%CI]:0.34-0.44),母亲从其他城市移民(OR:0.45; 95% CI :0.42-0.47)是不接受3剂HepB的决定因素;由低级医院出生的婴儿和当地母亲为TBD的管理做出了贡献。

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