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Effectiveness of quadrivalent human papillomavirus vaccine for the prevention of cervical abnormalities: case-control study nested within a population based screening programme in Australia

机译:四价人乳头瘤病毒疫苗预防宫颈异常的有效性:病例对照研究嵌套在澳大利亚基于人群的筛查计划中

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摘要

>Objective To measure the effectiveness of the quadrivalent human papillomavirus (HPV) vaccine against cervical abnormalities four years after implementation of a nationally funded vaccination programme in Queensland, Australia.>Design Case-control analysis of linked administrative health datasets.>Setting Queensland, Australia.>Participants Women eligible for free vaccination (aged 12-26 years in 2007) and attending for their first cervical smear test between April 2007 and March 2011. High grade cases were women with histologically confirmed high grade cervical abnormalities (n=1062) and “other cases” were women with any other abnormality at cytology or histology (n=10 887). Controls were women with normal cytology (n=96 404).>Main outcome measures Exposure odds ratio (ratio of odds of antecedent vaccination (one, two, or three vaccine doses compared with no doses) among cases compared with controls), vaccine effectiveness ((1−adjusted odds ratio)×100), and number needed to vaccinate to prevent one cervical abnormality at first screening round. We stratified by four age groups adjusted for follow-up time, year of birth, and measures of socioeconomic status and remoteness. The primary analysis concerned women whose first ever smear test defined their status as a case or a control.>Results The adjusted odds ratio for exposure to three doses of HPV vaccine compared with no vaccine was 0.54 (95% confidence interval 0.43 to 0.67) for high grade cases and 0.66 (0.62 to 0.70) for other cases compared with controls with normal cytology, equating to vaccine effectiveness of 46% and 34%, respectively. The adjusted numbers needed to vaccinate were 125 (95% confidence interval 97 to 174) and 22 (19 to 25), respectively. The adjusted exposure odds ratios for two vaccine doses were 0.79 (95% confidence interval 0.64 to 0.98) for high grade cases and 0.79 (0.74 to 0.85) for other cases, equating to vaccine effectiveness of 21%.>Conclusion The quadrivalent HPV vaccine conferred statistically significant protection against cervical abnormalities in young women who had not started screening before the implementation of the vaccination programme in Queensland, Australia.
机译:>目的:在澳大利亚昆士兰州实施一项国家资助的疫苗接种计划后四年,评估四价人乳头瘤病毒(HPV)疫苗对宫颈异常的有效性。>设计病例对照链接的行政健康数据集分析。>设置澳大利亚昆士兰州。>参与者符合免费疫苗接种条件的妇女(2007年年龄在12-26岁之间)并且参加了两次之间的首次宫颈涂片检查2007年4月和2011年3月。高等级病例是经组织学证实为高度宫颈异常的女性(n = 1062),“其他病例”是在细胞学或组织学上具有任何其他异常的女性(n = 10 887)。对照组是细胞学检查正常的女性(n = 96 404)。>主要结局指标病例之间的接触几率(先接种疫苗的几率比(一,两或三剂疫苗与无剂量相比)含对照),疫苗有效性((1-调整后的优势比)×100)以及在第一轮筛选中预防一次子宫颈异常所需的疫苗接种数量。我们根据四个年龄组进行了分层,这些年龄组根据随访时间,出生年份以及社会经济地位和偏远程度进行了调整。初步分析涉及首次涂片检查确定其作为病例或对照者身份的妇女。>结果与未接种疫苗相比,接触三剂HPV疫苗的调整后优势比为0.54(置信度为95%与细胞学正常的对照组相比,高等级病例的间隔为0.43至0.67),其他病例为0.66(0.62至0.70),分别相当于疫苗有效性为46%和34%。接种疫苗的调整后数字分别为125(95%置信区间97至174)和22(19至25)。对于两种情况,两种疫苗的调整后暴露几率比为0.79(95%置信区间0.64至0.98),其他情况下为0.79(0.74至0.85),相当于疫苗有效性为21%。>结论 >在澳大利亚昆士兰州实施疫苗接种计划之前,尚未开始筛查的年轻女性中,四价HPV疫苗具有统计学上显着的预防宫颈异常的保护作用。

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