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Effectiveness of the influenza a(H1N1)PDM09 vaccine in adults recommended for annual influenza vaccination: A case-control study

机译:推荐每年进行一次流感疫苗接种的成人a(H1N1)PDM09流感疫苗的有效性:病例对照研究

摘要

Background: Because of variability in published A(H1N1)pdm09 influenza vaccine effectiveness estimates, we aimed to assess the effectiveness of MF59-adjuvanted A(H1N1)pdm09 vaccine in a matched case-control study. Objectives: We aimed to assess the effectiveness of MF59- adjuvanted A(H1N1)pdm09 influenza vaccine in a matched case-control study. Methods: This study was conducted during the pandemic influenza season 2009-2010 in adults with underlying comorbidities and healthy subjects of 60 years and older recommended for annual influenza vaccination in the Netherlands. Sixteen laboratory- confirmed and eligible A(H1N1)pdm09 influenza cases registered by four Community Health Services of the Netherlands were included. The control population was retrieved from a general practice database and consisted of subjects who had not been registered with influenza code R80 (according to the International Classification of Primary Care) during the A(H1N1)pdm09 influenza season. The controls were matched to cases on sex, age and comorbidities. The primary outcome was laboratory-confirmed A(H1N1)pdm09 influenza. Odds ratios (OR) and their 95% confidence intervals (95% CI) were calculated. Vaccine effectiveness (VE) was expressed as VE = (1 - OR)∗100%. Results: The A(H1N1)pdm09 vaccination rates in cases and controls were 6% and 76% respectively. After matching cases with controls in a ratio of 1:10, vaccine effectiveness was 98% (95% CI 84-100%). Conclusions: Even though we cannot entirely rule out that selection bias has played a role in our study, the present results indicate that the MF59-adjuvanted A(H1N1)pdm09 influenza vaccine has been effective in preventing laboratory-confirmed A(H1N1)pdm09 influenza in adults with underlying comorbidities and healthy subjects of 60 years and older during the A(H1N1)pdm09 influenza pandemic.
机译:背景:由于已发表的A(H1N1)pdm09流感疫苗有效性评估中存在差异,我们旨在在匹配的病例对照研究中评估MF59佐剂的A(H1N1)pdm09疫苗的有效性。目的:我们旨在通过一项配对病例对照研究评估MF59佐剂的A(H1N1)pdm09流感疫苗的有效性。方法:本研究是在2009-2010年大流行性流感季节期间对患有潜在合并症的成人以及60岁及以上的健康人群进行的,建议他们在荷兰进行年度流感疫苗接种。荷兰的四个社区卫生服务机构共登记了16例经实验室确认且合格的A(H1N1)pdm09流感病例。从普通实践数据库中检索对照人群,这些人群包括在A(H1N1)pdm09流感季节未注册流感编码R80(根据国际初级保健分类)的受试者。对照与性别,年龄和合并症病例匹配。主要结果是实验室确认的A(H1N1)pdm09流感。计算赔率(OR)及其95%置信区间(95%CI)。疫苗有效性(VE)表示为VE =(1-OR)* 100%。结果:病例和对照组的A(H1N1)pdm09疫苗接种率分别为6%和76%。在将病例与对照组的比率为1:10匹配后,疫苗的有效性为98%(95%CI 84-100%)。结论:即使我们不能完全排除选择偏见在我们的研究中起作用,但目前的结果表明,MF59佐剂的A(H1N1)pdm09流感疫苗已有效预防实验室确认的A(H1N1)pdm09流感A(H1N1)pdm09流感大流行期间患有潜在合并症的成年人和60岁及以上的健康受试者。

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