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十价肺炎球菌结合疫苗预防鼓膜置管术的有效性:一项整群随机试验

Effectiveness of the Ten-valent Pneumococcal Conjugate Vaccine Against Tympanostomy Tube Placements in a Cluster-randomized Trial.

作者信息

Palmu Arto A, Jokinen Jukka, Nieminen Heta, Rinta-Kokko Hanna, Ruokokoski Esa, Puumalainen Taneli, Traskine Magali, Moreira Marta, Borys Dorota, Schuerman Lode, Kilpi Terhi M

机构信息

From the *Department of Vaccination and Immune Protection, National Institute for Health and Welfare, Finland; †GlaxoSmithKline Vaccines, Espoo, Finland; and ‡Global Vaccine Development, GlaxoSmithKline Vaccines, Wavre, Belgium.

出版信息

Pediatr Infect Dis J. 2015 Nov;34(11):1230-5. doi: 10.1097/INF.0000000000000857.

Abstract

BACKGROUND

We evaluated the impact of the new pneumococcal Haemophilus influenzae protein D conjugate vaccine (PHiD-CV10, GSK Vaccines) on tympanostomy tube placements (TTPs).

METHODS

Finnish Invasive Pneumococcal disease vaccine trial was a nationwide phase III/IV cluster-randomized, double-blind trial. Children younger than 19 months received PHiD-CV10 in two thirds of clusters (N = 52) or hepatitis B or A vaccine as control in 26 clusters according to 3 + 1 or 2 + 1 schedules (infants younger than 7 months) or catch-up schedules. A secondary objective of the trial was to assess vaccine effectiveness (VE) against TTPs in children who received at least one vaccine dose before or after 7 months of age. Blinded follow-up lasted from the date of first vaccination (from February 2009 through October 2010) to December 31, 2011. Outcome data were collected through the National Care register and Social Insurance Institution reimbursement register.

RESULTS

More than 47,000 children were enrolled. In 30,527 infants younger than 7 months of age at enrolment, 4369 TTPs were reported in 3594 subjects. The incidence was 7.9 per 100 person-years in the infant control cohort. The VE estimate was 13% [95% confidence interval (CI): -2% to 26%] for combined PHiD-CV10 3 + 1 and 2 + 1 infant schedules. The VE estimates for the 3 + 1 and 2 + 1 infant schedules when estimated separately were similar. For the catch-up schedules, the VE was 11% (95% CI: -7% to 26%) for children enrolled at 7-11 months of age and -1% (95% CI: -21% to 16%) for children enrolled at 12-18 months of age.

CONCLUSIONS

Our study results suggest that PHiD-CV10 immunization according to a 3 + 1 or 2 + 1 schedule initiated before 12 months of age may reduce the frequency of TTPs, although the primary analysis did not reach statistical significance.

摘要

背景

我们评估了新型肺炎球菌-流感嗜血杆菌蛋白D结合疫苗(PHiD-CV10,葛兰素史克疫苗公司)对鼓膜置管术(TTP)的影响。

方法

芬兰侵袭性肺炎球菌疾病疫苗试验是一项全国性的III/IV期整群随机双盲试验。19个月以下儿童在三分之二的群组(N = 52)中接种PHiD-CV10,或在26个群组中接种乙肝或甲肝疫苗作为对照,接种方案为3+1或2+1(7个月以下婴儿)或补种方案。该试验的一个次要目标是评估在7个月龄之前或之后至少接种一剂疫苗的儿童中,疫苗对TTP的有效性(VE)。盲法随访从首次接种日期(2009年2月至2010年10月)持续到2011年12月31日。结局数据通过国家医疗登记册和社会保险机构报销登记册收集。

结果

超过47000名儿童入组。在入组时7个月以下的30527名婴儿中,3594名受试者报告了4369次TTP。婴儿对照组的发病率为每100人年7.9次。联合PHiD-CV10 3+1和2+1婴儿接种方案的VE估计值为13%[95%置信区间(CI):-2%至26%]。分别估计时,3+1和2+1婴儿接种方案的VE估计值相似。对于补种方案,7至11个月龄入组儿童的VE为11%(95%CI:-7%至26%),12至18个月龄入组儿童的VE为-1%(95%CI:-21%至16%)。

结论

我们的研究结果表明,在12个月龄前按照3+1或2+1方案接种PHiD-CV10可能会降低TTP的发生率,尽管初步分析未达到统计学显著性。

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