Marshall Helen S, McMillan Mark, Koehler Ann, Lawrence Andrew, MacLennan Jenny M, Maiden Martin C J, Ramsay Mary, Ladhani Shamez N, Trotter Caroline, Borrow Ray, Finn Adam, Sullivan Thomas, Richmond Peter, Kahler Charlene M, Whelan Jane, Vadivelu Kumaran
Vaccinology and Immunology Research Trials Unit, Women's and Children's Hospital Adelaide, Adelaide, South Australia, Australia.
Robinson Research Institute and Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia.
BMJ Open. 2018 Jul 10;8(7):e020988. doi: 10.1136/bmjopen-2017-020988.
South Australia (SA) has the highest notification rate of invasive meningococcal disease in Australia with the majority of cases due to serogroup B. is carried in the pharynx, with adolescents having the highest rates of carriage. A vaccine designed to offer protection against serogroup B (4CMenB) is licensed in Australia. The SA MenB vaccine carriage study aims to assess the impact of 4CMenB on carriage of in adolescents.
This is a parallel cluster randomised controlled trial enrolling year 10, 11 and 12 school students (approximately 16-18 years of age) throughout SA, in metropolitan and rural/remote areas. Schools are randomised to intervention (4CMenB vaccination at baseline) or control (4CMenB vaccination at study completion) with randomisation stratified by school size and socioeconomic status, as measured by the Index of Community Socio-Educational Advantage (Australian Curriculum). Oropharyngeal swabs will be taken from all students at visit 1, and 12 months later from year 11 and 12 students. Students unvaccinated in 2017 will receive vaccine at the 12-month follow-up. Carriage prevalence of will be determined by PCR at baseline and 12 months following 4CMenB vaccination and compared with carriage prevalence at 12 months in unvaccinated students. A questionnaire will be completed at baseline and 12 months to assess risk factors associated with carriage. The primary outcome of carriage prevalence of disease causing at 12 months will be compared between groups using logistic regression, with generalised estimating equations used to account for clustering at the school level. The difference in carriage prevalence between groups will be expressed as an OR with 95% CI.
The study was approved by the Women's and Children's Health Network Human Research Ethics Committee (WCHN HREC). The protocol, informed consent forms, recruitment materials, social media and all participant materials have been reviewed and approved by the WCHN HREC and updated on ClinicalTrials.gov. Results will be published in international peer-reviewed journals and presented at national and international conferences. The study findings will be provided in public forums and to study participants and participating schools.
ACTRN12617000079347. NCT03089086; Pre-results.
南澳大利亚州(SA)的侵袭性脑膜炎球菌病通报率在澳大利亚最高,大多数病例由B群血清型引起。该病菌在咽部携带,青少年携带率最高。一种旨在预防B群血清型(4CMenB)的疫苗已在澳大利亚获得许可。南澳大利亚州B群脑膜炎球菌疫苗携带情况研究旨在评估4CMenB对青少年携带该病菌情况的影响。
这是一项平行整群随机对照试验,招募南澳大利亚州城市及农村/偏远地区10、11和12年级的在校学生(约16 - 18岁)。学校被随机分为干预组(基线时接种4CMenB疫苗)或对照组(研究结束时接种4CMenB疫苗),随机分组按学校规模和社会经济地位分层,社会经济地位通过社区社会教育优势指数(澳大利亚课程)衡量。在第1次访视时采集所有学生的口咽拭子,12个月后采集11和12年级学生的口咽拭子。2017年未接种疫苗的学生将在12个月随访时接种疫苗。将通过聚合酶链反应在基线时以及4CMenB疫苗接种后12个月确定该病菌的携带率,并与未接种疫苗学生12个月时的携带率进行比较。在基线和12个月时完成一份问卷,以评估与携带相关的风险因素。使用逻辑回归比较两组在12个月时引起疾病的该病菌携带率这一主要结局,使用广义估计方程来考虑学校层面的聚类情况。两组之间携带率的差异将表示为带有95%置信区间的比值比。
该研究已获得妇女与儿童健康网络人类研究伦理委员会(WCHN HREC)的批准。研究方案、知情同意书、招募材料、社交媒体及所有参与者材料均已得到WCHN HREC的审查和批准,并在ClinicalTrials.gov上更新。研究结果将发表在国际同行评审期刊上,并在国内和国际会议上展示。研究结果将在公共论坛上提供给研究参与者和参与学校。
ACTRN12617000079347。NCT03089086;预结果。