A neonatal pneumococcal conjugate vaccine trial in Papua New guinea: study population, methods and operational challenges.

Papua and New Guinea medical journal Pub Date : 2010-09-01
S Phuanukoonnon, J C Reeder, W S Pomat, A H J Van den Biggelaar, P G Holt, G Saleu, C Opa, A Michael, C Aho, M Yoannes, J Francis, T Orami, P Namuigi, P M Siba, P C Richmond, D Lehmann
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Abstract

Infants in Papua New Guinea (PNG) are at a high risk of invasive pneumococcal disease, and a substantial burden of this falls on children less than six months old. PNG is planning to introduce a pneumococcal conjugate vaccine for infants in the near future, but to make the maximum impact neonatal immunization will have to be considered. To provide evidence on safety and immunogenicity for neonatal and early infant immunization, we undertook an open randomized controlled trial of 7-valent pneumococcal conjugate vaccine (7vPCV). 318 children received 7vPCV at ages 0, 1 and 2 months or at 1, 2 and 3 months or not at all. All children received 23-valent pneumococcal polysaccharide vaccine at age 9 months. This was a large and complex trial: village reporters visited participants weekly during the first year and fortnightly for a further 6 months and nurses monitored self-reported morbidity and collected many thousands of biological samples. The study team was remarkably successful in achieving the study aims, with 18-month follow-up completed on 77% of enrolled children and over 80% of scheduled samples collected. While the results of the trial will be reported elsewhere, this paper discusses the design of the study and dissects out some of the main reasons for its successful completion. Strong community engagement was an essential factor in success and the principles of equitable partnership and service provision led to a strong research partnership. A two-stage consent process, comprising primary assent followed by later informed consent, led to a high drop-out before initial enrolment, but an outstanding retention of those enrolled in the study. We conclude that factors such as strong community participation, reciprocity and a good relationship between the study team and participants are just as important as the technical elements of laboratory testing and data handling in ensuring the success of a vaccine trial in PNG.

巴布亚新几内亚新生儿肺炎球菌结合疫苗试验:研究人群、方法和操作挑战
巴布亚新几内亚(PNG)的婴儿患侵袭性肺炎球菌疾病的风险很高,其中很大的负担落在了6个月以下的儿童身上。巴布亚新几内亚正计划在不久的将来为婴儿引入肺炎球菌结合疫苗,但为了产生最大的影响,必须考虑新生儿免疫接种。为了提供新生儿和早期婴儿免疫接种的安全性和免疫原性证据,我们进行了一项7价肺炎球菌结合疫苗(7vPCV)的开放随机对照试验。318名儿童在0、1、2个月或1、2、3个月或根本不接种7vPCV。所有儿童在9个月大时接种23价肺炎球菌多糖疫苗。这是一项大型而复杂的试验:村记者在第一年每周访问参与者,在接下来的6个月里每两周访问一次,护士监测自我报告的发病率,并收集数千份生物样本。研究小组非常成功地实现了研究目标,77%的入组儿童完成了18个月的随访,超过80%的计划样本收集。虽然试验结果将在其他地方报道,但本文讨论了研究的设计,并剖析了其成功完成的一些主要原因。强有力的社区参与是成功的关键因素,公平伙伴关系和提供服务的原则导致了强有力的研究伙伴关系。两阶段的同意过程,包括初步同意和随后的知情同意,导致在初始登记前的高辍学率,但参加研究的人保留得很好。我们的结论是,在确保巴布亚新几内亚疫苗试验成功方面,社区积极参与、互惠互利以及研究小组与参与者之间的良好关系等因素与实验室测试和数据处理的技术要素同样重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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