Rotarix in Japan: Expectations and Concerns.

Biologics in therapy Pub Date : 2011-12-14 eCollection Date: 2011-01-01 DOI:10.1007/s13554-011-0007-5
Osamu Nakagomi, Toyoko Nakagomi
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引用次数: 1

Abstract

A live-attenuated, orally-administered, monovalent, human rotavirus vaccine, Rotarix® (GlaxoSmithKline Biologicals, Rixensart, Belgium), was licensed and launched in 2011 as the first rotavirus vaccine in Japan. The rotavirus causes a substantial disease burden with an estimated 790,000 outpatient visits, 27,000-78,000 hospitalizations, and approximately 10 deaths each year in Japan. Since a recent clinical trial showed that Rotarix was as efficacious in Japan as in other industrialized countries, it is expected that the annual number of rotavirus hospitalizations will be reduced to between 1000-3000, and that outpatient visits will be reduced to 200,000. The universal rotavirus immunization program with Rotarix was calculated to be at the threshold of being cost-effective, even from the healthcare perspective, and it was highly cost-effective from the societal perspective, assuming that Rotarix is co-administered with other childhood vaccines. While Rotarix contains only a single G1P[8] human rotavirus, the postlicensure studies in Brazil showed that Rotarix provided a 75%-85% protective efficacy against severe dehydrating diarrhea or hospitalizations due to fully-heterotypic G2P[4] strains. While postlicensure studies detected a small and finite risk of intussusception associated with the administration of Rotarix, the authors conclude that Rotarix is safe to administer to infants between 6-12 weeks of age for the first dose and by 24 weeks of age for the second dose. However, the authors strongly discourage the delayed administration of the first dose between 13-20 weeks of age, which is allowed without any warning. Given the high incidence of naturally-occurring intussusception in Japan (185 cases per 100,000 children/year among children less than 1 year of age), this should prevent pediatricians and parents from having ill-perceptions of Rotarix being associated with an increased number of temporally-associated intussusception, and fully appreciate the benefit of the rotavirus vaccine.

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日本的扶轮社:期望与关注。
口服单价轮状病毒减毒活疫苗Rotarix®(GlaxoSmithKline Biologicals, Rixensart, Belgium)于2011年获得许可并在日本上市,成为首个轮状病毒疫苗。轮状病毒造成了巨大的疾病负担,据估计,日本每年有79万人次门诊就诊,2.7万至7.8万人次住院,约10人死亡。由于最近的一项临床试验表明,Rotarix在日本与其他工业化国家一样有效,预计每年因轮状病毒住院的人数将减少到1000至3000人之间,门诊人次将减少到20万人次。使用Rotarix的普遍轮状病毒免疫计划被计算为具有成本效益的门槛,甚至从医疗保健的角度来看,从社会的角度来看,假设Rotarix与其他儿童疫苗共同接种,它具有很高的成本效益。虽然Rotarix只含有一种G2P[8]人类轮状病毒,但巴西的许可后研究表明,Rotarix对由完全异型G2P[4]菌株引起的严重脱水腹泻或住院治疗具有75%-85%的保护功效。虽然许可后的研究发现与Rotarix给药相关的肠套叠的风险很小且有限,但作者得出结论,Rotarix对6-12周龄的婴儿第一次给药是安全的,对24周龄的婴儿第二次给药是安全的。然而,作者强烈反对在13-20周龄之间延迟给药,这是允许的,没有任何警告。鉴于日本自然发生的肠套叠发病率很高(1岁以下儿童每年每10万名儿童中有185例),这应该可以防止儿科医生和家长对轮状病毒疫苗与时间相关性肠套叠数量增加有关的错误看法,并充分认识到轮状病毒疫苗的好处。
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