Queensland Paediatric Infectious Diseases Laboratory, Queensland Children's Medical Research Institute, The University of Queensland, Royal Children's Hospital, Herston Road, Herston, QLD 4029, Australia.
Paediatr Drugs. 2010 Aug 1;12(4):235-56. doi: 10.2165/11537200-000000000-00000.
Rotaviruses are the most common cause of severe gastroenteritis in children. By 5 years of age virtually every child worldwide will have experienced at least one rotavirus infection. This leads to an enormous disease burden, where every minute a child dies because of rotavirus infection and another four are hospitalized, at an annual societal cost in 2007 of $US2 billion. Most of the annual 527 000 deaths are in malnourished infants living in rural regions of low and middle income countries. In contrast, most measurable costs arise from medical expenses and lost parental wages in high income countries. Vaccines are the only public health prevention strategy likely to control rotavirus disease. They were developed to mimic the immunity following natural rotavirus infection that confers protection against severe gastroenteritis and consequently reduces the risk of primary healthcare utilization, hospitalization and death. The two currently licensed vaccines--one a single human strain rotavirus vaccine, the other a multiple strain human-bovine pentavalent reassortant rotavirus vaccine--are administered to infants in a two- or three-dose course, respectively, with the first dose given at 6-14 weeks of age. In various settings they are safe, immunogenic and efficacious against many different rotavirus genotypes. In high and middle income countries, rotavirus vaccines confer 85-100% protection against severe disease, while in low income regions of Africa and Asia, protection is less, at 46-77%. Despite this reduced efficacy in low income countries, the high burden of diarrheal disease in these regions means that proportionately more severe cases are prevented by vaccination than elsewhere. Post-licensure effectiveness studies show that rotavirus vaccines not only reduce rotavirus activity in infancy but they also decrease rates of rotavirus diarrhea in older and unimmunized children. A successful rotavirus vaccination program will rely upon sustained vaccine efficacy against diverse and evolving rotavirus strains and efficient vaccine delivery systems. The potential introduction of rotavirus vaccines into the world's poorest countries with the greatest rates of rotavirus-related mortality is expected to be very cost effective, while rotavirus vaccines should also be cost effective by international standards when incorporated into developed countries immunization schedules. Nonetheless, cost effectiveness in each country still depends largely on the local rotavirus mortality rate and the price of the vaccine in relation to the per capita gross domestic product.
轮状病毒是导致儿童严重肠胃炎的最常见原因。全世界几乎每个孩子在 5 岁前都至少经历过一次轮状病毒感染。这导致了巨大的疾病负担,每分钟都有一名儿童因轮状病毒感染而死亡,还有四名儿童因轮状病毒感染住院,2007 年的全球社会成本为 20 亿美元。大多数年度 52.7 万例死亡发生在营养不良的婴儿中,这些婴儿生活在中低收入国家的农村地区。相比之下,在高收入国家,大多数可衡量的成本来自医疗费用和父母旷工的工资损失。疫苗是唯一可能控制轮状病毒病的公共卫生预防策略。它们是为了模仿自然轮状病毒感染后的免疫而开发的,这种免疫可以预防严重肠胃炎,并因此降低初级保健利用、住院和死亡的风险。目前有两种获得许可的疫苗——一种是单一人类株轮状病毒疫苗,另一种是多种人类-牛五价重配轮状病毒疫苗——分别以两剂或三剂的方式接种给婴儿,第一剂在 6-14 周龄时接种。在各种环境下,它们是安全的,对许多不同的轮状病毒基因型具有免疫原性和有效性。在高收入和中等收入国家,轮状病毒疫苗对严重疾病的保护率为 85-100%,而在非洲和亚洲的低收入地区,保护率较低,为 46-77%。尽管在低收入国家的效力有所降低,但这些地区腹泻病的高负担意味着疫苗接种比其他地区更能预防更多的严重病例。疫苗上市后有效性研究表明,轮状病毒疫苗不仅能降低婴儿期轮状病毒的活性,还能降低大龄和未免疫儿童的轮状病毒腹泻率。一个成功的轮状病毒疫苗接种计划将依赖于针对不同和不断演变的轮状病毒株的持续疫苗效力和有效的疫苗接种系统。预计在轮状病毒相关死亡率最高的世界最贫困国家引入轮状病毒疫苗将非常具有成本效益,而轮状病毒疫苗在发达国家免疫接种计划中纳入也将符合国际标准的成本效益。尽管如此,每个国家的成本效益在很大程度上仍取决于当地的轮状病毒死亡率和疫苗价格相对于人均国内生产总值的关系。