Sanofi, 1755 Steeles Avenue W, Toronto, Ontario M2R 3T4, Canada; University of Guelph, 50 Stone Road E, Guelph, Ontario N1G 2W1, Canada; York University, 4700 Keele St, Toronto, Ontario M3J 1P3, Canada.
Sanofi, Lyon, France.
Vaccine. 2022 Nov 28;40(50):7343-7351. doi: 10.1016/j.vaccine.2022.10.071. Epub 2022 Nov 5.
The World Health Organization (WHO) recommended 'pre-vaccination screening' as its preferred implementation strategy when using the licensed dengue vaccine (CYD-TDV; Dengvaxia, Sanofi), so that only individuals with previous dengue infection are vaccinated. The US Centers for Disease Control and Prevention (CDC) recommended use of CYD-TDV to prevent dengue in children with previous laboratory-confirmed dengue infection in regions where dengue is endemic. Here, we evaluate the public health impact and cost-effectiveness of a 'pre-vaccination screening' strategy in Puerto Rico.
The current analysis builds upon a previously published transmission model used to assess the benefits/risks associated with dengue vaccination. For 'pre-vaccination screening', three alternative testing methods were assessed: one using an immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA) dengue serotest, another with dengue serotesting using a rapid diagnostic test (RDT), and one using both sequentially (as recommended in Puerto Rico). The time horizon considered was 10 years.
In Puerto Rico, the disability-adjusted life years (DALYs) averted for 'pre-vaccination screening' with an ELISA-based program, RDT-based program, and both sequentially would be a median 1,192 (95% CI: 716-2,232), 2,812 (95% CI: 1,579-5,019), and 1,017 (95% CI: 561-1,738), respectively. These benefits would arise from the reduction in cases: median 24,961 (95% CI: 17,480-36,782), 58,273 (95% CI: 40,729-84,796), 20,775 (95% CI: 14,637-30,374) fewer cases, respectively. The cost per DALY averted from a payer perspective would be US$12,518 (95 %CI: US$4,749-26,922), US$10,047 (95% CI: US$3,350-23,852), and US$12,334 (95% CI: US$4,965-26,444), respectively. All three strategies would be cost saving from a societal perspective.
Our study supports the WHO and CDC 'pre-vaccination screening' guidance for CYD-TDV implementation. In Puerto Rico, regardless of the testing strategy and even with a relatively low rate of testing, it would be cost-effective from a payer perspective and cost saving from a societal perspective.
世界卫生组织(WHO)建议在使用已许可的登革热疫苗(CYD-TDV;Dengvaxia,赛诺菲)时采用“疫苗接种前筛查”作为其首选实施策略,以便仅对既往登革热感染的个体进行疫苗接种。美国疾病控制与预防中心(CDC)建议在登革热流行地区,对既往实验室确诊的登革热感染儿童使用 CYD-TDV 预防登革热。在此,我们评估了在波多黎各实施“疫苗接种前筛查”策略对公共卫生的影响和成本效益。
目前的分析基于之前发表的用于评估登革热疫苗接种相关风险/获益的传播模型。对于“疫苗接种前筛查”,评估了三种替代检测方法:一种使用免疫球蛋白 G(IgG)酶联免疫吸附试验(ELISA)登革热血清学检测,另一种使用快速诊断试验(RDT)进行登革热血清学检测,还有一种使用两者依次进行(如波多黎各所推荐的)。考虑的时间范围为 10 年。
在波多黎各,使用 ELISA 为基础的方案、RDT 为基础的方案和两者依次进行“疫苗接种前筛查”,可避免的残疾调整生命年(DALY)中位数分别为 1192(95%CI:716-2232)、2812(95%CI:1579-5019)和 1017(95%CI:561-1738)。这些获益将来自病例的减少:中位数分别为 24961(95%CI:17480-36782)、58273(95%CI:40729-84796)和 20775(95%CI:14637-30374)例。从支付者的角度来看,每避免一个 DALY 的成本分别为 12518 美元(95%CI:4749-26922 美元)、10047 美元(95%CI:3350-23852 美元)和 12334 美元(95%CI:4965-26444 美元)。从社会角度来看,这三种策略都是节省成本的。
我们的研究支持 WHO 和 CDC 关于 CYD-TDV 实施的“疫苗接种前筛查”指南。在波多黎各,无论采用哪种检测策略,甚至检测率相对较低,从支付者的角度来看,它具有成本效益,从社会角度来看,它是节省成本的。