- Research article
- Open Access
- Open Peer Review
Public health impact and cost effectiveness of routine childhood vaccination for hepatitis a in Jordan: a dynamic model approach
BMC Infectious Diseasesvolume 18, Article number: 119 (2018)
As the socioeconomic conditions in Jordan have improved over recent decades the disease and economic burden of Hepatitis A has increased. The purpose of this study is to assess the potential health and economic impact of a two-dose hepatitis A vaccine program covering one-year old children in Jordan.
We adapted an age-structured population model of hepatitis A transmission dynamics to project the epidemiologic and economic impact of vaccinating one-year old children for 50 years in Jordan. The epidemiologic model was calibrated using local data on hepatitis A in Jordan. These data included seroprevalence and incidence data from the Jordan Ministry of Health as well as hospitalization data from King Abdullah University Hospital in Irbid, Jordan. We assumed 90% of all children would be vaccinated with the two-dose regimen by two years of age. The economic evaluation adopted a societal perspective and measured benefits using the quality-adjusted life-year (QALY).
The modeled vaccination program reduced the incidence of hepatitis A in Jordan by 99%, 50 years after its introduction. The model projected 4.26 million avoided hepatitis A infections, 1.42 million outpatient visits, 22,475 hospitalizations, 508 fulminant cases, 95 liver transplants, and 76 deaths over a 50 year time horizon. In addition, we found, over a 50 year time horizon, the vaccination program would gain 37,502 QALYs and save over $42.6 million in total costs. The vaccination program became cost-saving within 6 years of its introduction and was highly cost-effective during the first 5 years.
A vaccination program covering one-year old children is projected to be a cost-saving intervention that will significantly reduce the public health and economic burden of hepatitis A in Jordan.
Hepatitis A virus (HAV) infections continue to pose significant public health issues in Jordan. Some studies over the past few decades had placed Jordan among countries with high HAV endemicity [1,2,3]. High endemicity is defined as seroprevalence ≥90% by age 10 years and intermediate endemicity is defined as ≥50% by age 15 years . However, the most recent study conducted in 2008 , found that a shift in HAV infection burden from children to young adults, that is, the number of children acquiring the infection has decreased while the number of infections in adolescents and adults has increased. This epidemiological pattern among older and relatively active cohorts may lead to serious outbreaks and significant burden of disease because HAV infection in older patients is usually more symptomatic.
The World Health Organization (WHO) recommends including hepatitis A vaccination in the national immunization schedule for children ≥1 year of age when indicated, based on: incidence of acute hepatitis A; change in endemicity from high to intermediate; and consideration of cost effectiveness. According to WHO guidelines, in countries transitioning to intermediate-endemicity where the majority of the adult population will likely be susceptible to hepatitis A infection, large-scale hepatitis A vaccination programs are likely to be cost-effective and are encouraged .
The National Immunization Technical Advisory Group (NITAG) of Jordan has voted to introduce several vaccines: pneumococcal conjugate, rotavirus, hepatitis A and varicella to the National Immunization Program. As of December 2015, only rotavirus was introduced. In view of financial and logistic obstacles facing new vaccines introduction, cost-effectiveness and disease burden studies are expected to help decision and policymakers determine prioritization of remaining in-plan vaccines including the hepatitis A vaccine in Jordan. The purpose of this paper is to test this evidence by assessing the potential health and economic impact of a hepatitis A vaccination program covering one-year old children in Jordan.
To assess the potential health and economic impact of a two-dose hepatitis A vaccination program targeting one-year-old children in Jordan, we used a deterministic, age-structured, epidemiologic dynamic model developed previously by Dhankhar, et al.  and adapted for the study of HAV transmission and vaccination against HAV infection in Jordan. The model divides the population of Jordan into several distinct classes: maternal antibodies, susceptible, exposed, asymptomatic infection, outpatient, hospitalized, fulminant, patients with recent liver transplant, patients with past liver transplant, recovered, and vaccinated (Fig. 1). Each compartment was further categorized into 101 age groups (0 to < 1, 1,.. .,99, and 100 years or older). The movement of populations between compartements in the model is described in detail in Dhankhar et al. 
The model used in the simulations consists of 1313 coupled differential equations corresponding to the 12 epidemiological classes (see Fig. 1) and demographic equations for 101 age groups. All differential equations and details of the epidemiologic model are given in the technical supplement.
Jordan does not have a national HAV vaccination program in place. Also, we were unable to find any data indicating signficant HAV vaccination through the private health sector. Hence, we assumed that before the start of universal vaccination no hepatitis A vaccination strategy was in place in Jordan and that, for our base case, a two-dose program covering oneyear-olds began in 2016. The program consisted of one dose at 12 months old and the second dose at 18 months old. .
In the model, the vaccination at age one year is incorporated by moving a fraction of infants from the susceptible class to the vaccination class before they are two years old. We compared routine universal vaccination of one year-olds to a no vaccine strategy.
Model parameters and data sources
We identified base case inputvalues of demographic, epidemiologic, vaccine, and economic inputs of the model through an extensive search of the published literature. The resulting input values are detailed in Table 1. Jordan specific data inputs were also identified and used where they were available.
We obtained age and gender-specific mortality from both the WHO Life Tables  and Jordan’s IndexMundi demographic profile . Population size of Jordan for 2014 was obtained from U.S. Census International Database  and includes Syrian refugee population.
Transmission rates and force of infection
The epidemiologic data on HAV in Jordan and the region suggest there is an ongoing shift from high endemicity to intermediate endemicity [3, 5]. The transmission of HAV in general is correlated with socioeconomic conditions and in particular sanitation and water supply infrastructure [3, 11, 12]. To account for this shift, we adjusted the age-specific force of infection by a universal (age independent) multiplier consisting of piecewise function of time that gradually reduces the force of infection. We allowed for two periods of change each at a different rate. Both the dates and the magnitude of the reduction in force of infection were determined from calibration to local data. To estimate the forces of infection before the vaccination program is initiated, we used least square methods to fit the model to data on age specific seroprevalence levels in 2008  and seroprevalence in 1988 data . In addition we used incidence data from Jordan Ministry of Health between 2004 and 2014 . Using these data, the force of infection multiplier function indicated a 4% per year decline in force of infection between 1984 and 1999 followed by a 1% reduction for the next 10 years (see Additional file 1). The timing and magnitude of the trends are consistent with the historical socioeconmic development of Jordan as well as specific sanitation and water supply improvement efforts over the past few decades [14, 15]. Additionally, the decline in force of infections ends in about 2009 as the Syrian crisis in the region  begins and ultimately strains resources as a significant new population with a different level of HAV endemicity is introduced into the Jordan population [17,18,19].
To estimate the proportion of non-outpatient cases we used unpublished HAV hospitalization data from King Abdullah University Hospital in Jordan over the years 2003 through 2013 (see Additional file 1). The proportion of icteric HAV infections is determined using an age specific probability of developing jaundice .
The modeling approach does not assume that the endemic disease has reached an equilibrium state before vaccination. Thus, force of infection estimates continue to change with time during the prevaccination period. Force of infection was modeled assuming proportionate mixing, and no exogenous effects, for example, exposure during foreign travel. The force of infection is dynamically modeled so that herd effects are naturally included. Detailed description of the forces of infection are available in the supplementary material (see Additional file 1). Other parameters of the natural history of HAV infection are summarized in Table 1.
Hepatitis a virus infection parameters
We modeled several health outcomes associated with the HAV infection including outpatient visits, hospitalizations, fulminant hepatitis disease, liver transplant, and death (Fig. 1). We assumed that asymptomatic hepatitis A cases do not require health care and only the management of icteric hepatitis A cases entails the use of health care resources. We further assumed that all reported and unreported icteric cases are treated and used the underreporting factor to identify the proportion of inpatient – hospitalized, fulminant hepatitis, or liver transplant – the remaining cases are assumed to receive outpatient care. Within the inpatient category the conditional probabilities shown in Table 1 are the result of dividing by the underreporting factor [7, 21].
Vaccine efficacy for one or two doses was based on data from VAQTA [Hepatitis A Vaccine, Purified Inactivated, Merck & Co., Inc., Kenilworth, NJ] and was determined to be 100% in the base case . We assumed the median duration of protection of a completed one-dose and two-dose hepatitis A vaccination in the base case was 21 and 32 years, respectively, and examined alternative assumptions in the sensitivity analysis . With respect to vaccine coverage, the base case assumed that 95% of one-year-olds will receive one-dose and that 95% of those will receive the second does before they are two years old. The base case vaccination coverage was chosen based on coverage achieved in similar childhood vaccinations in the Jordanian National Immunization Program [13, 24].
We adopted a societal perspective for economic evaluation. We included both direct and indirect costs in the evaluation. The direct costs included treatment costs of HAV-associated health outcomes and vaccination. Treatment costs included costs for outpatient visits, hospitalizations, fulminant hepatitis, and liver transplantations [25,26,27]. Wherever possible we used Jordanian cost data, however, in some cases we used costs from similarly economically situated countries and adjusted appropriately. We use $10.00 USD per dose for the vaccine price based on estimates of current regional pricing. We assumed $1.90 for vaccine administration costs based on estimates from King Abdullah University Hospital.
Indirect costs included the costs associated with the work loss due to different health outcomes. These were estimated by multiplying the days of work loss from an HAV disease outcome by the labor force participation rate and the daily wages of the patients’ age group (Table 1). We did not include public health disease control costs in the base case study as these were estimated to be very small in Jordan. However, we did include non-zero public health costs in the sensitivity analyses. All costs are reported in 2015 USD. Future costs were discounted at 3% per year. To interpret the cost-effectiveness of vaccination we used the WHO CHOICE criteria which set cost-effectiveness thresholds based on per capita GDP. According to this criteria, incremental cost-effectiveness ratio (ICER) less than one times per capita GDP is considered “very cost effective” while ICER greater than three times per capita GDP is “not cost-effective” .
We calculated quality-adjusted life-years (QALYs) by applying utility weights to time spent in each health state. We assumed a weight of 0.642 for all icteric outcomes related to hepatitis A, except liver transplant . For patients with liver transplants, we assumed a weight of 0.73 following transplantation . We assumed the quality-of-life weight of 0.83 for persons with anicteric hepatitis A. For all other health states we used a weight of 1.0. To account for the age-specific health utilities in the general population, all utility weights were multiplied by the age-specific US population norms  due to a lack of Jordanian-specific data.
The model was implemented in Mathematica 10.1 (Wolfram Research, Inc., Champaign, IL). We used the built-in function NDSolve to find numerical solutions to the system of ordinary differential equations. The built-in function NMinimize was used for model calibration. We used Mathematica for all simulations, and analyses and some figures; others were produced using Microsoft Excel 2010 (Microsoft Corp., Redmond, WA).
Base case and sensitivity analyses
We estimated expected health outcomes (total HAV infections, symptomatic HAV infections, outpatient visits, hospitalizations, fulminant hepatitis cases, number of liver transplants, deaths, QALYs) and costs over a time horizon of 50 years.
Deterministic sensitivity analyses were performed by varying vaccination parameters (efficacy, duration of protection, cost, coverage, and adherence), cost parameters, quality-of-life weights, and discount rate.
Probabilistic sensitivity analyses (PSA) were also performed using a subset of parameters including vaccine properties and uptake, clinical outcomes, costs, and quality-of-life weights were included in a PSA as described in Table 1. The rationale for the selection of the probability distribution function for each parameter and sampling techniques used in the PSA is discussed in the technical supplement. The results are summarized using the mean of outcomes and presented using a scatter plot in the incremental cost-effectiveness plane . The location of a point on the plane summarizes its cost and effectiveness. For example, all positive incremental QALYs represent health gains; negative costs represent a total cost savings for the program. If the costs are positive and the QALYs are positive then there is a threshold, the willingness to pay (WTP) for each QALY gained below which the program is considered cost-effective or cost-saving.
Model transparency and validation
To facilitate independent review and replication of our results according to industry recommendations  we provided a technical supplement which includes information on the model’s structure, equations, inputs, outputs, and detailed description of methods of the derivation. The face validity of the model is described in Dhankhar, et al.  Internal validity of the model code was verified using several tests including balanced inflow and outflow between compartments and constancy of total population throughout the calculations. The predictive validity of the model was evaluated by comparing model results with epidemiologic data reported in the literature (see Additional file 1).
The model predicts rapid and substantial decrease in overall incidence of Hepatitis A (Fig. 2). The model predicts a drop from 900 cases per 100,000 a year down to less than one case per 100,000 within five years of launching the vaccination program. Long-term health outcomes were predicted after the introduction of the vaccination program (Table 2). In terms of cumulative outcomes, on the 50 year time horizon there are 4.26 million infections avoided resulting in more than 1.4 million inpatient cases avoided over the 50 year time horizon.
The economic impact of the vaccination program is summarized in Table 3. The results for costs and QALYs are shown for the whole population. Costs savings are achieved by 6 years after the program begins saving $46.2 million in the first 50 years.
Deterministic sensitivity analysis
The number of years to reach cost savings was most sensitive to outpatient cost, vaccine dose cost, hospitalization costs, second dose vaccine adherence, and outpatient work-loss days. The outpatient costs parameter induced the largest change. In the low cost ($10) limit, the universal vaccination program takes more than 45 years to become cost saving while in the high cost limit ($100) cost saving is attained within 4 years. The sensitivity to this factor arises from the large proportion of cases that are treated as outpatient, approximately 99% of all symptomatic cases. The next most influential parameter was the vaccine cost. The vaccine cost lower limit ($8) leads to cost savings within 4 years while the upper limit ($14) extends time to cost savings to 14 years. This sensitivity is due to the vaccine cost being the only substantial contributor to the total cost of the vaccination program.
The other factors tested lead to between − 1.4 and 1.3 years difference in reaching the cost savings threshold. For example, the lower limit of the hospitalization costs ($80) results in 6 years to cost savings while the upper limit ($150) leads to 4.6 years to cost savings. Among factors that had little effect on years-to-cost savings were the 1st dose vaccine uptake and vaccine parameters such as vaccine efficacy and duration of protection. These likewise had little effect on health outcomes. For example, with the lowest uptake, 70%, the program still reaches less than one case per 100,000 people within the five years. In fact, as long as the 1st dose uptake is > 40% this threshold will be reached. In addition, since the population has not reached endemic equilibrium by 2016, we considered a range of vaccination program start years (tvstart) from 2016 through 2040. We found little qualitative difference in outcomes, for example, the time to cost savings ranged from approximately 2 to 5.4 years, with our base case, tvstart = 2016, being the worst case.
The total cost savings over 50 years was most sensitive to discount rate, outpatient costs, vaccine cost, median monthly earnings 25+, probability of death after 1st year liver transplant, outpatient work loss days, and hospitalization costs in that order. Discount rate produced the largest change reducing cost savings by $9.2 million between the low (0%) and high (5%) discount rates. Outpatient costs was the second most influential parameter increasing cost savings by $7.9 million between the low and high cost values. Vaccine cost was the third most influential parameter reducing cost savings by $3.3 million between the low and high limits. All other parameters were less influential leading to changes in cost savings between -$1.3 and $1.2 million.
Probabilistic sensitivity analysis (PSA)
We performed a PSA using 1024 Monte Carlo simulations. The results showed that the mean incremental cost savings for the population after 50 years was US $807,000 (95% confidence interval $41,000 to $2.1 M) with a median value of $560,000. The corresponding values for incremental QALYs gained was 460 (95% confidence interval 428 to 508) with a median value of 453. Additionally, the mean number of years to reach cost saving was 6.9 years (95% confidence interval 2.2 to 30 years) with a median value of 4.4 years.
The incremental cost-effectiveness plane shows that most (99.3%) of the PSA pairs fall in the fourth quadrant indicating they are cost saving (Fig. 3). The remaining 0.7% are in the first quadrant and are highly cost-effective. The average incremental cost-effectiveness ratio for the PSA pairs in the first quadrant is $86/QALY. The chart shows the line indicating a willingness-to-pay of $3600/QALY. This quantity is the one-times the per capita GDP of Jordan in 2014 below which therapies are considered “very cost-effective” according WHO CHOICE recommendations . All of the scenarios in these analyses fell well below the $3600/QALY threshold.
To our knowledge this is the first published modeling study of HAV in Jordan. We adapted a previously published dynamic transmission model to examine the potential impact of two-dose hepatitis A vaccination of one year-olds in Jordan. As compared with no vaccination, the model predicted that this vaccination program is cost-saving within 6 years of its introduction. The model showed the virtual elimination of HAV cases within five years of introducing a two-dose vaccination program targeting one-year olds.
Our health economic results are similar to those previously obtained from model-based analysis in other HAV intermediate endemic countries. Those analyses also support the clinical and economic value of universal mass vaccination against hepatitis A virus: > 98% reduction in incidence for toddlers and > 95% reduction for the rest of the population in the first five years in Israel ; a sharp disease rate decrease (88%) in Argentina ; total disease societal cost reduction while costing the health system <US$726 per QALY in Chile ; cost-saving -US $ 2.26 saved for each invested dollar- in Brazil [37, 38]; and 85 to 93% reduction for all HAV infections in Mexico .
Sensitivity analyses showed that outpatient costs, vaccine costs, probability of death after the 1st year of a liver transplant, were most influential in determining the time to reach cost saving. No scenarios failed to reach cost saving within 50 years. Health outcomes were not particularly sensitive to uptake or adherence. Regardless, suboptimal uptake and adherence is not expected considering consistently very high uptake levels reported by Jordanian National Immunization Program with other vaccination programs .
Despite similarity of overall economic value with above mentioned previous studies, their results show less optimistic health outcomes than our model’s predictions [26, 36, 39, 40]. Some of the differences could be due to methodological quality variation across studies , but the most significant effects are likely to be due to differences in the way exogenous effects are included in the force of infection.
Our study has several limitations. First, given the lack of directly measurable data on the force of infection parameters, we had to specify a particular functional form, make simplifying assumptions, and estimate the input parameters by fitting the model to real world data. For example, when considering exogenous factors affecting the force of infection, we excluded effects due to foreign travel, or immigration. This may be a good choice for the current state, but such factors, like the ongoing influx of refugees, may become important in the future. In addition, we have assumed that ongoing and future socioeconomic changes will not have significant influence on the force of infection in the future thereby potentially overestimating the benefit of a vaccination program. Second, limited availability of reliable historical data for seroprevalence and disease incidence adds uncertainty to the model calibration. Third, we assumed that certain parameters, e.g., population size and birth rate, stay constant over the time horizon. Fourth, due to the lack of data availability for Jordan, many economic and outcomes parameters were estimated, derived, or adapted from data from other countries. Finally, we did not incorporate uncertainty in the estimated parameters of the force of infection as part of the probabilistic sensitivity analysis.
Conclusion and recommendations
This model predicted that a universal 2-dose program vaccinating one year olds against hepatitis A led to significant reductions in hepatitis A morbidity and mortality and was cost saving within 6 years and highly cost-effective during the first 5 years.
Based on the study results, the safety profile of the vaccine [42, 43] and the WHO recommendations , the risk-benefit profile calls for the introduction of a two-dose program of vaccinating one-year olds against hepatitis A. These two doses, at 12 and 18 months of age, could ideally be administered simultaneously with other vaccines already included in the Jordanian National Pediatric Immunization Program.
Gross domestic product
Hepatitis A virus
Incremental cost-effectiveness ratio
National Immunization Technical Advisory Group
Probabilistic sensitivity analysis
World Health Organization
Willingness to pay
Battikhi MN, Battikhi EG. The seroepidemiology of hepatitis a virus in Amman, Jordan. New Microbiol. 2004;27:215–20.
Toukan AU, Sharaiha ZK, Abu-el-Rob OA. The seroepidemiology of hepatitis a virus infection in Jordan. Trop Gastroenterol. 1988;9:76–9.
Itani T, Jacobsen KH, Nguyen T, Wiktor SZ. A new method for imputing country-level estimates of hepatitis a virus endemicity levels in the eastern Mediterranean region. Vaccine. 2014;32:6067–74.
Jacobsen KH, Wiersma ST. Hepatitis a virus seroprevalence by age and world region, 1990 and 2005. Vaccine. 2010;28:6653–7.
Hayajneh WA, Balbeesi A, Faouri S. Hepatitis a virus age-specific sero-prevalence and risk factors among Jordanian children. J Med Virol. 2015;87:569–74.
World Health Organization. WHO position paper on hepatitis a vaccines: June 2012 -recommendations. Vaccine. 2013;31:285–6.
Dhankhar P, Nwankwo C, Pillsbury M, Lauschke A, Goveia MG, Acosta CJ, et al. Public health impact and cost-effectiveness of hepatitis a vaccination in the United States: a disease transmission dynamic modeling approach. Value Heal. 2015;18:358–67.
World Health Organization. Global Health Observatory: Life Tables by Country Jordan. World Health Organization; 2015 [cited 2015 Nov 11]. Available from: http://apps.who.int/gho/data/?theme=main&vid=60830
Jordan Demographics profile 2014. 2015 [cited 2015 Nov 16]. Available from: http://www.indexmundi.com/jordan/demographics_profile.html
United States Census Bureau. International Database: Demographics. Jordan: United States Census Bureau; 2015. [cited 2015 Sep 24]. Available from: http://www.census.gov/population/international/data/idb/region.php?N=Results&T=13&A=separate&RT=0&Y=2010,2011,2012,2013,2014,2015&R=−1&C=JO.
Jacobsen KH, Koopman JS. The effects of socioeconomic development on worldwide hepatis a virus seroprevalence patterns. Int J Epidemiol. 2005;34:600–9.
Jacobsen KH. The global prevalence of hepatitis a virus infection and susceptibility: a systematic review. Geneva: World Heal Organ; 2009.
Directorate of Vital information Studies Preparation. Ministry of Health Annual Statistical Book 2014. Amman: Jordan Ministry of Health; 2015. Available from: http://www.moh.gov.jo
Jiries A. Water resources in Jordan. Adv Water Supply Wastewater Treat A Road to Safer Soc Environ Springer. 2011:193–9.
WHO & UNICEF Progress on Sanitation and Drinking Water: 2015 Update and MDG assessment. UNICEF; 2015. Available from: http://www.unicef.org/publications/index_82419.html
UN Refugee Agency. Syrian Regional Refugee Response: Inter-agency Information Sharing Portal. 2015. Available from: http://data.unhcr.org/syrianrefugees/country.php?id=107
Carrion D. Syrian refugees in Jordan: confronting difficult truths. London; 2015. Available from: https://www.chathamhouse.org/sites/files/chathamhouse/field/field_document/20150921SyrianRefugeesCarrion.pdf
Slaih AA. Impact of Syrian refugees on Jordan’s health sector. 2013. Available from: https://data.unhcr.org/syrianrefugees/download.php?id=4345
UNDP. Analysis of Impact of Influx of Syrian Refugees on Host Communities. 2014. Available from: http://inform.gov.jo/en-us/By-Date/Report-Details/ArticleId/12/Analysis-of-Impact-of-Influx-of-Syrian-Refugees-on-Host-Communities
Armstrong GL, Bell BP. Hepatitis a virus infections in the United States: model-based estimates and implications for childhood immunization. Pediatrics. 2002;109
Rein DB, Hicks KA, Wirth KE, Billah K, Finelli L, Fiore AE, et al. Cost-effectiveness of routine childhood vaccination for hepatitis a in the United States. Pediatrics. 2007;119:e12–21.
Werzberger A, Mensch B, Kuter B, Brown L, Lewis J, Sitrin R, et al. A controlled trial of a formalin-inactivated hepatitis a vaccine in healthy children. N Engl J Med. 1992;327:453–7.
Wiens BL, Bohidar NR, Pigeon JG, Egan J, Hurni W, Brown L, et al. Duration of protection from clinical hepatitis a disease after vaccination with VAQTA. J Med Virol. 1996;49:235–41.
Nuseirat A, Qusous L, Ghanem M, editors. Jordan national drug formulary. Amman: Jordanian Food and Drug Administration; 2015. Available from: http://apps.who.int/medicinedocs/documents/s19468en/s19468en.pdf
Huda A, Newcomer R, Harrington C, Blegen MG, Keeffe EB. High rate of unemployment after liver transplantation: analysis of the united network for organ sharing database. Liver Transplant. 2012;18:89–99.
Lopez E, Debbag R, Coudeville L, Baron-Papillon F, Armoni J. The cost-effectiveness of universal vaccination of children against hepatitis a in Argentina: results of a dynamic health--economic analysis. J Gastroenterol. 2007;42:152–60.
World Health Organization. WHO-Choice: Estimates of Unit cost for Patient Services for Jordan. 2015 [cited 2015 Nov 19]. Available from: http://www.who.int/choice/country/jor/cost/en/
World Health Organization. WHO-Choice: Choosing Interventions that are cost-Effective. Geneva; 2015 [cited 2015 Dec 4]. Available from: htp://www.who.int/choice/en
Luyten J, Marais C, Hens N, De Schrijver K, Beutels P. Imputing QALYs from single time point health state descriptions on the EQ-5D and the SF-6D: a comparison of methods for hepatitis a patients. Value Heal. 2011;14:282–90.
Chong CAKY, Gulamhussein A, Heathcote EJ, Lilly L, Sherman M, Naglie G, et al. Health-state utilities and quality of life in hepatitis C patients. Am J Gastroenterol. 2003;98:630–8.
Hanmer J, Lawrence WF, Anderson JP, Kaplan RM, Fryback DG. Report of nationally representative values for the noninstitutionalized US adult population for 7 health-related quality-of-life scores. Med Decis Mak. 2006;26:391–400.
Black WC. The CE plane a graphic representation of cost-effectiveness. Med Decis Mak. 1990;10:212–4.
Eddy DM, Hollingworth W, Caro JJ, Tsevat J, McDonald KM, Wong JB. Model transparency and validation a report of the ISPOR-SMDM modeling good research practices task force--7. Med Decis Mak. 2012;32:733–43.
Dagan R, Leventhal A, Anis E, Slater P, Ashur Y, Shouval D. Incidence of hepatitis a in Israel following universal immunization of toddlers. JAMA. 2005;294:202–10.
Cervio G, Trentadue J, D’Agostino D, Luque C, Giorgi M, Armoni J, et al. Decline in HAV-associated fulminant hepatic failure and liver transplant in children in Argentina after the introduction of a universal hepatitis a vaccination program. Hepat Med. 2011;3:99–106.
Valenzuela MT, Jacobs RJ, Arteaga O, Navarrete MS, Meyerhoff AS, Innis BL. Cost-effectiveness of universal childhood hepatitis a vaccination in Chile. Vaccine. 2005;23:4110–9.
Sartori AMC, de Soárez PC, Novaes HMD, Amaku M, de Azevedo RS, Moreira RC, et al. Cost-effectiveness analysis of universal childhood hepatitis a vaccination in Brazil: regional analyses according to the endemic context. Vaccine. 2012;30:7489–97.
Zahdi MR, Maluf Junior I, Maluf EMCP. Hepatitis a: the costs and benefits of the disease prevention by vaccine, Paranà, Brazil. Braz J Infect Dis. 2009;13:257–61.
Van Effelterre TP, DeAntonio R, Cassidy A, Romano-Mazzotti L, Marano C. Model-based projections of the population-level impact of hepatitis a vaccination in Mexico. Hum Vaccin Immunother. 2012;8:1099–108.
Quezada A, Baron-Papillon F, Coudeville L, Maggi L. Universal vaccination of children against hepatitis a in Chile: a cost-effectiveness study. Rev Panam Salud Pública. 2008;23:303–12.
Anonychuk AM, Tricco AC, Bauch CT, Gilca V, Duval B, John-Baptiste A, et al. Cost-effectiveness analyses of hepatitis a vaccine. Pharmacoeconomics. 2008;26:17–32.
Black S, Shinefield H, Hansen J, Lewis E, Su L, Coplan P. A post-licensure evaluation of the safety of inactivated hepatitis a vaccine (VAQTA®, Merck) in children and adults. Vaccine. 2004;22:766–72.
Niu MT, Salive M, Krueger C, Ellenberg SS. Two-year review of hepatitis a vaccine safety: data from the vaccine adverse event reporting system (VAERS). Clin Infect Dis. 1998;26(6):1475.
Whitaker HJ, Farrington CP. Estimation of infections disease parameters from serological survey data: the impact of regular epidemics. Stat Med. 2004;23:2429–43.
Linder N, Karetnyi Y, Gidony Y, Dagan R, Ohel G, Levin E, et al. Decline of hepatitis a antibodies during the first 7 months of life in full-term and preterm infants. Infection. 1999;27:128–31.
Fiore AE, Wasley A, Bell BP. Prevention of hepatitis a through active or passive immunization: recommendations of the advisory committee on immunization practices (ACIP). MMWR Recomm Rep. 2006;55:1–23.
Leach CT. Hepatitis A in the United States. Pediatr Infect Dis J. 2004;23:551–2.
Amariei R, Willms AR, Bauch CT. The United States and Canada as a coupled epidemiological system: an example from hepatitis a. BMC Infect Dis. 2008;8:23.
Martin A, Lemon SM, Hepatitis A. Virus: from discovery to vaccines. Hepatology. 2006;43:S164–72.
Wolfe RA, Roys EC, Merion RM. Trends in organ donation and transplantation in the United States, 1999--2008. Am J Transplant. 2010;10:961–72.
Berge JJ, Drennan DP, Jacobs RJ, Jakins A, Meyerhoff AS, Stubblefield W, et al. The cost of hepatitis a infections in American adolescents and adults in 1997. Hepatology. 2000;31:469–73.
Mryyan N. Demographics, labor force participation, and unemployment in Jordan. In: Assaad R, editor. Jordanian Labour Mark. New Millenn. Oxford: Oxford University Press; 2014. p. 39–63.
Jordanian Employed Persons Age 15+ Years by Monthly Earnings Categories. Jordan Dep. Stat. 2014 [cited 2015 Nov 9]. Available from: http://jorinfo.dos.gov.jo/PXWeb2014R2/Menu.aspx?px_db=DOS+Database&px_language=en&rxid=e0c35eac-d04f-4689-ace3-8f29bf1f19da
Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, sponsored the study.
Availability of data and materials
The technical supplement providing model and analysis details supporting this article are included in additional files.
Ethics approval and consent to participate
Not applicable as this is a modelling study.
Consent for publication
Several authors are employees of or are contracted by Merck & Co., Inc., which produces and markets VAQTA® (hepatitis A vaccine, inactivated).
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Technical Supplement. Modeling and analysis details. (DOCX 231 kb)