| Literature DB >> 25921288 |
Conall H Watson1, W John Edmunds2.
Abstract
Despite a recommendation by the World Health Organization (WHO) that typhoid vaccines be considered for the control of endemic disease and outbreaks, programmatic use remains limited. Transmission models and economic evaluation may be informative in decision making about vaccine programme introductions and their role alongside other control measures. A literature search found few typhoid transmission models or economic evaluations relative to analyses of other infectious diseases of similar or lower health burden. Modelling suggests vaccines alone are unlikely to eliminate endemic disease in the short to medium term without measures to reduce transmission from asymptomatic carriage. The single identified data-fitted transmission model of typhoid vaccination suggests vaccines can reduce disease burden substantially when introduced programmatically but that indirect protection depends on the relative contribution of carriage to transmission in a given setting. This is an important source of epidemiological uncertainty, alongside the extent and nature of natural immunity. Economic evaluations suggest that typhoid vaccination can be cost-saving to health services if incidence is extremely high and cost-effective in other high-incidence situations, when compared to WHO norms. Targeting vaccination to the highest incidence age-groups is likely to improve cost-effectiveness substantially. Economic perspective and vaccine costs substantially affect estimates, with disease incidence, case-fatality rates, and vaccine efficacy over time also important determinants of cost-effectiveness and sources of uncertainty. Static economic models may under-estimate benefits of typhoid vaccination by omitting indirect protection. Typhoid fever transmission models currently require per-setting epidemiological parameterisation to inform their use in economic evaluation, which may limit their generalisability. We found no economic evaluation based on transmission dynamic modelling, and no economic evaluation of typhoid vaccination against interventions such as improvements in sanitation or hygiene.Entities:
Keywords: Cost utility analysis; Economic evaluation; Enteric fever; Immunisation; Mathematical model; Salmonella Typhi; Transmission dynamics; Typhoid; Typhoid fever; Vaccination
Mesh:
Substances:
Year: 2015 PMID: 25921288 PMCID: PMC4504000 DOI: 10.1016/j.vaccine.2015.04.013
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641
Summary of typhoid transmission model types.
| Characteristic | Number of models ( | References |
|---|---|---|
| Type of model | ||
| Compartmental | ||
| Deterministic | 6 | |
| Stochastic | 0 | |
| Individual-based stochastic | 1 | |
| Scope of model | ||
| Analytical/mathematical | ||
| Without data | 1 | |
| Uses data without fitting | 1 | |
| Exploratory/epidemiological | ||
| Uses data without fitting | 1 | |
| Fitted to data | 1 | |
| Policy-oriented/public health | ||
| Uses data without fitting | 2 | |
| Fitted to data | 1 | |
| Parameter-fitting method | ||
| Maximum likelihood estimation | 2 of 2 | |
| Bayesian | 0 | |
| Investigates vaccination | 4 | |
| Compares with improved sanitation, hygiene or water supply | 4 of 4 | |
| Include economic evaluation of vaccination | 2 of 4 | |
Summary of typhoid vaccine economic evaluation types.
| Characteristic | Number of studies ( | Reference |
|---|---|---|
| Based on field studies | 5 | |
| Perspective: | ||
| Public sector only | 2 | |
| Private only | 1 | |
| Societal (public and private) | 4 | |
| Include intangible costs of pain, suffering and disability | 3 | |
| Analytical approach: (a study can include more than one approach) | ||
| Cost-benefit analysis component | 4 | |
| Cost-effectiveness analysis component | 2 | |
| Cost-utility analysis component | 2 | |
| Willingness-to-pay component | 4 | |
| Price-optimisation model | 1 | |
| Include indirect protection of vaccines | 1 | |
| Include transmission dynamics | 0 | |
| Evaluates improve sanitation, hygiene or water supply as an alternative to or adjunct to vaccination | 0 | |
Components and main findings of typhoid vaccine economic evaluations.
| First author, year, reference | Analytical approach | Economic perspective | Setting | Burden of disease | Costs | Vaccine intervention modelled | Vaccine effectiveness | |
|---|---|---|---|---|---|---|---|---|
| 1 | Musgrove 1992 | CBA | Public sector | PAHO SIREVA countries | 150 cases per year per 100k population. | Vaccine programs and clinical/field trials or pilots. | Mass vaccination; reducing number of doses over time. | Estimated 90% |
| 2 | Shepard 1995 | CUA, cost per QALY | Public sector costs; societal benefit captured as QALYs | Countries with middle, high or very high U5MR | 1.5 cases per person per lifetime. | Marginal costs of additional vaccination within a childhood programme | By birth cohort, two doses | Anticipated 80% over 10 y |
| 3 | Poulos 2004 | CBA | Multi-dimensional public sector and societal | Kalkaji slum, New Delhi, India | As per | As above. Public funded vaccine programme. | Campaign with 80% coverage of: | 70% for 3 years |
| 4 | Canh 2006 | WTP, contingent valuation, CBA | Private | Hue, Vietnam | Raised incidence 1995–9; associated with outbreak in 1996 | Proposed USD | N/A | Proposed: |
| 5 | Cook 2008 | CUA | Public sector and societal | Kolkata, India; Karachi, Pakistan; North Jakarta, Indonesia; Hue, Vietnam | Highest in the sites within Karachi and Kolkata, lowest in Hue. | Private direct and indirect cost of illness obtained in interviews with confirmed cases, public costs obtained from health facilities. | Campaigns: | 65%, 3 y |
| 6 | Cook 2009 | CBA total economic benefits vs costs | Societal | Tiljala and Narkeldanga slums, Kolkata, India | 3.4 case per 1000 2–4 y | Total marginal vaccine cost USD (2007) $1.11 | Campaigns: | 65%, 3 y |
| 7 | Lauria 2009 | Optimisation model: different adult and child pricing, implicit CEA | Public sector | Hypothetical population | 3.5 annual cases per 1000 children and 1 per 1000 adults | As per | Price-dependent uptake | 70%, 3 y |
CBA, cost-benefit analysis; CE, cost-effective(ness); CEA, cost-effectiveness analysis; CFR, case-fatality rate (proportion of cases that result in death); CUA, cost-utility analysis; COI, cost of illness; DALY, Disability adjusted life-year; DALY weight, a scale from 0 (perfect health) to 1 (death). DOMI, Diseases of the most impoverished programme [39]; PAHO, Pan-American Health Organization; SIREVA, Sistema Regional de Vacunas (Regional Vaccine System); U5MR, under-five mortality rate; USD, United States Dollars; VE, vaccine effectiveness; WTP, willingness to pay.
Components and main findings of cost of illness studies and willingness to pay studies used in typhoid vaccine economic evaluations.
| First author, year, reference | Analytical approach | Economic perspective | Setting | Burden of disease | Costs | Vaccine intervention modelled | Vaccine effectiveness | |
|---|---|---|---|---|---|---|---|---|
| 1 | Bahl 2004 | Cost of illness | Multidimensional public sector and societal costs | Kalkaji slum, New Delhi, India | Culture confirmed incidence per year: 17 per 1000 under 5s; | Public sector/institutional and private costs, comprising direct medical, direct non-medical and indirect costs; for hospitalised and non-hospitalised | N/A | N/A |
| 2 | Poulos 2011 | COI | Public and private (direct and indirect) | Hechi, China; North Jakarta, Indonesia; Kolkata, India; Karachi, Pakistan; Hue, Vietnam. | Highest in the sites within Karachi and Kolkata, lowest in Hechi and Hue. | Measured by questionnaire, with estimates for nonmarket activities. Karachi costs from expert information. | N/A | N/A |
| 3 | Whittington 2009 | WTP | Private | Tiljala slum and Beliaghata neighbourhood, Kolkata, Inida | 2 case per 1000 population per year, peak incidence in older children and teenagers | Proposed USD (2007) | Price-dependent uptake | 70%, 3 y |
components and main findings of typhoid transmission models.
| First author and year | Model type | Disease states | Data source(s) | Fitting process | Interventions modelled | Time horizon | Sensitivity analysis | Findings | Comments | ||
|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | Cvjetanović 1971, 1978 | Compartmental deterministic with births = deaths, without age-structure | N S Es Ea Is Ia Ct Cl Rt Rl | Parameters estimated using literature and expert opinion. Considers an eidemiological scenario approximating Western Samoa. | None | Vaccination with whole-cell inactivated vaccines, VE 60%, 75% or 90%, coverage 60, 80 or 100%. | 60 years | Epidemiological/clinical parameters fixed. Effective contact rate (per capita per day) varied. | For both low and high VE, single vaccination campaigns achieve temporary reduction in incidence rates before return to a rate determined by the force of infection, where force of infection is above an elimination threshold. Sustained reduction in force of infection reduces incidence. Multiple vaccination campaigns reduce incidence will campaigns are sustained. | Multiple parameters are included without fitting. | |
| 2 | Briscoe 1980 | Deterministic analytical SIS | S I | N/A | N/A. Reviews Cvjetanović models. Analysis of role of force of infection and recovery on equilibrium prevalence. | N/A | N/A | N/A | Force of infection determines prevalence, and vice versa. | Intended as an analytical model rather than epidemiological simulation. | |
| 3 | Bailey 1982 | Compartmental deterministic with births = deaths, without age-structure | S E I C R | Rule-based simplification of Cvjetanović 1971 model | N/A | N/A | N/A, suggests an approach to sensitivity analysis | For a steady-state model, structural simplification results in compartment population estimates consistent with the unsimplified model for a given effective contact rate. | Reducing the number of compartments makes a model more suitable for validation with data. | ||
| 4 | Cvjetanović 1986 | Age-structured compartmental deterministic SIRS. | N S I Ct Cl Rt Rl | Demographic and typhoid surveillance data for Santiago and rest of Chile | Effective contact rate per capita per unit day (age-specific for acquisition) from linear interpolation of age-specific incidence. | Vaccination with Ty21a, 95% VE at 75% or 95% coverage of under 25s with 5 yrly revaccination. Food sanitation in schools reducing force of infection by 1/3 in ages 6 to 16 y. Sanitation with annual 2% or 5% improvement in force of infection over 10 years. | Interventions analysed over 25 y after run-in to equilibrium. | None | Vaccination campaigns would reduce age-specific incidence and increase the age of peak incidence | Somewhat simplified model structure, though now age structured. The model is not validated sufficiently against data, nor are outputs sufficiently clear to make strong policy conclusions. | |
| 5 | González-Guzmán 1989 | Compartmental deterministic SIS structure with births and deaths | S I V with environmental transmission | Parameter estimates for Chile | None, analytical model | Reductions in combinations of: | 10 y | N/A | Decline in incidence is not rapid, even with highly effective combined control measures. | Author cautions against using the model to estimate the effect of a vaccination programme but that it indicates areas for further epidemiological parameter determination. | |
| 6 | Saul 2013 | Individual-based stochastic, random-mixing. | S E Is Ia Ct Cl Rt Rl, Rc,;Rs; Vc Vs | Surveillance data from Dhaka, Bangladesh, and Kolkata India. | Maximum likelihood and visual inspection | None | 40 y to equilibrium and 40 y follow-up. 20 y for effects of carriage. | Sensitivity analysis on refractory period from birth. | Distinguishes between sterile immunity and clinical Immunity (in which individuals can be infected but not develop disease). Multiple infections needed to develop sterile immunity. | Complex agent based model, limited availability of epidemiological data results in issues of parameter identifiability. Plausible combinations of parameters identified. | |
| 7 | Pitzer 2014 | Compartmental, age-structured deterministic | S1 S2 I1 I2 R C W | Surveillance case series, Vellore, Tamil Nadu, India | Two-stage fitting with Latin hypercube sampling of starting parameters. Maximum likelihood estimation, simplex method. | Vaccination with: | 50 y to quasi-steady state and 25 y follow-up | Multi-parameter sensitivity analysis in model fitting. | Basic reproduction number is around 3 in Vellore and 7 in Dhaka. | Best fitting parameter sets were highly sensitive to initial parameter selection. |
VE = vaccine efficacy. Effective contact rate is the rate at which two individuals come into contact per unit time, with the nature of the contact being such that if one was infectious and the other susceptible, infection would be transmitted.
Disease states in typhoid models.
| Abbeviation | Disease state | Comment |
|---|---|---|
| N | Newborn | Susceptible in Cvjetanović’s model, refractory in Saul's |
| S | Susceptible; | |
| S1 S2 | Fully and partially susceptible | |
| E; | ‘Exposed’; | Infected but not (yet) infectious |
| Es; Ea | Symptomatic or asymptomatic | |
| I; | Infectious; | |
| Is Ia | Symptomatic or asymptomatic | Primary infection of a fully susceptible individual or asymptomatic/subclinical infection of a previously partially susceptible individual |
| I1 I2 | Primary or subclinical infection | |
| C; | Carrier; | |
| Ct; Cl | Temporary; long-term | |
| R; | Removed/resistant/refractory/recovered; | Not able to be infected, immune. |
| Rt; Rl; | Temporary immunity; long-term immunity; | Clinical immunity is against disease but allows infection and onward transmission. |
| Rc; Rs | Natural immunity to clinical disease; natural sterile immunity) | Sterile immunity is against any infection. |
| V | Vaccinated | |
| Vc; Vs | Vaccine-induced immunity to clinical disease; Vaccine-induced sterile immunity | |
| W | ‘Water’ | Long-cycle transmission from water or environmental contamination, contributed to by all infectious or carrier classes. |