| Literature DB >> 27012808 |
R M G J Houben1,2, M Lalli3,4, T Sumner3,4, M Hamilton5, D Pedrazzoli3,4, F Bonsu6, P Hippner7, Y Pillay8, M Kimerling9, S Ahmedov10, C Pretorius5, R G White3,4.
Abstract
Tuberculosis (TB) is the leading cause of death from infectious disease worldwide, predominantly affecting low- and middle-income countries (LMICs), where resources are limited. As such, countries need to be able to choose the most efficient interventions for their respective setting. Mathematical models can be valuable tools to inform rational policy decisions and improve resource allocation, but are often unavailable or inaccessible for LMICs, particularly in TB. We developed TIME Impact, a user-friendly TB model that enables local capacity building and strengthens country-specific policy discussions to inform support funding applications at the (sub-)national level (e.g. Ministry of Finance) or to international donors (e.g. the Global Fund to Fight AIDS, Tuberculosis and Malaria).TIME Impact is an epidemiological transmission model nested in TIME, a set of TB modelling tools available for free download within the widely-used Spectrum software. The TIME Impact model reflects key aspects of the natural history of TB, with additional structure for HIV/ART, drug resistance, treatment history and age. TIME Impact enables national TB programmes (NTPs) and other TB policymakers to better understand their own TB epidemic, plan their response, apply for funding and evaluate the implementation of the response.The explicit aim of TIME Impact's user-friendly interface is to enable training of local and international TB experts towards independent use. During application of TIME Impact, close involvement of the NTPs and other local partners also builds critical understanding of the modelling methods, assumptions and limitations inherent to modelling. This is essential to generate broad country-level ownership of the modelling data inputs and results. In turn, it stimulates discussions and a review of the current evidence and assumptions, strengthening the decision-making process in general.TIME Impact has been effectively applied in a variety of settings. In South Africa, it informed the first South African HIV and TB Investment Cases and successfully leveraged additional resources from the National Treasury at a time of austerity. In Ghana, a long-term TIME model-centred interaction with the NTP provided new insights into the local epidemiology and guided resource allocation decisions to improve impact.Entities:
Keywords: Capacity building; Mathematical modelling; Policy support; Tuberculosis
Mesh:
Year: 2016 PMID: 27012808 PMCID: PMC4806495 DOI: 10.1186/s12916-016-0608-4
Source DB: PubMed Journal: BMC Med ISSN: 1741-7015 Impact factor: 8.775
Fig. 1TIME Impact structure and link within Spectrum software suite. Figure illustrates how the TIME Impact tool is embedded in the Spectrum software suite, and linked to key modules and databases for demography, tuberculosis and HIV estimates (top row). The TIME box shows the basic model structure of TIME Impact (red boxes) and how TIME Impact fits within the other TIME modules
Fig. 2TIME Impact interface. TIME Impact’s user-friendly interface enables technical capacity building within National Tuberculosis Programmes. The user works through the different windows of (1) epidemiology, (2) care and control, and (3) interventions before visualising results (see drop down menus)
Fig. 3TIME Impact as part of the National Tuberculosis Programme (NTP) programming cycle. Figure and table illustrate how the TIME model can be a central focus of the NTP programming cycle and can support the process at each stage
Data for TIME Impact
| Included |
| • Demographic data and projections; UN Population Division |
| • Global Tuberculosis Programme (GTB) estimates for incidence, prevalence, mortality, notifications; GTB |
| • HIV burden and antiretroviral therapy (ART) coverage; UNAIDS |
| Required |
| • Estimated number of individuals screened (preferably trends); National Tuberculosis Programmes (NTPs) |
| • Diagnostic algorithms and coverage; NTP |
| • Linkage to care (trends, by multidrug resistance (MDR)); NTP, literature (MDR, GTB) |
| • Treatment success, by MDR (trends); GTB |
| • Drug susceptibility testing coverage; GTB |
| Desirable |
| • Prevalence survey results; NTP |
| • Drug resistance survey results; NTP |
| • HIV prevalence + ART coverage (required if high HIV burden setting); GTB, NTP |
| • Proportion of tuberculosis (TB) in children (<15 years old); NTP |
| • Current coverage and efficacy of TB programme activities; NTP |
| • Size of risk groups and TB prevalence; NTP |
Table provides a non-exhaustive list of data used to inform TIME Impact and suggested sources. ‘Included’ data are automatically provided by Spectrum, whereas those listed under ‘required’ and ‘desirable’ need to be provided by the user
Model fit to calibration targets
| South Africa | Ghana | |||
|---|---|---|---|---|
| Target (2012) | Model | Target (2013) | Model | |
| Notifications rate (per 100,000) | 667 | 622.7 | 61.9 | 60.3 |
| Prevalence rate (per 100,000) | 705 (388–1114) | 662 | 290 (113–548) | 312 |
| Incidence rate (per 100,000) | 900 (832–990) | 892 | 168 (81–286) | 167 |
| Mortality rate (per 100,000) | 179 (149–212) | 191 | 52 (24.8–88) | 64.6 |
| % prevalence MDR (treatment naïve) | 1.8 (1.5–2.3)a | 1.7 | 1.9 (0.1–5.3) | 2.9 |
| % prevalence MDR (retreatment) | 6.7 (5.5–8.1)a | 6.1 | 20 (0.1–40) | 13.7 |
| 15+ HIV prevalence | 15 (14–16) | 15.4 | 1.5 (1.2–2.0) | 1.34 |
| ART coverage | 36 (34–39) | 34 | 32 (24–41) | 27.5 |
a South Africa MDR prevalence based on 2002 survey data
ART, Antiretroviral therapy; MDR, Multidrug resistance
Fig. 4Model outputs for tuberculosis (TB) incidence and mortality in South Africa. The calibration focussed on matching 2012 data and aimed to fit within the confidence intervals around the Global TB Programme (GTB) estimates (thin solid lines). a TB Incidence: Modelled incidence (thick solid line) closely matches GTB estimates (dotted line). Model matches disaggregation by HIV status and annual decline in incidence in 2012. b Mortality: Modelled mortality (thick solid lines) match GTB estimates in 2012 (dotted line)
Fig. 5Global Fund to Fight AIDS, Tuberculosis and Malaria New Funding Model and country engagement timeline. TRP, Technical review panel; GAC, Grant approval committee. Figure adapted from the Global Fund to show visits to Ghana along the New Funding Model
Fig. 6Model outputs for notifications and prevalence in Ghana. a Notifications: Total notifications from model (thin solid line) closely match Global Tuberculosis Programme data (black dots). TIME Impact estimates the positive predictive value amongst notifications to be 75 %. True positive notifications are shown in the dark blue shaded area and false positive notifications are shown in shaded light blue. b Prevalence: Model was calibrated to adult prevalence estimates from the 2013 national prevalence survey (squares). Modelled smear positive adult prevalence is represented in red and all forms adult prevalence is represented in blue