|Year : 2019 | Volume
| Issue : 4 | Page : 517-527
Strategies for ending tuberculosis in the South-East Asian Region: A modelling approach
Nimalan Arinaminpathy1, Sandip Mandal2, Vineet Bhatia3, Ross McLeod4, Mukta Sharma3, Soumya Swaminathan5, Khurshid Alam Hyder3, Partha Pratim Mandal3, Swarup Kumar Sarkar3, Poonam Khetrapal Singh3
1 Department of Infectious Disease Epidemiology, St. Mary's Hospital, Imperial College, London, UK
2 Public Health Foundation of India, New Delhi, India
3 World Health Organization, South-East Asian Regional Office, New Delhi, India
4 eSYS Development, Sydney, Australia
5 Indian Council of Medical Research, New Delhi, India
|Date of Submission||14-Oct-2018|
|Date of Web Publication||16-Jul-2019|
Dr Nimalan Arinaminpathy
Department of Infectious Disease Epidemiology, St. Mary's Hospital, Imperial College London, London
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background & objectives: To support recent political commitments to end tuberculosis (TB) in the World Health Organization South-East Asian Region (SEAR), there is a need to understand by what measures, and with what investment, these goals could be reached. These questions were addressed by using mathematical models of TB transmission by doing the analysis on a country-by-country basis in SEAR.
Methods: A dynamical model of TB transmission was developed, in consultation with each of the 11 countries in the SEAR. Three intervention scenarios were examined: (i) strengthening basic TB services (including private sector engagement), (ii) accelerating TB case-finding and notification, and (iii) deployment of a prognostic biomarker test by 2025, to guide mass preventive therapy of latent TB infection. Each scenario was built on the preceding ones, in successive combination.
Results: Comprehensive improvements in basic TB services by 2020, in combination with accelerated case-finding to increase TB detection by at least two-fold by 2020, could lead to a reduction in TB incidence rates in SEAR by 67.3 per cent [95% credible intervals (CrI) 65.3-69.8] and TB deaths by 80.9 per cent (95% CrI 77.9-84.7) in 2035, relative to 2015. These interventions alone would require an additional investment of at least US$ 25 billion. However, their combined effect is insufficient to reach the end TB targets of 80 per cent by 2030 and 90 per cent by 2035. Model projections show how additionally, deployment of a biomarker test by 2025 could end TB in the region by 2035. Targeting specific risk groups, such as slum dwellers, could mitigate the coverage needed in the general population, to end TB in the Region.
Interpretation & conclusions: While the scale-up of currently available strategies may play an important role in averting TB cases and deaths in the Region, there will ultimately be a need for novel, mass preventive measures, to meet the end TB goals. Achieving these impacts will require a substantial escalation in funding for TB control in the Region.
Keywords: Burden - end TB - epidemiology - modelling - public health - SEAR - tuberculosis
|How to cite this article:|
Arinaminpathy N, Mandal S, Bhatia V, McLeod R, Sharma M, Swaminathan S, Hyder KA, Mandal PP, Sarkar SK, Singh PK. Strategies for ending tuberculosis in the South-East Asian Region: A modelling approach. Indian J Med Res 2019;149:517-27
|How to cite this URL:|
Arinaminpathy N, Mandal S, Bhatia V, McLeod R, Sharma M, Swaminathan S, Hyder KA, Mandal PP, Sarkar SK, Singh PK. Strategies for ending tuberculosis in the South-East Asian Region: A modelling approach. Indian J Med Res [serial online] 2019 [cited 2021 May 18];149:517-27. Available from: https://www.ijmr.org.in/text.asp?2019/149/4/517/262877
The World Health Organization (WHO) South-East Asian Region (SEAR) bears a disproportionate burden of tuberculosis (TB). In 2015, the 11 countries of this Region accounted for 25 per cent of the world's population but 40 per cent of global TB deaths, the highest of any of the WHO regions . The Region includes India and Indonesia, two countries with high absolute numbers of TB cases, that together account for an estimated 37 per cent of global TB incidence ,. Overall, therefore, progress in global TB control depends critically on the success of TB control in SEAR.
All countries in SEAR have adopted the end TB strategy, which sets ambitious targets for ending TB by 2035. Despite such broad political commitment, however, countries in the Region are faced with a range of challenges stemming from human and financial resource constraints and compounded by sociodemographic problems ,,. Many countries in the Region have a sizeable health sector outside the national TB programmes (NTPs) that often fails to notify TB cases to public health authorities ,,,,. Early detection of TB is additionally complicated by stigma, lack of awareness and underinvestment ,. Drug-resistant-TB (DR-TB) is becoming an increasing concern ,, while some countries also have a high burden of HIV co-infection. As a result of these and other challenges, TB incidence in the Region continues to decline at an estimated rate of only 1-2 per cent per year .
These circumstances raise important questions: how does the Region translate political commitment into interventions that lead towards ending TB? It is clear that current interventions (private sector engagement and accelerated case-finding, among other measures) will need to be taken to far larger scales than current levels, and that innovative interventions need to be developed and scaled up, with a focus on intensified case-finding. There is a need to estimate the levels of implementation, coverage and funding required to meet the end TB goals in the Region.
Here, we addressed these questions using mathematical models of TB transmission. Such models offer a helpful framework for capturing the dynamics of TB transmission, as well as the complexity of healthcare systems characteristic of many countries in the Region ,,. The analysis was conducted on a country-by-country basis. Input was gathered from each of the NTPs through WHO country offices in the Region and published literature on indicators, assumptions and intervention scenarios used in the model. As a guide to the resources needed, a costing exercise, fully integrated with the transmission model was additionally conducted.
| Material & Methods|| |
[Figure 1] shows the overall model structure. The model explicitly captures the national TB programme (NTP) and non-NTP sectors, and the respective standard of TB care in these sectors. In doing so, the model also captures the implications of diagnostic delays and treatment outcomes, for overall transmission. For simplicity, the model does not distinguish age groups and is nationally aggregated. However, it incorporates HIV/TB co-infection, as well as 'risk groups' bearing a disproportionate TB burden, and the generation and transmission of drug-resistant TB (DR-TB). Key structural elements were as follows:
|Figure 1: Illustration of the basic model structure, replicated by HIV, drug resistance and risk-group status. Compartments in red denote states that are infectious. The NTP (national TB programme) (left-hand side) sector is distinguished from the non-NTP sector (right-hand side). Among latent infection, it is assumed that those who are most at risk of developing disease within the next two years are detectable using a hypothetical, future diagnostic test. Not shown on this figure for clarity, the model also incorporates tuberculosis mortality, as well as recurrent tuberculosis (the latter including relapse of an existing infection, and exogenous reinfection).|
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Among people having latent TB infection, 'incipient TB' cases are distinguished as those who would develop active TB disease within the next two years . It is assumed that after patients develop active disease, they undergo an initial delay before first presenting for care (for example, as their symptoms develop in intensity) - often referred to as the 'patient delay'. This delay was estimated, together with the infectiousness per case, to country-specific epidemiological data (Supplementary files [Additional file 1]). It is to be noted that, because patients in this compartment have not yet visited a provider, they can only be reached through active/community-based case-finding strategies. In addition, any delay in diagnosis and initiation of treatment are captured in the 'diagnostic delay' in this model (also called 'provider delay').
On seeking care, it is assumed that a proportion p of patients visit the NTP, while the remainder seek care in the non-NTP sector: the latter broadly including pharmacies and traditional healers, as well as physicians and hospitals that are not involved with NTP. These 'non-NTP' providers generally have a lower standard of TB care than the NTP (substandard diagnosis as well as a general lack of treatment adherence) as well as not reporting TB cases to the programme ,,,. This difference was captured as a lower probability of TB diagnosis per patient visit, and a lower treatment completion rate, among non-NTP than among NTP providers. With limited systematic evidence to inform these parameters quantitatively, a range of values was assumed [Supplementary Table 2 [Additional file 2]]. To allow for exceptions such as Thailand, where non-NTP and NTP providers generally offer a similar quality of care, the same parameters were assumed for both. The proportion of patients approaching 'non-NTP' providers (p) is adjusted country-wise in such a way that simulated treatment initiations in the NTP agree with reported notifications from the public sector.
The model is constructed so that any patients missed from the TB care cascade (because of failed diagnosis, initial or subsequent default) enter the compartment B, representing those who have temporarily dropped out of careseeking. These patients are still infectious: they remain for an average of one month before seeking care, again with a probability p of choosing the NTP sector. Quantities governing the TB care cascade in the NTP and non-NTP sectors are shown in the [Supplementary Table 2].
The model captures the acquisition and transmission of drug resistance to first-line therapy: rifampicin-resistant and multi-drug-resistant TB (MDR-TB) were collectively referred to as 'drug-resistant' (DR)-TB, requiring second-line TB treatment. Laboratory-based drug susceptibility testing (e.g. through molecular tests or culture) is not universally available in the countries of the Region, and therefore, not routinely conducted. It was assumed that only a proportion g of cases identified in the public sector are subject to drug susceptibility testing: the value was calibrated to yield reported DR-TB notifications from the programme. Those not identified as DR-TB were assumed to undergo first-line treatment, and to remain infectious with DR-TB during this time: upon failing first-line treatment, a certain proportion were switched to second-line therapy.
We did not explicitly model the dynamics of HIV: instead, it was assumed that a time-dependent proportion h of new TB cases were HIV coinfected, drawing the value of h from WHO estimates. Individuals with HIV/TB infection have an elevated risk of developing active disease, with parameter values informed by the literature [Supplementary Table 2]. It was assumed that HIV-positive patients undergoing ART had the same risk of developing active disease, as HIV-negative TB infections.
We also considered the targeting of TB interventions. In particular, 'high-impact risk groups' were defined as population subgroups that bear a disproportionate TB burden, while also having sufficient contact with the general population, to play an important role in TB transmission. These groups may include, for example, slum populations or hospital outpatients . In practice, the most appropriate risk groups for a given country would depend on many country-level factors, including the size and relative burden of TB in a given group, as well as the feasibility of targeting such a group for intervention. We did not aim to identify these groups for each country in the current study. There are insufficient data to parameterize each risk factor, along with interactions between overlapping factors. Instead, an illustrative scenario was adopted, one where 10 per cent of the population had three times the prevalence of active TB as in the general population. This scenario was intended to be illustrative rather than prescriptive, and is consistent with, for example, urban slums in India . It was assumed that the concentrated burden in this high-impact risk group was mediated by an increased risk of reactivation relative to the general population, although we also explored other potential mechanisms in sensitivity analysis. We adopted broad uncertainty around these parameter values [Supplementary Table 2], while also exploring sensitivity of model findings to these assumptions.
Model calibration: Free parameters, calibrated separately to each country setting, included the mean annual infections per drug-susceptible TB case (β); the mean annual infections per DR-TB case (βDR); the mean, initial patient delay before first seeking care (d); the relative risk of re-activation following infection in the 'high-impact risk group' compared to the general population (m); the proportion of TB cases visiting an NTP provider at each care seeking attempt (p) and the proportion of TB diagnoses receiving a drug susceptibility test (g).
For each country setting, model inputs were calibrated to the following data: WHO estimates for incidence (all forms of TB) from 2006 to 2015; prevalence (all forms) in 2014 (the last year prevalence estimates were reported); estimated proportion of incident TB disease having DR-TB in 2015; TB notifications from 2000 to 2017 and DR-TB notifications from 2000 to 2017. India, the highest burden country in the Region, has also seen an upward revision of TB burden estimates : In this case, prevalence estimates were used from pooled subnational prevalence surveys . In addition, Indonesia recently saw a 15 per cent decrease in its estimated burden ; we used the most updated estimates, published in 2018.
The WHO estimates were used to construct independent log-normal distributions for each indicator and year. By evaluating the product of these likelihood terms, along with independent uniform priors for each of the model inputs, the posterior distribution for a given set of model inputs was evaluated. The Bayesian melding approach ,, was used to sample from the posterior distribution. This is a systematic way of propagating uncertainty from model inputs to outputs. We refer to the uncertainty intervals thus obtained as 'credible intervals' (CrI).
The WHO estimates suggest that TB incidence and mortality have been declining by 1-2 per cent annually over the last five years , 'background' trends that may arise from a variety of factors including socio-economic development. These secular trends were captured assuming a constant, annual decline in β and the per-capita mortality hazard for TB cases. However, there is little evidence for how these trends may continue in future: when simulating future projections; therefore, a range of scenarios was adopted, ranging from current trends continuing indefinitely, to a more conservative scenario where current trends stabilize by 2020 (yielding constant β and TB mortality hazard).
Implementing interventions: The interventions listed in the [Table 1] were modelled, successively adding each intervention in a combination strategy. Broadly, the interventions were grouped in three categories: strengthen, accelerate and prevent. The first of these, aimed at coordinating and improving basic TB services, focused on diagnostic facilities, private sector engagement and improving treatment initiation and outcomes. Such interventions are foundational, but contingent on a TB patient's presentation for care.
The 'accelerate' package of interventions builds on 'strengthening' activities and additionally includes measures to reach TB cases that have not yet presented for care: that is, enhanced case-finding measures (although as discussed below, this scenario could also include patient-focused mechanisms to encourage uptake of TB services). In risk groups, consistent with ongoing case-finding activities in some countries of the Region, we assumed sustained, systematic screening using mobile diagnostic units to screen for TB, at a given annual frequency . In the general population, however, such approaches are not feasible. Instead for this population, information was used from recent work in Vietnam, which demonstrated the potential value of contact investigation, for identifying undiagnosed TB . We modelled an 'extended contact investigation' scenario, where screening for TB incorporated not only household contacts of index TB patients but also social and occupational contacts.
Finally under 'prevent', interventions building on 'strengthen' and 'accelerate' were considered to additionally include population preventive measures. At present, the primary tool for TB prevention is preventive therapy . For example, recent WHO guidelines recommend that preventive therapy should be offered to clinical risk groups, including people living with HIV, and household contacts of those diagnosed with active TB . Ongoing modelling suggests that although these measures in the SEAR could have a meaningful impact on TB burden in the Region, these will not be sufficient to meet the end TB goals. Therefore, current preventive therapy was not explicitly considered in the current work. By contrast, a future scenario was considered where preventive therapy could be implemented in the general population without being constrained to any such clinical risk factors (hence the designation as 'population' preventive measures). It was assumed in particular that, by 2025, new 'biomarker' tools could allow the identification of those with TB infection who are most likely to develop disease within the next two years (that is, a tool for diagnosing 'incipient TB' in the model illustrated in [Figure 1]). Such tools together with the ongoing development of shorter, more effective regimens that are better suited for mass administration , could allow implementation of preventive therapy on a population level. This scenario is merely illustrative: it is contingent on the coverage of biomarker screening, as well as the effectiveness of future preventive regimens. To address both in a simple way, the 'effective prevention rate' was considered, as the multiple of these two factors.
It is important to note that this is just one example of population prevention, and other approaches may offer promise as well: for example, recent findings raise hope for a transmission-blocking TB vaccine , which would have a profound impact on TB control in the Region. Moreover, undernutrition is an important risk factor for TB in South Asia, accounting for one of the largest population attributable fractions of TB burden, in India . Therefore, 'intersectoral approaches' such as nutrition support initiatives could have an important population preventive impact  on TB. At present, all of these possibilities are equally untested and hypothetical: thus, the example of a biomarker test, which we adopted for the present study, remains only an illustrative one.
All interventions were assumed to be implemented with a steady (linear) scale-up, over five years starting from 2017 with the exception of population preventive measures, beginning from 2025.
For the 'strengthening' interventions the coverage scenarios shown in the [Table 1] were assumed, as such measures are a necessary foundation for the 'accelerate' and 'prevent' interventions. We then examined what levels of coverage were needed for the 'accelerate' and 'prevent' interventions, to meet the 2035 end TB goals for incidence and mortality. The 'accelerate' package builds upon the 'strengthening' package though these are not sequential. Different scenarios were explored for the coverage of these interventions in the high-impact risk group, and in the general population.
Finally, as an indication of the magnitude of investment that would be required, the resources required for scaling up the implementation of currently available tools were estimated. The 'prevent' scenario in the costing was not included, given that it featured diagnostic technologies and preventive therapy regimens that do not currently exist. Taking the programmatic perspective for the 'strengthen' and 'accelerate' packages, commodity and personnel costs were included, incorporating the number of diagnostic tests needed to identify one TB case, as well as 'false positive' TB, that is, the excess cost of treating patients wrongly diagnosed as having TB (Supplementary files). In practice, each SEAR country may adopt a different mix of interventions depending on local circumstances and programmatic experience. In the current study, capturing such programme optimization was not attempted.
| Results|| |
[Figure 2] shows the model outputs for incidence and prevalence for the three highest burden countries in the Region, illustrating the best parameter fits (black curves) as well as the different scenarios for future burden projections (blue and black curves, respectively). Although these figures show only the best-fitting parameter sets, for clarity, the model simulations additionally captured the uncertainty in WHO estimates for these epidemiological indicators.
|Figure 2: Model fits to World Health Organization estimates for incidence and mortality. Shown, for illustration, are the three countries accounting for 90 per cent of the population in South-East Asian Region: India (red), Indonesia (green) and Bangladesh (yellow). World Health Organization estimates account for recent trends, and it is not clear how these trends may continue in future. We adopted an 'optimistic' scenario (black curves) in which current trends persist until 2035, and a 'pessimistic' scenario in which current trends stabilize by 2020. Panels A and B show projections for incidence and mortality, respectively.|
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[Figure 3] shows illustrative dynamics for incidence and mortality, under the different intervention packages described above. The 'strengthen' scenario followed the levels of coverage shown in the [Table 1]. The 'accelerate' scenario assumed systematic screening in the high-impact risk group three times a year, along with extended contact investigation in the general population. Finally, the 'prevent' scenario assumed the use of a future biomarker test, together with preventive therapy, that successfully avertsed half of TB progressions from incipient to active disease, per year.
|Figure 3: Epidemic dynamics under different intervention scenarios. Shown are the dynamics aggregated over all 11 South-East Asian Region countries. Shaded regions show 95 per cent credible intervals (CrI), arising from uncertainty in input parameters (Table SII) and in potential future background trends in tuberculosis burden (illustrated in Fig. 2). The horizontal, dashed lines show the 2035 targets for incidence (left-hand panel) and mortality (right-hand panel).|
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The 'strengthen' package could reduce incidence rate by 43 per cent (95% CrI 32.0-49.4%) and TB deaths by 52.5 per cent (95% CrI 43.6-64.4%), the latter because of improvements in patient outcomes as well as reducing transmission. The addition of the 'accelerate' package of interventions increased these impacts to 67.3 per cent (95% CrI 65.3%-69.8%) and 80.9 per cent (95% CrI 77.9-84.7%), respectively. Although showing a considerable impact, these results suggested that even with the ambitious levels of implementation shown here, the end TB goals were not reached. It was observed that while such measures might be effective at controlling transmission, there is ultimately a dominant share of incidence coming from remote infection rather than recent transmission. It is only with the deployment of primary TB prevention, and of TB recurrence, that the end TB goals can ultimately be met [Figure 3]. We note that the 'population preventive' strategy modelled here is assumed to affect incipient TB among those recovered from previous TB episodes, as well as among new cases.
An accompanying, ingredient-based costing analysis (Supplementary files) suggested that the 'strengthen' and 'accelerate' intervention packages alone would require an additional programme investment of at least US$ 25 billion, between 2017 and 2035, additional to current spending. Translated to an annual investment need of US$ 1.3 billion, this is more than twice the current annual budget for the whole region . This is likely to be a conservative estimate, highlighting the substantial increase in investment that is needed in the Region.
These results showed just one illustrative scenario: we next explored the levels of coverage needed for the 'accelerate' and 'prevent' packages, scaled up, respectively, from 2017 to 2025, concentrating first on the numbers of active TB cases and incipient TB that were needed to be identified each year. [Figure 4] shows the coverage that would be needed in the general population. Curves showed the minimum required coverages of case-finding (horizontal axis) and population prevention (vertical axis), with each separate curve representing a different scenario for prioritization of the high-impact risk group. Screening in the risk group three times a year (green curve) can substantially reduce the amount of case-finding needed in the general population, compared to a strategy that addresses the risk group and the general population equally (blue curve). In practice, this would have important resource implications, as focused efforts in high-burden groups will mitigate the resources needed in the general population, where TB burden is more diffuse. However, addressing the risk group alone is not sufficient to meet the end TB goals. Moreover, these results suggested that under the parameters assumed here for the role of the risk group in TB burden there could be diminishing returns from screening more than three times a year in the risk group (see proximity of orange and green curves). Results from an alternative model (not shown here), where TB burden in the risk group arises not from higher rates of progression but from a higher risk of infection than the general population showed similar results to those shown in [Figure 4].
|Figure 4: Minimum coverage levels for meeting the end tuberculosis goals by 2035. The x-axis denotes the proportion of TB in the general group that is detected per year, while the y-axis denotes the proportion of incipient TB that is successfully diagnosed and treated in the general population, each year. Each curve represents a different scenario for the coverage of case-finding and population prevention in the risk group. For example, yellow curves involve, as well as full implementation of the 'strengthen' package, additionally the risk group being screened five times a year for active disease, and (after 2025) for 'incipient' disease. The Figure illustrates that focused interventions in the risk group can significantly lower the coverage needed in the general population. However, there is limited incremental benefit to be gained, between screening 3 or 5 times a year in the risk group (comparing green and yellow lines).|
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| Discussion|| |
The present work emerges in a context of increasing political commitment to end TB in SEAR. Here, a mathematical modelling was used which showed that ending TB in the Region could only be met through a massive mobilization of effort and resources, greatly exceeding current levels of TB activity. In particular, while there is a need to fix basic TB services (including engagement with the private healthcare sector) and accelerate TB diagnosis (including increases in case-finding), these measures alone will not be sufficient to meet the end TB goals. In addition, there is a pressing need to invest in the technology required for scalable, population-level preventive measures to be available by 2025. The Delhi ministerial meeting also called for the establishment of a regional 'Innovation to Implementation fund', to support sustained research into new technologies for TB control in the Region.
It is also to be noted that the interventions covered here are only examples of measures to realize the transmission impact of each of the three intervention scenarios. For example, the key feature of the 'accelerate' scenario is that it curtails the period of infectivity before a patient's first presentation for care. We considered case-finding as one way of realizing this impact, yet the same effect might also arise from interventions that aim to encourage uptake of TB services through social protection mechanisms for TB patients.
Second, current approaches to preventive therapy are restricted, by practical necessity, to specific risk factors, such as HIV co-infection and household contacts. By contrast, for the substantial reductions that will be needed in TB transmission before 2035, future preventive measures will need to be truly 'population-based', or unrestricted to any specific exposure or risk group. Here, as an illustrative example, we modelled a scenario where mass preventive therapy could be guided by the use of a biomarker tool, to identify incipient TB. In practice, it must be noted that the implementation of such a prognostic tool would carry its own challenges, involving testing in the general community, for a condition having less than one per cent prevalence. The specificity of such a test will therefore, be paramount, whether implemented alone or as part of a triage/confirmation algorithm. In addition, the delivery technology for the biomarker test would be critical in its implementation: for example, a point-of-care 'fingerprick' test could be deployed in primary care settings, not just for detecting incipient TB but also as part of routine screening for other conditions including diabetes. On the other hand, as illustrated in [Figure 4], where such a test is intensively implemented in high-burden settings such as urban slums, this could mitigate its required coverage in the rest of the population.
Our findings for the impact of the 'prevent' intervention scenario would apply to any primary prevention measure that is deployable on a population level, in addition to currently recommended strategies. A primary example is an effective transmission-blocking vaccine, which could have even more profound implications for TB control . Importantly, prevention need not be limited to biomedical tools; as discussed above, the impact of 'multisectoral approaches' aimed at addressing the determinants of TB, including poverty, diabetes and undernutrition may have an equally important effect on TB prevention. There is a pressing need for further evidence on such approaches in South-Asian settings.
As with any transmission model, this framework has some limitations. The model is nationally aggregated and thus does not address subnational heterogeneities, beyond high-impact risk groups. For simplicity, it was not aimed to capture certain secular trends in the Region, such as rapidly growing urbanization; a changing demography (namely an ageing population) and an increase in comorbidities such as diabetes. Further, different forms of TB were not distinguished, thus averaging over bacteriologically confirmed and clinically diagnosed, pulmonary and extrapulmonary TB. It was also assumed that all non-NTP providers involved in 'private sector engagement' were successfully trained to improve their standards of TB care. While initiatives in India have shown notable increases in notifications from the private sector, there is also an increasing body of evidence on the approaches that work best in engaging effectively with healthcare providers in the private sector . More broadly, illustrative scenarios for 'high-impact risk groups' were adopted, noting that the purpose of this element in the model was to be illustrative, rather than prescriptive. In particular, assumptions were made for two important parameters, the size and relative risk of TB in the risk group. An important question for future work is, for a given country setting, the values of these parameters specific to different risk groups. With ongoing case-finding efforts in India and elsewhere, data from these activities will be invaluable in addressing this important data gap. We have assumed efficient implementation and scale-up of TB services, whereas in practice, it is likely that challenges with recruitment, management, procurement and other issues would increase the costs of the activities that we have modelled. Moreover, the largest overall incremental costs are associated with active case-finding and preventive measures. There are limited studies on which these resource needs are based, and the cost per case found is likely to increase as prevalence declines, thus expanding overall resource needs. Further research is needed to better define active and preventive models and their costs. In this cost analysis, the potential for overlapping costs between different activities was ignored, for example, the fact that human resources needed to support the 'strengthen' package may also be able to support the 'accelerate' package of interventions.
Finally, we simulated declines in TB burden that have not previously been recorded on such a scale as in the SEAR. To some extent, this is because we simulated interventions at a scale that is equally unprecedented. A seminal study in Alaskan communities in the 1970s demonstrated that rapid declines in TB could indeed be achieved with population-based treatment of latent TB infection . As discussed above, however, to be replicated on the scale considered here, there is a need for mass preventive measures to be more targeted. In another example, while TB mortality in Western Europe declined up to 10 per cent per year in the early 1900s, this largely predated the availability of TB chemotherapy . Perhaps the most important similarity with modern-day SEAR is that much of TB incidence likely comes from recent transmission. In this respect, currently available tools for early detection and effective treatment would indeed be expected to yield more rapid declines in TB incidence than have previously been observed. It is important to note the limitations inherent in modelling at such levels of scale: for example, in modelling the 'accelerate' package of interventions, we have assumed that case-finding efforts can reduce the delay to diagnosis. Although plausible, as case-finding would tend to interrupt the initial 'patient delay', there remains a lack of systematic evidence for this impact . In future, there is a pressing need to address these evidence gaps, for the potential transmission impact of interventions at scale. Such studies could be facilitated if coupled with existing surveillance efforts (for example, studying the transmission impact of TB prevalence surveys).
In conclusion, our overall findings show that strengthening systems is a critical foundation for meeting the end TB goals in the SEAR; additional declines in TB incidence will require substantial acceleration in case-finding and that TB elimination will ultimately depend on population-level prevention. Achieving these impacts calls for a shift in the TB response in the Region: not only in funding and research effort but also in the ambitious scale at which currently available tools need to be deployed.
Financial support & sponsorship: This work was financially supported by the World Health Organization South-East Asia Region, New Delhi, India.
Conflicts of Interest: None.
| References|| |
Pai M, Memish ZA. New tuberculosis estimates must motivate countries to act. J Epidemiol Glob Health
World Health Organization. WHO End TB Strategy: Global strategy and targets for tuberculosis prevention, care and control after 2015
. Available from: http://www.who.int/tb/post2015_strategy/en/
, accessed on November 4, 2018.
Dye C, Lönnroth K, Jaramillo E, Williams BG, Raviglione M. Trends in tuberculosis incidence and their determinants in 134 countries. Bull World Health Organ
Lönnroth K, Castro KG, Chakaya JM, Chauhan LS, Floyd K, Glaziou P, et al.
Tuberculosis control and elimination 2010-50: Cure, care, and social development. Lancet
Oxlade O, Murray M. Tuberculosis and poverty: Why are the poor at greater risk in India? PLoS One
Zafar Ullah AN, Huque R, Husain A, Akter S, Islam A, Newell JN, et al.
Effectiveness of involving the private medical sector in the national TB control programme in Bangladesh: Evidence from mixed methods. BMJ Open
. pii: e001534.
Mahendradhata Y, Lestari T, Probandari A, Indriarini LE, Burhan E, Mustikawati D, et al.
How do private general practitioners manage tuberculosis cases? A survey in eight cities in Indonesia. BMC Res Notes
Probandari A, Lindholm L, Stenlund H, Utarini A, Hurtig AK. Missed opportunity for standardized diagnosis and treatment among adult tuberculosis patients in hospitals involved in public-private mix for directly observed treatment short-course strategy in Indonesia: A cross-sectional study. BMC Health Serv Res
Udwadia ZF, Pinto LM, Uplekar MW. Tuberculosis management by private practitioners in Mumbai, India: Has anything changed in two decades? PLoS One
Das J, Kwan A, Daniels B, Satyanarayana S, Subbaraman R, Bergkvist S, et al.
Use of standardised patients to assess quality of tuberculosis care: A pilot, cross-sectional study. Lancet Infect Dis
Baral SC, Karki DK, Newell JN. Causes of stigma and discrimination associated with tuberculosis in Nepal: A qualitative study. BMC Public Health
Pai M, Daftary A, Satyanarayana S. TB control: Challenges and opportunities for India. Trans R Soc Trop Med Hyg
Banu S, Rahman MT, Ahmed S, Khatun R, Ferdous SS, Hosen B, et al.
Multidrug-resistant tuberculosis in Bangladesh: Results from a sentinel surveillance system. Int J Tuberc Lung Dis
Falzon D, Jaramillo E, Wares F, Zignol M, Floyd K, Raviglione MC, et al.
Universal access to care for multidrug-resistant tuberculosis: An analysis of surveillance data. Lancet Infect Dis
Mandal S, Chadha VK, Laxminarayan R, Arinaminpathy N. Counting the lives saved by DOTS in India: A model-based approach. BMC Med
Sun AY, Pai M, Salje H, Satyanarayana S, Deo S, Dowdy DW, et al.
Modeling the impact of alternative strategies for rapid molecular diagnosis of tuberculosis in Southeast Asia. Am J Epidemiol
Houben RMGJ, Menzies NA, Sumner T, Huynh GH, Arinaminpathy N, Goldhaber-Fiebert JD, et al.
Feasibility of achieving the 2025 WHO global tuberculosis targets in South Africa, China, and India: A combined analysis of 11 mathematical models. Lancet Glob Health
Achkar JM, Jenny-Avital ER. Incipient and subclinical tuberculosis: Defining early disease states in the context of host immune response. J Infect Dis
(Suppl 4) : S1179-86.
Wells WA, Ge CF, Patel N, Oh T, Gardiner E, Kimerling ME, et al.
Size and usage patterns of private TB drug markets in the high burden countries. PLoS One
Dhanaraj B, Papanna MK, Adinarayanan S, Vedachalam C, Sundaram V, Shanmugam S, et al.
Prevalence and risk factors for adult pulmonary tuberculosis in a metropolitan city of South India. PLoS One
Nadda JP, Singh PK. New evidence of the tuberculosis burden in Asia demands national action. Lancet
Pandey S, Chadha VK, Laxminarayan R, Arinaminpathy N. Estimating tuberculosis incidence from primary survey data: A mathematical modeling approach. Int J Tuberc Lung Dis
Poole D, Raftery AE. Inference for deterministic simulation models: The Bayesian melding approach. J Am Stat Assoc
Menzies NA, Cohen T, Lin HH, Murray M, Salomon JA. Population health impact and cost-effectiveness of tuberculosis diagnosis with xpert MTB/RIF: A dynamic simulation and economic evaluation. PLoS Med
Fox GJ, Nhung NV, Sy DN, Hoa NLP, Anh LTN, Anh NT, et al.
Household-contact investigation for detection of tuberculosis in Vietnam. N Engl J Med
Moonan PK, Nair SA, Agarwal R, Chadha VK, Dewan PK, Gupta UD, et al.
Tuberculosis preventive treatment: The next chapter of tuberculosis elimination in India. BMJ Glob Health
Sterling TR, Villarino ME, Borisov AS, Shang N, Gordin F, Bliven-Sizemore E, et al.
Three months of rifapentine and isoniazid for latent tuberculosis infection. N Engl J Med
Van Der Meeren O, Hatherill M, Nduba V, Wilkinson RJ, Muyoyeta M, Van Brakel E, et al.
Phase 2b controlled trial of M72/AS01E vaccine to prevent tuberculosis. N Engl J Med
Bhargava A. Undernutrition, nutritionally acquired immunodeficiency, and tuberculosis control. BMJ
Oxlade O, Huang CC, Murray M. Estimating the impact of reducing undernutrition on the tuberculosis epidemic in the central eastern States of India: A dynamic modeling study. PLoS One
World Health Organization, Regional Office for South-East Asia. Call for action: ministerial meeting towards ending TB in the South-East Asia.
New Delhi: WHO; 2017. Available from: https://apps.who.int/iris/handle/10665/255553
, accessed on February 18, 2019.
Pai M, Dewan P. Testing and treating the missing millions with tuberculosis. PLoS Med
Comstock GW, Baum C, Snider DE Jr. Isoniazid prophylaxis among alaskan eskimos: A final report of the bethel isoniazid studies. Am Rev Respir Dis
Mcdonald JC, Springett VH. The decline of tuberculosis mortality in Western Europe. Br Med Bull
Kranzer K, Afnan-Holmes H, Tomlin K, Golub JE, Shapiro AE, Schaap A, et al.
The benefits to communities and individuals of screening for active tuberculosis disease: A systematic review. Int J Tuberc Lung Dis
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