An economic evaluation of expanding hookworm control strategies to target the whole community
© Turner et al. 2015
Received: 16 September 2015
Accepted: 23 October 2015
Published: 5 November 2015
The WHO treatment guidelines for the soil-transmitted helminths (STH) focus on targeting children for the control of morbidity induced by heavy infections. However, unlike the other STHs, the majority of hookworm infections are harboured by adults. This untreated burden may have important implications for controlling both hookworm’s morbidity and transmission. This is particularly significant in the context of the increased interest in investigating STH elimination strategies.
We used a deterministic STH transmission model and parameter estimates derived from field epidemiological studies to evaluate the impact of child-targeted (2–14 year olds) versus community-wide treatment against hookworm in terms of preventing morbidity and the timeframe for breaking transmission. Furthermore, we investigated how mass treatment may influence the long-term programmatic costs of preventive chemotherapy for hookworm.
The model projected that a large proportion of the overall morbidity due to hookworm was unaffected by the current child-targeted strategy. Furthermore, driving worm burdens to levels low enough to potentially break transmission was only possible when using community-wide treatment. Due to these projected reductions in programme duration, it was possible for community-wide treatment to generate cost savings – even if it notably increases the annual distribution costs.
Community-wide treatment is notably more cost-effective for controlling hookworm’s morbidity and transmission than the current child-targeted strategies and could even be cost-saving in many settings in the longer term. These calculations suggest that it is not optimum to treat using the same treatment strategies as other STH. Hookworm morbidity and transmission control require community-wide treatment.
The most common neglected tropical diseases (NTDs) are the soil-transmitted helminths (STH) which include Ascaris lumbricoides, Trichuris trichiura and the hookworms (Ancylostoma duodenale and Necator americanus). In the 2010 Global Burden of Disease study, the hookworms were estimated to be responsible for over 65 % of the total disability-adjusted life years (DALY) lost due to STH infections  and, worldwide, are the second leading cause of anaemia .
In addition, there has recently been an increasing interest in considering different strategies for breaking the transmission of STH [5–7] since it is widely recognised that in the absence of effective water, sanitation and hygiene (WASH) programmes, childhood treatment alone is unlikely to break transmission. Previous STH modelling studies have illustrated that even in low transmission settings it is not possible to eliminate hookworm with preventative chemotherapy alone when only targeting children [8, 9, 10].
Expanding treatment programmes to include adults through community-wide treatment is under consideration. However, it should be noted that this would be a major shift in STH control policy, and require an increase in resources and international commitment. Consequently, it is important to evaluate how cost-effective expanding control programmes to include adults is, and understand if it could potentially generate long term cost-savings.
The aim of this paper is to investigate the impact, long-term cost and cost-effectiveness of using community-wide treatment for the control of hookworm.
This analysis was performed with a fully age-structured deterministic model of the dynamics of STH transmission (described in [8–10]), using the parameters pertaining to hookworm (Additional file 1: Table S1). The model can estimate the number of treatment rounds of a given strategy required to theoretically achieve elimination – defined as crossing the breakpoint in transmission where infection levels settle to the equilibrium of extinction .
The relative exposure of the different age groups to the infectious reservoir defined in the model was estimated using likelihood methods and the age intensity profile of infection reported by Bradley et al.  (Fig. 1). This fit is presented in Additional file 1: Figure S1.
The efficacy of albendazole (400 mg) against hookworm (defined within the model as the proportion of worms expelled per treatment) was assumed to be 94.8 % . In the sensitivity analyses we also considered a much lower efficacy of 64.2 % . Individuals under two years of age were considered ineligible for drug treatment.
Scenarios and output
The model was used to compare child-targeted annual and biannual treatment (targeting Pre-SAC and SAC, 2–14 year olds [3, 4]) to annual community-wide treatment (targeting ≥2 year olds). Two different transmission settings were explored; intermediate (R0 = 2.5), and high (R0 = 5) – as measured by the basic reproductive number (R0) which defines the average number of female worm offspring generated by a single female worm in her lifespan who survive to reproductive maturity in the absence of density-dependent or mate-availability constraints . We considered a range of different coverage levels of adults (35–75 %).
Age-specific worm burden thresholds for morbidity 
Age class (years)
Due to the absence of cost data for community-wide STH treatment , a range of relative increases in the economic distribution cost (total per year) when using community-wide compared to child-targeted treatment were assumed (+50, +100, +150, and +200 % i.e. if the full economic cost of a child-targeted programme was US$100,000 per year, this would increase to US$150,000, US$200,000, US$250,00 and US$300,000 per year respectively when using community-wide treatment). Though the relative increase in costs were not based on any primary cost data, this wide range would capture a very broad range of settings/scenarios. Due to the notable variation in reported costs of STH control programmes , the cost of annual child-targeted treatment was assumed to be arbitrary – as we are only considering the relative increase in cost/cost-effectiveness of community-wide treatment.
As MDA programmes have substantial economies of scale, assuming constant cost per treatment and varying treatment coverage within a model can be highly misleading [20, 21]; as the fixed costs of MDA are not accounted for, this method can notably underestimate the costs of treating at a lower coverage within a given transmission setting. Due to this, we assumed a range of different relative increases in the total cost per year of the treatment programme when using community-wide treatment. This reflects that the increase in cost will vary across different settings due to a range of programmatic factors i.e. it is possible to have a relatively inexpensive programme with a high coverage and an expensive programme with a low coverage.
It was assumed that after elimination was achieved, the distribution cost stopped immediately. This reflects that although using a community-wide treatment strategy will initially increase the programmatic distribution costs, it may generate cost savings compared to using a child-targeted strategy for the full time horizon depending on the reduction in the required programme duration (due to the capacity to break transmission). It is important to note that the potential programmatic costs are only considered within the assumed time horizon for the simulations (the potential cost savings achieved by elimination will be greater the longer the assumed time horizon, which is assumed to be finite in the simulations, but could, in theory, be infinite).
It is also important to note that the costs were considered from the perspective of the health care service provider (since the costs of accessing the intervention are likely to be negligible).
The model was used to estimate the relative increase in cost-effectiveness of community-wide treatment in terms of preventing years lived with morbidity (Table 1). This was done by comparing the incremental cost (based on assumed percentage increase in cost of community-wide treatment) and incremental benefit of community-wide treatment in terms of preventing years lived with morbidity in both adults and children to that of annual child-targeted treatment, as estimated from the modelling.
Discounting is the process of adjusting the future values of costs to reflect the fact that society prefers to receive benefits sooner and pay costs later. The discount rate reflects the strength of this time reference. As recommended by the WHO , a discount rate of 3 % per year was applied to the costs and effects. The sensitivity of the results to the use of different discount rates was also explored .
The number of morbidity case years averted for the three different strategies
Intensity thresholds for morbidity
Annual child-targeted treatment
Biannual child-targeted treatment (a)
Community-wide treatment (a)
498 (35 %)
3136 (748 %)
3.2 (33 %)
9.8 (317 %)
1638 (33 %)
6075 (394 %)
135 (46 %)
583 (527 %)
The sensitivity to the relative increase in the number of morbidity case years averted by annual community-wide treatment to the level of coverage in adults
Intensity thresholds for morbidity
Adult coverage: 75 %
Adult coverage: 55 %
Adult coverage: 35 %
Cost-effectiveness of morbidity control
The increase in the cost-effectiveness of preventing morbidity when using annual community-wide versus child-targeted treatment
Intensity thresholds for morbidity
Relative increase in the distribution costs (total per year) of community-wide versus child-targeted treatment
Coverage of adults: 75 %
Coverage of adults: 35 %
When using the higher intensity threshold for morbidity (which corresponds to >160 worms in adults (Table 1)), the relative increase in cost-effectiveness was lower in intermediate transmission settings than for a lower morbidity threshold because the prevalence of these infections was so low in these settings (Table 2 and Additional file 1: Figure S2). Note that the results in Table 4 only investigate the impact of two treatment rounds, and therefore do not account for any potential cost savings resulting from breaking transmission with community-wide treatment – which would increase cost-effectiveness even further.
Even when assuming that the drug efficacy was lower than previously assumed (64.2 % versus 94.8 %), community-wide treatment was still predicted to generate notable benefits and therefore it appears that the general conclusions are robust (Additional file 1: Figure S3).
Feasibility of and timeframe for breaking transmission
Total programme costs and cost savings
The relative total cost of annual community-wide versus child-targeted treatment in an intermediate transmission setting
Relative increase in the distribution costs (total per year) of community-wide versus child-targeted treatment
Coverage of adults: 75 %
Coverage of adults: 55 %
Coverage of adults: 35 %
For a given incease in cost, the chance of cost-savings from comminity-wide treatment were smaller the lower the level of coverage achivied in adults (Table 5) – though were notable even if the coverage was relatively low (55 %) (Table 4). When assuming the coverage of adults was 35 %, cost savings were projected to be unlikely without long time horizons for the modelled setting (Table 4) .
When assuming a lower drug efficacy of 64.2 %, the number of rounds required to break transmission was higher (Additional file 1: Figure S4) and therefore cost-savings was lower/less likely. With this pessimistic assumption on efficacy, it was not possible to eliminate in high transmission settings with MDA alone (Additional file 1: Figure S4) and therefore no cost savings were projected in this scenario.
The projected timeframes for elimination and cost savings were consistent when using a different parameter for the strength of the density dependence in egg production by female worms (Additional file 1: Table S3) and were even more pronounced when using an alternative dataset for the baseline age profile of infection intensity (particularly for lower coverages) (Fig. 1 and Additional file 1: Table S4).
The employed discount rate had a major impact on the potential cost savings generated by reaching elimination through community-wide treatment (Additional file 1: Table S5). The higher the discount rate, the lower the potential cost savings (as these savings occur in the future – illustrated by the gradient of the solid curve in Fig. 5). However, even with a high discount rate of 6 %, community-wide treatment could still generate notable cost savings (depending on the time horizon and transmission settings).
Our projections indicate that the current STH control strategy, which focuses on targeting children, is ineffective in reducing the overall burden of disease induced by hookworm infection – though it is effective in the context of controlling morbidity in children (Fig. 2). This occurs because the burden of infection lies largely in adults due to the rising burden of infection with age (Fig. 1) . Consequently, the disease burden is projected to be higher in adults compared to children (Fig. 2). This is important because hookworm is estimated to be responsible for over 65 % of the DALYs lost due to STH infections , and worldwide it is the second leading cause of anaemia . Our analyses show that in order to control the overall disease burden of hookworm with preventive chemotherapy, programmes must include adults through community-wide treatment (Fig. 2), which is projected to be notably more cost-effective in terms of preventing morbidity (Table 4).
In areas with a STH prevalence greater than 50 %, WHO guidelines recommend that treatment frequency in children is increased to at least twice a year . Though this would have a notable benefit for Ascaris and Trichuris [8, 23], our calculations indicate that this strategy was projected to generate only very small additional reductions in both morbidity (Fig. 2), and the level of overall transmission (Fig. 3) for hookworm [Turner et al., ‘Analysis of the population-level impact of co-administering ivermectin with albendazole or mebendazole for the control and elimination of Trichuris trichiura’, submitted].
It is important to note that the motivation for focusing on treating children for STH is in part due to the potential developmental consequences of infection in children (though this is an area that needs more investigation ) and in part due to the ease with which SAC can be accessed through the school. Though the evidence that intestinal worms directly interfere with productivity and wage earning capacity in adults (reviewed in ) is circumstantial, many of the health consequences of hookworm (especially anaemia [27, 28]) have been proven to affect productivity in working teenagers and adults . Consequently, treating adults for hookworm could generate economic gains and accelerate economic development in endemic countries.
Over the past decade, many areas may have received community-wide treatment which impacts STH through lymphatic filariasis control programmes (which also use albendazole). Where the impacts of lymphatic filariasis control programmes on STH have been measured the impact on hookworm has been notable . Another important route for adult treatment is through the treatment of women of reproductive age within other programmes – such as iron supplementation campaigns, but the level of treatment coverage is typically uncertain.
Timeframe for elimination
Our projections indicate that targeting children alone does not notably impact the overall level of hookworm transmission (Fig. 3). Consequently, it is not possible to break transmission with drug administration alone without including the treatment of adults [8-10] (Fig. 4). These results are supported in part by a previous modelling study by Chan et al. , which investigated the effect of various mixing patterns between children and adults on the impact of hookworm treatment. Furthermore, in a recent field trial in an area with a low baseline hookworm infection, two semi-annual community-wide treatments with albendazole were enough to almost completely eliminate hookworm , which as such supports these model predictions. The level of treatment coverage in adults was the major determinant of the feasibility of eliminating hookworm transmission (Fig. 4). This finding contrasts with the model projections for Ascaris and Trichuris, where the coverage of children is often the major determinate [8-10], Turner et al., ‘Analysis of the population-level impact of co-administering ivermectin with albendazole or mebendazole for the control and elimination of Trichuris trichiura’, submitted.
Due to the projected reductions in programme duration, it is possible for community-wide treatment to generate cost savings compared to the current child-targeted strategy. The extent of these costing savings was sensitive to the assumed increase in distribution costs when using community-wide treatment and the achieved coverage of adults (Table 5 and Additional file 1: Table S2). However, even when assuming it increases the programme’s distribution costs by 200 %, the analysis indicates potential cost savings in intermediate transmission settings when achieving a moderate to high coverage of adults (Table 5).
The higher the transmission setting and lower the coverage in adults, the lesser the possibility of cost savings from community-wide treatment (Fig. 5 and Table 5 and Additional file 1: Table S2). This occurs because the duration of community-wide treatment required to break transmission (Fig. 4), and therefore its total cost, increases with the intensity of the transmission setting (Fig. 5). However, it should be noted that these high transmission settings would have a higher prevalence of morbidity (Fig. 2). Therefore, though the cost savings of community-wide treatment are more uncertain in these settings, the benefits regarding morbidity and accelerating socioeconomic development will be more positive (Fig. 2).
Costs of community-wide versus child-targeted treatment
Due to the absence of data, we calculated the distribution costs of community-wide treatment as a relative increase over the cost per year of child-targeted treatment. This reflects that the increase in cost for community-wide treatment will vary in different settings (see Methods).
It should be noted that it is often not possible to simply separate the costs of treating adults versus children – as they employ overlapping distribution systems . For example, if many un-enrolled SAC or Pre-SAC are treated in the community rather than at the school, it would reduce the observed cost of community-based treatment (changing the apparent cost of treating adults). Consequently, the relative cost per treatment of the different strategies will also be influenced by the local demography (due to economies of scale) . In addition, there will be fixed costs (i.e. those which do not depend on the number treated) shared between both distribution methods. Consequently, expanding treatment to target adults may generate economies of scale for the school-based programme, lowering the cost per treatment for children [19, 20, 32].
Better cost data will permit more detailed cost-effectiveness analysis, using absolute and not relative costs  and an understanding of how the costs may be influenced by coverage.
Programmatic considerations of treating adults as well as children
Since the 2012 London Declaration on NTDs , the availability of donated drugs is no longer the major barrier to achieving the current WHO 2020 goals for STH control . However, focus has now shifted to scaling up the implementation of STH programmes . Expanding treatment programmes to include adults will require more programmatic resources and may not always be practical – particularly in countries which are struggling to achieve a high coverage of children. This highlights the fact that expanding treatment to communities will require further international aid support. However, experiences with lymphatic filariasis and onchocerciasis control programmes which use community-wide MDA clearly demonstrate that expansion is programmatically feasible and can be highly successful .
It is important to note that adding a community drug distributor (CDD) to treat adults would likely improve coverage of children (as the CDD may reach unenrolled children and Pre-SAC within the community more effectively). Where resources are limited to permit the expansion to community-wide treatment, a potential solution could be to further encourage the treatment of the parents of SAC within the school-based programmes. Ensuring the economic productivity of the children’s parents may also reduce school dropout rates.
GSK currently donates 400 million albendazole tablets each year for STH control . Expanding programmes to target adults would increase the number of drugs doses needed considerably. This has important economic implications for donation programmes. However, it is important to acknowledge that the total amount of drugs required for donation could potentially decrease in the long term (due to the capacity to break transmission). Unfortunately, mebendazole is less effective against hookworm , so in this context programmes may have to rely on albendazole alone.
A further important programmatic consideration of treating continuously across entire communities is the potential risk of drug resistance developing. Restricting drug treatment to children creates a reservoir of untreated worms in adults that can effectively dilute any resistant gene pool in children. This issue needs careful monitoring with more research to define markers to track via molecular epidemiological studies.
Uncertainty still surrounds some aspects of hookworm biology and epidemiology. Consequently there is also uncertainty surrounding model structure and parameter estimation (and how these may differ for the different hookworm species). However, the results of this analysis depend largely on the observed age profiles of infection intensity and the observation that the adults harbour the majority of the worms – which was found to be robust across a range of different settings (Fig. 1a) and for both hookworm species (Fig. 1b); with the assumed host demography used within the model (from Uganda) , the proportion of worms harboured by adults was between 70 and 85 % for the different settings (Fig. 1). This range is also supported by . It should be noted that the potential cost-savings were even more pronounced when using an alternative dataset for the baseline age profile of infection intensity (Fig. 1 and Additional file 1: Table S4). They were also robust when changing the parameter for the strength of the density dependence in egg production by female worms (Additional file 1: Table S3).
Within the model, a worm burden above previously established intensity thresholds (Table 1) was used as a proxy for morbidity . It should be acknowledged that these thresholds (Table 1) are uncertain and are likely to be influenced by a number of host specific factors [38, 39]. Furthermore, the thresholds were based on a study where N. americanus was the predominant hookworm species and may be too high for A. duodenale (which is associated with higher rates of blood loss per worm) . More research is needed for statistical models that relate the disease burden of hookworm to experience of infection and the impact of treatment, to allow models to accurately estimate a cost per DALY averted.
This analysis assumed that once hookworm transmission is broken the costs of control stop immediately. However, in reality, certifying elimination would require a period of post-intervention surveillance with associated costs. Furthermore, STH control programmes also target Ascaris and Trichuris and therefore may need to be continued even if hookworm is eliminated (though community-wide treatment would also accelerate the timeframe for breaking transmission for these infections as well [8, 9, 10]).
The model does not currently address the possibility of systematic non-compliance. If a high proportion of adults were systematically non-compliant, the timeframe for elimination would be increased, reducing the potential cost savings of community-wide treatment (though the general principles still apply).
Annual community-wide treatment is predicted to be markedly more cost-effective in controlling both hookworm’s disease burden and the level of on-going transmission. Furthermore, because it is possible to break transmission when using community-wide treatment (which reduces the required programme duration), expanding programmes can generate long term cost savings– even if it notably increases the annual distribution costs of the programme when achieving a moderate to high coverage of adults.
Although expanding programmes to target adults will require greater programmatic resources and drug donations, the calculations highlight the notable benefits it can generate and the importance of further considering this strategy in any ongoing revisions of the treatment and control guidelines for STH. These results highlight that the current WHO guidelines, which recommend treating all STH the same way (regardless of which age groups have the highest burden), may lead to an inefficient use of available drug donations and associated resources.
HCT, AAB, KVS, and JCD are supported by London Centre for Neglected Tropical Disease Research (funded by GSK). JET and TDH are supported by the Bill & Melinda Gates Foundation (#OPP1033751) and the Partnership for Child Development. SJB is supported by a Wellcome Trust Senior Fellowship in Basic Biomedical Science (098045). RMA is supported by the Bill & Melinda Gates Foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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- Pullan RL, Smith JL, Jasrasaria R, Brooker SJ. Global numbers of infection and disease burden of soil transmitted helminth infections in 2010. Parasit Vectors. 2014;7:37.PubMed CentralView ArticlePubMedGoogle Scholar
- Kassebaum NJ, Jasrasaria R, Naghavi M, Wulf SK, Johns N, Lozano R, et al. A systematic analysis of global anemia burden from 1990 to 2010. Blood. 2014;123(5):615–24.PubMed CentralView ArticlePubMedGoogle Scholar
- WHO. Preventive Chemotheraphy in Human Helminthiasis. Geneva, Switzerland: World Health Organization; 2006. http://apps.who.int/iris/bitstream/10665/43545/1/9241547103_eng.pdf.
- World Health Organization. Eliminating soil-transmitted helminthiasis as a public health problem in children: progress report 2001–2010 and strategic plan 2011–2020. 2012. http://apps.who.int/iris/bitstream/10665/44804/1/9789241503129_eng.pdf.
- Brooker SJ, Nikolay B, Balabanova D, Pullan RL. Global feasibility assessment of interrupting the transmission of soil-transmitted helminths: a statistical modelling study. Lancet Infect Dis. 2015.Google Scholar
- Global Partners Are Taking the “Neglect” out of “Neglected Tropical Diseases”. [http://www.gatesfoundation.org/Media-Center/Press-Releases/2014/04/Global-Partners-Are-Taking-the-Neglect-out-of-Neglected-Tropical-Diseases].
- Anderson RM, Turner HC, Truscott JE, Hollingsworth TD, Brooker SJ. Should the Goal for the Treatment of Soil Transmitted Helminth (STH) Infections Be Changed from Morbidity Control in Children to Community-Wide Transmission Elimination? PLoS Negl Trop Dis. 2015;9(8), e0003897.PubMed CentralView ArticlePubMedGoogle Scholar
- Anderson RM, Truscott JE, Hollingsworth TD. The coverage and frequency of mass drug administration required to eliminate persistent transmission of soil-transmitted helminths. Philos Trans R Soc Lond B Biol Sci. 2014;369(1645):20130435.PubMed CentralView ArticlePubMedGoogle Scholar
- Truscott JE, Hollingsworth TD, Brooker SJ, Anderson RM. Can chemotherapy alone eliminate the transmission of soil transmitted helminths? Parasit Vectors. 2014;7(1):266.PubMed CentralView ArticlePubMedGoogle Scholar
- Truscott JE, Turner HC, Anderson RM. What impact will the achievement of the current World Health Organisation targets for anthelmintic treatment coverage in children have on the intensity of Soil Transmitted Helminth infections? Parasit Vectors 2015. 2015;8:551.Google Scholar
- Anderson RM, May RM. Infectious diseases of humans: dynamics and control. Oxford: Oxford Science; 1991.Google Scholar
- Bradley M, Chandiwana SK, Bundy DA, Medley GF. The epidemiology and population biology of Necator americanus infection in a rural community in Zimbabwe. Trans R Soc Trop Med Hyg. 1992;86(1):73–6.View ArticlePubMedGoogle Scholar
- Vercruysse J, Behnke JM, Albonico M, Ame SM, Angebault C, Bethony JM, et al. Assessment of the anthelmintic efficacy of albendazole in school children in seven countries where soil-transmitted helminths are endemic. PLoS Negl Trop Dis. 2011;5(3), e948.PubMed CentralView ArticlePubMedGoogle Scholar
- Keiser J, Utzinger J. Efficacy of current drugs against soil-transmitted helminth infections: systematic review and meta-analysis. JAMA. 2008;299(16):1937–48.View ArticlePubMedGoogle Scholar
- Bundy D, Chan M, Medley G, Jamison D, Savioli L. Intestinal nematode infections (Chapter 9). In: Murray CJL, Lopez AD, Mathers CD, editors. Global Epidemiology of Infectious Disease Volume IV. Geneva: WHO; 2004.Google Scholar
- Lwambo NJ, Bundy DA, Medley GF. A new approach to morbidity risk assessment in hookworm endemic communities. Epidemiol Infect. 1992;108(3):469–81.PubMed CentralView ArticlePubMedGoogle Scholar
- Chan MS, Medley GF, Jamison D, Bundy DA. The evaluation of potential global morbidity attributable to intestinal nematode infections. Parasitology. 1994;109(Pt 3):373–87.View ArticlePubMedGoogle Scholar
- Brooker S. Estimating the global distribution and disease burden of intestinal nematode infections: adding up the numbers - a review. Int J Parasitol. 2010;40(10):1137–44.PubMed CentralView ArticlePubMedGoogle Scholar
- Turner HC, Truscott JE, Hollingsworth TD, Bettis AA, Brooker SJ, Anderson RM. Cost and cost-effectiveness of soil-transmitted helminth treatment programmes: systematic review and research needs. Parasit Vectors. 2015;8:355.PubMed CentralView ArticlePubMedGoogle Scholar
- Turner HC, Truscott JE, Fleming FM, Hollingsworth TD, Brooker SJ, Anderson RM. Cost-effectiveness of scaling up mass drug administration for the control of soil-transmitted helminths: a comparison of cost function and constant costs analyses Lancet Infect Dis (in press).Google Scholar
- Brooker S, Kabatereine NB, Fleming F, Devlin N. Cost and cost-effectiveness of nationwide school-based helminth control in Uganda: intra-country variation and effects of scaling-up. Health Policy Plan. 2008;23(1):24–35.PubMed CentralView ArticlePubMedGoogle Scholar
- World Health Organization. Making choices in health: WHO guide to cost-effectiveness analysis. Geneva: World Health Organization; 2003. http://www.who.int/choice/publications/p_2003_generalised_cea.pdf.
- Truscott J, Hollingsworth TD, Anderson R. Modeling the Interruption of the Transmission of Soil-Transmitted Helminths by Repeated Mass Chemotherapy of School-Age Children. PLoS Negl Trop Dis. 2014;8(12), e3323.PubMed CentralView ArticlePubMedGoogle Scholar
- Anderson RM, Truscott JE, Pullan RL, Brooker SJ, Hollingsworth TD. How effective is school-based deworming for the community-wide control of soil-transmitted helminths? PLoS Negl Trop Dis. 2013;7(2), e2027.PubMed CentralView ArticlePubMedGoogle Scholar
- Brooker S, Bethony J, Hotez PJ. Human hookworm infection in the 21st century. Adv Parasitol. 2004;58:197–288.PubMed CentralView ArticlePubMedGoogle Scholar
- Guyatt H. Do intestinal nematodes affect productivity in adulthood? Parasitol Today. 2000;16(4):153–8.View ArticlePubMedGoogle Scholar
- Brooker S, Hotez PJ, Bundy DA. Hookworm-related anaemia among pregnant women: a systematic review. PLoS Negl Trop Dis. 2008;2(9), e291.PubMed CentralView ArticlePubMedGoogle Scholar
- Smith JL, Brooker S. Impact of hookworm infection and deworming on anaemia in non-pregnant populations: a systematic review. Trop Med Int Health. 2010;15(7):776–95.PubMed CentralView ArticlePubMedGoogle Scholar
- Haas JD, Brownlie T. Iron deficiency and reduced work capacity: a critical review of the research to determine a causal relationship. J Nutr. 2001;131(2S-2):676S–88. discussion 688S-690S.PubMedGoogle Scholar
- Pion SD, Chesnais CB, Bopda J, Louya F, Fischer PU, Majewski AC, et al. The impact of two semiannual treatments with albendazole alone on lymphatic filariasis and soil-transmitted helminth infections: a community-based study in the republic of congo. Am J Trop Med Hyg. 2015;92(5):959–66.View ArticlePubMedGoogle Scholar
- Chan MS, Bradley M, Bundy DA. Transmission patterns and the epidemiology of hookworm infection. Int J Epidemiol. 1997;26(6):1392–400.View ArticlePubMedGoogle Scholar
- Leslie J, Garba A, Oliva EB, Barkire A, Tinni AA, Djibo A, et al. Schistosomiasis and soil-transmitted helminth control in Niger: cost effectiveness of school based and community distributed mass drug administration [corrected]. PLoS Negl Trop Dis. 2011;5(10), e1326.PubMed CentralView ArticlePubMedGoogle Scholar
- Ending the neglect and reaching 2020 goals. [http://unitingtocombatntds.org/downloads/press/ntd_event_london_declaration_on_ntds.pdf].
- From promises to progress: The first anniversary report on the London Declaration on NTDs. [http://unitingtocombatntds.org/resource/promises-progress-first-report-london-declaration-ntds].
- Krentel A, Fischer PU, Weil GJ. A Review of Factors That Influence Individual Compliance with Mass Drug Administration for Elimination of Lymphatic Filariasis. PLoS Negl Trop Dis. 2013;7(11), e2447.PubMed CentralView ArticlePubMedGoogle Scholar
- The campaign to control soil-transmitted helminths Protecting children and communities. [http://www.gsk.com/media/267956/Soil-transmitted-helminths-factsheet-PDF.pdf].
- Olsen A. The proportion of helminth infections in a community in western Kenya which would be treated by mass chemotherapy of schoolchildren. Trans R Soc Trop Med Hyg. 1998;92(2):144–8.View ArticlePubMedGoogle Scholar
- Mascarini-Serra L. Prevention of Soil-transmitted Helminth Infection. J Glob Infect Dis. 2011;3(2):175–82.PubMed CentralView ArticlePubMedGoogle Scholar
- Gilles HM, Williams EJ, Ball PA. Hookworm infection and anaemia. An epidemiological, clinical, and laboratory study. Q J Med. 1964;33:1–24.PubMedGoogle Scholar
- Haswell-Elkins MR, Elkins DB, Manjula K, Michael E, Anderson RM. An investigation of hookworm infection and reinfection following mass anthelmintic treatment in the south Indian fishing community of Vairavankuppam. Parasitology. 1988;96(Pt 3):565–77.View ArticlePubMedGoogle Scholar
- Pritchard DI, Quinnell RJ, Slater AF, McKean PG, Dale DD, Raiko A, et al. Epidemiology and immunology of Necator americanus infection in a community in Papua New Guinea: humoral responses to excretory-secretory and cuticular collagen antigens. Parasitology. 1990;100(Pt 2):317–26.View ArticlePubMedGoogle Scholar
- Ye XP, Wu ZX, Sun FH. The population biology and control of Necator americanus in a village community in south-eastern China. Ann Trop Med Parasitol. 1994;88(6):635–43.PubMedGoogle Scholar
- Anderson RM, Schad GA. Hookworm burdens and faecal egg counts: an analysis of the biological basis of variation. Trans R Soc Trop Med Hyg. 1985;79(6):812–25.View ArticlePubMedGoogle Scholar