Citation: Anderson RM, Turner HC, Truscott JE, Hollingsworth TD, Brooker SJ (2015) 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 9(8): e0003897. https://doi.org/10.1371/journal.pntd.0003897
Editor: Serap Aksoy, Yale School of Public Health, UNITED STATES
Published: August 20, 2015
Copyright: © 2015 Anderson et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Funding: RMA and SJB receive funding from the Bill and Melinda Gates Foundation (OPP1033751). SJB is supported by the Wellcome Trust through a Senior Fellowship in Basic Biomedical Science (098045). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: I have read the journal’s policy and the authors of this manuscript have the following competing interests: RMA is non-executive member of the board of GlaxoSmithKline (GSK). GlaxoSmithKline played no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. This does not alter our adherence to all PLOS policies on sharing data and materials.
Morbidity induced by infection with the major soil transmitted infections (STH—Ascaris lumbricoides, Trichuris trichiura, and hookworms) results in an estimated 5.19 million disability-adjusted life years (DALYs) . The World Health Organization’s (WHO) policy for control centres on three groups, preschool aged children (pre-SAC), school-aged children (SAC), and women of child bearing age, on the basis that heavy infection in these groups will have a detrimental impact on anaemia, child growth, and development. The current WHO guidelines focus on school-aged children, both for monitoring infection and as a target for treatment, although treatment of pre-SAC and women of childbearing age is also recommended where sustainable delivery mechanisms exist, especially in areas of intense transmission [2,3]. The guidelines recommend treating SAC annually where any STH prevalence falls between 20% and 50% and twice a year where it exceeds 50% .
The London Declaration on Neglected Tropical Diseases in 2012 endorsed WHO goals to scale up mass drug administration (MDA) for STH, so that by 2020, 75% of the pre-SAC and SAC in need will be treated regularly . Building on an existing roadmap, WHO announced an intention to meet the target [2,5,6]. Progress has been good in some areas, but less so in others. In 2012, global coverage of those in need was 37% for SAC and 29% for pre-SAC . Data for the more recent years is as yet to be published by WHO , but a huge gain in coverage is not expected, despite increased drug donations from the pharmaceutical companies who manufacture the main anthelmintics. This is due in part to the logistical challenges in getting even donated drugs to these populations, who are often beyond “the end of the road.” At present, many countries with endemic STH infections are not availing themselves of the freely donated drugs to treat children.
We are still a long way from the 2020 target of 75%. Even if this target is reached, will it be enough to eliminate transmission and the disease arising from heavy infections with STH? If not, how should the guidelines be changed to push towards morbidity control, and ideally, the eventual elimination of transmission?
Basing Policy on Quantitative Calculations
To answer these questions, calculations are required to assess the impact of MDA targeted at particular age groupings, especially pre-SAC and SAC, on overall transmission in communities with differing levels of infection exposure. In many areas of infectious disease epidemiology and the design of interventions, the impact of control is today assessed by simulations based on mathematical models using parameter estimates from epidemiological studies (e.g., HIV and Plasmodium falciparum [7,8]). The neglected tropical disease (NTD) field lags behind, in the sense of largely basing target treatment levels on discussion and consensus, without detailed calculations. Much of the basic framework for the study of the transmission dynamics of helminth infections was laid down in the 1960s and 1980s [9,10]). Rather little has been achieved since that time in model development and parameter estimation. Concomitantly, little use has been made of the insights gained from these analyses in the design of public health policy for the control of STH and schistosome infections. The tools now available can rectify this shortcoming, and they can easily be adapted to include costs and benefits as outlined in this article. They should be used to refine WHO policy on treatment to aim for a robust framework that will eliminate transmission.
Demography and Epidemiology
A key issue concerns demography in sub-Saharan Africa and other areas with endemic infection. Typically, there are as many adults as there are pre-SAC and SAC . This implies that, depending on the distribution of worms across the age classes, the adults themselves may be able to sustain transmission within a community, even when a very high fraction of the children are treated effectively. This is especially the case for hookworm where adults typically harbour the majority of worms (in some areas, more than 80% of the total population of parasites, (Fig 1—see inset in graph C)), but also applies for Ascaris and Trichuris, where up to 30% of worms and egg counts are in those older than 15 years of age , irrespective of the intensity of transmission in a defined area.
These are typical age intensity profiles for the three most important STH species, where the colours denote the age groupings: pre-SAC (blue), SAC (red), and adults (orange). Data for A from , data for B , and data for C . The inset in Graph C represents five worm expulsion studies of Necator americanus showing consistent patterns in a rise in burden with age in different geographical locations .
The impact of this substantial reservoir of infection in adults on reinfection in children can be better illuminated using deterministic and stochastic models of STH transmission, based on parameter estimates derived from cross-sectional and longitudinal worm expulsion studies and observations on demography and the mean intensity distribution across the major age groupings (pre-SAC, SAC, and adults—see Fig 1 [12,13]). A series of general conclusions emerge that support the observational studies based on demography and cross-sectional epidemiological data on age specific intensities of infection.
Impact of Current Treatment Strategies
We focus on three major issues concerning MDA, namely: who to treat, how frequently to treat, and how long to treat. In our calculations, we use a fully aged structured deterministic STH transmission model (described in [12,13]). Stochastic individual-based models for the mean worm burden give identical results to the deterministic predictions. For illustration, we compare the impact of annual and biannual treatment of pre-SAC and SAC, with annual mass treatment, in communities with Ascaris and hookworm. As a case study, we focus on an area of medium transmission (R0 values around 2–3, true prevalence (not adjusted for diagnostic sensitivity) around 70% in SAC). As illustrated in Fig 2, which records simulated MDA strategies focusing on once and twice yearly treatment of pre-SAC and SAC combined (at a coverage level of 75%), compared with community-wide treatment (at the same coverage level). Increasing the frequency of MDA in children is predicted to be marginally more effective than annual mass treatment, in terms of reducing the overall burden of Ascaris. In contrast, for hookworm, the analyses illustrate that increasing the frequency of MDA for pre-SAC and SAC alone has limited additional impact. Expanding the annual treatment programme to also include adults actually reduces the intensity of hookworm infections both in children and the community as a whole (Fig 2). This occurs because the adults have the majority share of the infectious reservoir (i.e., are a core group), and consequently, treating children alone does not significantly impact the level of transmission. The children get reinfected after treatment because of the reservoir in adults. This suggests that WHO guidelines to increase treatment to twice a year in high prevalence areas is unlikely to have the desired impact in areas with high hookworm prevalence. The best treatment strategy is highly dependent on the local age distribution of infection of the different STH species.
The coloured lines represent different treatment strategies: green—annual community-wide MDA (75% coverage of all age groupings (pre-SAC, SAC, and adults) and 95% drug efficacy); red—biannual age group targeted MDA (pre-SAC and SAC with 75% coverage and 95% drug efficacy); and blue—annual age group targeted MDA (pre-SAC and SAC with 75% coverage and 95% drug efficacy). Graphs A–C and D–F correspond to Hookworm and Ascaris respectively. Graphs A and D record the overall mean number of worms across all ages. Graphs B and E record the mean number of worms in children (pre-SAC and SAC, 2–15-year-olds). Graphs C and F record the mean number of worms in adults (>15 year olds). Calculations based on a basic reproductive number, Ro, of 2.5 (medium to high transmission setting). Model parameters described in .
It is important to note that monitoring and evaluation programmes that only measure the impact of a school-based hookworm treatment programme in the treated age group record a much bigger impact on the children (Fig 2b) than the true impact on the entire population, as reflected by persisting worm burdens in adults (Fig 2c). School-age group-based surveillance programmes can give good estimates of the reduced morbidity in children but can lead to misleading estimates of the impact of these programmes on overall transmission in the community. A revision in the monitoring and evaluation (M & E) guidelines is required to address this problem. Current guidelines recommend that monitoring is conducted in schools, as school children are the main targets of control . More recently, transmission assessment surveys (TAS) for lymphatic filariasis have been proposed as an alternative platform for monitoring STH infection , and the implementation of TAS in the wider community provides the opportunity to reliably track STH across a range of age classes .
To cross the transmission “breakpoint” , where transmission is eliminated, requires many years of continual treatment (Fig 2b) at moderate to high coverage (>75%), depending on the intensity of transmission (the value of R0). Elimination requires the treatment of adults for hookworm, and the time required to achieve this is accelerated (and required in areas of high transmission) for Ascaris. This conclusion also applies for Trichuris, and in most circumstances for the schistosome infections for which praziquantel is employed in MDA. Pre-SAC treatment for the control of morbidity induced by schistosome infections has been suggested by Stothard . The practical feasibility of providing mass treatment to adults in addition to pre-SAC and SAC is demonstrated by the mass treatment campaigns for onchocerciasis and lymphatic filariasis (LF), which provide albendazole plus ivermectin or diethylcarbamazine citrate to entire communities, using community drug distributors . The albendazole and ivermectin used in these programmes are also highly effective against STH [18,19], although there has been no systematic attempt to quantify the impact of the global onchocerciasis and LF control programmes on the transmission of STH despite the potential insight they afford into the impact of expanding current school-based deworming programmes.
Costs of Different Strategies
A key issue in scaling up treatment to the whole community is cost, and this in turn depends on demography (the proportions of the population in each age grouping), who is treated, at what coverage level, how often, and for how long. If transmission is not interrupted by only focusing on pre-SAC and SAC, treatment must continue forever if no other conditions change . Water, sanitation, and hygiene (WASH) programmes have the potential to radically change the picture, if they can be designed to permanently supress transmission, but progress has been limited in many areas of endemic infection . Hopefully, this situation may change in the coming decades as economic growth improves in parts of Africa and Asia, leading to better sanitation and hygiene.
Under the pessimistic assumption that treating adults is twice as expensive as treating children (many studies reporting a much lower difference ), we calculate that the total costs of community-wide treatment over a 20 year period (discounting at 3% per year) are much less (approximately 60%) than that for repeated annual treatment of pre-SAC and SAC, given that the former has only to continue for three years (with the assumptions in Fig 2), while the latter must continue beyond the 20-year time horizon in hookworm transmission areas of intermediate intensity (Turner et al. manuscript in preparation).
New Treatment Guidelines and a New Strategy
Our calculations suggest that the current guidelines need modification, particularly regarding the recommendation to increase treatment frequency if the prevalence of any STH is greater than 50% in SAC. Calculations suggest that in most areas where hookworm is the dominate infection, it is better to broaden treatment across all age classes instead of treating children twice a year. This leads to the more efficient use of limited resources in the longer term. For high transmission Ascaris areas, the best option is both increasing frequency and broadening coverage across all age classes.
Drug efficacy for Trichuris is known to be low with monotherapy using either Albendazole or Mebendazole (the standard treatments for STH) , and hence in settings where Trichuris is the dominant STH, alternative approaches will be required. One such approach that has been shown to notably increase the treatment efficacy against Trichuris is coadministering Ivermectin with the benzimidazoles or using other drug combinations . With dual therapy, broadening the coverage of age groupings to include adults may also be beneficial (depending on the local age intensity profile [Fig 1]).
What are the barriers to changing the quidelines for treatment, monitoring and evaluation? The school has many advantages for treatment delivery since high treatment coverage can be achieved for regular attenders and for surveillance as schools provide a ready sampling frame. In contrast, in some settings it has proven difficult to achieve high coverage (and good surveillance) in adults for STH (although the experience with MDA for lymphatic filariasis argues that it can be achieved ), and the cost of treating one adult may at times be higher when compared with treating children in a school setting. Community-wide coverage also requires an increase in drug donations. Despite this, the longer term cost calculations are compelling, given that one strategy has to be continued forever while the other offers the hope of interrupting transmission permanently. On this basis, it would seem highly desirable to change the WHO guidelines, with a concomitant emphasis on education, sustainability of current WASH programmes (to reduce transmission intensity and thereby enhance the impact of MDA), communication to encourage high treatment uptake amongst adults and better integration of STH control with that of LF where community-wide coverage has been a target for some time. The coverage levels predicted to eliminate LF transmission are much less stringent than those required for hookworm or Ascaris, so integrated STH and LF control is desirable, but reported coverage and frequency of treatment with Albendazole for LF must be increased to stop STH transmission. A revision of the guidelines is especially desirable when hookworm is the dominant infection, since most worms are typically harboured by adults. The cross-sectional age intensity profiles for Ascaris and Trichuris (Fig 1), and for the schistosomes, suggest that in high transmission areas, infections across the community may be maintained by adults even when children are effectively treated twice a year at high coverage levels. Of course, treating the whole community will also lead to more rapid reductions in transmission. But the effect will not be as extreme as for hookworm. To achieve the 2020 goals, treatment coverage in children must be increased significantly, but in many areas reductions in morbidity, and the highly desirable goal of stopping transmission, would both be more likely and much more rapid, if coverage is broadened to encompass adults. The debate on what is the best strategy to manage STH infection should shift from morbidity control to transmission interruption. Concomitantly, there is a need to broaden the scope of research to investigate the cost-effectiveness and feasibility of alternative treatment strategies in achieving the interruption of transmission across a range of settings. Linked to any shift from age group targeting to community-wide control is the risk of enhancing selection for drug resistant strains of the parasites, where the refugium of untreated adults no longer dilutes the gene pool of those parasites exposed to selection. But the experience with community-wide control in LF programmes, where the Albendazole drug also impacts STH, suggests this concern may not materialize in practice. However, this needs careful monitoring.
We thank Don Bundy for discussions on Trichuris and issues surrounding the implementation of STH control.
- 1. Pullan RL, Smith JL, Jasrasaria R, Brooker SJ (2014) Global numbers of infection and disease burden of soil transmitted helminth infections in 2010. Parasit Vectors 7: 37. pmid:24447578
World Health Organization (2012) Accelerating work to overcome the global impact of neglected tropical diseases: a roadmap for implementation. Geneva: World Health Organization; 2012 WHO/HTM/NTD/2012.1. Available: http://www.who.int/neglected_diseases/NTD_RoadMap_2012_Fullversion.pdf. Accessed 27th April 2015.
World Health Organization (2006) Preventive Chemotheraphy in Human Helminthiasis. Geneva, Switzerland: World Health Organization. Available: http://whqlibdoc.who.int/publications/2006/9241547103_eng.pdf. Accessed 27th April 2015.
The London Declaration on Neglected Tropical Diseases. Available: www.UnitingToCombatNTDs.org. Accessed 27th April 2015.
World Health Organization (2015) Investing to overcome the global impact of neglected tropical diseases. Third WHO report on neglected tropical diseases. Available: http://apps.who.int/iris/bitstream/10665/152781/1/9789241564861_eng.pdf?ua=1. Accessed 27th April 2015.
WHO Resolution 66.12 http://www.who.int/neglected_diseases/mediacentre/WHA_66.12_Eng.pdf. Accessed 27th April 2015.
- 7. Griffin JT, Hollingsworth TD, Okell LC, Churcher TS, White M, et al. (2010) Reducing Plasmodium falciparum malaria transmission in Africa: a model-based evaluation of intervention strategies. PLoS Med 7: e 1000324.
- 8. Hallett TB, Menzies NA, Revill P, Keebler D, Borquez A, et al. (2014) Using modeling to inform international guidelines for antiretroviral treatment. AIDS 28 Suppl 1: S1–4. pmid:24468942
- 9. Macdonald G (1965) The dynamics of helminth infections, with special reference to schistosomes. Trans R Soc Trop Med Hyg 59: 489–506. pmid:5860312
- 10. Anderson RM, May RM (1985) Helminth infections of humans: mathematical models, population dynamics, and control. Adv Parasitol 24: 1–101. pmid:3904343
- 11. Anderson RM, Truscott JE, Pullan RL, Brooker SJ, Hollingsworth TD (2013) How effective is school-based deworming for the community-wide control of soil-transmitted helminths? PLoS Negl Trop Dis 7: e2027. pmid:23469293
- 12. Anderson RM, Truscott JE, Hollingsworth TD (2014) 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 369: 20130435. pmid:24821921
- 13. Truscott JE, Hollingsworth TD, Brooker SJ, Anderson RM (2014) Can chemotherapy alone eliminate the transmission of soil transmitted helminths? Parasit Vectors 7: 266. pmid:24916278
World Health Organization (2011) Helminth Control in School-Age Children: A Guide for Managers of Control Programmes. Geneva: World Health Organization. Available: http://whqlibdoc.who.int/publications/2011/9789241548267_eng.pdf. Accessed 27th April 2015.
World Health Organization (2015) Assessment of Soil-Transmitted Helminthiases during a Transmission Assessment Survey (TAS) Conducted in the Context of the Programme for the Elimination of Lymphatic Filariasis. Available: http://apps.who.int/iris/bitstream/10665/153240/1/9789241508384_eng.pdf. Accessed 23th June 2015.
- 16. Smith JL, Sturrock HJ, Assefa L, Nikolay B, Njenga SM, et al. (2015) Factors associated with the performance and cost-effectiveness of using lymphatic filariasis transmission assessment surveys for monitoring soil-transmitted helminths: a case study in Kenya. Am J Trop Med Hyg 92: 342–353. pmid:25487730
- 17. Stothard JR, Sousa-Figueiredo JC, Betson M, Bustinduy A, Reinhard-Rupp J (2013) Schistosomiasis in African infants and preschool children: let them now be treated! Trends Parasitol 29: 197–205. pmid:23465781
- 18. Gutman J, Emukah E, Okpala N, Okoro C, Obasi A, et al. (2010) Effects of annual mass treatment with ivermectin for onchocerciasis on the prevalence of intestinal helminths. Am J Trop Med Hyg 83: 534–541. pmid:20810817
- 19. Gunawardena NK, Amarasekera ND, Pathmeswaran A, de Silva NR (2008) Effect of repeated mass chemotherapy for filariasis control on soil-transmitted helminth infections in Sri Lanka. Ceylon Med J 53: 13–16. pmid:18590264
- 20. Pullan RL, Freeman MC, Gething PW, Brooker SJ (2014) Geographical Inequalities in Use of Improved Drinking Water Supply and Sanitation across Sub-Saharan Africa: Mapping and Spatial Analysis of Cross-sectional Survey Data. PLoS Med 11: e1001626. pmid:24714528
Turner HC, Truscott JE, Hollingsworth TD, Bettis AA, Brooker SJ, et al. (2015) Cost and cost-effectiveness of soil-transmitted helminth treatment programmes: systematic review and research needs. Parasit Vectors, In press.
- 22. Keiser J, Utzinger J (2008) Efficacy of current drugs against soil-transmitted helminth infections: systematic review and meta-analysis. JAMA 299: 1937–1948. pmid:18430913
- 23. Knopp S, Mohammed KA, Speich B, Hattendorf J, Khamis IS, et al. (2010) Albendazole and mebendazole administered alone or in combination with ivermectin against Trichuris trichiura: a randomized controlled trial. Clin Infect Dis 51: 1420–1428. pmid:21062129
- 24. Krentel A, Fischer PU, Weil GJ (2013) A Review of Factors That Influence Individual Compliance with Mass Drug Administration for Elimination of Lymphatic Filariasis. PLoS Negl Trop Dis 7: e2447. pmid:24278486
- 25. Elkins DB, Haswell-Elkins M, Anderson RM (1986) The epidemiology and control of intestinal helminths in the Pulicat Lake region of Southern India. I. Study design and pre- and post-treatment observations on Ascaris lumbricoides infection. Trans R Soc Trop Med Hyg 80: 774–792. pmid:3603617
- 26. Bundy DA, Cooper ES, Thompson DE, Anderson RM, Didier JM (1987) Age-related prevalence and intensity of Trichuris trichiura infection in a St. Lucian community. Trans R Soc Trop Med Hyg 81: 85–94. pmid:3445330
- 27. Bradley M, Chandiwana SK, Bundy DA, Medley GF (1992) The epidemiology and population biology of Necator americanus infection in a rural community in Zimbabwe. Trans R Soc Trop Med Hyg 86: 73–76. pmid:1566314
- 28. Brooker S, Bethony J, Hotez PJ (2004) Human hookworm infection in the 21st century. Adv Parasitol 58: 197–288. pmid:15603764