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Modelling mass drug administration strategies for reducing scabies burden in Monrovia, Liberia

Published online by Cambridge University Press:  18 August 2023

Nefel Tellioglu
Affiliation:
School of Computing and Information Systems, The University of Melbourne, Melbourne, VIC, Australia
Rebecca H. Chisholm
Affiliation:
Department of Mathematical and Physical Sciences, La Trobe University, Bundoora, VIC, Australia Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia
Patricia Therese Campbell
Affiliation:
Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia Department of Infectious Diseases, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia
Shelui Collinson
Affiliation:
Clinical Research Department, Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK
Joseph Timothy
Affiliation:
Department of Disease Control, Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK
Karsor Kollie
Affiliation:
Ministry of Health, Monrovia, Liberia
Samuel Zayzay
Affiliation:
Ministry of Health, Monrovia, Liberia
Angela Devine
Affiliation:
Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia Global and Tropical Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, NT, Australia
Jodie McVernon
Affiliation:
Department of Infectious Diseases, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia Victorian Infectious Diseases Reference Laboratory, The Royal Melbourne Hospital at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia
Michael Marks
Affiliation:
Clinical Research Department, Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK Hospital for Tropical Diseases, University College London Hospital, London, UK Division of Infection and Immunity, University College London, London, UK
Nicholas Geard*
Affiliation:
School of Computing and Information Systems, The University of Melbourne, Melbourne, VIC, Australia
*
Corresponding author: Nicholas Geard; Email: ngeard@unimelb.edu.au
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Abstract

Scabies is a parasitic infestation with high global burden. Mass drug administrations (MDAs) are recommended for communities with a scabies prevalence of >10%. Quantitative analyses are needed to demonstrate the likely effectiveness of MDA recommendations. In this study, we developed an agent-based model of scabies transmission calibrated to demographic and epidemiological data from Monrovia. We used this model to compare the effectiveness of MDA scenarios for achieving scabies elimination and reducing scabies burden, as measured by time until recrudescence following delivery of an MDA and disability-adjusted-life-years (DALYs) averted. Our model showed that three rounds of MDA delivered at six-month intervals and reaching 80% of the population could reduce prevalence below 2% for three years following the final round, before recrudescence. When MDAs were followed by increased treatment uptake, prevalence was maintained below 2% indefinitely. Increasing the number of and coverage of MDA rounds increased the probability of achieving elimination and the number of DALYs averted. Our results suggest that acute reduction of scabies prevalence by MDA can support a transition to improved treatment access. This study demonstrates how modelling can be used to estimate the expected impact of MDAs by projecting future epidemiological dynamics and health gains under alternative scenarios.

Type
Original Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2023. Published by Cambridge University Press

Background

Scabies is a parasitic infestation commonly observed in tropical and resource-poor settings [Reference Engelman and Steer1]. The primary manifestations of scabies are severe pruritic skin lesions on the host [Reference Engelman2, Reference McCarthy3]. Scratching due to scabies infestation often leads to secondary bacterial infections such as Group A Streptococcus infections [Reference Currie and Carapetis4, Reference Engelman5]. In 2016, it was estimated that scabies caused 3.8 million disability-adjusted life-years (DALYs) globally [Reference Hay6].

To reduce the scabies burden, an ivermectin-based mass drug administration (MDA) strategy is recommended when the community-level scabies prevalence is above 10% [7]. Several clinical studies in island populations have shown a significant reduction in scabies prevalence one year after a single round of MDA [Reference Romani8Reference Romani10]; however, one study did not demonstrate a reduction, which was believed to be due to high human mobility [Reference Kearns11]. Longer-term follow-up has demonstrated some rebound in prevalence following cessation of MDA delivery [Reference Romani8, Reference Marks12, Reference Romani13]. To date, most MDA studies have taken place in isolated communities [Reference Romani8, Reference Romani10, Reference Kearns11, Reference Rinaldi and Porter14, Reference Lake15], making their direct application to larger areas and to highly interconnected urban settings uncertain.

Based on previous observations and practical considerations around programme delivery, the current recommendation is for three to five rounds of MDA applied at annual intervals [7]. Surveillance of the population should be continued for at least one year following the last MDA round to assess whether the prevalence has reached the target level of less than 2%. When the observed prevalence is below this ‘stopping threshold’, it is proposed that annual MDA rounds can be stopped [Reference Engelman2]. Following cessation of MDA, health systems need to be strengthened to ensure access to ongoing treatment of scabies for sustained control [7]. As there are no clear recommendations for communities with a prevalence between 2% and 10%, and existing recommendations are based on limited evidence and expert opinion, the World Health Organization (WHO) has highlighted the need for further modelling research to estimate the likely effectiveness of MDA strategies [7].

Previous modelling studies have estimated the likely impact of scabies interventions including MDAs [Reference Kinyanjui16Reference Lydeamore19], but have not explicitly investigated the current MDA recommendations. In this study, we use an agent-based model of scabies transmission, calibrated to demographic and epidemiologic data from Monrovia, to estimate the effectiveness of alternative recurring MDA strategies in an urban population with a starting prevalence of around 10%, and estimate their longer-term impact, independently and in combination with improved treatment access.

Methods

Demographic and epidemiologic model and data

A cross-sectional survey conducted in New Kru Town, Monrovia, Liberia (population size of over 20,000 [20]) in 2020 found a community-level scabies prevalence of 9.3% [Reference Collinson21]. Since the prevalence is in the range of 2–10%, it is not clear whether an MDA should be applied in Monrovia, and whether an MDA strategy would be effective to reduce the scabies burden. We extended an existing framework of disease transmission in an age- and household-structured population [Reference Geard22] (Supplementary material S1). We calibrated demographic parameters so that the model generated household size and age distributions corresponding to those observed in Monrovia, Liberia [Reference Collinson21] (Supplementary material S2.1).

Historical (and unrepeatable) studies indicate that prior infection can reduce the intensity of parasite burden in adult individuals [Reference Mellanby23]. However, there is insufficient evidence of such apparent immunity to assign an immune state or related parameters in the model. We, therefore, used a susceptible-infectious-susceptible (SIS) model to generate the dynamics of scabies infestation and transmission in this population. We assumed that clearance of a scabies infestation was primarily driven by treatment rather than natural recovery and that the duration of infestation therefore corresponds to the time until treatment [Reference Mellanby23]. As the average time until scabies treatment is not known for Liberia, we assumed a mean infestation duration of 90 days, based on health system visit data from Liberia [Reference Kruk24]. We used Bayesian inference [Reference Gutmann and Corander25] to calibrate transmission coefficients to match age- and household-size-specific patterns of scabies incidence observed in Monrovia [Reference Collinson21] (Supplementary material S2.2).

MDA scenarios

We defined MDA scenarios in terms of the number of rounds, time interval between rounds, population coverage (percentage of population receiving treatment), population selection (whether individuals or households are selected randomly), and treatment efficacy (the probability of recovery of an infested person following treatment) (Table 1). In the individual-based population selection method, the participation of individuals was independent across each round, for example an individual had the same probability of participating in rounds 1, 2, and 3. In the household-based selection, we assumed that the participation of a household was consistent across rounds and within each household every member either did or did not receive MDA. While we assumed that each MDA round consists of two doses of ivermectin given at 7–14 days intervals, and that every selected individual in each round received two doses, we also considered participating individuals who do not receive one or both doses (Supplementary material S6) [7]. We considered scenarios with large population coverages as 93% population coverage has been achieved in an MDA targeting malaria in Monrovia [Reference Kuehne26]. We simulated scenarios for all combinations of MDA parameters shown in Table 1. We conducted sensitivity analyses around the average infestation days (Supplementary material S5 and S7), treatment efficacy (Supplementary material S6.1), systematic non-treatment (where the duration of infestation for 10% of individuals was increased from 90 days to 5 years), and systematic non-compliance (where 20% of the individuals or households never receive treatment through MDA) (Supplementary material S6 and S7).

Table 1. MDA parameters and their values

a Results with 85% and 95% treatment efficacy are presented in Supplementary material S6.1.

We compared the effectiveness of the selected MDA strategies in the absence and presence of importation (Supplementary material S6.2). For each run, we recorded whether a prevalence of less than 2% was achieved one year after the last MDA round, whether scabies was eliminated (zero infestations), the number of undiscounted and discounted DALYs averted per 10,000 people over 20 years, and the time until prevalence recrudesced to its baseline (pre-MDA) level (Supplementary material S4). As the simulation model is stochastic, we ran each scenario 100 times and calculated means and 95% quantiles. We used these values to calculate the probability of decreasing prevalence to below the proposed stopping threshold of 2%, the probability of achieving elimination, estimation of discounted and undiscounted DALYs averted, and the distribution of the time gained until another MDA strategy would be necessary (when the prevalence reaches pre-MDA levels).

Systemic changes

The long duration of infestation is a likely contributor to high scabies prevalence. This duration corresponds to the time until treatment as there is no natural recovery from scabies [Reference Mellanby23]. Access to health services and healthcare-seeking behaviour (normalisation) are factors that affect the time until treatment [Reference Middleton and Bowen30, Reference Yeoh31]. MDAs may provide an opportunity to decrease the average duration of infestation in several ways. By reducing prevalence, MDA strategies may help break the normalisation of scabies and encourage people to seek treatment earlier [Reference Middleton and Bowen30, Reference Yeoh31]. Second, a healthcare system will be better able to provide treatment for every affected person when there are fewer such individuals in society [Reference Engelman2]. However, in order for MDAs to be followed by systemic changes, post-MDA drug treatment must be available in the primary healthcare system. We selected two MDA strategies (MDA strategies applied with random individual selection in three annual rounds and 60% and 80% population coverage) to understand the impact of systemic changes. For selected scenarios, we estimated the additional impact of longer-term changes to the health system by reducing the time it takes for someone to receive effective treatment for scabies by 10% and 20% after the last MDA round.

Results

The probability of decreasing scabies prevalence below the stopping threshold increases as the time interval between rounds is reduced

We observed that the probability of achieving a prevalence below 2% increases with a shorter time interval between MDA rounds (Figure 1).

Figure 1. The scabies prevalence in 20 years with MDA strategies consisting of three rounds, 80% population coverage, random individual selection, and (a) six-month (b) two-year time intervals. The green dashed lines show when MDA rounds are applied. The red dotted lines represent MDA stopping threshold (2%). It is assumed that there is no scabies importation.

For an annual MDA strategy with three rounds, at least 80% population coverage was necessary to reach the stopping threshold in at least 75% of the simulations (Figure 2). At 90% coverage, prevalence less than the stopping threshold was achieved in more than 90 out of 100 runs, irrespective of number of rounds, interval between rounds, and method of selection. In contrast, at the lowest level of coverage tested (60%), this same result could only be achieved when five rounds of MDA were conducted at an interval of six months between rounds. Household-based selection almost always produced a higher proportion of simulations with less than 2% prevalence than random selection.

Figure 2. The proportion of simulation runs with less than 2% prevalence is achieved in differing MDA strategies. The first column (a & c) shows the MDA strategies with household-based selection and the second column (b & d) shows the MDA strategies with random individual selection. The first row (a & b) shows the MDA strategies with three rounds and the second row (c & d) shows the MDA strategies with five rounds. Each panel is grouped by the population coverage in MDAs and MDA intervals. Each value is calculated one year after the last MDA round from 100 simulation runs. In these scenarios, it is assumed that there is no scabies importation.

Both the probability of scabies elimination and overall DALYs averted increase as the number of MDA rounds and population coverage are increased

We found that an MDA strategy consisting of five annual rounds with 90% population coverage resulted in elimination in only 18% of simulations (Table 2). We observed more DALYs averted with more MDA rounds and a higher population coverage (Table 2). The probability of scabies elimination one year after program cessation increased when we considered shorter time intervals between rounds, as previously described [Reference Lydeamore19]. We also found that the average number of DALYs averted was higher when the time interval between MDA rounds was reduced. In addition, we did not observe a notable impact of the method of population selection on DALYs averted in 20 years.

Table 2. Percentage of simulations with <=2% prevalence one year after the last MDA round, percentage of simulations with scabies elimination, DALYs averted per 10,000 people (mean, 2.5–97.5 quantiles), and time until prevalence reaches baseline are presented for MDA strategies with at least 80% population coverage

Note: Time until prevalence returns to baseline is calculated among the runs in which scabies is not eliminated. MDA strategies are ordered from best to worst in terms of discounted DALYs averted. Undiscounted DALYs averted results are presented in Supplementary material S6.

Systemic changes coupled with MDA strategies can help us sustainably maintain the scabies prevalence at a lower level

We observed that reducing the time to routine treatment of scabies by 20% after the final MDA round of an MDA strategy consisting of three annual rounds and 80% population coverage results in the elimination of scabies in 36% of simulations, compared to 0% of simulations in scenarios with no reduction in the time to treatment. This suggests that, following MDA, health system or behavioural changes which result in a reduction in the infestation duration can sustainably maintain scabies prevalence at a lower level (Figure 3a). These sustained reductions in prevalence post MDA occur because the shortened duration of infestation corresponds to reductions in the basic reproduction number, R0, from 1.24 (baseline) to 1.10 with a 10% reduction, and to 0.99 with a 20% reduction (Supplementary material S3).

Figure 3. Scabies prevalence over 20 years with (orange) and without (blue) an MDA strategy. Green dashed lines show when MDA rounds are applied (years 0, 1, and 2). Solid pink line (year 2) shows when the duration of infestation is reduced. Solid lines represent scenarios with an average of 90 days (baseline – 0% reduction) duration of infestation throughout the simulation, while dashed and dotted lines represent an average of 81 (10% reduction) and 72 (20% reduction) days duration of infestation after year 2, respectively. MDA strategies were applied with random individual selection in three annual rounds and 80% population coverage. There was no scabies importation.

In a hypothetical scenario, where health system or behavioural changes suddenly occur at year 2, a reduction in scabies prevalence is also sustainably maintained at a low level (Figure 3b). However, without an MDA strategy, it is unlikely that the ‘normalisation cycle’ of scabies that inhibits clinical presentations will be reversed. Also, given the high baseline prevalence of scabies, treatment seeking at this level would exceed the capacity of the healthcare system. For instance, in order to achieve a 20% reduction in the infestation duration without an MDA (difference between blue solid and dotted lines in Figure 3b), more than 1,000 additional people are needed to seek treatment between years 2 and 3 in New Kru Town, Monrovia, Liberia.

We evaluated the sensitivity of the impact of MDAs to systematic non-treatment, scabies importation, and systematic non-compliance. If the main driver of endemic prevalence is assumed to be systematic non-treatment, MDA strategies can be highly effective to reduce transmission (Supplementary material S7). However, if scabies importation is a dominant source of new infections, the efficacy of MDA strategies decreases as the seeding rate increases (Supplementary material S6.2). We also evaluated the sensitivity of the impact of MDAs to the assumption that every selected individual in each round received two doses of treatment within 7–14 days. When individuals do not receive one or two doses in each MDA round, the effectiveness of MDA decreases (Supplementary material S6). We also observed that systematic non-compliance, where individuals not receiving treatment in previous rounds do not receive treatment in the following rounds, has only a limited impact on MDA effectiveness when there is a high population coverage (Supplementary material S7).

Discussion

In this study, we evaluated the effectiveness of various MDA strategies for reducing the scabies prevalence using an agent-based model calibrated to survey data collected in Monrovia, Liberia [Reference Collinson21]. We observed that while MDAs can have short- and medium-term success [Reference Romani8, Reference Lawrence9, Reference Carapetis32, Reference Taplin33], it remains likely that prevalence will return to pre-MDA levels over longer time periods, especially in the absence of health system or systemic behavioural changes [Reference Lydeamore19]. However, sustainable improvements to scabies control can be achieved when MDAs are coupled with systemic changes that reduce the time it takes for scabies infestations to be successfully treated (Figure 3). When post-MDA treatment is available in the healthcare system, MDAs may naturally provide an environment for systemic changes by breaking the normalisation cycle and increasing the per capita rate of healthcare access of individuals with scabies [Reference Middleton and Bowen30, Reference Yeoh31], which highlights the importance of post-MDA treatment accessibility. Moreover, MDAs are likely to have a higher chance of sustainably maintaining scabies prevalence at a low level when supported by other interventions such as improved education and health system accessibility [Reference Engelman and Steer1, Reference Engelman2, Reference Marks34, Reference Hay35].

The current recommendation is for 3–5 rounds of MDA, stopping when prevalence is reduced below 2% [Reference Engelman2, 7]. We observed that prevalence can be reliably reduced below 2% provided that the population coverage is sufficient (Figure 2). We also observed that it is unlikely that MDAs will be sufficient to eliminate scabies without broader health system changes that reduce delays in treatment of scabies beyond the MDA setting (Figure 3).

Several existing studies use modelling to compare the effectiveness of scabies interventions including MDAs [Reference Kinyanjui16Reference Lydeamore19]. However, to our knowledge, this is the first modelling analysis to estimate the efficacy of recommended MDA strategies, as well as the first to quantify the role of community transmission in a sub-Saharan African setting. For instance, our model showed that among MDA strategies with >80% coverage, the discounted DALYs averted per 10,000 people increased from 104 to 271 years when the population coverage and number of rounds increased. Our study provides a flexible modelling framework for scabies that can be calibrated to other settings to compare community-level interventions using DALYs and incidence statistics.

As with any modelling study, our results depend on assumptions made and are subject to some limitations. First, limited data were available to calibrate some model parameters, including duration of infestation, which may be longer in the presence of systematic non-treatment, and importation rate. Our sensitivity analyses established that estimates of MDA efficacy were sensitive to these parameters. Collection of additional data on time to treatment of scabies and population mobility may reduce the uncertainty around model estimates. Second, in this study, we report the ‘true’ prevalence of scabies in the modelled population. In reality, estimates of prevalence will depend on the sampling strategy used to detect infestations [Reference Tellioglu36]. Monitoring the impact of MDAs and responding appropriately will thus require effective surveillance in addition to effective interventions. We also found that when population coverage is high, systematic non-compliance has a limited impact on MDA efficacy. Finally, we estimated DALYs averted under various MDA scenarios and found that high population coverage in MDA rounds increased the number of DALYs averted. We did not consider the differing costs associated with each scenario; however, strategies that were likely to avert most DALYs were also likely to be the most resource intensive. The results presented here could form the basis of future cost-effectiveness analyses to provide a more robust basis for comparison [Reference Romani8, Reference Mow37].

In summary, our modelling study suggests that MDAs can play a critical role in scabies control by reducing the prevalence and maintaining it at a low level when combined with systemic changes. This study demonstrates how modelling can be used to refine and define effective interventions in reducing scabies burden in large populations with endemic prevalence.

Supplementary material

The supplementary material for this article can be found at https://doi.org/10.1017/S0950268823001310.

Data availability statement

Code and data are available at https://github.com/nefeltellioglu/simodd-scabies.

Author contribution

Conceptualization: N.G., J.M., M.M., N.T.; Supervision: N.G., P.T.C., J.M., M.M., R.H.C.; Writing – review & editing: N.G., P.T.C., J.M., A.D., J.T., M.M., R.H.C.; Methodology: A.D., R.H.C., N.T.; Data curation: J.T., K.K., S.Z., S.C.; Formal analysis: R.H.C., N.T.; Validation: N.T.; Visualization: N.T.; Writing – original draft: N.T.

Financial support

The authors received no specific funding for this work.

Competing interest

The authors declare none.

References

Engelman, D and Steer, AC (2018) Control strategies for scabies. Tropical Medicine and Infectious Disease 3, 98.10.3390/tropicalmed3030098CrossRefGoogle ScholarPubMed
Engelman, D, et al. (2021) A framework for scabies control. PLoS Neglected Tropical Diseases 15, e0009661.10.1371/journal.pntd.0009661CrossRefGoogle ScholarPubMed
McCarthy, JS, et al. (2004) Scabies: More than just an irritation. Postgraduate Medical Journal 80, 382387.10.1136/pgmj.2003.014563CrossRefGoogle Scholar
Currie, BJ and Carapetis, JR (2000) Skin infections and infestations in aboriginal communities in northern Australia. Australasian Journal of Dermatology 41, 139143.CrossRefGoogle ScholarPubMed
Engelman, D, et al. (2019) The public health control of scabies: Priorities for research and action. Lancet 394, 8192.10.1016/S0140-6736(19)31136-5CrossRefGoogle ScholarPubMed
Hay, SI, et al. (2017) Global, regional, and national disability-adjusted life-years (DALYs) for 333 diseases and injuries and healthy life expectancy (HALE) for 195 countries and territories, 1990–2016: A systematic analysis for the global burden of disease study 2016. Lancet 390, 12601344.10.1016/S0140-6736(17)32130-XCrossRefGoogle Scholar
World Health Organization (2020) WHO informal consultation on a framework for scabies control meeting report. Manila, Philippines, February 2020.Google Scholar
Romani, L, et al. (2019) Efficacy of mass drug administration with ivermectin for control of scabies and impetigo, with coadministration of azithromycin: A single-arm community intervention trial. Lancet Infectious Diseases 19, 510518.CrossRefGoogle ScholarPubMed
Lawrence, G, et al. (2005) Control of scabies, skin sores and haematuria in children in the Solomon Islands: Another role for ivermectin. Bulletin of the World Health Organization 83, 3442.Google ScholarPubMed
Romani, L, et al. (2015) Mass drug administration for scabies control in a population with endemic disease. New England Journal of Medicine 373, 23052313.10.1056/NEJMoa1500987CrossRefGoogle Scholar
Kearns, TM, et al. (2015) Impact of an ivermectin mass drug administration on scabies prevalence in a remote Australian aboriginal community. PLoS Neglected Tropical Diseases 9, e0004151.10.1371/journal.pntd.0004151CrossRefGoogle Scholar
Marks, M, et al. (2020) Prevalence of scabies and impetigo 3 years after mass drug administration with ivermectin and azithromycin. Clinical Infectious Diseases 70, 15911595.10.1093/cid/ciz444CrossRefGoogle ScholarPubMed
Romani, L, et al. (2019) Mass drug administration for scabies - 2 years of follow-up. New England Journal of Medicine 381, 186187.CrossRefGoogle ScholarPubMed
Rinaldi, G and Porter, K (2021) Mass drug administration for endemic scabies: A systematic review. Tropical Diseases, Travel Medicine and Vaccines 7, 21.CrossRefGoogle ScholarPubMed
Lake, SJ, et al. (2022) Mass drug administration for the control of scabies: A systematic review and meta-analysis. Clinical Infectious Diseases 75, 959967.CrossRefGoogle ScholarPubMed
Kinyanjui, T, et al. (2018) Scabies in residential care homes: Modelling, inference and interventions for well-connected population sub-units. PLoS Computational Biology 14, e1006046.CrossRefGoogle ScholarPubMed
Bhunu, CP, Mushayabasa, S and Monera, TG (2013) Assessing the impact of vaccination on controlling the spread of human scabies. ISRN Computational Biology 2013, 362973.CrossRefGoogle Scholar
Gilmore, SJ (2011) Control strategies for endemic childhood scabies. PLoS One 6, e15990.CrossRefGoogle ScholarPubMed
Lydeamore, MJ, et al. (2019) A biological model of scabies infection dynamics and treatment informs mass drug administration strategies to increase the likelihood of elimination. Mathematical Biosciences 309, 163173.CrossRefGoogle ScholarPubMed
UNDP (2018) President Weah Launches Coastal Project in New Kru Town. Available at https://www.lr.undp.org/content/liberia/en/home/presscenter/articles/2018/president-weah-launches-coastal-project-in-new-kru-town.html (accessed 19 May 2023).Google Scholar
Collinson, S, et al. (2020) The prevalence of scabies in Monrovia, Liberia: A population-based survey. PLoS Neglected Tropical Diseases 14, e0008943.CrossRefGoogle ScholarPubMed
Geard, N, et al. (2015) The effects of demographic change on disease transmission and vaccine impact in a household structured population. Epidemics 13, 5664.CrossRefGoogle Scholar
Mellanby, K (1944) The development of symptoms, parasitic infection and immunity in human scabies. Parasitology 35, 197206.CrossRefGoogle Scholar
Kruk, ME, et al. (2011) Population preferences for health care in Liberia: Insights for rebuilding a health system. Health Services Research 46, 20572078.CrossRefGoogle ScholarPubMed
Gutmann, MU and Corander, J (2016) Bayesian optimization for likelihood-free inference of simulator-based statistical models. Journal of Machine Learning Research 17, 147.Google Scholar
Kuehne, A, et al. (2016) Impact and lessons learned from mass drug administrations of malaria chemoprevention during the Ebola outbreak in Monrovia, Liberia, 2014. PLoS One 11, e0161311.CrossRefGoogle ScholarPubMed
Romani, L, et al. (2015) Prevalence of scabies and impetigo worldwide: A systematic review. Lancet Infectious Diseases 15, 960967.CrossRefGoogle ScholarPubMed
Matthewman, J, et al. (2020) A randomized controlled trial comparing the effectiveness of individual versus household treatment for scabies in Lambaréné, Gabon. PLoS Neglected Tropical Diseases 14, e0008423.CrossRefGoogle ScholarPubMed
Marks, M, et al. (2018) Exploration of a simplified clinical examination for scabies to support public health decision-making. PLoS Neglected Tropical Diseases 12, e0006996.CrossRefGoogle ScholarPubMed
Middleton, K and Bowen, AC (2021) Addressing normalization using culturally relevant approaches: An important adjunct to reducing the burden of impetigo and scabies. Lancet Regional Health - Western Pacific 7, 100102.CrossRefGoogle ScholarPubMed
Yeoh, DK, et al. (2017) Are scabies and impetigo “normalised”? A cross-sectional comparative study of hospitalised children in Northern Australia assessing clinical recognition and treatment of skin infections. PLoS Neglected Tropical Diseases 11, e0005726.CrossRefGoogle ScholarPubMed
Carapetis, JR, et al. (1997) Success of a scabies control program in an Australian aboriginal community. Pediatric Infectious Disease Journal 16, 494499.CrossRefGoogle Scholar
Taplin, D, et al. (1991) Community control of scabies: A model based on use of permethrin cream. Lancet 337, 10161018.CrossRefGoogle Scholar
Marks, M, et al. (2015) Long term control of scabies fifteen years after an intensive treatment programme. PLoS Neglected Tropical Diseases 9, e0004246.CrossRefGoogle ScholarPubMed
Hay, RJ, et al. (2012) Scabies in the developing world–Its prevalence, complications, and management. Clinical Microbiology and Infection 18, 313323.CrossRefGoogle ScholarPubMed
Tellioglu, N, et al. (2022) The efficacy of sampling strategies for estimating scabies prevalence. PLoS Neglected Tropical Diseases 16, e0010456.CrossRefGoogle ScholarPubMed
Mow, M, et al. (2022) Costs of mass drug administration for scabies in Fiji. PLoS Neglected Tropical Diseases 16, e0010147.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. MDA parameters and their values

Figure 1

Figure 1. The scabies prevalence in 20 years with MDA strategies consisting of three rounds, 80% population coverage, random individual selection, and (a) six-month (b) two-year time intervals. The green dashed lines show when MDA rounds are applied. The red dotted lines represent MDA stopping threshold (2%). It is assumed that there is no scabies importation.

Figure 2

Figure 2. The proportion of simulation runs with less than 2% prevalence is achieved in differing MDA strategies. The first column (a & c) shows the MDA strategies with household-based selection and the second column (b & d) shows the MDA strategies with random individual selection. The first row (a & b) shows the MDA strategies with three rounds and the second row (c & d) shows the MDA strategies with five rounds. Each panel is grouped by the population coverage in MDAs and MDA intervals. Each value is calculated one year after the last MDA round from 100 simulation runs. In these scenarios, it is assumed that there is no scabies importation.

Figure 3

Table 2. Percentage of simulations with <=2% prevalence one year after the last MDA round, percentage of simulations with scabies elimination, DALYs averted per 10,000 people (mean, 2.5–97.5 quantiles), and time until prevalence reaches baseline are presented for MDA strategies with at least 80% population coverage

Figure 4

Figure 3. Scabies prevalence over 20 years with (orange) and without (blue) an MDA strategy. Green dashed lines show when MDA rounds are applied (years 0, 1, and 2). Solid pink line (year 2) shows when the duration of infestation is reduced. Solid lines represent scenarios with an average of 90 days (baseline – 0% reduction) duration of infestation throughout the simulation, while dashed and dotted lines represent an average of 81 (10% reduction) and 72 (20% reduction) days duration of infestation after year 2, respectively. MDA strategies were applied with random individual selection in three annual rounds and 80% population coverage. There was no scabies importation.

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