It depends on how you tell: a qualitative diagnostic analysis of the implementation climate for community-wide mass drug administration for soil-transmitted helminth

Euripide Avokpaho, Sarah Lawrence, Amy Roll, Angelin Titus, Yesudoss Jacob, Saravanakumar Puthupalayam Kaliappan, Marie Claire Gwayi-Chore, Félicien Chabi, Comlanvi Innocent Togbevi, Abiguel Belou Elijan, Providence Nindi, Judd L Walson, Sitara Swarna Rao Ajjampur, Moudachirou Ibikounle, Khumbo Kalua, Kumudha Aruldas, Arianna Rubin Means, Euripide Avokpaho, Sarah Lawrence, Amy Roll, Angelin Titus, Yesudoss Jacob, Saravanakumar Puthupalayam Kaliappan, Marie Claire Gwayi-Chore, Félicien Chabi, Comlanvi Innocent Togbevi, Abiguel Belou Elijan, Providence Nindi, Judd L Walson, Sitara Swarna Rao Ajjampur, Moudachirou Ibikounle, Khumbo Kalua, Kumudha Aruldas, Arianna Rubin Means

Abstract

Objectives: Current soil-transmitted helminth (STH) morbidity control guidelines primarily target deworming of preschool and school-age children. Emerging evidence suggests that community-wide mass drug administration (cMDA) may interrupt STH transmission. However, the success of such programmes depends on achieving high treatment coverage and uptake. This formative analysis was conducted to evaluate the implementation climate for cMDA and to determine barriers and facilitators to launch.

Settings: Prior to the launch of a cMDA trial in Benin, India and Malawi.

Participants: Community members (adult women and men, children, and local leaders), community drug distributors (CDDs) and health facility workers.

Design: We conducted 48 focus group discussions (FGDs) with community members, 13 FGDs with CDDs and 5 FGDs with health facility workers in twelve randomly selected clusters across the three study countries. We used the Consolidated Framework for Implementation Research to guide the design of the interview guide and thematic analysis.

Results: Across all three sites, aspects of the implementation climate that were facilitators to cMDA launch included: high community member demand for cMDA, integration of cMDA into existing vaccination campaigns and/or health services, and engagement with familiar health workers. Barriers to launching cMDA included mistrust towards medical interventions, fear of side effects and limited perceived need for interrupting STH transmission. We include specific recommendations from community members regarding cMDA distribution sites, personnel requirements, delivery timing and incentives, leaders to engage and methods for mobilising participants.

Conclusions: Prior to launching the cMDA programme as an alternative to school-based MDA, cMDA was found to be generally acceptable across diverse geographical and demographic settings. Community members, CDDs and health workers felt that engaging communities and tailoring programmes to the local context are critical for success. Potential barriers may be mitigated by identifying local concerns and addressing them via targeted community sensitisation prior to implementation.

Trial registration number: NCT03014167; Pre-results.

Keywords: community child health; public health; qualitative research; tropical medicine.

Conflict of interest statement

Competing interests: None declared.

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.

References

    1. Hotez PJ, Molyneux DH, Fenwick A, et al. . Control of neglected tropical diseases. N Engl J Med 2007;357:1018–27. 10.1056/NEJMra064142
    1. Jamison D, Breman J, Measham A. Disease Control Priorities in Developing Countries. In: Helminth infections: Soil-transmitted helminth infections and schistosomiasis, 2006.
    1. WHO. Guideline: preventive chemotherapy to control soil-transmitted helminth infections in at-risk population groups, 2017.
    1. Brooker SJ, Nikolay B, Balabanova D, et al. . Global feasibility assessment of interrupting the transmission of soil-transmitted helminths: a statistical modelling study. Lancet Infect Dis 2015;15:941–50. 10.1016/S1473-3099(15)70042-3
    1. Pullan RL, Halliday KE, Oswald WE, et al. . Effects, equity, and cost of school-based and community-wide treatment strategies for soil-transmitted helminths in Kenya: a cluster-randomised controlled trial. Lancet 2019;393:2039–50. 10.1016/S0140-6736(18)32591-1
    1. Lo NC, Bogoch II, Blackburn BG, et al. . Comparison of community-wide, integrated mass drug administration strategies for schistosomiasis and soil-transmitted helminthiasis: a cost-effectiveness modelling study. Lancet Glob Health 2015;3:e629-e38. 10.1016/S2214-109X(15)00047-9
    1. Farrell SH, Truscott JE, Anderson RM. The importance of patient compliance in repeated rounds of mass drug administration (MDA) for the elimination of intestinal helminth transmission. Parasit Vectors 2017;10:291. 10.1186/s13071-017-2206-5
    1. Shuford KV, Turner HC, Anderson RM. Compliance with anthelmintic treatment in the neglected tropical diseases control programmes: a systematic review. Parasit Vectors 2016;9:29. 10.1186/s13071-016-1311-1
    1. Yajima A, Mikhailov A, Mbabazi PS, et al. . Preventive chemotherapy and transmission control (PCT) databank: a tool for planning, implementation and monitoring of integrated preventive chemotherapy for control of neglected tropical diseases. Trans R Soc Trop Med Hyg 2012;106:215–22. 10.1016/j.trstmh.2012.01.003
    1. 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:e2447. 10.1371/journal.pntd.0002447
    1. Gyapong JO, Owusu IO, da-Costa Vroom FB, et al. . Elimination of lymphatic filariasis: current perspectives on mass drug administration. Res Rep Trop Med 2018;9:25–33. 10.2147/RRTM.S125204
    1. Silumbwe A, Halwindi H, Zulu JM. How community engagement strategies shape participation in mass drug administration programmes for lymphatic filariasis: the case of Luangwa district, Zambia. PLoS Negl Trop Dis 2019;13:e0007861. 10.1371/journal.pntd.0007861
    1. Stetler CB, Legro MW, Wallace CM, et al. . The role of formative evaluation in implementation research and the QUERI experience. J Gen Intern Med 2006;21 Suppl 2:S1–8. 10.1007/s11606-006-0267-9
    1. Lugtenberg M, Burgers JS, Westert GP. Effects of evidence-based clinical practice guidelines on quality of care: a systematic review. Qual Saf Health Care 2009;18:385–92. 10.1136/qshc.2008.028043
    1. Ásbjörnsdóttir KH, Ajjampur SSR, Anderson RM, et al. . Assessing the feasibility of interrupting the transmission of soil-transmitted helminths through mass drug administration: the DeWorm3 cluster randomized trial protocol. PLoS Negl Trop Dis 2018;12:e0006166. 10.1371/journal.pntd.0006166
    1. Curran GM, Bauer M, Mittman B, et al. . Effectiveness-implementation hybrid designs: combining elements of clinical effectiveness and implementation research to enhance public health impact. Med Care 2012;50:217. 10.1097/MLR.0b013e3182408812
    1. Means AR, Ajjampur SSR, Bailey R, et al. . Evaluating the sustainability, scalability, and replicability of an STH transmission interruption intervention: the DeWorm3 implementation science protocol. PLoS Negl Trop Dis 2018;12:e0005988. 10.1371/journal.pntd.0005988
    1. Damschroder LJ, Aron DC, Keith RE, et al. . Fostering implementation of health services research findings into practice: a consolidated framework for advancing implementation science. Implement Sci 2009;4:50. 10.1186/1748-5908-4-50
    1. Means AR, Kemp CG, Gwayi-Chore M-C, et al. . Evaluating and optimizing the consolidated framework for implementation research (CFIR) for use in low- and middle-income countries: a systematic review. Implementation Science 2020;15:1–9. 10.1186/s13012-020-0977-0
    1. Kirk MA, Kelley C, Yankey N, et al. . A systematic review of the use of the consolidated framework for implementation research. Implementation Science 2015;11:72. 10.1186/s13012-016-0437-z
    1. Cassell C, Symon G. Essential guide to qualitative methods in organizational research. Sage, 2004.
    1. Nowell LS, Norris JM, White DE. Thematic analysis: Striving to meet the trustworthiness criteria. Int.J.Qual. Methods 2017;16. 10.1177/1609406917733847
    1. Babu BV, Satyanarayana K. Factors responsible for coverage and compliance in mass drug administration during the programme to eliminate lymphatic filariasis in the East Godavari district, South India. Trop Doct 2003;33:79–82. 10.1177/004947550303300208
    1. Gunawardena S, Ismail M, Bradley M, et al. . Factors influencing drug compliance in the mass drug administration programme against filariasis in the Western Province of Sri Lanka. Trans R Soc Trop Med Hyg 2007;101:445–53. 10.1016/j.trstmh.2006.09.002
    1. Ahorlu CSK, Koka E, Adu-Amankwah S, et al. . Community perspectives on persistent transmission of lymphatic filariasis in three hotspot districts in Ghana after 15 rounds of mass drug administration: a qualitative assessment. BMC Public Health 2018;18:238. 10.1186/s12889-018-5157-7
    1. Legge H, Kepha S, Prochazka M, et al. . Implementer and recipient perspectives of community-wide mass drug administration for soil-transmitted helminths in Kwale County, Kenya. PLoS Negl Trop Dis 2020;14:e0008258. 10.1371/journal.pntd.0008258
    1. Babu BV, Mishra S. Mass drug administration under the programme to eliminate lymphatic filariasis in Orissa, India: a mixed-methods study to identify factors associated with compliance and non-compliance. Trans R Soc Trop Med Hyg 2008;102:1207–13. 10.1016/j.trstmh.2008.05.023
    1. Dial NJ, Ceesay SJ, Gosling RD, et al. . A qualitative study to assess community barriers to malaria mass drug administration trials in the Gambia. Malar J 2014;13:47. 10.1186/1475-2875-13-47
    1. Wanzira H, Naiga S, Mulebeke R, et al. . Community facilitators and barriers to a successful implementation of mass drug administration and indoor residual spraying for malaria prevention in Uganda: a qualitative study. Malar J 2018;17:474. 10.1186/s12936-018-2624-7
    1. Lahariya C, Mishra A. Strengthening of mass drug administration implementation is required to eliminate lymphatic filariasis from India: an evaluation study. J Vector Borne Dis 2008;45:313–20.
    1. Kisoka WJ, Simonsen PE, Malecela MN, et al. . Factors influencing drug uptake during mass drug administration for control of lymphatic filariasis in rural and urban Tanzania. PLoS One 2014;9:e109316. 10.1371/journal.pone.0109316
    1. Vaz Nery S, Pickering AJ, Abate E, et al. . The role of water, sanitation and hygiene interventions in reducing soil-transmitted helminths: interpreting the evidence and identifying next steps. Parasit Vectors 2019;12:273. 10.1186/s13071-019-3532-6
    1. Kisoka WJ, Tersbøl BP, Meyrowitsch DW, et al. . Community members' perceptions of mass drug administration for control of lymphatic filariasis in rural and urban Tanzania. J Biosoc Sci 2016;48:94–112. 10.1017/S0021932015000024
    1. Sousa-Figueiredo JC, Pleasant J, Day M, et al. . Treatment of intestinal schistosomiasis in Ugandan preschool children: best diagnosis, treatment efficacy and side-effects, and an extended praziquantel dosing pole. Int Health 2010;2:103–13. 10.1016/j.inhe.2010.02.003
    1. Musuva RM, Matey E, Masaku J, et al. . Lessons from implementing mass drug administration for soil transmitted helminths among pre-school aged children during school based deworming program at the Kenyan coast. BMC Public Health 2017;17:575. 10.1186/s12889-017-4481-7
    1. Omedo MO, Matey EJ, Awiti A, et al. . Community health workers' experiences and perspectives on mass drug administration for schistosomiasis control in Western Kenya: the score project. Am J Trop Med Hyg 2012;87:1065–72. 10.4269/ajtmh.2012.12-0435
    1. Cantey PT, Rout J, Rao G, et al. . Increasing compliance with mass drug administration programs for lymphatic filariasis in India through education and lymphedema management programs. PLoS Negl Trop Dis 2010;4:e728. 10.1371/journal.pntd.0000728
    1. Garfield RM, Vermund SH. Health education and community participation in mass drug administration for malaria in Nicaragua. Soc Sci Med 1986;22:869–77. 10.1016/0277-9536(86)90241-8
    1. De Martin S, von Seidlein L, Deen JL, et al. . Community perceptions of a mass administration of an antimalarial drug combination in the Gambia. Trop Med Int Health 2001;6:442–8. 10.1046/j.1365-3156.2001.00723.x
    1. Mulugeta A, Gebregergs GB, Asfaw S, et al. . Coverage, social mobilization and challenges of mass Zithromax administration campaign in South and South East zones of Tigray, Northern Ethiopia: a cross sectional study. PLoS Negl Trop Dis 2018;12:e0006288. 10.1371/journal.pntd.0006288

Source: PubMed

Подписаться