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Stated preferences for anti-malarial drug characteristics in Zomba, a malaria endemic area of Malawi
BACKGROUND: The evidence on determinants of individuals’ choices for anti-malarial drug treatments is scarce. This study sought to measure the strength of preference for adult antimalarial drug treatment attributes of heads of urban, rural and peri-urban households in a resource-limited malaria-ende...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108233/ https://www.ncbi.nlm.nih.gov/pubmed/25005466 http://dx.doi.org/10.1186/1475-2875-13-259 |
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author | Medina-Lara, Antonieta Mujica-Mota, Ruben E Kunkwenzu, Esthery D Lalloo, David G |
author_facet | Medina-Lara, Antonieta Mujica-Mota, Ruben E Kunkwenzu, Esthery D Lalloo, David G |
author_sort | Medina-Lara, Antonieta |
collection | PubMed |
description | BACKGROUND: The evidence on determinants of individuals’ choices for anti-malarial drug treatments is scarce. This study sought to measure the strength of preference for adult antimalarial drug treatment attributes of heads of urban, rural and peri-urban households in a resource-limited malaria-endemic area of sub-Saharan Africa. METHODS: Discrete choice experiments were conducted with 508 heads of household interviewed face-to-face for a household population survey of health-seeking behavior in Zomba District, Malawi. The interviews were held in Chichewa and the choice experiment questions were presented with cartoon aids. The anti-malarial drug attributes included in the stated preference experiment were: speed of fever resolution, side effects (pruritus) risk, protection (duration of prophylactic effect), price, duration of treatment course and recommendation by a health professional. Sixteen treatment profiles from a fractional factorial design by orthogonal array were paired into choice scenarios, and scenarios were randomly assigned to participants so that each participant was presented with a series of eight pairwise choice scenarios. Respondents had the option to state indifference between the two profiles or decline to choose. Data were analysed in a mixed logit model, with normally distributed coefficients for all six attributes. RESULTS: The sex ratio was balanced in urban areas, whereas 63% of participants in rural areas were male. The proportion of individuals with no education was considerably higher in the rural group (25%) than in the urban (5%) and peri-urban (6%) groups. All attributes investigated had the expected influence, and traded-off in most respondents’ choices. There were heterogeneous effects of price, pruritus risk, treatment recommendation by a professional, and duration of prophylaxis across respondents, only partly explained by their differences in education, household per capita expenditure, sex and age. Individuals´ demand elasticity (simulated median, inter-quartile range) was highest (most responsive) to speed of symptom resolution (0.88, 0.80-0.89) and pruritus risk (0.25, 0.08-0.62). CONCLUSIONS: Most adult antimalarial users are willing to use treatments without recommendation from health professional, and may be influenced by price. Future studies should investigate the magnitude of differences in price and treatment attribute sensitivity between adult anti-malarial drug users in rural, peri-urban and urban areas in order to determine optimal price subsidies. |
format | Online Article Text |
id | pubmed-4108233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41082332014-08-04 Stated preferences for anti-malarial drug characteristics in Zomba, a malaria endemic area of Malawi Medina-Lara, Antonieta Mujica-Mota, Ruben E Kunkwenzu, Esthery D Lalloo, David G Malar J Research BACKGROUND: The evidence on determinants of individuals’ choices for anti-malarial drug treatments is scarce. This study sought to measure the strength of preference for adult antimalarial drug treatment attributes of heads of urban, rural and peri-urban households in a resource-limited malaria-endemic area of sub-Saharan Africa. METHODS: Discrete choice experiments were conducted with 508 heads of household interviewed face-to-face for a household population survey of health-seeking behavior in Zomba District, Malawi. The interviews were held in Chichewa and the choice experiment questions were presented with cartoon aids. The anti-malarial drug attributes included in the stated preference experiment were: speed of fever resolution, side effects (pruritus) risk, protection (duration of prophylactic effect), price, duration of treatment course and recommendation by a health professional. Sixteen treatment profiles from a fractional factorial design by orthogonal array were paired into choice scenarios, and scenarios were randomly assigned to participants so that each participant was presented with a series of eight pairwise choice scenarios. Respondents had the option to state indifference between the two profiles or decline to choose. Data were analysed in a mixed logit model, with normally distributed coefficients for all six attributes. RESULTS: The sex ratio was balanced in urban areas, whereas 63% of participants in rural areas were male. The proportion of individuals with no education was considerably higher in the rural group (25%) than in the urban (5%) and peri-urban (6%) groups. All attributes investigated had the expected influence, and traded-off in most respondents’ choices. There were heterogeneous effects of price, pruritus risk, treatment recommendation by a professional, and duration of prophylaxis across respondents, only partly explained by their differences in education, household per capita expenditure, sex and age. Individuals´ demand elasticity (simulated median, inter-quartile range) was highest (most responsive) to speed of symptom resolution (0.88, 0.80-0.89) and pruritus risk (0.25, 0.08-0.62). CONCLUSIONS: Most adult antimalarial users are willing to use treatments without recommendation from health professional, and may be influenced by price. Future studies should investigate the magnitude of differences in price and treatment attribute sensitivity between adult anti-malarial drug users in rural, peri-urban and urban areas in order to determine optimal price subsidies. BioMed Central 2014-07-08 /pmc/articles/PMC4108233/ /pubmed/25005466 http://dx.doi.org/10.1186/1475-2875-13-259 Text en Copyright © 2014 Medina-Lara et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Medina-Lara, Antonieta Mujica-Mota, Ruben E Kunkwenzu, Esthery D Lalloo, David G Stated preferences for anti-malarial drug characteristics in Zomba, a malaria endemic area of Malawi |
title | Stated preferences for anti-malarial drug characteristics in Zomba, a malaria endemic area of Malawi |
title_full | Stated preferences for anti-malarial drug characteristics in Zomba, a malaria endemic area of Malawi |
title_fullStr | Stated preferences for anti-malarial drug characteristics in Zomba, a malaria endemic area of Malawi |
title_full_unstemmed | Stated preferences for anti-malarial drug characteristics in Zomba, a malaria endemic area of Malawi |
title_short | Stated preferences for anti-malarial drug characteristics in Zomba, a malaria endemic area of Malawi |
title_sort | stated preferences for anti-malarial drug characteristics in zomba, a malaria endemic area of malawi |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108233/ https://www.ncbi.nlm.nih.gov/pubmed/25005466 http://dx.doi.org/10.1186/1475-2875-13-259 |
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