Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/10486
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dc.contributor.authorMcCarthy, AE-
dc.contributor.authorCoyle, D-
dc.date.accessioned2015-03-24T10:12:30Z-
dc.date.available2010-
dc.date.available2015-03-24T10:12:30Z-
dc.date.issued2010-
dc.identifier.citationMalaria Journal, 9: 92, (2010)en_US
dc.identifier.issn1475-2875-
dc.identifier.urihttp://www.malariajournal.com/content/9/1/92-
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/10486-
dc.description© 2010 McCarthy and Coyle; licensee BioMed Central Ltd. 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 cited.en_US
dc.description.abstractBackground. Chemoprophylaxis for travellers' malaria is problematic. Decision modeling may help determine optimal prevention strategies for travellers' malaria. Such models can fully assess effect of drug use and disease on quality of life, and help travellers make informed values based decisions. Such models require utility values reflecting societal preferences over different health states of relevance. To date, there are no published utility values relating to clinical malaria or chemoprophylaxis adverse events. Methods. Utility estimates for health states related to falciparum malaria, sequelae and drug-related adverse events were obtained using a self-administered visual analogue scale in 20 individuals. Utility values for health states related to clinical malaria were obtained from a survey of 11 malaria experts questioned about length of hospital stay or equivalent disability with simple and severe travellers' malaria. Results. The general public (potential travellers), were more tolerant of taking prophylaxis if associated with no or mild AEs and least tolerant of mild sequelae from malaria and severe drug related events. The rating value reported for taking no prophylaxis was quite variable. Tropical medicine specialists estimated a mean hospital stay 3.23 days (range 0.5-4.5 days) for simple and 6.36 days (range 4.5 - 7 days) for severe malaria. Conclusions. This study provides a benchmark for important utility value estimates for modeling malaria and drug-related outcomes in non-immune travellers.en_US
dc.languageeng-
dc.language.isoenen_US
dc.publisherBioMed Centralen_US
dc.subjectMalariaen_US
dc.subjectChemoprophylaxisen_US
dc.subjectUtility value estimatesen_US
dc.subjectNon-immune travellersen_US
dc.titleDetermining utility values related to malaria and malaria chemoprophylaxisen_US
dc.typeArticleen_US
dc.identifier.doihttp://dx.doi.org/10.1186/1475-2875-9-92-
dc.relation.isPartOfMalaria Journal-
dc.relation.isPartOfMalaria Journal-
dc.relation.isPartOfMalaria Journal-
pubs.issue1-
pubs.issue1-
pubs.issue1-
pubs.volume9-
pubs.volume9-
pubs.volume9-
pubs.organisational-data/Brunel-
pubs.organisational-data/Brunel/Brunel Staff by College/Department/Division-
pubs.organisational-data/Brunel/Brunel Staff by College/Department/Division/College of Health and Life Sciences-
pubs.organisational-data/Brunel/Brunel Staff by College/Department/Division/College of Health and Life Sciences/Dept of Life Sciences-
pubs.organisational-data/Brunel/Brunel Staff by College/Department/Division/College of Health and Life Sciences/Dept of Life Sciences/Biological Sciences-
pubs.organisational-data/Brunel/Brunel Staff by Institute/Theme-
pubs.organisational-data/Brunel/Brunel Staff by Institute/Theme/Institute of Environmental, Health and Societies-
pubs.organisational-data/Brunel/Brunel Staff by Institute/Theme/Institute of Environmental, Health and Societies/Health Economics-
pubs.organisational-data/Brunel/Specialist Centres-
pubs.organisational-data/Brunel/Specialist Centres/HERG-
Appears in Collections:Health Economics Research Group (HERG)

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