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Published:
Apr 23, 2011Keywords:
malaria morbidity mortality diagnosis treatment Tanzania
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Mwanziva, C., Manjurano, A., Mbugi, E., Mweya, C., Mkali, H., Kivuyo, M. P., Sanga, A., Ndaro, A., Chambo, W., Mkwizu, A., Kitau, J., Kavishe, R., Dolmans, W., Chilongola, J., & Mosha, F. W. (2011). Defining malaria burden from morbidity and mortality records, self treatment practices and serological data in Magugu, Babati District, northern Tanzania. Tanzania Journal of Health Research, 13(2), 93–96. https://doi.org/10.4314/thrb.v13i2.62980
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Author Biographies
Charles Mwanziva, Kilimanjaro Clinical Research Institute
Research Scientist, PhD candidateAlphaxard Manjurano, Joint Malaria Programme (JMP)
Molecular biologist, PhDErasto Mbugi, Muhimbili University of Health and Allied Sciences (MUHAS), Dar es Salaam,Tanzania
molecular biologist, PhDClement Mweya, National Institute for Medical Research (NIMR), Tukuyu Centre, P. O. Box 538, Tukuyu, Tanzania;South African Centre for Infectious Diseases Surveillance (SACIDS), Sokoine University of Agriculture (SUA), P. O. Box 3297, Morogoro, Tanzania
Entomologist, PhD candidateHumphrey Mkali, National Institute for Medical Research (NIMR), Tabora Medical Centre, P. O. Box 482, Tabora, Tanzania
Statistician, MScMaggie P. Kivuyo, National Institute for Medical Research (NIMR), Ngongongare Research Station, P. O. Box 514, Usa River, Arumeru, Tanzania
EntomologistArnold Ndaro, Kilimanjaro Clinical Research Institute (KCRI)
Laboratory Technician, BSC laboratory science student
Abas Mkwizu, Magugu Health Centre, Box 679, Babati Manyara Tanzania
Clinical Officer
Jovin Kitau, Kilimanjaro Christian Medical College (KCMC) P. O Box 2240, Moshi, Tanzania;
Research Scientist, PhD candidateReginald Kavishe, Kilimanjaro Christian Medical College (KCMC) P. O Box 2240, Moshi, Tanzania;Kilimanjaro Clinical Research Insitute (KCRI), P. O. Box 2236, Moshi, Tanzania
Molecular Biologist, PhDWilliam Dolmans, Radboud University-Nijmegen,Netherlands
PhD
Jaffu Chilongola, Kilimanjaro Christian Medical College (KCMC) P. O Box 2240, Moshi, Tanzania;Kilimanjaro Clinical Research Insitute (KCRI), P. O. Box 2236, Moshi, Tanzania
Deputy Director Training, PhDFranklin W. Mosha, Kilimanjaro Christian Medical College (KCMC) P. O Box 2240, Moshi, Tanzania;Kilimanjaro Clinical Research Insitute (KCRI), P. O. Box 2236, Moshi,
Director, PhDMain Article Content
Defining malaria burden from morbidity and mortality records, self treatment practices and serological data in Magugu, Babati District, northern Tanzania
Charles Mwanziva
Kilimanjaro Clinical Research Institute
Alphaxard Manjurano
Joint Malaria Programme (JMP)
Erasto Mbugi
Muhimbili University of Health and Allied Sciences (MUHAS), Dar es Salaam,Tanzania
Clement Mweya
National Institute for Medical Research (NIMR), Tukuyu Centre, P. O. Box 538, Tukuyu, Tanzania;South African Centre for Infectious Diseases Surveillance (SACIDS), Sokoine University of Agriculture (SUA), P. O. Box 3297, Morogoro, Tanzania
Humphrey Mkali
National Institute for Medical Research (NIMR), Tabora Medical Centre, P. O. Box 482, Tabora, Tanzania
Maggie P. Kivuyo
National Institute for Medical Research (NIMR), Ngongongare Research Station, P. O. Box 514, Usa River, Arumeru, Tanzania
Alex Sanga
St John University of Tanzania, Dodoma
Arnold Ndaro
Kilimanjaro Clinical Research Institute (KCRI)
William Chambo
National Institute for Medical Research (NIMR), Amani Centre, P. O. Box 81, Muheza, Tanzania
Abas Mkwizu
Magugu Health Centre, Box 679, Babati Manyara Tanzania
Jovin Kitau
Kilimanjaro Christian Medical College (KCMC) P. O Box 2240, Moshi, Tanzania;
Reginald Kavishe
Kilimanjaro Christian Medical College (KCMC) P. O Box 2240, Moshi, Tanzania;Kilimanjaro Clinical Research Insitute (KCRI), P. O. Box 2236, Moshi, Tanzania
William Dolmans
Radboud University-Nijmegen,Netherlands
Jaffu Chilongola
Kilimanjaro Christian Medical College (KCMC) P. O Box 2240, Moshi, Tanzania;Kilimanjaro Clinical Research Insitute (KCRI), P. O. Box 2236, Moshi, Tanzania
Franklin W. Mosha
Kilimanjaro Christian Medical College (KCMC) P. O Box 2240, Moshi, Tanzania;Kilimanjaro Clinical Research Insitute (KCRI), P. O. Box 2236, Moshi,
Abstract
Malaria morbidity and mortality data from clinical records provide essential information towards defining disease burden in the area and for planning control strategies, but should be augmented with data on transmission intensity and serological data as measures for exposure to malaria. The objective of this study was to estimate the malaria burden based on serological data and prevalence of malaria, and compare it with existing self-treatment practices in Magugu in Babati District of northern Tanzania. Prospectively, 470 individuals were selected for the study. Both microscopy and Rapid Diagnostic Test (RDT) were used for malaria diagnosis. Seroprevalence of antibodies to merozoite surface proteins (MSP-119) and apical membrane antigen (AMA-1) was performed and the entomological inoculation rate (EIR) was estimated. To complement this information, retrospective data on treatment history, prescriptions by physicians and use of bed nets were collected. Malaria prevalence in the area was 6.8% (32/470). Of 130 individuals treated with artemisinin combination therapy (ACT), 22.3 % (29/130) were slide confirmed while 75.3% (98/130) of them were blood smear negative. Three of the slides confirmed individuals were not treated with ACT. Fever was reported in 38.2% of individuals, of whom 48.8 % (88/180) were given ACT. Forty-two (32.3%) of those who received ACT had no history of fever. About half (51.1%) of those treated with ACT were children <10 years old. Immunoglobulin against MSP-119 was positive in 16.9% (74/437) while against AMA-1 was positive in 29.8 % (130/436). Transmission intensity was estimated at <0.2 infectious bites per person per year. The RDT was highly specific (96.3%) but with low sensitivity (15.6%). Magugu is a low endemic area. There is substantial over diagnosis, over treatment and self treatment in the community. The burden of malaria based on medical records is over estimated as was mostly presumptive. The low sensitivity of RDT reflects the low number of immune individuals as well as the low parasite density.