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Viral haemorrhagic fevers and malaria co-infections among febrile patients seeking health care in Tanzania
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Abstract
BACKGROUND: In recent years there have been reports of viral haemorrhagic fever (VHF) epidemics in sub-Saharan Africa where malaria is endemic. VHF and malaria have overlapping clinical presentations making differential diagnosis a challenge. The objective of this study was to determine the prevalence of selected zoonotic VHFs and malaria co-infections among febrile patients seeking health care in Tanzania. METHODS: This facility-based cross-sectional study was carried out between June and November 2018 in Buhigwe, Kalambo, Kyela, Kilindi, Kinondoni, Kondoa, Mvomero, and Ukerewe districts in Tanzania. The study involved febrile patients seeking health care from primary healthcare facilities. Blood samples were collected and tested for infections due to malaria, Crimean-Congo haemorrhagic fever (CCHF), Ebola virus disease (EVD), Marburg virus disease (MVD), Rift Valley fever (RVF) and yellow fever (YF). Malaria infections were tested using rapid diagnostics tests while exposure to VHFs was determined by screening for immunoglobulin M antibodies using commercial enzyme-linked immunosorbent assays. The Chi-square test was used to compare the proportions. RESULTS: A total of 308 participants (mean age = 35 ± 19 years) were involved in the study. Of these, 54 (17.5%) had malaria infection and 15 (4.8%) were positive for IgM antibodies against VHFs (RVF = 8; CCHF = 2; EBV = 3; MBV = 1; YF = 1). Six (1.9%) individuals had both VHF (RVF = 2; CCHF = 1; EVD = 2; MVD = 1) and malaria infections. The highest co-infection prevalence (0.6%) was observed among individuals aged 46‒60 years (P < 0.05). District was significantly associated with co-infection (P < 0.05) with the highest prevalence recorded in Buhigwe (1.2%) followed by Kinondoni (0.9%) districts. Headache (100%) and muscle, bone, back and joint pains (83.3%) were the most significant complaints among those infected with both VHFs and malaria (P = 0.001). CONCLUSIONS: Co-infections of VHF and malaria are prevalent in Tanzania and affect more the older than the younger population. Since the overlapping symptoms in co-infected individuals may challenge accurate diagnosis, adequate laboratory diagnosis should be emphasized in the management of febrile illnesses.
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Seroprevalence estimates of MVD and EVD are often reported together, with estimates for MVD consistently lower than for EVD.
“Seroprevalence estimates of MVD and EVD are often reported together, with estimates for MVD consistently lower than for EVD, e.g. (35,36,44,54).”
From Marburg virus disease outbreaks, mathematical models, and disease parameters: a systematic review (2024) · cites this paper as [44]
The Results (Table 2) report EVD and MVD together, with three EVD-positive participants versus one MVD-positive participant. The Background also reports a separate Tanzanian study with EVD seroprevalence of 3.4% and MVD seroprevalence of 1.2%. These examples support lower MVD estimates, but this paper does not establish that estimates are often reported together or that MVD is consistently lower across studies. (LLM, conf=0.82)
Experimental — accuracy not yet measuredThe evidence gathered indicates high susceptibility to MVD among populations in the surveyed regions, including Tanzania.
“Overall, the evidence gathered here indicates high susceptibility to MVD among populations in the surveyed regions, including Tanzania, where one of the subsequent 2023 MVD outbreaks occurred (44).”
From Marburg virus disease outbreaks, mathematical models, and disease parameters: a systematic review (2024) · cites this paper as [44]
The citation is attached to the clause about a 2023 MVD outbreak in Tanzania, rather than clearly to the citing authors’ conclusion about susceptibility. The source’s Background describes Tanzania as at high risk but says no clinical MVD case had been reported there; our copy does not address a subsequent 2023 outbreak (searched: 2023 Marburg outbreak in Tanzania). (LLM, conf=0.76)
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Cites
Emergence of Zaire Ebola Virus Disease in Guinea
Baize, S., Pannetier, D., Oestereich, L., Rieger, T., Koivogui, L., Magassouba, N., Soropogui, B., Sow, M. S., Keïta, S., De Clerck, H., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1404505 · Cited by 1,366
Flagged first, then by citations
Research works printed but not linked: 34
- Asogun DA, Gunther S, Akpede GO, Ihekweazu C, Zumla A. Lassa fever: epidemiology, clinical features, diagnosis, management and prevention. Infect Dis Clin North Am. 2019;33:933–51. https://doi.org/10.1016/j.idc.2019.08.002. · DOI
- Zumla A, Hui DSC. Emerging and re-emerging infectious diseases: global overview. Infect Dis Clin North Am. 2019. https://doi.org/10.1016/j.idc.2019.09.001. · DOI
- Iannetta M, Di Caro A, Nicastri E, Vairo F, Masanja H, Kobinger G, et al. Viral hemorrhagic fevers other than Ebola and Lassa. Infect Dis Clin North Am. 2019;33:977–1002. https://doi.org/10.1016/j.idc.2019.08.003. · DOI
- Rugarabamu S, Mwanyika G, Rumisha SF, Sindato C, Lim H-Y, Misinzo G, et al. Seroprevalence of selected zoonotic viral haemorrhagic fevers and associated risk factors in Tanzania. Int J Infect Dis. 2021;109:174–81. https://doi.org/10.1016/j.ijid.2021.07.006. · DOI
- Swanepoel R, Shepherd AJ, Leman PA, Shepherd SP, McGillivray GM, Erasmus MJ, et al. Epidemiologic and clinical features of Crimean-Congo hemorrhagic fever in southern Africa. Am J Trop Med Hyg. 1987;36(1):120–32. https://doi.org/10.4269/ajtmh.1987.36.120. · DOI
- Swanepoel R. Nairovirus infections. In: Porterfield JS, editor. Exotic Viral Infections. London: Chapman and Hall; 1995. p. 285–93.
- Sindato C, Karimuribo ED, Pfeiffer DU, Mboera LEG, Kivaria F, Dautu G, et al. Spatial and temporal pattern of Rift Valley fever outbreaks in Tanzania; 1930 to 2007. PLoS One. 2014;9(2):E8889. https://doi.org/10.1371/journal.pone.0088897. · DOI
- Smith DH, Johnson BK, Isaacson M, Swanepoel R, Johnson KM, Killey M, et al. Marburg-virus disease in Kenya. Lancet. 1982;1(8276):816–20. https://doi.org/10.1016/s0140-6736(82)91871-2. · DOI · Paper page
- Kwallah AO, Inoue S, Thairu-Muigai AW, Kuttoh N, Morita K, Mwau M. Sero-prevalence of yellow fever virus in selected health facilities in Western Kenya from 2010 to 2012. Jap J Infect Dis. 2014;68(3):230–4. · DOI
- Siya A, Bazeyo W, Tuhebwe D, Tumwine G, Ezama A, Manirakza L, et al. Lowland grazing and Marburg virus disease (MVD) outbreak in Kween district, Eastern Uganda. BMC Public Health. 2019;19:136. https://doi.org/10.1186/s12889-019-6477-y. · DOI
- Rugarabamu S, George J, Mbanzulu KM, Mwanyika G, Misinzo G, Mboera LEG. Estimating risk of introduction of Ebola virus disease from the Democratic Republic of Congo to Tanzania: a qualitative assessment. Epidemiol. 2021. https://doi.org/10.3390/epidemiologia3010007. · DOI
- Chacky F, Runge M, Rumisha SF, Machafuko P, Chaki P, Massaga JJ, et al. Nationwide school malaria parasitaemia survey in public primary schools, the United Republic of Tanzania. Malar J. 2018;17:452. https://doi.org/10.1186/s12936-018-2601-1. · DOI · Paper page
- Mboera LEG, Rumisha SF, Chiduo MG, Mangu CD, Lyimo EP, Mremi IR, et al. Cause-specific mortality patterns among hospital deaths in Tanzania. PLoS One. 2018;13(10):e0205833. https://doi.org/10.1371/journal.pone.0205833. · DOI
- Abbate JL, Becquart P, Leroy E, Ezenwa VO, Roche B. Exposure to Ebola virus and risk for infection with malaria parasites, rural Gabon. Emerg Infect Dis. 2020;26(2):229–37. https://doi.org/10.3201/eid2602.181120. · DOI
- Sow A, Loucoubar C, Diallo D, Faye O, Ndiaye Y, Senghor CS, et al. Concurrent malaria and arbovirus infections in Kedougou, south-eastern Senegal. Malar J. 2016;15:47. https://doi.org/10.1186/s12936-016-1100-5. · DOI
- Kolawole OM, Ayodeji AO, Ogah JI. Prevalence of Rift Valley fever virus in febrile malaria patients using serological and molecular-based evidence. Ann Sci Technol. 2018;3(1):1–6. https://doi.org/10.2478/ast-2018-0008. · DOI
- Kratz T, Roddy P, Tshomba Oloma A, Jeffs B, Pou Ciruelo D, de la Rosa O, et al. Ebola virus disease outbreak in Isiro, Democratic Republic of the Congo, 2012: signs and symptoms, management and outcomes. PLoS One. 2015;10(6):e0129333. https://doi.org/10.1371/journal.pone.0129333. · DOI
- Edwards HM, Counihan H, Bonnington C, Achan J, Hamade P, Tibenderana K. The impact of malaria co-infection on Ebola virus disease outcomes: a systematic review and meta-analysis. PLoS One. 2021;16(5):e0251101. https://doi.org/10.1371/journal.pone.0251101. · DOI
- Hassan A, Wlodarczyk MF, Benamar M, Bassot E, Salvioni A, Kassem S, et al. A virus hosted in malaria-infected blood protects against T cell-mediated inflammatory diseases by impairing DC function in a Type I IFN-dependent manner. MBio. 2020;11(2):e03394-e3419. https://doi.org/10.1128/mBio.03394-19. · DOI
- Baba M, Logue CH, Oderinde B, Abdulmaleek H, Williams J, Lewis J, et al. Evidence of arbovirus co-infection in suspected febrile malaria and typhoid patients in Nigeria. J Infect Develop Countr. 2013;7(1):51–9. https://doi.org/10.3855/jidc.2411. · DOI
- Rosenke K, Adjemian J, Munster VJ, Marzi A, Falzarano D, Onyango CO, et al. Plasmodium parasitemia associated with increased survival in Ebola virus-infected patients. Clin Infect Dis. 2016;63(8):1026–33. https://doi.org/10.1093/cid/ciw452. · DOI
- Waxman M, Aluisio AR, Rege S, Levine AC. Characteristics and survival of patients with Ebola virus infection, malaria, or both in Sierra Leone: a retrospective cohort study. Lancet Infect Dis. 2017;17:654–60. https://doi.org/10.1016/S1473-3099(17)30112-3. · DOI
- World Health Organization. Guidance on temporary malaria control measures in Ebola-affected countries. Geneva: World Health Organization; 2014.
- Karimuribo ED, Mutagahywa E, Sindato C, Mboera LE, Mwabukusi M, Kariuki Njenga M, et al. A smartphone app (AfyaData) for innovative one health disease surveillance from community to national levels in Africa: Intervention in disease surveillance. JMIR Public Health Surveill. 2017;3(4): e94. https://doi.org/10.2196/publichealth.7373. · DOI
- Bwire GM, Ngasala B, Kilonzi M, Mikomangwa WP, Felician FF, Kamuhabwa AAR, et al. Diagnostic performance of CareStart™ malaria HRP2/pLDH test in comparison with standard microscopy for detection of uncomplicated malaria infection among symptomatic patients, Eastern Coast of Tanzania. Malar J. 2019;18:354. https://doi.org/10.1186/s12936-019-2990-9. · DOI
- Mohamed M, Mosha F, Mghamba J, Zaki SR, Shieh WJ, Paweska J, et al. Epidemiologic and clinical aspects of a Rift Valley fever outbreak in humans in Tanzania, 2007. Am J Trop Med Hyg. 2010;83(2 Suppl):22–7. https://doi.org/10.4269/ajtmh.2010.09-0318. · DOI
- Heinrich N, Saathoff E, Weller N, Clowes P, Kroidl I, Ntinginya E, et al. High seroprevalence of Rift Valley fever and evidence for endemic circulation in Mbeya region, Tanzania, in a cross-sectional study. PLoS Negl Trop Dis. 2012;6: e1557. https://doi.org/10.1371/journal.pntd.0001557. · DOI
- Barry M, Traoré FA, Sako FB, Kpamy DO, Bah EI, Poncin M, et al. Ebola outbreak in Conakry, Guinea: epidemiological, clinical, and outcome features. Med Mal Infect. 2014;44:491–4. https://doi.org/10.1016/j.medmal.2014.09.009. · DOI
- Ahmed A, Makame J, Robert F, Julius K, Mecky M. Seroprevalence and spatial distribution of Rift Valley fever infection among agro-pastoral and pastoral communities during Interepidemic period in the Serengeti ecosystem, northern Tanzania. BMC Infect Dis. 2018;18:276. https://doi.org/10.1186/s12879-018-3183-9. · DOI
- Kolawole OM, Irekeola AA, Seriki AA, Bellow KE. Investigation of risk factors associated with malaria and yellow fever coinfection among febrile patients in Ilorin. Nigeria J Med Soc. 2018;32:33–9. https://doi.org/10.4103/0972-4958.213955. · DOI
- Glynn JR. Age-specific incidence of Ebola Virus disease. Lancet. 2015;386(9992):432. https://doi.org/10.1016/S0140-6736(15)61446-5. · DOI
- Muga GO, Onyango-Ouma W, Sang R, Affognon H. Sociocultural and economic dimensions of Rift Valley fever. Am J Trop Med Hyg. 2015;92(4):730–8. https://doi.org/10.4269/ajtmh.14-0363. · DOI
- Omoleke SA, Mohammed I, Saidu Y. Ebola Viral Disease in West Africa: a threat to global health, economy and political stability. J Public Health Afr. 2016;7(1):534. https://doi.org/10.4081/jphia.2016.534. · DOI
- Thawer SG, Chacky F, Runge M, Reaves E, Mandike R, Lazaro S, et al. Sub-national stratification of malaria risk in mainland Tanzania: a simplified assembly of survey and routine data. Malar J. 2020;19:177. https://doi.org/10.1186/s12936-020-03250-4. · DOI · Paper page
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Marburg virus disease outbreaks, mathematical models, and disease parameters: a systematic review
Cuomo-Dannenburg, G., McCain, K., McCabe, R., Unwin, H. J. T., Doohan, P., Nash, R. K., Hicks, J. T., Charniga, K., Geismar, C., Lambert, B., et al. (2024) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(23)00515-7 · Cited by 65
“Overall, the evidence gathered here indicates high susceptibility to MVD among populations in the surveyed regions, including Tanzania, where one of the subsequent 2023 MVD outbreaks occurred (44).”
Metadata
- Authors
- Rugarabamu, S., Rumisha, S. F., Mwanyika, G. O., Sindato, C., Lim, H.-Y., Misinzo, G., & Mboera, L. E. G.
- Affiliations
- Muhimbili University of Health and Allied Sciences (TZ)
- The Kids Research Institute Australia (AU)
- Mbeya University of Science and Technology (TZ)
- Southern African Centre for Infectious Disease Surveillance (TZ)
- Korea Disease Control and Prevention Agency (KR)
- Corresponding author
- Mboera, Leonard E. G.
- ORCID
- Venue
- Infectious Diseases of Poverty
- Published
- 2022-04-25
- Volume
- 11
- Issue
- 1
- Pages
- 33-33
- ISSN
- 2049-9957 (ISSN-L)
- PMC
- PMC9036688
- OpenAlex
- W4226044412
- Cited by
- 29
- References
- 1
- Citations by year
- 2026: 8 · 2025: 8 · 2024: 4 · 2023: 8 · 2022: 1
- FWCI
- 2.57
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Infectious Diseases of Poverty (publishedVersion, cc-by)
- Research Square (acceptedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Korea Centers for Disease Control and Prevention (4845-300-340-01))
- Topics
- Health Sciences › Medicine › Infectious Diseases › Viral Infections and Vectors
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Mosquito-borne diseases and control
- Health Sciences › Medicine › Infectious Diseases › Viral Infections and Outbreaks Research
- Keywords
- viral hemorrhagic fever, malaria co-infection, Crimean-Congo hemorrhagic fever, Ebola virus disease, Marburg virus disease, Rift Valley fever, yellow fever, zoonoses, IgM, febrile illness, differential diagnosis, Tanzania, sub-Saharan Africa, clinical symptoms, primary care patients
- MeSH terms
- Adolescent, Adult, Animals, Antibodies, Viral, Hemorrhagic Fever Virus, Crimean-Congo, Cross-Sectional Studies, Delivery of Health Care, Fever, Hemorrhagic Fever, Crimean, Hemorrhagic Fevers, Viral, Humans, Immunoglobulin M, Malaria, Middle Aged, Tanzania, Hemorrhagic Fever, Ebola, Young Adult, Coinfection
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