Vol 75, No 2 (2024)
Original article
Published online: 2024-06-28

open access

Page views 1023
Article views/downloads 410
Get Citation

Connect on Social Media

Connect on Social Media

Prevalence of malaria in Arusha Region in the northern Tanzania

Daria Kołodziej1, Heriel Zacharia Ammi2, Wanesa Richert1, Małgorzata Marchelek-Myśliwiec3, Krzysztof Korzeniewski1
DOI: 10.5603/imh.100440
Pubmed: 38949218
Int Marit Health 2024;75(2):103-108.

Abstract

Background: The World Health Organization (WHO) reported an estimated 249 million malaria cases globally in 2023, of which 94% were reported from Africa. Tanzania, a Sub-Saharan African country, has an exceptionally high malaria prevalence (3.6 million in 2023). The aim of the present study was to assess malaria prevalence rates in the Arusha Region, northern Tanzania. This region is famous for its national parks and wildlife reserves, and it is visited by thousands of tourists from all over the world each year. The assessment of malaria prevalence in the region is important in the context of the necessity to administer antimalarial chemoprophylaxis to international travellers.

Material and methods: The study group consisted of 101 people, residents of the Karatu District in the Arusha Region, aged between 1 and 73 years, who volunteered to participate in the screening. Phase I of the study was conducted in July 2022 in the Karatu Lutheran Hospital in Karatu Town (located close to the Ngorongoro Conservation Area and the Serengeti National Park). During this phase a venous blood sample was collected from each patient. The samples were tested for malaria using a rapid diagnostic test (mRDT); the same samples were also used to measure haemoglobin concentration and next they were applied onto the Whatman FTA micro cards for further molecular diagnostics in Poland (phase II).

Results: mRDT detected two (2.0%) infections caused by Plasmodium (the etiological factor of malaria), the molecular tests (RT-PCR) confirmed the two positive results by mRDT but also detected infections in six other samples (7.9% in total). The study found that six patients were infected with the Plasmodium falciparum species, while two other subjects had co-infections (P. falciparum + P. ovale, P. falciparum + P. vivax + P. malariae).

Conclusions: The study findings confirm the prevalence of malaria in areas located close to national parks in northern Tanzania and support the use of antimalarial chemoprophylaxis in international travellers visiting the area. The present study found co-infections caused by four different species of Plasmodium species which supports the prevalence of different parasitic species in Sub-Saharan Africa and is in line with CDC reports but contrary to WHO reports which estimate that 100% of malaria cases in Sub-Saharan Africa are caused by P. falciparum.

Article available in PDF format

View PDF Download PDF file

References

  1. Plewes K, Leopold SJ, Kingston HWF, et al. Malaria: What's New in the Management of Malaria? Infect Dis Clin North Am. 2019; 33(1): 39–60.
  2. Douglas RG, Amino R, Sinnis P, et al. Active migration and passive transport of malaria parasites. Trends Parasitol. 2015; 31(8): 357–362.
  3. WHO. World Malaria Report 2023. Geneva: World Health Organization, 30 November 2023. Available from:. https://www.who.int/teams/global-malaria-programme/reports/world-malaria-report-2023. (Accessed: 31 March 2024).
  4. CDC Yellow Book 2024. Atlanta: Centers for Disease Control and Prevention, 2023. Available from:. https://wwwnc.cdc.gov/travel/yellowbook/2024/preparing/yellow-fever-vaccine-malaria-prevention-by-country/tanzania#seldyfm1118. (Accessed: 31 March 2024).
  5. Weiss DJ, Bertozzi-Villa A, Rumisha SF, et al. Indirect effects of the COVID-19 pandemic on malaria intervention coverage, morbidity, and mortality in Africa: a geospatial modelling analysis. Lancet Infect Dis. 2021; 21(1): 59–69.
  6. Mboera LE, Kitua AY. Malaria epidemics in Tanzania: An overview. Afr J Health Sci. 2001; 8(1-2): 17–23.
  7. STATISTA. Number of visitors at national parks in Tanzania. Available from:. https://www.statista.com/statistics/1248942/most-visited-national-parks-in-tanzania/. (Accessed: 30 March 2024).
  8. MD Doctors Direct GmbH. Alltest Malaria Pf/Pv/Pan. Available from:. https://www.mddoctorsdirect.com/wp-content/uploads/2023/04/145894100-IMPVF-402-Alltest-CE-EN-PI.pdf. (Accessed: 01 April 2024).
  9. Qiagen Group. WHAWB120211 QIAcard™ Indicating FTA™ Cards. Available from:. https://www.sigmaaldrich.com/PL/pl/product/sigma/whawb120211#product-documentation. (Accessed: 01 April 2024).
  10. A&A Biotechnology. Sherlock AX. Available from:. https://www.aabiot.com/ pobierz?code=120d24be129231125ec37a0b300ce6c551e668c0. (Acessed: 01 April 2024).
  11. European Centre for Disease Prevention and Control. Malaria – Annual Epidemiological Report for 2019. http://www.ecdc.europa.eu/en/publications-data/malaria-annual-epidemiological-report-2019. (Accessed: 30 April 2022).
  12. National Institute of Public Health of the Republic of Poland.Cases of selected infectious diseases in Poland from January 1 to December 31, 2023 and in a comparable period in 2022. Department of Infectious Disease Epidemiology and Surveillance. Available from:. https://wwwold.pzh.gov.pl/oldpage/epimeld/2023/INF_23_12B.pdf (Accessed: 01 April 2024).
  13. WHO. World Malaria Report 2021. Geneva: World Health Organization, 2022. Available from:. https://www.who.int/publications/i/item/9789240015791. (Accessed: 30 April 2022).
  14. WHO. Recommended selection criteria for procurement of malaria rapid diagnostic tests. Global Malaria Programme. Geneva: World Health Organization, January 2018. Available from:. https://www.who.int/malaria/publications/atoz/rdt_selection_criteria/en/. (Accessed: 07 May 2022).
  15. Bylicka-Szczepanowska E, Korzeniewski K. Asymptomatic malaria infections in the time of COVID-19 pandemic: experience from the Central African Republic. Int J Environ Res Public Health. 2022; 19(6).
  16. Korzeniewski K, Bylicka-Szczepanowska E, Lass A. Prevalence of asymptomatic malaria infections in seemingly healthy children, the Rural Dzanga Sangha Region, Central African Republic. Int J Environ Res Public Health. 2021; 18(2).
  17. Bylicka-Szczepanowska E, Korzeniewski K, Lass A. Prevalence of spp. in symptomatic BaAka Pygmies inhabiting the rural Dzanga Sangha region of the Central African Republic. Ann Agric Environ Med. 2021; 28(3): 483–490.
  18. Milligan R, Daher A, Graves PM. Primaquine at alternative dosing schedules for preventing relapse in people with Plasmodium vivax malaria. Cochrane Database Syst Rev. 2019; 7(7): CD012656.
  19. Briolant S, Pradines B, Basco LK. Role of primaquine in malaria control and elimination in French-speaking Africa. Bull Soc Pathol Exot. 2017; 110(3): 198–206.
  20. Escalante AA, Ferreira MU, Vinetz JM, et al. Malaria molecular epidemiology: lessons from the international centers of excellence for malaria research network. Am J Trop Med Hyg. 2015; 93(3 Suppl): 79–86.
  21. Cuu G, Asua V, Tukwasibwe S, et al. Species infecting children presenting with malaria in Uganda. Am J Trop Med Hyg. 2017; 97(3): 753–757.
  22. Zimmerman PA. Infection in duffy-negative people in Africa. Am J Trop Med Hyg. 2017; 97(3): 636–638.
  23. Twohig KA, Pfeffer DA, Baird JK, et al. Growing evidence of Plasmodium vivax across malaria-endemic Africa. PLoS Negl Trop Dis. 2019; 13(1): e0007140.