Blood and Urinary Parasites and Associated Risk Factors in A Rural Community in Abia State, Nigeria

Authors

  • C. Okosa Department of Zoology and Environmental Biology, Michael Okpara University of Agriculture, Umudike. P.M.B 7267, Umuahia, Abia State, Nigeria
  • O. M. Ukpai Department of Zoology and Environmental Biology, Michael Okpara University of Agriculture, Umudike. P.M.B 7267, Umuahia, Abia State, Nigeria
  • Q. O. Lawrence Department of Zoology and Environmental Biology, Michael Okpara University of Agriculture, Umudike. P.M.B 7267, Umuahia, Abia State, Nigeria
  • B. C. Chukwuemeka Department of Zoology and Environmental Biology, Michael Okpara University of Agriculture, Umudike. P.M.B 7267, Umuahia, Abia State, Nigeria
  • P. O. Ikpi Department of Zoology and Environmental Biology, Michael Okpara University of Agriculture, Umudike. P.M.B 7267, Umuahia, Abia State, Nigeria

Keywords:

ITN usage, associated risk factors, parasites, urine, Blood

Abstract

The environment, climate, social behaviour, and economic factors make developing countries vulnerable to parasitic infections. A cross-sectional study was conducted (Dec 2017-May 2018) to determine the prevalence of blood and urine parasites in Obizi,Amakama-Olokoro, a rural community in Umuahia South LGA,Abia State. Blood and urine samples were collected from 284 respondents. Sample analyses were done using Rapid Diagnostic Test (RDT) kits and microscopy for blood and centrifugal sedimentation method for urine. Socio-demographic data and risk factors were collected with structured questionnaires. Statistical analysis was done using the Pearson’s Chi-square, with the PAST Statistical package. The results showed an overall blood parasitic prevalence of 32.4%. Plasmodium falciparum recorded the highest prevalence of 28.17% by RDT and 30.6% by microscopy. Trypanosoma brucei gambiense occurred as a mixed infection (1.8%). Schistosoma haematobium had a prevalence of 3.9%. Socio-demographic data showed there were more females (67.3%); more persons in the age group 61-70 years (31.0%) and more farmers (38.0%) in the studied population. More females were infected with Plasmodium falciparum (34.6%) while more males were infected with Schistosoma haematobium (8.6%) P. falciparum occurred in all the age groups. S. haematobium occurred only in three age groups with the highest prevalence found in the age group (11-20) years (26.9%). Malaria infection was higher in those who did not use ITNs (37.1%). Some reasons given for the non-usage of ITNs were high cost/non-availability and discomfort. Farming activities and swimming have been recognized as risk factors to the acquisition of Trypanosoma brucei gambiense and Schistosoma haematobium, respectively. Plasmodium falciparum, Trypanosoma brucei gambiense and Schistosoma haematobium still pose a serious health threat to the community. Eliminating vector breeding sites, the use of ITNs and changes in social behaviours will help reduce blood and urinary parasites and ensure a healthier and economically viable community.

Purchase

References

Centers for Disease Control and Prevention: Parasites: Parasitic Disease and Malaria Strategic Priorities: 2015-2020. Available on lineat

www.cdc.gov/parasites/features/dpdm_strategic

World Health Organization. (2001). Global prevalence and incidence of selected curable sexually transmitted infections: overviews and estimates. WHO/HIV- AIDS. Available online at https://www.who.int/reproductivehealth/publications/rtis/HIV_AIDS_2001_2/en/

World Health Organisation (2009). WHO World Malaria Report Geneva. Available online at https://www.mmv.org/newsroom/publicatio

ns/world-malaria-report-2009

World Health Organization. World Health Report (2002). Reducing Risks, Promoting Healthy Life. Geneva: World Health Organization, Geneva 2002. Available at https://apps.who.int/iris/bitstream/handle/10665/42510/WHR_2002.pdf

World Health Organization (2006). Human African trypanosomiasis (sleeping sickness): epidemiological update. Weekly Epidemiological Record. 81(8): 71–80.

Retmanasari, A., Widartono, B. S., Wijayanti, M. A., and Artama, W. T. (2017). Prevalence and Risk Factors for Toxoplasmosis in Middle Java, Indonesia. Ecology and Health Alliance, 14(1), 162–170.

Jin, S., Zhu, Y.C., Xu, M., Cao, L.M., He, W., Liang, Y. S., and Guan, X. H. (2005). Fast Dipsticks Dye for detection of immunoglobulin G (1gG) and IgMantibodies for human toxoplasmosis.American Society for Microbiology. 12: 198-201.

Brant, T.A., Okorie, P.N., Ogunmola, O., Ojeyode, N.B., Fatunade, S.B., Yisa Saka, E. D., Stanton, M.C., Molyneux, D.H., Stothard, J.R., and Kelly-Hope, L.A. (2018). Integrated risk mapping and landscape characterisation of lymphatic filariasis and loiasis in South-West Nigeria.

Parasite Epidemiology and Control. 3 (1):21-35.

The Carter Center (2008). Schistosomiasis Control Program. Retrieved January 2022 from https://web.archive.org/web/20080720091015/http://cartercenter.org/health/schistosomiasis/index.html

World Health Organisation. (WHO)(2014). "Schistosomiasis Fact sheet N°115". Retrieved 5 March 2021 from http://www.who.int/mediacentre/factsheets/fs115/en/

Usman,A. M. I., and Babeker, E.A. (2017). A Study on the Aspects of Epidemiology of Urinary and Intestinal Schistosomiasis in

Bauchi State, Nigeria. Science World Journal. 12(4).

Onyebiguwa, P. G., Nworsi, C. I., Igho, B. I., and Umukoro, D. P. A. (2010). Human African trypanosomiasis in an endemic focus of Abraka, Nigeria: Asian Pacific Journal of Tropical Medicine. 448-450

Cheesbrough, M. (2005). District Laboratory in Tropical Countries, Part 1. 2nd Edition, Cambridge. UK. 159-162.

Cheesbrough, M. (2009). District Laboratory Practice in Tropical Countries, Part I, Cambridge University Press, Cambridge, UK. 8, 190-120.

Nmor, J. C, Onojafe, J. O. and Omu, B. A. (2009). Anthropogenic Indices of SoilTransmitted Helminthiasis among children in Delta state, southern Nigeria. IranianJournal of Public Health. 38: 31–38.

Wogu, M. N., and Nduka, F.O. (2018). Evaluating Malaria Prevalence Using Clinical Diagnosis Compared with Microscopy and Rapid Diagnostic Test in a Tertiary Healthcare facility in Rivers State, Nigeria. Journal of Tropical Medicine. 4:39-50.

Ubiaru, P. C., Ukpai, O.M. and Ohaeri C.C. (2018). Evaluation of Microscopy and Rapid Diagnostic Tests in Screening Clinically Suspected Malaria Patients in a Hospital Setting in Umuahia, Nigeria. Nigeria Journal of Parasitology, 39(1): 80- 99.

Ukaga, C. N., Nwoke B. E. B., Udujih O. S., Udujih, O. G., OhaeriA.A.,Anosike, J. C., Udujih, B. U., and Nwachukwu, M. I. (2007). Placental Malaria in Owerri, Imo State, South-Eastern Nigeria. Tanzanian Health Research Bulletin (9): 180-185.

Ukpai, O, M and Ajoku, E, I. (2001). The Prevalence of Malaria in Okigwe and Owerri Areas of Imo State, Nigeria. Nigerian Journal of Parasitology. (22) (1&2): 43-48.

Nmorsi, O. P. G. Isaac, C., Igbinosa, I. B., Umukoro, O. and Aitaikuru, D. P. (2010). Human African Trypanosomiasis in Endemic Focus of Abraka, Nigeria. Asian Pacific Journal of Tropical Medicine. 448- 450.

Singh K. and Muhammad (2017). Incidence of Parasitic Diseases among Noma Patients in Sokoto State Nigeria. International Journal of Pharma Research and Health Sciences. 5(6): 1984-1988.

Doolan, D. L., Dobano, C. and Baird, J. K (2009). Acquired Immunity to Malaria. Clinical Microbiology Reviews. 22 (1): 13-36.

Sam Wobo, S. O., Adekunle, N. O., Adeleke, M. A., Dedeke, G. A., Oke, O. A., Abimbola, W. A., and Surakat, O. A. (2014). Epidemiological Factors in Prevalence of Malaria Parasites in Primary Health Facilities Attendees, Ogun State. Malaria Chemotherapy Control and Elimination. 3:111.

Bola, O., Omissakin, C., Ayodele, E. and Owoseni, M. F. (2014). Prevalence of Filaria worm among Prospective Blood Donors Attending a Tertiary Health Institution in South-West Nigeria. Journal of Dental and Medical Services. 13 (1): 2279-2286.

Kalu, M. K., Obasi,A. N., Nduka, F.O. and Otuchristian, G. (2012). Comparative Study of the Prevalence of Malaria and in Aba Umuahia Urban Areas of Abia State, Nigeria. Research Journal of Parasitology. (7): 17-24.

Awobode, H.O., Okunkola, D.O., Oyekunle, A.O., and Adekeye, T.A. (2016). Prevalence of Schistosomiasis and other parasites among Female Residents in some Communities in Oyo, state. Journal of Public Health and Epidemiology. 8 (3): 38- 44.

Okoli, C. G. and Iwuala, M. O. E. (2004). The Prevalence, Intensity and Clinical Signs of Urinary Schistosomiasis in Imo State, Nigeria. Journal of Helminthology. 78 (4): 337-342.

Morenikeji, O. A., Azubike, N. C. and Ige, A. O. (2009). Prevalence of Intestinal and Vector-Borne Urinary Parasites in Communities in South-West Nigeria. Journal of Vector Borne Diseases. 46 (2): 164-167.

Published

2022-03-01

How to Cite

Okosa, C., Ukpai, O. M., Lawrence, Q. O., Chukwuemeka, B. C., & Ikpi, P. O. (2022). Blood and Urinary Parasites and Associated Risk Factors in A Rural Community in Abia State, Nigeria. Nigerian Journal of Parasitology, 43(1), 67–77. Retrieved from https://njpar.com.ng/index.php/home/article/view/269

Similar Articles

1 2 3 4 5 6 7 8 9 10 > >> 

You may also start an advanced similarity search for this article.