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Comparative Use of RDT and Thick Film Microscopy in the Diagnosis of Malaria in Sub-urban Settlements in Makurdi, Nigeria

Received: 16 January 2017     Accepted: 31 January 2017     Published: 1 March 2017
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Abstract

In as much as accurate diagnosis seems to be the only way of effecting rational therapy, it has been the most neglected area of malaria research. Thick blood film microscopy and Rapid diagnostic test (RDT) was comparatively used to study malaria prevalence in Makurdi, Nigeria. A total of 328 blood samples were collected from consented respondents and analyzed using Blood film examination with Field’s stains A and B staining techniques and Care Start TM rapid diagnostic test (RDT) manufactured by Access Bio Inc, USA to detect the presence of malaria parasites in blood. Questionnaires were used to get demographics of the respondents. Of the 328 participants examined, 164(50.0%) were positive for malaria parasites by light microscopy and 32(9.8%) were positive for malaria by RDT Care Start TM HRP2. The sensitivity and specificity of RDT was found to be 16.5% and 97.0% respectively while the Positive Predictive Value (PPV) and Negative Predictive Value (NPV) was found to be 84.4% and 53.7% respectively. The females 92(51.7%) and 20(11.2%) were slightly more infected than the males 72(48.0%) and 12(8.0%) using both methods, but result was not statistically significant (P>0.05). Malaria prevalence was higher among those with no formal education and least among those with tertiary education (P>0.05). The prevalence of malaria in respect to location was significantly higher in New GRA by RDT and Chile by light microscopy and least in High level and Agwan Jukum in order of RDT and microscopy (P=0.000). This study revealed that malaria can affect all sexes irrespective of their educational cadre and location. The Care Start TM RDT showed very poor sensitivity in contrast to light microscopy. In as much as light microscopy in poor set ups cannot be used routinely, the RDT has not proven to be a good replacement.

Published in International Journal of Infectious Diseases and Therapy (Volume 2, Issue 2)
DOI 10.11648/j.ijidt.20170202.11
Page(s) 25-34
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2017. Published by Science Publishing Group

Keywords

Malaria, Makurdi, RDT, Microscopy

References
[1] L. U. Amazu, O. O. Ebong, C. C. A. Azikiwe, P. C. Unekwe, M. I. Simialayi and P. J. C. Nwosu. Effects of methanolic seeds extract of Carica papaya on Plasmodium berghei infected mice. Asian Pacific Journal of Tropical Medicine, 2 (3): 1–6, 2009.
[2] S. Nandwani, M. Mathur and S. Rawat. Evaluation of the polymerase chain reaction analysis for diagnosis of falciparum malaria in Delhi India. Indian Journal of Medical Microbiology, 23 (3): 176–178, 2005.
[3] WHO. World Malaria Report 2013 - World Health Organization. Geneva Switzerland 2013. Retrieved from www.who.int/iris/bitstream/10665/97008/1/9789241564694_eng.pdf.
[4] A. E. Orimadegun, O. Fawole, J. O. Okereke, F. O. Akinbami and O. Sodeinde. Increasing burden of childhood severe malaria in a Nigerian tertiary hospital: Implications for control. Journal of Tropical Pediatricians, 53: 185-189, 2007.
[5] S. O. Adewole. The influence of environmental and ecological Factors in the transmission of malaria. Journal of Research in Science and Management, 7 (1): 57-62, 2009.
[6] L. A. Salako. National malaria day awareness week: A text of address given on the occasion of the malaria awareness day held in Abuja. Journal of Malaria in Tropical Africa, 1: 6-7, 2006.
[7] S. O. Adewole. Prevalence of malaria in Children, adults and pregnant women in Akure, Nigeria. International Journal of Biological Science, 1 (3): 185-190, 2010.
[8] WHO. Global Malaria Program. Updated WHO Policy Recommendation (October 2012): Intermittent Preventive Treatment of Malaria in Pregnancy Using Sulfadoxine-Pyrimethamine (IPTp-SP). Geneva, Switzerland, 2012.
[9] E. Klinkenberg, K. A. Onwona-Agyeman and P. J. McCall. Cohort trial reveals community impact of insecticide-treated nets on malariometric indices in urban Ghana. Transactions of the Royal Society of Tropical Medicine and Hygiene, 104 (7). 496–503, 2010.
[10] M. Yé, V. Hoshen, S. Louis, I. T. Séraphin and R. Sauerborn. Housing conditions and Plasmodium falciparum infection: protective effect of iron-sheet roofed houses. Malaria Journal, 5: 8, 2006.
[11] S. Shillcutt, C. Morel, C. Goodman, P. Coleman, D. Bell and C. J. Whitty. Cost-effectiveness of malaria diagnostic methods in sub-Saharan Africa in an era of combination therapy. Bulletin of World Health Organisation.86: 101–110, 2008.
[12] K. Krafts, E. Hempelmann and B. Oleksyn. The color purple: from royalty to laboratory, with apologies to Malachowski. Biotechnology and Histochemistry 86 (1): 7–35, 2011.
[13] C. J. Sutherland and R. Hallett. Detecting malaria parasites outside the blood. Journal of Infectious Diseases, 199 (11): 1561–3, 2009.
[14] I. T. Ling, S. Cooksley, P. A. Bates, E. Hempelmann and R. J. M. Wilson. Antibodies to the glutamate dehydrogenase of Plasmodium falciparum". Parasitology, 92 (2): 313–24, 1986.
[15] P. F. Mens, G. J. Schoone, P. A. Kager and H. D. F. H. Schallig. Detection and identification of human Plasmodium species with real-time quantitative nucleic acid sequence-based amplification. Malaria Journal, 5 (80): 80, 2006.
[16] L. B. Melanie, M. M. Clifford and A. K. Randall. Current Policy and Status of DDT Use for Malaria Control in Ethiopia, Uganda, Kenya and South,Nicholas School of Environment and Earth Sciences, Duke University, Africa. Working Paper 95 International Water management Institute, South Africa, 2004.
[17] Wikipedia. www.wikkiepedia.org/wikki/makurdi 2000. Retrieved on 25th September 2014
[18] M. Cheesbrough. District Laboratory practice in Tropical Countries part 2 ed. Cambridge University Press, New York pp 320- 329, 2010.
[19] I. O. Okonko, O. O. B. Donbraye-Emmanuel, E. Donbraye, J. A. Alli, O. A. Adekolurejo, M. O. Ojezele, E. T. Babalola, O. K. Mejeha and T. A. Amusan. Malaria parasitaemia among patients in Ibadan, Southwestern Nigeria. Journal of Applied Biosciences, 29: 1774-1780, 2010.
[20] O. Amali, G. Okwori and N. O. Awodi. Malaria and Anaemia among Pregnant Women in Makurdi, Benue State. Nigerian Journal of Parasitology, 32 (2): 193-196, 2011.
[21] G. T. A. Jombo, E. M. Mbaawuaga, A. S. Ayegba and M. A. Araoye. Anaemia, malaria burden and its control methods among pregnant women in a semi-urban community of Northern Nigeria. Journal of Public Health and Epidemiology, 3 (7): 317-323, 2011.
[22] E. Amuta, R. Houmsou, E. Wama and M. Ameh. Malarial infection among antenatal and maternity clinics attendees at the Federal Medical Centre, Makurdi, Benue State, Nigeria. Infectious Disease Reports, 6: 5050, 2014.
[23] C. I. Anumudu, A. Adepoju, M. Adeniran, O. Adeoye and I. Kassim. Malaria prevalence and treatment seeking behavior of young Nigerian adults. Annals of African Medicine, 15: 82-88, 2006.
[24] Igbeneghu, C., Odaibo, A. B. and Olaleye, D. O. (2011). Impact of asymptomatic malaria on some hematological parameters in the Iwo community in Southwestern Nigeria. Medical Principle and Practice, 20: 459-463.
[25] Federal Ministry of Health of Nigeria. Malaria Desk Situation Analysis. Federal Ministry of Health. Publication of the FMH, FGN Publication, Nigeria, 27, 2005a.
[26] K. M. Kalu, N. A. Obasi, F. O. Nduka and G. Otuchristian. A comparative study of the prevalence of malaria in Aba and Umuahia urban areas in Abia State, Nigeria. Research Journal of Parasitology, 7: 17-24, 2012.
[27] A. E. Onyido, N. C. Obi, P. U. Umeanaeto, M. O. Obiukwo and M. C. Egbuche, M. C. Malaria Prevalence and Indoor-Biting Mosquito Vector Abundance in Ogbunike, Oyi Local Government Area, Anambra State, Nigeria. African Research Review, 5 (3): 1-13, 2011a.
[28] Nwuzo, A. C., Onyeagba, R. A., Iroha, I. R., Nworie, O. and Oji, A. E. (2009). Parasitological, bacteriological, and cultural determination of prevalence of malaria parasite (Plasmodium falciparum) and typhoid fever co-infectionin Abakaliki, Ebonyi State. Scientific Research and Essay, 4 (10): 966-971.
[29] O. J. Nebe, G. O. Adeoye and P. U. Agomo. Prevalence and clinical profile of malaria among the coastal dwellers of Lagos State, Nigeria. Nigerian Journal of Parasitology, 23: 61-68, 2007.
[30] C. I. Ezeanya. Seasonal variation in malaria episodes among residents in Udi, a semi urban community in Southeast Nigeria. Nigerian Journal of Parasitology, 19:39-43, 1998.
[31] H. K. Kimbi, F. C. Keka, H. N. Nyabeyeu, H. U. Ajeagah and C. F. Tonga. An update of asymptomatic falciparum malaria in school children in Muea, Southwest Cameroon. Journal of Bacteriology and Parasitology. 3: 154, 2012.
[32] S. O. Sam Wobo, N. O. Adekunle, M. A. Adeleke, G. A. Dedeke and O. A. Oke. Epidemiological Factors in Prevalence of Malaria Parasites in Primary Health Facilities Attendees, Ogun State, Nigeria. Malaria Chemotherapy Control and Elimination, 3: 111, 2014.
[33] O. M. Ukpai and E. J. Ajoku. The prevalence of malaria in Okigwe and Owerri areas of Imo state, Nigeria. Journal of Parasitology, 22: 83-84, 2001.
[34] S. P. Kachur, E. Nicolas, V. Jean-Francois, A. Benitez and P. B. Bloland. Prevalence of malaria parasitemia and accuracy of microscopic diagnosis in Haiti, October 1995. Rev. Panamericana de Salud Publica, 3: 35-39, 1998.
[35] D. Syafruddin, A. Krisin, P. Sekartuti, R. M. and Dewi. Seasonal prevalence of malaria in West Sumba district, Indonesia. Malaria Journal, 8: 8, 2009.
[36] G. C. Ejezie. The Nigerian environment and parasitic infections. Folia Parasitologica (Praha) 30: 89-95, 1983.
[37] H. D. Mazigo, E. Obasy, W. Mauka, P. Manyiri, M. Zinga and E. J. Kweka. Knowledge, attitudes, and practices about Malaria andits control in rural Northwest Tanzania. Malaria Research and Treatment, 79 (42): 61, 2010.
[38] A. Hanafi-Bojd, H. Vatandoost, M. Oshaghi, M. Eshraghian, A. Haghdoost, F. Abedi, G. Zamani, M. Sedaghat, A. Rashidian and A. Madani. Knowledge, attitudes and practices regarding malaria control in an endemic area of southern Iran. Southeast Asian Journal of Tropical Medicine and Public Health, 42: 491, 2011.
[39] K. Koram, S. Bennett, J. Adiamah and B. Greenwood. Socio-economic determinants are not major risk factors for severe malaria in Gambian children. Transactions of the Royal Society Tropical Medicine and Hygiene, 89: 151-154, 1995.
[40] H. M. Asl, M. Motabar, G. Zamani, D. Naserinejad and H. Vatandoost. A Case–control Study of Determinative Factors on Malaria Morbidity in Minab, Jask and Roodan Counties, in Hormozgan Province, Southern Iran, 2001. Iran Journal of Public Health, 32: 14-18, 2001.
[41] S. Xiaodong, E. Tambo, W. Chun, C. Zhibin, D. Yan, W. Jian, W. Jiazhi and Z. Xiaonong. Diagnostic performance of CareStart™ malaria HRP2/pLDH (Pf/pan) combo test versus standard microscopy on falciparum and vivax malaria between China-Myanmar endemic borders. Malaria Journal. 12: 6, 2013.
[42] M. Beyene, A. Bemnet, B. Yeshambel, T. Zinaye, G. Muchiye, W. Meseret, G. Amare, W. Desalegn, M. Andargachew and K. Afework. Comparison of CareStart™ HRP2/pLDH COMBO Rapid Malaria Test With Light Microscopy in North-west Ethiopia. Malaria journal, 11: 234, 2012.
[43] Z. Sheyin and I. E. Bigwan. Comparison of CARE START HRP2 rapid malaria test with light microscopy for guiding patient’s treatment of fever in Nigerian endemic areas. Journal of medicine and Medical Sciences, 4 (9): 353-356, 2013.
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  • APA Style

    Faith Odije Okita, Elizabeth Uneh Amuta. (2017). Comparative Use of RDT and Thick Film Microscopy in the Diagnosis of Malaria in Sub-urban Settlements in Makurdi, Nigeria. International Journal of Infectious Diseases and Therapy, 2(2), 25-34. https://doi.org/10.11648/j.ijidt.20170202.11

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    Faith Odije Okita; Elizabeth Uneh Amuta. Comparative Use of RDT and Thick Film Microscopy in the Diagnosis of Malaria in Sub-urban Settlements in Makurdi, Nigeria. Int. J. Infect. Dis. Ther. 2017, 2(2), 25-34. doi: 10.11648/j.ijidt.20170202.11

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    AMA Style

    Faith Odije Okita, Elizabeth Uneh Amuta. Comparative Use of RDT and Thick Film Microscopy in the Diagnosis of Malaria in Sub-urban Settlements in Makurdi, Nigeria. Int J Infect Dis Ther. 2017;2(2):25-34. doi: 10.11648/j.ijidt.20170202.11

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  • @article{10.11648/j.ijidt.20170202.11,
      author = {Faith Odije Okita and Elizabeth Uneh Amuta},
      title = {Comparative Use of RDT and Thick Film Microscopy in the Diagnosis of Malaria in Sub-urban Settlements in Makurdi, Nigeria},
      journal = {International Journal of Infectious Diseases and Therapy},
      volume = {2},
      number = {2},
      pages = {25-34},
      doi = {10.11648/j.ijidt.20170202.11},
      url = {https://doi.org/10.11648/j.ijidt.20170202.11},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijidt.20170202.11},
      abstract = {In as much as accurate diagnosis seems to be the only way of effecting rational therapy, it has been the most neglected area of malaria research. Thick blood film microscopy and Rapid diagnostic test (RDT) was comparatively used to study malaria prevalence in Makurdi, Nigeria. A total of 328 blood samples were collected from consented respondents and analyzed using Blood film examination with Field’s stains A and B staining techniques and Care Start TM rapid diagnostic test (RDT) manufactured by Access Bio Inc, USA to detect the presence of malaria parasites in blood. Questionnaires were used to get demographics of the respondents. Of the 328 participants examined, 164(50.0%) were positive for malaria parasites by light microscopy and 32(9.8%) were positive for malaria by RDT Care Start TM HRP2. The sensitivity and specificity of RDT was found to be 16.5% and 97.0% respectively while the Positive Predictive Value (PPV) and Negative Predictive Value (NPV) was found to be 84.4% and 53.7% respectively. The females 92(51.7%) and 20(11.2%) were slightly more infected than the males 72(48.0%) and 12(8.0%) using both methods, but result was not statistically significant (P>0.05). Malaria prevalence was higher among those with no formal education and least among those with tertiary education (P>0.05). The prevalence of malaria in respect to location was significantly higher in New GRA by RDT and Chile by light microscopy and least in High level and Agwan Jukum in order of RDT and microscopy (P=0.000). This study revealed that malaria can affect all sexes irrespective of their educational cadre and location. The Care Start TM RDT showed very poor sensitivity in contrast to light microscopy. In as much as light microscopy in poor set ups cannot be used routinely, the RDT has not proven to be a good replacement.},
     year = {2017}
    }
    

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  • TY  - JOUR
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    AB  - In as much as accurate diagnosis seems to be the only way of effecting rational therapy, it has been the most neglected area of malaria research. Thick blood film microscopy and Rapid diagnostic test (RDT) was comparatively used to study malaria prevalence in Makurdi, Nigeria. A total of 328 blood samples were collected from consented respondents and analyzed using Blood film examination with Field’s stains A and B staining techniques and Care Start TM rapid diagnostic test (RDT) manufactured by Access Bio Inc, USA to detect the presence of malaria parasites in blood. Questionnaires were used to get demographics of the respondents. Of the 328 participants examined, 164(50.0%) were positive for malaria parasites by light microscopy and 32(9.8%) were positive for malaria by RDT Care Start TM HRP2. The sensitivity and specificity of RDT was found to be 16.5% and 97.0% respectively while the Positive Predictive Value (PPV) and Negative Predictive Value (NPV) was found to be 84.4% and 53.7% respectively. The females 92(51.7%) and 20(11.2%) were slightly more infected than the males 72(48.0%) and 12(8.0%) using both methods, but result was not statistically significant (P>0.05). Malaria prevalence was higher among those with no formal education and least among those with tertiary education (P>0.05). The prevalence of malaria in respect to location was significantly higher in New GRA by RDT and Chile by light microscopy and least in High level and Agwan Jukum in order of RDT and microscopy (P=0.000). This study revealed that malaria can affect all sexes irrespective of their educational cadre and location. The Care Start TM RDT showed very poor sensitivity in contrast to light microscopy. In as much as light microscopy in poor set ups cannot be used routinely, the RDT has not proven to be a good replacement.
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Author Information
  • Department of Biological Sciences, Faculty of Science, Benue State University, Makurdi, Nigeria

  • Department of Biological Sciences, College of Science, Federal University of Agriculture, Makurdi, Nigeria

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