Abstract / Summary
Department of Medical Microbiology, University of Benin Teaching Hospital Benin City, Nigeria.
ABSTRACT
Background: Intestinal parasite infection is one of the main Public health issue, particularly in developing countries like Sub-Saharan Africa. Around 450 million people, primarily children, are believed to be unwell as a result of such diseases, with an estimated 3.5 billion people affected globally. Intestinal helminths infections have continued to occur in Nigeria as a result of low living standards, unsanitary surroundings, and a lack of knowledge about fundamental health-promoting behaviours. The majority of those afflicted are children, and Children in developing nations are most often affected because of their typical hand-mouth conduct, uncontrolled faecal activity, and immature immune systems. These diseases are more common in the less affluent neighbourhoods. They share several characteristics, including poor household income, filthy living circumstances, crowded living quarters, limited access to potable water, tropical weather, and low altitude.Among the top 10 most common infections in the world are intestinal parasitic disorders, including trichiuriasis, ascariasis, and hookworm infestation. The severity of intestinal parasite infections and their determinants among patients at University Of Benin Teaching Hospital, Benin-city, Nigeria, are poorly understood.
Aims: To estimate the prevalence of intestinal helminthic parasites among patients attending University Benin Teaching hospital, Benin-city.
Method: The study is a Retrospective Cross Sectional Study. It involved a review of Case notes of Patients that were admitted in UBTH and managed for Intestinal parasitic diarrhoea diseases from June 2016 to December 2019. Also a review of their Medical microbiology laboratory test records during management especially their Stool Microscopy results was done. Patients with incomplete or missing medical data were excluded from the study. Data were analyzed using SPSS version 26.0 statistical software.
Results: A total of 200 stool samples were processed during the period under review, and 40(20%) Stool samples were positive for intestinal helminths,28 (14%)stool samples were positive for Protozoa, while 132(66%) stool samples showed no parasites .
The Prevalence of intestinal parasite over these three year and 7 months period was 20% (40/200). With Male prevalence 13%(26/200) and Female 7%(14/200).
Of the Forty(40) intestinal helminths isolated,Twenty-six (65%) were from male Stool samples, while 14 (35%) were from female stool samples.
Hookworm (Ancyclostoma duodenale and Necator americanus) was the most isolated intestinal parasite accounting for8 (20%) of the total intestinal isolates. This was followed by Ascaris lumbricoides which accounted for 6(15%) of the total intestinal helminths isolated. In Male stool samples Hookworm and Ascaris lumbricoides were the most isolated intestinal parasite, while Schistosoma haematobium and Ascaris lumbricoides were the most isolated intestinal parasites in female stool samples. The least identified intestinal parasite were Hymenolopsisnana and Schistosomajapanicum. Seven different kinds of intestinal helminths were identified.
There was no significant relationship between the Sex of patients and the acquisition of intestinal parasites (as P= 0.460)
There was a significant relationship between the age group of patients and the Species of intestinal parasites isolated (P= 0.000).
Conclusion: In adults and school-age children, intestinal parasite infections were highly prevalent. The findings suggest that in order to reduce intestinal parasite infections, coordinated eradicated measures must be strengthened. The results of this study will be a valuable contribution to any modifications made to intestinal parasite prevention and control programmes by the federal, state or local governments.
Keywords: Intestinal helminths, Patients, University of Benin Teaching Hospital, Prevalence, Benin-city
INTRODUCTION
Intestinal parasite infection is one of the main public health issues, particularly in developing countries like Sub-Saharan Africa. Around 450 million people, primarily children, are believed to be unwell as a result of such diseases, with an estimated 3.5 billion people affected globally [1].
|
Intestinal helminths infections have continued to occur in Nigeria as a result of low living standards, unsanitary surroundings, and a lack of knowledge about fundamental health-promoting behaviours [2, 3]. Kids attending school have a higher probability of acquiring intestinal helminths infections, and they also tend to have them more frequently [4, 5, 6]. The majority of those afflicted are children, and Children in developing nations are most often affected because of their typical hand-mouth conduct, uncontrolled faecal activity, and immature immune systems(7).
Parasitic illnesses have been associated with a higher risk of nutritional anaemias, protein energy shortages, and stunted child growth. They may also result in a high risk of morbidity and mortality [10], as well as physical illness and subpar academic performance among pupils [8, 9]. Parasitic diseases are regulated by behaviour. Key components of health systems include biological, environmental, and social elements. The probability of disease transmission, infection, and associated death and morbidity is influenced by social and professional factors like education, local circumstances like well-maintained residential and rural infrastructure, and economic factors like monthly income [11, 12].
These diseases are more common in the less affluent neighbourhoods. They share several characteristics, including poor household income, filthy living circumstances, crowded living quarters, limited access to potable water, tropical weather, and low altitude. Among the top 10 most common infections in the world are intestinal parasitic disorders, including trichiuriasis, ascariasis, and hookworm infestation [13].
Intestinal helminths have a major role in the development of gastrointestinal problems, including dysentery, vomiting, diarrhoea, anorexia, haematuria, abdominal distension, and sometimes cognitively associated disorders. [14, 15]. Malnutrition and anaemia can be caused by severe chronic infections with Ascaris lumbricoides and hookworms (Ancylostomadoudenaleor Necator americanus) in high-risk individuals. [16, 17, 18].
The severity of intestinal parasite infections and their determinants among patients at University Of Benin Teaching Hospital, Benin-city, Nigeria, are poorly understood.
In order to ascertain the types and prevalence of human intestinal helminthic parasites among patients arriving at the University of Benin Teaching Hospital in Benin City,the current retrospective Study was carried out.
MATERIAL AND METHODS
Study setting:
The study was conducted in UBTH and the department of medical microbiology of the University of Benin Teaching Hospital, a 900-bedded tertiary centre located in Benin-city, south south Nigeria. The hospital is dedicated to teaching, research and specialist services and serves Lagos State and neighbouring States in south south Nigeria.
Study design:
The study was a Retrospective Cross Sectional Study. It involved a review of Case notes of patients that were admitted in UBTH and managed for Intestinal parasitic diarrhoea diseases from June 2016 to December 2019. Also, a review of their medical microbiology laboratory test records during management especially their Stool Microscopy results was done.
Patients with incomplete or missing medical data were excluded from the study.
Ethical considerations
Ethical approval for the study was obtained from University of Benin Teaching Hospital Research and Ethics Committee, with PROTOCOL NUMBER: ADM/E22/A/VOL.VII/14830112981. As data were retrospectively obtained from the laboratory records and did not involve contact with patients nor was recruitment of patients done, informed consent was not deemed necessary. However, privacy and confidentiality of patients’ data were protected in accordance with the Declaration of Helsinki.
RESULTS
A total number of 200 stool samples were processed during the period of review(Table 1). 40(20%) Stool samples were positive for intestinal helminths,28 (14 %) stool samples were positive for Protozoa, while 132(66%) stool samples showed no parasites. (Table 2)
The Prevalence of intestinal parasite over these three year and 7 months period was 20%( 40/200). With Male prevalence of intestinal parasite of 13%(26/200) and Female prevalence of intestinal parasite of 7%(14/200).
Of the Forty (40) intestinal helminths isolated , Twenty-six( 65%) were from male Stool samples, while 14 (35%) were from female stool samples. (Table 3, Fig1)
Table 1: Socio-demographic characteristics of subjects
|
VARIABLE |
TOTAL NUMBER OF STOOL SAMPLES |
NUMBER OF STOOL SAMPLES POSITIVE FOR HELMINTHS ISOLATION |
||||||
|
AGE GROUPS |
MALE |
FEMALE |
MALE |
FEMALE |
||||
|
(n) |
(%) |
(n) |
(%) |
(n) |
(%) |
(n) |
(%) |
|
|
1-5 |
13 |
10.83 |
7 |
8.75 |
0 |
0.00 |
0 |
0.00 |
|
6-10 |
17 |
14.17 |
10 |
12.5 |
6 |
5.00 |
3 |
3.75 |
|
11-15 |
6 |
5.00 |
5 |
6.25 |
3 |
2.50 |
2 |
2.50 |
|
16-20 |
5 |
4.17 |
5 |
6.25 |
2 |
1.67 |
0 |
0.00 |
|
21-25 |
18 |
15.00 |
15 |
18.75 |
3 |
2.50 |
2 |
2.50 |
|
26-30 |
19 |
15.83 |
10 |
12.5 |
4 |
3.33 |
2 |
2.50 |
|
31-35 |
16 |
13.33 |
10 |
12.5 |
5 |
4.17 |
3 |
3.75 |
|
36-40 |
5 |
4.17 |
8 |
10.00 |
0 |
0.00 |
1 |
1.25 |
|
41-45 |
11 |
9.17 |
5 |
6.25 |
3 |
2.50 |
0 |
0.00 |
|
46-50 |
10 |
8.33 |
5 |
6.25 |
0 |
0.00 |
1 |
1.25 |
|
Total |
120 |
100 |
80 |
100 |
26 |
21.67 |
14 |
17.5 |
Table 2: Isolates from stool sample and their percentages
PARASITE IN STOOL SAMPLE NUMBER %
Intestinal helminth 40 20
Protozoan 28 14
No parasite 132 66
Total stool sample 200 100
`
Table 3: Age and Sex
|
|
STOOL SAMPLE WITH INTESTINAL HELMINTHS |
|
|
||
|
MALE |
FEMALE |
||||
|
Age range |
6-10 |
6 |
3 |
|
|
|
11-15 |
3 |
2 |
|
|
|
|
16-20 |
2 |
0 |
|
|
|
|
21-25 |
3 |
2 |
|
|
|
|
26-30 |
4 |
2 |
|
|
|
|
31-35 |
5 |
3 |
|
|
|
|
36-40 |
0 |
1 |
|
|
|
|
41-45 |
3 |
0 |
|
|
|
|
46-50 |
0 |
1 |
|
|
|
|
Total |
26 |
14 |
|
|
|
Figure 1: Age and sex of patients with helminths infected stool sample.
Hookworm ( Ancyclostoma duodenale and Necator americanus) was the most isolated intestinal parasite accounting for 8 (20%) of the total intestinal isolates. This was followed by Ascaris lumbricoides which accounted for 6( 15%) of the total intestinal helminths isolated. In Male stool samples, Hookworm and Ascaris lumbricoides were the most isolated intestinal parasite, while Schistosoma haematobium andAscaris lumbricoides were the most isolated intestinal parasites in female stool samples. The least identified intestinal parasite were Hymenolopsis nana and Schistosoma japanicum.Seven different kinds of intestinal helminths were identified. (Figure 4)
Figure 4: Gender and parasites isolated
There was no significant relationship between the Sex of patients and the acquisition of intestinal parasites ( as P= 0.460). (Table 4)
Table4: Gender and Parasite isolated.
|
|
INFECTED STOOL SAMPLE |
X2 |
P-VALUE |
||
|
MALE |
FEMALE |
||||
|
Parasite seen in microscopy |
Hook worm |
8 |
2 |
5.678 |
0.460 |
|
Ascaris lumbricoides |
6 |
3 |
|
|
|
|
Strongiloidesstercoralis |
3 |
0 |
|
|
|
|
Trichuris trichura |
5 |
3 |
|
|
|
|
Hymenolopsis nana |
1 |
1 |
|
|
|
|
Schistosoma japanicum |
1 |
1 |
|
|
|
|
Schistosoma haematobium |
2 |
4 |
|
|
|
There was a significant relationship between the age group of patients and the Species of intestinal parasites isolated( P= 0.000). (Table 5)
Table 5. Frequency of parasite species seen across the various age groups
|
|
PARASITE SPECIE |
||||||||||
|
Hook worm |
A. lumbricordes |
Strongihoidessterlorcicin |
Trichuris trichura |
Hymenolopsis nana |
Schistostonrejapanicum |
Schistosoma haematobium |
X2 |
P-value |
|
||
|
Age range |
1-5 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
97.872 |
0.000 |
|
|
6-10 |
5 |
2 |
0 |
1 |
0 |
0 |
1 |
|
|
|
|
|
11-15 |
1 |
1 |
0 |
1 |
0 |
0 |
2 |
|
|
|
|
|
16-20 |
0 |
0 |
1 |
0 |
1 |
0 |
0 |
|
|
|
|
|
21-25 |
1 |
1 |
0 |
2 |
0 |
0 |
1 |
|
|
|
|
|
26-30 |
2 |
0 |
0 |
2 |
0 |
0 |
2 |
|
|
|
|
|
31-35 |
1 |
5 |
0 |
2 |
0 |
0 |
0 |
|
|
|
|
|
36-40 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
|
|
|
|
|
41-45 |
0 |
0 |
2 |
0 |
1 |
0 |
0 |
|
|
|
|
|
46-50 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
|
|
|
|
|
|
Total |
10 |
9 |
3 |
8 |
2 |
2 |
6 |
|
|
|
DISCUSSION
In this Study, the Prevalence of intestinal helminths over the 43months period was 20%( 40/200).This Findings were similar to another study done in North eastern Nigeria by Ibrahim et al(19). Another study done in Irrua reported prevalence of 40% intestinal parasitic infection [20] which was not consistent with the findings in this study.
The Male prevalence of intestinal parasite (13%) was higher than the Female prevalence of intestinal parasite (7%.). This was similar to a study done by Ibrahim at tal (19).
Hookworm (Ancyclostoma duodenale and Necator americanus) was the most isolated intestinal parasite (accounting for 20%of the total intestinal isolates) in this study. This was followed by Ascaris lumbricoides.This was similar to findings of Elemuwa e tal (21) .
The finding that gender doesnot affect the acquisition of intestinal parasite in this study was similar to other previous studies (22-24).
In this Study, Age did not affect the acquisition of intestinal parasites. This was similar to the study by Elemuwa e tal(21), but contrary to some studies which found higher prevalence within the age groups ( 22, 25).
CONCLUSION
In conclusion, a prevalence of 20% of intestinal Helminthic infections was observed in this study and the parasites that was most frequently isolated from patients accessing care in the University of Benin Tertiary Care centre was Hookworm (Ancyclostoma duodenale and Necator americanus).
REFERENCES
1. WHO. Conquering suffering enriching humanity. World Health Organisation: Geneva;
2000.
2. Brooker S, Bethony J, Hotez PJ. Human hookworm infection in the 21st century. Advances in parasitology. 2004; 58:197.
3. Mohammed K, Gulma MK, Yahaya M, Spencer TH, Nataala SU, Garba MK, Imam AU, Aschroft OF, Micheal U. Prevalence of Intestinal Parasitic Infections among Patients Attending UsmanuDanfodiyo University Teaching Hospital, Sokoto, Nigeria. Asian Journal of Research in Infectious Diseases. 2019 Jan 29;2(1):1-9.
4. Albonico M, Wright V, Jape K, Haji HJ,Taylor M, Savioli L, Bickle O. Soil transmitted nematode infections and mebendazole treatment in Mafia Island School children. Annal Trop MedParasitol.2002;96:717-726.
5. Alvañiz AFA, De Castro EC, Tablizo BJB, Flores MJC, Maghirang ESV, Esmeli LAR, Pacificador AY, Sumalapao DEP. Prevalence, physiologic effects, and risk factors of soil-transmitted helminth infections among grade school children. National Journal of Physiology, Pharmacy and Pharmacology. 2017;7(9):907-913.
6. Flores MJC, Bautista YM, Carandang LGE, Go KM, Olalia MBIT, Maghirang ESV, De Peralta AS, Esmeli LAR, Sumalapao DEP. Risk factors associated with intestinal parasitic infections among school children. Annual Research & Review in Biology. 2018;24(4):1-6.
7. Opara K, Udoidung Okon D, Edosomwan E, Udoh A. The Impact of Intestinal Parasitic Infections on the Nutritional Status of Rural and Urban School-Aged Children in Nigeria. International Journal of MCH and AIDS. 2012;1(1):73–82.
8. Taylor‐Robinson DC, Maayan N, Soares‐Weiser K, Donegan S, Garner P. Deworming drugs for soil‐transmitted intestinal worms in children: effects on nutritional indicators, haemoglobin and school performance. Cochrane Database of Systematic Reviews. 2012(11).
9. Crompton DW, Nesheim MC. Nutritional impact of intestinal helminthiasis during the human life cycle. Annual review of nutrition. 2002 Jul;22(1):35-59.
10. Sackey ME, Weigel MM, Armijos RX. Predictors and nutritional consequences of intestinal parasitic infections in rural Ecuadorian children. J. Trop. Pediatr.2003;49:17-23.
11. Yakubu N, Musa G, Yakubu SE. Seasonal changes in the distrinution and infection rate of Schistosoma intermediate hosts in River Kubanni and its tributaries. Bio Res Com. 2003; 15:207-214.
12.Wang K, Tang D, Wang M, Lu J, Yu H, Liu J. Journal of Cell Science. 2009; 122(Pt12):20556.
13. Alum A, Rubino JR, Ijaz MK. The global war against intestinal parasites—should we use a holistic approach? International journal of infectious diseases. 2010 Sep 1;14(9):732-738.
14.Bethony, J., Brooker, S., Albanico, M., Geiger, S.M., Loukas, A., Diemert, D. & Hotez, P.J. (2006) Soil-transmitted helminth infections; Ascaris, Trichuriasis and hookworm. Lancet 367, 1521.
15.Garcia, L.S.H. (2004) Diagnostic Medical Parasitology, 4th edition, ASM Press 2004.
16. Chaparro CM, Suchdev PS. Anemia epidemiology, pathophysiology, and etiology in low‐and middle‐income countries. Annals of the New York Academy of Sciences. 2019 Aug;1450(1):15-31.
17.Awasti, S., Bundy, D.A.P. &Savioli L. (2003) Helminthic infections. Brazil Medical Journal 327, 431-433.
18.Hotez, P.J., Brooker, S., Bethony, J.M., Bottazzi, M.E., Loukas, A. & Xiao S. (2004) Hookworm infection. New England Journal of Medicine, 351, 799-807.
19. Ibrahim M. Muhammad, Askira M. Umoru, Tom M. Isyaka. Intestinal parasitic infections among patients attending a Tertiary Health Institution in Northeastern Nigeria. American Journal of Research Communication, 2014, 2(6): 88-96} www.usa-journals.com,ISSN: 2325-4076.
20. Iyevhobu KO, Obodo BN (2020) Prevalence of parasitic infections in relation to CD4+ and antiretroviral (ART) usage of HIV sero-positive patients attending Irrua Specialist Teaching Hospital (ISTH) Irrua, Edo State, Nigeria. International Journal of Innovative Research and Advanced Studies 7(6): 205-211.
21. Elemuwa CO, Isibor JO, Inyang NJ, Elemuwa GU, Omoregie R, Ayanlere M and Akpan Emma. Prevalence of Intestinal Parasites among Patients Accessing care in Secondary and Tertiary Healthcare Institutions in Edo State, Nigeria. Am J Biomed Sci & Res. 2023 18(3) AJBSR.MS.ID.002467, DOI:10.34297/AJBSR.2023.18.00247.
22.Akinbo FO, Omoregie R, Eromwon R, Igbarumah IO, Airueghiomon UE (2011b) Prevalence of intestinal parasites among patients of a tertiary hospital in Benin City, Nigeria. N Am J Med Sci 3(10): 462-464.
23. Akinbo FO, Okaka CE, Omoregie R (2010b) Prevalence of intestinalparasitic infections among HIV patients in Benin City, Nigeria. Libyan J Med 5: 5506
24. Akinbo FO, Okaka CE, Omoregie R (2011a) Seasonal variations of intestinal parasitic infections among HIV-positive patients in Benin City, Nigeria. Ethiopian Journal of Health Sciences 21(3): 191-194.
25. Oladeinde BH, Omoregie R, Olley M, Anunibe JA, Odia I (2014) Intestinal parasitic infections in rural community of Okada, Edo State, Nigeria: a four-year retrospective study. Healthcare in Low-resource Setting 2(1): 35