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. 2018 Aug 6;18:373. doi: 10.1186/s12879-018-3291-6

Prevalence of helminthic infections and determinant factors among pregnant women in Mecha district, Northwest Ethiopia: a cross sectional study

Berhanu Elfu Feleke 1,, Tadesse Hailu Jember 2
PMCID: PMC6080381  PMID: 30081837

Abstract

Background

Intestinal parasites are the most common infections in developing countries. Prevalence and impacts of these parasites are high in pregnant women. The aims of this study were to determine prevalence of helminthic infection and evaluate the determinant factors during pregnancy.

Methods

A cross-sectional study was conducted in Mecha district from November 2015 to January 2016. The data were collected by interview technique and collecting the stool sample from each pregnant woman. Descriptive statistics and binary logistic regression were used.

Results

A total of 783 pregnant women were included. The prevalence of intestinal parasite among pregnant women was 70.6% [95% CI 67 -74%]. Ascaris lumbricoides (32.7%) was the predominant intestinal parasite species. Intestinal parasitic infection were 2.94 folds higher in the absence of latrine (AOR: 2.94 [95% CI: 1.5–5.8]). Absence of regular hand washing habit increase the odds of infection by 3.33 folds higher (AOR: 3.33 [95% CI: 1.54–7.14]). Not wearing shoe increased the odds of helminthic infection by 6.87 folds higher (AOR: 6.87 [95% CI: 3.67–12.9]). Illiteracy increases the odds of intestinal parasitic infection by 2.32 folds higher (AOR: 2.32 [95% CI: 1.04–5.26]). Ingestion of raw vegetables increases the odds of intestinal parasitic infection by 2.65 folds higher (AOR: 2.65 [95% CI: 3.23–9.9]). The odds of intestinal parasitic infection were higher in rural areas (AOR: 2 [95% CI: 5–10]). Intestinal parasitic infection was higher in women aged less than 21 years (AOR: 6.48 [95% CI: 2.91–14.4]).

Conclusion

The prevalence of helminthic infection is high in this study. Latrine utilization, hand washing habit, eating raw vegetables and bare foot were the major determinant factors for the high prevalence. Therefore, health education and improvements in sanitary infrastructure could achieve long-term and sustainable reductions in helminth prevalence.

Keywords: Prevalence, Determinants, Intestinal parasite, Pregnant women, Ethiopia

Background

Intestinal parasites especially geohelmenths are the most common and widespread of human parasites in the developing world [1]. Thousands of rural and impoverished villagers are often chronically infected with different species of parasitic worms [2]. More than 1.5 billion people, or 24% of the world’s population, are infected with soil-transmitted helminthic infections worldwide. Infections are widely distributed in tropical and subtropical areas, with the greatest numbers occurring in sub-Saharan Africa, the Americas, China and East Asia [3].

Intestinal parasitic infection is very common in Ethiopia [4] and the magnitude of infection varies from place to place [5]. Intestinal parasitic infections account the second most predominant causes of outpatient morbidity in the country [6]. High prevalence of parasitic infection in Ethiopia were due to the unsafe and inadequate provision of water, unhygienic living conditions, the absence of proper utilization of latrine and habit of walking with a bare foot [7, 8].

Pregnant women are also at high risk of parasitic infection due to their close relationship with children [9]. Recently, a study done on pregnant women indicated that pregnancy has been associated with an increasing prevalence of parasitic infections compared to non-pregnant women [10].

Infections with helminth were associated with a modest decrease in hemoglobin levels and indicators of poor nutritional status. Helminthic infections, such as Hookworm, Trichuriasis, and Schistosomiasis, have been shown to directly contribute to severe anemia in patients through blood loss and micronutrient deficiencies [11]. Low hemoglobin level is associated within areas where with a high prevalence of Hookworm infection [12]. Hookworm is the leading cause of pathologic blood loss in endemic areas [13].

Anemia accounts 20% of maternal death globally [14]. Anemia in these highly endemic regions is common among pregnant women and often multi-factorial. Anemia has a devastating effect on pregnant women and has been associated with stillbirth, prematurity and low birth weight [15].

Although there are a lot of factors that causes anemia, intestinal parasites like Hookworm, Trichuriasis trichuira and schistosoma are highly associated to cause anemia in pregnant women in endemic parts of Ethiopia. These parasites cause anemia directly by feeding the red blood cells or indirectly by causing bleeding, feeding the micronutrients and infiltrating the blood forming organs. The complication of intestinal parasitic infection during pregnancy leads to stillbirth, prematurity and low birth weight. To minimize the burden of parasitic infection during pregnancy, studying the prevalence of intestinal parasitic infections in pregnant women is very ideal. Therefore, the aims of this study were to determine the prevalence and determinants of intestinal helminth among pregnant women in Northwest Ethiopia.

Methods and materials

A cross sectional study was conducted in Mecha district. Mecha district was located 40 km to the north of Bahir dar city and the district contains 376,000 residents. The data were collected from November 2015 to January 2016. The target population was all pregnant women residing in Mecha district. Pregnant women absent during the data collection period or unable to give stool sample were excluded from the study.

The sample size was calculated using single population proportion formula with the assumption of 95% CI, 50% proportion of intestinal parasite in pregnant women, 5% margin of error, none response rate of 10% and a design effect of 2 gives 846 pregnant women’s. Multistage sampling technique was used. First 10 kebeles (the smallest administrative unit in Ethiopia) were selected from 40 kebeles of Mecha district using simple random sampling technique. Then simple random sampling technique was used to select pregnant women from these 10 kebeles using the kebele health extension workers registration list as a sampling frame.

The data collection procedure was conducted using interview technique and collecting stool sample from each interviewed pregnant women. Fifteen health extension workers were recruited for the data collection and 5 clinical nurses were recruited for supervision. The stool sample was collected from each pregnant woman, preserved with 10 ml sodium acetate- acetic acid-formalin solution (SAF) and transported to Bahir dar regional laboratory for analysis. From each pregnant woman, one gram stool sample was collected. Concentration technique was used. The stool sample was well mixed and filtered using a funnel with gauze then centrifuged for one minute at 2000 RPM (revolution per minute) and the supernatant was discarded. 7 ML (Milliliter) normal saline was added, mixed with a wooden stick, 3 ML ether was added and mixed well then centrifuged for 5 min at 2000 RPM. Finally, the supernatant was discarded and the whole sediment was examined for parasites [16].

To ensure the quality of this research, training was given for all data collectors and supervisors. The pre-test was conducted in 50 pregnant women then the necessary correction was done on the questionnaire after the pre-test. The whole data collection procedures were closely supervised by field supervisors and investigators.

We say the women practice proper hand hygiene if she washed her hands after visiting the toilet, before cooking food and before feeding her child. We say the women properly utilize toilets if the household members consistently utilize the toilets.

The data were entered into the computer using Epi-info software and transported to SPSS software for analysis. Descriptive statistics were used to estimate the prevalence of intestinal parasite and binary logistic regression was used to identify the determinants of intestinal parasite and variable with a p-value less than 0.05 was declared as determinants of intestinal parasite. Adjustments were done for age, gravidity, parity, ANC visit, religion, ethnicity, residence, ingestion of raw vegetables, latrine utilization, hand washing practice, bare foot and educational status.

Results

A total of 783 pregnant women were included giving a response rate of 92.55%. The mean age of the responders was 20.3 years (Standard deviation [SD] 2.95 years). The majority (91.8%) of respondents were orthodox Christian by religion. Amhara ethnicity constituted 87.9% of the study participants (Table 1).

Table 1.

Socio-demographic profile of pregnant women in Mecha district, Northwest Ethiopia (n = 783)

SNa Population profile Nb Percentage
1. Age 16–20 489 62.5
21–25 291 37.2
> 25 3 0.4
2. Residence Urban 181 23.1
Rural 602 76.9
3. Religion Orthodox 719 91.8
Muslim 64 8.2
4. Ethnicity Amhara 688 87.9
Agaw 74 9.5
Others 21 2.6
5. Educational status Illiterate 194 24.5
Elementary 458 58.5
Secondary 36 4.6
Certificate 43 5.5
Diploma 16 2
First degree 35 4.5
Second degree 1 0.1
6. Gravidity 1 263 33.6
2 329 42
3 185 23.6
4 6 0.8
7. Frequency of ANC visit 0 275 35.1
1 314 40.1
2 189 24.1
3 5 0.6
8. Gestational age in weeks 14–23 157 20.1
24–33 293 37.4
34–42 333 42.5

aSN serial number

bN number of women

The prevalence of intestinal parasite among pregnant women was 70.6% [95% CI 67 -74%].

60.8% of the infection was on high intensity of infection, 18.3% of the infection was on moderate intensity of infection and 21% of the infection was on low intensity of infection (Table 2).

Table 2.

The helminthic infection status of pregnant women

Parasites Number of women infected Percentage of women infected
Ascaris lumbricoides 256 32.7
Schistosoma mansoni 136 17.4
Hookworm 111 14.2
Strongyloides stercolaris 50 6.4
Mixed infection 42 5.36

The absence of latrine increases the odds of intestinal parasitic infection by 2.94 folds higher. The odds of intestinal parasitic infection were 3.33 folds higher among pregnant women that didn’t have regular hand washing habit. Not wearing shoe increases the odds of intestinal parasitic infection by 6.87 times higher. Illiteracy increases the odds of intestinal parasitic infection by 2.32 folds higher. The odds of helminthic infections were 2.65 times higher in pregnant women that ingest raw vegetables. Pregnant women whose age less than or equal to 21 years old were 6.48 times more likely to be infected with helminth than the others. The odds of intestinal parasitic infections were 2 folds higher in the rural areas (Table 3).

Table 3.

Determinants of helminthic infection among pregnant women in Mecha district, Northwest Ethiopia (n = 783)

Variables aIP Infected IP Not infected bCOR[95%CI] cAOR[95%CI] p-value
Latrine Absent 136 24 2.8 [1.72–4.58] 2.94 [1.5–5.8] < 0.01
Present 417 206
Hand washing habit Absent 182 15 7.03 [3.94–12.74] 3.33 [1.54–7.14] < 0.01
Present 371 215
Residence Rural 530 72 50.57 [29.82–86.4] 2 [5–10] 0.01
Urban 23 158
Bare footed Yes 199 105 0.67 [0.48–0.93] 6.87 [3.67–12.9] < 0.01
No 354 125
Educational status Illiterate 135 59 0.94 [0.65–1.35] 2.32 [1.04–5.26] < 0.01
Literate 418 171
Habit of eating raw vegetables Yes 426 142 2.08 [1.47–2.94] 2.65 [3.23–9.9] < 0.01
No 127 88
Age in years <= 21 179 42 2.44 [1.44–3.19] 6.48 [2.91–14.4] < 0.01
> 21 374 188

aIP=intestinal parasites

bCrude odds ratio

cAdjusted odds ratio

Discussion

The prevalence of helminthic infection was 70.6% (95% CI: 67 - 74%). This result was comparable with previous studies conduct in Uganda [17] and Venezuela [18], but higher than previous studies conducted in Ethiopia [1921], and Kenya [22]. This might be due to difference in the socio-demographic factors and lack of awareness on prevention of parasitic infection.

The current high prevalence of Ascaris lumbricoides (32.7%) is comparable with the previous study conducted in southern Ethiopia [20], Venezuela [18], and Kenya [22], but higher than studies done in western Ethiopia [21]. This difference may be due to the difference in altitude and awareness in the prevention of parasitic disease.

14.2% of pregnant women were infected with hookworm. This result was higher than studies conducted in southern Ethiopia [23], and Niger Delta regions of Nigeria [24], but lower than previously reported data in western Ethiopia [21].

The prevalence of schistosoma among pregnant women was 17.4%. This result was higher than studies conducted in Southeast Ethiopia [19, 23].

This study identified that intestinal helminth is underestimated public health problem among pregnant women and that socioeconomic factors play an important role in the establishment and spread of the infections in the communities.

Intestinal parasitic infection among pregnant women was determined by age, walking with bare foot, utilization of latrine, hand washing habit, and habit of eating raw vegetables.

Illiteracy increases the odds of intestinal parasitic infection in pregnant women by 2.32 folds higher. This result was in accordance with the previous study conducted in Kenya [25]. This might be due to the health-seeking behavior of literate pregnant women. The odds of intestinal parasitic infection were 2 folds higher in pregnant women living in the rural areas. This finding agrees with finding from south Ethiopia [23]. This is due to the reason that rural pregnant women have less access to the primary healthcare interventions. The odds of intestinal parasitic infections were 3.33 folds higher among pregnant women that didn’t have regular hand washing habit. This finding was in line with previous study conducted in Nigeria [26]. This is due to the reason that proper hand washing practices breaks the chain of transmission for intestinal parasites. Not wearing shoe increases the odds of intestinal parasitic infection by 6.87 times higher. This finding was similar to the previous study conducted in Ethiopia [21]. This is due to the reason that soil-transmitted helminth like hookworm infection will be prevented from entering the susceptible host. Ingestion of raw vegetables increases the odds of intestinal parasitic infection by 2.32 folds higher. A similar previous finding was recorded in Southeast Ethiopia [19, 27]. This is due to the reason that raw vegetables acts as vehicle for transporting intestinal parasites [2830].

Conclusion

A high prevalence of intestinal parasites was observed in pregnant women. Walking with bare foot, living in the rural area, illiteracy, age less than 21 years, the absence of proper utilization of latrine, poor hand washing practice and eating raw vegetables were associated factors with a high prevalence of intestinal parasitic infection during pregnancy. Therefore, health educations on hand wash and shoe wearing practice and improvements in sanitary infrastructure could achieve long-term and sustainable reductions in helminth prevalence among pregnant women.

Acknowledgments

We would like to acknowledge federal democratic republic of Ethiopia for financially sponsoring this research work. The funder has no role in data collection, analysis of data and interpretation of data, writing of the manuscript and decision to send the manuscript for publication. We would also like to acknowledge Mecha Woreda health office for their unreserved cooperation during data collection stage. At last but not least we would also like to acknowledge all organizations and individuals that contributed to this work.

Author contribution

BEF conceived the experiment; BEF and THJ performed the experiment, BEF plan the data collection process, BEF, and THJ analyzed and interpreted the data. BEF and THJ wrote the manuscript and approved the final draft for publication.

Funding

This research work was financially supported by the federal democratic republic of Ethiopia ministry of health. The funder has no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Abbreviation

A.lumbricoides

Ascaris lumbricoides

AOR

Adjusted odds ratio

CI

Confidence interval

COR

Crude odds ratio

ML

Milliliters

P-VALUE

Probability value

RPM

Revolution per minute

SAF

Sodium acetate- acetic acid-formalin solution

SD

Standard deviation

Competing interest

The authors declare that they have no competing interests.

Ethics approval and consent to participate

Ethical clearance was obtained from Amhara national regional state health bureau with protocol number of 314/10–2015. Permission was obtained from Mecha Woreda health office. Written informed consent was obtained from each study participants. The name was not written on the questionnaire and the confidentiality of the data was kept properly. Pregnant women with intestinal parasitic infection were referred to the nearby health center for further investigation.

Consent for publication

Not applicable.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Berhanu Elfu Feleke, Phone: +251918312095, Email: elfufeleke@gmail.com, Email: belfu@yahoo.com.

Tadesse Hailu Jember, Email: tadessehailu89@yahoo.com.

References

  • 1.Hotez PJ, Brindley PJ, Bethony JM, King CH, Pearce EJ, Jacobson J. Helminth infections: the great neglected tropical diseases. J Clin Invest. 2008;118(4):1311–1321. doi: 10.1172/JCI34261. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Hotez J, Molyneux H, Fenwick A. Control of neglected tropical diseases. N Engl J Med. 2007;357(10):1018–1027. doi: 10.1056/NEJMra064142. [DOI] [PubMed] [Google Scholar]
  • 3.WHO: Soil-transmitted helminth infections. Fact sheet In. Geneva: World health organization; 2015.
  • 4.Tada I, Otomo H, Kaneko K, Yamaguchi T. Detecting techniques of parasite eggs in feces (in Japanese, Author’s translation) Ishiyaku Pub. Inc: Tokyo; 1987. [Google Scholar]
  • 5.Mengistu A, Gebre-Selassie S, Kassa T. Prevalence of intestinal parasitic infections among urban dwellers in Southwest Ethiopia. Ethiop J Health Dev. 2007;21(1):12–17. [Google Scholar]
  • 6.Samuel F. Status of soil-transmitted helminthes infection in Ethiopia. American Journal of Health Research. 2015;3(3):170–176. doi: 10.11648/j.ajhr.20150303.21. [DOI] [Google Scholar]
  • 7.Habtamu B, Kloos H. The epidemiology and ecology of health and diseases in Ethiopia Addis Ababa. Ethiopia: Shama Books; 2006. [Google Scholar]
  • 8.Alemu M, Hailu A, Bugssa G. Prevalence of intestinal schistosomiasis and soil-transmitted helminthiasis among primary schoolchildren in Umolante district. South Ethiopia Clin Med Res. 2014;3(6):174–180. doi: 10.11648/j.cmr.20140306.14. [DOI] [Google Scholar]
  • 9.Van Eijk AM, Lindblade KA, Odhiambo F, Peterson E, Rosen DH, Karanja D, Ayisi JG, Shi YP, Adazu K, Slutsker L. Geohelminth infections among pregnant women in rural western Kenya; a cross-sectional study. PLoS Negl Trop Dis. 2009;3(1):e370. doi: 10.1371/journal.pntd.0000370. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Hotez PJ, Molyneux DH, Fenwick A, Kumaresan J, Sachs SE, Sachs JD, Savioli L. Control of neglected tropical diseases. N Engl J Med. 2007;357(10):1018–1027. doi: 10.1056/NEJMra064142. [DOI] [PubMed] [Google Scholar]
  • 11.Steketee RW. Pregnancy, nutrition and parasitic diseases. J Nutr. 2003;133(5):1661S–1667S. doi: 10.1093/jn/133.5.1661S. [DOI] [PubMed] [Google Scholar]
  • 12.Luoba AI, Wenzel Geissler P, Estambale B, Ouma JH, Alusala D, Ayah R, Mwaniki D, Magnussen P, Friis H. Earth-eating and reinfection with intestinal helminths among pregnant and lactating women in western Kenya. Tropical Med Int Health. 2005;10(3):220–227. doi: 10.1111/j.1365-3156.2004.01380.x. [DOI] [PubMed] [Google Scholar]
  • 13.Brooker S, Bethony J, Hotez PJ. Human hookworm infection in the 21st century. Adv Parasitol. 2004;58:197–288. doi: 10.1016/S0065-308X(04)58004-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Driskell JA. Nutritional AnemiaThe guidebook: nutritional Anemia. JAMA. 2008;299(22):2690–2691. doi: 10.1001/jama.299.22.2690. [DOI] [Google Scholar]
  • 15.Elliott AM, Ndibazza J, Mpairwe H, Muhangi L, Webb EL, Kizito D, Mawa P, Tweyongyere R, Muwanga M. Treatment with anthelminthics during pregnancy: what gains and what risks for the mother and child? Parasitology. 2011;138(12):1499–1507. doi: 10.1017/S0031182011001053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Institute S: Methods in Parasitology . In: Sodium acetate-acetic acid-formalin solution method for stool specimen. Basel: Swiss TPH: Swiss Tropical Institute; 2005. pp. 1–18. [Google Scholar]
  • 17.Ndibazza J, Muhangi L, Akishule D, Kiggundu M, Ameke C, Oweka J, Kizindo R, Duong T, Kleinschmidt I, Muwanga M. Effects of deworming during pregnancy on maternal and perinatal outcomes in Entebbe, Uganda: a randomized controlled trial. Clin Infect Dis. 2010;50(4):531–540. doi: 10.1086/649924. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Rodríguez-Morales AJ, Barbella RA, Case C, Arria M, Ravelo M, Perez H, Urdaneta O, Gervasio G, Rubio N, Maldonado A: Intestinal parasitic infections among pregnant women in Venezuela Infect. Dis. Obstet. Gynecol. 2006, 2006. [DOI] [PMC free article] [PubMed]
  • 19.Kefiyalew F, Zemene E, Asres Y, Gedefaw L. Anemia among pregnant women in Southeast Ethiopia: prevalence, severity and associated risk factors. BMC Research Notes. 2014;7(1):1. doi: 10.1186/1756-0500-7-771. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Tesfaye DJ, Beshir WG, Dejene T, Tewelde T: Prevalence of intestinal helminthiases and associated factors among pregnant women attending antenatal Clinic of Nigist Eleni Mohammed Memorial Hospital, Hossana, Southern Ethiopia Open Access Library Journal 2015, 2.
  • 21.Getachew M, Tafess K, Zeynudin A, Yewhalaw D: Prevalence soil transmitted helminthiasis and malaria co-infection among pregnant women and risk factors in Gilgel gibe dam area, Southwest Ethiopia BMC. Res. Notes 2013, 6(1):1. [DOI] [PMC free article] [PubMed]
  • 22.Wekesa A, Mulambalah C, Muleke C, Odhiambo R: Intestinal helminth infections in pregnant women attending antenatal clinic at Kitale District hospital, Kenya J. Parasitol. Res. 2014, 2014. [DOI] [PMC free article] [PubMed]
  • 23.Gedefaw L, Ayele A, Asres Y, Mossie A. Anaemia and associated factors among pregnant women attending antenatal care clinic in Walayita Sodo town, southern Ethiopia. Ethiopian journal of health sciences. 2015;25(2):155–164. doi: 10.4314/ejhs.v25i2.8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Green KI, Ojule JD. Helminthiasis in pregnancy in the Niger-Delta region of Nigeria. The Nigerian Health Journal. 2016;15(2):69. [Google Scholar]
  • 25.McClure EM, Meshnick SR, Mungai P, Malhotra I, King CL, Goldenberg RL, Hudgens MG, Siega-Riz AM, Dent AE. The association of parasitic infections in pregnancy and maternal and fetal anemia: a cohort study in coastal Kenya. PLoS Negl Trop Dis. 2014;8(2):e2724. doi: 10.1371/journal.pntd.0002724. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Amuta E, Houmsou R, Mker S. Knowledge and risk factors of intestinal parasitic infections among women in Makurdi, Benue state. Asian Pac J Trop Med. 2010;3(12):993–996. doi: 10.1016/S1995-7645(11)60016-3. [DOI] [Google Scholar]
  • 27.Mahande AM, Mahande MJ. Prevalence of parasitic infections and associations with pregnancy complications and outcomes in northern Tanzania: a registry-based cross-sectional study. BMC Infect Dis. 2016;16(1):1. doi: 10.1186/s12879-016-1413-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Omowaye O, Audu P. Parasites contamination and distribution on fruits and vegetables in Kogi,Nigeria. Cibtech Journal of Bio-Protocols. 2012;1(1):44–47. [Google Scholar]
  • 29.Al-Binali AM, Bello CS, El-Shewy K, Abdulla SE. The prevalence of parasites in commonly used leafy vegetables in south western Saudi Arabia. Saudi Medical Journal. 2006;27(5):613–616. [PubMed] [Google Scholar]
  • 30.Slifko TR, Smith HV, Rose JB. Emerging parasite zoonoses associated with water and food. Int J Parasitol. 2000;30(12–13):1379–1393. doi: 10.1016/S0020-7519(00)00128-4. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.


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