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Prevalence and clinical outcomes of Plasmodium falciparum and intestinal parasitic infections among children in Kiryandongo refugee camp, mid-Western Uganda: a cross sectional study



The prevalence of Plasmodium falciparum and Intestinal Parasitic Infections (IPIs) - with the corresponding pathogenesis among children remain uncertain. This study aimed at determining the prevalence and the outcomes (including anaemia) of the respective infections and co-infections. Anaemia is a condition in which the number of red blood cells transporting oxygen to the various body parts is not sufficient to meet the needs of the body.


This was a cross sectional study conducted among 476-refugee camp school children. Kato-Katz technique was used to screen stool samples for intestinal parasites. Microscopy was used for malaria testing while the portable Haemoglobin (Hb) calorimeter was used to measure haemoglobin concentration.


The overall prevalence of the mixed infections was 63.03%. Plasmodium falciparum was most prevalent of the single infections 262(55.04%) followed by Taenia spp. 14 (2.9%), Schistosoma mansoni 12(2.5%), Giardia lamblia 7 (2.9%), Trichuris trichiura 2(0.4%), Hookworm 2(0.4%) and Strongyloides stercoralis 1(0.2%). The odds of developing simple or uncomplicated malaria infection or anaemia was 14 times higher in individuals with dual co-infection with Plasmodium falciparum + Taenia sp. compared to single parasitic infection (Odds = 14.13, P = 0.019). Co-infection with Plasmodium falciparum + Taenia spp, was a strong predictor of Malaria and anaemia.


This study shows that Plasmodium falciparum and Taenia spp. co-infections is a stronger predictor of malaria and anaemia. The prevalence of malaria and anaemia remains higher than the other regions in Uganda outside restricted settlements. The findings of this study underline the need for pragmatic intervention programmes to reduce burden of the co-infections in the study area and similar settlements.

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Uganda currently hosts the highest number of refugees in the country’s history and also continues to receive simultaneous emergency influxes from South Sudan, Democratic Republic of Congo (DRC) and Burundi. The Kiryandongo refugee camp has been one of largest camps created to resettle the increasing number of Sudanese refugees in Uganda which has exceeded one million, and the daily arrival rate remains high [1, 2]. Malaria and IPIs are diseases of public health importance particularly among children in Africa. In 2015, Sub-Saharan Africa had 88% malaria cases, 90% of which were fatal [3]. According to Walldorf and others, “School-age children represent an underappreciated reservoir of malaria infection and have less exposure to antimalarial interventions” [4].

Several studies have had limited contribution of intestinal metazoan and protozoa co-infections with malaria in children [5]. Similarly, the interaction between malaria and the different intestinal parasites whenever co-infection is present is inadequately reported.

The most common diseases in the Kiryandongo refugee camp have been previously reported and remain as malaria, upper respiratory tract infections and watery diarrhoea [6]. No study had been performed in a Ugandan refugee resettlement Camp to determine the interaction between malaria and IPIs among children. This study was designed to determine the prevalence of parasitic infections and the respective disease characteristics among the children in the refugee camp.


Study area

This study was carried out from October 3, 2017 to May 10, 2018, at Kiryandongo refugee settlement camp in Kiryandongo district, Mid-Western region of Uganda, as shown in Fig. 1 [7]. The Camp is about 255.47 km along Kampala-Gulu road and is surrounded by Lake Albert and Kyoga. The population of Kiryandongo is 280,000 people according to 2014 census and the refugee camp has 52, 613 refugees [8]. The study site was chosen because it falls into a stable malaria transmission zone. Similarly, at 64.9%, the prevalence of anaemia in children aged 6–59 months indicates an increasing trend in Kiryandongo.

Target population

The primary target population were divided into two groups aged < 5 and 5–14 years as per the local Uganda Ministry of health guidelines. The secondary study population were the care takers/guardians respectively residing within the refugee resettlement camp.

Inclusion and exclusion criteria

The study included all children who provided both parental consent and assent in addition to providing blood and stool samples. Children below 3 years and above 14 years were excluded from the study.

Study design

An analytical cross-sectional study design was used to investigate the relationship between Plasmodium falciparum and intestinal parasitic co-infection of children. Eligible children aged 3–14 years were recruited and screened for malaria and intestinal parasitic infection. Parents/guardians were interviewed to provide socio-demographic information related to sanitary and malaria prevention practices.

Sample size calculations

Sample size was determined using the formula for estimating single proportion at the level of 95% confidence interval [Zα/2 = 1.96] by taking the proportion of metazoa and protozoa co-infection prevalence in the study area. However, since the prevalence of co-infection is unknown, was used 0.50 to have the largest sample size. The expected margin of error was taken to be 5% (d = 0.05). Using the formula, n = Z2 x P x (1-P)/d2. A minimum of 437 samples (n) was estimated as shown: n = Z2 P (1-P)/d2 [9]. Where, n-sample size, P- average prevalence, Z2- value at 95% CI, from table, d – expected marginal error. n = (1.96)2 × 0.5x (1–0.50) / (0.05)2 = 437. Therefore, once the minimum sample was obtained, a contingency of 8% was added for the sample size to reach 476.

Sampling strategy

Random sampling of children visiting the Panyadoli Health Centre III (HC III) based on the selection criteria was used to obtain blood film and stool sample by the law of voluntarism. Using roll numbers, random numbers were generated using Microsoft Excel 2013. This technique provided each participant with an equal chance of participating in the study. Along with sample collection, face-to-face interview of parents/guardians was conducted using a questionnaire constituting socio-demographic information. The data collection form has been included as Additional file 1.

Fig. 1.

Map of Uganda showing location of Kiryandongo District and the resettlement camp[7].

Data collection

A researcher developed structured questionnaire based on the objectives of the study, conceptual framework and guided by the literature review was used to collect data from the respondents. The data collection tool with the questionnaire has been included as Additional file 1.

Laboratory methods

The choice of diagnostic techniques was dependent on available equipment, reagents, experience of the technician and considerations of cost. The techniques used in this study for analysis of stool and blood samples included malaria microscopic examinations using Giemsa Staining technique, intestinal parasitic detection using Kato Katz and Calorimetric Hb estimation. Microscopy was used for detecting malaria because it is a gold standard putting in mind the limitation of rapid diagnostic kits (RDT) since it detects malaria antigen 4 weeks even after treatment and does not allow differentiation of malaria species.

Data management

Completed questionnaires were serialized and coded. Data was entered and cross checked for errors using Microsoft Excel 2013 before running the analysis.

Data analysis

The preliminary data was entered into Microsoft Excel 2013 and exported into STATA 14. Descriptive statistics was done to analyse the background characteristics of participants and the factors associated with Plasmodium falciparum infection, intestinal parasitic infection and co-infection. Chi-square test and Fishers Exact test was used to determine the association between the factors associated with Plasmodium falciparum and intestinal parasites. Statistical significance of the differences in the prevalence of single and co-infection with each factor was determined via Chi-square analysis and Fishers Exact test. Multivariate logistic regression analysis was used to predict the extent of the association with the different infection status as the dependent variable. The study was able to control for confounding factors during analysis by adjusting for age, sex and nutritional status, while the association between helminth and Plasmodium infections, and related outcomes was evaluated.


Table 1: Descriptive demographic characteristics of the study population (N = 476)

Table 1 above shows the socio-demographic profile of the 476 participants. Most of the study participants were refugees from the South Sudan, Uganda, DRC, Rwanda and Burundi respectively. Of the 476 participants, 364 (83.3%) wash their hands every time after using the toilet and only 73 (16.4%) participants do not wash their hands after using the toilet. 471 (98.9%) wash their hands before eating; and those who do not wash their hands before eating were 6. Most of the participant use borehole 267 (56.1%) and tap water 201 (42.3) as main sources of drinking water. 432 (90.8%) of the participants had previously been infected with malaria. 454 (95.4%) of the children had ever slept under a mosquito net.

Table 1 Descriptive demographic characteristics of the study population (N = 476)

Nutritional status assessment using mid upper arm circumference (MUAC), showed no evidence of malnutrition of 100% of children who had median MAUC of 18.8 cm. Out of the 476 children examined, 300 (63.03%) had a mono-infection, 28(5.88%) were co-infected with malaria and IPIs whereas 148 (31.09%) were not, as shown in Table 2 above. It is worth noting that the overall prevalence of parasitic infections in the study population was 63.03%, of which Plasmodium falciparum accounted for the highest prevalence 262(55.04%).

Table 2 Descriptive study related factors of the study population (N = 476)

From table 3, the most infected age group by Plasmodium falciparum was (5–14 years) with the prevalence of 55.7%. The younger age group (< 5 years) had a prevalence of 52.7% and the difference was statistically significant (P = 0.000). A total of 256 (53.8%) males and 220 (46.2%) females were enrolled in the study. Overall, 72.27% (159/220) of the females were slightly more infected with all the intestinal helminths as compared to 55.1% (141/256) of the males but this and the difference was not statistically significant (P > 0.05).

Table 3 Prevalence of Plasmodium falciparum and intestinal parasitic infection, stratified by age and sex

As shown in table 4 above, the most prominent co-infection combinations were of Plasmodium falciparum + Taenia spp. 5 (1.05%), Plasmodium falciparum + Giardia lamblia 2 (0.42%) and Plasmodium falciparum + Schistosoma mansoni 1(0.21%).

Table 4 Logistic regression analysis of interaction of Plasmodium falciparum and intestinal parasitic co-infections on malaria in the study population

The results above further indicate that the odds of developing simple or uncomplicated malaria infection was 14 times higher in individuals double infected with Plasmodium falciparum + Taenia spp. compared to single parasitic infection (Odds = 14.13, P = 0.019).

From table 5 above, the occurrence of co-infection of Plasmodium falciparum + Taenia spp. (P = 0.019, Odds = 14.13) showed a strong predictor of anaemia in the study population. No single infection was a strong predictor of anaemia.

Table 5 Logistic regression analysis predicting occurrence of anaemia in relation to parasitic infections in the study population

From table 6 above, it is evident that the highest prevalence of anaemia was among the children with no infection at 24.1%.

Table 6 Prevalence of anaemia in health children, mono-infection and co-infection in the study population


More than half of the study population tested positive for one parasite (63.03%). The results of this study are similar to the previous report in Tach Gayint, Ethiopia [10] and in the different settlements of Gabon, Central Africa [11]. Similar studies conducted in Cameroon reported higher prevalence of malaria but lower prevalence of anaemia; 64 and 31% respectively [12]. However, in their report the prevalence of anaemia was attributed to malaria [12]. Higher prevalence of anaemia (56.1%) was observed in this study among children infected with Plasmodium falciparum followed by Taenia spp. at 2.94%. However, studies conducted in North Western Uganda reported a lower prevalence of anaemia (34.4%) of children aged 1-14 years [13]. This was attributed to study setting and intervention strategies by government of Uganda. A higher prevalence of anaemia was previously reported among school children (age 6–14 years) in two Ugandan studies [14, 15].

The current finding of the higher prevalence of malaria and anaemia, is comparable to the previous report by Green et al., 2011 among children living along shores of Lake Albert and in the Islands of Lake Victoria [16]. It is necessarily so, because, in this study the most prevalent helminth was Taenia spp. (2.9%). Therefore, the current finding suggests that the co-infection of Plasmodium falciparum and Taenia spp. is a stronger predictor of anaemia. These results differ from previous reports where the prevalence of the co-infection of 22% [17]. This is perhaps because the malaria prevalence of 77% was higher than of this study conducted in a refugee settlement camp.

The high prevalence of Plasmodium falciparum reported in this study is four times higher than previously reported Mid-Western region of Uganda [18]. These discrepancies could be due to the fact that the present study was based in a refugee setting in which febrile children were enrolled, compared to the other studies. Other regional prevalence of 39.7% were reported in East Central, 33.8% in North East, 27.4% West Nile, 20.4% Central 2, 15.3% Mid Northern, 14.1% Mid-Eastern, 10.7% Central-1, 4.2% South Western and Kampala 0.4% among children under the age of five years were reported in Uganda [18]. The difference in the finding could be attributed to the study design, method used, age group and sample size. The study by Roberts and Matthews used data collected from the 2014 Malaria Indicator Survey conducted in Uganda for children under 5 years and the sample size was 10 times (N = 4939) higher compared to our sample size.

In this study, the prevalence of intestinal parasitic infection (IPIs) was 7.9%, which is lower compared to the 34.7% reported in communities around Dschang, in the West Region of Cameroon [19], 36.5% in Bushenyi district, western Uganda [20], 22.7% in Thailand [21] and 34.2% in Ethiopia [22]. These discrepancies could be attributed to the geographical differences, regular deworming campaigns by the Ministry of Health, Uganda, sanitation practices and the study sample size. This study reported 53.6% of the study population had taken anti-helminthiasis medication, 99.2% of the sources of drinking water safe and 83.3 and 98.9% children washed their hands after using a toilet and before eating respectively, which may account for the lower prevalence of IPIs.

It is important to note that low socioeconomic status, poor living conditions, insufficient knowledge and practice of correct sanitation, and limited access to safe water are known risk factors for IPIs, are also common in populations from these settlements. This argument is consistent with reports from Ethiopia (70.8% in rural area versus 5.2% in a urban city) and Rwanda (54.5% in a remote area versus 20% in a peri urban area) [11], but contrast with our findings, where most of the children had received long lasting insecticide treated mosquito nets, had safe drinking water and practice good personal hygiene and thus the observed general lower prevalence of intestinal protozoal and helminth infections. Previous studies have shown that intestinal parasitic infections were more prevalent in children aged 5–14 years and attributed to differences in exposure levels in children as they grow [23].

The prevalence of intestinal protozoa was higher than that of intestinal metazoa (1.5 vs. 0.8%), which is in contrast with some studies but in agreement with others due to the urbanization, the public investments in basic sanitation, and improvement of general living conditions, and the accessibility to health services [19, 22, 24]. The observed low prevalence of soil transmitted helminths (STHs) and intestinal protozoa could be attributed to the clean habits of washing hands before eating and after visiting the toilet among the children. This is contrary to the previous reports of higher prevalence of STHs observed among the school children due to poor hygiene practices [25].

A higher prevalence of 13.15 and 9.6% Taenia spp. were reported in studies conducted in Ghana [26] and Nigeria [27] respectively. However, this study reported a low prevalence of 2.9% Taenia spp., which is similar to reports previously published across Africa demonstrating taeniasis prevalence ranging from 0 to 8.7%, although these studies do not use a standardized diagnostic protocol [28]. This is in agreement with study conducted in Western Kenya which reported a similarly a very low prevalence of 0.02%, which lies within the previously reported range [29]. This supports the hypothesis that spatial heterogeneity in the distribution of infections may be influenced by environmental conditions, highlighting the interplay between socio-economic, behavioural and environmental factors in Taenia spp. infection risk in humans.

In this study, individuals infected with Plasmodium falciparum were significantly more likely to harbor Taenia spp. 5 (1.05%) and Schistosoma mansoni 1(0.21%) compared to individuals without malaria. The most prominent co-infection combinations were of Plasmodium falciparum + Taenia spp. 5 (1.05%), Plasmodium falciparum + Giardia lamblia 2 (0.42%) and Plasmodium falciparum + Schistosoma mansoni 1(0.21%). The factors that supported the co-infections in this study include humidity, surrounding water bodies of Lake Kyoga and Albert, bushes and poor sanitary disposal. The co-infection of Schistosoma mansoni and Plasmodium falciparum observed in this study has been previously observed [30]. The findings of this study are similar to the previous report from Uganda [31].

The current study shows that the odds of developing malaria and anaemia was 14 times higher in individuals co-infected with Plasmodium falciparum + Taenia spp. compared with single parasitic infection. The co-infection of Plasmodium falciparum + Taenia spp. showed a stronger prediction of malaria and anaemia (Odds = 14.13, P = 0.019). The reason for this co-infection leading to malaria is due to the established immunological antagonism of Th1 and Th2 for Plasmodium falciparum and Taenia control as has been reported previously in a similar study with other helminthes. Plasmodium falciparum and Taenia infections are established risk factors of anaemia. Therefore, this co-infection is expected for the observed prevalence of anaemia. Helminthiasis has been shown to significantly contribute to the problem of anaemia in studies conducted in Rwanda, Kenya and Uganda [32,33,34].

In this study, we did not find statistical relationship between single helminthes infection and anaemia (P > 0.05) possibly due to our sample size and the extremely low prevalence. This finding agrees with studies conducted in Uganda around the lake side and island communities of lake Victoria that reported declined prevalence of Schistosomiasis from 42.4 to 17.9% in 2005, while hookworm prevalence reduced from 50.9 to 10.7%, Ascariasis and Trichuriasis from 2.8 and 2.2% in 2003, to very undetectable levels in 2005 [35].


This is the first study conducted in a refugee settlement camp in Uganda, assessing the prevalence and disease characteristics of Plasmodium falciparum, intestinal metazoa and protozoa infections. Our findings show that malaria, intestinal protozoa and helminthes were more prevalent in children aged 3–14 years. Multiple infections with malaria, intestinal protozoa and helminths were common. However, the only significant association observed was between Plasmodium falciparum and Taenia spp. This co-infection constitutes an important risk to anaemia and malaria. Secondly, the co-infection impairs the immunological function of the individuals leading to other infections, as established elsewhere. The prevalence of malaria and anaemia remains higher than the other regions in Uganda outside restricted settlements. The findings of this study underline the need for pragmatic intervention programmes to reduce burden of the co-infections in the study area and similar settlements.



Giardia lamblia




Health Centre III




Intestinal Parasitic Infections


Mid Upper Arm Circumference


Plasmodium falciparum


Schistosoma mansoni


Strongyloides stercoralis


Soil Transmitted Helminths

T. spp:

Taenia spp.


Trichuris trichiura


United Nations High Commission for Refugees


  1. 1.

    UNHCR. Uganda Factsheet Kiryandongo Gap Analysis: The UN Refugee Agency. 2018.

  2. 2.

    UNHCR. UNHCR Uganda Factsheet. 2018.

  3. 3.

    World Health Organization. World malaria report. Geneva; 2016.

  4. 4.

    Walldorf JA, Cohee LM, Coalson JE, Bauleni A, Nkanaunena K, Kapito-Tembo A, et al. School-age children are a reservoir of malaria infection in Malawi. PLoS One. 2015;10:e0134061.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  5. 5.

    Degarege A, Legesse M, Medhin G, Animut A, Erko B. Malaria and related outcomes in patients with intestinal helminths: a cross-sectional study. BMC Infect Dis. 2012;12:291.

    Article  PubMed  PubMed Central  Google Scholar 

  6. 6.

    Akezi LE. Refugee health risks in northern Uganda: a case study project of Kiryangdongo refugee settlement: Bweyale Sub County, Kibanda County, Kiryangdongo District. University of York; 2014.

  7. 7.

    Uganda Bureau of Statistics. Uganda’s Sub county administrative Boundaries. Kampala, Uganda: 2014.

  8. 8.

    Uganda Bureau of Statistics. National Population and Housing Census 2014 Area Specific Profiles Kiryandongo District. Kampala, Uganda: 2017.

  9. 9.

    Kish L. Survey sampling 1965.

  10. 10.

    Chanyalew MD, Gurara MK. Malaria and intestinal parasite infections and co- infections in tach Gayint District , South Gondar zone. Sci J Public Heal. 2010;2:546–53.

    Article  Google Scholar 

  11. 11.

    M’bondoukwé NP, Kendjo E, Mawili-Mboumba DP, Koumba Lengongo JV, Offouga Mbouoronde C, Nkoghe D, et al. Prevalence of and risk factors for malaria, filariasis, and intestinal parasites as single infections or co-infections in different settlements of Gabon, Central Africa. Infect Dis Poverty. 2018;7:6.

    Article  PubMed  PubMed Central  Google Scholar 

  12. 12.

    Nkuo-Akenji TK, Chi PC, Cho JF, Ndamukong KKJ, Sumbele I. Malaria and helminths co-infection in children living in a malaria endemic setting of Mount Cameroon and predictors of Anaemia. J Parasitol. 2006;92:1191–5.

    Article  PubMed  Google Scholar 

  13. 13.

    Legason ID, Atiku A, Ssenyonga R, Olupot-Olupot P, Barugahare JB. Prevalence of Anaemia and associated risk factors among children in North-Western Uganda: a cross sectional study. BMC Hematol. 2017;17:10.

    Article  PubMed  PubMed Central  Google Scholar 

  14. 14.

    Barugahara E, Kikafunda J, Gakenia W. Prevalence and risk factors of nutritional Anaemia among female school children in Masindi District, Western Uganda. African J Food, Agric Nutr Dev. 2013;13:7679–92.

    CAS  Google Scholar 

  15. 15.

    Turyashemererwa FM, Kikafunda J, Annan R, Tumuhimbise GA. Dietary patterns, anthropometric status, prevalence and risk factors for anaemia among school children aged 5-11 years in Central Uganda. J Hum Nutr Diet. 2013;26:73–81.

    Article  PubMed  Google Scholar 

  16. 16.

    Green HK, Sousa-Figueiredo JC, BasÑez M-G, Betson M, Kabatereine NB, Fenwick A, et al. Anaemia in Ugandan preschool-aged children: the relative contribution of intestinal parasites and malaria. Parasitology. 2011;138:1534–45.

    Article  PubMed  Google Scholar 

  17. 17.

    Zeukeng F, Tchinda VHM, Bigoga JD, Seumen CHT, Ndzi ES, Abonweh G, et al. Co-infections of malaria and Geohelminthiasis in two rural communities of Nkassomo and Vian in the Mfou Health District, Cameroon. PLoS Negl Trop Dis. 2014;8:e3236.

    Article  PubMed  PubMed Central  Google Scholar 

  18. 18.

    Roberts D, Matthews G. Risk factors of malaria in children under the age of five years old in Uganda. Malar J. 2016;15:246.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  19. 19.

    Fusi-Ngwa C, Besong E, Pone JW, Mbida M. A cross-sectional study of intestinal parasitic infections in children in Ghettoed, diverse and affluent communities in Dschang, west region, Cameroon. Open Access Libr J. 2014;01:1–14.

    Article  Google Scholar 

  20. 20.

    Ntulume I, Tibyangye J, Aliero AA, Banson BJ, Zhou Z. Prevalence of intestinal protozoan infections and the associated risk factors among children in Bushenyi District, Western Uganda. Int J Trop Dis Heal. 2017;23:1–9.

    Article  Google Scholar 

  21. 21.

    Bodhidatta L, Wongstitwilairoong B, Serichantalergs O, Srijan A, Fukuda CD, MASON CJ, et al. Intestinal parasitic infections among pre-school children in Sangkhlaburi, Thailand. Am J Trop Med Hyg. 2007;76:345–50.

    Article  PubMed  Google Scholar 

  22. 22.

    Gelaw A, Anagaw B, Nigussie B, Silesh B, Yirga A, Alem M, et al. Prevalence of intestinal parasitic infections and risk factors among schoolchildren at the University of Gondar Community School, Northwest Ethiopia: a cross-sectional study. BMC Public Health. 2013;13:304.

    Article  PubMed  PubMed Central  Google Scholar 

  23. 23.

    Hélène V, Tchinda M, Ponka R, Ndzi ES, Kamdem Madocgne A, Amédée M, et al. Prevalence of malaria and soil-transmitted helminth infections and their association with undernutrition in schoolchildren residing in Mfou health district in Cameroon. J Public Heal Epidemiol. 2012;4:253–60.

    Article  Google Scholar 

  24. 24.

    Ngrenngarmlert W, Lamom C, Pasuralertsakul S, Yaicharoen R, Wongjindanon N, Sripochang S, et al. Intestinal parasitic infections among school children in Thailand. Trop Biomed. 2007;24:83–8.

    Google Scholar 

  25. 25.

    Uneke C, Eze KO, Oyibo PG, Azu NC, Ali E. Soil-transmitted helminth infection in school children in south-eastern Nigeria: the public health implication. Internet J Third World Med. 2007;4:1–10.

    Google Scholar 

  26. 26.

    Bimi L, Laar AK, Anto F. Prevalence and risk factors of Taeniasis in the Bunkpurugu-Yunyoo District of northern Ghana. J Bacteriol Parasitol. 2012;03:1000129.

    Article  Google Scholar 

  27. 27.

    Agbolade OM, Agu NC, Adesanya OO, Odejayi AO, Adigun AA, Adesanlu EB, et al. Intestinal helminthiases and schistosomiasis among school children in an urban center and some rural communities in Southwest Nigeria. Korean J Parasitol. 2007;45:233–8.

    Article  PubMed  PubMed Central  Google Scholar 

  28. 28.

    Assana E, Lightowlers MW, Zoli AP, Geerts S. Taenia solium taeniosis/cysticercosis in Africa: risk factors, epidemiology and prospects for control using vaccination. Vet Parasitol. 2013;195:14–23.

    Article  PubMed  Google Scholar 

  29. 29.

    Wardrop NA, Thomas LF, Atkinson PM, de Glanville WA, Cook EAJ, Wamae CN, et al. The influence of socio-economic, Behavioural and environmental factors on Taenia spp. transmission in Western Kenya: evidence from a cross-sectional survey in humans and pigs. PLoS Negl Trop Dis. 2015;9:e0004223.

    Article  PubMed  PubMed Central  Google Scholar 

  30. 30.

    Midzi N, Sangweme D, Zinyowera S, Mapingure MP, Brouwer KC, Munatsi A, et al. The burden of polyparasitism among primary schoolchildren in rural and farming areas in Zimbabwe. Trans R Soc Trop Med Hyg. 2008;102:1039–45.

    CAS  Article  PubMed  Google Scholar 

  31. 31.

    Shapiro AE, Tukahebwa EM, Kasten J, Clarke SE, Magnussen P, Olsen A, et al. Epidemiology of helminth infections and their relationship to clinical malaria in Southwest Uganda. Trans R Soc Trop Med Hyg. 2005;99:18–24.

    Article  PubMed  Google Scholar 

  32. 32.

    Marcelline U, Noella U, Tharcisse M, Corine K, Josephat M, Jonh Banson B. The impact of malaria and gastrointestinal helminthiasis co-infection on Anaemia and severe malaria among children in Bugesera District, Rwanda. Int J Trop Dis Heal. 2016;13:1–7.

    Article  Google Scholar 

  33. 33.

    Brooker S, Peshu N, Warn PA, Mosobo M, Guyatt HL, Marsh K, et al. The epidemiology of hookworm infection and its contribution to anaemia among pre-school children on the Kenyan coast. Trans R Soc Trop Med Hyg. 1999;93:240–6.

    CAS  Article  PubMed  Google Scholar 

  34. 34.

    Standley CJ, Adriko M, Alinaitwe M, Kazibwe F, Kabatereine NB, Stothard JR. Intestinal schistosomiasis and soil-transmitted helminthiasis in Ugandan schoolchildren: a rapid mapping assessment. Geospat Health. 2009;4:39.

    Article  PubMed  Google Scholar 

  35. 35.

    Kabatereine NB, Brooker S, Koukounari A, Kazibwe F, Tukahebwa EM, Fleming FM, et al. Impact of a national helminth control programme on infection and morbidity in Ugandan schoolchildren. Bull World Health Organ. 2007;85:91–9.

    Article  PubMed  PubMed Central  Google Scholar 

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This work forms part of PO’s Masters of Public Health dissertation at Busitema University Faculty of Health Sciences, Uganda. We thank the field and technical staff especially laboratory personnel and clinicians from the Panyadoli HC III in the refugee settlement camp for their collaboration and hard work during data collection. Sincere thanks also go to the refugee children and their parents/guardians for their participation and assistance in conducting fieldwork. Final thanks go to Mr. Amanya Geoffrey and his team at the Infectious Diseases Institute, Makerere University for the M&E role they played during the course of the project and final guidance in regards to the analysis of the data.


The study was supported by the Makerere University – Swedish International Development Agency (Mak-SIDA) Research Cooperation Fund with Public Partner Universities in Uganda. The funders only provided funds to facilitate the research approval and data collection process. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Availability of data and materials

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

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This work was collaboratively carried out. Author PO is the first author in this study right from conception, execution, data analysis and work review. Authors BJB and YG supported the supervision, manuscript writing and revision, and reading and confirmation of the final manuscript. All authors were involved in the manuscript preparation and approval of the final version submitted.

Corresponding author

Correspondence to Yahaya Gavamukulya.

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Ethics approval and consent to participate

The study was approved by the Busitema University Faculty of Health Sciences Higher Degrees and Research Committee as well as the Mbale Regional Referral Hospital Research and Ethics Committee (Ref No: MRRH-REC OUT-COM 064/2017). Permission to conduct the study was further obtained from the Office of the Prime Minister through the office of the Kiryandongo Refuge Settlement Commandant (Ref No: OPM/KIRY/010). Informed consent was attained based on the WHO guidelines. Parents/guardians whose children participated provided written parental consent while the children assented to participating in the study. Only those children who had both parental consent and their assent participated in the study.

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The authors declare that they have no competing interests.

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Additional files

Additional file 1

The developed data collection form which contains questionnaire and the associated data collection criterion used in the study. (DOCX 17 kb)

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Oboth, P., Gavamukulya, Y. & Barugahare, B.J. Prevalence and clinical outcomes of Plasmodium falciparum and intestinal parasitic infections among children in Kiryandongo refugee camp, mid-Western Uganda: a cross sectional study. BMC Infect Dis 19, 295 (2019).

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  • Malaria
  • Intestinal parasites
  • Intestinal parasitic infections
  • Coinfection
  • Anaemia
  • Children
  • Prevalence
  • Mid-Western Uganda