Skip to main content

Diarrheal diseases prevalence among children of Sudan and socio cultural risks related; systematic review and meta analysis

Abstract

It is estimated that more than 4% of the causes of inpatient deaths in 2017 were due to diarrheal diseases. The current study is aimed to provide pooled prevalence of microorganisms causing diarrhea among Sudanese as well as determine any socio-cultural risk factors associated. A systematic review of the literature was conducted and regulated in accordance to PRISMA. After abstract and full text screening Twenty-one research articles were recruited to the study. Among witch eighteen research articles determined prevalence of causative microorganisms of Diarrhea; eight research articles determining prevalence of causative microorganisms of Diarrhea were conducted in Khartoum State, five in Gezira State, two in White Nile State, one in Kordofan State while two studies were conducted in several States. Moreover, majority of studies were concerned of prevalence among children while two studies were toward general population as well as mothers of children. The pooled prevalence of viral diarrhea in less than five years old children was 22.90% [15.37, 30.43] among more than 14 thousands’ participants, the pooled prevalence of parasitic diarrhea was 31.40% [19.53, 43.27] among participants from different age groups while the pooled prevalence of bacterial diarrhea was 36.20% [14.00, 58.40]. No associated risk factors were able to be synthesized from included studies.

Peer Review reports

Introduction

Bearing in mind the political issues that have weighed down Sudan with war and enmity for the last 30 years, health care has become an afterthought and basically lost in the midst of what governments might believe to be more pressing matters. The country faces escalating humanitarian devastation, almost 8 million people facing critical problems related to mental and physical wellbeing, including more than 1.5 million internally displaced people and almost 1 million refugees. Resources are scarce, economic output is shrunken by two-thirds between 2017 and 2018 and the country's health system is unprepared to respond to growing and neglected needs. Adding insult to injury, Sudan still has a long way to go to achieve the Sustainable Development Goals (SDGs). According to the WHO as well as the Sudan Health Observatory in the federal ministry of health, the major communicable diseases contributing (SHO) to morbidity are Malaria, Tubercelosis, Schistosomiasis, Pneumonia and Diarrheal diseases [1, 2].

Diarrheal diseases and despite of the encouraging trends in the positive direction regarding water quality and good sanitation nationally in Sudan, diarrheal deaths attributable to lack of tolerable water, sanitation as well as hygiene remain a considerable challenge. In 2015, 26% of people in Sudan were reported to practice open defecation and a further 30% relied on unimproved forms of sanitation, while access to basic and safely managed drinking water was reported to be variable; ranging from 95% in Khartoum State down to 30% in North Darfur State. SHO estimated that more than 4% of the causes of inpatient deaths in 2017 were due to diarrheal diseases, specific determination causative pathogen prevalence determination is rarely conducted in Sudan as even reference hospitals in several localities are not equipped to detect and identify several microorganisms causing diarrhea [1, 2]. For research purposes; several studies investigated fecal specimens collected from children with diarrhea in Sudan; they determined varying estimates ranged from 2% up to 20% for different viral pathogens (rotavirus, norovirus, adenovirus, bocavirus), a range of 1% up to 15% for different bacterial pathogens (Shigella, E.coli, Vibrio spp, and Salmonella spp) and a range of 16% up to 35% for different parasitic pathogens [3,4,5,6,7,8].

Knowledge of causative agents that cause diarrheal disease is critical in the implementation of suitable actions to prevent and control these diseases. The current study is aimed to provide pooled prevalence of microorganisms causing diarrhea among Sudanese as well as to determine any socio-cultural risk factors associated.

Materials and methods

Search strategy

To identify relevant studies; a systematic review of the literature was conducted in the 1st of June 2022 as described in details previously [9]. The review was regulated in accordance with the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) Statement [10] (S1 Table). A comprehensive search was operated in PubMed, Embase, Google scholar, Scopus, Index Copernicus, DOAJ, EBSCO-CINAHL, Cochrane databases without language limits. To obtain a current situation evidence; only studies published in or after 2010 were included. Furthermore, all studies where the data collection process took place before 2010 were also excluded, the only exception was if the collection process started in or before 2010 and ended in 2010 or afterwards.

As medical literature in Sudan is generally scarce in international databases as well as socio-cultural factors may be differently reported, socio-cultural factors were not used in keyword formulation and their related results were later extracted from included studies, the keywords used in PubMed was as follow:

Diarrhea[Mesh] OR Gastroenteritis[Mesh] OR gastrointestinal infection[Mesh] OR enteritis[Mesh] OR dysentery[Mesh]AND Sudan*[tiab]. As previously described [11].

Moreover, to optimize our search, hand searches of reference lists of included articles were also performed.

Study selection and data extraction

Titles and abstracts were assessed for preliminary eligibility. A copy of the full text was obtained for all research articles that were available and approved in principle to be included. Abstraction of data was in accordance with the task separation method; method and result sections in each study were separately abstracted in different occasions to reduce bias. Moreover, data abstraction was conducted with no consideration of author’s qualifications or expertise. Each research article was screened for all relevant information and recorded in the data extraction file (Microsoft Excel), data from each method section was extracted using a predefined set of variables; study characteristics, type of participants, study population size, geographical region, methodology used in prevalence or risk assessment and the period of the study conduction as described in details previously [9].

After inclusion, studies were further classified into studies determining prevalence, studies determining socio-cultural risk factors and studies determining both prevalence and socio-cultural risk factors. Furthermore, as risk factors-related keywords were not formulated in the search strategy, each study was fully screened to check the nature of the risk investigated by authors, studies determining risk factors in which socio-cultural risks have not been assessed, were later excluded.

Although age grouping is available alongside their corresponding included study in (Table 1), it was not possible to be included in the Meta analysis due to the complexity and diversity of categorization of “age” variable among studies included.

Table 1 Characteristics of included studies

Assessment of quality

Each included article was evaluated based on a framework for making a summary assessment of the quality. The related published literature was crossed, then a framework was structured specifically to determine the level of representativeness of the studied population and to judge the strength of the estimates provided. Five questions were to be answered in each article, each answer represent either 1 score for yes, 0 score for No or 0 score for not available; a total score for risk of bias and quality was calculated by adding up the scores in all five domains, resulting in a score of between 0 and 5. The highest score indicates the highest quality, only studies with a score for quality greater or equal to 3 (higher quality) were included. The five domains were: is the study objective clearly defined?, is the study sample completely determined?, is the study population clearly defined and specified?, is the methodology rigorous? And is the data analysis rigorous?, as described in details previously [9].

Secondary analysis

Among all included studies reporting either prevalence or risk factor estimates, articles were crossed whether Standard Error (SE) is reported. In studies where the SE is not reported; the following formula was used to calculate it: SE = √p (1-p)/ n, where p stands for Prevalence as described in details previously [9]. Regarding risk factors, as each included study may have different objective influencing thereby their result demonstration (i.e. adjusted OR, unadjusted OR, frequencies), each individual category in a given socio-cultural variable investigated the Odd Ratio (OR) was calculated (whenever possible) to provide univariate analysis for the given category among investigated population.

Quantitative analysis

Meta-analysis was performed—whenever possible using Review Manager Software (Version 5.3). The software automatically provided the Confidence Interval (CI) according to the calculated SE, if the CI is provided in a study; it was introduced accordingly. The heterogeneity of each meta-analysis was assessed as well, the random effect was favored over the fixed effect model in all meta-analysis established as variations between studies is predicted to be probable due to the diversity of the study populations. Sensitivity analysis was also approached to determine the effect of studies conducted in populations proposed to behave in indifference manners or proposed to have low risk on the overall pooled data. Moreover, subgroup analysis was also conducted -whenever suitable to determine prevalence of specific pathogen or risk level in specific State or population. An outcome to take part in the meta-analysis has to be included in at least two studies as described in details previously [9].

Trim and Fill method was used to assess the risk of publication bias in each Meta analysis conducted [33].

Results

Studies included

A total of 450 articles were identified from the search strategy. From these, 399 articles were excluded. After abstract as well as full text screening twenty-one articles met the inclusion criteria and passed the quality assessment protocol. The articles reported prevalence among specific population and/or risk factors. (Fig. 1) illustrates the PRISMA diagram. The included articles are available in (Table 1). Assessment of the quality of included studies is depicted in (Table S2).

Fig. 1
figure 1

PRISMA flow diagram

Study characteristics

Twenty-one research articles were recruited to the study. Among witch eighteen research articles determined prevalence of causative microorganisms of Diarrhea [12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32]. The oldest were published in 2013 while the recent was published in 2022. Eight research articles determining prevalence of causative microorganisms of Diarrhea were conducted in Khartoum State, five in Gezira State, two in White Nile State, one in Kordofan State while two studies were conducted in several States. Moreover, 15 articles were conducted among both genders, while the remaining three studies did not determine the gender of their participants. Furthermore, majority of studies were concerned of prevalence among children while two studies were toward general population as well as mothers of children. All characteristics of included studies are depicted in (Table 1). Publication bias assessment indicated no major asymmetry.

Prevalence of diarrhea

Prevalence estimates were synthesized to represent the overall burden as well as to estimate subgroup burden related to causative agents, study population and geographic location –whenever possible as illustrated below, summary of prevalence estimates synthesized from Diarrhea related included studies is available in (Table 2).

Table 2 Summary of prevalence estimates synthesized from diarrhea related included studies

Prevalence of viruses causing diarrhea among children

Among the eighteen studies concerned with prevalence; eleven included studies provided viruses prevalence among participants, five studies were conducted in Khartoum State, four in Gezira State and two studies were conducted in different States representing a total sample size of 14,132 participants. The studies investigated prevalence of Rotavirus, Adenovirus, Astrovirus and Bocavirus. All studies targeted suspected children less than five years old from both gender. Only one study did not determine the gender of their participants. The pooled prevalence of viral diarrhea was 22.90% [15.37, 30.43]. Heterogeneity was high (I2 = 100%) (Fig. 2).

Fig. 2
figure 2

Meta analysis of prevalence of viral diarrhea among Sudanese children

Prevalence of rotavirus causing diarrhea among children

Six included studies provided Rotavirus prevalence among participants; studies were conducted in Khartoum, Gezira as well as different States representing a total sample size of 12,758 participants concerning suspected children from both gender. The pooled prevalence was 22.21% [9.97, 34.46]. Heterogeneity was high (I2 = 100%) (Fig. 3).

Fig. 3
figure 3

Meta analysis of prevalence of Rotavirus causing diarrhea among Sudanese children

Prevalence of parasites causing diarrhea

Five included studies provided parasites prevalence among participants, among which two studies were conducted in each of Khartoum State, as well as White Nile State while the last study participants were from Kordofan State representing a total sample size of 1,100 participants. The related articles covered E.Histolytica, G.Lambilia, G.Intestinalis, H.Nana, E.vermicularis, A.Lumbricoids, S.Mansonia, Teania spp, S.Stercoralis prevalence. Three studies concerned with children and another study was toward primary school adolescents of up to fourteen years old while one study was conducted among general population of all ages. The pooled prevalence was 31.40% [19.53, 43.27]. Heterogeneity was high (I2 = 100%) (Fig. 4).

Fig. 4
figure 4

Meta analysis of prevalence of parasite causing diarrhea among Sudanese population

Prevalence of Hymenolepis nana causing diarrhea

Three included studies provided Hymenolepis nana prevalence among participants, the related studies were conducted in Khartoum, Gezira and Kordofan States representing a total sample size of 634 participants including suspected children as well as children and adolescents of up to 16 years old from both gender. The pooled prevalence was 44.83% [-11.57, 101.24]. Heterogeneity was high (I2 = 100%).

Prevalence of Giardia and Entamoeba histolytica causing diarrhea

Five included studies provided Giardia as well as E. histolytica prevalence estimates among participants. The related studies were conducted in Khartoum, Gezira, Kordofan and White Nile States representing a total sample size of 1,350 participants. The majority of included research articles targeted suspected children as well as children and adolescents of up to 16 years old from both genders. Only one study was conducted among general population of all ages did not determine the gender of their participants. The pooled prevalence estimates were 13.86% [CI: 4.73, 22.99] and 8.82% [CI: 5.08, 12.56] for Giardia and E. histolytica, respectively. Heterogeneity was high in both Meta analysis (I2 = 100%) (Figs. 5 and 6).

Fig. 5
figure 5

Meta analysis of prevalence of E. histolytica causing diarrhea among Sudanese participants

Fig. 6
figure 6

Meta analysis of prevalence of Gardia causing diarrhea among Sudanese participants

Prevalence of bacteria causing diarrhea

Three included studies investigated bacteria causing Diarrhea prevalence among participants; all studies were conducted in Khartoum State representing a total sample size of 1,774 participants. Studies investigated prevalence estimates of Escherichia Coli, Shigella spp, Salmonella spp, Campylobacter spp, Aeromohydrophila, Morganella Morgani, Y. Enterocolitica and Non-Cholera vibrio. Two studies were conducted among suspected children from both genders while the third study was carried out among children and adults without gender determination. The pooled prevalence was 36.20% [14.00, 58.40]. Heterogeneity was high (I2 = 100%).

Prevalence of Escherichia Coli, Shigella spp and Salmonella spp causing diarrhea

Three included studies provided E.Coli, Shigellaspp and Salmonella spp prevalence estimates among participants. All studies were conducted in Khartoum State representing a total sample size of 1,774 participants. Two studies were conducted among suspected children from both genders while the third study was carried out among children and adults without gender determination. The pooled prevalence estimates were 23.52% [CI: 10.12, 36.93], 7.04% [CI: 3.84, 10.24] and 1.94% [CI: 0.66, 3.21] for E. Coli, Shigella spp and Salmonella spp, respectively. Heterogeneity was high in all Meta analysis (I2 = 100%).

Socio-cultural risk factors of diarrhea

Education

Parent’s education was investigated as a possible socio-cultural risk factor toward children Diarrhea in 2 included studies among participants from different States. Among which; 6378 parents were classified as illiterates, the pooled odd ratio of their children having diarrhea was 5.34 [0.17, 167.93] with insignificant p value z = 0.95 (P = 0.34).

Discussion

Prevalence of viral Diarrhea among children was investigated in seven States in Sudan, representing a total sample size of 14,132 participants recruited in eleven included studies; the overall pooled prevalence was 22.90% [CI:15.37, 30.43]. Moreover, prevalence of Rotaviral Diarhhea among children was investigated in seven States in Sudan, representing a total sample size of 12,758 participants recruited in seven included studies, the overall pooled prevalence was 22.21% [CI:9.97, 34.46]. This high prevalence may be due to the low level of sanitation reported previously in East African countries [34]. The pooled prevalence of diarrhea diseases among children generated from this study is considered high when compared to a study done in India (18%) [35], Egypt (19.5%) [36] and Ghana (19.2%) [37]. However, this finding is low compared to estimates concluded in India (25.2%) [38] as well as Ethiopia (23.1%) [39], this dissimilarity is possibly attributable to a difference in socio-demographic characteristics, climate, culture of stool disposal, water access, and the attitude of hand washing.

Prevalence of parasite causing Diarhhea was investigated in three States in Sudan representing a total sample size of 1,100 participants in five included studies; the overall pooled prevalence was 31.40% [CI:19.53, 43.27]. Moreover, prevalence of Hymenolepis nana was investigated in three States in Sudan representing a total sample size of 634 participants in three included studies; the overall pooled prevalence was 44.83% [CI:-11.57, 101.24]. Lower prevalence of protozoa was reported as (21.4%) [95% CI: 17.0 – 26.6] among children of northern Mozambique [40]. Moreover, studies from Nepal and Ethiopia indicated lower estimates as well (0.7%, 15.6%, respectively) [41, 42]. Nevertheless, in a recent study titled “Molecular prevalence of intestinal parasites infections in children with diarrhea in Franceville, Southeast of Gabon “ prevalence of pediatric diarrhea was concluded to be (61%) and that Hymenolepis species was the most common pathogen accounting for 31% of cases. Moreover, similar findings were reported from Burkina-Faso as well [43], Tanzania and South Africa reported higher estimates (55.6%, 68%, respectively) [44, 45]. However, the fact that some of these studies used molecular diagnostics with higher sensitivity is to be considered.

Prevalence of Giardia lamblia was investigated in four States in Sudan representing a total sample size of 1,350 participants in five included studies; the overall pooled prevalence was 13.86% [CI:4.73, 22.99]. Moreover, prevalence of Entameba. histolytica was investigated in four States in Sudan representing a total sample size of 1,350 participants in five included studies; the overall pooled prevalence was 8.82% [CI:5.08, 12.56]. However, lower as well as higher estimates have been reported for G. lamblia as (9.7%) and (17.2%) in several studies while lower E. histolytica as (0.4%) and (1%) were reported as well [40, 46, 47].

Prevalence of bacterial Diarhhea was investigated in Khartoum State representing a total sample size of 1,774 participants in three included studies; the overall pooled prevalence was 36.20%[CI:14.00, 58.40]. This finding is considered comparable to some extent of findings in United States as bacterial diarrhea was estimated to be approximately 31% of all diarrheas [48]. Moreover, prevalence of Escherichia Coli was investigated in Khartoum State representing a total sample size of 1,774 participants in three included studies; the overall pooled prevalence was 23.79%[CI:6.17, 41.41]. Furthermore, prevalence of Shigella spp. was investigated in Khartoum State representing a total sample size of 1,774 participants in three included studies; the overall pooled prevalence was 7.04% [CI:3.84, 10.24], while prevalence of Salmonella spp. was investigated in Khartoum State representing a total sample size of 1,774 participants in three included studies; the overall pooled prevalence was 1.94% [CI:0.66, 3.21]. Global estimates for the prevalence of E.coli causing diarrhea was reported as 10% to 25% which is in accordance to the findings of the current study. Moreover, pooled prevalence synthesized regarding Shigella spp as well as salmonella spp causing diarrhea is lower than estimates reported from Argentina and Djibouti as 10% and 3% for Shigella spp and Salmonella spp, respectively [49, 50].

Determining diarrheal causative pathogens to the strain level is crucial in understanding specific patterns of geographically related strain distributions [51], no study among included in the current review was found adopting typing of specific strains to better investigate the epidemiological burden of specific genotype causing diarrhea among children in Sudan.

The strengths of this review are that we systematically identified and included prevalence estimates, all studies with good quality were enrolled. Moreover, we have conducted meta-analysis to derive a pooled prevalence estimate of all included prevalence studies. Furthermore, we carried out a quality assessment of the included studies based on criteria specifically developed to determine the quality and the degree of selection bias in the studied populations.

However, several limitations are to be considered when interpreting study findings. First, gray literature evidence was not fully assessed, although all included studies are of good quality, several good studies might have been missed. Furthermore, the included studies used in the current study to determine pooled prevalence estimates adopted different approaches toward prevalence determination as molecular detection techniques [52] are not used for diagnosis purposes in Sudan. Lastly, the heterogeneity was high among the meta-analysis conducted and as consequence of the low sample size; sensitivity analysis was not able to be synthesized.

Conclusion

The pooled prevalence of viral diarrhea was 22.90% among more than 14 thousands participants; the pooled prevalence of parasitic diarrhea was 31.40% while the pooled prevalence of bacterial diarrhea was 36.20%. No associated risk factors were able to be synthesized from included studies. Further research with larger sample sizes targeting prevalence, risk factors of diarrhea, molecular detection of virulence or specific pathological determinants among Sudanese children is needed to be conducted.

Availability of data and materials

All related data are available in the manuscript.

References

  1. Federal Ministry of Health, Department of Health Information, Research & Evidence, Sudan Health Observatory [Internet]. 2021. Available from: http://www.sho.gov.sd/

  2. World Health Organization. (WHO), (n.d. a), Accessed 03–112017. Available from: http://www.who.int/maternal_child_adolescent/epidemiology/about/en.

  3. Elhag WI, Saeed HA, Omer EFE, Ali AS. Prevalence of rotavirus and adenovirus associated with diarrhea among displaced communities in Khartoum, Sudan. BMC Infect Dis. 2013;13(1).

  4. Magzoub MA, Bilal NE, Bilal JA, Osman OF. Rotavirus infection among Sudanese children younger than 5 years of age: a cross sectional hospital-based study. Pan Afr Med J. 2013;16:88.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Mustafa A, Makki A, Siddig O, Haithami S, Teleb N, Trivedi T, et al. Baseline burden of rotavirus disease in Sudan to monitor the impact of vaccination. Pediatr Infect Dis J. 2014;33(SUPPL. 1).

  6. Wang J, Xu Z, Niu P, Zhang C, Zhang J, Guan L, et al. A two-tube multiplex reverse transcription PCR assay for simultaneous detection of viral and bacterial pathogens of infectious diarrhea. Biomed Res Int. 2014;2014.

  7. Adam M, Shen H, Enan K-A, Wang H, Musa ABM, El Hussein AR, et al. Molecular survey of certain protozoan agents that cause diarrhea in children in Sudan. F1000Research. 2022;11:1401.

    Article  CAS  Google Scholar 

  8. Saeed A, Abd H, Sandstrom G. Microbial aetiology of acute diarrhoea in children under five years of age in Khartoum. Sudan J Med Microbiol. 2015;64(4):432–7.

    Article  PubMed  Google Scholar 

  9. Badawi MM, Atif MS, Mustafa YY. Systematic review and meta-analysis of HIV, HBV and HCV infection prevalence in Sudan. Virol J. 2018;15:148.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Moher D, Liberati A, Tetzlaff J, Altman DGTPG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009;6(7):e1000097.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Alebel A, Tesema C, Temesgen B, Gebrie A, Petrucka PKG. Prevalence and determinants of diarrhea among under-five children in Ethiopia: a systematic review and meta-analysis. PLoS ONE. 2018;13(6):e0199684.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Abdalla AE, Nagi AM, Elawa HE. Frequency of rotavirus infection among children with diarrhea in Omdurman pediatric hospital. Sudan Sudan J Med Sci. 2013;8(4):163–8.

    Google Scholar 

  13. Adam MA, Wang J, Enan K-A, Shen H, Wang H, El Hussein AR, et al. Molecular survey of viral and bacterial causes of childhood diarrhea in Khartoum state. Sudan Front Microbiol. 2018;9:112.

    Article  PubMed  Google Scholar 

  14. Ahmed AB, Mohammed AA, Mohammed EA, Ibrahim MEA, Elawad HE, Abdalla AE. Frequency of rotavirus infection among vaccinated and non-vaccinated children with diarrhea in Omdurman pediatric hospital. Sudan Am J Res Commun. 2015;3(3):96–107.

    Google Scholar 

  15. Algahtani FD, Elhassan NE. RISK factors of diarrhea in children less THAN 5 years of age in east Medni. Sudan Pharmacophore. 2020;11(1):85–91.

    Google Scholar 

  16. Ali MA, Kamal F, Mohamed ITE, Rahoud SAG. The impact of rotavirus vaccination on the diarrhea admission and mortality rate in children at WMTHC, Gezira state. Sudan SMU Med J. 2015;2(2):10–20.

    Google Scholar 

  17. Eisa AI, Elfaki TEM, Abdellah MA, Mohammed IA. Detection of gastrointestinal parasites among primary school children by using different parasitological techniques in rural of Kordofan state-Sudan. Int J Acad Heal Med Res. 2019;3(4):1–4.

    Google Scholar 

  18. Elmanssury A, Elnadif D, Safa A. Prevalence of diarrhea and association with socio-demographic factors among children under five in Mayo Camp-Khartoum state Sudan. Pakistan J Med Heal Sci. 2022;16(03):1100.

    Article  Google Scholar 

  19. Hassan HA, Abd Alla AB, Elfaki TEM, Saad MBEA. Frequencies of gastrointestinal parasites among students of primary school in Al Kalakla Locality, Khartoum State, Sudan: A cross-sectional study. F1000Research. 2019;8:1719.

    Article  Google Scholar 

  20. Hussein SH. Risk factors of diarrhea disease among under five in Ibrahim Malik Teaching Hospital, Khartoum state–Sudan 2017. University of Gezira; 2018.

  21. Ibrahim MBA. Prevalence of rotavirus infection among vaccinated children suffering from diarrhea in Wad Madani pediatric Teaching Hospital, Gezira state, Sudan (2014). University of Gezira; 2015.

  22. EL Imam N. Laboratory diagnosis and risk factors of gastrointestinal parasites among basic school children in greater wad Madani locality, Gezira State, Sudan (2011–2014). University of Gezira; 2014.

  23. Khogali EMI. Bacterial causes of diarrhea among some Sudanese patients–Khartoum State, Sudan. University of Gezira; 2013.

  24. Magzoub MA, Bilal NE, Bilal JA, Osman OF. Rotavirus infection among Sudanese children younger than 5 years of age: a cross sectional hospital-based study. Pan Afr Med J. 2013;16(88).

  25. Mohamed AS, Elkhidir IM, Enan KA, Mohamed HA. Detection of norovirus RNA among hospitalized children with acute gastroenteritis in Gazeera State, Sudan. Afr J Med Sci. 2019;4(12).

  26. Mohamed EE, El Hussein ARM, Mustafa MO, Elkhidir IM, Enan KA. Molecular detection of rotavirus (A and B) and astrovirus in children less than 5 years with gastroenteritis in Khartoum and Aljazeera states. Sudan IJSRSET. 2018;4(10):2394–4099.

    Google Scholar 

  27. Mohammed HY, Magboul AM, Suliman MA. Investigation of cryptosporidium species antigen by ELISA method in stool specimens obtained from patients with diarrhoea in Kosti teaching hospital, White Nile State, Sudan. Eur Acad Res. 2018;6(1).

  28. Mustafa A, Makki A, Siddig O, Haithami S, Teleb N, Trivedi T, et al. Baseline burden of rotavirus disease in Sudan to monitor the impact of vaccination. Pediatr Infect Dis J. 2014;33(Suppl 1):S23–7.

    Article  PubMed  Google Scholar 

  29. Netsereab TB, Xenos P. Factors associated with diarrhea among children less than 5 years old in Sudan: a secondary analysis of sudan multiple indicator cluster survey 2014. J Heal Res. 2017;31(Suppl. 2):S209-15 https://www.thaiscience.info/Journals/Article/JHRE/10989080.pdf.

    Google Scholar 

  30. Saeed A, Abd H, Sandstrom G. Microbial aetiology of acute diarrhoea in children under five years of age in Khartoum, Sudan. J Med Microbiol. 2015;64(4):432–7 http://www.ncbi.nlm.nih.gov/pubmed/25713206.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Subahi OB, Rahama AB, Hassan MM, Hago MA, Ahmed MA, Yassin ME. Frequency rate of rotavirus infection among vaccinated children with diarrhea in Khartoum State, Sudan. Afr J Med Sci. 2017;2(6).

  32. Tamomh AG, Agena AEM, Elamin E, Suliman MA, Elmadani M, Omara AB, et al. Prevalence of cryptosporidiosis among children with diarrhoea under five years admitted to Kosti teaching hospital, Kosti City, Sudan. BMC Infect Dis. 2021;21(1):349.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Duval S, Tweedie R. Trim and fill: a simple funnel-plot-based method of testing and adjusting for publication bias in meta-analysis. Biometrics. 2000;56(2):455–63.

    Article  CAS  PubMed  Google Scholar 

  34. Morgan C, Bowling M, Bartram J, Lyn KG. Water, sanitation, and hygiene in schools: status and implications of low coverage in Ethiopia, Kenya, Mozambique, Rwanda, Uganda, and Zambia. Int J Hyg Environ Health. 2017;220(6):950–9.

    Article  PubMed  Google Scholar 

  35. Ganguly E, Sharma PK, Bunker CH. Prevalence and risk factors of diarrhea morbidity among under-five children in India: a systematic review and META-analysis. Indian J Child Health. 2015;02(04):152–60.

    Article  Google Scholar 

  36. Yassin K. Morbidity and risk factors and diarrheal diseases among under-five children in rural upper Egypt. J Trop Pediatr. 2000;46(5):282–7.

    Article  CAS  PubMed  Google Scholar 

  37. Kwasi OB, Markku K. Childhood diarrheal morbidity in the Accra metropolitan area, Ghana: socio-economic, environmental and behavioral risk determinants childhood diarrheal morbidity in the Accra Metropolitan Area, Ghana: socio-economic, environmental and behavioral risk. J Heal Popul Dev Ctries. 2005;7(1):1–13 http://www.jhpdc.unc.edu.

    Google Scholar 

  38. Ahmed SF, Farheen A, Muzaffar A, Mattoo GM. Prevalence of diarrhoeal disease, its seasonal and age variation in under-fives in Kashmir. India Int J Health Sci (Qassim). 2008;2(2):126–33 http://www.ncbi.nlm.nih.gov/pubmed/21475494%0A.

    PubMed  Google Scholar 

  39. Workie GY, Akalu TY, Baraki AG. Environmental factors affecting childhood diarrheal disease among under-five children in Jamma district, south Wello zone, Northeast Ethiopia. BMC Infect Dis. 2019;19(1):804.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Acácio S, Mandomando I, Nhampossa T, Quintó L, Vubil D, Sacoor C, Kotloff K, Farag T, Nasrin D, Macete E, Levine MM, Alonso P, Bassat Q. Risk factors for death among children 0-59 months of age with moderate-to-severe diarrhea in Manhiça district, southern Mozambique. BMC Infect Dis. 2019;19(1):322.

  41. Firdu T, Abunna F, Girma M. Intestinal protozoal parasites in diarrheal children and associated risk factors at Yirgalem hospital, Ethiopia: a case-control study. Int Sch Res Not. 2014;2014:1–8.

    Google Scholar 

  42. Ansari S, Sherchand JB, Parajuli K, Paudyal BM, Adhikari RP, Shrestha S, et al. Pattern of acute parasitic diarrhea in children under five years of age in Kathmandu. Nepal Open J Med Microbiol. 2012;02(03):95–100.

    Article  Google Scholar 

  43. Karou SD, Sanou D, Ouermi D, Pignatelli S, Pietra V, Moret R, et al. Enteric parasites prevalence at Saint Camille medical centre in Ouagadougou, Burkina Faso. Asian Pac J Trop Med. 2011;4(5):401–3.

    Article  PubMed  Google Scholar 

  44. Ngosso BE, Nkwengulila G, Namkinga LA. Identification of pathogenic intestinal parasitic protozoa associated with diarrhea among under-fives children in Dar Es Salaam, Tanzania. Int Invent J Med Med Sci. 2015;2(4):2408 http://internationalinventjournals.org/journals/IIJMMS.

    Google Scholar 

  45. Samie A, Guerrant RL, Barrett L, Bessong PO, Igumbor EO, Obi CL. Prevalence of intestinal parasitic and bacterial pathogens in diarrhoeal and non-diarroeal human stools from Vhembe district, South Africa. J Heal Popul Nutr. 2009;27(6):739–45.

    CAS  Google Scholar 

  46. Bauhofer AFL, Cossa-Moiane ILC, Marques SDA, Guimarães ELAM, Munlela BA, Anapakala EM, et al. Intestinal protozoa in hospitalized under-five children with diarrhoea in Nampula-a cross-sectional analysis in a low-income setting in northern Mozambique. BMC Infect Dis. 2021;21(1).

  47. Tellevik MG, Moyo SJ, Blomberg B, Hjøllo T, Maselle SY, Langeland N, et al. Prevalence of Cryptosporidium parvum/hominis, Entamoeba histolytica and Giardia lamblia among young children with and without diarrhea in Dar es Salaam, Tanzania. PLoS Negl Trop Dis. 2015;9(10).

  48. Talan DA, Moran GJ, Newdow M, Ong S, Mower WR, Nakase JY, et al. Etiology of bloody diarrhea among patients presenting to United States emergency departments: prevalence of Escherichia coli O157:H7 and other enteropathogens. Clin Infect Dis. 2001;32(4):573–80.

    Article  CAS  PubMed  Google Scholar 

  49. Mikhail IA, Fox E, Haberberger RL, Ahmed MH, Abbatte EA. Epidemiology of bacterial pathogens associated with infectious diarrhea in Djibouti. J Clin Microbiol. 1990;28(5):956–61.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  50. Notario R, Borda N, Gambande T, Sutich E. Species and serovars of enteropathogenic agents associated with acute diarrheal disease in Rosario, Argentina. Rev Inst Med Trop Sao Paulo. 1996;38(1):5–7.

    Article  CAS  PubMed  Google Scholar 

  51. Ranjbar R, Bolandian M, Behzadi P. Virulotyping of Shigella Spp. isolated from pediatric patients in Tehran, Iran. Acta Microbiol Immunol Hung. 2017;64(1):71–80.

    Article  CAS  PubMed  Google Scholar 

  52. Behzadi P, Najafi A, Behzadi E, Ranjbar R. Microarray long oligo probe designing for escherichia coli: An in-silico DNA marker extraction. Central Eur J Urol. 2016;69:105–11.

    CAS  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

Not applicable.

Author information

Authors and Affiliations

Authors

Contributions

Conceptualization; BMM, methodology; SMA, IAB, IEB, MSG and BMM, Validation; BMM, SMA, formal analysis SMA, writing—original draft preparation; SMA, IAB, IEB, MSG, writing—review and editing; BMM, visualization; SMA, IAB, IEB and MSG, supervision; BMM and SMA, project administration; BMM. All authors have read and agreed to the published version of the manuscript.

Corresponding author

Correspondence to MM Badawi.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

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

Supplementary Information

Additional file 1: Table S1.

PRISMA checklist of included studies. Table S2. Quality assessment of included studies.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Badawi, M., SalahEldin, M., Idris, A. et al. Diarrheal diseases prevalence among children of Sudan and socio cultural risks related; systematic review and meta analysis. BMC Infect Dis 24, 30 (2024). https://doi.org/10.1186/s12879-023-08920-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12879-023-08920-7

Keywords