Prevalence and correlates of soil-transmitted helminths in schoolchildren aged 5 to 18 years in low- and middle-income countries: a systematic review and meta-analysis

Background: According to the Global Burden of Disease (GBD) 2019 report, up to 1.5 million disability-adjusted life years (DALYs) are lost due to soil-transmitted helminths (STHs), and 5.9 million people are at risk of acquiring STHs. Regions with the highest prevalence of STH infections include Sub-Saharan Africa, China, South America, and Asia. While there are numerous fragmented studies on STH, comprehensive information on the prevalence and geographic distribution of different species, as well as their regional variations in the context of STHs is limited. The present systematic review and meta-analysis study attempts to provide a summary of the prevalence, geographical variation, and determinants of STHs among schoolchildren aged 5 to 18 years.

Methods: An extensive literature search was carried out using PubMed, Embase, Cinhal, and Psychinfo for studies published between 1999 and 2022 that reported the rate of STH infection in school-going children aged 5–18 years. A random effects model was employed in this meta-analysis due to expected heterogeneity. Subgroup analysis was carried out based on sex and STH species because of expected geographical variation.

Results: A total of 19,725 of the 49,630 children examined were infected with STH, yielding an overall pooled prevalence of 37.16% (95% CI: 29.74–44.89). The prevalence was highest in the Western Pacific region at 50.41% (95% CI: 33.74–67.04) followed by Europe at 39.74% (95% CI: 20.40–61.0) and Africa at 37.10% (95% CI: 26.84–47.95). Ascaris lumbricoides was found to be the most prevalent helminth with a prevalence of 24.07% (95% CI: 17.07–31.83).

Conclusion: The Western Pacific region is classified as a High-risk Zone (HRZ), while Southeast Asia, Africa, Europe, and the Eastern Mediterranean are classified as moderate-risk zones (MRZs). We found a 12% reduction in the pooled prevalence of STH infection from 1999 to 2012. Ascaris lumbricoides was the predominant species among schoolchildren. Mass Drug Administration (MDA) of Albendazole tablets and improved water, sanitation, and hygiene (WASH) practices are effective in controlling and preventing STH. Ensuring their implementation and access is crucial to addressing the problem.

Systematic review registration: https://www.crd.york.ac.uk/prospero/#loginpage, CRD42022333341.

Background

Soil-transmitted helminths (STHs) are a group of neglected tropical diseases (NTDs) that affect over 1.5 billion people (24% of the world’s population) as per the World Health Organization (WHO) (1). According to the Global Burden of Disease (GBD) 2019, the reported global Disability-Adjusted Life Years (DALYs) due to STHs were as high as 1.5 million (2, 3). Additionally, approximately 5.9 billion people worldwide are at risk of acquiring STHs (4). Of the various age groups, children are the most vulnerable and at the highest risk of acquiring STH infections because of their immature immune system, tendency to play on the ground, and poor hygiene practices (5, 6). Furthermore, they are more susceptible to the pathological consequences of STH infections. More than 260 million preschool children, 654 million school-age children, and 108 million adolescent girls are estimated to live in regions where transmission of STH parasites is intense (1).

STHs are a group of parasites including Ascaris lumbricoides, Trichuris trichiura, Hookworms (Ancylostoma duodenale and Necator americanus). Infections caused by STHs have a greater impact on poor and disadvantaged communities that lack access to clean water, sanitation, and hygiene facilities in tropical and subtropical regions (7). The regions with the highest prevalence of STH infections are Sub-Saharan Africa, China, South America, and Asia (8). This is due to the fact that the life cycle of STHs requires fecal contamination of the soil, and as a result, the burden of their infection is higher in areas where hygiene practices are poor and sanitation facilities are scarce.

STHs are primarily transmitted through the feces of infected individuals, which contain eggs or larvae. Adult worms living in the gut of an infected person can produce large quantities of eggs daily, leading to contamination of the environment and food sources that lack proper sanitation (9). The tropical and sub-tropical climates in certain regions are suitable for the survival of STH eggs and larvae, as they require warm temperatures and moist soil (10, 11). In children, STH infections have profound implications, affecting their nutritional well-being, physical growth, and overall health. These infections bring about a range of issues such as gut blood loss, impaired nutrient absorption, diminished appetite, and anemia, all of which contribute to hindered cognitive development (4). Furthermore, the impact of STH infections on cognitive performance and learning abilities cannot be underestimated. Various studies have shed light on the adverse effects of these infections on children’s health, manifesting as stunted growth, anemia, malnutrition, and decreased school attendance (12, 13) and involve a loss of disability-adjusted life-years in affected children (4, 14, 15).

In 2012, the World Health Organization (WHO) released a detailed plan to address Neglected Tropical Diseases (NTDs) with the goal of eliminating them by 2020. One of the key strategies developed was the Mass Drug Administration (MDA) approach, which aimed to provide medication to at least 75% of affected individuals where STHs were present (16). The WHO subsequently set a target of STH elimination by 2030 (17). To this end, it is important to have evidence of the burden of STH, especially in low- and middle-income countries (LMICs), due to its high prevalence.

Nevertheless, numerous fragmented studies have been carried out to assess the prevalence of STHs among preschool children (PSAC) and SAC in different countries, but comprehensive data on the prevalence, geographic distribution of different species, patterns as well as regional variations among different regions of the country are lacking in the context of STHs. As a result, the current study aimed to provide a summary of the prevalence, geographical variation, species-specific prevalence, and various determinants of STHs among schoolchildren aged 5 to 18 years, which could assist the government and other relevant bodies in prioritizing and developing context-appropriate strategies to control and prevent STH infection among school-age children.

Methods

Protocols and standards

This systematic review was prospectively registered with the International Prospective Register of Systematic Reviews (Registration ID: CRD42022333341) which was registered on 13th June 2022 (18). It was conducted and reported according to the Preferred Reporting Items for Systematic Reviews and Meta-analysis (PRISMA) guidelines (19).

Eligibility criteria

Original observational studies reporting prevalence and determinants of STH, studies with a population including schoolchildren aged 5 to 18 years, conducted either in a community-based setting or primary studies from LMICs between 1999 and 2022 were included. The diagnostic methods used for STH detection (such as fecal concentration, Kato-Katz method, McMaster, and the flotac technique) were evaluated. Additionally, all included studies were published in English.

Research papers that reported the prevalence of STH among (human immunodeficiency virus, TB, malaria, and other health issues), preschool children, and students undergoing treatment were higher, thus they were excluded from the analysis, as were hospital-based prevalence studies. Additionally, systematic reviews, randomized controlled trials, and reviews were also excluded from this study.

STH infections can be affected by other health issues, especially in people with weakened immune systems, such as those with HIV. These interactions can make it difficult to understand how common STH infections are in the general population. So, this is what we are focusing on to get a clearer picture of how widespread STH infections are by themselves, without these other factors coming into play.

We also excluded preschoolers and students under treatment, focusing on untreated individuals in the general population. Hospital-based prevalence studies were excluded due to their potential bias toward severe cases. Additionally, systematic reviews, randomized controlled trials, and reviews were excluded to ensure a clear focus on primary cross-sectional studies. These decisions were made to provide a more accurate representation of the prevalence of STH infections in the general population and to streamline the analysis for the research objectives.

Information sources and search strategy

We searched the medical literature databases to make our search exclusive. A comprehensive search was carried out using the electronic databases Medline through PubMed and Embase along with Cinhal and Psychinfo. The basic search syntax comprised four main concepts: prevalence, soil-transmitted helminths, school-going children, and low- and middle-income countries. The search was conducted in Medline and PubMed using search terms such as “STH,” “Soil-Transmitted Helminth,” and “Animal helminthiases” along with medical subject heading (MeSH) terms identifying soil-transmitted Helminthes such as “helminth,” “Ascaris lumricoide,” “trichurias,” “Necator americanus,” “hookworm,” “hookworm infection.” “Trichuris trichiura,” “roundworm” and “ancyclostoma duodenale” were searched along with LMICs using the individual names of the country and “school-going children.” These relevant keywords were combined by using the Boolean operators “AND” and “OR.” However, for other databases the terms were used together with other keywords to make the search strategy more comprehensive. The search strategy was then refined to include only data from LMICs. The detailed search strategy is provided in Supplementary material S1.

Study selection, data extraction, and synthesis

The researchers combined and filtered studies from multiple databases to remove duplicates. Three reviewers (RA, JSS and SP) independently screened the articles based on their titles and abstracts, categorizing them as relevant, irrelevant, or uncertain. If all three reviewers marked an article as irrelevant, it was eliminated. The full texts of the included articles from the primary screening were then reviewed by the same three independent reviewers to determine eligibility based on the inclusion and exclusion criteria. Disagreements were resolved by consensus with the help of other reviewers (JSS, SPati, and SPalo).

Relevant data from the studies were collected using a pre-designed data extraction sheet and entered by two independent reviewers (RA and SP). Two reviewers (JSS, SPati and SPalo) checked the data for any discrepancies, with inconsistencies resolved by consensus of the entire team. If any data were unclear, the team contacted the respective authors for clarification. After determining the relevance of the articles, the full texts were downloaded for detailed review. We extracted information on the name of the first author and year of publication, study design, sex, region of study, country, laboratory method for parasite identification, total sample size, species-specific prevalence, the number of positive cases for STHs, and a quality assessment for each research paper included in this study. We have adapted the Johanna Bricks Institute (JBI) checklist to evaluate the quality of each study. Scoring was achieved by assessing specific questions related to the study, and each entity was scored accordingly. It is crucial to remember that the JBI checklist doesn’t have a comprehensive numerical scoring system and set score criteria. Rather, the emphasis is on assessing the study’s quality by determining if it satisfies the checklist’s requirements (20). The detailed grading and method adopted for quality assessment of the included research studies is presented in Supplementary material S2.

Statistical analysis

The findings were summarized as a quantitative summary of the evidence, with pooled prevalence estimates representing the quantitative summary. We used R Software version 4.2.2 for data analysis. Forest plots were used to estimate the pooled effect size and the effect of each study, along with their confidence intervals, to provide a visual summary of the data. A random effects model was employed in this meta-analysis due to expected heterogeneity. The I² statistic was used to assess the variability between studies; this statistic can take values between 0 and 100%, with high values indicative of strong heterogeneity. We anticipated high heterogeneity due to the nature of the selected studies such as nationally representative samples vs. primary studies with relatively smaller sample sizes; and age group considered in the study. Given the anticipated regional diversity and the likelihood that socioeconomic circumstances may differ considerably between studies, subgroup analysis was conducted depending on STH type and gender. The asymmetry of the funnel plot was used to detect publication bias; furthermore, quantitative assessments of the potential for publication bias were conducted using Egger’s regression and Begg’s correlation tests. Visual inspection for publication bias by plot symmetry with a p value of <0.05 was considered statistically significant (Supplementary material S3). The results of Begg’s correlation test and Egger’s regression test were found to be non-significant (p value of ˃0.05).

Patient and public involvement

We did not involve any patients or the public during the designing, conducting, reporting, or dissemination plans of our research.

Results

Literature searches and selection

Our initial search of electronic databases such as Medline via PubMed, Embase, Cinhal and Psychinfo yielded 2,626 articles, of which 2,382 records remained after removing duplications (244). Upon screening the articles, 2,299 articles were further excluded; 2,117 were irrelevant because they were of different study designs, had different outcomes, or had different study populations. A total of 23 studies were intervention studies about the sensitivity and specificity of STH diagnostics, and 159 articles were not about humans. Upon further assessment for eligibility, 7 studies that were review articles, 1 literature review and 2 case reports were excluded. After provisional screening of the title and abstract, 87 articles were included for full-text screening. Finally, 58 (21–72) published studies fulfilling the criteria were included in the final analysis (Table 1). The detailed list of included studies is given in Supplementary material S4. The PRISMA flow diagram for the selection of studies is given in Figure 1. The PRISMA checklist for this study is also given in the Supplementary material S5.

Table 1

Table 1. Pooled prevalence of STH infection by region.

Figure 1

Figure 1. PRISMA flow diagram showing the selection of studies included in this systematic review.

General characteristics of selected studies

The sample sizes of the included studies ranged from 139 (64) to 6,421 (43). A total of 48,782 children aged 5–18 were recruited for the studies. We categorized the regional distribution of our studies according to the World Health Organization’s classification of various countries into six regions. In total, 21 studies were from the African region (AFR) (21–35, 73–78), 1 study was from the American region (AMR) (36), 14 studies were from the Southeast Asia region (SER) (37–50), 4 studies were from the European region (EUR) (51–54), 9 studies were from the Eastern Mediterranean region (EMR) (55–63), and 9 studies were from the Western Pacific region (WPR) (64–72). All of our included studies were cross-sectional. The diagnostic methods used to detect STH infection in various studies include the Kato-Katz method (30), the Formol-ether concentration method (FEC) (7), the Cellophane thick smear (2), Direct microscopy (3), Formol-ether concentration with other methods (10), Direct wet mount with other methods (5), and the Kato-Katz smear with ELISA (1). A detailed description can be found in Figure 1. We assessed the quality of each study using the JBI critical appraisal tools and also reported the publication bias of the included studies using the funnel plot asymmetry in Supplementary material S2, S3.

Pooled prevalence estimates of soil-transmitted helminths and heterogeneity

Among a total of 57 studies from different regions, 49,630 school-going children (5–18 years) as study participants, the pooled prevalence and regional prevalence of STH infection were estimated. Among the total study participants, 19,725 children were found to be positive for STH infection, giving a pooled prevalence estimate of 37.16 (95% CI: 29.74–44.89) with considerable heterogeneity (χ2 = 17,346.5, p < 0.001; I² = 99.70%) (Figure 2). The prevalence of STH was 37.10% (95% CI: 26.84–47.95) in Africa, 60.20% (95% CI: 55.76–64.52) in the America, 39.60% (95% CI: 25.67–54.41) in Southeast Asia, 22.87% (9.27–40.30) in the Eastern Mediterranean, 50.41% (95% CI: 33.74–67.04) in the Western Pacific and 35.10% (10.03–65.67) in the European region (Table 1). The forest plot showing the prevalence of STH in different regions is shown in Supplementary material S6.

Figure 2

Figure 2. Pooled prevalence of STH among school-going children in LMICs.

Pooled prevalence of species-specific soil-transmitted helminths

In the species-specific estimation of the pooled prevalence of various soil-transmitted helminths, the prevalence of Ascaris lumbricoides was found to be the highest [24.07% (95% CI: 17.07–31.83)] from the fifty-one included studies. From forty four studies, the prevalence of Trichuris trichiura was found to be 16.04% (95% CI: 10.92–21.91) followed by hookworm with a prevalence of 10.20 (95% CI: 6.63–14.41). The lowest prevalence was found for Enterobius vermicularis at 5.97% (95%CI: 1.56–12.90) from ten studies (Table 2).

Table 2

Table 2. Species-specific pooled prevalence of STH infection.

Subgroup analysis based on species of soil-transmitted helminths and sex by species

Pooled prevalence estimates of Ascaris lumbricoides and heterogeneity

Fifty-one studies consisting of 38,972 school-going children reported that the pooled prevalence of Ascaris lumbricoides was 24.07% (95% CI: 17.07–31.83) with substantial heterogeneity (χ2 = 14484.92, p < 0.001; I² = 99.70%) (Supplementary material S7). The prevalence was 34.64% (95% CI: 21.16–50.0) in Southeast Asia, 28.20% (95% CI: 13.60–45.61) in Western pacific followed by 25% (95% CI: 14.70–37.0) in the African region. The detailed description is presented in Table 3.

Table 3

Table 3. Regional subgroup analysis to estimate the pooled prevalence of different soil-transmitted helminths.

Pooled prevalence estimates of hookworm and heterogeneity

Forty-four studies involving 31,496 children also reported the pooled prevalence of hookworm. Hence, the pooled prevalence of hookworm was 10.20% (6.63–14.41) with substantial heterogeneity (χ2 = 5349.50, p < 0.001; I² = 99.20%) (Supplementary material S7). The prevalence of hookworm was 13.40% (95% CI: 7.20–21.10) in Southeast Asia, 12.42% (95% CI: 5.43–21.70) in Africa, followed by 6.63% (95% CI: 1.97–13.70) in Western Pacific region (Table 3).

Pooled prevalence estimates of Trichuris trichiura and heterogeneity

Forty-four studies involving 30,536 children reported that the pooled prevalence of Trichuris trichiura was 16.04% (95% CI: 10.92–21.91) with variable heterogeneity (χ2 = 7187.60, p < 0.001; I² = 99.40%) (Supplementary material S7). The pooled prevalence of Trichuris trichiura was 36.84 (15.80–61.0) in the Western Pacific region, 10.80 (5.24–17.91) in the African region, 9.85 (9.30–10.43) in the Southeast Asia region followed by 2.21 (0.33–5.57) in the Eastern Mediterranean region (Table 3).

Subgroup analysis based on sex

The prevalence of Ascaris lumbricoides was found to be higher in male subjects 28.75% (95% CI: 21.20–37.0) compared with female subjects 28.30% (95% CI: 20.90–36.34). A detailed description can be found in Table 4.

Table 4

Table 4. Sex-specific subgroup analysis for estimation of the pooled prevalence of different soil-transmitted helminths.

Regional distribution of eligible studies and risk zones for STH infections

The highest number of studies was from the African region with 21 (36.2%) and from Southeast Asia with 14 (24.1%) studies, respectively. These were followed by the Eastern Mediterranean and Western Pacific regions with 9 studies each (15.5%). Studies from Europe and the America were 4 (6.8%) and 1 (1.72%), respectively. The Western Pacific region is classified as a High-risk Zone (HRZ) with a prevalence of 50.41% according to the WHO risk classification (79). As the America contains only one study having STH of 60%, still we cannot classify it according to WHO risk classification (79). With STH prevalence values of 39.6, 37.1, 35.1, and 22.8%, respectively, Southeast Asia, Africa, Europe, and the Eastern Mediterranean area have been defined as moderate risk zones (MRZs). None of the regions were classified as low-risk zones (LRZs) based on the study findings.

Trends of STH infection in different regions according to the included studies from 1999 to 2022

To understand the trend, the time period was divided into two groups, i.e., (i) from 1999 to 2012 and, (ii) from 2013 to 2022. We observed that the overall prevalence of STH (soil-transmitted helminth) infection decreased by 12% from 1999 to 2012, from 44.61% (with a confidence interval of 33.90 to 55.61%) to 32.61% (with a confidence interval of 22.70 to 43.40%) in the years 2013–2022. The details of the included studies and the change in trend are shown in Table 5. The regional distribution of STH infection is shown in Figure 3.

Table 5

Table 5. Subgroup analysis for pooled STH prevalence during the years 1999 to 2012 and 2013 to 2022.

Figure 3

Figure 3. Regional trends of STH infection from 1999 to 2022.

Discussion

This study aimed to assess the prevalence of soil-transmitted helminths (STH) and identify associated factors among school-aged children. The results indicate a high overall pooled prevalence of STH, estimated at approximately 37.16% [95% CI: 29.74–44.89]. Additionally, the prevalence of STH showed regional differences, with the highest rates observed in the Western Pacific region (50.41%) and the lowest in the Eastern Mediterranean region (19.86%).

Species-specific analysis revealed that Ascaris lumbricoides was the most common STH, with a prevalence of 24.07%, followed by Trichuris trichiura at 16.04%. Notably, the Western Pacific region fell into the high-risk zone (HRZ) according to the World Health Organization’s risk classification for STH, while Southeast Asia, Africa, Europe, and the Eastern Mediterranean region fell into the moderate-risk zones (MRZs).

The primary purpose of conducting a systematic review and meta-analysis of the prevalence of soil-transmitted helminth infections, particularly among school-aged children, is to gain a thorough understanding of the disease burden in LMICs. This knowledge will aid in assessing the efficacy of current control and prevention strategies in these countries to control and eliminate these important NTDs. Furthermore, this study will help determine the benefits of various strategies aimed at managing and preventing soil-transmitted helminth infections and NTDs which in turn contribute to vivid outcomes like anemia, stunting, malnutrition, and developmental delays that further affect children’s education and their future prospects. Such policies could be further strengthened by supplementing national epidemiological data to maximize the impact of these diseases. STH infection is a major health concern in LMICs, and it has a direct or indirect impact on the population’s general health due to limited resources to address the problem.

The studies included in this systematic review offer helpful data that provides a bird’s-eye view of different regions organized according to the WHO regional classification from 1999 to 2022. Organizing and spatially distributing this information has the ability to help establish an integrated approach to STH infection control and prevention which requires the utmost urgency. The overall pooled prevalence of STH infection in LMICs is estimated at approximately 37.16% which is higher than systematic reviews conducted in Ethiopia 33 and 33.4%, respectively (80, 81). Some studies conducted in the Eastern Mediterranean (9.48%) (82) and South America (27.1%) (83), reported lower rates of STH prevalence than the present study. However, studies from Sub-Saharan regions such as Nigeria reported a prevalence of about 54.8%, which is higher than this study (84). Differences in results could be due to differences in the sensitivity and specificity of the diagnostics used, and climatic conditions (such as moisture content, precipitation, and temperature). Furthermore, WASH (Water, Sanitation and Health) indicators among study participants and the number of studies completed during this period may have contributed to these discrepancies. Also, we only focused on prevalence studies that detected all cases, avoiding studies that took into account ongoing Mass Drug Administration (MDA) protocols and the provision of anthelminthic drugs to identified cases.

The WHO regional classification was used to estimate the burden of STHs. The present study revealed that STH infections were more prevalent in the Western Pacific followed by Europe and Southeast Asia regions and that they were not distributed uniformly across the globe. The majority of these STHs are exacerbated by poor living conditions, low socioeconomic levels, poor personal hygiene, and insufficient environmental sanitation. These conditions can increase the likelihood of exposure to infectious agents and could contribute to an environment conducive to disease transmission and persistence, particularly in remote and high-risk areas.

The time trend analysis showed a significant decline in the overall prevalence over time from 1999 to 2022 There are large regional variations in the trend of decline in STH cases on an annual basis. This variation could be attributed to a multitude of factors including increased awareness and adoption of hygienic practices, coordinated deworming programs at the national level, and the implementation of educational campaigns. Although the prevalence of STHs has decreased, this drop has been relatively slow at almost 10% with the prevalence falling from 44.61% in 1999–2012 to 32.61% in 2013–2022. This may be related to increasing population estimates in LMICs as well as the widespread use of a single treatment regimen for deworming, which may lead to drug-resistant strains of STHs, resulting in a slower rate of decline in the prevalence of STHs (85, 86).

Ascaris lumbricoides was found to be the most common (24.07%) form of STH in the present study. This finding is consistent with a study conducted in Sri Lanka (87), India (88), Malaysia (89), and Cuba (90), respectively where the prevalence of A. lumbricoides was found to be highest. On the other hand, higher prevalence rates were observed in Nigeria (44.6%), Rwanda (38.6%), Uganda (43.5%) (91), and Kenya (24.3%) (92) than in the present study. School-going children tend to spend their leisure time playing outdoors with sand and eating unclean food leftovers under trees with unwashed hands. This ultimately keeps them at a higher risk of exposure to the infective stage of Ascaris parasites compared to preschool children (87). Similarly, the pooled prevalence of hookworm, followed by A. lumbricoides, was 10.20%. Specifically, the prevalence found in the current study was lower than the prevalence reported in previous studies conducted in Uganda (91) and Nigeria (84) and higher than in studies conducted in Cameroon (93) and Rwanda (94). The third most common species was Trichuris trichiura with a pooled prevalence estimated at 16.04%. The results of this study show that the observed prevalence is significantly higher than in studies from Malaysia (2.7%) (95), China (2.4%) (96), and Bangladesh (10.52%) (97). The variation in species between different regions can be attributed to a multitude of factors, including environmental permissibility, geographic distribution, agricultural practices, precipitation levels, and climatic variations, among others. These factors may contribute to the prevalence of a particular species in one region over another. Interestingly, it is possible for multiple species to coexist within a single region, resulting in mixed infections in the general population.

At least 120 countries are affected by endemic STH, accounting for more than 5 million DALYs to date (98). Nonetheless, the number of DALYs caused by STH has decreased by 3.5 million as a result of the global rise in the use of preventative chemotherapy treatments for STH management, which went from 5 to 60% between 2000 and 2019. Despite continuous efforts to bring awareness and curb the incidence of new cases the countries preferably with low resource settings and urban poor are still under the vicious clutch of helminth infection. To effectively reduce STH infections, several challenges must be tackled, including the potential for anthelmintic drug resistance, inadequate diagnosis during program implementation, the limited effectiveness of existing treatments, and shortages in the pharmaceutical supply (99). To address these challenges, it is critical to develop novel STH control targets and tactics that go beyond the existing practice of delivering anthelmintic medications only to schoolchildren. This may involve creating novel diagnostic tools to detect high-risk individuals and tailoring interventions to the specific requirements of different communities.

Furthermore, encouraging responsible use of anthelmintic drugs and exploring alternative therapies that are less susceptible to resistance can aid in the fight against drug resistance. We conducted an in-depth search of numerous databases and sources to discover relevant papers on STH-infected populations. Our study offers insightful data to assist policymakers in deciding whether to strengthen or change current control and preventative measures. In order to support international efforts to eradicate STH, we selected geographic regions at high risk of STH infection that should be prioritized for MDA and other interventions. To reduce the burden of STH and other parasite diseases, it is critical to prioritize these areas and ensure the implementation of appropriate management methods. Furthermore, because there is an urgent need to enhance the accuracy of STH diagnosis and management, we advocate for large-scale research employing sensitive diagnostic methods on repeated stool samples to measure the degree of STH infection in children.

Strengths and limitations

This systematic review is a groundbreaking effort to better understand STH infection among school-aged children in low- and middle-income countries. This is the first complete assessment of the overall burden of STH infection in this population, and it takes into account regional helminth infestation prevalence, sex-specific prevalence, and age group prevalence. This systematic review includes all cross-sectional studies of STH infection in school-going children in LMICs, which is a major strength in itself. Additionally, this study sheds light on the prevalence of helminth infection in different locations, providing a more comprehensive picture of helminth occurrence. This information is critical for the creation of species-specific anti-infection targets. Our study also has certain limitations. First, the inclusion and exclusion criteria necessarily resulted in some publication and translation bias. Publication bias refers to the tendency of journals to publish positive or statistically significant results more often than negative or null findings, potentially skewing the available literature. Translation bias occurs when research from one language or region is disproportionately represented, potentially leading to cultural or regional specificity in the findings. It is critical to address the extent and potential magnitude of these biases in order to accurately assess their generalizability and reliability. Without a thorough understanding, the validity and applicability of the study findings may be compromised, ultimately affecting the ability to make informed decisions and draw accurate conclusions. Some studies that measured moderate prevalence were excluded from meta-analyses due to insufficient data on the total number of participants and/or the number of participants by sex. Several studies have used the Kato-Katz diagnostic test; however, more precise diagnostic procedures, particularly those based on multi-parallel quantitative polymerase chain reaction (qPCR), are essential for lower-prevalence settings and lower-intensity investigations (100). Despite the substantial risk of bias, this review identified all the cross-sectional studies that still offer useful information and could be more widely used in scientific research.

While we used the JBI checklist to evaluate the quality of the studies, it is clear that there is a wide range in how well these cross-sectional studies adhere to rigorous methodology. The JBI checklist does not rely on fixed scores, which means we can look at the bigger picture. After a thorough evaluation, we found that some studies closely aligned with the checklist criteria, while others fell short in important aspects. These differences in methodological quality highlight the potential for bias in the cross-sectional studies we reviewed. It is important to keep this potential bias in mind when interpreting the results and implications of this review. Despite these methodological challenges, it is worth noting that these studies still offer valuable insights, and although we need to interpret their findings carefully, they remain relevant and useful in the field of scientific research.

The overall prevalence was 37% which is still a high prevalence of STH across school-going children in LMICs. DALYs due to soil-transmitted helminthiases (STH), which are related to both the severity of the infection and the source of the disability along with nutritional deficiency and growth retardation. This decreases the quality of life in places with few resources and a high risk of transmission alongside increasing the DALY. Albendazole MDA and the WASH technique have been proven to be important controlling factors in the prevention of STH, but in retrospect, a progressive approach is needed to reduce the prevalence.

Future implications

While the administration of MDA has a major positive impact on children, there is still a scarcity of data on the completion of deworming treatment among school-going children. Incomplete administration further leads to helminthic resistance, which contributes to other health problems that will be difficult to treat in the future. Monitoring of deworming among young female children will help keep STH-induced anemia under control along with Weekly Iron Folic Acid Supplementation (WIFS). This will not only prevent anemia but also reduce complications associated with anemia in the reproductive years. Regions with high levels of helminthic infection still lack extensive longitudinal studies, which may lead to an evidence gap and hamper burden estimation. Continuous assessment of high-burden areas and rampant evaluation can provide an overview of the overall situation and help focus on preventive treatment.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding authors.

Author contributions

RA: Conceptualization, Data curation, Formal analysis, Methodology, Software, Visualization, Writing – original draft, Writing – review & editing. SwP: Conceptualization, Data curation, Formal analysis, Methodology, Software, Visualization, Writing – original draft, Writing – review & editing. JSK: Conceptualization, Data curation, Investigation, Resources, Software, Supervision, Validation, Visualization, Writing – review & editing. SK: Methodology, Supervision, Validation, Visualization, Writing – review & editing. NM: Methodology, Supervision, Validation, Visualization, Writing – review & editing. SuP: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Resources, Supervision, Visualization, Writing – review & editing. SaP: Conceptualization, Data curation, Funding acquisition, Methodology, Resources, Software, Supervision, Validation, Visualization, Writing – review & editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpubh.2024.1283054/full#supplementary-material

References

1. World Health Organization (WHO), Soil transmitted helminth infection fact sheet (2023). Available at: https://www.who.int/news-room/fact-sheets/detail/soil-transmitted-helminth-infections (Accessed February 6, 2023).

Google Scholar

2. Institute for Health Metrics and Evaluation (IHME) (2019) GBD 2019 cause and risk summary. Seattle, USA: IHME, University of Washington. (Accessed February 6, 2023).

Google Scholar

3. Incani, RN, Mughini-Gras, L, Homan, T, Sequera, I, Sequera, L, Serrano, R, et al. Risk of acquiring Ascaris lumbricoides infection in an endemically infected rural community in Venezuela. Epidemiol Infect. (2022) 150:e151. doi: 10.1017/S0950268822001273

PubMed Abstract | Crossref Full Text | Google Scholar

4. Pullan, RL, Smith, JL, Jasrasaria, R, and Brooker, SJ. Global numbers of infection and disease burden of soil transmitted helminth infections in 2010. Parasit Vectors. (2014) 7:37–9. doi: 10.1186/1756-3305-7-37

Crossref Full Text | Google Scholar

5. Hotez, PJ, Brindley, PJ, Bethony, JM, King, CH, Pearce, EJ, and Jacobson, J. Helminth infections: the great neglected tropical diseases. J Clin Invest. (2008) 118:1311–21. doi: 10.1172/JCI34261

PubMed Abstract | Crossref Full Text | Google Scholar

6. Shrestha, A, Six, J, Dahal, D, Marks, S, and Meierhofer, R. Association of nutrition, water, sanitation and hygiene practices with children’s nutritional status, intestinal parasitic infections and diarrhoea in rural Nepal: a cross-sectional study. BMC Public Health. (2020) 20:1–21. doi: 10.1186/s12889-020-09302-3

Crossref Full Text | Google Scholar

7. Moncayo, AL, Lovato, R, and Cooper, PJ. Soil-transmitted helminth infections and nutritional status in Ecuador: findings from a national survey and implications for control strategies. BMJ Open. (2018) 8:e021319. doi: 10.1136/bmjopen-2017-021319

PubMed Abstract | Crossref Full Text | Google Scholar

8. Akinsanya, B, Taiwo, A, Adedamola, M, and Okonofua, C. An investigation on the epidemiology and risk factors associated with soil-transmitted helminth infections in Ijebu east local government area, Ogun state, Nigeria. Sci Afr. (2021) 12:e00757. doi: 10.1016/j.sciaf.2021.e00757

Crossref Full Text | Google Scholar

9. Tefera, T, Biruksew, A, Mekonnen, Z, and Eshetu, T. Parasitic contamination of fruits and vegetables collected from selected local markets of Jimma town, Southwest Ethiopia. Int Sch Res Notices. (2014) 2014:1–7. doi: 10.1155/2014/382715

PubMed Abstract | Crossref Full Text | Google Scholar

10. Salam, N, and Azam, S. Prevalence and distribution of soil-transmitted helminth infections in India. BMC Public Health. (2017) 17:1–2. doi: 10.1186/s12889-017-4113-2

Crossref Full Text | Google Scholar

11. Hassan, A, and Oyebamiji, D. Intensity of soil transmitted helminths in relation to soil profile in selected public schools in Ibadan metropolis. J Epidemiol Infect Dis. (2018) 1:73–7. doi: 10.15406/jeid.2018.01.00011

Crossref Full Text | Google Scholar

12. Garrison, A, Boivin, M, Khoshnood, B, Courtin, D, Alao, J, Mireku, M, et al. Soil-transmitted helminth infection in pregnancy and long-term child neurocognitive and behavioral development: a prospective mother-child cohort in Benin. PLoS Negl Trop Dis. (2021) 15:e0009260. doi: 10.1371/journal.pntd.0009260

Crossref Full Text | Google Scholar

13. Sari, MP, Nathasaria, T, Majawati, ES, and Pangaribuan, HU. Soil-transmitted helminth infections, Anemia, and undernutrition among school-children in an elementary School in North Jakarta, Indonesia. Maj Kedokt Bandung. (2020) 52. doi: 10.15395/mkb.v52n4.2137

Crossref Full Text | Google Scholar

14. Hall, A, Hewitt, G, Tuffrey, V, and De Silva, N. A review and meta-analysis of the impact of intestinal worms on child growth and nutrition. Matern Child Nutr. (2008) 4:118–236. doi: 10.1111/j.1740-8709.2007.00127.x

PubMed Abstract | Crossref Full Text | Google Scholar

15. Östan, İ, Kilimcioğlu, AA, Girginkardeşler, N, Özyurt, BC, Limoncu, ME, and Ok, ÜZ. Health inequities: lower socio-economic conditions and higher incidences of intestinal parasites. BMC Public Health. (2007) 7:1–8. doi: 10.1186/1471-2458-7-342

Crossref Full Text | Google Scholar

16. World Health Organization; Accelerating work to overcome the global impact of neglected tropical diseases: a roadmap for implementation: executive summary. World Health Organization. (2012). Available at: https://apps.who.int/iris/handle/10665/70809 (Accessed February 6, 2023).

Google Scholar

17. World Health Organization. 2030 targets for soil-transmitted helminthiases control programmes. Available at: https://apps.who.int/iris/handle/10665/330611 (Accessed February 6, 2023).

Google Scholar

18. International Prospective register of Systematic Reviews. Available at: https://www.crd.york.ac.uk/prospero/ (Accessed February 6, 2023).

Google Scholar

19. Page, MJ, Moher, D, Bossuyt, PM, Boutron, I, Hoffmann, TC, Mulrow, CD, et al. PRISMA 2020 explanation and elaboration: updated guidance and exemplars for reporting systematic reviews. BMJ. (2021) 372:n160. doi: 10.1136/bmj.n160

Crossref Full Text | Google Scholar

20. JBI Critical Appraisal Tools. Available at: https://jbi.global/sites/default/files/2020-07/Checklist_for_Analytical_Cross_Sectional_Studies.pdf (Accessed October 20, 2023).

Google Scholar

21. Anagha, LI, Inegbenosun, CU, and Inegbenosun, H. Prevalence of intestinal helminthic infections among secondary school students in Edo state, Nigeria. Afr J Clin Exp Microbiol. (2020) 21:156–63. doi: 10.4314/ajcem.v21i2.9

Crossref Full Text | Google Scholar

22. Abe, EM, Echeta, OC, Ombugadu, A, Ajah, L, Aimankhu, PO, and Oluwole, AS. Helminthiasis among school-age children and hygiene conditions of selected schools in Lafia, Nasarawa state, Nigeria. Trop Med Infect Dis. (2019) 4:112. doi: 10.3390/tropicalmed4030112

PubMed Abstract | Crossref Full Text | Google Scholar

23. Gyang, VP, Chuang, TW, Liao, CW, Lee, YL, Akinwale, OP, Orok, A, et al. Intestinal parasitic infections: current status and associated risk factors among school aged children in an archetypal African urban slum in Nigeria. J Microbiol Immunol Infect. (2019) 52:106–13. doi: 10.1016/j.jmii.2016.09.005

Crossref Full Text | Google Scholar

24. Olopade, BO, Idowu, CO, Oyelese, AO, and Aboderin, AO. Intestinal parasites, nutritional status and cognitive function among primary school pupils in Ile-Ife, Osun state, Nigeria. Afr J Infect Dis. (2018) 12:21–8. doi: 10.21010/ajid.v12i2.4

PubMed Abstract | Crossref Full Text | Google Scholar

25. Okafor, NM, Onwuzulike, IV, Nzeukwu, CI, Irikannu, KC, Onyebueke, AC, and Nwankwo, A. Soil-transmitted helminths infection and associated risk factors among primary school pupils in Omogho and Awa communities, Anambra state, Nigeria. Int J Trop Dis Health. (2021) 42:56–64. doi: 10.9734/ijtdh/2021/v42i830478

Crossref Full Text | Google Scholar

26. Kirorei, JK, Mwinzi, P, Chelimo, K, and Ogonda, L. Epidemiology of helminths in primary school children in Kisumu municipality, Western Kenya. Int J Infect Dis. (2014) 21:298–9. doi: 10.1016/j.ijid.2014.03.1038

Crossref Full Text | Google Scholar

27. Rebollo, M, Tchuente, T, Perea, C, Polentinos, E, Bueno, A, and Sobron, B. Prevalence of soil transmitted helminthiasis on school age children in South Cameroon In: Tropical medicine & international health, vol. 16. Commerce place, 350 main st malden 02148, ma USA: Wiley Blackwell (2011). 223–3.

Google Scholar

28. Ezeagwuna, D, Okwelogu, IS, Ekejindu, IM, and Ogbuagu, C. The prevalence and socio-economic factors of intestinal helminth infections among primary school pupils in Ozubulu, Anambra state, Nigeria. Internet J Epidemiol. (2009) 9:87–91.

Google Scholar

29. Egwunyenga, OA, and Ataikiru, DP. Soil-transmitted helminthiasis among school age children in ethiope east local government area, delta state, Nigeria. Afr J Biotechnol. (2005) 4

Google Scholar

30. Eyayu, T, Yimer, G, Workineh, L, Tiruneh, T, Sema, M, Legese, B, et al. Prevalence, intensity of infection and associated risk factors of soil-transmitted helminth infections among school children at Tachgayint woreda, northcentral Ethiopia. PLoS One. (2022) 17:e0266333. doi: 10.1371/journal.pone.0266333

PubMed Abstract | Crossref Full Text | Google Scholar

31. Erismann, S, Diagbouga, S, Odermatt, P, Knoblauch, AM, Gerold, J, Shrestha, A, et al. Prevalence of intestinal parasitic infections and associated risk factors among schoolchildren in the plateau central and Centre-Ouest regions of Burkina Faso. Parasit Vectors. (2016) 9:1–4. doi: 10.1186/s13071-016-1835-4

Crossref Full Text | Google Scholar

32. Coulibaly, JT, Fürst, T, Silué, KD, Knopp, S, Hauri, D, Ouattara, M, et al. Intestinal parasitic infections in schoolchildren in different settings of Côte d’Ivoire: effect of diagnostic approach and implications for control. Parasit Vectors. (2012) 5:135. doi: 10.1186/1756-3305-5-135

Crossref Full Text | Google Scholar

33. Tomlinson, M, Adams, V, Chopra, M, Jooste, P, Strydom, E, and Dhansay, A. Survey of iodine deficiency and intestinal parasitic infections in school-going children: Bie Province, Angola. Public Health Nutr. (2010) 13:1314–8. doi: 10.1017/S1368980010000510

PubMed Abstract | Crossref Full Text | Google Scholar

34. Raso, G, Vounatsou, P, Gosoniu, L, Tanner, M, N'Goran, EK, and Utzinger, J. Risk factors and spatial patterns of hookworm infection among schoolchildren in a rural area of western Côte d'Ivoire. Int J Parasitol. (2006) 36:201–10. doi: 10.1016/j.ijpara.2005.09.003

PubMed Abstract | Crossref Full Text | Google Scholar

35. Moser, W, Labhardt, ND, Cheleboi, M, Muhairwe, J, and Keiser, J. Unexpected low soil-transmitted helminth prevalence in the Butha-Buthe district in Lesotho, results from a cross-sectional survey. Parasit Vectors. (2017) 10:1–5. doi: 10.1186/s13071-017-1995-x

Crossref Full Text | Google Scholar

36. Kaminsky, RG, Ault, SK, Castillo, P, Serrano, K, and Troya, G. High prevalence of soil-transmitted helminths in southern Belize-highlighting opportunity for control interventions. Asian Pac J Trop Biomed. (2014) 4:345–53. doi: 10.12980/APJTB.4.201414B3

PubMed Abstract | Crossref Full Text | Google Scholar

37. Pasaribu, AP, Alam, A, Sembiring, K, Pasaribu, S, and Setiabudi, D. Prevalence and risk factors of soil-transmitted helminthiasis among school children living in an agricultural area of north Sumatera, Indonesia. BMC Public Health. (2019) 19:1–8. doi: 10.1186/s12889-019-7397-6

Crossref Full Text | Google Scholar

38. Rajan, VX, Sivamani, M, and Appalaraju, BJ. Prevalence and the factors influencing soil-transmitted helminths among school age children (5–14 years age) in a rural area of Coimbatore district. Trop Parasitol. (2020) 10:74. doi: 10.4103/tp.TP_33_19

Crossref Full Text | Google Scholar

39. Nasution, RK, Nasution, BB, Lubis, M, and Lubis, IN. Prevalence and knowledge of soil-transmitted helminth infections in Mandailing Natal, north Sumatera, Indonesia. Open Access Maced J Med Sci. (2019) 7:3443–6. doi: 10.3889/oamjms.2019.441

PubMed Abstract | Crossref Full Text | Google Scholar

40. Shrestha, A, Schindler, C, Odermatt, P, Gerold, J, Erismann, S, Sharma, S, et al. Intestinal parasite infections and associated risk factors among schoolchildren in Dolakha and Ramechhap districts, Nepal: a cross-sectional study. Parasit Vectors. (2018) 11:1–5. doi: 10.1186/s13071-018-3105-0

PubMed Abstract | Crossref Full Text | Google Scholar

41. Singh, HL, Singh, NB, and Singh, YI. Helminthic infestation of the primary school-going children in Manipur. J Commun Dis. (2004) 36:111–6.

PubMed Abstract | Google Scholar

42. Sharma, M, Sapkota, J, Jha, B, Mishra, B, and Bhatt, CP. Prevalence of intestinal parasitic infestation among public school children of a community. JNMA J Nepal Med Assoc. (2020) 58. doi: 10.31729/jnma.4892

Crossref Full Text | Google Scholar

43. Ganguly, S, Barkataki, S, Karmakar, S, Sanga, P, Boopathi, K, Kanagasabai, K, et al. High prevalence of soil-transmitted helminth infections among primary school children, Uttar Pradesh, India, 2015. Infect Dis Poverty. (2017) 6:1–9. doi: 10.1186/s40249-017-0354-7

Crossref Full Text | Google Scholar

44. Ragunathan, L, Kalivaradhan, SK, Ramadass, S, Nagaraj, M, and Ramesh, K. Helminthic infections in school children in Puducherry, South India. J Microbiol Immunol Infect. (2010) 43:228–32. doi: 10.1016/S1684-1182(10)60036-9

PubMed Abstract | Crossref Full Text | Google Scholar

45. Deka, S, Barua, D, Bahurupi, Y, and Kalita, D. Assessment of the prevalence of soil-transmitted helminth infections and associated risk factors among school-aged children in a flood-affected area of Northeast India. Am J Trop Med Hyg. (2021) 105:480–9. doi: 10.4269/ajtmh.20-1238

PubMed Abstract | Crossref Full Text | Google Scholar

46. Khanal, LK, Choudhury, DR, Rai, SK, Sapkota, J, Barakoti, A, Amatya, R, et al. Prevalence of intestinal worm infestations among school children in Kathmandu, Nepal. Nepal Med Coll J. (2011) 13:272–4.

PubMed Abstract | Google Scholar

47. Atukorala, TS, and Lanerolle, P. Soil transmitted helminthic infection and its effect on nutritional status of adolescent schoolgirls of low socioeconomic status in Sri Lanka. J Trop Pediatr. (1999) 45:18–22. doi: 10.1093/tropej/45.1.18

PubMed Abstract | Crossref Full Text | Google Scholar

48. Naish, S, McCarthy, J, and Williams, GM. Prevalence, intensity and risk factors for soil-transmitted helminth infection in a south Indian fishing village. Acta Trop. (2004) 91:177–87. doi: 10.1016/j.actatropica.2004.04.004

PubMed Abstract | Crossref Full Text | Google Scholar

49. Wani, SA, Ahmad, F, Zargar, SA, Ahmad, Z, Ahmad, P, and Tak, H. Prevalence of intestinal parasites and associated risk factors among schoolchildren in Srinagar City, Kashmir, India. J Parasitol. (2007) 93:1541–3. doi: 10.1645/GE-1255.1

PubMed Abstract | Crossref Full Text | Google Scholar

50. Gupta, A, Acharya, AS, Rasania, SK, Ray, TK, and Jain, SK. Prevalence and risk factors of soil-transmitted helminth infections in school age children (6–14 years)–a cross-sectional study in an urban resettlement colony of Delhi. Indian J Public Health. (2020) 64:333–8. doi: 10.4103/ijph.IJPH_120_20

PubMed Abstract | Crossref Full Text | Google Scholar

51. Steinmann, P, Usubalieva, J, Imanalieva, C, Minbaeva, G, Stefiuk, K, Jeandron, A, et al. Rapid appraisal of human intestinal helminth infections among schoolchildren in Osh oblast, Kyrgyzstan. Acta Trop. (2010) 116:178–84. doi: 10.1016/j.actatropica.2010.06.008

PubMed Abstract | Crossref Full Text | Google Scholar

52. Ulukanligil, M, and Seyrek, A. Demographic and parasitic infection status of schoolchildren and sanitary conditions of schools in Sanliurfa, Turkey. BMC Public Health. (2003) 3:1–7. doi: 10.1186/1471-2458-3-29

Crossref Full Text | Google Scholar

53. Matthys, B, Bobieva, M, Karimova, G, Mengliboeva, Z, Jean-Richard, V, Hoimnazarova, M, et al. Prevalence and risk factors of helminths and intestinal protozoa infections among children from primary schools in western Tajikistan. Parasit Vectors. (2011) 4:1–3. doi: 10.1186/1756-3305-4-195

Crossref Full Text | Google Scholar

54. Sherkhonov, T, Yap, P, Mammadov, S, Sayfuddin, K, Martinez, P, Amoss, WP, et al. National intestinal helminth survey among schoolchildren in Tajikistan: prevalences, risk factors and perceptions. Acta Trop. 126:93–8. doi: 10.1016/j.actatropica.2013.01.013

PubMed Abstract | Crossref Full Text | Google Scholar

55. Farghly, AM, Mohamed, SM, Abdel-Rahman, SA, Mohammed, FE, El-Bahaie, ES, and El-Shafey, MA. The relation between the prevalence of soil transmitted parasites in the soil and among school children in Zagazig district, Sharkyia governorate, Egypt. J Parasit Dis. (2016) 40:1021–9. doi: 10.1007/s12639-014-0627-z

PubMed Abstract | Crossref Full Text | Google Scholar

56. Daryani, A, Sharif, M, Nasrolahei, M, Khalilian, A, Mohammadi, A, and Barzegar, G. Epidemiological survey of the prevalence of intestinal parasites among schoolchildren in Sari, northern Iran. Trans R Soc Trop Med Hyg. (2012) 106:455–9. doi: 10.1016/j.trstmh.2012.05.010

PubMed Abstract | Crossref Full Text | Google Scholar

57. Rostami, M, Tohidi, F, Sharbatkhori, M, Taherkhani, H, Eteraf, A, Mohammadi, R, et al. The prevalence of intestinal parasitic infections in primary school students in Gorgan, Iran. Med Lab J. (2012) 6:42–6.

Google Scholar

58. Taheri, F, Namakin, K, Zarban, A, and Sharifzadeh, G. Intestinal parasitic infection among school children in South Khorasan Province, Iran. J Res Health Sci. (2011) 11:45–50.

Google Scholar

59. Gabrielli, AF, Ramsan, M, Naumann, C, Tsogzolmaa, D, Bojang, B, Khoshal, MH, et al. Soil-transmitted helminths and haemoglobin status among afghan children in world food Programme assisted schools. J Helminthol. (2005) 79:381–4. doi: 10.1079/JOH2005316

PubMed Abstract | Crossref Full Text | Google Scholar

60. Rahimi, BA, Mahboobi, BA, Wafa, MH, Sahrai, MS, Stanikzai, MH, and Taylor, WR. Prevalence and associated risk factors of soil-transmitted helminth infections in Kandahar, Afghanistan. BMC Infect Dis. (2022) 22:361. doi: 10.1186/s12879-022-07336-z

PubMed Abstract | Crossref Full Text | Google Scholar

61. Ahmed, AK, Malik, B, Shaheen, B, Yasmeen, G, Dar, JB, Mona, AK, et al. Frequency of intestinal parasitic infestation in children of 5–12 years of age in Abbottabad. J Ayub Med Coll Abbottabad. (2003) 15:28–30.

Google Scholar

62. Ali, SA, Niaz, S, Aguilar-Marcelino, L, Ali, W, Ali, M, Khan, A, et al. Prevalence of Ascaris lumbricoides in contaminated faecal samples of children residing in urban areas of Lahore, Pakistan. Sci Rep. (2020) 10:21815. doi: 10.1038/s41598-020-78743-y

PubMed Abstract | Crossref Full Text | Google Scholar

63. Khan, W, Panhwar, WA, Mehmood, SA, Ahmed, S, Ahmed, MS, Khan, N, et al. Pinworm infection in school children of four districts of Malakand region, Khyber Pakhtunkhwa, Pakistan. Braz J Biol. (2021) 82:82. doi: 10.1590/1519-6984.238769

Crossref Full Text | Google Scholar

64. Jeyaprakasam, NK, and Mohamed Kamel, AG. Soil-transmitted helminthiases amongst the orang Asli (aboriginal) school children at Sungai Raba Village Gerik, Perak, Malaysia. Int Med J. (2019) 26:109–11.

Google Scholar

65. De Gier, B, Nga, TT, Winichagoon, P, Dijkhuizen, MA, Khan, NC, Van De Bor, M, et al. Species-specific associations between soil-transmitted helminths and micronutrients in Vietnamese schoolchildren. Am J Trop Med Hyg. (2016) 95:77–82. doi: 10.4269/ajtmh.15-0533

PubMed Abstract | Crossref Full Text | Google Scholar

66. Hung, BK, Van De, N, and Chai, JY. Prevalence of soil-transmitted helminths and molecular clarification of hookworm species in ethnic Ede primary schoolchildren in Dak Lak province, southern Vietnam. Korean J Parasitol. (2016) 54:471–6. doi: 10.3347/kjp.2016.54.4.471

PubMed Abstract | Crossref Full Text | Google Scholar

67. Belizario, V Jr, Chua, PL, Liwanag, HJ, Naig, JR, and Erfe, JM. Soil-transmitted helminthiases in secondary school students in selected sites in two provinces in the Philippines: policy implications. J Trop Pediatr. (2014) 60:303–7. doi: 10.1093/tropej/fmu018

PubMed Abstract | Crossref Full Text | Google Scholar

68. Liu, C, Luo, R, Yi, H, Zhang, L, Li, S, Bai, Y, et al. Soil-transmitted helminths in southwestern China: a cross-sectional study of links to cognitive ability, nutrition, and school performance among children. PLoS Negl Trop Dis. (2015) 9:e0003877. doi: 10.1371/journal.pntd.0003877

PubMed Abstract | Crossref Full Text | Google Scholar

69. Al-Mekhlafi, MS, Atiya, AS, Lim, YA, Mahdy, AK, Ariffin, WA, Abdullah, HC, et al. An unceasing problem: soil-transmitted helminthiases in rural Malaysian communities. Southeast Asian J Trop Med Public Health. (2007) 38:998–1007.

PubMed Abstract | Google Scholar

70. Lee, JD, Yen, CM, Wang, JJ, Lin, RJ, and Chung, LY. A school-based soil-transmitted helminths survey in the Guadalcanal Province, the Solomon Islands. Trop Dr. (2021) 51:167–70. doi: 10.1177/0049475520970055

Crossref Full Text | Google Scholar

71. Ahmed, A, Al-Mekhlafi, HM, Choy, SH, Ithoi, I, Al-Adhroey, AH, Abdulsalam, AM, et al. The burden of moderate-to-heavy soil-transmitted helminth infections among rural malaysian aborigines: an urgent need for an integrated control programme. Parasit Vectors. (2011) 4:1–7. doi: 10.1186/1756-3305-4-242

Crossref Full Text | Google Scholar

72. Belizario, VY Jr, Totañes, FI, de Leon, WU, Lumampao, YF, and Ciro, RN. Soil-transmitted helminth and other intestinal parasitic infections among school children in indigenous people communities in Davao del Norte, Philippines. Acta Trop. (2011) 120:S12–8. doi: 10.1016/j.actatropica.2011.02.010

PubMed Abstract | Crossref Full Text | Google Scholar

73. Hailu, GG, and Ayele, ET. Assessment of the prevalence of intestinal parasitic infections and associated habit and culture-related risk factors among primary schoolchildren in Debre Berhan town, Northeast Ethiopia. BMC Public Health. (2021) 21:1–2. doi: 10.1186/s12889-020-10148-y

Crossref Full Text | Google Scholar

74. Alemu, G, Abossie, A, and Yohannes, Z. Current status of intestinal parasitic infections and associated factors among primary school children in Birbir town, Southern Ethiopia. BMC Infect Dis. (2019) 19:1–8. doi: 10.1186/s12879-019-3879-5

Crossref Full Text | Google Scholar

75. Bello-Manga, H, Mamman, A, Suleiman, H, Olayinka, A, Musa, A, and Musa, K. Prevalence and pattern of parasitic infestations among nomadic Fulani children in a grazing reserve in northwestern Nigeria. Annals of tropical medicine and public. Health. (2017) 10:1799. doi: 10.4103/ATMPH.ATMPH_664_17

Crossref Full Text | Google Scholar

76. Ito, EE, and Egwunyenga, AO. Soil-transmitted helminthiasis in aviara community: an observation from primary school children in Nigeria. Int Med J. (2017) 24:205–8.

Google Scholar

77. Nnolim, C, Adekeye, TA, and Awobode, HO. Intestinal helminth infection and malnutrition among public primary school children in Ibadan, Nigeria. Niger J Parasitol. (2020) 41:49–55. doi: 10.4314/njpar.v41i1.8

Crossref Full Text | Google Scholar

78. Ibrahim, A, Tijani, M, and Nwuba, R. Soil transmitted helminthiasis and stunting among school-aged children in Ibadan: prevalence and risk factors. Int J Infect Dis. (2020) 101:425. doi: 10.1016/j.ijid.2020.09.1116

Crossref Full Text | Google Scholar

79. World Health Organization. (2017). Helminth control in school-age children: a guide for managers of control programmes. Available at: https://apps.who.int/iris/bitstream/handle/10665/44671/9789241548267_eng.pdf?sequence= (Accessed February 22, 2023).

Google Scholar

80. Chelkeba, L, Mekonnen, Z, Emana, D, Jimma, W, and Melaku, T. Prevalence of soil-transmitted helminths infections among preschool and school-age children in Ethiopia: a systematic review and meta-analysis. Glob Health Res Policy. (2022) 7:1–23. doi: 10.1186/s41256-022-00239-1

Crossref Full Text | Google Scholar

81. Hailegebriel, T, Nibret, E, and Munshea, A. Prevalence of soil-transmitted helminth infection among school-aged children of Ethiopia: a systematic review and meta-analysis. Infect Dis. (2020) 13:1178633720962812. doi: 10.1177/1178633720962812

Crossref Full Text | Google Scholar

82. Daryani, A, Hosseini-Teshnizi, S, Hosseini, SA, Ahmadpour, E, Sarvi, S, Amouei, A, et al. Intestinal parasitic infections in Iranian preschool and school children: a systematic review and meta-analysis. Acta Trop. (2017) 169:69–83. doi: 10.1016/j.actatropica.2017.01.019

PubMed Abstract | Crossref Full Text | Google Scholar

83. Chammartin, F, Scholte, RG, Guimarães, LH, Tanner, M, Utzinger, J, and Vounatsou, P. Soil-transmitted helminth infection in South America: a systematic review and geostatistical meta-analysis. Lancet Infect Dis. (2013) 13:507–18. doi: 10.1016/S1473-3099(13)70071-9

PubMed Abstract | Crossref Full Text | Google Scholar

84. Karshima, SN . Prevalence and distribution of soil-transmitted helminth infections in Nigerian children: a systematic review and meta-analysis. Infect Dis Poverty. (2018) 7:1, 1–4. doi: 10.1186/s40249-018-0451-2

Crossref Full Text | Google Scholar

85. Keiser, J, and Utzinger, J. Efficacy of current drugs against soil-transmitted helminth infections: systematic review and meta-analysis. JAMA. (2008) 299:1937–48. doi: 10.1001/jama.299.16.1937

PubMed Abstract | Crossref Full Text | Google Scholar

86. Levecke, B, Montresor, A, Albonico, M, Ame, SM, Behnke, JM, Bethony, JM, et al. Assessment of anthelmintic efficacy of mebendazole in school children in six countries where soil-transmitted helminths are endemic. PLoS Negl Trop Dis. (2014) 8:e3204. doi: 10.1371/journal.pntd.0003204

PubMed Abstract | Crossref Full Text | Google Scholar

87. Galgamuwa, LS, Iddawela, D, and Dharmaratne, SD. Prevalence and intensity of Ascaris lumbricoides infections in relation to undernutrition among children in a tea plantation community, Sri Lanka: a cross-sectional study. BMC Pediatr. (2018) 18:1–9. doi: 10.1186/s12887-018-0984-3

Crossref Full Text | Google Scholar

88. Traub, RJ, Robertson, ID, Irwin, P, Mencke, N, and Andrew Thompson, RC. The prevalence, intensities and risk factors associated with geohelminth infection in tea-growing communities of Assam, India. Trop Med Int Health. (2004) 9:688–701. doi: 10.1111/j.1365-3156.2004.01252.x

PubMed Abstract | Crossref Full Text | Google Scholar

89. Ngui, R, Ishak, S, Chuen, CS, Mahmud, R, and Lim, YA. Prevalence and risk factors of intestinal parasitism in rural and remote West Malaysia. PLoS Negl Trop Dis. (2011) 5:e974. doi: 10.1371/journal.pntd.0000974

Crossref Full Text | Google Scholar

90. Escobedo, AA, Cañete, R, and Núñez, FA. Prevalence, risk factors and clinical features associated with intestinal parasitic infections in children from San Juan y Martínez, Pinar del Río, Cuba. West Indian Med J. (2008) 57:377–82. doi: 10.1258/004947507782332991

PubMed Abstract | Crossref Full Text | Google Scholar

91. Ojja, S, Kisaka, S, Ediau, M, Tuhebwe, D, Kisakye, AN, Halage, AA, et al. Prevalence, intensity and factors associated with soil-transmitted helminths infections among preschool-age children in Hoima district, rural western Uganda. BMC Infect Dis. (2018) 18:1–2. doi: 10.1186/s12879-018-3289-0

Crossref Full Text | Google Scholar

92. Ngonjo, T, Okoyo, C, Andove, J, Simiyu, E, Lelo, AE, Kabiru, E, et al. Current status of soil-transmitted helminths among school children in kakamega county, western Kenya. J Parasitol Res. (2016) 2016:1–9. doi: 10.1155/2016/7680124

Crossref Full Text | Google Scholar

93. Tchuenté, L-AT, Ngassam, RIK, Sumo, L, Ngassam, P, Noumedem, CD, Nzu, DDL, et al. Mapping of schistosomiasis and soil-transmitted helminthiasis in the regions of Centre, east and West Cameroon. PLoS Negl Trop Dis. (2012) 6. doi: 10.1371/journal.pntd.0001553

Crossref Full Text | Google Scholar

94. Staudacher, O, Heimer, J, Steiner, F, Kayonga, Y, Havugimana, JM, Ignatius, R, et al. Soil-transmitted helminths in southern highland R wanda: associated factors and effectiveness of school-based preventive chemotherapy. Trop Med Int Health. (2014) 19:812–24. doi: 10.1111/tmi.12321

PubMed Abstract | Crossref Full Text | Google Scholar

95. Lim-Leroy, A, and Chua, TH. Prevalence and risk factors of geohelminthiasis among the rural village children in Kota Marudu, Sabah, Malaysia. PLoS One. (2020) 15:e0239680. doi: 10.1371/journal.pone.0239680

PubMed Abstract | Crossref Full Text | Google Scholar

96. Yang, D, Yang, Y, Wang, Y, Yang, Y, Dong, S, Chen, Y, et al. Prevalence and risk factors of Ascaris lumbricoides, Trichuris trichiura and Cryptosporidium infections in elementary school children in southwestern China: a school-based cross-sectional study. Int J Environ Res Public Health. (2018) 15:1809. doi: 10.3390/ijerph15091809

PubMed Abstract | Crossref Full Text | Google Scholar

97. Ahmed, T, Khanum, H, and Hossain, A. Prevalence of Trichuris trichiura among the children of age under five years. Bangladesh J Zool. (2013) 41:97–103. doi: 10.3329/bjz.v41i1.23303

Crossref Full Text | Google Scholar

98. Means, AR, Werkman, M, and Walson, JL. Prospects for elimination of soil-transmitted helminths. Curr Opin Infect Dis. (2017) 30:482–8. doi: 10.1097/QCO.0000000000000395

Crossref Full Text | Google Scholar

99. Freeman, MC, Akogun, O, Belizario, V Jr, Brooker, SJ, Gyorkos, TW, Imtiaz, R, et al. Challenges and opportunities for control and elimination of soil-transmitted helminth infection beyond 2020. PLoS Negl Trop Dis. (2019) 13:e0007201. doi: 10.1371/journal.pntd.0007201

PubMed Abstract | Crossref Full Text | Google Scholar

100. Easton, AV, Oliveira, RG, O’Connell, EM, Kepha, S, Mwandawiro, CS, Njenga, SM, et al. Multi-parallel qPCR provides increased sensitivity and diagnostic breadth for gastrointestinal parasites of humans: field-based inferences on the impact of mass deworming. Parasit Vectors. (2016) 9:38. doi: 10.1186/s13071-016-1314-y

PubMed Abstract | Crossref Full Text | Google Scholar

Glossary