Tinea capitis among schoolchildren in Ethiopia: A systematic review and meta analysis

Abstract

Background

Tinea capitis accounts for25 to 30% of all fungal infections, but it is often ignored because it is not life threatening in nature. It is more common among schoolchildren particularly in developing countries. Due to the presence of significant variability among the previous studies, this study was conducted to provide a pooled prevalence and associated factors of tinea capitis in Ethiopian schoolchildren.

Method

We conducted a systematic search in five major databases for articles similar to our topic. This review included school-based cross-sectional studies that were reported in English and conducted from 2006 through 2022. The data were extracted using Microsoft Excel and further analysis was done using Stata^TM Version 17.0 statistical software. Forest plots were used to assess the presence of heterogeneity with 95% confidence intervals. A random effects meta- analysis model was used to pool primary estimates. To declare the presence or absence of association, 95% confidence interval with odds ratio was used.

Results

Fourteen studies with a total of 9465 schoolchildren were included. The pooled prevalence was 29.03% (95%CI: 15.37–42.71). There was observed heterogeneity, which could be explained by publication bias (P = 0.04). Family history of tinea capitis (OR: 9.18, 95%CI: 3.5–24.02), under the age of 10 years (OR: 1.65, 95%CI: 1.17–2.33) were factors increasing the development of tinea capitis among schoolchildren and schoolchildren who had hair wash at least once a week (OR: 0.31, 95%CI: 0.24–0.42) was significantly associated with reduced risk for tinea capitis.

Conclusion

One of the most prevalent childhood health condition in Ethiopia is tinea capitis, which affects over one in every four schoolchildren. Schoolchildren who had family history of tinea capitis and under the age of 10 years were the identified risk factors but they had hair wash at least once a week was the protective factor of tinea capitis among schoolchildren. Clinical and public engagement activities are needed to overcome the burden of the disease.

Introduction

Tinea capitis is a fungal infection of the hairs on the scalp, eyelash and brows [1]. It is caused mostly by Trichophyton and Microsporum that can infect keratin, keratinized tissue, and hair [2]. It affects people of all ages, but children aged from 3 to 14 are the most affected [3,4]. It is responsible for up to 92.5% of all dermatophytoses in children under the age of ten [5,6]. It can be diagnosed clinically and using laboratory investigation. Hence, to identify tinea capitis from its differential diagnosis, clinicians used different diagnosising approach of tinae capitis like clinical (history taking and physical examination) as well as laboratory investigation (wet mount and culture). It is clinically presents as single or multiple scaly alopecia patches and alopecia patches with black dots at follicular orifices representing broken hairs, a little erythematous papule around a hair shaft on the scalp, eyebrows, or eyelashes are the most common clinical findings [7]. It can be inflammatory or non-inflammatory, with the inflammatory type causing kerion (painful pus-filled nodules) and scarring alopecia [8]. Definitive diagnosis can be made by demonstrating the presence of fungal elements via potassium hydroxide (KOH) wet mount or isolating of pathogenic fungi on appropriate media. KOH wet mount has a high sensitivity but low specificity and may be the only available technique. Addition of fluorescent brighteners such as calcofluor white may improve the demonstration of fungal elements. Fungal culture is the gold standard and has a better specificity with the added advantage of allowing for antifungals susceptibility testing, to influence the drug of choice for treatment [9]. In recent times, genomic and proteomics techniques such as polymerase chain reaction (PCR) and matrix-assisted laser desorption and ionization time of flight (MALDI-TOF) play a significant role in identifying rare etiological agents [10,11]. The most and second common agent aisolated for tinea capitis were Microsporum cani and Trichophyton rubrumin in Korea [12], Trichophyton verrucosum and T. tonsurans in Ethiopian schoolchildren respectively [13].

Tinea capitis is treated using antifungal and the drug of choice is determined by the strain of tinea, the degree of inflammation, and the patient’s immunologic and nutritional status [12]. Nowadays, antifungal resistance is increasing, making patient management more difficult [14]. To prevent this resistance, antifungal susceptibility tests, particularly for difficult-to-treat infections, should be performed to determine the best drug of choice and dosage [15]. Antifungal sensitivity tests conducted previously revealed that amphotericin was the most effective antifungal agent, followed by terbinafine and itraconazole [16,17]. It is a highly contagious disease that can transmitted from another human or an animal through direct contact and most prevalent in rural areas. Poor personal hygiene, overcrowding, under the age of 10 years, male gender, and a low socioeconomic status are all factors that contribute to the spread of the infection [1,18].

As the previous studies revealed that the prevalence of tinea capitis among schoolchildren in Ethiopia is high with significant variation and prevention and treatment efforts of the disease has not improved [19–21]. As a result, the goal of this study was to determine the pooled prevalence and associated factors of tinea capitis among schoolchildren in Ethiopia. The findings of this study may lay the scientific groundwork for a better appreciation of the updated epidemiology of Tinea capitis in Ethiopia to guide the development of effective preventive and management approach.

Research question: what is the prevalence and associated factors of tinea capitis among Ethiopian primary schoolchildren?

Condition:Tinea capitis

Context: Ethiopia

Population: Primary schoolchildren in Ethiopia

Methods

Study area

This study was carried out in Ethiopia which is organized as a Federal Democratic Republic with nine regional states (Afar, Amhara, Benishangul-Gumuz, Gambella, Harari, Oromia, Somali, Southern Nations Nationalities and People’s Region, and Tigray) and two city administrations (Addis Ababa and Dire Dawa). It covers an area of 1,100,000 km², and its regional states are divided into zones, which are further subdivided into districts, which are further subdivided into kebeles, the lowest administrative divisions [22]. Ethiopia is the second most populous country in Africa with a population of about 112 million people (56,010, 000 females and 56, 069, 000 males in 2019) [23] (Fig 1).

[Figure omitted. See PDF.]

Data source and searches

The Preferred Reporting Items for Systematic Review and Meta Analysis (PRISMA) guideline was used to report this review [24]. (S1 File). We systematically searched five major databases (PubMed/MEDLINE, CINAHL, EMBASE, Google Scholar, and Science Direct) for previous studies similar to our topic. Additionally, important articles were found by searching the reference lists of eligible studies. The search was carried out independently by three authors (MYB SSJ, and HT). Endnote X9 was used to retrieve and manage studies found through a systematic search. The following terms were used in the above-mentioned databases searches: "tinea capitis" OR "prevalence" AND "schoolchildren" OR "associated factor" AND "Ethiopia." The searching strategy was began in 28 June 2022 up to 20 July 2022.

Study selection criteria

Inclusion criteria. All studies conducted on tinea capitis among Ethiopian schoolchildren were included.

Exclusion criteria. Articles were excluded when they were not fully accessed after two email contacts with the correesponding authors.

Design: Systematic review and Meta analysis

Publication status: All published and unpublished articles

Language: English language

Screening procedure

All titles/abstracts found in electronic databases were independently screened by five authors (MYB, GMB, MD, DBK, SSJ). Disagreements were settled through discussion. Four authors (MYB, SSJ, TG, GMB) independently screened the full text of screened and included articles for title and abstract. Disagreements were settled through discussion. In the event of a disagreement, the third author (HT) was consulted.

Data extraction process and quality assessment

The data were extracted using the data extraction Cheklist prepared from a Microsoft Excel spreadsheet. To ensure consistency, three authors (MYB, SSJ, and DBK) extracted data independently using a predefined extraction checklist. After the source of the disagreements was identified, disagreements between or among authors were resolved through discussion. The prevalence of tinea capitis in schoolchildren, the study setting, region, year of publication, sample size, and the first author name were all the extracted data from the primary article during extraction.

The Newcastle-Ottawa Quality Assessment Scale (NOQAS) [25] was used to evaluate the quality of the included primary studies based on study representativeness, adequate sample size, acceptable non-response rate, use of validated measurement tool, comparability of the study, description of outcome assessment, and use of appropriate statistical tests as parameters. During the quality assesment of articles, the articles that scored seven out of ten were declared as high-quality article [26,27] (S2 File)

Outcome variable and measures

In this systematic review and meta analysis, prevalence of tinea capitis was the main outcome of interest. It was calculated by pooling the prevalence of tinea capitis among Ethiopian schoolchildren from previous studies. The second outcome of interest was associated factors of tinea capitis and measured by computing binary meta regression using random effects meta regression model with 95% confidence level and p-value < 0.05.

Data management and synthesis

The extracted data were exported to Stata^TM Version 17.0 software for further analysis. The metaprop stata command was used to compute the pooled estimate. Using a binominal distribution assumption, the standard errors were calculated from the reported estimates and population denominators.The presence of heterogeneity between studies was checked using Cochran’s-Q test and quantified using I-square statistics and significant heterogeneity was found. Thus, a random-effect model based on DerSimonian and Laird was used to estimate the effect size [28]. Accordingly, heterogeneity was classified as low, moderate, or high when the values of I-square were 25, 50, and 75%, respectively [19]. Additionally, the dispersion of individual results in the forest plot was also used to evaluate the presence of heterogeneity visually. Egger’s linear regression test at a p-value < 0.05 was used to assess the presence of publication bias [20]. A 95% confidence interval was used to calculate and report an overall synthesised measure of effect size.To identify the possible sources of heterogeneity, additional statistical analyses such as subgroup analyses, publication bias, and meta-regression were performed. We conducted a subgroup analysis using geographical regions, the study setting (urban Vs rural), sample size (above mean Vs below the mean), and study period(before 2015 Vs after 2015). Finally, the results were presented in tables and forest plots.

Patient and public involvement statement

Patients were not directly involved in the study, only previously conducted studies were employed. Hence, new study participants were not recruited and participants were not involved in the dissemination of findings.

Results

Search results

A total of 1073 studies were found through electronic and other searches (like organizational records and websites) on PubMed/ MEDLINE, CINAHL, EMBASE, Google Scholar, and Science Direct. About 824 articles were excluded due to duplication, 191 articles were excluded due to different in study setting/context [29–32], 33 articles were excluded due to different in interest of outcome [33–38], and 11 articles were excluded due to different in study population [39–41]. Finally, 14 cross-sectional studies were identified to be included in the current systematic review and meta-analysis (Fig 2).

[Figure omitted. See PDF.]

Characteristics of included studies

About 14 studies qualified for inclusion and analysis with a total of 9465 primary schoolchildren in Ethiopia.This meta-analysis and systematic review included three regions and one city administration. Among them were the Amhara region (n = 4) [20,42–44], the Oromia region (n = 4) [13,19,45,46], the SNNPR (n = 3) [21,47,48], and Addis Ababa (n = 3) [49–51]. About 5 studies out of the total included studies identified the causative agent of tinea capitis, T. violaceum, and the rest did not identify the species. Five of the included studies used culture to diagnosis and identify the species, while the others used clinical and KOH to diagnose and identify the causative agent. The study with the smallest and largest sample sizes, 288 and 1869, both conducted in the SNNPR’s Hawassa and Wolita zone, respectively, followed by a study with a sample size of 1122 in Merkato, Addis Ababa’s administrative city (Table 1).

[Figure omitted. See PDF.]

The pooled prevalence of tinea capitis

In Ethiopia, the prevalence of tinea capitis among primary schoolchildren was 29.03% (95%CI: 17.63–40.42). When we looked at it by region, Addis Ababa city administration had the highest prevalence of tinea capitis at 58.57 percent, followed by the southern nation and nationality of people at 39.87 percent, and Oromia regional state had the lowest prevalence at 12.68 percent (Fig 3).

[Figure omitted. See PDF.]

Subgroup meta–analysis

It was computed using study setting, region, sampling method, sample size, and study period. It was discovered that there were no identified sources of heterogeneity identified using subgroup analysis despite the presence of strong evidence supporting the existence of heterogeneity (means study setting I² = 99.6 with p-value 0.0001 (Fig 4), region I² = 99.6 with p-value 0.001, sampling method I² = 99.6, and publication year I² = 99.6 with p-value 0.0001(Fig 5), sample size I² = 99.8 with p-value 0.0001) (Fig 6).

[Figure omitted. See PDF.]

[Figure omitted. See PDF.]

[Figure omitted. See PDF.]

Meta-regression

The publication year and sample size were used as covariates in random-effects meta-regression. The analysis revealed that sample size (p = 0.603) and publication year (p = 0.440) had no effect on heterogeneity (Table 2).

[Figure omitted. See PDF.]

Publication bias (Bias detection)

A funnel plot was used to determine the presence or absence of publication bias, and the scatter plots were asymmetrical, indicating that the small-study had effects on the heterogeneity of tinea capitis prevalence among Ethiopian primary schoolchildren (Fig 7), and contour-enhanced funnel plots were used to see if the plot asymmetry could be attributed to publication bias, and the contours show the p-value level where there is strong evidence for the presence of publication bias (Fig 8). In addition to contour-enhanced funnel plots, the egger linear regression test was used to objectively assess the presence or absence of publication bias. As a result, there was statistically significant publication bias (P = 0.040) (Table 3).

[Figure omitted. See PDF.]

[Figure omitted. See PDF.]

[Figure omitted. See PDF.]

Factors associated with tinea capitis

Factors associated with tinea capitis in schoolchildren was determined based on sex (including five studies) [19,47,48,50,51], age (including four studies) [19,42,47,48], frequency of shower(including three studies) [42,46,47], frequency of hair wash(including two studies) [42,47], sharing of combs(including four studies) [20,44,46,47], and family history of tinea capitis(including three studies) [20,42,48]. As a result tinea capitis was associated with age, family history of tinea capitis, and weekly hair washing practice.

Being male had a 1.09 (95% CI: 0.56, 2.13), taking shower atleast once a week had a 0.69 (95% CI: 0.45–1.06), and sharing of comb had a 1.89 (95% CI: 0.59–6.06) times larger chance of experiencing tinea capitis than their corresponding counterparts. However, these differences were not statistically significant.

The odds of tinea capitis among those schoolchildren who were under the age of 10 years were 1.65(95% CI: 1.17–2.33) times greater than those schoolchildren who were greater than 10 years (Fig 9). Schoolchildren who had hair wash at least once a week had a 0.31 (95% CI: 0.24–0.42) times lower chance of developing tinea capitis than schoolchildren who washed their hair more than a week (Fig 10). Schoolchildren who had family history of tinea capitis had a 9.18 (95% CI: 3.5–24.02) times greater chance of developing tinea capitis than students who had no family history of tinea capitis (Fig 11).

[Figure omitted. See PDF.]

[Figure omitted. See PDF.]

[Figure omitted. See PDF.]

Discussion

This systematic review and meta-analysis incorporated 14 articles conducted between 2006 and 2022 with 9465 schoolchildren. Each study’s sample size ranged from 288 to 1869 schoolchildren.The study participants were selected using a simple and systematic random sampling approach in each study.

The pooled prevalence of tinea capitis among schoolchildren in Ethiopia was 29.03% (95%CI: 15.37–42.71). which is consistent with a study carried out in Africa (23%) among schoolhildren conducted through a systematic review and meta analysis [30] and epidemiological trends of tinea capitis in Northen California (23.7%) [4]. Schoolchildren may feel ashamed and abashed due to the impact of tinea capitis on the external features like unsightly appearance of their scalp, leading to poor psychosocial interaction with their classmates and the society at large. Secondary bacterial infection can occur in tinea capitis patients due to the presence of moist or occluded skin, significant erosions, ulceration, or malodor, which may leads to hospitalization due to bacterial comorbidity. As a result of poor psychosocial interaction and secondary bacterial infection, students become ineffective in their education and have a low quality of life in general.

Tinea capitis affected more schoolchildren in Ethiopia than it did in lilongwe urban, Malawi among elementary schoolchildren which was 14.6% [53]. This could be as a result of the fact that maintaining personal hygiene (since it prevents the spreading of the causative agent in an individual who are already infected as well as the cross transmission of it) of schoolchildren and betterment of socioeconomic (due to a better health seeking habits) standing among lilongwe urban, Malawi parents relative to Ethiopian parents could reduce the prevalence of tinea capitis in lilongwe urban, Malawi schoolchildren compared to Ethiopian schoolchildren.

The burden of tinea capitis in Ethiopia is higher than the disease in Nigeria (14.3%) [54], Tanzania (15.3%) [55]. This may be the diagnosis approach used in Ethiopian research, which mostly rely on physical examinations alone and rarely direct microscopic examination using standard potassium hydroxide (KOH), as opposed to the culture investigation used in the Indian study, which is the gold standard examination method for fungal infections due to its high sensitivity and specificity [11]. Due to a lack of the gold standard laboratory diagnosiswhich is usedd to confirm for rule out other dermatological abnormalities, but using of physical diagnosis alone or/and direct microscopic examination having a high sensitive KOH method has/have a propensity to include any dermological disorder as tinea capitis. This could be the cause of the tinea capitis being more prevalent among Ethiopian schoolchildren as compared to Indian.

The odds of experiencing tinea capitis among schoolchildren who had family history of tinea capitis were 9.18 (95%CI: 3.5–24.02) times greather than their counterparts. This is consistent with the study conducted in Nigeria [56]. This might be, Microsporum and Trichophyton the most common etiology of tinea capitis can viable on the shared materials like towel, comb, and pillow for long periods and schoolchildrens are known by sharing their parents towel,comb, and pillow [57]. This could cause tinea capitis to spread from students’ parents to schoolchildren, and students with a family history of tinea capitis were more likely to experience the disease than their peers.

The odds of experiencing tinea capitis among schoolchildren who were under the age of 10 years old were 1.65 (95%CI: 1.17–2.33) times greater than those schoolchildren who were greater than 10 years old. This is supported by the study conducted at Southern Ethiopia [48]. This could be due to younger children having poor personal hygien practice secondary to having less knowledge and a poor attitude in order to prevent and control communicable diseases in general and tinea capitis in particular [58] as well as a lack of saturated fatty acids, which act as a natural anti-dermatophytosis mechanism [59].

The odds of experiencing tinea capitis among schoolchildren who had hair wash at least once a week were 0.31 (95%CI: 0.24–0.42) times less than those schoolchildren who had hair wash greater than a week. This consistent with the study conducted in Iraq [60]. This could be due to the fact that keeping good personal hygiene like hair washing is one method of preventing tinea capitis. So study participants who wash their hair at least once a week using soaps or shampoos which has active antifungal ingredient such as ketoconazole or selenium sulfide,can prevent tinea capitis [61]. As a result, schoolchildren who was their hair at least once a week had less tinea capitis than their counterparts. This study’s pooled prevalence of tinea capitis may not exactly represent the burden of Ethiopian schoolchildren because it was conducted using primary studies only from Amhara, South nation nationalities and people, Oromia, and Addis Ababa. In addition to the foregoing, this study only included articles published in English, which may affect the prevalence of tinea capitis and taken as a limitation of this study.

Conclusion

One of the most prevalent childhood health condition in Ethiopia is tinea capitis, which affects over one in every four schoolchildren. Having family history of tinea capitis and under the age of 10 years old were the identified risk factors and having hair wash at least once a week was the protective factor of tinea capitis. Clinical and public engagement activities are needed to address the burden of this disease. Public engament activities like providing health education for parents and students to promot good hygiene and clinical engament activities like early diagnosis and treatment of tinea capitis need to be given great emphasis.

Supporting information

S1 File. PRISMA 2020 checklist.

https://doi.org/10.1371/journal.pone.0280948.s001

(DOCX)

S2 File. Newcastle-Ottawa Quality assessment scale (NOQAS).

https://doi.org/10.1371/journal.pone.0280948.s002

(DOCX)

Citation: Birhanu MY, Temesgen H, ketema DB, Desta M, Getaneh T, Bekele GM, et al. (2023) Tinea capitis among schoolchildren in Ethiopia: A systematic review and meta analysis. PLoS ONE 18(2): e0280948. https://doi.org/10.1371/journal.pone.0280948

About the Authors:

Molla Yigzaw Birhanu

Roles: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing

E-mail: [email protected]

Affiliation: Department of Public Health, College of Health Sciences, Debre Markos University, Debre Markos, Ethiopia

ORICD: https://orcid.org/0000-0001-6286-446X

Habtamu Temesgen

Roles: Data curation, Formal analysis

Affiliation: Department of Human Nutrition and Food Science, College of Health Sciences, Debre Markos University, Debre Markos, Ethiopia

Daniel Bekele ketema

Roles: Conceptualization

Affiliation: Department of Public Health, College of Health Sciences, Debre Markos University, Debre Markos, Ethiopia

ORICD: https://orcid.org/0000-0002-7464-7814

Melaku Desta

Roles: Conceptualization

Affiliation: Department of Midwifery, College of Health Sciences, Debre Markos University, Debre Markos, Ethiopia

Temesgen Getaneh

Roles: Data curation

Affiliation: Department of Midwifery, College of Health Sciences, Debre Markos University, Debre Markos, Ethiopia

Getamesay Molla Bekele

Roles: Conceptualization

Affiliation: Department of Gynecology and Obstetric, School of Medicine, Debre Markos university, Debre Markos, Ethiopia

Balew Zeleke

Roles: Conceptualization, Data curation

Affiliation: Department of Pediatrics and Child Health Nursing, School of Health Sciences, College of Medicine and Health Sciences, Bahir Dar University, Bahir Dar, Ethiopia

Selamawit Shita Jemberie

Roles: Data curation, Formal analysis, Methodology, Validation, Writing – original draft

Affiliation: Department of Midwifery, College of Health Sciences, Debre Markos University, Debre Markos, Ethiopia

References

1. Abdel-Rahman SM, Farrand N, Schuenemann E, Stering TK, Preuett B, Magie R, et al: The prevalence of infections with Trichophyton tonsurans in schoolchildren: the CAPITIS study. Pediatrics 2010, 125(5):966–973. pmid:20403937

2. Al Aboud AM, Crane JS: Tinea capitis. 2019.

3. Hillary T, Suys E: An outbreak of tinea capitis in elderly patients. International Journal of Dermatology 2014, 53(2):e101–e103. pmid:23488592

4. Mirmirani P, Tucker L-Y: Epidemiologic trends in pediatric tinea capitis: a population-based study from Kaiser Permanente Northern California. Journal of the American Academy of Dermatology 2013, 69(6):916–921. pmid:24094452

5. Silverberg NB, Weinberg JM, DeLeo VA: Tinea capitis: focus on African American women. Journal of the American Academy of Dermatology 2002, 46(2):S120–S124. pmid:11807474

6. Abdel-Rahman SM, Herron J, Fallon-Friedlander S, Hauffe S, Horowitz A, Rivière G-J: Pharmacokinetics of terbinafine in young children treated for tinea capitis. The Pediatric infectious disease journal 2005, 24(10):886–891. pmid:16220086

7. Dei‐Cas I, Carrizo D, Giri M, Boyne G, Domínguez N, Novello V, Acuña K, et al: Infectious skin disorders encountered in a pediatric emergency department of a tertiary care hospital in Argentina: a descriptive study. International Journal of Dermatology 2019, 58(3):288–295. pmid:30246865

8. Souissi A, Lagha B, Toukabri N, Mama M, Mokni M: Morse code-like hairs in tinea capitis disappear after successful treatment. International Journal of Dermatology 2018, 57(12):e150–e151. pmid:30264392

9. Goldstein B, Goldstein A, Levy ML: Approach to the patient with a scalp disorder. Uptodate Apr 2019, 17.

10. Ely JW, Rosenfeld S, Stone MS: Diagnosis and management of tinea infections. American family physician 2014, 90(10):702–710. pmid:25403034

11. Levitt JO, Levitt BH, Akhavan A, Yanofsky H: The sensitivity and specificity of potassium hydroxide smear and fungal culture relative to clinical assessment in the evaluation of tinea pedis: a pooled analysis. Dermatology research and practice 2010, 2010. pmid:20672004

12. Gupta A, Summerbell R: Tinea capitis. Medical mycology 2000, 38(4):255–287. pmid:10975696

13. Pérez-Tanoira R, Marín I, Berbegal L, Prieto-Pérez L, Tisiano G, Cuadros J, et al: Mycological profile of tinea capitis in schoolchildren in rural southern Ethiopia. Medical mycology 2017, 55(3):262–268. pmid:27555558

14. Pfaller M, Boyken L, Hollis R, Messer S, Tendolkar S, Diekema D: In vitro susceptibilities of clinical isolates of Candida species, Cryptococcus neoformans, and Aspergillus species to itraconazole: global survey of 9,359 isolates tested by clinical and laboratory standards institute broth microdilution methods. Journal of clinical microbiology 2005, 43(8):3807–3810. pmid:16081915

15. Arikan S: Current status of antifungal susceptibility testing methods. Medical mycology 2007, 45(7):569–587. pmid:17885947

16. Doss RW, El-Rifaie A-A, Radi N, El-Sherif AY: Antimicrobial susceptibility of tinea capitis in children from Egypt. Indian Journal of Dermatology 2018, 63(2):155. pmid:29692458

17. Mock M, Monod M, Baudraz-Rosselet F, Panizzon R: Tinea capitis dermatophytes: susceptibility to antifungal drugs tested in vitro and in vivo. Dermatology 1998, 197(4):361–367. pmid:9873175

18. Rebollo N, López-Barcenas A, Arenas R: Tinea capitis. Actas Dermo-Sifiliográficas (English Edition) 2008, 99(2):91–100.

19. Alemayehu A, Minwuyelet G, Andualem G: Prevalence and etiologic agents of dermatophytosis among primary school children in Harari Regional State, Ethiopia. Journal of Mycology 2016, 2016.

20. Dessie AM, Feleke SF, Workie SG, Abebe TG, Chanie YM, Yalew AK: Prevalence of Skin Disease and Its Associated Factors Among Primary Schoolchildren: A Cross-Sectional Study from a Northern Ethiopian Town. Clinical, Cosmetic and Investigational Dermatology 2022, 15:791–801.

21. Kelbore AG, Owiti P, Reid AJ, Bogino EA, Wondewosen L, Dessu BK: Pattern of skin diseases in children attending a dermatology clinic in a referral hospital in Wolaita Sodo, southern Ethiopia. BMC dermatology 2019, 19(1):1–8.

22. [Ethiopia] CSA: Population Projections for Ethiopia. Addis ABaba;. 2013.

23. Nations U: World population prospects-population division-united nations. World Population Prospects-Revision 2015.

24. Rethlefsen ML, Kirtley S, Waffenschmidt S, Ayala AP, Moher D, Page MJ, et al: PRISMA-S: an extension to the PRISMA statement for reporting literature searches in systematic reviews. Systematic reviews 2021, 10(1):1–19.

25. Fazel S, Khosla V, Doll H, Geddes J: The prevalence of mental disorders among the homeless in western countries: systematic review and meta-regression analysis. PLoS medicine 2008, 5(12):e225. pmid:19053169

26. Islam MM, Iqbal U, Walther B, Atique S, Dubey NK, Nguyen P-A, et al: Benzodiazepine use and risk of dementia in the elderly population: a systematic review and meta-analysis. Neuroepidemiology 2016, 47(3–4):181–191. pmid:28013304

27. Leshargie CT, Alebel A, Kibret GD, Birhanu MY, Mulugeta H, Malloy P, et al: The impact of peer pressure on cigarette smoking among high school and university students in Ethiopia: A systemic review and meta-analysis. PLoS One 2019, 14(10):e0222572. pmid:31603930

28. DerSimonian R, Laird N: Meta-analysis in clinical trials. Controlled clinical trials 1986, 7(3):177–188. pmid:3802833

29. Mubanga B, Siziya S, Malumani M: Prevalence and Associated Factors of Tinea Capitis among School-Aged Children at Buseko Primary School in Buchi Compound, Kitwe, Zambia.

30. Bongomin F, Olum R, Nsenga L, Namusobya M, Russell L, de Sousa E, et al: Estimation of the burden of tinea capitis among children in Africa. Mycoses 2021, 64(4):349–363. pmid:33251631

31. Coloe JR, Diab M, Moennich J, Diab D, Pawaskar M, Balkrishnan R, et al: Tinea capitis among children in the Columbus area, Ohio, USA. Mycoses 2010, 53(2):158–162. pmid:19302461

32. Pérez-González M, Torres-Rodríguez JM, Martínez-Roig A, Segura S, Griera G, Triviño L, et al: Prevalence of tinea pedis, tinea unguium of toenails and tinea capitis in school children from Barcelona. Revista Iberoamericana de Micologia 2009, 26(4):228–232. pmid:19766517

33. Gupta A, Mays R, Versteeg S, Piraccini B, Shear N, Piguet V, et al: Tinea capitis in children: a systematic review of management. Journal of the European Academy of Dermatology and Venereology 2018, 32(12):2264–2274. pmid:29797669

34. Kakourou T, Uksal U: Guidelines for the management of tinea capitis in children. Pediatric dermatology 2010, 27(3):226–228. pmid:20609140

35. Hay R, Clayton Y, De Silva N, Midgley G, Rossor E: Tinea capitis in south‐east London—a new pattern of infection with public health implications. British Journal of dermatology 1996, 135(6):955–958. pmid:8977718

36. Ali S, Graham TA, Forgie SE: The assessment and management of tinea capitis in children. Pediatric emergency care 2007, 23(9):662–665. pmid:17876261

37. Bennassar A, Grimalt R: Management of tinea capitis in childhood. Clinical, cosmetic and investigational dermatology: CCID 2010, 3:89. pmid:21437064

38. González U, Seaton T, Bergus G, Jacobson J, Martínez‐Monzón C: Systemic antifungal therapy for tinea capitis in children. Cochrane database of systematic reviews 2007(4). pmid:17943825

39. PIPKIN JL: Tinea capitis in the adult and adolescent. AMA Archives of Dermatology and Syphilology 1952, 66(1):9–40. pmid:14932501

40. Chen BK, Friedlander SF: Tinea capitis update: a continuing conflict with an old adversary. Current opinion in pediatrics 2001, 13(4):331–335. pmid:11717558

41. Bergson CL, Fernandes NC: Tinea capitis: study of asymptomatic carriers and sick adolescents, adults and elderly who live with children with the disease. Revista do Instituto de Medicina Tropical de Sao Paulo 2001, 43:87–91. pmid:11340482

42. Tizazu Getahun mW, Hailemariam Abiy: PREVALENCE AND ASSOCIATED FACTORSOF TINEA CAPITIS AMONG CHILDREN IN FINOTE SELAM TOWN, NORTH WEST ETHIOPIA. 2022.

43. Moges F, Tiruneh M, Belyhun Y, Kebede Y, Mulu A, Kassu A: INTESTINAL PARASITIC INFECTIONS IN ASSOCIATION WITH CUTANEOUS FUNGAL INFECTION AND NUTRITIONAL STATUS AMONG TSEDA SCHOOL CHILDREN, NORTHWEST ETHIOPIA. Ethiopian Journal of Health and Biomedical Sciences 2010, 3(I):35–44.

44. Lulekal S, Abera S, Misganaw S, Urgie S, Asfaw S: Assessment on Prevalence of Tinea Capitis and Its Associated Factors among School Children in Addis Zemen, Northwest Ethiopia, 2016. Central African Journal of Public Health 2019, 5(4):172.

45. Leiva-Salinas M, Marin-Cabanas I, Betlloch I, Tesfasmariam A, Reyes F, Belinchon I, et al: Tinea capitis in schoolchildren in a rural area in southern Ethiopia. Int J Dermatol 2015, 54(7):800–805. pmid:25557908

46. Lulu Y, Tolesa G, Cris J: Prevalence and associated factors of skin diseases among primary school children in Illuababorzone, Oromia Regional State, South West Ethiopia. Indo Am J Pharm Res 2017, 7(1):7374–7383.

47. Amare HH, Lindtjorn B: Risk factors for scabies, tungiasis, and tinea infections among schoolchildren in southern Ethiopia: A cross-sectional Bayesian multilevel model. PLoS neglected tropical diseases 2021, 15(10):e0009816. pmid:34613968

48. Hibstu DT, Kebede DL: Epidemiology of Tinea Capitis and Associated Factors among School Age Children in Hawassa Zuria District, Southern Ethiopia, 2016. J Bacteriol Parasitol 2017, 8(2).

49. Betelhem Yilma AB: Prevalence and spectrum of dermatophytes and non-dermatophyte mold isolated from patients with Tinea Capitis, attending Rank Higher Specialized Dermatology Clinic, Addis Ababa, Ethiopia. 2021.

50. Araya S, Abuye M, Negesso AE: Epidemiological characterization of dermatomycosis in Ethiopia. Clinical, cosmetic and investigational dermatology 2021, 14:83. pmid:33519223

51. Woldeamanuel Y, Leekassa R, Chryssanthou E, Mengistu Y, Petrini B: Clinico-mycological profile of dermatophytosis in a reference centre for leprosy and dermatological diseases in Addis Ababa. Mycopathologia 2006, 161(3):167–172. pmid:16482389

52. Leiva‐Salinas M, Marin‐Cabanas I, Betlloch I, Tesfasmariam A, Reyes F, Belinchon I, Ramos JMet al: Tinea capitis in schoolchildren in a rural area in southern E thiopia. International Journal of Dermatology 2015, 54(7):800–805.

53. Sichone S: PREVALENCE OF TINEA CAPITIS AMONG PRIMARY SCHOOL CHILDREN AT KALONGA PRIMARY SCHOOL IN LILONGWE URBAN.

54. Fienemika A, Alikor E, Opara P: Prevalence and Risk Factors Associated with Tinea Capitis among Primary School Children in a Semi-Urban Area of Rivers State, Nigeria. West African Journal of Medicine 2020, 37(7):805–811.

55. Magreth EM, Mariam RM, Gerald M: Prevalence and identification of fungi associated with Tinea capitis in school children of Morogoro municipality, Tanzania. African Journal of Medical and Health Sciences 2020, 19(7):103–109.

56. Dogo J, Afegbua SL, Dung EC: Prevalence of Tinea capitis among school children in Nok community of Kaduna State, Nigeria. Journal of pathogens 2016, 2016.

57. Ameen M: Epidemiology of superficial fungal infections. Clinics in dermatology 2010, 28(2):197–201. pmid:20347663

58. Aldinger C, Zhang X-W, Liu L-Q, Pan X-D, Yu S-H, Jones J, Kass Jet al: Changes in attitudes, knowledge and behavior associated with implementing a comprehensive school health program in a province of China. Health Education Research 2008, 23(6):1049–1067.

59. Kligman AM, Ginsberg D: Immunity of the adult scalp to infection with Microsporum audouini. Journal of Investigative Dermatology 1950, 14(5).

60. Fathi H, Al Samarai A: Prevalence of tinea capitis among schoolchildren in Iraq. EMHJ-Eastern Mediterranean Health Journal, 6 (1), 128–137, 2000 2000. pmid:11370324

61. Chen X, Jiang X, Yang M, Gonzalez U, Lin X, Hua X, Xue S, Zhang M, Bennett Cet al: Systemic antifungal therapy for tinea capitis in children. Cochrane Database of Systematic Reviews 2016(5).