Head Lice Infestation among Internally Displaced Persons in Tikrit Camp/
Iraq
DhefafRadhiMadhi*1, AwadJasim Muhammad2, QasimSharhan Al-Mayah3
1Department of Biology/ College of Science/ Tikrit University/ Iraq
2Department of Plant Protection-Entomology/ College of Agriculture/ Tikrit University/ Iraq
3Medical Research Unit/ College of Medicine/ Al-Nahrain University/ Iraq
*Corresponding author email is: [email protected]
Abstract
Background and Objectives: Head lice infestation is a health issue that frequently affects crowded populations with low social-hygiene status. This study aimed to investigate the prevalence and associated risk factors for head lice among internally displaced persons in Tikrit camp.
Subjects and Methods: This is a cross-sectional study which was conducted in the camps of internally displaced persons (IDPs) in Tikrit province, North of Iraq. The study included a total of 372 subjects (194 males and 178 females), mean age was 12.62± 8.65 years. All participants were examined in the inspection room. Visual inspection and dry comb test were used for detection of different developmental stage of lice in the head. A subject was considered infested when at least one of the developing stages of the parasite is detected. Demographic and personal characteristics of each subject were obtained using structural questionnaire.
Results: The prevalence of head lice infestation amonginternally displaced persons in Tikrit camp was (47.85%).Each of older age (<12 years) (OR= 0.53, 95%CI=0.25-0.98, p=0.048) and mother’s secondary or above educational level (OR= 0.012, 95%CI= 0.02-0.06, p<0.001) were independent protective factors against pediculosis. In contrast, each of female sex (OR= 7.2, 95%CI=4.0-12.94, p<0.001), family size ≥8 (OR= 3.17, 95%CI= 1.37-13.25, p=0.039) and sharing others with the same bed (OR= 1.76, 95%CI=1.01-3.71, p= 0.044) were independent risk factors for pediculosis.
Conclusions: There is a relatively high prevalence of head lice infestation among internally displaced persons in Tikrit camp. Younger age, female sex, mother’s educational level, increased family member and sharing others with the same bed are the main factors associated with this infestation.
Keywords: pediculosiscapitis, infestation, internally displaced persons Introduction
Despite the modern hygiene standards and marked promotion in health and medical education, several ectoparasitic diseases still prevalent worldwide. Perhaps the most important disease in this regard is pediculosis, the infestation of head with the ectoparasitePediculushumanuscapitis.
It was estimated that 6 to 12 million head lice infestations occur every year [1]. However,
infestations occur almost exclusively in vulnerable groups: school children, homeless people, refugees, and slum dwellers [2]. Thus the infestation rate can range from 5.8% to 35% depending on the cultural behavior, crowding, and treatment option [3].
The impact of pediculosis should be considered form three aspects: medical, social and economic. From medical point of view, the disease associated with blood loss, itching, inflammation of scalp and neck secondary bacterial skin infections (impetigo, cellulitis), conjunctivitis, and lymphadenopathy [4]. On the other hand, it is now evidenced that lice can transmit several pathogens. Acinetobacterbaumannii DNA was detected in 33% of head lice collected from 245 children in 44 schools in France [5]. Moreover, the nucleic acid of Bartonellaquintana (the agent of trench fever, endocarditis, bacillary angiomatosis and other disease manifestations) was frequently reported in these lice [6,7].
Sociologically, the stigma and mental health impact of pediculosis is arguably the most concerning aspect of the infestation. The negative social effects of this perception create more problematic issues than pediculosis itself [8]. These negative impacts include: formal social isolation via exclusion from school, voluntary home isolation, overtreatment with harsh chemicals, and a potentially negative psychological impact upon the infected person and family involved [9].
Aside from medical and social impact, head lice infestation has a substantial economic impact.
The estimated annual direct and indirect costs of this infested in the United State was 367 million US dollars including consumer costs, lost wages, and school system expenses [10].
As such, the assessment of pediculosis incidence and related risk factors are of paramount importance and are considered a cornerstone for controlling programs. Most related previous studies whether local [11] or international [12,13,14,15] have focused on school children in main cities, while other occupational classes in counties were neglected. Therefore, the present study aimed to evaluate the incidence of pediculosis among general population in city/Tikrit.
Subjects and Methods
This is a cross-sectional study which was conducted in the camps of internally displaced persons (IDPs) in Tikrit province, North of Iraq (figure 1). The city has an area of about 2836 k2. The city's population is 260,000. And located between latitudes 34° 35' 59.99" N and longitude 43°
40' 59.99" E.Tikrit has warm climate. The annual average rainfall is 180 mm.
The study included a total of 372 subjects (194 males and 178 females), mean age was 12.62±
8.65 years (range 5- 23 years) residing the United Nation camp (figure 2) for at least one years.
Most families in the camp have come from a nearby Mosul province. The selected subjects were attending Ibn-Rushd Medical Center for primary health care during the period from 1st January to 30th April 2019 due to different complains other than lice infestation. A consent form was obtained from each participant or his/her parent before including in the study.
Figure 1: Map showing the provinces of Iraq, highlighting the location of Salahiddin province and study city (Tikrit) where the camps are located
All participants were examined in the inspection room. Lice detection was performed with the aid of lenses and LED pen light along with fine-tooth comb. Firstly, the entire head was visually inspected for about 3 min, paying a special attention to the nape of head and areas behind the ears. Secondly, the head was systematically combed from the scalp to the end of the hair onto a white paper sheet. The comb was cleaned with a tissue and the tissue was carefully inspected to detect any developmental stage. A subject was considered infested when at least one of the developing stages of the parasite is detected[16].
Age, the chief illness, gender, parent educational level, family size, sleeping arrangement, bathing time/week, sharing personal tools, hair nature were obtained using preformed questionnaire.
Figure 2: Tents of the Tikrit camp for internally displaced persons Statistical Analysis
The Statistical Package for the Social Sciences (SPSS) for Windows (version 15.0 SPSS Inc., Illinois, USA) was used for all statistical analysis. Descriptive statistics was used to demonstrate percentage, means, and frequencies of the different variables. Cross tabulation and Chi square test were applied to determine the statistical significance of different factors. Variables which had p-value≤0.2 in this test were candidates for multivariable logistic regression for the final model [Ethiopia} The Omnibus test was used to test model performance. A p-value of ≤ 0.05 was considered significant.
Results
Demographic and personal Characteristics of the Study Population
The demographic characteristics of the study population are listed in table 1. The most common age class was 9-12 years accounting for about half of the population. All participants were attending Ibn-Rushd Medical Center/ Tikrit because they were complaining different illnesses other than pediculosis. The most common illness was diarrhea which was reported in 30.11% of the participant followed by anemia (12.53%) and diabetes (7.53%). Many other illnesses like common cold, influenza, psoriasis, hepatitis, leukemia, Hodgkin lymphoma and rickets were reported with minor frequencies. Males were predominant accounting for about two-third of study population. The percentage of illiterate fathers and mothers was 22.58% and 50.54%, respectively. Individual tent can have 2 to 9 family member, with the majority of tents (77.15%)
had 5-7 members. Slightly more than half of the subjects (56.45%) were a school attendant in different stages of elementary and secondary schools. About two-third of investigated subjects share the same bed with the others during sleeping, while 82.26% of them was sharing their combs. Due to the shortage in water supply, the vast majority (87.63%) of the subject had on 1 or 2 times bathing/week.
Table 1: Demographic characteristics of the study population
Variables Frequency Percentage
Age, years 5-8
9-12
>12
79 184 109
21.23%
49.46%
29.3%
Principle Comorbidity Diarrhea
Anemia Diabetes Others
112 38 28 194
30.11%
12.22%
7.53%
52.15%
Sex Male Female
261 111
70.16%
29.84%
Father’s education Illiterate
Primary
Secondary and above
84 248
40
22.58%
66.67%
10.75%
Mother’s education Illiterate
Primary
Secondary and above
188 156 28
50.54%
41.94%
7.53%
Family size 2-4
5-7 ≥8
23 287
62
6.18%
77.15%
16.67%
School attendance No
Yes
162 210
43.55%
56.45%
Sleeping arrangement Alone
With others
116 256
31.18%
68.82%
Sharing combs
No Yes
66 306
17.74%
82.26%
Bathing (times/week) 1-2
≥3
326 46
87.63%
12.37%
Hair Nature Straight Curly
249 123
66.94%
33.06%
Proportion of PediculosisCapitis
Out of 372 subjects included in this study, 178 (47.85%) were found to have at least one developmental stage of the Pediculushumanuscapitisin their hair or scalp according to visual and comb test.
Association of Demographic Characteristics with Pediculosis
Three demographic characteristics, out of six, were found to be significantly associated with pediculosis (Table 2). Younger ages (5-8 years) represented 26.97% versus 15.98% in infested and non-infested subjects respectively. Likewise, female accounted for about half of infested subjects compared with only 12.37% of non-infested subjects with a highly significant difference. Finally, mother of 65.73% of infested subjects were illiterate compared with 36.6%
of non-infested subjects who had such a characteristic.
Although illiterate fathers and larger family size were markedly more frequent among infested than non-infested subjects, the differences were insignificant.
Table 2: Association of demographic characteristics with pediculosis
Variables Infested (n= 178)
Non-infested (194)
p-value Age, years
5-8 9-12
>12
48(26.97%) 84(46.07%) 46(25.84%)
31(15.98%) 100(51.55%)
63(32.47%)
0.03
Chief morbidity Diarrhea
Anemia Diabetes Others
51(20.79%) 21(11.8%)
13(7.3%) 93(60.11%)
61(31.44%) 17(8.76%) 15(7.73%) 101(52.06%)
0.777
Sex Male Female
91(51.12%) 87(48.89%)
170(87.63%) 24(12.37%)
<0.001
Father’s education Illiterate
Primary
Secondary and above
32(17.98%) 129 (72.47%)
17(9.55%)
52(26.8%) 119(5.67%) 23(11.86%)
0.068
Mother’s education Illiterate
Primary
Secondary and above
117(65.73%) 56(31.46%)
5(2.81%)
71(36.6%) 100(51.55%)
23(11.85%)
<0.001
Family size 2-4
5-7 ≥8
8(4.49%) 134(75.38%)
36(20.22%)
15(7.73%) 153(78.87%)
26(13.4%)
0.115
Association of Personal Characteristics with Pediculosis
Table 3 demonstrates the association of personal characteristics with pediculosis. Only sleeping arrangement had significant association with pediculosis as 76.4% of infested versus 61.86%
non-infested subjects share their beds with the others. Marginal significant association was found between fewer bathing (1-2 times/week) and pediculosis (p= 0,054).
Table 3: Association of personal characteristics with pediculosis
Variables Infested (n= 178)
Non-infested (194)
p-value School attendance
No Yes
73(41.0%) 105(59.0%)
89(45.88%) 105(54.12%)
0.334
Sleeping arrangement Alone
With others
42(23.6%) 136(76.4%)
74(38.14%) 120(61.86%)
0.02
Sharing combs No
Yes
26(14.61%) 152(85.39%)
40(20.62%) 154(79.38%)
0.129
Bathing (times/week) 1-2
≥3
162(91.0%) 16(9.0%)
164(84.54%) 30(15.46%)
0.054
Hair Nature Straight Curly
117(65.73%) 61(34.27%)
132(68.04%) 62(31.96%)
0.636
Multivariate Analysis
Multivariate logistic regression model was used to find out independent risk factors for pediculosis. All variables that give significant association as well as those having p-value ≤0.2 were entered in this model (Table 4). Almost the same variables (except family size) that had significant through χ2, remained significant in multivariate analysis. Each of older age (<12 years) (OR= 0.53, 95%CI=0.25-0.98, p=0.048) and mother’s secondary or above educational level (OR= 0.012, 95%CI= 0.02-0.06, p<0.001) were independent protective factors against pediculosis. In contrast, each of female sex (OR= 7.2, 95%CI=4.0-12.94, p<0.001), family size
≥8 (OR= 3.17, 95%CI= 1.37-13.25, p=0.039) and sharing others with the same bed (OR= 1.76, 95%CI=1.01-3.71, p= 0.044) were independent risk factors for pediculosis.
Table 4: multivariate analysis of factors associated with pediculosis
Variables p-value Odds ratio
(95%CI) Age, years
5-8 9-12
>12
0.224 0.365 0.048
1.0 0.74(0.38-1.43 0.53(0.25-0.98) Sex
Male Female
<0.001 1.0
7.2(4.0-12.94) Father’s education
Illiterate Primary
Secondary and above
0.285 0.184 0.947
1.0 1.52(0.82-2.83) 0.97(0.38-2.47) Mother’s education
Illiterate Primary
Secondary and above
<0.001
<0.001
<0.001
1.0 0.37(0.22-0.63) 0.12(0.28-0.67) Family size
2-4 5-7 ≥8
0.041 0.067 0.039
1.0
3.17 (1.48-12.62) 4.32(1.37-13.25) Sleeping arrangement
Alone With others
0.044 1.0
1.76(1.01-3.71 Sharing combs
No Yes
0.141 1.0
1.64(0.85-3.17)
Bathing (times/week) 1-2
≥3
0.274 1.0
0.65(0.3-1.41)
Discussion
Iraq has witnessed a lot of forced displacement after 2014 when of Islamic State of Iraq and Syria (ISIS) controlled over large parts in the North of the country. Camps used for settling the displaced families were usually lacking the standards hygiene. Accordingly, many epidemics can occur. This study aimed to investigate the prevalence of head lice infestation among IDPs in Tikrit. The overall prevalence of pediculosis in the present study was 47.85%. This is a very high figure compared with many studies [11,14,17,18,19). However, all these studies were conducted on elementary school children which implies that there are some educational programs and continuous monitoring of the general health of the pupils. Alternatively, there are several studies which reported almost similar or even higher rate than the present rate when the hygiene standards were extremely low. For example, a previous Iraqi study showed that 48.9% of pupil in primary schools in Baghdad were infested [20]. In one Iranian study, Soleimani-Ahmadi [21]
investigated pediculosis in school children in 6 villages and reported an overall prevalence of 67.3%. In another study, Suleman et al. [22]reported 42% infestation rate among general population in Pakistan., while Saddozi et al. [23] found that 87% of primary schools in some Pakistani cities were infested.
Surprisingly, a previous local study on the refugees in Sulaimani Province, North of Iraq showed that only 1.12% of the camp residence were infested [24], while a similar Chinese study revealed 14.2% [25]. This high discrepancy between the two study is related to several factors the most important of which are the detection methods, sample size and the season of the year in which the study was conducted. It is well known that combing is highly sensitive method (has a sensitivity of 90%) for detection of active head lice infestation (presence of trophic stages and/or viable eggs) in children with low infestation intensity [26], and it is much better than visual examination. Supporting this conception is an Egyptian study in which the infestation arte was 14.9% and 33% using visual inspection and dermoscopy respectively [14]. Furthermore, studies during Winter season may reveal higher incidence than that conducted during summer season because of the frequent bathing during summer [27].
In the present study, multivariable logistic regression was used to identify the independent factors that may associate with the prevalence of pediculosis. Five factors were found to be independently affect such prevalence. Being older than 12 years was significantly associated with about two-fold protection against the infestation. Such a results echo several previous studies [17,28,29,30]. However, in most studies the age class 9-12 were the most affected ages, because at this age, children usually depend on themselves. The younger ages may less prone to infestation because of a complete dependence on parents for combing and washing or cleaning
their hair which helps to early detection of infestation before its establishment. Usually older ages (<12 years) are more conscious and aware of personal hygiene, while young children are more prone to behaviors like clos contact and touching with friends and playmates.
The odds of being infested head lice was 7.2-time higher in female than males. This preponderance is in line with previous studies from Bangkok [31], Iran [32,33] Argentina [34]
and Colombia [35]. This might be due to the habit of female students to have long hairs that can harbor the parasite. However, whether hair length indeed affects pediculosiscapitis infestation is still discussed controversially in the literature. [36,37]. Females also have close relationships with other girls, involving multiple and intimate body contact[38].On the other hand, boys have a tendency to brief contact, during their activities outside their houses [11]. Furthermore, using scarves, hats, combs, hair bushes, and other accessories can increase the transmission of lice between girls.
According to the present study, children with secondary or above educational level mothers have about 8.3-time less risk to have head lice compared with those with illiterate mothers. This is in agreement with other studies [15]. This might be because education is correlated with eagerness and ability to gain new knowledge and knowledge may help to have good personal hygiene practice which reduces infestation. However, in other studies maternal education was not associated [33,39].
The present finding revealed that family size ≥8 persons exposes the subjects to 4.3-fold increased risk of pediculosis. This results is consistent with studies from Greece, Malaysia and Iran, which show a significant positive association of family size with the occurrence of pediculosis [40,41]. In an overcrowded home, close contact between family members facilitates the transmission of head lice. Moreover, having more children may lead to higher infestation rates because parents pay less time per child to perform laundry and personal cleansing [15].
Finally, a person sharing the same bed with other will have 1.76-fold increase infestation risk compared with a person having a separated bed. In accordance with this result are studies in Nigeria, Venezuela, Yemen and Iran [36,39,42,43] However, some other studies did not found such association [14,44].Sharing beds is a sign of crowding and facilitates the direct and indirect head lice transmission through head-to-head contact and fomites. The trend is seemed logical because lying on the same bed with the same pillow certainly facilitate transmission the lice either through direct contact or indirectly throw the pillow.
Collectively, these data brought attention to the high prevalence of pediculosis among internally displaced persons in Tikrit camp. Each of younger age, female sex, illiterate mother’s increased family member and sharing others with the same bed are the main risk factors associated with this infestation. Thus, policymakers should take the initiative step to deal with public health issue.
Acknowledgments
The author is grateful to all staff member of Ibn-Rushd Medical Center for their help and cooperation
Conflict of Interest
The authors declare that they have no competing interests.
References
1. CDC. Parasites-lice-head lice-epidemology. www.cdc.gov/parasites/lice/head/epi.html, August 2016.
2. Meister L, Ochsendorf F. Head Lice. DtschArztebl Int. 2016;113(45):763–772.
3. Amirkhani MA, Alavian SM, Maesoumi H, Aminaie T, Dashti M, Ardalan G, et al. A nationwide survey of prevalence of pediculosis in children and adolescents in Iran. Iran Red Crescent Med J 2011;13:167-70.
4. Canpolat F. Infestations and neoplasms of the scalp, hair and scalp disorder. IntechOpen, DOI: 10.5772/67278.
5. Bouvresse S, Socolovshi C, Berdjane Z, Durand R, Izri A, Raoult D, et al. No evidence of Bartonellaquintana but detection of Acinetobacterbaumannii in head lice from elementary schoolchildren in Paris. Comp ImmunolMicrobiol Infect Dis 2011;34:475- 477
6. Cutler S, Abdissa A, Adamu H, Tolosa T, Gashaw A. Bartonellaquintana in Ethiopian lice. Comp ImmunolMicrobiol Infect Dis 2012;35:17-21
7. Angelakis E, Rolain JM, Raoult P, Brouqui P. Bartonellaquintana in head louse nits FEMS Immunol Med Microbiol 2011;62:244-246
8. Parison J, Speare R, Canyon DV. Uncovering family experiences with head lice: the difficulties of eradication. Open Dermatol J 2008; 2: 9–17.
9. Parison JC, Speare R, Canyon DV. Head lice: the feelings people have. Int J Dermatol 2013,52, 169–171
10. Hansen RC, O’Haver J. Economic considerations associated with Pediculushumanuscapitis infestation. ClinPediatr. 2004;43:523-527
11. Mahmood SA. Head pediculosis among Baghdad area elementary school children. Iraqi J Sci 2010;51(1):49-55.
12. Kassiri H, Gatitif A. The frequency of head lice, health practices and its associated factors in primary schools in Khorramshahr, Iran. Health Scope 2016;5(4):e31570.
13. Mohamed K, Elmubarak A, Zaghloul D, Zahrani M, Jefri M, Alfaqish K, et al.
Prevalence of head lice (Pediculushumanuscapitis) infestation among pupils in elementary school in Makkah, Saudi Arabia. Int J Med Res Health Sci 2018;7(8):66-76.
14. El-Sayed MM, Toama MA, Abdelshafy AS, Esawy AM, El-Naggar SA. Prevalence of pediculosiscapitis among primary school students at Sharkia governorate by using dermoscopy. Egyptian J DermatolVenereol 2017;37:33–42.
15. Soleimani-Ahmadi M, Jaberhashemi SA, Zare M, Sanei-Dehkordi A. Prevalence of head lice infestation and pediculicidal effect of permethrine shampoo in primary school girls in a low-income area in southeast of Iran. BMC Dermatol. 2017;17(1):10.
16. Wananukul S, Chatproedprai S, Tempark T, Wananukul W. Clinical response and safety of malathion shampoo for treatment of head lice in a primary school. J Med Assoc Thai 2011; 94: 465-469.
17. Mahmud S, Pappas G, Hadden WC. Prevalence of head lice and hygiene practices among women over twelve years of age in Sindh, Balochistan, and North West Frontier Province: National Health Survey of Pakistan, 1990-1994. Parasit Vectors2011;4:11.
18. Manrique-Saide P, Pavla-Ruz N, Rodriguez-Buenfil JC, Herrera RH, Gomez-Ruiz P, Pilger D. Prevalence of pediculosiscapitis in children from rural school in Yucatan, Mexico. Rev Inst Med Trop Sao Paulo 2011;53(6):325-327.
19. Khamaiseh AM. Head lice among governmental primary school students in Southern Jordan: prevalence and risk factors. J Global Infect Dis 2018;10:11-15.
20. Al-kubiassy W, Abdul Karim ET. Head lice in pupils of two primary schools in Baghdad.
J Bahrain Med Soc 2003; 15: 34-38
21. Soleimani-Ahmadi M, Jaberhashemi SA, Zare M, Sanei-Dehkordi A. Prevalence of head lice infestation and pediculicidal effect of permethrine shampoo in primary school girls in a low-income area in southeast of Iran. BMC Dermatol. 2017;17(1):10.
22. Suleman M, Jabeen N: Head lice infestation in some urban localities of NWFP, Pakistan.
Ann Trop Med Parasitol 1989, 83:539-547
23. Saddozai S, Kakarsulemankhel KK. Infestation of head lice, Pediculushumanuscapitis in schoolchildren at Quetta City and its suburban areas, Pakistan. Pakistan J Zool 2008; 40:
45-52.
24. Ali FM, Hama AA. Prevalence of head pediculosis among refugees in Sulaimani Governorate/Kurdistan-Iraq. Iraqi J Sci 2018;59(2C):1012-1018.
25. Fan CK, Liao CW, Wu MS, Hu NY, Su KE. Prevalence of Pediculuscapitis infestation among schoolchildren of Chinese refugees residing in mountainous areas of northern Thailand. Kaohsiung. J Med Sci 2004;20:183–187.
26. Jahnke C, Bauer E, Hengge UR, Feldmeier H. Accuracy of diagnosis of pediculosiscapitis: visual inspection vs wet combing. Arch Dermatol 2009;145:309–313 27. Henderson CA. Skin disease in rural Tanzania. Int J Dermatol 1996;35:640-2
28. Hodjati MH, Mousavi N, Mousavi M.Head lice infestation in school children of a low socio-economy area of Tabriz city, Iran. Afr J Biotechnol 2008;7:2292-2294
29. Leung AK, Fong JH, Pinto-Rojas A. Pediculosiscapitis. J Pediatr Health Care.
2005;19:369–73.
30. Moosazadeh M, Afshari M, Keianian H, Nezammahalleh A, Enayati AA. Prevalence of head lice infestation and its associated factors among primary school students in Iran: a systematic review and meta-analysis. Osong Public Health Res Perspect 2015;6:346–56
31. Rassami W, Soonwera M. Epidemiology of pediculosiscapitis among schoolchildren in the eastern area of Bangkok, Thailand. Asian Pac J Trop Biomed 2012;2(11):901–904.
32. Nejati J, Keyhani A, Kareshk AT, Mahmoudvand H, Saghafpour A, Khoraminasab M, et al. Prevalence and risk factors of pediculosis in primary school children in South West of Iran. Iran J Public Health 2018;47(12):1923.
33. Shayeghi M, Paksa A. Epidemiology of head lice infestation in primary school pupils, in Khajeh city, East Azerbaijan province, Iran. Iran J Arthropod-borne Dis 2010;4(1):42 34. Gutiérrez MM, González JW, Stefanazzi N, Serralunga G, Yañez L, Ferrero AA.
Prevalence of Pediculushumanuscapitis infestation among kindergarten children in Bahía Blanca city, Argentina. Parasitol Res 2012;111(3):1309–1313.
35. López-Valencia D, Medina-Ortega Á, Vásquez-Arteaga LR. Prevalence and variables associated with pediculosiscapitis in kindergarten children from Popayán, Colombia.
Revista de la Facultad de Medicina. 2017;65(3):425–428.
36. Al-Maktari MT. Head louse infestations in Yemen: prevalence and risk factors determination among primary schoolchildren, Al-Mahweet Governorate, Yemen. J Egypt SocParasitol 2008;38:741-748.
37. Ríos SM, Fernández JA, Rivas F, Sáenz ML, Moncada LI. Pediculosis prevalence and associated risk factors in a nursery school, Bogotá, Colombia. Biomedica 2008;28:245- 251.
38. Heukelbach J, Wilcke T, Winter B, Feldmeier H. Epidemiology and morbidity of scabies and pediculosiscapitis in resource-poor communities in Brazil. Br J Dermatol.
2005;153(1):150–156.
39. Nazari M, Goudarztalejerdi R, Payman MA. Pediculosiscapitis among primary and middle school children in Asadabad, Iran: an epidemiological study. Asian Pac J Trop Biomed 2016;6(4):367–370.
40. Bachok N, Nordin RB, Awang CW, Ibrahim NA, Naing L. Prevalence and associated factors of head lice infestation among primary schoolchildren in Kelantan, Malaysia.
Southeast Asian J Trop Med Public Health 2006;37:536-543
41. Soultana V, Euthumia P, Antonios M, Angeliki RS. Prevalence of pediculosiscapitis among schoolchildren in Greece and risk factors: A questionnaire survey.
PediatrDermatol 2009;26:701-705.
42. Austin NI. Pediculosis among school children, in Owerri north local government area of Imo State, South Eastern Nigeria. Int J Infect Dis 2016;45(1):352-353.
43. Cazorla D, Ruiz A, Acosta M. Clinical and epidemiological study of pediculosiscapitis in schoolchildren from Coro, Venezuela. Invest Clin 2007;48:445-457.
44. Dagne H, Aba Biya A, Tirfie A, Yallew WW, Dagnew B. Prevalence of Pediculushumanuscapitisand associated factors among schoolchildren in Woreta town, Northwest Ethiopia. BMC Res Note 2019;12:465.