Prevalence and associations of active trachoma among rural preschool children in Wadla district, northern Ethiopia

doi:10.21203/rs.2.14562/v7

PDF

Research article

Prevalence and associations of active trachoma among rural preschool children in Wadla district, northern Ethiopia

https://doi.org/10.21203/rs.2.14562/v7

This work is licensed under a CC BY 4.0 License

Journal Publication

published 26 Aug, 2020

Read the published version in BMC Ophthalmology →

You are reading this latest preprint version

Background: Trachoma is a neglected eye disease and an important cause of preventable corneal blindness. In endemic areas, initial infection can occur in early childhood and following a recurrent episodes, it progresses to scarring and visual impairment. Trachoma disappeared from high income countries through enhancements of hygiene and sanitation but the disease is still a challenge in developing countries. In Ethiopia, data indicate that Amhara is the region with the highest prevalence of active trachoma. The aim of this study was to assess the prevalence and associations of active trachoma among rural preschool children in Wadla district, Amhara region, Ethiopia.

Methods: In this study, 596 children were screened for signs of active trachoma by using cluster-sampling technique. Following pre-testing of the survey instrument in a different district, questions about socio-demographic status were delivered for heads of households. Integrated eye care workers, previously trained to undertake trachoma screening for one month, performed eye examination. The logistic regression model was used to look for associations of active trachoma.

Results: The prevalence of active trachoma among rural preschool children in Wadla district was 22%. Low economic status (adjusted odds ratio [AOR]3.8 (95%CI 1.3–11.4), being 37–48 months old (4.2;1.5–12.0), living in a house with thatched roof (4.4;1.4–13.6), presence of flies in a home (4.6;2.1–9.9), once-weekly face-washing frequency (8.6;2.5–29.3), having a face that had not been washed for longer than a week (10.6;2.9–37.7), and not using soap (4.5;1.8–11.3) had association to active trachoma

Conclusion: The prevalence of active trachoma among rural pre-school children in Wadla district was high. This indicates that Trachoma is still a public health problem in the district. This high prevalence calls for further interventions to prevent future trachomatis blindness.

Ophthalmology

Active Trachoma

Associations

Water

Sanitation

Hygiene

Wadla district

Ethiopia

Trachoma is a neglected eye disease and an important cause of preventable corneal blindness (1, 2), which is categorized into active and cicatricial types of trachoma (2, 3). In endemic areas, cycles of infection with Chlamydia trachomatis progress to scarring, trachomatis trichiasis, and corneal opacity (4, 5, 6). Trachoma is a disease of poverty and poor hygiene (7) that found primarily in children (4), with the late-stage disease more frequently seen in adult women than adult men, possibly because of women's greater time spent in proximity to children. Pieces of literature indicate that preschool children are the main pool of ocular C. trachomatis infection (8, 9). Active trachoma can be an extremely common problem in children, with prevalence estimates of 60-90% (10). Ocular C. trachomatis is believed to be transmitted through hand-to-hand contact, sharing of towels, fomites, pillows, and eye-seeking flies (11).

Globally, an estimated 2.5 million people had trachomatis trichiasis, needing surgery (S) to prevent ongoing visual impairment. Another nearly 142 million people lived in districts in which the prevalence of active trachoma met WHO-defined criteria for intervention with antibiotics (A) and interventions to promote facial cleanliness (F) and improve the environment (E), in order to prevent future trichiasis cases. Ethiopia is the most trachoma affected country: more than half of the 142 million people needing the A, F and E components of the “SAFE strategy” in 2019 lived here, Ethiopia (12). Within Ethiopia, Amhara region has the highest trachoma burden (13), although, the prevalence and associations of active trachoma vary from setting to setting. Hence, studying the differences may help to tailor local control approaches. This is why we undertook investigations in Wadla district, Amhara region after 5 successive years of Zithromax administration in order to re-estimate the prevalence of active trachoma and examine its associations.

Study design, period and setting

A community-based cross-sectional study design was used. Fieldwork was undertaken from March 11, 2017 to April 26, 2107. The estimated population of Wadla district was 128,170 with 64,574 males and 63,596 females. There were 28,414 households in this district with an average of 4.5 persons per house. The district had 1 general hospital, 7 health centers, and 20 health posts.

Population

The sampling frame was children aged 1 to 5 years old in 150 rural villages of Wadla district. The study units were heads from the selected rural households that also had preschool children.

Sample size determination

We estimated the required sample size using the single population proportion formula. We assumed, based on previous surveys, an observed prevalence of active trachoma (12.1%) (14), which we wished to estimate with 95% confidence within ±5%. We used a design effect of 1.5, and allowed for 10% non- response rate. Through multiplying the sample size by the design effect, 1.5 and incorporating a 10% non-response rate, we estimated 273 children that were needed to be framed in selected households.

Sampling technique

A multistage cluster sampling technique was applied. Wadla district had 20 kebeles (sub-districts) that comprise 247 villages. Twelve of the kebeles were rural, whereas eight of the kebeles were urban. Regarding the villages, 150 of the 247 villages were rural. We used simple random sampling to select 30 of the 150 rural villages. There were 967 households in the selected 30 villages, but only 499 of those households had preschool children. Thus, those 499 households were visited. Heads of households were interviewed for socio-demographic and economic information, plus housing and environmental conditions, and all children aged between 1 and 5 years who had been resident in the district for at least six months were invited to be examined. Eye examiners used the WHO simplified trachoma grading scheme to grade signs of trachoma (15) (Figure1).

The sample size calculated was 273 using single population proportion formula, but as the sampling procedure was cluster sampling, the numbers of screened children were 596 from all 30 villages.

Definitions

Clean face: A face of child that was free of eye discharges, nose discharges or flies at the time of eye examination

Preschool: Children whose age were greater than and equal to 1 year and less than or equal to 5 years old.

Village: A grouping of homes that contained at least 30 households organized as one peasant association

Fly in a home: When there is/are a countable fly in a house during data collection, despite the number of flies

Active trachoma: The presence of at least one of the two signs of active trachoma according to the WHO simplified trachoma grading scheme (TF or TI) in at least one eye (16).

Trachomatis inflammation—follicular (TF): The presence of five or more follicles each having a diameter of at least 0.5mm in the central part of the upper tarsal conjunctiva (16).

Trachomatis inflammation—intense (TI): A pronounced inflammatory thickening of the upper tarsal conjunctiva that obscures more than half of the normal deep tarsal blood vessels (16).

Trachomatis scarring (TS): The presence of easily visible scarring in the upper tarsal conjunctiva (16)

Trachomatis trichiasis (TT): The presence of at least one eyelash rubs on the eyeball or evidence of removal of in-turned eyelashes in the two weeks before examination (16).

Corneal opacity (CO): the presence of easily visible corneal opacity over the pupil (16)

Exclusion and inclusion criteria

All the children belong to the appropriate age range mentioned above and who had lived in the district for at least 6 months, who were resident in selected villages and available at the time of study were invited to be included. Children who were seriously ill or for whom informed consent was not given by parents or guardians were excluded.

Measurements

The outcome variable was active trachoma and measured by physical examination. A number of dependent variables were considered that includes socio-demographic, environmental, hygiene and sanitation, and children’s demographic data.

Data collection tools and procedures

In collecting the data, face to face interviews, observation using a checklist and clinical eye examination were used. Experienced health informatics professionals were using structured interview questions that prepared from pieces of literature (17, 18), while they collected the data on a socio-demographic status, environmental, and housing conditions. All the questionnaires of socio-demographic status, housing, and environmental condition, observation checklist, and eye examination tools were pretested and validated before data collection in Kosomender, Meket district, a district bordering Wadla to the north. A household wealth index was developed using composite indicators for rural residents’ assets: livestock ownership, size of agricultural land and quantity of crop production.

Two integrated eye care workers performed the eye examination. Those integrated eye care workers are ophthalmic nurses who had been previously trained for a total duration of one month for the purposes of contributing to the 2013–2014 national trachoma survey. The Carter Center delivered that previous training using both pictures and live patients as media of instruction. However, for the purpose of this study, the trachoma graders undertook refreshment training for 5 days. This training considers examination of 58 live patients and 100 pictures of different trachoma signs. Trainers, whose grades were used as the gold-standard assessment assessed graders. The training was also delivered for interviewers. Interviewers assisted graders by recording clinical grades, and data related to each household's socio-demographic status and environmental situation. The trainers emphasized on the objectives, procedures of data collection and mode of communication between graders and interviewers. When undertaking the fieldwork, graders initially observed the eyelashes and cornea of study subjects, looking for TT and CO, then everted the upper lid and inspected the upper tarsal conjunctiva for TF, TI, or TS. Binocular lenses (×2.5) and penlight torches were used (4) to magnify the examined eye.

Data analysis and presentation

The data were checked for completeness, coded and entered into Epi-info version 7, and transferred to SPSS version 23 for analysis. The data were checked for normality using Hosmer-Lemeshow-goodness-of-fit. A univariate analysis model were carried out, and variables that had a p-value of <0.25 in a binary logistic regression model were included to the multivariate logistic regression analysis. Potential co-linearity was also considered and tested using multi co-linearity model in considering tolerance and variance inflection factor (VIF). Variables with a p-value of <0.05 in the multivariate logistic regression analysis were considered as statistically significant. A principal component analysis was performed to categorize households’ wealth into poorer, poorest, middle, richer, and richest. However, for the presentation of the variables, the wealth index was grouped into three; lowest, middle, and highest. The procedure of eye examination and result reporting presented in figure2. Both active trachoma and cicatricial trachoma were modeled as outcome variables. Thus, children were screened for both Active and cicatricial types of trachoma (Figure2).

Data quality assurance

The questionnaire was prepared in English and translated to Amharic, then re-translated to English (to check for accuracy) by individuals, who are fluent in both English and Amharic. Both graders and one of the researchers, principal investigator had been participated in a community-based trachoma survey and training before starting the present study. The interviewers had also previous experience in a community-based data collection.

In the study villages, there were 610 preschool children from 499 households. However, only 596 preschool children were examined and gave a response rate of 100%. The remaining 14 children were not involved in the screening phase because of the exclusion criteria and absenteeism after repeated household visit. More than three-fourths 383 (77%) of households had male heads. The range in the number of residents per household was 2 to 10 with a median of five. The range in the number of 1 to 5 years old children per household was 1 to 3 with a median of one. All the 499 families were Amhara in ethnicity and followed Ethiopian orthodox Christianity, and 325 (65%) fathers, and 380 (76%) mothers were unable to read and write. Four hundred and sixty-six (93%) fathers were farmers and 16 (3%) fathers were government employees (Table1).

In addition to the socio-demographic characteristics, the environmental characteristics of households are shown in Table2

Among children examined for signs of active trachoma, 301 (51%) were males, and 295 (49%) were females. The median age of children was 36 months (Table3).

Of the 596 screened children for signs of trachoma, 56.2% of female children had trachoma. One hundred and thirty children had active trachoma, giving a prevalence of 22% [95%CI, 18–25%)]. One hundred and six children had TF, 13 had TI, and 11 had both TF and TI. There were no signs of TS, TT or CO. Two hundred and eighty (47%) children had clean face, 89 (15%) had ocular discharge, 75 (13%) had nasal discharge, 34 (6%) had both ocular and nasal discharge and 55 (9%) children had nasal discharge, ocular discharge, and fly on their face.

Factors associated with active trachoma

On binary logistic regression analysis, lowest economic status, being in the age group of 24-36 months old, unable to read and write educational status of fathers, unable to read and write educational status of mothers, living in a house with a thatched grass roof, fly in a house, and a MUAC of children <13.9cm associated with active trachoma (Table4). However, on the multivariable logistic regression analysis, only lowest economic status (AOR (95% CI), (3.80 (1.27-11.42)), being 37–48 months old (4.21 (1.47-12.03)), living in a house with a thatched grass roof (4.40 (1.42-13.59)), or presence of fly in a home (4.6 (2.1-9.9)) were increasing the odds of active trachoma (Table4).

The objective of this study was to assess the current prevalence of active trachoma and to identify its associations among children aged 1 to 5 years old in rural communities of Wadla district. The prevalence of active trachoma in this age group was 22%, [95%CI, 18–25%], whereas the prevalence of TF was 21%. Although the usual indicator age group for determining the need or otherwise for the A, F and E components of the SAFE strategy is the prevalence of TF in 1 to 9 years-old children, the prevalence that we estimate here suggests that three further years of antibiotic mass drug administration is likely to be required, according to WHO recommendation(19). However, a study from northern Ethiopia reported that azithromycin mass treatment coverage in 2012 was 92.9% (20). That reported mass azithromycin coverage was greater than the minimum coverage set by WHO, 80% (21). The prevalence agreed with a review that indicated 70 million people in Ethiopia required MDA. This was the largest need of any other country in the world (22).

The prevalence of TI among 1 to 5 years old children here was 3.4%. Severe inflammatory trachoma is a risk factor for later cicatricial disease, particularly when the sign is observed repeatedly over a time (23). In our subjects, reportedly face washing once weekly and having a face that had remained unwashed for longer than a week were associated with active trachoma. Similar associations had been seen elsewhere (18, 24). We also found that3963

the absence of a toilet or presence of human excreta near to a home increased the odds of there being active trachoma. Recent multi-country observational data support the link between inadequate access to sanitation and the likelihood of active trachoma (25). In general, the associations that we found agreed with the previous published literature that suggests a strong links between trachoma and environmental factors related to water, sanitation, and hygiene. Some of these associations implicate the fly Musca sorbens, which oviposit in human excreta left exposed on the soil, as an important vector (26-28). In this study, grassed and thatched house roof (AOR (95% CI), 4.402 (1.425-13.597) were increasing the odds of active trachoma. This association evidenced from central Ethiopia (29). In this study, not using soap was increasing the odds of active trachoma [(AOR (95% CI), 4.49 (1.79-11.29)]. This agreed with studies that were conducted in Dessie city and Gonder, Ethiopia (13, 30). Unfortunately, we did not have any entomological data for this site. Other limitations of our analyses include our reliance on self-report for many of the exposure variables, and the exclusion of children aged 6 to 9 years old. However, this research estimates the prevalence of active trachoma among preschool children from rural area, and its associations, for the attention of policymakers interested in trachoma elimination in Wadala district, Amhara region, Ethiopia.

The prevalence of active trachoma among rural preschool children in Wadla district was high, suggesting that active trachoma is still a public health problem in Wadla district. Environmental factors were found to be associated with active trachoma. This might suggest an ongoing need for implementation of the F and E components of the SAFE strategy for trachoma elimination in this district to prevent future trachomatis blindness.

Ethics approval and consent to participate

The study was approved by the Health Research Ethics Review Committee [HRERC0917/2017], College of Health Sciences, Mekelle University. A written permission to implement the study was obtained from Woldia zonal health department and Wadla district health office. A written informed consent was obtained from children’s parents or guardians for interview and examination. Confidentiality was maintained by omitting the name and personal identification of respondents within datasets used for analyses.

Consent for publish

The participants were requested their consent for publication of the outcomes, and agreed on the publication of the outcome in international repeatable, and a peer-reviewed journal.

Availability of data and materials

The data generated in this study will be available to researchers wishing to use the data for non-commercial purposes.

Competing interests

The authors have no competing interests

Funding

This study was sponsored by Mekelle University, College of Health Sciences, and Wadla district health office, northern Ethiopia. Both of the funders did not contribute in collecting, analyzing, writing, and other scientific content of this paper except the full financial expense.

Authors’ Contributions

For this study MWK, AMA, MAG, KDT, and WTB conceived the title and designed the study, conducting a field study, analyzed the data, critically revising the work and writing the final manuscript. All the authors read and approved the final version of this manuscript and agreed to be accountable for all aspects of this work.

Acknowledgments

We would like to acknowledge nursing department, college of health science, Mekelle University, and Wadla district health office for providing funds. We are also grateful to Mr. Semagn Gubala, Mr. Mulugeta Wodaje, Mr. Matiyas Munye, Mr. Melak Menberu, and Mr. Eskeziaw Abebe for their immense contribution in drafting and finalizing the paper. Lastly, we are thankful to the community of the study area, Wadla district and respondents whose participation made the work possible.

COR – Crude odds ratio, AOR- Adjusted odds ratio, CI – Confidence interval, AT-Active Trachoma, SAFE-Surgery, Antibiotics, Facial cleanliness, Environmental improvement, GET2020- Global elimination of Trachoma by 2020, WHO- World Health Organization, TT- trachomatis trichiasis, TF- trachomatis inflammation—follicular, TI- trachomatis inflammation—intense, TT- trachomatis trichiasis, CO- corneal opacity, MUAC-Mid upper arm circumference, MDA-mass drug administration

Jawetz, Melnick, and Adelberg. Lange Medical Microbiology. The 24^th United States of America, McGraw-Hill. 2007, ISBN / ASIN: 0071476660. P 531
Victoria Francis and Virginia Turner. Achieving Community Support for Trachoma Control, A guide for district health work. The Edna McConnell Clark Foundation, New York and WHO. United States of America, Helen Keller International.1995.
David CW. Mabey, Anthony W Solomon, Allen Foster. Trachoma seminar. Lancet, 2003. 362. Available from thelancet.com
Imtiaz A, Chaudhry, Yonca O., Arat and Waleed Al-Rashed. Trachoma and conjunctivitis, conjunctivitis as a complex and multifaceted disorder. (INTECH open science. 2011. ISBN: 978-953-307-750-5. Available at: http://www.intechopen.com/books/conjunctivitis-a-complex-and-multifaceteddisorder/trachoma-and-conjunctivitis
Hugh R Taylor. Trachoma as a blinding scourge from the bronze age to the twentieth century. Centre for Eye Research, Australia, 2008.
Gambhir M, Basanez MG, Burton MJ, et al. The development of age-structured model for trachoma transmission dynamics, pathogenesis and control. PLoS Negl Trop Dis 2009; 3(6): e462
Habtamu E, Wondie T, Aweke S, et al. Trachoma and relative poverty: A Case-Control Study. PLoS Negl Trop Dis 2015; 9(11): e0004228
Solomon AW, Holland MJ, Burton MJ, et al. Strategies for control of trachoma: observational study with quantitative PCR. Lancet 2003; 362(9379): 198-204.
Last A, Burr S, Alexander N, et al. Spatial clustering of high load ocular Chlamydia trachomatis infection in trachoma: A cross-sectional population-based study. Pathog Dis 2017.
Ngondi J, Onsarigo A, Matthews F, et al. The effect of 3 years of SAFE (surgery, antibiotics, facial cleanliness, and environmental change) strategy for trachoma control in southern Sudan : a cross-sectional study. Lancet 2006; 368(9535): 589-95.)
Last A., Versteeg B, Shafi Abdurahman O, et al. Detecting extra-ocular Chlamydia trachomatis in a trachoma-endemic community in Ethiopia: Identifying potential routes of transmission. PLoS Negl Trop Dis. 2020; 14(3):e0008120. DOI: 10.1371/journal.pntd.0008120. PMID: 32130213
World Health Organization. WHO Alliance for the Global Elimination of Trachoma by 2020: progress report on elimination of trachoma, 2018. Wkly Epidemiol Rec 2019; 29(94): 317-28.
Yemane Berhane, Dr. Alemayehu Worku, Dr. Abebe Bejiga. A national survey on blindness, low vision and Trachoma in Ethiopia. Federal Ministry of Health of Ethiopia with a support from a consortium of NGOs, Ophthalmological Society of Ethiopia, and the Ethiopian Public Health Association. Addis Ababa, Ethiopia. September 2006.
Muluken Asres, Mulualem Endeshaw, and MeleseYeshambaw. Prevalence and Risk Factors of Active Trachoma among Children in Gondar Zuria District, North Gondar, Ethiopia. Preventive medicine. 2016. 1 (1:5).
World Health Organization. Primary Health Care Level Management of Trachoma. Geneva: [WHO/PBL/93.33]; 1993; 4(2):461–466.
Thylefors B, Dawson CR, Jones BR, West SK, Taylor HR. A simple system for the assessment of trachoma and its complications. Bull World Health Organ. 1987; 65(4):477-83. PMID: 0003500800
Endale Berta. Prevalence and risk factors of active trachoma among children of rural south Gonder, Ethiopia. Addis Ababa University, Thesis. 2004.
Alemayehu Mesfin. Assessing the prevalence of active trachoma among young children in relation to the implementation of safe strategy in Ebinat and East Belesa woreda, North West Ethiopia. Ethiopia, Addis Ababa University, Thesis, 2005.
Solomon AW., Zondervan M., Kuper H., Buchan JC., Mabey DC., Foster A. Trachoma control: a guide for program managers. Geneva: World Health Organization; 2006.
Zelalem Tilahun, Teferi Gedif Fenta. Coverage of azithromycin mass treatment for trachoma elimination in Northwestern Ethiopia: a community based cross-sectional study. BMC Ophthalmology, (2018) 18:193; https://doi.org/10.1186/s12886-018-0868-1
Melese M., Chidambaram JD., Alemayehu W., Lee DC., Cevallos V, Zhou Z, Donnellan C, Saidel M, Whitcher JP, Gaynor BD. Feasibility of eliminating ocular chlamydia trachomatis with repeated mass antibiotic treatments. JAMA, 2004; 292:721–5)
The WHO alliance for the global elimination of trachoma by the year 2020. Wkly Epidemiol Rec 2014; 89: 421–8.)
West SK., Munoz B, Mkocha H, Hsieh YH, Lynch MC. Progression of active trachoma to scarring in a cohort of Tanzanian children. Ophthalmic Epidemiol 2001; 8(2-3): 137-44.
The report during the six meetings of the WHO alliance for the global elimination of blinding trachoma. WHO, Switzerland, Geneva, 2001.
Garn JV., Boisson S., Willis R. et al. Sanitation and water supply coverage thresholds associated with active trachoma: modeling cross-sectional data from 13 countries. PLoS Negl Trop Dis, 2018; 12(1): e0006110.
Emerson PM, Bailey RL, Mahdi OS, Walraven GE, Lindsay SW. Transmission ecology of the fly Musca sorbens, a putative vector of trachoma. Trans R Soc Trop Med Hyg 2000; 94(1): 28-32.
Emerson PM, Bailey RL, Walraven GE, Lindsay SW. Human and other feces as breeding media of the trachoma vector Musca sorbens. Med Vet Entomol 2001; 15(3): 314-20.
Miller K, Pakpour N. et al. Pesky trachoma suspect finally caught. Br J Ophthalmol 2004; 88(6): 750-1.
Jeremiah Ngondi et al. Risk factors for active trachoma in children and trichiasis in adults: a household survey in Amhara Regional State, Ethiopia. ScienceDirect, Transactions of the Royal Society of Tropical Medicine and Hygiene, 2008, 102, 432— 438
Michael J. Mahande, Humphrey D. Mazigo and Eliningaya J. Kweka. Association between water related factors and active trachoma in Hai district, northern Tanzania. Infectious diseases of poverty. 2012, 1:10

Table1: Socio-demographic characteristics of households in rural Wadla district, northern Ethiopia, 2017, (n=499)

Variables	Frequency	Percent (%)
Sex of head of a household
Male Female	383	76.8
Male Female	116	23.2
Marital status of head of a household
Married	492	98.6
Divorce	7	1.4
Wealth index
Poor	144	28.9
Medium	279	55.9
Rich	76	15.2
Occupation of head of a household
Farmer	466	93.4
Merchant	17	3.4
Government employee	16	3.2
Educational status of head of a household
Unable to read and write	325	65.1
Able to read and write	109	21.8
Up to grade 8	35	7
Grade 9 to 12	19	3.8
Diploma and above	11	2.2
Educational status of mothers
Unable to read and write	380	76.2
Able to read and write	55	11
Up to grade 8	23	4.6
Grade 9 to 12	35	7
Diploma	6	1.2
Number of rooms in the house (observation)
One	424	85
Two and more	75	15
Family size
Less than 6	286	57.3
Greater than and equal to 6	213	42.7
Total number of children less than five years in a house
One	424	85
Two	69	13.8
Three	6	1.2
Number of children less than ten years in a house
One	132	26.5
Two	240	48.1
Three	102	20.4
Four	25	5
Adult face washing habit (self-report)
At least one times per a day	417	83.6
Less than 7 times per a week	82	16.4

In addition to the socio-demographic characteristics, the environmental characteristics of households are shown in Table2

Table2: The environmental conditions in rural Wadla district, northern Ethiopia, 2017, (n=499)

Variables	Frequency				Percent (%)
Presence of fly in or around a house (observation)
Present Absent		242			48.5
		257			51.5
Source of water (self-report)
River		30			6.0
Unprotected well		12			2.4
Protected well		56			11.2
Pipe		401			80.4
Amount of water in a litter (self -report)
Less than 20		180			36.1
20-40		162			32.5
40-60		92			18.4
60-80		49			9.8
Greater than 80		16			3.2
Total time taken to reach to water source (self-report)
Less than and equal to 1/2 hr.		459			92
Greater than 1/2 hr.		40			8
Place of cooking (observation)
In the same room of living house		157			31.7
In the same house but in a kitchen		166			33.3
A kitchen constructed against outside wall of the house		3			.6
Isolated kitchen		173			34.7
Presence of window in a kitchen (observation)
Yes		248			49.7
No		251			50.3
Household waste removal (self-report)
Burn it		312			62.5
Bury it		90			18
Dispose in the farm		93			18.8
Dispose in another place		4			.8
Presence of latrine (observation)
Present		371			74.3
Absent		128			25.7
Presence of feces at open field in nearby a house (observation)
Present		243			48.7
Absent		256			51.3
Presence of cattle in a household (observation)
Present				439	87.9
Absent				60	12.1
Cattle sheltering (n=439) (observation)
In the same room where family lives			128		29.1
In the same living house but in a separate room			203		46.2
Attached shelter against outside of the house			6		1.6
Isolated shelter far from the house			102		23.1

Among children examined for signs of active trachoma, 301 (51%) were males, and 295 (49%) were females. The median age of children was 36 months (Table3).

Table3: Socio-demographic characteristics of pre-school children in rural Wadla district, northern Ethiopia, 2017, (n=596)

Variables	Frequency	Percent
Sex of children
Male Female	301	50.5
Male Female	295	49.5
Age of children in months (kebele registration book)
12 – 24	208	34.9
25 – 36	102	17.10
37 – 48	129	21.6
49 – 59	157	26.3
Current breast-feeding status of children
Yes	239	40.1
No	357	59.9
Face washing frequency of children (self-report)
2 or more times per a day	108	18.1
Once daily	79	13.3
2 to 6 times per week	149	25
Once weekly	167	28
Stays unwashed for longer than a week.	93	15.6
Habit of child bathing for at least one times per a week (self-report)
Yes	445	74.7
No	151	25.3
Use of soap for face washing(self-report)
Yes	264	44.3
No	332	55.7
Use of soap for hand washing(self-report)
Yes	254	42.6
No	342	57.4
Face of children on observation (observation)
Clean face	280	47
Ocular discharge	89	14.9
Nasal discharge	75	12.6
Flies on the face of child		10.6
Ocular and nasal discharge	34	5.7
Ocular and nasal discharge and flies on the face	55	9.2
Presence of another eye problem(self-report)
Yes	146	24.5
No	450	75.5
Type of eye problem (n=146)
Discharge	96	65.6
Itching	8	5.3
Excessive tear	25	17.1
Redness of eye	18	12.2
Took drug during mass drug administration in the last year(self-report)
Yes	515	86.4
No	81	13.6

Table4: Factors associated with active trachoma among pre-school children in rural Wadla district, northern Ethiopia, 2017, (n=596)

Variables

Trachoma

OR (95% CI)

Presence (%)

Absence (%)

COR

AOR

Type of house roof (observation)

Clean iron

Thatch iron

Clean grass

Thatch grass

15 (11.5)

24 (18.5)

27 (20.8)

64 (49.2)

82 (17.6)

141 (30.3)

144 (30.9)

99 (21.2)

1.00

0.9(0.5-1.9)

1.0(0.5-2.0)

3.5 (1.9-6.7) *

1.00

0.9 (0.3-2.8)

0.7 (0.2-2.2)

4.4 (1.4-13.6) *

Fly in a house or in nearby (observation)

Yes

96(73.8)

34 (26.2)

206 (44.2)

260 (55.8)

3.6 (2.3-5.5)

1.00

4.6 (2.1-9.9) *

1.00

Face washing frequency (self-report)

Two and more times

Once daily

2 to 6 times per a week

Once weekly

Unwashed for a week

9 (6.9)

2 (1.5)

15 (11.5)

63 (48.5)

41(31.5)

99 (21.2)

77 (16.5)

134 (28.8)

104 (22.3)

52 (11.2)

1.00

0.3 (0.1-1.4)

1.2 (0.5-2.9)

6.7 (3.1-14.1) *

8.7 (3.9-19.2) *

1.00

0.2 (0.03-1.3)

1.366 (.365-5.114)

8.7 (2.6-29.3) *

10.6 (2.9-37.7) *

Soap for face washing(self-report)

Used

Not used

26 (20)

104 (80)

238 (51.1)

228 (48.9)

1.00

4.2 (2.6-6.7) *

1.00

4.5 (1.8-11.3) *

Soap for hand washing(self-report)

Used

Not used

35 (26.9)

95(73.1)

219 (47.0)

247 (53.0)

1.00

2.4 (1.6-3.7) *

1.00

1.6 (0.8-3.6)

Household latrine (observation)

Present

Absent

7 (21.2)

26 (78.8)

364 (78.1)

102 (21.9)

1.00

2.0 (1.3-3.0) *

1.00

5.0 (2.0-12.9) *

Household waste around the house (observation)

Exist

Not exist

80(61.5)

50 (38.5)

214 (45.9)

252 (54.1)

1.9 (1.3-2.8) *

1.00

3.4 (1.6-7.6) *

1.00

Mothers educational status

Unable to read and write

Able to read and write

Attend formal education

Wealth index

Poor

Medium

Rich

MUAC of children

Less than 13.9

Greater than 14

Age of children (in months)

12-24

25-36

37-48

49-59

Fathers education

Unable to read and write

Able to read and write

Formal education

111 (85.4)

12 (9.2)

7 (5.4)

73 (56.2%)

45 (34.6%)

12 (9.2%)

81(62.3)

49(37.7)

42 (32.3)

14 (10.8)

36 (27.7)

38 (29.2)

93 (71.5)

28 (21.5)

9 (6.9)

348 (74.7)

53 (11.4)

65 (13.9)

101 (21.7)

288 (61.8)

77(16.5)

230 (49.4)

236 (50.6)

166 (35.6)

88 (18.9)

93 (20)

119 (25.5)

299 (64.2)

102 (21.9)

65 (13.9)

2.9 (1.3-6.6) *

2.1 (0.8-5.7)

1.00

4.6 (2.3-9.1) *

1.003 (.506-1.988)

1.000

1.7 (1.1-2.52) *

1.00

0.8 (0.5-1.3)

0.5 (0.3-0.9) *

1.2 (0.7-2.1)

1,00

2.3 (1.1-4.7) *

1.9(0.9-4.5)

1.00

0.8 (0.2-3.2)

0.3 (0.1-1.6)

1.00

4.2 (1.5-12.0)

0.5(0.2-1.4)

1.00

1.3 (0.6-2.6)

1.00

0.7 (0.3-1.8)

0.7(0.2- 2.1)

2.7(.1.0-7.2)

1.00

1.4 (0.3-6.2)

2.1 (0.5-9.7)

1.00

*= p < 0.05

PDF

Journal Publication

published 26 Aug, 2020

Read the published version in BMC Ophthalmology →

Submission checks completed at journal
25 Jul, 2020
Editorial decision: Accept
24 Jul, 2020

You are reading this latest preprint version

Prevalence and associations of active trachoma among rural preschool children in Wadla district, northern Ethiopia

Status:

Journal Publication

Version 7

Abstract

Figures

Background

Methods

Results

Discussion

Conclusions

Declarations

Abbreviations

References

Tables

Supplementary Files

Status:

Journal Publication

Version 7