Onchocercal skin disease in Benue state, Nigeria: integrated assessment of burden and psychosocial impact, and associated factors

U. Ugbomoiko, Asen Bem, Abdulkareen Olarewaju Babamale, Rukayat Queen Adegbola, Nyamngee Amase, C. Alencar, J. Heukelbach
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Abstract

Aim: We aimed to measure the degree to which onchocercal skin disease (OSD) impairs quality of life (QoL) in endemic resource-poor communities in the Ushongo, Kwande, and Katsina-ale local government areas of Benue State, Nigeria. Methods: We evaluated the skin characteristics and QoL of 307 children and adults with OSD using a modified dermatological life quality index (mDLQI). Assessment of OSD was conducted and scored using mDLQI from 0 (no effects) to 18 (large effects). Thereafter, structured questionnaires were applied to assess the knowledge, attitudes, and predictors of moderate and severe OSD patients. Results: In total, 235/307 (76.5%) participants presented onchocercal nodules; chronic papular dermatitis was found in 68 (22.1%). A total of 288 (93.8%) had two or more OSD-associated symptoms. The median mDLQI score was 0 [interquartile range (IQR): 0-0] in children and 5 in adults (IQR: 2-8). A higher mDLQI median score was observed in farmers. There was a statistically significant difference between children and adults (P < 0.001). The most frequently reported impairments were social exclusion, embarrassment/shame, and restriction from work/leisure activities. In logistic regression analysis, there was a significant association with increasing age (adjusted odds ratio (AOR) = 1.44; 95%CI: 1.21-1.71; P < 0.001) and visual impairment (AOR = 1.78; 95%CI: 1.02-3.10; P = 0.040) with severe mDLQI. Papular rash was an independent protective factor (AOR = 0.50; 95%CI: 0.27-0.93; P = 0.030). Conclusion: Onchocerciasis-related morbidity has a profound measurable impact on the individual QoL, affecting the overall socioeconomic well-being of the affected community, if left untreated. Therefore, strict supervision and follow-up of home-based mass treatment with ivermectin are vital for successful control of the disease and to reduce the burden on affected communities.
尼日利亚贝努埃州盘尾虫性皮肤病:负担和心理社会影响及相关因素的综合评估
目的:我们旨在衡量盘尾蚴性皮肤病(OSD)对尼日利亚贝努埃州Ushongo、Kwande和Katsina-ale地方政府地区地方性资源贫乏社区生活质量(QoL)的影响程度。方法:采用改良皮肤生活质量指数(mDLQI)评价307例儿童和成人OSD的皮肤特征和生活质量。对OSD进行评估,并使用mDLQI评分,评分范围从0(无影响)到18(大影响)。随后,采用结构化问卷对中重度OSD患者的认知、态度和预测因素进行评估。结果:总共有235/307(76.5%)参与者出现盘尾结节;慢性丘疹性皮炎68例(22.1%)。共有288人(93.8%)有两种或两种以上的osd相关症状。儿童mDLQI评分中位数为0[四分位间距(IQR): 0-0],成人为5 (IQR: 2-8)。农民的mDLQI中位数得分较高。儿童与成人的差异有统计学意义(P < 0.001)。报告中最常见的障碍是社交排斥、尴尬/羞耻以及工作/休闲活动受限。在logistic回归分析中,与年龄增加有显著相关(校正优势比(AOR) = 1.44;95%置信区间:1.21—-1.71;P < 0.001)和视力障碍(AOR = 1.78;95%置信区间:1.02—-3.10;P = 0.040),重度mDLQI。丘疹是独立的保护因素(AOR = 0.50;95%置信区间:0.27—-0.93;P = 0.030)。结论:盘尾丝虫病相关发病率对个体生活质量有深远的可衡量的影响,如果不及时治疗,会影响受影响社区的整体社会经济福祉。因此,严格监督和跟踪以家庭为基础的伊维菌素大规模治疗对于成功控制该病和减轻受影响社区的负担至关重要。
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