印度恰蒂斯加尔邦部落集中的巴斯塔尔地区麻风病患者所经历的知识、态度和耻辱

Swapan Kumar Kolay
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引用次数: 2

摘要

目的:了解印度恰蒂斯加尔邦部落集中的巴斯塔尔地区麻风病患者的知识、态度和病耻感。方法:本横断面研究纳入2012年4月至2013年6月在一个麻风治疗中心登记的101例麻风患者。数据收集工具(预先测试的封闭式问卷)基于麻风病相关的社会人口变量,了解患者/参与者所经历的不同类型的问题和问题。调查人员通过面对面访谈和家访收集数据。结果:总体上,受访者年龄在16 - 60岁之间的占85.1%。74.3%为男性,80.2%为已婚,54.5%为文盲。大多数(67.3%)对疾病的传播有积极的认识,75.3%的人知道手麻木是早期症状,88.12%的人知道手麻木是可以治愈的,91.1%的人有未经治疗的畸形。报告的经历包括婚姻关系(90.1%)或社交生活(94.1%)受到干扰,失业(54.5%),与人交谈(29.7%),家庭成员不分享食物(94.1%);被迫离开家庭(54.45%)。健康教育干预提高了91.1%的参与者的知识水平。多杆菌性麻风病在新登记病例中较高,手脚(60.4%)和眼睛(29.7%)残疾程度较高。9.9%的世卫组织二级残疾是由于诊断延误造成的。67.5%患有某种形式残疾的患者/参与者经历了长达12个月的诊断延迟。结论:该研究指出,麻风病对部落人民的影响不仅体现在身体问题上,而且还体现在影响其社会参与的污名化上。需要通过国家麻风病规划的进展来解决这些问题。关键词:麻风病,社会污名,残疾分级,印度
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Knowledge, attitude and stigma experienced by leprosy patients in tribal concentrated Bastar district of Chhattisgarh, India
Objective: To study leprosy patients in tribal concentrated Bastar district of Chhattisgarh, India in terms of their knowledge, attitudes and the stigma they have experienced. Method: This cross-sectional study included 101 registered Leprosy patients, in a single leprosy treatment centre between April, 2012 - June, 2013. The data collection tool (a pre tested close-ended questionnaire) was based on leprosy related socio-demographic variables, knowled geregarding different kinds of problems and issues experienced by the patients/participants. The investigators collected the data in face to face interviews and house hold visit. Results: Overall the majority of the respondents (85.1%) were between 16 and 60 years of age. 74.3% were males, 80.2% were married, and 54.5% were literate. The majority (67.3%) articulated positive knowledge about transmission of the disease, 75.3% knew that numbness of hands is an early symptom, 88.12% that it is curable, 91.1% had untreated deformities. Experiences reported included disturbed marital relationships (90.1%) or social life (94.1%), loss of employment (54.5%), isolation with the sitation to talk to people (29.7%), family members not sharing food (94.1%); being forced to leave the family (54.45%). Health education interventions improved the knowledge of 91.1% of participants. Multi-Bacillary leprosy was higher in newly registered cases with higher disabilities in the hands and feet (60.4%), eyes (29.7%). 9.9% of WHO grade-2 disabilities were due to a delayed diagnosis. 67.5% of the patients/participants with some form of disability had experienced a delay in diagnosis up to 12 months. Conclusion: The study noted that the tribal people were affected by leprosy not only in terms of the physical problems, but also by the stigmatization that affects their social participation. These need to be addressed by the progress of the national leprosyp rogram. Keywords: Leprosy, social stigma, disability grading, India
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