N. Bari, L. Muthupalaniappen, S. NarulAida, M. Diana
{"title":"马来西亚人类免疫缺陷病毒感染者的自我认知耻辱及其对生活质量的影响","authors":"N. Bari, L. Muthupalaniappen, S. NarulAida, M. Diana","doi":"10.17576/MH.2017.1202.08","DOIUrl":null,"url":null,"abstract":"Human Immunodeficiency Virus (HIV) epidemic remains a significant burden in Malaysia. Stigma related to HIV and its effect on the quality of life (QOL) of persons living with HIV (PLHIV) remains under-reported. The aim of the present study was to assess self-perceived stigma amongst PLHIV attending an urban community clinic and its influence on their QOL. Data was collected using HIV Stigma Scale and WHO-QOL HIV BREF Scale. The overall stigma experienced by PLHIV in this community was higher than previous studies (mean ± SD; 103.37 ±18.14). Majority participants had fear disclosing their disease status, while personalized stigma or the experience of prejudice and rejection was the least experienced. The overall QOL was low and was significantly impaired in social relationship domain (mean ± SD; 12.72 ± 3.59). However, their ability to perform daily activities was not affected by the illness (mean ± SD; 14.48 ± 2.91). PLHIV with higher spiritual values demonstrate lower perception of negative self-image and inferiority (r= -0.54). This finding was unique to PLHIV in this study and suggested the importance of spirituality and personal beliefs on their self-esteem. In conclusion, stigma remains as a significant problem among PLHIV in this community. Primary care offers the best platform to promote a holistic management of PLHIV, where the integration between counselors, religious experts, family and non-governmental associations could come together. The management of PLHIV is unique in every community, hence individualized approach based on cultural norms and beliefs could assist in the overall management of PLHIV.","PeriodicalId":53946,"journal":{"name":"Medicine and Health","volume":"5 1","pages":"230-243"},"PeriodicalIF":0.1000,"publicationDate":"2017-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Self-perceived stigma and its effect on quality of life among Malaysians living with human immunodeficiency virus\",\"authors\":\"N. Bari, L. Muthupalaniappen, S. NarulAida, M. Diana\",\"doi\":\"10.17576/MH.2017.1202.08\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Human Immunodeficiency Virus (HIV) epidemic remains a significant burden in Malaysia. Stigma related to HIV and its effect on the quality of life (QOL) of persons living with HIV (PLHIV) remains under-reported. The aim of the present study was to assess self-perceived stigma amongst PLHIV attending an urban community clinic and its influence on their QOL. Data was collected using HIV Stigma Scale and WHO-QOL HIV BREF Scale. The overall stigma experienced by PLHIV in this community was higher than previous studies (mean ± SD; 103.37 ±18.14). Majority participants had fear disclosing their disease status, while personalized stigma or the experience of prejudice and rejection was the least experienced. The overall QOL was low and was significantly impaired in social relationship domain (mean ± SD; 12.72 ± 3.59). However, their ability to perform daily activities was not affected by the illness (mean ± SD; 14.48 ± 2.91). PLHIV with higher spiritual values demonstrate lower perception of negative self-image and inferiority (r= -0.54). This finding was unique to PLHIV in this study and suggested the importance of spirituality and personal beliefs on their self-esteem. In conclusion, stigma remains as a significant problem among PLHIV in this community. Primary care offers the best platform to promote a holistic management of PLHIV, where the integration between counselors, religious experts, family and non-governmental associations could come together. The management of PLHIV is unique in every community, hence individualized approach based on cultural norms and beliefs could assist in the overall management of PLHIV.\",\"PeriodicalId\":53946,\"journal\":{\"name\":\"Medicine and Health\",\"volume\":\"5 1\",\"pages\":\"230-243\"},\"PeriodicalIF\":0.1000,\"publicationDate\":\"2017-12-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medicine and Health\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.17576/MH.2017.1202.08\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medicine and Health","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.17576/MH.2017.1202.08","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 2
摘要
人体免疫缺陷病毒(艾滋病毒)流行病仍然是马来西亚的一个重大负担。与艾滋病毒相关的耻辱感及其对艾滋病毒感染者生活质量(QOL)的影响仍未得到充分报道。本研究的目的是评估在城市社区诊所就诊的艾滋病毒感染者的自我感觉耻感及其对生活质量的影响。采用HIV污名量表和WHO-QOL HIV BREF量表收集数据。该社区PLHIV患者的总体耻辱感高于以往的研究(mean±SD;103.37±18.14)。大多数参与者害怕透露自己的疾病状况,而个性化的耻辱或偏见和拒绝的经历是最少的。总体生活质量较低,在社会关系领域显著受损(mean±SD;12.72±3.59)。然而,他们进行日常活动的能力不受疾病的影响(mean±SD;(14.48±2.91)。精神价值越高的hiv患者自我负面形象和自卑感越低(r= -0.54)。这一发现在本研究中是PLHIV独有的,表明精神和个人信仰对他们自尊的重要性。总之,耻辱感仍然是该社区PLHIV中的一个重要问题。初级保健为促进艾滋病毒感染者的全面管理提供了最好的平台,辅导员、宗教专家、家庭和非政府组织之间的整合可以走到一起。PLHIV的管理在每个社区都是独特的,因此基于文化规范和信仰的个性化方法可以帮助整体管理PLHIV。
Self-perceived stigma and its effect on quality of life among Malaysians living with human immunodeficiency virus
Human Immunodeficiency Virus (HIV) epidemic remains a significant burden in Malaysia. Stigma related to HIV and its effect on the quality of life (QOL) of persons living with HIV (PLHIV) remains under-reported. The aim of the present study was to assess self-perceived stigma amongst PLHIV attending an urban community clinic and its influence on their QOL. Data was collected using HIV Stigma Scale and WHO-QOL HIV BREF Scale. The overall stigma experienced by PLHIV in this community was higher than previous studies (mean ± SD; 103.37 ±18.14). Majority participants had fear disclosing their disease status, while personalized stigma or the experience of prejudice and rejection was the least experienced. The overall QOL was low and was significantly impaired in social relationship domain (mean ± SD; 12.72 ± 3.59). However, their ability to perform daily activities was not affected by the illness (mean ± SD; 14.48 ± 2.91). PLHIV with higher spiritual values demonstrate lower perception of negative self-image and inferiority (r= -0.54). This finding was unique to PLHIV in this study and suggested the importance of spirituality and personal beliefs on their self-esteem. In conclusion, stigma remains as a significant problem among PLHIV in this community. Primary care offers the best platform to promote a holistic management of PLHIV, where the integration between counselors, religious experts, family and non-governmental associations could come together. The management of PLHIV is unique in every community, hence individualized approach based on cultural norms and beliefs could assist in the overall management of PLHIV.