{"title":"脱发患者在工作场所遭受欺凌的经历:一项横断面调查研究。","authors":"Sara J Li, Sophia Reyes-Hadsall, Lara Drake, Kathie Huang, Arash Mostaghimi","doi":"10.1159/000529924","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Alopecia areata (AA) is an immune-mediated hair loss condition with substantial psychosocial impact. The impact of AA on social interactions at work has not been established.</p><p><strong>Methods: </strong>We administered the Negative Acts Questionnaire-Revised Scale to the National Alopecia Areata Foundation database to evaluate workplace bullying in patients with AA.</p><p><strong>Results: </strong>Ultimately, 673/1,120 individuals who met inclusion criteria completed the survey. Most respondents were female (<i>n</i> = 537, 79.8%), Caucasian (<i>n</i> = 508, 75.5%), with an average age of 46.8 ± 14, and employed full-time (<i>n</i> = 427, 63.4%). Our results demonstrate 21.7% (<i>n</i> = 146) of respondents experienced workplace bullying. Participants most frequently faced having their opinions ignored (53.8%, <i>n</i> = 362), being excluded (47.7%, <i>n</i> = 321), and having gossip spread about them (44.0%, <i>n</i> = 296). Notably, 75.0% (<i>n</i> = 120/160) of individuals who self-reported bullying addressed the behavior; however, 30.8% of participants noted the bully continued (30.8%, <i>n</i> = 37). Stress associated with filing a complaint (43.5%, <i>n</i> = 293) and effect on future career options (36.1%, <i>n</i> = 243) were common barriers to report bullying.</p><p><strong>Conclusion: </strong>This study expands our understanding of the psychosocial impact of AA by confirming individuals with AA experience workplace bullying. Stigma against patients may play a role in this phenomenon. Future work is warranted to identify strategies to reduce bullying against patients with AA.</p>","PeriodicalId":21844,"journal":{"name":"Skin Appendage Disorders","volume":"9 4","pages":"258-261"},"PeriodicalIF":1.4000,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10410103/pdf/","citationCount":"0","resultStr":"{\"title\":\"Experiencing Workplace Bullying in Patients with Alopecia Areata: A Cross-Sectional Survey Study.\",\"authors\":\"Sara J Li, Sophia Reyes-Hadsall, Lara Drake, Kathie Huang, Arash Mostaghimi\",\"doi\":\"10.1159/000529924\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Alopecia areata (AA) is an immune-mediated hair loss condition with substantial psychosocial impact. The impact of AA on social interactions at work has not been established.</p><p><strong>Methods: </strong>We administered the Negative Acts Questionnaire-Revised Scale to the National Alopecia Areata Foundation database to evaluate workplace bullying in patients with AA.</p><p><strong>Results: </strong>Ultimately, 673/1,120 individuals who met inclusion criteria completed the survey. Most respondents were female (<i>n</i> = 537, 79.8%), Caucasian (<i>n</i> = 508, 75.5%), with an average age of 46.8 ± 14, and employed full-time (<i>n</i> = 427, 63.4%). Our results demonstrate 21.7% (<i>n</i> = 146) of respondents experienced workplace bullying. Participants most frequently faced having their opinions ignored (53.8%, <i>n</i> = 362), being excluded (47.7%, <i>n</i> = 321), and having gossip spread about them (44.0%, <i>n</i> = 296). Notably, 75.0% (<i>n</i> = 120/160) of individuals who self-reported bullying addressed the behavior; however, 30.8% of participants noted the bully continued (30.8%, <i>n</i> = 37). Stress associated with filing a complaint (43.5%, <i>n</i> = 293) and effect on future career options (36.1%, <i>n</i> = 243) were common barriers to report bullying.</p><p><strong>Conclusion: </strong>This study expands our understanding of the psychosocial impact of AA by confirming individuals with AA experience workplace bullying. Stigma against patients may play a role in this phenomenon. Future work is warranted to identify strategies to reduce bullying against patients with AA.</p>\",\"PeriodicalId\":21844,\"journal\":{\"name\":\"Skin Appendage Disorders\",\"volume\":\"9 4\",\"pages\":\"258-261\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2023-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10410103/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Skin Appendage Disorders\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1159/000529924\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/4/27 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"DERMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Skin Appendage Disorders","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000529924","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/4/27 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"DERMATOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
简介斑秃(AA)是一种免疫介导的脱发疾病,对社会心理有很大影响。AA 对工作中社会交往的影响尚未确定:我们在全国脱发基金会的数据库中使用了消极行为问卷-修订版量表,以评估 AA 患者在工作场所受到欺凌的情况:最终,符合纳入标准的 673/1,120 人完成了调查。大多数受访者为女性(n = 537,79.8%)、白种人(n = 508,75.5%),平均年龄为 46.8 ± 14 岁,从事全职工作(n = 427,63.4%)。我们的研究结果表明,21.7% 的受访者(n = 146)曾遭受过职场欺凌。受访者最常遇到的情况是自己的意见被忽视(53.8%,n = 362)、被排斥(47.7%,n = 321)和被人说闲话(44.0%,n = 296)。值得注意的是,75.0%(n = 120/160)的自我报告者对欺凌行为进行了处理;然而,30.8% 的参与者指出欺凌行为仍在继续(30.8%,n = 37)。与投诉相关的压力(43.5%,n = 293)和对未来职业选择的影响(36.1%,n = 243)是报告欺凌行为的常见障碍:本研究证实 AA 患者会遭受工作场所欺凌,从而加深了我们对 AA 的社会心理影响的了解。对患者的成见可能在这一现象中起到了一定的作用。我们有必要在未来开展工作,确定减少 AA 患者遭受欺凌的策略。
Experiencing Workplace Bullying in Patients with Alopecia Areata: A Cross-Sectional Survey Study.
Introduction: Alopecia areata (AA) is an immune-mediated hair loss condition with substantial psychosocial impact. The impact of AA on social interactions at work has not been established.
Methods: We administered the Negative Acts Questionnaire-Revised Scale to the National Alopecia Areata Foundation database to evaluate workplace bullying in patients with AA.
Results: Ultimately, 673/1,120 individuals who met inclusion criteria completed the survey. Most respondents were female (n = 537, 79.8%), Caucasian (n = 508, 75.5%), with an average age of 46.8 ± 14, and employed full-time (n = 427, 63.4%). Our results demonstrate 21.7% (n = 146) of respondents experienced workplace bullying. Participants most frequently faced having their opinions ignored (53.8%, n = 362), being excluded (47.7%, n = 321), and having gossip spread about them (44.0%, n = 296). Notably, 75.0% (n = 120/160) of individuals who self-reported bullying addressed the behavior; however, 30.8% of participants noted the bully continued (30.8%, n = 37). Stress associated with filing a complaint (43.5%, n = 293) and effect on future career options (36.1%, n = 243) were common barriers to report bullying.
Conclusion: This study expands our understanding of the psychosocial impact of AA by confirming individuals with AA experience workplace bullying. Stigma against patients may play a role in this phenomenon. Future work is warranted to identify strategies to reduce bullying against patients with AA.