Department of Dermatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA; Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA; Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Department of Family Medicine and Community Health, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
J Invest Dermatol. 2019 Aug;139(8):1672-1679.e1. doi: 10.1016/j.jid.2018.12.032. Epub 2019 Feb 6.
In the United States, black patients are less likely than white patients to receive biologic treatment for their psoriasis. We conducted a qualitative free-listing study to identify patient-generated factors that may explain this apparent racial disparity in psoriasis treatment by comparing the perceptions of biologics and other psoriasis therapies between white and black adults with psoriasis. Participants included 68 white and black adults with moderate to severe psoriasis who had and had not received biologic treatment. Each participant was asked to list words in response to verbal probes querying five psoriasis treatments: self-injectable biologics, infliximab, methotrexate, apremilast, and phototherapy. Salience scores indicating the relative importance of each word were calculated, and salient words were compared across each race/treatment group. Participants who had experience with biologics generally associated positive words with self-injectable biologics. Among biologic-naïve participants, "apprehension," "side effects," and "immune suppression" were most salient. "Unfamiliar" and "dislike needles" were salient only among black participants who were biologic naïve. Participants were generally unfamiliar with the other psoriasis therapies except phototherapy. Unfamiliarity with biologics, particularly among black, biologic-naïve patients, may partly explain the existing racial disparity in biologic treatment for psoriasis and might stem from lack of exposure to or poor understanding of biologics.
在美国,黑人患者接受生物治疗银屑病的可能性低于白人患者。我们进行了一项定性自由列表研究,通过比较有和没有接受生物治疗的白人成年人和黑人成年人对生物制剂和其他银屑病治疗方法的看法,来确定可能导致银屑病治疗中这种明显种族差异的患者产生的因素。参与者包括 68 名患有中重度银屑病且接受过和未接受过生物治疗的白人和黑人成年人。每个参与者都被要求列出五个银屑病治疗方法的词:自我注射生物制剂、英夫利昔单抗、甲氨蝶呤、阿普米司特和光疗。计算出表示每个词相对重要性的显着性得分,并比较每个种族/治疗组的显着词。有生物制剂治疗经验的参与者通常将积极的词与自我注射生物制剂联系起来。在生物制剂初治者中,“焦虑”、“副作用”和“免疫抑制”是最突出的。“不熟悉”和“不喜欢针”仅在初治的黑人参与者中突出。除光疗外,参与者通常对其他银屑病治疗方法不熟悉。对生物制剂的不熟悉,特别是在黑人初治的生物制剂患者中,可能部分解释了银屑病生物治疗中现有的种族差异,并且可能源于对生物制剂缺乏接触或理解不足。