Georgios Kokolakis, Eva Vilarrasa, Amit Garg, Ivette Alarcon, Mei Go, Gillian Newbold, Aikaterini Mamareli, Craig Richardson, Barry M. McGrath, Philippe Guillem
{"title":"患者对化脓性汗腺炎影响的看法:来自全球“HS未发现”疾病负担调查的结果","authors":"Georgios Kokolakis, Eva Vilarrasa, Amit Garg, Ivette Alarcon, Mei Go, Gillian Newbold, Aikaterini Mamareli, Craig Richardson, Barry M. McGrath, Philippe Guillem","doi":"10.1002/jvc2.70071","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Hidradenitis suppurativa (HS) is a chronic, painful inflammatory skin disease. There is a need to evaluate how patients experience their disease.</p>\n </section>\n \n <section>\n \n <h3> Objectives</h3>\n \n <p>The HS Uncovered survey was conducted to understand patient activation, the patient journey and burden of disease.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>HS Uncovered was a real-world, quantitative, online survey completed by adults who self-reported a diagnosis/suspected diagnosis of HS. The survey included patient-reported outcome measures (PROMs) and non-PROM-related questions and was conducted between December 2022 to March 2023 in six countries (US, UK, Germany, France, ltaly, Spain). PROMs included the Patient Activation Measure (PAM13; primary endpoint), Dermatology Life Quality Index (DLQI), Work Productivity and Activity Impairment (WPAI) and Hospital Anxiety and Depression Scale (HADS) tools (Spain excluded from PROM analyses).</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Overall, 656 participants were included (<i>N</i> = 505, diagnosed HS; <i>N</i> = 151, suspected HS). Of 425 diagnosed participants, 66% reported high (level 3/4) PAM13 scores. A very large (DLQI score 11–20) and extremely large (DLQI score 21–30) effect of HS on QoL was reported by 41% and 28% of participants, respectively. A very large to extremely large effect of HS on QoL (DLQI score 11–30) was reported by 67% and 73% of patients with level 3 and 4 PAM13 scores, respectively. Overall, 53% and 29% of diagnosed participants reported abnormal anxiety and depression, respectively. The percentage of work impairment due to HS in employed diagnosed participants (<i>N</i> = 302) was 52%. Of diagnosed females, 52% considered HS a concern for family planning. Overall (<i>N</i> = 656), 58% of participants considered pain relief the most important treatment feature.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>Despite participants having high activation levels, HS had a negative impact on QoL, mental health, work and activity. There is an unmet need for effective treatments that provide sustained pain reduction and improve work productivity in HS.</p>\n </section>\n </div>","PeriodicalId":94325,"journal":{"name":"JEADV clinical practice","volume":"4 4","pages":"920-929"},"PeriodicalIF":0.5000,"publicationDate":"2025-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jvc2.70071","citationCount":"0","resultStr":"{\"title\":\"Patient Perspectives on the Impact of Living With Hidradenitis Suppurativa: Results From the Global ‘HS Uncovered’ Burden of Disease Survey\",\"authors\":\"Georgios Kokolakis, Eva Vilarrasa, Amit Garg, Ivette Alarcon, Mei Go, Gillian Newbold, Aikaterini Mamareli, Craig Richardson, Barry M. McGrath, Philippe Guillem\",\"doi\":\"10.1002/jvc2.70071\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>Hidradenitis suppurativa (HS) is a chronic, painful inflammatory skin disease. There is a need to evaluate how patients experience their disease.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Objectives</h3>\\n \\n <p>The HS Uncovered survey was conducted to understand patient activation, the patient journey and burden of disease.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>HS Uncovered was a real-world, quantitative, online survey completed by adults who self-reported a diagnosis/suspected diagnosis of HS. The survey included patient-reported outcome measures (PROMs) and non-PROM-related questions and was conducted between December 2022 to March 2023 in six countries (US, UK, Germany, France, ltaly, Spain). PROMs included the Patient Activation Measure (PAM13; primary endpoint), Dermatology Life Quality Index (DLQI), Work Productivity and Activity Impairment (WPAI) and Hospital Anxiety and Depression Scale (HADS) tools (Spain excluded from PROM analyses).</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Overall, 656 participants were included (<i>N</i> = 505, diagnosed HS; <i>N</i> = 151, suspected HS). Of 425 diagnosed participants, 66% reported high (level 3/4) PAM13 scores. A very large (DLQI score 11–20) and extremely large (DLQI score 21–30) effect of HS on QoL was reported by 41% and 28% of participants, respectively. A very large to extremely large effect of HS on QoL (DLQI score 11–30) was reported by 67% and 73% of patients with level 3 and 4 PAM13 scores, respectively. Overall, 53% and 29% of diagnosed participants reported abnormal anxiety and depression, respectively. 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Patient Perspectives on the Impact of Living With Hidradenitis Suppurativa: Results From the Global ‘HS Uncovered’ Burden of Disease Survey
Background
Hidradenitis suppurativa (HS) is a chronic, painful inflammatory skin disease. There is a need to evaluate how patients experience their disease.
Objectives
The HS Uncovered survey was conducted to understand patient activation, the patient journey and burden of disease.
Methods
HS Uncovered was a real-world, quantitative, online survey completed by adults who self-reported a diagnosis/suspected diagnosis of HS. The survey included patient-reported outcome measures (PROMs) and non-PROM-related questions and was conducted between December 2022 to March 2023 in six countries (US, UK, Germany, France, ltaly, Spain). PROMs included the Patient Activation Measure (PAM13; primary endpoint), Dermatology Life Quality Index (DLQI), Work Productivity and Activity Impairment (WPAI) and Hospital Anxiety and Depression Scale (HADS) tools (Spain excluded from PROM analyses).
Results
Overall, 656 participants were included (N = 505, diagnosed HS; N = 151, suspected HS). Of 425 diagnosed participants, 66% reported high (level 3/4) PAM13 scores. A very large (DLQI score 11–20) and extremely large (DLQI score 21–30) effect of HS on QoL was reported by 41% and 28% of participants, respectively. A very large to extremely large effect of HS on QoL (DLQI score 11–30) was reported by 67% and 73% of patients with level 3 and 4 PAM13 scores, respectively. Overall, 53% and 29% of diagnosed participants reported abnormal anxiety and depression, respectively. The percentage of work impairment due to HS in employed diagnosed participants (N = 302) was 52%. Of diagnosed females, 52% considered HS a concern for family planning. Overall (N = 656), 58% of participants considered pain relief the most important treatment feature.
Conclusions
Despite participants having high activation levels, HS had a negative impact on QoL, mental health, work and activity. There is an unmet need for effective treatments that provide sustained pain reduction and improve work productivity in HS.