Treatment satisfaction of adult patients with moderate-to-severe atopic dermatitis treated with baricitinib in France, Germany, and the United Kingdom: results from a cross-sectional international patient survey

被引:1
|
作者
Augustin, Matthias [1 ,7 ]
Nosbaum, Audrey [2 ]
Werfel, Thomas [3 ]
Grond, Susanne [4 ]
Reed, Catherine [4 ]
Lampropoulou, Anastasia [4 ]
Tietz, Nicole [4 ]
Irvine, Alan D. [5 ]
Riedl, Elisabeth [6 ]
机构
[1] Univ Med Ctr Hamburg Eppendorf, Inst Hlth Serv Res Dermatol & Nursing, Hamburg, Germany
[2] Hosp Civils Lyon, Ctr Hosp, Dept Allergy & Clin Immunol, Lyon Sud, Pierre Benite, France
[3] Hannover Med Sch, Dept Dermatol & Allergy, Hannover, Germany
[4] Eli Lilly & Co Ltd, Indianapolis, IN USA
[5] Our Ladys Childrens Hosp Crumlin, Dermatol Clin, Dublin, Ireland
[6] Med Univ Vienna, Dept Dermatol, Vienna, Austria
[7] Univ Med Ctr Hamburg Eppendorf, Inst Hlth Serv Res Dermatol & Nursing, Martinistr 52, Hamburg, Germany
关键词
Atopic dermatitis; patient-centered care; oral Janus kinase inhibitors; baricitinib; patient satisfaction; CARE;
D O I
10.1080/09546634.2023.2276047
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Introduction We explored patient satisfaction with baricitinib, an oral Janus kinase inhibitor, in patients with atopic dermatitis (AD) treated in routine clinical practice.Methods Adults with moderate-to-severe AD treated with baricitinib in clinical practice for >= 4 weeks in France, Germany, and the UK completed a one-time online survey under market research methodologies. Treatment satisfaction was assessed using a Likert scale and abbreviated Treatment Satisfaction Questionnaire for Medication (TSQM-9). Patients reported demographic, disease, and treatment information. Data were analyzed descriptively.Results The survey was completed by 170 patients with a mean age of 39.3 years (SD = 13.5), 59% (n = 101) were female. At baricitinib initiation, 79% rated their AD as "Severe", yet 28% reported body surface area (BSA) involvement >= 10%. Most were "Satisfied" or "Very satisfied" (76%/18%) with baricitinib, with high rates reported for controlling itch (36%/56%). Itch improvements were noted by 97% of patients. Some tapered/stopped (50%/32%) topical corticosteroid use, aligned with reported improvements on the patient global assessment and BSA. Mean TSQM-9 convenience score was 78.0 (SD = 14.0).Conclusions Satisfaction with itch control was particularly high, reflected in rates of improvement in itch since starting baricitinib. On the TSQM-9, the convenience score was the highest. Many patients tapered/stopped concomitant topicals, indicating baricitinib's effect in controlling AD symptoms.
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页数:8
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