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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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