Eczema control and treatment satisfaction in atopic dermatitis patients treated with dupilumab - a cross-sectional study from the BioDay registry
Oosterhaven, Jart A F; Spekhorst, Lotte S; Zhang, Junfen; Voorberg, Angelique N; Romeijn, Geertruida L E; Boesjes, Celeste M; de Graaf, Marlies; de Bruin-Weller, Marjolein S; Schuttelaar, Marie L A
(2022) The journal of dermatological treatment, volume 33, issue 4, pp. 1986 - 1989
(Article)
Abstract
BACKGROUND: Eczema control is a new construct to be measured in atopic dermatitis (AD). OBJECTIVES: Measuring patient-perceived eczema control and treatment satisfaction in AD patients, treated with dupilumab between 16 and 52 weeks. METHODS: Cross-sectional questionnaire study. Patients from the Dutch BioDay registry completed the Atopic Dermatitis Control Test (ADCT), Recap
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of Atopic Eczema (RECAP) and Treatment Satisfaction Questionnaire for Medication, Version II (TSQM v. II), along with other Patient Reported Outcome Measures (PROMs). RESULTS: 104/157 patients responded (response rate 66.2%). Median ADCT score was 4 (interquartile range [IQR] 5); median RECAP score was 5 (IQR 6); median TSQM v.II global satisfaction score was 83.3 (IQR 25.0). According to the ADCT, 38.5-66.3% perceived their AD was 'in control', depending on the interpretability method used. Minimally clinically important difference (MCID) of ≥4 points for the DLQI and POEM was achieved respectively in N = 66 (84.6%) and N = 63 (78.8%) patients. CONCLUSION: When considering the favorable scores on other PROMs and the TSQM v. II, and comparing these to the relatively low percentage of patients perceiving control according to the ADCT, interpretability of eczema control still appears difficult. Treatment satisfaction in the studied cohort was high.
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Keywords: Atopic dermatitis, atopic dermatitis control test, dupilumab, eczema control, recap of atopic eczema, treatment satisfaction questionnaire for medication, Dermatology
ISSN: 0954-6634
Publisher: Informa Healthcare
Note: Funding Information: Marjolein S. de Bruin-Weller has been a consultant, advisory board member, and/or speaker for AbbVie, Almirall, Eli Lilly, Galderma, Janssen, Leo Pharma, Pfizer, Regeneron, Sanofi-Genzyme, and UCB. Marie L. A. Schuttelaar: Sanofi Genzyme, Pfizer, LEO Pharma, Eli Lilly – advisory board member; AbbVie, Novartis, Regeneron Pharmaceuticals, Inc., Sanofi Genzyme – investigator; Regeneron Pharmaceuticals, Inc. – consultant; Sanofi Genzyme, Novartis – research grant. Marlies de Graaf has been an advisory board member and/or speaker for Sanofi-Genzyme, Eli Lilly and Leo Pharma. The other authors report no conflict of interest. Publisher Copyright: © 2021 The Author(s). Published with license by Taylor and Francis Group, LLC.
(Peer reviewed)