TY - JOUR
T1 - The Family Impact of Atopic Dermatitis in the Pediatric Population
T2 - Results from an International Cross-sectional Study
AU - Barbarot, Sebastien
AU - Silverberg, Jonathan I.
AU - Gadkari, Abhijit
AU - Simpson, Eric L.
AU - Weidinger, Stephan
AU - Mina-Osorio, Paola
AU - Rossi, Ana B.
AU - Brignoli, Lysel
AU - Mnif, Tarek
AU - Guillemin, Isabelle
AU - Fenton, Miriam C.
AU - Pellan, Marine
AU - Mahajan, Puneet
AU - Delevry, Dimittri
AU - Bansal, Ashish
AU - Eckert, Laurent
N1 - Funding Information:
Funded by Sanofi and Regeneron Pharmaceuticals. S.B. has received research grants from Pierre Fabre Laboratory and Fondation pour la dermatite atopique; personal fees from Bioderma, Laboratoire La Roche Posay, Sanofi-Genzyme, Novalac, and Ferring; and nonfinancial support from AbbVie, Novartis, and Janssen. J.S. has acted as a consultant for and/or received grants/honoraria from AbbVie, AnaptysBio, Asana Biosciences, LLC, Eli Lilly and Company, Galderma Research & Development, LLC, GlaxoSmithKline, Glenmark Generics Inc., Kiniksa Pharmaceuticals, Ltd., Leo Pharma Inc., Medimmune, Menlo Therapeutics, Pfizer Inc., PuriCore, Inc., Regeneron, and Sanofi. E.S. has received grants/research support from Amgen, Celgene, Chugai, Galderma, Genentech, Medimmune, Sanofi/Regeneron Pharmaceuticals, Tioga, Vanda, and Lilly, and is a consultant for Anacor, Celgene, Galderma, Genentech, Medicis, Sanofi/Regeneron Pharmaceuticals, and Merck. S.W. is co-principal investigator of the German Atopic Dermatitis Registry TREATgermany, and has received institutional research grants from Novartis, Pfizer, L'Oreal, and LEO; has performed consultancies for Sanofi-Genzyme, Regeneron, LEO Pharma, Incyte, and Novartis; has lectured at educational events sponsored by Sanofi-Genzyme, Regeneron, LEO Pharma, AbbVie, and Galderma; and is involved in performing clinical trials with many pharmaceutical industries that manufacture drugs used for the treatment of psoriasis and atopic eczema. L.B., T.M., and M.P. are employees of Kantar Health Division, who received funding from Sanofi to conduct the study. A.R. and L.E. are employees of and stockholders in Sanofi. P.M. and I.G. were employees of Sanofi at the time the study was conducted. D.D. and A.B. are employees of and stockholders in Regeneron Pharmaceuticals Inc. P.O. was an employee of and stockholder in Regeneron Pharmaceuticals Inc at the time the study was conducted; she is a current employee of Aurinia Pharmaceuticals. A.G. was an employee of and stockholder in Regeneron Pharmaceuticals at the time of the study; he is a current employee of Boehringer Ingelheim Corporation. M.F. was an employee of Sanofi at the time of study and is currently employed at Syneos Health.We thank E. Jay Bienen, PhD, for medical writing support, which was funded by Sanofi and Regeneron Pharmaceuticals, Inc.
Funding Information:
We thank E. Jay Bienen, PhD, for medical writing support, which was funded by Sanofi and Regeneron Pharmaceuticals, Inc.
Publisher Copyright:
© 2022
PY - 2022/7
Y1 - 2022/7
N2 - Objective: To evaluate the impact of atopic dermatitis on families of pediatric patients. Study design: This cross-sectional, web-based survey of children/adolescents (6 months to <18 years old) with atopic dermatitis and their parents and caregivers was conducted in 18 countries encompassing North America, Latin America, Europe, Middle East/Eurasia, and East Asia. Children and adolescents with atopic dermatitis and their parents and caregivers were identified by the International Study of Asthma and Allergies in Childhood criteria and ever being told by a physician that they had “eczema”. Atopic dermatitis severity was assessed using the Patient-Oriented Eczema Measure and the Patient Global Assessment. Atopic dermatitis impact on families’ lives was evaluated using the Dermatitis Family Impact questionnaire and stand-alone questions on hours of atopic dermatitis-related care (past week) and missed work days (past 4 weeks) owing to their child's atopic dermatitis. Results: A total of 7465 pairs of pediatric participants with atopic dermatitis and their parents or caregivers were surveyed. Across age groups, the Dermatitis Family Impact questionnaire total score for all regions ranged from 7.1 to 8.6, 13.2 to 14.9, and 17.0 to 17.2 for Patient-Oriented Eczema Measure mild, moderate, and severe atopic dermatitis, respectively. Subscale scores showed that greater atopic dermatitis severity had a greater impact on all family life domains, including sleep and tiredness. No specific patterns or trends were observed across age groups. Time spent on childcare and missed work days increased with atopic dermatitis severity. Conclusions: Across pediatric age groups and geographic regions, greater atopic dermatitis severity was associated with a greater negative impact on physical, emotional, social, and economic components of family life.
AB - Objective: To evaluate the impact of atopic dermatitis on families of pediatric patients. Study design: This cross-sectional, web-based survey of children/adolescents (6 months to <18 years old) with atopic dermatitis and their parents and caregivers was conducted in 18 countries encompassing North America, Latin America, Europe, Middle East/Eurasia, and East Asia. Children and adolescents with atopic dermatitis and their parents and caregivers were identified by the International Study of Asthma and Allergies in Childhood criteria and ever being told by a physician that they had “eczema”. Atopic dermatitis severity was assessed using the Patient-Oriented Eczema Measure and the Patient Global Assessment. Atopic dermatitis impact on families’ lives was evaluated using the Dermatitis Family Impact questionnaire and stand-alone questions on hours of atopic dermatitis-related care (past week) and missed work days (past 4 weeks) owing to their child's atopic dermatitis. Results: A total of 7465 pairs of pediatric participants with atopic dermatitis and their parents or caregivers were surveyed. Across age groups, the Dermatitis Family Impact questionnaire total score for all regions ranged from 7.1 to 8.6, 13.2 to 14.9, and 17.0 to 17.2 for Patient-Oriented Eczema Measure mild, moderate, and severe atopic dermatitis, respectively. Subscale scores showed that greater atopic dermatitis severity had a greater impact on all family life domains, including sleep and tiredness. No specific patterns or trends were observed across age groups. Time spent on childcare and missed work days increased with atopic dermatitis severity. Conclusions: Across pediatric age groups and geographic regions, greater atopic dermatitis severity was associated with a greater negative impact on physical, emotional, social, and economic components of family life.
KW - atopic dermatitis
KW - dermatitis family impact questionnaire
KW - family burden
KW - parents/caregivers
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UR - http://www.scopus.com/inward/citedby.url?scp=85131803715&partnerID=8YFLogxK
U2 - 10.1016/j.jpeds.2022.04.027
DO - 10.1016/j.jpeds.2022.04.027
M3 - Article
C2 - 35490745
AN - SCOPUS:85131803715
SN - 0022-3476
VL - 246
SP - 220-226.e5
JO - Journal of Pediatrics
JF - Journal of Pediatrics
ER -