TY - JOUR
T1 - Psychometric properties of the itch numeric rating scale, skin pain numeric rating scale, and atopic dermatitis sleep scale in adult patients with moderate-to-severe atopic dermatitis
AU - Silverberg, Jonathan I.
AU - DeLozier, Amy
AU - Sun, Luna
AU - Thyssen, Jacob P.
AU - Kim, Brian
AU - Yosipovitch, Gil
AU - Nunes, Fabio P.
AU - Gugiu, P. Cristian
AU - Doll, Helen A.
AU - Eichenfield, Lawrence F.
N1 - Funding Information:
This study was funded by Eli Lilly and Company.
Funding Information:
JIS has received honoraria as a consultant and/or advisory board member for Abbvie, Afyx, Arena, Asana, Bluefin, Boehringer-Ingelheim, Celgene, Dermavant, Dermira, Eli Lilly, Galderma, GlaxoSmithKline, Incyte, Kiniksa, Leo, Luna, Menlo, Novartis, Pfizer, RAPT, Regeneron, Sanofi; speaker for Regeneron, Sanofi; institution received grants from Galderma. AD, LS and FN are employees of Eli Lilly and Company and may hold stock and/or stock options in the company. JPT reports personal fees from Pfizer, personal fees from Eli Lilly & Co, personal fees from Abbvie, personal fees from LEO Pharma, grants and personal fees from Regeneron, grants and personal fees from Sanofi-Genzyme, outside the submitted work. GY has been on advisory boards for and received honoraria from Sanofi and Regeneron Pharmaceuticals, Inc. TREVI, Pfizer, Novartis, Eli Lilly, Kiniksa, LEO, Galderma, Kiniksa, GSK, and his research has been funded by Pfizer, Galderma, Novartis, LEO, Kinksa, Sanofi Regeneron and Sun Pharma. LFE has received honoroaria for his work as a consultant for Abbvie, Dermavant, Dermira, Leo, Eli Lilly, Novartis, Regeneron, Sanofi-Genzyme and Ortho Dermatology, been an investigator/received grants for Abbvie, Galderma Laboratories, Ortho Dermatology and Pfizer. BK reports personal fees from AbbVie, personal fees from Almirall, personal fees from Boehringer Ingelheim, grants and personal fees from Cara Therapeutics, personal fees from AstraZeneca, personal fees from Menlo Therapeutics, personal fees from Regeneron, personal fees from Sanofi Genzyme, grants and personal fees from LEO Pharma, personal fees from Trevi Therapeutics, personal fees from Daewoong, personal fees from OM Pharma, personal fees from Incyte, personal fees from Amagma, personal fees from Maruho, outside the submitted work; In addition, BK has a patent on JAK inhibitors for chronic itch pending to None. PCG and HAD report no conflict of interest. Fabio P. Nunes was an employee of Eli Lilly and Company, Indianapolis, Indiana, USA at the time of conducting this study. Currently he is an employee of Janssen Pharmaceutical Companies of Johnson & Johnson, Raritan, New Jersey, USA.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12
Y1 - 2021/12
N2 - Background: The Itch Numeric Rating Scale (NRS), Skin Pain NRS, and Atopic Dermatitis Sleep Scale (ADSS) are self-administered patient-reported outcome (PRO) instruments developed to assess symptoms in patients with atopic dermatitis (AD). The objective of this study was to evaluate the psychometric properties (reliability, validity, and responsiveness) and interpretability thresholds of these PROs using data from three pivotal Phase 3 studies in adults. Methods: BREEZE-AD1, BREEZE-AD2, and BREEZE-AD5 evaluated the safety and efficacy of baricitinib in adults with moderate-to-severe AD. Clinician-reported outcomes and other PROs commonly assessed in patients with AD were used to estimate meaningful changes and evaluate test–retest reliability, convergent and divergent validity, known-groups validity, responsiveness, and meaningful change thresholds (MCTs) of the Itch NRS, Skin Pain NRS, and ADSS. Results: The test–retest reliability of the Itch NRS, Skin Pain NRS, and ADSS was evidenced by generally large intraclass correlation coefficients (> 0.7) in stable groups of patients between baseline and Week 1 and Weeks 4 and 8. Moderate-to-large correlations (r > 0.4) at baseline and Week 16 were generally observed between each measure and other PROs measuring the same concept, supporting convergent validity. Small-to-moderate correlations with clinician-reported outcomes demonstrated divergent validity. Each instrument was able to distinguish between known groups of disease severity as assessed using other indicators of AD severity. The responsiveness of the Itch NRS, Skin Pain NRS, and ADSS scales was demonstrated through significant differences in their change scores from baseline to Week 16 between categories of change in another PRO also from baseline to Week 16. Thresholds for interpreting meaningful change were estimated as − 4.0 for the 0–10 Itch and Skin Pain NRS items; − 1.25 for the 0–4 ADSS Items 1 and 3 and; − 1.50 for the 0–29 ADSS Item 2, these equivalent to moderate degrees of change. Conclusions: Results of this study demonstrate that the psychometric properties of the Itch NRS, Skin Pain NRS, and ADSS are good to excellent. These findings support the use of these instruments in daily assessment of AD symptoms in adults with moderate-to-severe AD. Trial registration ClinicalTrials.gov numbers: NCT03334396, NCT03334422, and NCT03435081.
AB - Background: The Itch Numeric Rating Scale (NRS), Skin Pain NRS, and Atopic Dermatitis Sleep Scale (ADSS) are self-administered patient-reported outcome (PRO) instruments developed to assess symptoms in patients with atopic dermatitis (AD). The objective of this study was to evaluate the psychometric properties (reliability, validity, and responsiveness) and interpretability thresholds of these PROs using data from three pivotal Phase 3 studies in adults. Methods: BREEZE-AD1, BREEZE-AD2, and BREEZE-AD5 evaluated the safety and efficacy of baricitinib in adults with moderate-to-severe AD. Clinician-reported outcomes and other PROs commonly assessed in patients with AD were used to estimate meaningful changes and evaluate test–retest reliability, convergent and divergent validity, known-groups validity, responsiveness, and meaningful change thresholds (MCTs) of the Itch NRS, Skin Pain NRS, and ADSS. Results: The test–retest reliability of the Itch NRS, Skin Pain NRS, and ADSS was evidenced by generally large intraclass correlation coefficients (> 0.7) in stable groups of patients between baseline and Week 1 and Weeks 4 and 8. Moderate-to-large correlations (r > 0.4) at baseline and Week 16 were generally observed between each measure and other PROs measuring the same concept, supporting convergent validity. Small-to-moderate correlations with clinician-reported outcomes demonstrated divergent validity. Each instrument was able to distinguish between known groups of disease severity as assessed using other indicators of AD severity. The responsiveness of the Itch NRS, Skin Pain NRS, and ADSS scales was demonstrated through significant differences in their change scores from baseline to Week 16 between categories of change in another PRO also from baseline to Week 16. Thresholds for interpreting meaningful change were estimated as − 4.0 for the 0–10 Itch and Skin Pain NRS items; − 1.25 for the 0–4 ADSS Items 1 and 3 and; − 1.50 for the 0–29 ADSS Item 2, these equivalent to moderate degrees of change. Conclusions: Results of this study demonstrate that the psychometric properties of the Itch NRS, Skin Pain NRS, and ADSS are good to excellent. These findings support the use of these instruments in daily assessment of AD symptoms in adults with moderate-to-severe AD. Trial registration ClinicalTrials.gov numbers: NCT03334396, NCT03334422, and NCT03435081.
KW - Atopic dermatitis
KW - Atopic dermatitis sleep scale
KW - Convergent-divergent validity
KW - Itch NRS
KW - Numeric rating scale
KW - Patient-reported outcome
KW - Psychometric
KW - Reliability
KW - Responsiveness
KW - Skin pain NRS
KW - Validity
UR - http://www.scopus.com/inward/record.url?scp=85117690795&partnerID=8YFLogxK
U2 - 10.1186/s12955-021-01877-8
DO - 10.1186/s12955-021-01877-8
M3 - Article
C2 - 34688290
AN - SCOPUS:85117690795
SN - 1477-7525
VL - 19
JO - Health and Quality of Life Outcomes
JF - Health and Quality of Life Outcomes
IS - 1
M1 - 247
ER -