4 results on '"Silyuk T"'
Search Results
2. A Global eDelphi Exercise to Identify Core Domains and Domain Items for the Development of a Global Registry of Alopecia Areata Disease Severity and Treatment Safety (GRASS).
- Author
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Wall D, Meah N, York K, Bhoyrul B, Bokhari L, Abraham LS, Adams R, Bergfeld W, Betz RC, Blume-Peytavi U, Callender V, Campbell C, Chambers J, Chen G, Chitreddy V, Cotsarelis G, Craiglow B, Dhurat R, Dlova N, Donovan J, Duque-Estrada B, Eisman S, Ellison A, Farrant P, Barberá JF, Gadzhigoroeva A, Grimalt R, Harries M, Hordinsky M, Irvine AD, Jolliffe V, Jones L, King B, Lee WS, Lortkipanidze N, McMichael A, Messenger A, Mirmirani P, Olsen E, Orlow SJ, Ovcharenko Y, Piraccini BM, Pirmez R, Rakowska A, Reygagne P, Riley M, Rudnicka L, Saceda Corralo D, Shapiro J, Sharma P, Silyuk T, Kaiumov S, Tobin DJ, Tosti A, Vañó-Galván S, Vogt A, Wade M, Yip L, Zlotogorski A, Zhou C, and Sinclair R
- Subjects
- Alopecia Areata diagnosis, Consensus, Delphi Technique, Humans, Internationality, Severity of Illness Index, Surveys and Questionnaires, Alopecia Areata epidemiology, Alopecia Areata therapy, Registries
- Abstract
Importance: A recent expert consensus exercise emphasized the importance of developing a global network of patient registries for alopecia areata to redress the paucity of comparable, real-world data regarding the effectiveness and safety of existing and emerging therapies for alopecia areata., Objective: To generate core domains and domain items for a global network of alopecia areata patient registries., Evidence Review: Sixty-six participants, representing physicians, patient organizations, scientists, the pharmaceutical industry, and pharmacoeconomic experts, participated in a 3-round eDelphi process, culminating in a face-to-face meeting at the World Congress of Dermatology, Milan, Italy, June 14, 2019., Findings: Ninety-two core data items, across 25 domains, achieved consensus agreement. Twenty further noncore items were retained to facilitate data harmonization in centers that wish to record them. Broad representation across multiple stakeholder groups was sought; however, the opinion of physicians was overrepresented., Conclusions and Relevance: This study identifies the domains and domain items required to develop a global network of alopecia areata registries. These domains will facilitate a standardized approach that will enable the recording of a comprehensive, comparable data set required to oversee the introduction of new therapies and harness real-world evidence from existing therapies at a time when the alopecia areata treatment paradigm is being radically and positively disrupted. Reuse of similar, existing frameworks in atopic dermatitis, produced by the Treatment of Atopic Eczema (TREAT) Registry Taskforce, increases the potential to reuse existing resources, creates opportunities for comparison of data across dermatology subspecialty disease areas, and supports the concept of data harmonization.
- Published
- 2021
- Full Text
- View/download PDF
3. Lichen simplex chronicus of the scalp: dermoscopy and reflectance confocal microscopy features.
- Author
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Starace, M., Mandel, V.D., Francesca, B., Alessandrini, A., Misciali, C., Apalla, Z., Iorizzo, M., Pellacani, G., Silyuk, T., Patrizi, A., and Piraccini, B.M.
- Subjects
CONFOCAL microscopy ,SCALP ,REFLECTANCE ,SKIN diseases ,ALOPECIA areata - Abstract
RCM detects broom hair fibres that present a distal split of the hair tips into two or three tiny hair endings (d). Therefore, short hairs (maximum 1-2 mm length) of similar thickness were observed, which emerged as a single stem from the follicular opening and may present an additional distal split of the hair tips into two or three tiny hair endings (broom hair fibres). Scalp lichen simplex chronicus (LSC) is rare and can be a challenging and frustrating condition for both patient and physician. [Extracted from the article]
- Published
- 2021
- Full Text
- View/download PDF
4. A Global eDelphi Exercise to Identify Core Domains and Domain Items for the Development of a Global Registry of Alopecia Areata Disease Severity and Treatment Safety (GRASS)
- Author
-
Jeff C. Donovan, Cheng Zhou, Valerie D. Callender, Dmitri Wall, Ncoza C. Dlova, Leonardo Spagnol Abraham, Laita Bokhari, Martin S Wade, Sergio Vano-Galvan, Bruna Duque-Estrada, Alan D. Irvine, Wilma F. Bergfeld, Antonella Tosti, Abby Ellison, David Saceda Corralo, Jen Chambers, Pooja Sharma, Seth J. Orlow, Andrew G. Messenger, Bianca Maria Piraccini, Ulrike Blume-Peytavi, Spartak Kaiumov, Brett A. King, Roisin Adams, Rodney Sinclair, Annika Vogt, Melissa Riley, Katherine York, Rachita Dhurat, Won Soo Lee, Brittany G. Craiglow, Bevin Bhoyrul, Aida Gadzhigoroeva, Leslie Jones, Chel Campbell, V. Jolliffe, Juan Ferrando Barberá, Gang Chen, Regina C. Betz, Adriana Rakowska, Elise A. Olsen, Amy J. McMichael, Samantha Eisman, Abraham Zlotogorski, Matthew Harries, George Cotsarelis, Jerry Shapiro, Paul Farrant, Vijaya Chitreddy, Paradi Mirmirani, Leona Yip, Lidia Rudnicka, Nino Lortkipanidze, Yuliya Ovcharenko, Ramon Grimalt, Pascal Reygagne, Maria K. Hordinsky, Tatiana Silyuk, Rodrigo Pirmez, Desmond J. Tobin, Nekma Meah, Wall D., Meah N., York K., Bhoyrul B., Bokhari L., Abraham L.S., Adams R., Bergfeld W., Betz R.C., Blume-Peytavi U., Callender V., Campbell C., Chambers J., Chen G., Chitreddy V., Cotsarelis G., Craiglow B., Dhurat R., Dlova N., Donovan J., Duque-Estrada B., Eisman S., Ellison A., Farrant P., Barbera J.F., Gadzhigoroeva A., Grimalt R., Harries M., Hordinsky M., Irvine A.D., Jolliffe V., Jones L., King B., Lee W.-S., Lortkipanidze N., McMichael A., Messenger A., Mirmirani P., Olsen E., Orlow S.J., Ovcharenko Y., Piraccini B.M., Pirmez R., Rakowska A., Reygagne P., Riley M., Rudnicka L., Saceda Corralo D., Shapiro J., Sharma P., Silyuk T., Kaiumov S., Tobin D.J., Tosti A., Vano-Galvan S., Vogt A., Wade M., Yip L., Zlotogorski A., Zhou C., and Sinclair R.
- Subjects
medicine.medical_specialty ,Consensus ,Internationality ,Alopecia Areata ,Delphi Technique ,Delphi method ,MEDLINE ,Redress ,Consensu ,Dermatology ,Disease ,Subspecialty ,Severity of Illness Index ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,Surveys and Questionnaires ,Global network ,medicine ,Humans ,Surveys and Questionnaire ,Registries ,skin and connective tissue diseases ,Pharmaceutical industry ,integumentary system ,business.industry ,Alopecia areata ,medicine.disease ,030220 oncology & carcinogenesis ,Family medicine ,business ,Human - Abstract
Importance A recent expert consensus exercise emphasized the importance of developing a global network of patient registries for alopecia areata to redress the paucity of comparable, real-world data regarding the effectiveness and safety of existing and emerging therapies for alopecia areata. Objective To generate core domains and domain items for a global network of alopecia areata patient registries. Evidence Review Sixty-six participants, representing physicians, patient organizations, scientists, the pharmaceutical industry, and pharmacoeconomic experts, participated in a 3-round eDelphi process, culminating in a face-to-face meeting at the World Congress of Dermatology, Milan, Italy, June 14, 2019. Findings Ninety-two core data items, across 25 domains, achieved consensus agreement. Twenty further noncore items were retained to facilitate data harmonization in centers that wish to record them. Broad representation across multiple stakeholder groups was sought; however, the opinion of physicians was overrepresented. Conclusions and Relevance This study identifies the domains and domain items required to develop a global network of alopecia areata registries. These domains will facilitate a standardized approach that will enable the recording of a comprehensive, comparable data set required to oversee the introduction of new therapies and harness real-world evidence from existing therapies at a time when the alopecia areata treatment paradigm is being radically and positively disrupted. Reuse of similar, existing frameworks in atopic dermatitis, produced by the Treatment of Atopic Eczema (TREAT) Registry Taskforce, increases the potential to reuse existing resources, creates opportunities for comparison of data across dermatology subspecialty disease areas, and supports the concept of data harmonization.
- Published
- 2021
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