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).
Обработка статьи · этапы, ошибки и управление
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Wall Dmitri, Meah Nekma, York Katherine, Bhoyrul Bevin, Bokhari Laita, Abraham Leonardo Spagnol, Adams Roisín, Bergfeld Wilma, Betz Regina C, Blume-Peytavi Ulrike, Callender Valerie, Campbell Chel, Chambers Jen, Chen Gang, Chitreddy Vijaya, Cotsarelis George, Craiglow Brittany, Dhurat Rachita, Dlova Ncoza, Donovan Jeff, Duque-Estrada Bruna, Eisman Samantha, Ellison Abby, Farrant Paul, Barberá Juan Ferrando, Gadzhigoroeva Aida, Grimalt Ramon, Harries Matthew, Hordinsky Maria, Irvine Alan D, Jolliffe Victoria, Jones Leslie, King Brett, Lee Won-Soo, Lortkipanidze Nino, McMichael Amy, Messenger Andrew, Mirmirani Paradi, Olsen Elise, Orlow Seth J, Ovcharenko Yuliya, Piraccini Bianca Maria, Pirmez Rodrigo, Rakowska Adriana, Reygagne Pascal, Riley Melissa, Rudnicka Lidia, Saceda Corralo David, Shapiro Jerry, Sharma Pooja, Silyuk Tatiana, Kaiumov Spartak, Tobin Desmond J, Tosti Antonella, Vañó-Galván Sergio, Vogt Annika, Wade Martin, Yip Leona, Zlotogorski Abraham, Zhou Cheng, Sinclair Rodney
Аннотация
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.