TY - JOUR
T1 - Development and implementation of the AIDA International Registry for patients with undifferentiated systemic autoinflammatory diseases
AU - Della Casa, Francesca
AU - Vitale, Antonio
AU - Lopalco, Giuseppe
AU - Ruscitti, Piero
AU - Ciccia, Francesco
AU - Emmi, Giacomo
AU - Cattalini, Marco
AU - Wiesik-Szewczyk, Ewa
AU - Maggio, Maria Cristina
AU - Ogunjimi, Benson
AU - Sfikakis, Petros P.
AU - Tufan, Abdurrahman
AU - Al-Mayouf, Sulaiman M.
AU - Del Giudice, Emanuela
AU - Aragona, Emma
AU - La Torre, Francesco
AU - Sota, Jurgen
AU - Colella, Sergio
AU - Di Cola, Ilenia
AU - Iacono, Daniela
AU - Mattioli, Irene
AU - Jahnz-Rózyk, Karina
AU - Joos, Rik
AU - Laskari, Katerina
AU - Gaggiano, Carla
AU - Abbruzzese, Anna
AU - Cipriani, Paola
AU - Rozza, Gelsomina
AU - Alsaleem, Alhanouf
AU - Yildirim, Derya
AU - Tarsia, Maria
AU - Ragab, Gaafar
AU - Ricci, Francesca
AU - Cardinale, Fabio
AU - Korzeniowska, Marcelina
AU - Frassi, Micol
AU - Caggiano, Valeria
AU - Saad, Moustafa Ali
AU - Pereira, Rosa Maria
AU - Berlengiero, Virginia
AU - Gentileschi, Stefano
AU - Guerriero, Silvana
AU - Giani, Teresa
AU - Gelardi, Viviana
AU - Iannone, Florenzo
AU - Giardini, Henrique Ayres Mayrink
AU - Almaghlouth, Ibrahim A.
AU - Kardas, Riza Can
AU - Ait-Idir, Djouher
AU - Frediani, Bruno
AU - Balistreri, Alberto
AU - Fabiani, Claudia
AU - Rigante, Donato
AU - Cantarini, Luca
PY - 2022
Y1 - 2022
N2 - Objective: This paper points out the design, development and deployment of the AutoInflammatory Disease Alliance (AIDA) International Registry dedicated to pediatric and adult patients affected with Undifferentiated Systemic AutoInflammatory Diseases (USAIDs). Methods: This is a physician-driven, population- and electronic-based registry employed for real-world data collection about demographics, clinical, laboratory, instrumental and socioeconomic data of USAIDs patients. Data recruitment, based on the Research Electronic Data Capture (REDCap) tool, is thought to gain standardised information for real-life research and has been developed to change over time according to the scientific acquisitions and potentially communicate with other similar instruments; this platform ensures security, data quality and data governance. Results: The focus of the AIDA project is connecting physicians and researchers from all over the world to shed a new light on heterogeneous rare diseases. Since its birth, 99 centres from 20 countries and 4 continents have joined the AIDA project. Forty-eight centres have already obtained the approval from their local Ethics Committees. Currently, the platform counts 265 users (99 Principal Investigators, 162 Site Investigators, 2 Lead Investigators, and 2 data managers). The Registry is collecting baseline and follow-up data using 3357 fields organised into 23 instruments, which include demographics, history, symptoms, trigger/risk factors, therapies, and healthcare access for USAIDs patients. Conclusions: The development of the AIDA International Registry for USAIDs patients will facilitate the on-line collection of standardised data, connecting a worldwide group of researchers: the Registry constitutes an international multicentre observational groundwork aimed at increasing the study cohort of patients with USAIDs in order to improve our knowledge of this peculiar cluster of autoinflammatory diseases.
AB - Objective: This paper points out the design, development and deployment of the AutoInflammatory Disease Alliance (AIDA) International Registry dedicated to pediatric and adult patients affected with Undifferentiated Systemic AutoInflammatory Diseases (USAIDs). Methods: This is a physician-driven, population- and electronic-based registry employed for real-world data collection about demographics, clinical, laboratory, instrumental and socioeconomic data of USAIDs patients. Data recruitment, based on the Research Electronic Data Capture (REDCap) tool, is thought to gain standardised information for real-life research and has been developed to change over time according to the scientific acquisitions and potentially communicate with other similar instruments; this platform ensures security, data quality and data governance. Results: The focus of the AIDA project is connecting physicians and researchers from all over the world to shed a new light on heterogeneous rare diseases. Since its birth, 99 centres from 20 countries and 4 continents have joined the AIDA project. Forty-eight centres have already obtained the approval from their local Ethics Committees. Currently, the platform counts 265 users (99 Principal Investigators, 162 Site Investigators, 2 Lead Investigators, and 2 data managers). The Registry is collecting baseline and follow-up data using 3357 fields organised into 23 instruments, which include demographics, history, symptoms, trigger/risk factors, therapies, and healthcare access for USAIDs patients. Conclusions: The development of the AIDA International Registry for USAIDs patients will facilitate the on-line collection of standardised data, connecting a worldwide group of researchers: the Registry constitutes an international multicentre observational groundwork aimed at increasing the study cohort of patients with USAIDs in order to improve our knowledge of this peculiar cluster of autoinflammatory diseases.
KW - Autoinflammation
KW - Registry
KW - Autoinflammation
KW - Registry
UR - http://hdl.handle.net/10807/211457
U2 - 10.3389/fmed.2022.908501
DO - 10.3389/fmed.2022.908501
M3 - Article
SN - 2296-858X
VL - 2022
SP - 1
EP - 10
JO - Frontiers in Medicine
JF - Frontiers in Medicine
ER -