|
Depot Institutionnel de l'UMBB >
Publications Scientifiques >
Publications Internationales >
Veuillez utiliser cette adresse pour citer ce document :
http://dlibrary.univ-boumerdes.dz:8080/handle/123456789/10374
|
Titre: | Development and implementation of the AIDA international registry for patients with undifferentiated systemic autoInflammatory diseases |
Auteur(s): | Della Casa, Francesca Vitale, Antonio Lopalco, Giuseppe Ruscitti, Piero Ait-Idir, Djouher |
Mots-clés: | Autoinflammatory diseases International Registry Personalized medicine Precision medicine Rare diseases |
Date de publication: | 2022 |
Collection/Numéro: | Frontiers in Medicine/ Vol.9 (2022);pp. 1-10 |
Résumé: | 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 by Undifferentiated Systemic AutoInflammatory
Diseases (USAIDs).
Methods: This is an electronic 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 designed to obtain standardized information for real-life research. The instrument
is endowed with flexibility, and it could change over time according to the scientific
acquisitions and potentially communicate with other similar tools; 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,
110 centers from 23 countries and 4 continents have joined the AIDA project. Fifty-four
centers have already obtained the approval from their local Ethics Committees. Currently,
the platform counts 290 users (111 Principal Investigators, 179 Site Investigators, 2 Lead
Investigators, and 2 data managers). The Registry is collecting baseline and follow-up
data using 3,769 fields organized into 23 instruments, which include demographics,
history, symptoms, trigger/risk factors, therapies, and healthcare information access for
USAIDs patients.
Conclusions: The development of the AIDA International Registry for USAIDs patients
will facilitate the online collection of real standardized data, connecting a worldwide
group of researchers: the Registry constitutes an international multicentre observational
groundwork aimed at increasing the patient cohort of USAIDs in order to improve our
knowledge of this peculiar cluster of autoinflammatory diseases. NCT 05200715 available
at https://clinicaltrials.gov/ |
URI/URL: | DOI: 10.3389/fmed.2022.908501 https://pubmed.ncbi.nlm.nih.gov/35755024/ http://dlibrary.univ-boumerdes.dz:8080/handle/123456789/10374 |
ISSN: | 2296858X |
Collection(s) : | Publications Internationales
|
Fichier(s) constituant ce document :
|
Tous les documents dans DSpace sont protégés par copyright, avec tous droits réservés.
|