Literature DB >> 30181934

National information system for rare diseases with an approach to data architecture: A systematic review.

Simin Derayeh1, Alireza Kazemi1, Reza Rabiei1, Azamossadat Hosseini1, Hamid Moghaddasi1.   

Abstract

The study aims to systematically review literature on the rare diseases information system to identify architecture of this system from a data perspective. The search for relevant English language articles, based on keywords in title, abstract, Mesh and Emtree terms, was done in Pubmed and Embase (from 1980 to June 2017), Scopus, Science Direct and Cochran (from 1980 to July 2017). Articles were selected if they addressed data architecture of information systems with a focus on rare disease, and if at least one of their objectives dealt with design, implementation, and development of rare diseases information systems. Thirty-five studies met the inclusion criteria. The findings were categorized into six groups. This first group addressed organizations acting as data generators, data users, and data governors. The second group was related to data sources and databases. Datasets and data elements formed the third group of findings, including common datasets, specific datasets, and complementary datasets. The fourth group of findings was in relation to data standards. Data sharing and interactions among relevant bodies included the fifth group of the findings. The last group of findings was pertinent to procedures and criteria used for checking the quality of data, as cross review checking was a main procedure assessing the accuracy, consistency, and completeness of data. Design and development of an integrated information system for rare diseases considering data architecture principles in practice could help eliminating issues with management of rare diseases through facilitating sharing information and experiences.

Keywords:  Rare disease; data architecture; data set; information system; registry

Year:  2018        PMID: 30181934      PMCID: PMC6119672          DOI: 10.5582/irdr.2018.01065

Source DB:  PubMed          Journal:  Intractable Rare Dis Res        ISSN: 2186-3644


  37 in total

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Authors:  Peipei Song; Jianjun Gao; Yoshinori Inagaki; Norihiro Kokudo; Wei Tang
Journal:  Biosci Trends       Date:  2012-04       Impact factor: 2.400

2.  A model for the European platform for rare disease registries.

Authors:  L Vittozzi; S Gainotti; E Mollo; C Donati; D Taruscio
Journal:  Public Health Genomics       Date:  2014-02-03       Impact factor: 2.000

3.  CEMARA an information system for rare diseases.

Authors:  Paul Landais; Claude Messiaen; Ana Rath; Loïc Le Mignot; Eric Dufour; Mohamed Ben Said; Jean-Philippe Jais; Laurent Toubiana; Geneviève Baujat; Eva Bourdon-Lanoy; Marion Gérard-Blanluet; Christine Bodemer; Rémi Salomon; Ségolène Aymé; Martine Le Merrer; Alain Verloes
Journal:  Stud Health Technol Inform       Date:  2010

4.  A modular approach to disease registry design: successful adoption of an internet-based rare disease registry.

Authors:  Matthew I Bellgard; Andrew Macgregor; Fred Janon; Adam Harvey; Peter O'Leary; Adam Hunter; Hugh Dawkins
Journal:  Hum Mutat       Date:  2012-07-02       Impact factor: 4.878

5.  Building a Semantic Interoperability Framework for Care and Research in Fibromuscular Dysplasia.

Authors:  Marie-Christine Jaulent; Ariane Assélé-Kama; Sébastien Savard; Alessandra Giavarini; Emmanuel Touzé; Xavier Jeunemaître; Adrien Ugon; Pierre-François Plouin; Laurent Toubiana
Journal:  Stud Health Technol Inform       Date:  2015

6.  National registries of rare diseases in Europe: an overview of the current situation and experiences.

Authors:  Domenica Taruscio; Luciano Vittozzi; Remy Choquet; Ketil Heimdal; Georgi Iskrov; Yllka Kodra; Paul Landais; Manuel Posada; Rumen Stefanov; Christiane Steinmueller; Elfriede Swinnen; Herman Van Oyen
Journal:  Public Health Genomics       Date:  2014-09-09       Impact factor: 2.000

7.  TOSCA - first international registry to address knowledge gaps in the natural history and management of tuberous sclerosis complex.

Authors:  John C Kingswood; Paolo Bruzzi; Paolo Curatolo; Petrus J de Vries; Carla Fladrowski; Christoph Hertzberg; Anna C Jansen; Sergiusz Jozwiak; Rima Nabbout; Matthias Sauter; Renaud Touraine; Finbar O'Callaghan; Bernard Zonnenberg; Stefania Crippa; Silvia Comis; Guillaume Beaure d'Augères; Elena Belousova; Tom Carter; Vincent Cottin; Maria Dahlin; José Carlos Ferreira; Alfons Macaya; Mirjana Perkovic Benedik; Valentin Sander; Sotirios Youroukos; Ramon Castellana; Bulent Ulker; Martha Feucht
Journal:  Orphanet J Rare Dis       Date:  2014-11-26       Impact factor: 4.123

8.  Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registry.

Authors:  Teresinha Evangelista; Libby Wood; Roberto Fernandez-Torron; Maggie Williams; Debbie Smith; Peter Lunt; Judith Hudson; Fiona Norwood; Richard Orrell; Tracey Willis; David Hilton-Jones; Karen Rafferty; Michela Guglieri; Hanns Lochmüller
Journal:  J Neurol       Date:  2016-05-09       Impact factor: 4.849

9.  The RUDY study platform - a novel approach to patient driven research in rare musculoskeletal diseases.

Authors:  M K Javaid; L Forestier-Zhang; L Watts; A Turner; C Ponte; H Teare; D Gray; N Gray; R Popert; J Hogg; J Barrett; R Pinedo-Villanueva; C Cooper; R Eastell; N Bishop; R Luqmani; P Wordsworth; J Kaye
Journal:  Orphanet J Rare Dis       Date:  2016-11-08       Impact factor: 4.123

10.  Design of a framework for the deployment of collaborative independent rare disease-centric registries: Gaucher disease registry model.

Authors:  Matthew I Bellgard; Kathryn R Napier; Alan H Bittles; Jeffrey Szer; Sue Fletcher; Nikolajs Zeps; Adam A Hunter; Jack Goldblatt
Journal:  Blood Cells Mol Dis       Date:  2017-01-27       Impact factor: 3.039

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  3 in total

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Authors:  Mahnaz Samadbeik; Ali Garavand; Marzieh Kordi; Atefeh Abtin; Heshmatollah Asadi
Journal:  Iran J Nurs Midwifery Res       Date:  2020-11-07

2.  Incidence, prevalence, and national burden of interstitial lung diseases in India: Estimates from two studies of 3089 subjects.

Authors:  Sahajal Dhooria; Inderpaul Singh Sehgal; Ritesh Agarwal; Valliappan Muthu; Kuruswamy Thurai Prasad; Soundappan Kathirvel; Mandeep Garg; Amanjit Bal; Ashutosh Nath Aggarwal; Digambar Behera
Journal:  PLoS One       Date:  2022-07-21       Impact factor: 3.752

3.  Cerebral palsy information system with an approach to information architecture: a systematic review.

Authors:  Mina Afzali; Korosh Etemad; Alireza Kazemi; Reza Rabiei
Journal:  BMJ Health Care Inform       Date:  2019-12
  3 in total

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