Literature DB >> 36167994

[Healthcare networks for people with rare diseases: integrating data and expertise].

Holm Graessner1, Holger Storf2, Franz Schaefer3.   

Abstract

In the European Union (EU), rare diseases (RDs) are diseases that affect no more than 5 in 10,000 people. Due to their rarity, clinical expertise and quality-assured care structures are scarce, and research is more difficult compared to other diseases. However, these problems can be overcome by means of national and transnational RD care networks. Data and expertise are pooled in these networks.In the EU, the European Reference Networks (ERNs) for Rare and Complex Diseases cooperate across borders. Important services provided by ERNs using health data include diagnostic coding of RDs, conducting virtual cross-border case conferences, and establishing European registries that are used to measure and improve the quality of care. In ERNs, local data generation and documentation combine with network-wide data infrastructures. This paper describes the data-based services in and for RD healthcare networks: (1) diagnostic coding, (2) cross-border case conferences, and (3) ERN registries for RD patient care. The final section discusses the integration of the networks into national healthcare systems.In order to achieve the best possible benefit for SE patients, ERN activities and structures need to be better integrated into national healthcare systems. In Germany, the Medical Informatics Initiative and the German Reference Networks play a central role in this regard.
© 2022. The Author(s).

Entities:  

Keywords:  Diagnostic coding; European Reference Networks; Integration; Registries; Virtual case conferences

Year:  2022        PMID: 36167994     DOI: 10.1007/s00103-022-03592-1

Source DB:  PubMed          Journal:  Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz        ISSN: 1436-9990            Impact factor:   1.595


  10 in total

1.  [Improving the visibility of rare diseases in health care systems by specific routine coding].

Authors:  Magdalena María Marx; Franzisca Marie Dulas; Katja Maria Schumacher
Journal:  Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz       Date:  2017-05       Impact factor: 1.513

Review 2.  The Team-Based Approach to Undiagnosed and Rare Diseases.

Authors:  Robert M Kliegman; Barbara E Ruggeri; Molly Marquardt Smith
Journal:  Pediatr Clin North Am       Date:  2017-02       Impact factor: 3.278

3.  Implementation of EXABO - An Expert Advisory Board for the European Reference Network for Rare Respiratory Diseases.

Authors:  Désirée Walther; Olivia Steinmann; Thomas O F Wagner; Holger Storf
Journal:  Stud Health Technol Inform       Date:  2020-06-16

Review 4.  Health professional networks as a vector for improving healthcare quality and safety: a systematic review.

Authors:  Frances C Cunningham; Geetha Ranmuthugala; Jennifer Plumb; Andrew Georgiou; Johanna I Westbrook; Jeffrey Braithwaite
Journal:  BMJ Qual Saf       Date:  2011-11-30       Impact factor: 7.035

5.  Collaborative research networks in health: a pragmatic scoping study for the development of an imaging network.

Authors:  Tracy Elizabeth Robinson; Nicole Rankin; Anna Janssen; Deborah Mcgregor; Stuart Grieve; Timothy Shaw
Journal:  Health Res Policy Syst       Date:  2015-12-09

6.  Comparative Accuracy of Diagnosis by Collective Intelligence of Multiple Physicians vs Individual Physicians.

Authors:  Michael L Barnett; Dhruv Boddupalli; Shantanu Nundy; David W Bates
Journal:  JAMA Netw Open       Date:  2019-03-01

7.  An ontological foundation for ocular phenotypes and rare eye diseases.

Authors:  Panagiotis I Sergouniotis; Emmanuel Maxime; Dorothée Leroux; Annie Olry; Rachel Thompson; Ana Rath; Peter N Robinson; Hélène Dollfus
Journal:  Orphanet J Rare Dis       Date:  2019-01-09       Impact factor: 4.123

8.  The FAIR Guiding Principles for scientific data management and stewardship.

Authors:  Mark D Wilkinson; Michel Dumontier; I Jsbrand Jan Aalbersberg; Gabrielle Appleton; Myles Axton; Arie Baak; Niklas Blomberg; Jan-Willem Boiten; Luiz Bonino da Silva Santos; Philip E Bourne; Jildau Bouwman; Anthony J Brookes; Tim Clark; Mercè Crosas; Ingrid Dillo; Olivier Dumon; Scott Edmunds; Chris T Evelo; Richard Finkers; Alejandra Gonzalez-Beltran; Alasdair J G Gray; Paul Groth; Carole Goble; Jeffrey S Grethe; Jaap Heringa; Peter A C 't Hoen; Rob Hooft; Tobias Kuhn; Ruben Kok; Joost Kok; Scott J Lusher; Maryann E Martone; Albert Mons; Abel L Packer; Bengt Persson; Philippe Rocca-Serra; Marco Roos; Rene van Schaik; Susanna-Assunta Sansone; Erik Schultes; Thierry Sengstag; Ted Slater; George Strawn; Morris A Swertz; Mark Thompson; Johan van der Lei; Erik van Mulligen; Jan Velterop; Andra Waagmeester; Peter Wittenburg; Katherine Wolstencroft; Jun Zhao; Barend Mons
Journal:  Sci Data       Date:  2016-03-15       Impact factor: 6.444

9.  Telemedicine strategy of the European Reference Network ITHACA for the diagnosis and management of patients with rare developmental disorders.

Authors:  Michael Smith; Elizabeth Alexander; Ruta Marcinkute; Dorica Dan; Myfanwy Rawson; Siddharth Banka; Jason Gavin; Hany Mina; Con Hennessy; Florence Riccardi; Francesca Clementina Radio; Marketa Havlovicova; Matteo Cassina; Adela Chirita Emandi; Melanie Fradin; Lianne Gompertz; Ann Nordgren; Rasa Traberg; Massimiliano Rossi; Aurelién Trimouille; Rasika Sowmyalakshmi; Bruno Dallapiccola; Alessandra Renieri; Laurence Faivre; Bronwyn Kerr; Alain Verloes; Jill Clayton-Smith; Sofia Douzgou
Journal:  Orphanet J Rare Dis       Date:  2020-04-25       Impact factor: 4.123

  10 in total

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