Literature DB >> 29663119

Multicenter data banking in management of dizzy patients: first results from the DizzyNet registry project.

Eva Grill1,2,3, Gülden Akdal4, Sandra Becker-Bense5,6, Steffen Hübinger7,5, Doreen Huppert5,8, Erna Kentala9, Ralf Strobl7,5, Andreas Zwergal5,6, Nese Celebisoy10.   

Abstract

PURPOSE: Comprehensive phenotypical data across countries is needed to understand the determinants, prognosis and consequences of vestibular disease. The registry is a data repository for the members of the European DizzyNet. We report results from a pilot study using data from Turkey and Germany.
METHODS: The pilot study included a convenience sample of patients aged 18 or above referred to Ege University Medical School Hospital, Dokuz Eylül University Hospital, Izmir, Turkey, and the German Center for German Center for Vertigo and Balance Disorders, University on Munich, Germany, with symptoms of vertigo or dizziness. Health-related quality of life was assessed with the EQ5-D and the Dizziness Handicap Inventory (DHI). To obtain comparable groups we matched data from the two countries for age, sex and diagnosis by propensity score.
RESULTS: We included 80 adult patients, 40 from each country (60% female, mean age 54.1, SD 12.4). Matching was successful. Vestibular migraine (34%) was the most frequent diagnosis, followed by benign paroxysmal positional vertigo (29%) and Menière's disease (12%). Clinical signs and symptoms were comparable in both countries. Patients from Turkey were more likely to report headaches (65 vs. 32%) and to show gait unsteadiness (51 vs. 5%). Patients from Germany reported significantly higher quality of life and lower values of the DHI score.
CONCLUSIONS: Sharing data facilitates research, enhances translation from basic science into clinical applications, and increases transparency. The DizzyNet registry is a first step to data sharing in vestibular research across Europe.

Entities:  

Keywords:  Activities of daily living; Dizziness; Quality of life; Registries; Vertigo

Mesh:

Year:  2018        PMID: 29663119     DOI: 10.1007/s00415-018-8864-1

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  26 in total

1.  Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.

Authors:  Paul A Harris; Robert Taylor; Robert Thielke; Jonathon Payne; Nathaniel Gonzalez; Jose G Conde
Journal:  J Biomed Inform       Date:  2008-09-30       Impact factor: 6.317

2.  The International Classification of Headache Disorders, 3rd edition (beta version).

Authors: 
Journal:  Cephalalgia       Date:  2013-07       Impact factor: 6.292

3.  DizzyReg: the prospective patient registry of the German Center for Vertigo and Balance Disorders.

Authors:  Eva Grill; Thomas Müller; Sandra Becker-Bense; Robert Gürkov; Florian Heinen; Doreen Huppert; Andreas Zwergal; Ralf Strobl
Journal:  J Neurol       Date:  2017-03-07       Impact factor: 4.849

4.  Quality of life in elderly patients with dizziness: analysis of the Short-Form Health Survey in 197 patients.

Authors:  Li-Chi Hsu; Han-Hwa Hu; Wen-Jang Wong; Shuu-Jiun Wang; Yun-On Luk; Chang-Ming Chern
Journal:  Acta Otolaryngol       Date:  2005-01       Impact factor: 1.494

5.  Vestibular migraine: diagnostic criteria.

Authors:  Thomas Lempert; Jes Olesen; Joseph Furman; John Waterston; Barry Seemungal; John Carey; Alexander Bisdorff; Maurizio Versino; Stefan Evers; David Newman-Toker
Journal:  J Vestib Res       Date:  2012       Impact factor: 2.435

6.  Mine, yours, ours? Sharing data on human genetic variation.

Authors:  Nicola Milia; Alessandra Congiu; Paolo Anagnostou; Francesco Montinaro; Marco Capocasa; Emanuele Sanna; Giovanni Destro Bisol
Journal:  PLoS One       Date:  2012-06-05       Impact factor: 3.240

7.  Biomedical Data Sharing and Reuse: Attitudes and Practices of Clinical and Scientific Research Staff.

Authors:  Lisa M Federer; Ya-Ling Lu; Douglas J Joubert; Judith Welsh; Barbara Brandys
Journal:  PLoS One       Date:  2015-06-24       Impact factor: 3.240

8.  Open sharing of genomic data: Who does it and why?

Authors:  Tobias Haeusermann; Bastian Greshake; Alessandro Blasimme; Darja Irdam; Martin Richards; Effy Vayena
Journal:  PLoS One       Date:  2017-05-09       Impact factor: 3.240

9.  Improving the transparency of prognosis research: the role of reporting, data sharing, registration, and protocols.

Authors:  George Peat; Richard D Riley; Peter Croft; Katherine I Morley; Panayiotis A Kyzas; Karel G M Moons; Pablo Perel; Ewout W Steyerberg; Sara Schroter; Douglas G Altman; Harry Hemingway
Journal:  PLoS Med       Date:  2014-07-08       Impact factor: 11.069

10.  Health-related quality of life and emotional distress in patients with dizziness: a cross-sectional approach to disentangle their relationship.

Authors:  Steffi Weidt; Annette B Bruehl; Dominik Straumann; Stefan C A Hegemann; Gerhard Krautstrunk; Michael Rufer
Journal:  BMC Health Serv Res       Date:  2014-07-22       Impact factor: 2.655

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  2 in total

1.  Development and validation of a classification algorithm to diagnose and differentiate spontaneous episodic vertigo syndromes: results from the DizzyReg patient registry.

Authors:  Michael Groezinger; Doreen Huppert; Ralf Strobl; Eva Grill
Journal:  J Neurol       Date:  2020-07-13       Impact factor: 4.849

2.  Primary or secondary chronic functional dizziness: does it make a difference? A DizzyReg study in 356 patients.

Authors:  Maximilian Habs; Ralf Strobl; Eva Grill; Marianne Dieterich; Sandra Becker-Bense
Journal:  J Neurol       Date:  2020-08-27       Impact factor: 4.849

  2 in total

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