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Genetic Testing of Patients with Inherited Retinal Diseases in the European Countries: An International Survey by the European Vision Institute.
Calzetti, Giacomo; Schwarzwälder, Kerstin; Ottonelli, Giorgia; Kaminska, Karolina; Strauss, Rupert Wolfgang; Baere, Elfride De; Leroy, Bart P; Audo, Isabelle; Zeitz, Christina; Cursiefen, Claus; Stingl, Katarina; Boon, Camiel J F; Marques, João Pedro; Santos, Cristina; Ayuso Garcia, Carmen; Escher, Pascal; Cordeiro, M Francesca; D'Esposito, Fabiana; Charbel Issa, Peter; Lotery, Andrew; Lin, Siying; Michaelides, Michel; Rivolta, Carlo; Scholl, Hendrik P N.
Afiliação
  • Calzetti G; Institute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland, giacomo.calzetti@iob.ch.
  • Schwarzwälder K; Department of Ophthalmology, University of Basel, Basel, Switzerland, giacomo.calzetti@iob.ch.
  • Ottonelli G; Vista Vision Eye Clinic, Brescia, Italy, giacomo.calzetti@iob.ch.
  • Kaminska K; Institute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
  • Strauss RW; Vista Vision Eye Clinic, Brescia, Italy.
  • Baere E; Institute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
  • Leroy BP; Department of Ophthalmology, Medical University Graz, Graz, Austria.
  • Audo I; Center for Medical Genetics, Ghent University Hospital and Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
  • Zeitz C; Center for Medical Genetics, Ghent University Hospital and Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
  • Cursiefen C; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Stingl K; Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts, Centre de Référence Maladies Rares REFERET and INSERM-DGOS CIC 1423, Paris, France.
  • Boon CJF; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Marques JP; Department of Ophthalmology, Faculty of Medicine, University of Cologne, University Hospital Cologne, Cologne, Germany.
  • Santos C; University Eye Hospital, Center for Ophthalmology, University of Tübingen, Tübingen, Germany.
  • Ayuso Garcia C; Department of Ophthalmology, Leiden University Medical Center, Leiden, The Netherlands.
  • Escher P; Amsterdam University Medical Center, Department of Ophthalmology, Amsterdam, The Netherlands.
  • Cordeiro MF; Ophthalmology Unit, Centro Hospitalar e Universitario de Coimbra (CHUC), Coimbra, Portugal.
  • D'Esposito F; University Clinic of Ophthalmology, Faculty of Medicine, University of Coimbra (FMUC), Coimbra, Portugal.
  • Charbel Issa P; Clinical and Academic Centre of Coimbra (CACC), Coimbra, Portugal.
  • Lotery A; Instituto de Oftalmologia Dr Gama Pinto, Lisbon, Portugal.
  • Lin S; Department of Genetics, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), Madrid, Spain.
  • Michaelides M; Center for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.
  • Rivolta C; Department of Ophthalmology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
  • Scholl HPN; Imperial College Ophthalmic Research Group (ICORG) Unit, Imperial College, London, UK.
Ophthalmic Res ; 67(1): 448-457, 2024.
Article em En | MEDLINE | ID: mdl-39079514
ABSTRACT

INTRODUCTION:

The purpose of this project was to explore the current standards of clinical care genetic testing and counseling for patients with inherited retinal diseases (IRDs) from the perspective of leading experts in selected European countries. Also, to gather opinions on current bottlenecks and future solutions to improve patient care.

METHODS:

On the initiative of the European Vision Institute, a survey questionnaire with 41 questions was designed and sent to experts in the field from ten European countries. Each participant was asked to answer with reference to the situation in their own country.

RESULTS:

Sixteen questionnaires were collected by November 2023. IRD genetic tests are performed in clinical care settings for 80% or more of tested patients in 9 countries, and the costs of genetic tests in clinical care are covered by the public health service to the extent of 90% or more in 8 countries. The median proportion of patients who are genetically tested, the median rate of genetically solved patients among those who are tested, and the median proportion of patients receiving counseling are 51-70%, 61-80%, and 61-80%, respectively. Improving the education of healthcare professionals who facilitate patient referrals to specialized centers, improving access of patients to more thorough genotyping, and increasing the number of available counselors were the most advocated solutions.

CONCLUSION:

There is a significant proportion of IRD patients who are not genetically tested, whose genetic testing is inconclusive, or who do not receive counseling. Educational programs, greater availability of state-of-the-art genotyping and genetic counselors could improve healthcare for IRD patients.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Testes Genéticos Limite: Humans País/Região como assunto: Europa Idioma: En Revista: Ophthalmic Res Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Testes Genéticos Limite: Humans País/Região como assunto: Europa Idioma: En Revista: Ophthalmic Res Ano de publicação: 2024 Tipo de documento: Article