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Press release

Minister Donnelly welcomes approval for Irish hospitals to join European Reference Networks on rare diseases

Minister for Health Stephen Donnelly has welcomed formal notification from the European Commission that 15 applications (mainly consortia) submitted by five Irish academic hospitals to join European Reference Networks have been approved.

European Reference Networks (ERNs) are virtual networks for clinicians and researchers across the EU to share expertise, knowledge and resources on rare diseases. ERNs convene virtual advisory panels of medical specialists across different disciplines, using a dedicated IT platform and telemedicine tools, to review a patient with a rare disease’s diagnosis and treatment.

The five academic hospitals joining ERNs are Beaumont Hospital, Children’s Health Ireland, Mater Hospital, St. Vincent's University Hospital, and Tallaght University Hospital.

Minister Donnelly said:

"Access to these networks for our healthcare workers, enabling them to engage with their peers across the EU on best practice in the treatment of rare diseases, is a significant development for healthcare in Ireland. These networks help foster developments in the diagnosis and multidisciplinary treatment of rare diseases including kidney diseases, neuromuscular diseases, paediatric and adult cancers, and immunodeficiency, autoinflammatory and autoimmune diseases.

"Most importantly, this is a very positive development for individuals and families affected by rare diseases in Ireland. Rare disease patients will be able to benefit from improved care and access to treatment, embodying the Sláintecare principles of right care, right place, right time."


Notes

ERN are networks for clinicians and researchers to share expertise, knowledge and resources across the EU on rare diseases. There are 24 ERNs working on a range of thematic issues including bone disorders, childhood cancer and immunodeficiency. The first ERNs were launched in March 2017, involving more than 900 highly specialised healthcare units from over 300 hospitals in 26 EU countries. ERNs are part of the legal framework of the EU Directive on Patients' Rights in Cross-Border Healthcare Directive adopted in 2011.

Five Irish academic hospitals have been approved to join the following 15 ERNs:

ERN Hospital
Endo-ERN (endocrine conditions) Beaumont Hospital
ERKNet (kidney diseases) Beaumont Hospital
EURO-NMD (neuromuscular diseases) Beaumont Hospital
MetabERN (hereditary metabolic disorders) Children’s Health Ireland
ITHACA (congenital malformations and rare intellectual disability) Children’s Health Ireland
PaedCan (paediatric cancer) Children’s Health Ireland
CRANIO (craniofacial anomalies and ear, nose and throat (ENT) disorders) Children’s Health Ireland
TRANSPLANTCHILD (conditions and complications linked to the transplantation in children) Children’s Health Ireland
ERN-EYE (eye diseases) Mater Misericordiae University Hospital
GUARD-HEART (diseases of the heart) Mater Misericordiae University Hospital
EURACAN (adult cancers - solid tumours) St. Vincent's University Hospital
ERN-LUNG (respiratory diseases) St. Vincent's University Hospital
BOND (bone disorders) St. Vincent’s University Hospital and Children’s Health Ireland
ERN-RND (neurological diseases) Tallaght University Hospital
RITA (immunodeficiency, autoinflammatory and autoimmune diseases) Tallaght University Hospital

For more information visit: https://ec.europa.eu/health/european-reference-networks/work-erns_en

A ‘rare disease’ is defined in Europe as a life-threatening or chronically debilitating disease affecting no more than 5 people per 10,000. There are an estimated 6-8,000 known rare diseases affecting up to 6% of the total EU population, (at least 30 million Europeans), and perhaps up to 300,000 Irish people during their lives.