derick mitchell, ipposi, rare disease day 2016 presentation
TRANSCRIPT
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February 29th, 2016
Rare Disease Day 2016
Derick Mitchell
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I #rarediseaseday
“It’s rare when you have everything going perfectly
all at the same time”
Sigourney Weaver
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What we know….
• Irish health system is unique + requires an Irish solution
• 2014: 9 ODs assessed, majority eventually approved
• High budget impact = decisions take longer
• No funding process in place
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What we don’t know…..
• What the final decisions are based on?
• How many ODs are currently available in Ireland?
• What reimbursement of ODs actually costs?
• How ODs are being prescribed/monitored?
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IPPOSI views
• Separate assessment system with different criteria for assessing OD in Ireland
• Criteria should consider • where patient perspective can be incorporated
• the cost to the state of not treating someone
• Transparency and Communication
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Health Technology Assessment
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Active Partnership with HIQA + NCPE
• HIQA have patient involvement on the advisory board of individual HTAs
• Annual HTA Training for patients through IPPOSI
• Acknowledgement that data provided by patient organisations is invaluable to NCPE assessments
• Irish patient groups exploring measuring patient outcomes with the NCPE
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Irish National Platform
• John Dowling, Men Against Cancer
• Caitriona Dunne, Fighting Blindness
• Joan Jordan, MS Ireland
• Katie Murphy, CF Ireland
• Rachel Lynch, FibroIreland
• Damien Peelo, COPD Support Ireland
• Julie Power, Vasculitis Ireland Awareness
• Sharon Thompson, Rare Dis. + Palliative care
8 Irish Trainees
The project is receiving support from the Innovative Medicines Initiative Joint Undertaking under grant agreement n° 115334, resources of which are composed of financial contribution from the European Union's Seventh Framework Programme (FP7/2007-2013) and EFPIA companies.
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I #rarediseaseday
“May you live in interesting times”