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Medicinal Products

Dáil Éireann Debate, Tuesday - 17 October 2023

Tuesday, 17 October 2023

Questions (547)

Cathal Crowe

Question:

547. Deputy Cathal Crowe asked the Minister for Health when the rapid HTA, undertaken by HIQA in November 2022, reviewing the evidence of the clinical and cost-effectiveness of continuous (includes the Dexcom, Medtronic and GlucoRx CGMs) and intermittent (Freestyle Libre) glucose monitoring systems for people with type 1 diabetes will be published; and if it recommends the widening of access to these devices; and if funding will be provided to do so. [44911/23]

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Written answers

The Health Service Executive (HSE) has statutory responsibility for decisions on pricing and reimbursement under the community schemes, in accordance with the Health (Pricing and Supply of Medical Goods) Act 2013.

In making a relevant reimbursement decision, the HSE is required under the Act to have regard to a number of criteria including clinical efficacy, the health needs of the public, cost effectiveness and potential or actual budget impact.

I, as the Minister for Health, have no role in these decisions.

The Health Information and Quality Authority completed a Health Technology Assessment (HTA) in respect of the provision of glucose monitoring systems to adults with Type I diabetes in Ireland. This was published on 29 September 2023 and can be read at www.hiqa.ie/reports-and-publications/health-technology-assessment/rapid-health-technology-assessment-continuous.

The HTA advises the HSE that a single managed access programme with clearly defined eligibility criteria would improve equity of access and could help to control costs.

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