Go raibh maith agat. I welcome all our guests. As Minister for Health, I extend a particular welcome to the nurses or retired nurses who are here with us today. I have had the great pleasure of visiting University Hospital Kerry on several occasions. There has been a transformation at the hospital in recent years. It has been under intense pressure. When I went there first, I was told about consultants having to do paperwork in their cars because they could not get offices. Our nursing staff were under sustained pressure for a significant period. In recent years, it has been fantastic to see the change. We are not remotely done. We are probably only halfway done. We have a very big block of new beds coming in, which will be a game-changer. Much more capital investment is being made and many more staff are going in. I have seen first-hand the difference our healthcare workers in that hospital are making for patients. I know it is not easily achieved; it is bloody hard work. I salute our healthcare workers and thank them for everything they have done.
I am very pleased to have the opportunity to address the Seanad today on what is normally quite a technical Bill concerning amendments to health insurance legislation that nobody really pays much attention to. However, this Bill is also what we will use to legislate for the provision of free hormone replacement therapy, HRT, products. That makes it much more interesting than the annual health insurance Bill.
The Bill started its journey through the Houses as the health insurance Bill, and I received Government approval to move amendments on Committee Stage in Dáil Éireann to provide the legislative basis for these measures to introduce fully State-funded HRT relating to menopause.
Parts 1 and 2 of the Bill provide for free HRT products to women experiencing the symptoms of menopause. This means that where a woman has been prescribed HRT by her healthcare provider to alleviate the systems associated with all stages of menopause, the costs of these medications or products will be met by the State.
Part 3 provides for amendments to the health insurance legislation that are required each year to update the level of risk equalisation credits and stamp duty levies necessary to fund the credits. I approved the risk equalisation credits to apply next year and the Minister for Finance has approved the corresponding stamp duty levies.
In addition, this Bill will amend the definition of “high cost claim”. The definition of high cost claim was to have included all HSE-approved drugs, but it did not. An amendment to the definition was required to ensure the original policy intent was met.
I will now outline the specific sections of the Bill for colleagues.
Section 1 provides for the Short Title, commencement, collective citations and construction of the Bill.
Section 2 defines the Health Act 1970 as the “Act of 1970”.
Section 3 provides that the new section being introduced, section 67F of the Health Act 1970, is included for reference within section 47A of the Health Act 1970. Section 67F gives effect to the provision of free hormone replacement therapy products related to menopause to women. The existing section 47A allows the Minister for Health to issue guidance related to the concept of a person being ordinarily resident. The amendment is now required because the provision of free hormone replacement therapy products related to menopause will now be available to women who are ordinarily resident within the State.
Section 4 inserts a new section 67F into the Health Act 1970. It contains the main provisions for free menopause products to women. Within this proposed new section 67F, there are six subsections. Subsection (1) provides that the HSE will make available without charge menopause products on the HSE reimbursement list to women ordinarily resident in the State who have been prescribed menopause products by a relevant healthcare provider, that is, a registered medical practitioner, a registered nurse or a registered midwife. Subsection (2) provides that a woman shall receive the menopause product from a pharmacy that has entered into an agreement with the HSE for the dispensing of menopause products to women. Subsection (3) provides that, separate to the provisions outlined within this legislation, women with full eligibility - medical card holders - will continue to receive free menopause products under section 59(1) of the Health Act 1970. Section 59(1) provides for the provision of free drugs, medicines and medical and surgical appliances to medical card holders. Subsection (4) provides that the Minister, following consultation with the HSE, may by regulation prescribe the form and manner in which the HSE may reimburse pharmacy providers for the supply of menopause products to women, the form and manner in which the pharmacy providers may claim for the reimbursement, and the forms that would be used to make the claims and reimbursements. Subsection (5) provides that every regulation made under this section must be laid before the Oireachtas. Subsection (6) provides for the definitions.
Section 5 contains a number of consequential amendments to the Health (Pricing and Supply of Medical Goods) Act 2013. These are necessary to provide the legislative framework for the HSE’s conditional supply and reimbursement of listed menopause products, meaning hormone replacement therapy drugs, medicines and surgical and medical appliances used to alleviate the symptoms of menopause and which are on the reimbursement list as administered by the HSE. This section of the Bill allows for the introduction of a measure which will mean that where a woman has been prescribed HRT by her healthcare provider to treat her menopause symptoms at any stage in the menopause journey, the cost of those medications will be met by the State, thereby relieving some of the cost burden of menopause.
This is for any HRT medications or products prescribed for the treatment of menopause symptoms that are on the HSE’s reimbursement list. At this time, this measure does not cover the cost of consultations with healthcare providers, the costs associated with the insertion or removal of a coil, or charges that a pharmacist may be required to apply because, in many cases, the pharmacist will make their margin by either adding a percentage or charging an administrative or prescription fee. This does not cover that.
Section 6 defines the Health Insurance Act 1994 as the “Act of 1994”.
Section 7 amends the definition of high cost claim. This Bill amends the definition to include a number of HSE-published lists of drugs and all drugs that are approved under the HSE drugs approval process. It also includes immunoglobulins, a group of drugs that were approved prior to the establishment of the current HSE drugs approval process in 2013. The revised definition will apply from the date of the introduction of the high cost claim credit, which is 1 April 2022. This will ensure that the State will remain in compliance with the European Commission approval of the risk equalisation scheme.
Section 8 amends section 11C of the principal Act to provide for 1 April 2025 as the effective date for revised credits payable from the risk equalisation fund. Section 9 replaces table 2 in Schedule 4 of the principal Act. This table revises the applicable age-related health credits payable from the risk equalisation fund. The amounts are applicable on or after 1 April 2025. The amount of the credit depends on the person’s age, sex and whether they have advanced or non-advanced cover. Non-advanced contracts provide for mostly public hospital cover, while advanced contracts provide a higher level of cover and cover in private hospitals. Age-related health credits for advanced products will increase for all ages and genders. This is to meet the expected increase in claims in these segments of the market. Most of the age-related health credits will decrease for non-advanced products for all ages and genders. It is expected that there will be a reduction in claims for these sections of the market.
Section 10 amends section 125A of the Stamp Duties Consolidation Act 1999 to specify the stamp duty rates to apply in the market for 2025. The amount of stamp duty levy is calculated to align with the expected risk equalisation credits. The risk equalisation scheme is Exchequer-neutral. It is not funded by the State and the State does not derive any funds from it. When the Health Insurance Authority makes a recommendation on the amount of stamp duty levy, it must also avoid sustaining surpluses or deficits in the risk equalisation fund. The amount of stamp duty payable on a health insurance contract depends on whether a contract is advanced or non-advanced. The stamp duty payable on non-advanced health insurance contracts will decrease from 1 April 2025. It will be €94 per adult, a decrease of €11, and €31 per child, a decrease of €4. On advanced health insurance contracts, the stamp duty will increase to €469 per adult, an increase of €49, and €156 per child, an increase of €16. I commend this Bill to the House.