The national cancer strategy includes provision for the introduction of breast cancer screening on a phased basis for women aged 50 to 64. Phase I will cover the Eastern, North Eastern and Midland Health Board areas and will target 120,000 women in the age cohort 50 to 64, which represents 50 per cent of the national target population.
The decision to proceed on a phased basis was not based on financial constraints. Instead, it is a reflection of the complexities involved in the screening process and the importance of ensuring that the Irish programme meets the necessary quality assurance criteria. Specifically, the phasing will take account of the following critical success factors: the achievement of acceptable compliance levels among the target population; ongoing evaluation of the programme from a quality assurance perspective; and availability of the necessary clinical expertise to conduct the programme.
As Minister for Health, I am very much aware of the unnecessary trauma and anguish that could be caused to women and their families as a result of mistakes in an organised screening programme. For this reason the Irish national breast screening programme must be driven by international quality assurance standards and best practice.
To this end, a national steering committee, under the chairmanship of Dr. Sheelah Ryan, chief executive officer, Western Health Board, was established in March 1997 to manage and oversee the implementation of phase I of the programme. In addition, a national quality assurance committee has been established under the chairmanship of Professor Joe Ennis, who was the director of the Eccles Street Pilot Screening Programme. The quality assurance committee, which is a sub-committee of the national steering committee, is charged with the responsibility for drawing up protocols for the programme to ensure it meets the necessary quality assurance criteria.
To start screening by I September 1998, it is critical that all the quality assurance requirements are satisfied. In this regard, I am pleased that considerable progress has been made on the development of the clinical and administrative systems and on the establishment of a national population register. It is expected that the appointment of the project director will be finalised in the near future.
In terms of identifying an appropriate model of delivery for the programme, the key concern in this regard was the need to achieve acceptable compliance levels and at the same time to meet the necessary quality assurance criteria. After careful deliberation and much discussion on the issue, the decision was made to develop two central units based at the Mater and St. Vincent's hospitals, where the screening, assessment and treatment will be carried out, using a multi-disciplinary team approach involving the key clinical disciplines, including the screening radiologist. In addition, two mobile units will bring the screening services to the women in the more remote or rural areas within the three health boards in Phase I. Each mobile unit will be linked with one of the central units. This should ensure uniformity of standards and continuity of care.
I am confident that the decisions to date in relation to phase I of the programme are very much in line with international quality assurance standards and best practice. I reiterate that my Department is committed to making the necessary capital and revenue resources available for the successful implementation of the programme.