John O'Mahony (Mayo, Fine Gael)
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Question 297: To ask the Minister for Health and Children when the Pollock Report from the Health Service Executive Cystic Fibrosis working group will be implemented; and if she will make a statement on the matter. [11537/08]

John O'Mahony (Mayo, Fine Gael)
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Question 298: To ask the Minister for Health and Children when the Pollock Report from the Health Service Executive Cystic Fibrosis working group will be released; and if she will make a statement on the matter. [11538/08]

Mary Harney (Dublin Mid West, Progressive Democrats)
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I propose to take Questions Nos. 297 and 298 together.

I take it that the Deputy is referring to the report by Dr Ronnie Pollock which was commissioned by the Cystic Fibrosis Association of Ireland.

Following publication of the Pollock Report in 2005, the Health Service Executive established a Working Group to undertake a detailed review of cystic fibrosis services. The Group, which was multi-disciplinary in its composition, was asked to review the current configuration and delivery of services to persons with cystic fibrosis in Ireland. The Group identified a range of service improvements required for persons with Cystic Fibrosis, including the need to increase the level of clinical, nursing and allied health professional staffing in Cystic Fibrosis units around the country.

Arising from the Pollock Report and the emerging recommendations of the Working Group, I identified the development of cystic fibrosis services as a policy priority in the Estimates process. In 2006 and 2007, additional revenue funding of €6.78 million was provided to the Health Service Executive (HSE) to develop services.

My Department is advised by the HSE that 44 additional staff dealing with cystic fibrosis were recruited on foot of this additional funding and that the necessary funding is available to facilitate the recruitment of a further 37 staff nationally.

The HSE was asked to place a particular focus on the development of services at the National Adult Tertiary Referral Centre at St. Vincent's Hospital. A number of capital projects have recently been completed at the hospital and have helped to improve facilities.

However, it is accepted that these developments do not fully address the immediate needs of patients. The HSE has been working intensively with the Hospital and with representatives of the Cystic Fibrosis Association of Ireland to progress options for further interim improvements.

In the longer term, a new ward block is to be built and will include 120 replacement beds in single en-suite accommodation. The new facility will accommodate cystic fibrosis patients and will include appropriate isolation facilities.

Beaumont Hospital operates as a regional centre in providing services to adults with cystic fibrosis. In the 2008 Budget, a special allocation of €2.5m capital funding was provided to enable the hospital to develop out patient facilities for cystic fibrosis patients.

My Department has requested the Parliamentary Affairs Division of the Executive to respond directly to the Deputy in relation to the publication of the report of the Working Group.