Michael Noonan (Limerick East, Fine Gael)
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Question 35: To ask the Minister for Health and Children if she will provide an undertaking that there will be no further delay in the implementation of the recommendations of the Pollock Report; and if she will make a statement on the matter. [2694/08]

Caoimhghín Ó Caoláin (Cavan-Monaghan, Sinn Fein)
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Question 41: To ask the Minister for Health and Children if she will expedite measures to provide high standard facilities for persons with cystic fibrosis in order to address the low life expectancy of CF sufferers here compared to Ireland's EU neighbours; and if she will make a statement on the matter. [2198/08]

Seán Barrett (Dún Laoghaire, Fine Gael)
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Question 68: To ask the Minister for Health and Children if it is intended to provide a dedicated cystic fibrosis unit to meet the urgent and critical needs of cystic fibrosis sufferers; if she has plans to provide isolation units for CF patients at hospitals here; and if she will make a statement on the matter. [1592/08]

Bernard Durkan (Kildare North, Fine Gael)
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Question 133: To ask the Minister for Health and Children the action she proposes to take to meet the requirements of cystic fibrosis sufferers with a view to bringing the quality of service here into line with that available in other jurisdictions; and if she will make a statement on the matter. [2966/08]

Mary Harney (Dublin Mid West, Progressive Democrats)
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I propose to take Questions Nos. 35, 41, 68 and 133 together.

I acknowledge the need to improve services to persons with cystic fibrosis. The negative experience recounted by some patients is a matter of much concern to me.

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 and included representation from my Department, was asked to review the current configuration and delivery of services to persons with cystic fibrosis in Ireland. The Group idenitified 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.

44 additional staff dealing with cystic fibrosis have been appointed to date across a number of hospitals, including St Vincent's, Beaumont, Temple Street, Crumlin, Tallaght, Cork University Hospital, Galway, Limerick and Waterford. 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. These include a new ambulatory care centre, the refurbishment of St. Camillus Ward, and a new Accident and Emergency Department which includes single room accommodation.

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. My Department is advised that the option of developing a modular unit is being examined in this context and the position will be clarified shortly.

The HSE advises that it is fast-tracking the re-development of a ward which is adjacent to the main cystic fibrosis treatment area. The project is to commence within the next few weeks and will provide six single rooms. On completion, additional work will begin to provide a further eight single rooms. The HSE advise that this will result in a total of fourteen single rooms for cystic fibrosis patients by the end of the summer.

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. Planning permission has been obtained and financial provision has been included in the HSE Capital Plan. The HSE advises that contract notices will be published by the end of February 2008 and the contract is to be awarded in 2008. It will be a condition of the contract that the design build period be not more than 24 months from the date of contract award.

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 Beaumont hospital to provide out patient facilities for cystic fibrosis patients.

An independent registry for cystic fibrosis has been established. As yet, the data is not available to fully inform analysis relating to median survival in this country. When it is available, the data from the Registry will allow for benchmarking against comparable countries around the world to measure the performance of our healthcare system.