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The annual report of the Cystic Fibrosis Registry of Ireland (CFRI) provides a comprehensive overview of the health status, clinical outcomes, and demographic characteristics of people living with Cystic Fibrosis in Ireland. It summarises key data on prevalence, treatment patterns, and long-term trends; helping to monitor disease progression and the impact of therapies. The report also highlights improvements and ongoing challenges in patient care, supports healthcare planning, and serves as a valuable resource for clinicians, researchers, policymakers, and patient advocacy groups working to improve quality of life and outcomes for individuals with Cystic Fibrosis.
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Kirwan et al. (2026) studied this question.
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