Longitudinal Trends in Real-World Outcomes after Initiation of Ivacaftor. A Cohort Study from the Cystic Fibrosis Registry of Ireland

Author:

Kirwan Laura1,Fletcher Godfrey1,Harrington Mary1,Jeleniewska Paulina1,Zhou Shijun1,Casserly Brian2,Gallagher Charles G.3,Greally Peter4,Gunaratnam Cedric5,Herzig Mary6,Linnane Barry78,McElvaney Noel Gerard5,McKone Edward F.3,McNally Paul9,Mullane David10,Ní Chróinín Muireann10,O’Mahony Michael11,Plant Barry J.12,Jackson Abaigeal D.1

Affiliation:

1. Cystic Fibrosis Registry of Ireland, Woodview House, University College Dublin, Belfield, Dublin, Ireland

2. University Hospital Limerick, Dooradoyle, Limerick, Ireland

3. National Referral Centre for Adult Cystic Fibrosis, St. Vincent’s University Hospital, Dublin, Ireland

4. Children’s Hospital Group, Rialto, Dublin, Ireland

5. Cystic Fibrosis Unit, Beaumont Hospital, Dublin, Ireland

6. Paediatrics Department and

7. Graduate Entry Medical School and Centre for Interventions in Infection, Inflammation, and Immunity, University of Limerick, Limerick, Ireland

8. National Children’s Research Centre, Crumlin, Dublin, Ireland

9. Royal College of Surgeons in Ireland, Our Lady’s Children’s Hospital, Crumlin, Dublin, Ireland; and

10. Cork Paediatric Cystic Fibrosis Centre and

11. Respiratory Department, University Hospital Galway, Galway, Ireland

12. Cork Adult Cystic Fibrosis Centre, University College Cork, Cork University Hospital, Cork, Ireland

Publisher

American Thoracic Society

Subject

Pulmonary and Respiratory Medicine

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