Journal of Cystic Fibrosis
Volume 8, Issue 5 , Pages 295-315, September 2009

Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: A European consensus☆

  • Harry Heijerman

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: +31 702100000; fax: +31 702102150.
    • ,
  • Elsbeth Westerman
    • ,
  • Steven Conway
    • ,
  • Daan Touw
    • ,
  • Gerd Döring for the consensus working group

      Affiliations

    • Baroukh Assael, Cystic Fibrosis Center, Verona, Italy; Ian Balfour-Lynn, Royal Brompton & Harefield NHS Trust, Sydney Street, London, United Kingdom; Gabriel Bellon, Hôpital Debrousse, Lyon, France; Celeste Barreto, Hospital de Santa Maria, Lisbon, Portugal; Cesare Braggion, Ospedale Civile Maggiore, Verona, Italy; Steven Conway, St James University Hospital, Leeds, UK; Christiane De Boeck, University Hospital Gasthuiberg, Leuven, Belgium; Gerd Döring, Institute of Medical Microbiology and Hygiene, Eberhard-Karls-Universität, Tübingen, Germany; Jean-Christophe Dubus, Faculté de Médecine, Marseille, France; Irmgard Eichler, EMEA, London; Mark Elkins, Royal Prince Alfred Hospital, Sydney Australia; Henderik Frijlink, University of Groningen, Groningen, The Netherlands; Charles Gallagher, St Vincent's Hospital, Dublin, Ireland; Silvia Gartner, University Hospital Vall d'Hebron, Barcelona, Spain; David Geller, Nemours Children's Clinic, Orlando, USA; Matthias Griese, University of Munich, Munich, Germany; Harry Heijerman, Haga Teaching Hospital, The Hague, The Netherlands; Lena Hjelte, Karolinska University Hospital Huddinge, Stockholm, Sweden; Margaret Hodson, Royal Brompton Hospital, London, United Kingdom; Niels Høiby, Rigshospitalet, Copenhagen, Denmark; James Littlewood, St. James's University Hospital, Leeds, UK; Anne Malfroot, Academisch Ziekenhuis, Vrije Universiteit Brussel, Brussels, Belgium; Alexander Möller, University Children's Hospital, Zurich, Switzerland; Petr Pohunek, Charles University 2nd Medical School, Prague, Czech Republic; Tanja Pressler, Rigshospitalet, Copenhagen, Denmark; Alexandra Quittner, University of Miami, Miami, USA; Felix Ratjen, Hospital for Sick Children, Toronto, Canada; Martin Schöni, University of Berne, Berne, Switzerland; Giovanni Taccetti, Ospedale Meyer, Florence, Italy; Harm Tiddens, Erasmus University Medical Center, Rotterdam, The Netherlands; Daan Touw, Apotheek Haagse Ziekenhuizen, The Hague, The Netherlands; Elsbeth Westerman, Apotheek Haagse Ziekenhuizen, The Hague, The Netherlands.

Haga Teaching Hospital, Department of Pulmonology, Leyweg 275, 2545 CH The Hague, The Netherlands

Received 31 January 2009; received in revised form 5 April 2009; accepted 8 April 2009.

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☆ This meeting, held on April 4 to 6, 2008 in Artimino, Tuscany, Italy, was organized by the European Cystic Fibrosis Society. Supported by AOP Orphan Pharmaceuticals AG, Austria; Aradigm Corporation, USA; Bayer Healthcare, Germany; Boehringer Ingelheim GmbH, Germany; Chiesi Farmaceutici, Italy; Forest Pharmaceuticals Inc., USA; Gilead Sciences, USA; Grünenthal GmbH, Germany; Novartis UK, Profile Pharma Limited/Respironics, UK; Roche, Switzerland.

PII: S1569-1993(09)00035-6

doi:10.1016/j.jcf.2009.04.005

Journal of Cystic Fibrosis
Volume 8, Issue 5 , Pages 295-315, September 2009

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