Respiratory Medicine
Volume 103, Issue 12 , Pages 1832-1837, December 2009

Peak inspiratory flow through the Genuair® inhaler in patients with moderate or severe COPD

  • H. Magnussen

      Affiliations

    • Pulmonary Research Institute, Hospital Grosshansdorf, Center for Pneumology and Thoracic Surgery, Woehrendamm 80, 22927 Grosshansdorf, Germany
    • Corresponding Author InformationCorresponding author. Tel.: +49 4102601151; fax: +49 4102601245.
  • ,
  • H. Watz

      Affiliations

    • Pulmonary Research Institute, Hospital Grosshansdorf, Center for Pneumology and Thoracic Surgery, Woehrendamm 80, 22927 Grosshansdorf, Germany
  • ,
  • I. Zimmermann

      Affiliations

    • Pulmonary Research Institute, Hospital Grosshansdorf, Center for Pneumology and Thoracic Surgery, Woehrendamm 80, 22927 Grosshansdorf, Germany
  • ,
  • S. Macht

      Affiliations

    • Pulmonary Research Institute, Hospital Grosshansdorf, Center for Pneumology and Thoracic Surgery, Woehrendamm 80, 22927 Grosshansdorf, Germany
  • ,
  • R. Greguletz

      Affiliations

    • Almirall Sofotec GmbH, Benzstrasse 1, D-61352 Bad Homburg v. d. Hoehe, Germany
  • ,
  • M. Falques

      Affiliations

    • Almirall, R&D Centre, Laureà Miró 408-410, 08980 Sant Feliu de Llobregat, Barcelona, Spain
  • ,
  • D. Jarreta

      Affiliations

    • Almirall, R&D Centre, Laureà Miró 408-410, 08980 Sant Feliu de Llobregat, Barcelona, Spain
  • ,
  • E. Garcia Gil

      Affiliations

    • Almirall, R&D Centre, Laureà Miró 408-410, 08980 Sant Feliu de Llobregat, Barcelona, Spain

Received 13 February 2009; accepted 13 July 2009. published online 03 August 2009.

Summary 

The Genuair® inhaler is a new multidose dry powder inhaler for the delivery of aclidinium bromide – a novel, long-acting, muscarinic antagonist in development for the treatment of chronic obstructive pulmonary disease (COPD). The primary aim of this study was to assess the inspiratory flow characteristics through Genuair® in patients with moderate or severe COPD.

Using a three-period cross-over design, 48 patients were randomised to inhale placebo powder through Genuair®, HandiHaler® A (slow, deep inhalation as per manufacturer's instructions) or HandiHaler® B (fast, forceful inhalation). Three measurements of peak inspiratory flow (PIF), 10min apart, were recorded for each method of administration.

The highest and average PIFs for the three attempts (mean±standard deviation) generated through the Genuair® inhaler were 97.7±15.7 and 92.0±15.4L/min, respectively. Furthermore, 97% of inhalations with the Genuair® inhaler were successful (activation of trigger threshold mechanism) and optimal (PIF45L/min). The highest and average PIFs generated through HandiHaler® A and B were significantly lower than with the Genuair® inhaler.

In conclusion, patients with moderate or severe COPD were able to generate sufficient inspiratory airflow through the Genuair® inhaler to reliably inhale the full dose and reset the inhaler.

Keywords: Chronic obstructive pulmonary disease, Dry powder inhaler, Genuair® inhaler, Peak inspiratory flow

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PII: S0954-6111(09)00239-X

doi:10.1016/j.rmed.2009.07.006

Respiratory Medicine
Volume 103, Issue 12 , Pages 1832-1837, December 2009