Cystic Fibrosis Clinical Trial
Official title:
Randomized Cross-over Physiologic Study of High Flow Nasal Oxygen Cannula Versus Non-invasive Ventilation in Cystic Fibrosis. The HIFEN Study
Many patients with cystic fibrosis (CF) require hospitalization and/or Intensive Care Unit
(ICU) admission because of acute exacerbation of chronic respiratory failure or for any acute
deterioration of clinical status. Non-invasive ventilation (NIV) is the first option for the
clinical management of CF patients with moderate-to-severe respiratory distress and NIV has
been shown to improve gas exchange, reduce respiratory muscle work and improve pulmonary
function in patients with obstructive lung disease in general and those with acute CF
exacerbation. High-flow nasal oxygen cannula (HFN) is a relatively new system providing
heated and humidified, high-flow (50L/min) oxygen through the nostrils. This device provides
a small positive pressure, probably washes-out the pharyngeal dead space, reduces inspiratory
resistance, and possibly facilitates secretion clearance. The technique is very well
tolerated. From a physiologic standpoint, this device could help CF patients by improving gas
exchange, reducing respiratory workload, and facilitating mucus clearance. Non-interrupted
delivery may be possible given better clinical tolerance in contrast with bi-level positive
pressure NIV. Whether the short-term physiological efficacy of HFN is comparable to NIV is
unknown and there is no study on the benefit of HFN in CF patients.
The aim of this study is to compare the physiological effects of HFN and NIV in CF patients
requiring ventilatory support. Our hypothesis is that HFN will not be inferior to NIV, as
evaluated by breathing pattern, gas exchange, and respiratory workload and will decrease dead
space. In addition, comfort and preference between the two techniques will be evaluated.
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