TY - JOUR
T1 - Oronasal mask versus helmet in acute hypercapnic respiratory failure
AU - Pisani, Lara
AU - Mega, Chiara
AU - Vaschetto, Rosanna
AU - Bellone, Andrea
AU - Scala, Raffaele
AU - Cosentini, Roberto
AU - Musti, Muriel
AU - Forno, Manuela Del
AU - Grassi, Mario
AU - Fasano, Luca
AU - Navalesi, Paolo
AU - Nava, Stefano
N1 - Publisher Copyright:
Copyright ©ERS 2015.
PY - 2015/3/1
Y1 - 2015/3/1
N2 - The choice of the interface for noninvasive ventilation (NIV) is a key factor in NIV success. We hypothesised that a new helmet specifically design to improve performance in hypercapnic patients would be clinically equivalent to a standard oronasal mask. In a multicentre, short-term, physiological, randomised trial in chronic obstructive pulmonary disease patients facing an acute hypercapnic respiratory failure episode, we compared the changes in arterial blood gases (ABGs) and tolerance score obtained using the helmet or mask, and, as secondary end-points, dyspnoea, vital signs, early NIV discontinuation and rate of intubation. 80 patients were randomly assigned to receive NIV either with the helmet (n=39) or mask (n=41), using an intensive care unit ventilator. Compared with baseline, in the first 6 h, NIV improved ABGs, dyspnoea and respiratory rate (p<0.05) in both groups. Changes in ABGs and discomfort were similar with the two groups, while dyspnoea decreased more (p<0.005) using the mask. The rate of intubation and the need for interface change during the whole period of NIV were very low and not different between groups. The new helmet may be a valid alternative to a mask in improving ABGs and achieving a good tolerance during an episode of acute hypercapnic respiratory failure.
AB - The choice of the interface for noninvasive ventilation (NIV) is a key factor in NIV success. We hypothesised that a new helmet specifically design to improve performance in hypercapnic patients would be clinically equivalent to a standard oronasal mask. In a multicentre, short-term, physiological, randomised trial in chronic obstructive pulmonary disease patients facing an acute hypercapnic respiratory failure episode, we compared the changes in arterial blood gases (ABGs) and tolerance score obtained using the helmet or mask, and, as secondary end-points, dyspnoea, vital signs, early NIV discontinuation and rate of intubation. 80 patients were randomly assigned to receive NIV either with the helmet (n=39) or mask (n=41), using an intensive care unit ventilator. Compared with baseline, in the first 6 h, NIV improved ABGs, dyspnoea and respiratory rate (p<0.05) in both groups. Changes in ABGs and discomfort were similar with the two groups, while dyspnoea decreased more (p<0.005) using the mask. The rate of intubation and the need for interface change during the whole period of NIV were very low and not different between groups. The new helmet may be a valid alternative to a mask in improving ABGs and achieving a good tolerance during an episode of acute hypercapnic respiratory failure.
UR - http://www.scopus.com/inward/record.url?scp=84923862727&partnerID=8YFLogxK
U2 - 10.1183/09031936.00053814
DO - 10.1183/09031936.00053814
M3 - Article
SN - 0903-1936
VL - 45
SP - 691
EP - 699
JO - European Respiratory Journal
JF - European Respiratory Journal
IS - 3
ER -