[HTML][HTML] A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis

…, EG Belousova, W Xuan, PTP Bye - … England Journal of …, 2006 - Mass Medical Soc
Background Inhaled hypertonic saline acutely increases mucociliary clearance and, in short-term
trials, improves lung function in people with cystic fibrosis. We tested the safety and …

Mechanisms and applications of hypertonic saline

MR Elkins, PTP Bye - Journal of the Royal Society of …, 2011 - journals.sagepub.com
Hypertonic saline is a strong sterile solution of salt water that can be inhaled as a nebulized
medication for people with cystic fibrosis (CF). To examine how it should be applied clinically…

Inhaled hypertonic saline as a therapy for cystic fibrosis

MR Elkins, PTP Bye - Current opinion in pulmonary medicine, 2006 - journals.lww.com
… Elkins, Mark R a,b,c ; Bye, Peter TP a,b,c … Correspondence to Peter TP Bye MBBS, FRACP,
PhD, Department of Respiratory Medicine, Royal Prince Alfred Hospital, Missenden Road …

Treatment of respiratory failure during sleep in patients with neuromuscular disease: positive-pressure ventilation through a nose mask

ER Ellis, PTP Bye, JW Bruderer… - American Review of …, 1987 - atsjournals.org
Severe nocturnal hypoxemia may occur in patients with respiratory muscle weakness caused
by neuromuscular disorders. Negative pressure ventilators may be partially effective in …

The role of exercise in maintaining health in cystic fibrosis

TJ Dwyer, MR Elkins, PTP Bye - Current opinion in pulmonary …, 2011 - journals.lww.com
Although its effects on some outcomes are unclear, the overall effect of exercise on quality
of life is substantially beneficial and the evidence available for other specific outcomes is …

Noninvasive ventilatory support during sleep improves respiratory failure in kyphoscoliosis

ER Ellis, RR Grunstein, S Chan, PTP Bye, CE Sullivan - Chest, 1988 - Elsevier
We investigated the effect on daytime respiratory function and quality of sleep, of providing
adequate ventilation either by intermittent positive pressure ventilation (EPPV) or by …

Inhaled mannitol improves lung function in cystic fibrosis

…, P Cooper, RG Stirling, CF Robertson, PTP Bye… - Chest, 2008 - Elsevier
Background The airways in patients with cystic fibrosis (CF) are characterized by the accumulation
of tenacious, dehydrated mucus that is a precursor for chronic infection, inflammation, …

Effects of exercise on respiratory flow and sputum properties in patients with cystic fibrosis

…, JA Alison, ZJ McKeough, E Daviskas, PTP Bye - Chest, 2011 - Elsevier
Background The physiologic mechanisms by which exercise may clear secretions in subjects
with cystic fibrosis (CF) are unknown. The purpose of this study was to compare ventilation, …

Studies of oxygenation during sleep in patients with interstitial lung disease

PTP Bye, F Issa, M Berthon-Jones… - American Review of …, 1984 - atsjournals.org
The pattern of change in arterial oxyhemoglobin saturation (Sa O 2 %) during sleep was
characterized in 13 patients with interstitial lung disease (ILD), 12 off whom had restrictive …

[HTML][HTML] Evaluation of the SenseWear activity monitor during exercise in cystic fibrosis and in health

…, JA Alison, ZJ McKeough, MR Elkins, PTP Bye - Respiratory …, 2009 - Elsevier
OBJECTIVE: Determine the SenseWear Pro3 Armband (SWA) accuracy for estimating energy
expenditure (EE) and step count during treadmill walking in cystic fibrosis (CF) compared …