Oxygen and helium gas mixtures for dyspnoea.

PURPOSE OF REVIEW: Recent reports of the benefits of helium/oxygen gas mixtures (heliox) use for the relief of dyspnoea and exercise limitation have stimulated interest in the use of heliox in the palliation of dyspnoea especially in chronic obstructive pulmonary disease patients. With better understanding of the mechanistic causes of dyspnoea in these patients theoretical benefits of heliox have been suggested. This report considers the evidence to support this role and reviews the current position on heliox administration and use as a carrier gas for nebulization therapies. RECENT FINDINGS: Heliox can effectively improve exercise limitations, decrease the work of breathing and reduce dyspnoea in lung cancer and chronic obstructive pulmonary disease patients; in the latter it works by reducing dynamic hyperinflation. The evidence comes from short-term assessments of single exercise tests and additional benefits are seen when used in conjunction with other current therapies such as supplemental oxygen and nebulization. Dedicated devices with better comprehensive guidelines for administration have been developed to alleviate some of the reluctance of use. SUMMARY: Heliox use could prove beneficial either administered alone or as an addition to current therapies for the palliation of dyspnoea and give significant improvement in outcomes of rehabilitation programmes. There is still an urgent need to identify which patients are the best candidates for heliox use and translate the significant short-term benefits into long-term improvements in functioning and quality of life.

The effect of helium and oxygen on exercise performance in chronic obstructive pulmonary disease: a randomized crossover trial.

RATIONALE: Breathing supplemental oxygen reduces breathlessness during exercise in patients with chronic obstructive pulmonary disease (COPD). Replacing nitrogen with helium reduces expiratory flow resistance and may improve lung emptying. Combining these treatments should be independently effective. OBJECTIVES: Study the effect of changing oxygen or helium concentration in inspired gas during exercise in patients with stable COPD. METHODS: In 82 patients (mean age, 69.7 yr; mean FEV(1), 42.6% predicted), we measured endurance shuttle walking distance, resting and exercise oxygen saturation, and end-exercise dyspnea (Borg scale) while patients breathed Heliox28 (72% He/28% O(2)), Heliox21 (79% He/21% O(2)), Oxygen28 (72% N(2)/28% O(2)), or medical air (79% N(2)/21% O(2)). Gases were administered using a randomized, blinded, crossover design via a face mask and an inspiratory demand valve. RESULTS: Breathing Heliox28 increased walking distance (mean+/-SD, 147+/-150 m) and reduced Borg score (-1.28+/-1.30) more than any other gas mixture. Heliox21 significantly increased walking distance (99+/-101 m) and reduced dyspnea (Borg score, -0.76+/-0.77) compared with medical air. These changes were similar to those breathing Oxygen28. The effects of helium and oxygen in Heliox28 were independent. The increase in walking distance while breathing Heliox28 was inversely related to baseline FEV(1) breathing air. CONCLUSION: Reducing inspired gas density can improve exercise performance in COPD as much as increasing inspired oxygen. These effects can be combined as Heliox28 and are most evident in patients with more severe airflow obstruction.

Hypoxia of sleep apnoea: cardiopulmonary and cerebral changes after intermittent hypoxia in rats.

Sleep apnoea (SA) is common, especially in elderly people. In severe cases, arterial P(O2) may be lowered for a third or more in a night of sleep. To simulate the degree and duration of severe SA we exposed rats in a normobaric environmental chamber to 10% O(2) for 4h daily for 56 days (intermittent hypoxia: IH group) and compared them with rats continuously exposed for 8 weeks (continuous hypoxia: CH group) and control rats breathing room air (normoxic: N group). We found significant cardiopulmonary and cerebral changes. Right ventricular hypertrophy developed in IH and to a greater extent in CH. Small peripheral lung vessels developed thicker walls (assessed by a new method), which reduced their lumen, more in CH than IH. Coronal brain sections were immunostained for the glucose-transporter 1 (GLUT1) and the vascular endothelial growth factor (VEGF). The percentages of immunoreactivity in the frontal and temporal cortex, hippocampus, accumbens and putamen were determined by image-capture analysis. We noted GLUT1 immunoreactivity of the capillaries was similarly increased in all regions after CH but less so after IH. However, there was a significant linear trend in GLUT1 reactivity from N to IH to CH (R(2) = 0.73, P = 0.007) that was also confirmed by analysis of variance. The extent of VEGF-stained neurones and glial cells was significantly increased in all regions after IH but not after CH. This suggests that the signals for angiogenesis were complete or arrested after CH. Our findings have implications for the elderly subjected to hypoxic episodes during sleep apnoea.