Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
---|---|---|---|---|---|
Sztrymf et al. September 2011, France. | 38 adult patients admitted to intensive care with acute respiratory failure, defined as requiring more than 9 l/min oxygen to achieve an SpO2 > 92% or exhibiting persistent signs of respiratory distress (respiratory rate > 25 bpm, thoraco-abdominal asynchrony or supraclavicular retraction) despite oxygen administration. Patients requiring immediate endotracheal intubation or with hypercapnic respiratory failure were excluded. | Prospective, observational study. High flow, humidified nasal oxygen therapy compared to conventional oxygen therapy (delivered by non-rebreathing face mask). | PaO2 after 1h of high flow nasal oxygen | Significantly increased (p=0.009) | No control, small study. |
Respiratory rate on high flow nasal oxygen (all time points from 15 minutes to 48h) | Significantly decreased (p=0.009) | ||||
Dyspnoea on high flow nasal oxygen (all time points from 15 minutes to 48h) | Significantly decreased (p=0.012) | ||||
Tolerance of therapy | No patients required cessation of therapy because of intolerance | ||||
Lenglet et al. November 2012, France. | 17 adult patients admitted to the emergency department with acute respiratory failure, defined as requiring ore than 9l/min oxygen or ongoing signs of respiratory distress despite oxygen therapy. | Prospective, observational, feasibilty study. | SpO2 after 15 minutes of high flow nasal oxygen | Significantly increased (p<0.0001) | No control, small study. |
Respiratory rate after 15 minutes of high flow nasal oxygen | Significantly decreased (p<0.0001) | ||||
Dyspnoea intensity after 15, 30 and 45 minutes of high flow nasal oxygen (Borg score and VAS) | Significantly decreased (p< 0.05) | ||||
Parke et al. March 2011, New Zealand. | 60 adult patients admitted to intensive care with hypoxaemic respiratory failure. Patients requiring immediate endotracheal intubation and those not for mechanical ventilation were excluded. | Prospective, randomised, controlled trial. | Desaturations | Significantly fewer in group receiving high flow nasal oxygen (p=0.009) | Unclear how hypoxaemic respiratory failure was defined. Mixed aetiologies including post-operative patients. Blinding not possible. Unclear how to power such studies given effect size unknown. |
Respiratory rate | No significant difference | ||||
PaO2 / FiO2 | No significant difference | ||||
Length of intensive care stay | No significant difference | ||||
Length of hospital stay | No significant difference | ||||
Cuquemelle et al. October 2012, France. | 37 adult patients admitted to intensive care with acute hypoxaemic respiratory failure, defined as requiring at least 4l/min oxygen to maintain an SpO2 above 95%. patients requiring non-invasive or invasive ventilation were excluded. | Prospective, randomized, crossover design, single centre. High flow, humidified nasal oxygen compared to standard oxygen therapy (not humidifed, delivered by mask or nasal cannulae). | Mouth, nose and throat dryness score after 24 hours on high flow nasal oxygen | Significantly reduced (p=0.004) | Soft endpoints. |
Preferred oxygen delivery device | Significantly more people preferred high flow nasal oxygen (p=0.01) | ||||
Roca et al. April 2010, Spain. | 20 adult patients admitted to intensive care with acute respiratory failure, defined as SpO2 < 96% while receiving humidified oxygen via facemask with an FiO2 greater than or equal to 0.5. Patients with an unstable clinical state, need for endotracheal intubation, decreased consciousness, haemodynamic instability despite fluid therapy and vasopressors, severe failure of > 2 organs apart from respiratory failure, pregnancy or lack of co-operation were excluded. | Prospective, observational study. High flow, humidified nasal oxygen compared to the preceding period of conventional oxygen therapy (delivered by facemask or nasal cannulae). | PaO2 after 30 minutes on high flow nasal oxygen | Significantly increased (p=0.002) | No control, small study. |
SpO2 after 30 minutes on high flow nasal oxygen | Significantly increased (p=0.02) | ||||
Respiratory rate after 30 minutes on high flow nasal oxygen | Significantly decreased (p<0.001) | ||||
Dyspnea after 30 minutes on high flow nasal oxygen | Significantly reduced (p=0.01) | ||||
Mouth dryness after 30 minutes on high flow nasal oxygen | Significantly reduced (p<0.01) |