Breathe Easy Early Study (BEES): A randomised control study assessing the efficacy of early intervention with humidified high flow nasal cannula in the emergency department-Optimising outcomes in the Golden Hour of Respiratory failure.
- Conditions
- Respiratory illnessesChronic respiratory conditionsCongestive Heart FailureAcute Respiratory illnessesCardiovascular - Other cardiovascular diseasesRespiratory - Other respiratory disorders / diseases
- Registration Number
- ACTRN12616000587404
- Lead Sponsor
- Ipswich Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 268
18 years and over
Symptomatic breathlessness- increased respiratory rate > 25 breaths per min and observed increased work of breathing.
Patients requiring oxygen supplementation to maintain Sp02 > 94% for acutely unwell patient OR 88% to 92% for those at risk of hypercapnic respiratory failure (in line with recruiting site hospital).
Recent ENT surgery
Epistaxis/ nasal trauma/ sinus problems
Altered level of consciousness
Pregnancy
Non invasive ventilation at point of triage
Pneumothorax/chest trauma
History of trauma eg. post fall
Falling GCS or GCS <9
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome will be the proportion of patients who experience relief of dyspnea. This will be defined as a reduction of 20 points on a 100mm visual analogue scale (VAS), reduction in heart and respiratory rate prior to discharge from ED. The proportion of patients who achieve dyspnea relief in each group will be reported and the differences between each group (with a 95% confidence interval of the difference) will be reported.[Baseline visual analogue scale( VAS) - Included as part of the initial assessment (prior to any or just as initial intervention takes place), then will continue 30minutely for 90minutes whilst in the ED. If patient is admitted to the ward then hourly-4hrly depending on the patients clinical condition or wards protocol.]
- Secondary Outcome Measures
Name Time Method