Overview
We aim to investigate whether the use of Continuous Positive Airway Pressure using a Helmet device (Helmet CPAP) will increase the number of days alive and free of ventilator within 28 days compared to the use of a High Flow Nasal Cannula (HFNC) in patients admitted to Helsingborg Hospital, Sweden, suffering from COVID-19 and an acute hypoxic respiratory failure.
Description
A detailed description can be found in the study protocol which is pending submission for peer-review.
Eligibility
Inclusion Criteria (all of the following):
- Age 18 years
- Sars-Cov-2 found in the upper or lower respiratory tract by PCR during the current disease episode
- Peripheral oxygen saturation (SpO2) < 92 % despite conventional low-flow oxygen therapy of at least 6 L /min for at least 15 min
- A decision to initiate HFNC or Helmet CPAP by the attending ward physician
- The patient has given written informed consent to participate.
Exclusion Criteria (any of the following):
- Need for direct admission to the intensive care unit for mechanical ventilation
- Unconsciousness or drowsiness
- Pneumothorax
- Carbon dioxide pressure (pCO2) > 6 kPa in venous blood gas (VBG)
- Underlying chronic obstructive pulmonary disease stage III-IV
- A decision not to participate
- Inability to comprehend the study content and give informed consent