Timed Awake Prone and Repositioning for Patients With Covid-19-induced Hypoxic Respiratory Failure.
Corona Virus Infection, Hypoxic Respiratory Failure
About this trial
This is an interventional treatment trial for Corona Virus Infection focused on measuring Awake prone positioning
Eligibility Criteria
Inclusion Criteria: Adults ≥ 18 years of age Awake patients without endotracheal intubation Suspected or confirmed infection of COVID-19 Hypoxemia requiring oxygen supplementation ≥ 0.4 FiO2 or ≥ 5L/min via nasal cannula Bilateral or unilateral chest infiltrates on x-ray or HRCT Admitted to the ICU or an acute care unit where hemodynamic and respiratory Willingness to comply with the protocol and provide written informed consent Exclusion Criteria: Risk of airway obstruction or even asphyxia Need for emergent intubation after admission Respiratory failure caused by cardiogenic pulmonary edema Unable to implement timed prone and repositioning due to any cause Injury or wound on the ventral body surface affecting the prone position Unstable fracture of cervical vertebra and spine Glaucoma or other sharp increases in intraocular pressure Intracranial hypertension caused by traumatic brain injury etc. Significantly high risk of pulmonary embolism Acute hemorrhagic disease Respiratory rate >40 breaths/min, with significant dyspnea Transcutaneous oxygen saturation can not be continuously monitored Hemodynamic instability requiring vasoactive drugs (systolic blood pressure <90 mmHg or mean arterial pressure <65 mmHg despite adequate volume resuscitation) Awareness disorder or inability to accept instructions, communication barrier with the nursing team, inability to use language or pager to call for help Difficulty or limitation in autonomous movement, inability to adjust the position without assistance from others Body mass index > 37 kg/m2
Sites / Locations
- Changxing People's Hospital
- The Second Affiliated Hospital Zhejiang University School of Medicine
- Lishui Municipal Central Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Awake timed prone and repositioning group
Standard care group
Patients' cumulative prone and repositioning time is encouraged to reach 8-10 hours per day for 4 days following a timed prone and repositioning strategy.
Patients can change their positions freely according to their own needs. Health providers do not take the initiative to give guidance on prone and repositioning.