The severity of COVID-19 is related to the level of hypoxemia, respiratory failure, how long it lasts and how refractory it is at increasing concentrations of inspired oxygen. The inability to perform hematosis due to edema that occurs from acute inflammation could be attenuated by the administration of hyperbaric oxygen (HBO). Recently, it has been reported benefits in this matter in patients with SARS-CoV-2 hypoxemic pneumonia in China; where the administration of repeated HBO sessions decreased the need for mechanical ventilation (MV) in patients admitted to the Intensive Care Unit due to COVID-19. Hyperbaric oxygen is capable of increasing drastically the amount of dissolved oxygen in the blood and maintain an adequate supply oxygen to the tissues. In addition to this, it can influence immune processes, both humoral and cellular, allowing to reduce the intensity of the response inflammatory and stimulate antioxidant defenses. HBO is considered safe and it has very few adverse events, it is a procedure approved by our authorities regulatory for several years. In the current context of the pandemic by COVID-19 and worldwide reports of mortality associated with severe cases of respiratory failure, it is essential to propose therapeutical strategies to limit or decrease respiratory compromise of severe stages by COVID-19. That is why, it is proposed to carry out this research to assess whether HBO treatment can improve the evolution of patients with COVID-19 severe hypoxemia.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
40
Hyperbaric oxygen therapy (HBOT): inhalation of pressurized oxygen through a hyperbaric chamber (Revitalair430)
Hospital Central de San Isidro Dr. Angel Melchor Posse
San Isidro, Buenos Aires, Argentina
Hospital de Infecciosas F. J. Muñiz
Buenos Aires, Buenos Aires F.D., Argentina
Hospital General de Agudos D.F Santojanni
Buenos Aires, Buenos Aires F.D., Argentina
Time to normalize the oxygen requirement (oxygen dependence)
Time to normalize the oxygen requirement: Allowing a pulse oximetry value in ambient air greater than or equal 93% and/or arterial blood gas with PaO2 value greater than 60 mmHg in ambient air.
Time frame: 15-30 days.
Need for Invasive Mechanical Ventilation (IMV) and / or Respiratory Distress Syndrome Acute (ARDS)
Number of patients who required IMV after being enrolled
Time frame: 30 days
Development of Acute Respiratory Distress Syndrome (ARDS)
Number of patients who required IMV and / or had a diagnosis of ARDS after being enrolled.
Time frame: 30 days
30-day mortality
Number of patients who died in that period since enrollment
Time frame: 30 days
Hypotension with vasopressor requirement
Number of patients with hypotension who were administered vasopressors in this period
Time frame: 30 days
Mortality
Number of patients who died in that period since enrollment.
Time frame: 45 days / 60 days / 90 days and 180 days
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