This open label randomized controlled multicenter phase II trial will evaluate the clinical impact of the use of HFNC vs. conventional oxygen therapy in patients with moderate and severe hypoxemic acute respiratory failure secondary to SARS-CoV-2 infection.
Acute hypoxemic respiratory failure is a condition in which rapid-onset impairment in gas exchange between the lungs and the blood, lead to hypoxemia with or without hypercapnia. Usual management of this condition relies on oxygen supplementation throughout different respiratory support modalities (i.e., low flow oxygen devices, high-flow nasal cannulas, mechanical ventilation, ECMO, etc.) aiming to restore gas exchange and to support respiratory effort. In most cases, initial management of acute hypoxemic respiratory failure might be provided through low-flow oxygen systems, but more severe cases will require more advanced life-supporting strategies. Respiratory compromise by SARS-CoV-2 infection widely varies between subjects. Thus, respiratory system elastance, intrapulmonary shunt, pulmonary perfusion/ventilation inequalities and lung weight can range between almost normal up to very high values. Consequently, modalities to provide initial support in acute severe hypoxemic respiratory failure in SARS-CoV-2 infection should not be limited to immediate invasive mechanical ventilation support as such respiratory support modalities should be adapted to individual requirements. Unfortunately, similar values of initial PaO2/FiO2 ratios (especially when PaO2/FiO2 ratio is \< 200) are not clearly related with more or less severe lung affectation, high or low respiratory system elastance patterns, high or low adaptive hypoxic vasoconstriction, and far beyond clinical signs, there are no widely available methods able to rapidly decide which patients would be more benefit from a relative "conservative" management or on the contrary, which patient would benefit from immediate invasive respiratory support. Use of high-flow nasal cannulas (HFNC) in acute hypoxemic respiratory failure from different etiologies has rapidly increased during the last years. Certainly, randomized controlled trials suggest that HFNC might prevent intubation and the need for invasive mechanical ventilation in patients with moderate and severe hypoxemia. Nevertheless, impact of HFNC on mortality rates and other important clinical outcomes in this condition remains controversial. Initial observational reports of patients with severe SARS-CoV-2 infection subjected to invasive mechanical ventilation showed a consistent and very high mortality. Indeed, some experts claimed for using such non-invasive respiratory support devices in patients with moderate or even high pulmonary shunt values arguing about possible harm induced by mechanical ventilation especially in patients with a relative normal respiratory system elastance. Nevertheless, others recommended against HFNC use because safety concerns for health care workers, which clearly limited its use at the initial phases of the pandemic. Thus, the impact and safety of using HFNC at very early stages of acute hypoxemic respiratory failure induced by severe SARS-CoV-2 infection remain to be elucidated. This is how the HiFlo-COVID trial propose to assess the impact HFNC vs. conventional oxygen therapy on the need for intubation / invasive mechanical ventilation support and the clinical status (at days-14 and -28) as assessed by a modified 7-point ordinal scale in patients with moderate / severe hypoxemic respiratory failure secondary to SARS-CoV-2 infection.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
199
Oxygen therapy by conventional nasal cannula / prongs, venturi mask, or mask with reservoir
Breathing support with High-flow nasal cannula
Fundacion Valle del Lili
Cali, Valle del Cauca Department, Colombia
Intubation rate
Need for intubation / support with invasive mechanical ventilation.
Time frame: 28 days
Clinical recovery
Time to improvement of clinical status according to the 7-point ordinal scale. Modified 7-point ordinal scale: * An ordinal scale of 7 points where 1= Ambulatory/no limitation of activities and 7= Death. Low scores denote a better outcome and high scores denote a worse outcome. * Time to reduction in scale score will be measured (daily scale scoring).
Time frame: 28 days
Proportion of patients with requirement of early mechanical ventilation.
Whether or not each patient required mechanical ventilation during the first 7 and 14 days after randomization will be assessed. Proportion of patients with early mechanical ventilation will be calculated for each group.
Time frame: 7 and 14 days
Mechanical ventilation-free days
Days off from mechanical ventilation
Time frame: 28 days
Renal replacement therapy-free days
Days off from renal replacement therapy
Time frame: 28 days
Length of ICU stay
Duration of stay in ICU
Time frame: 28 days
Length of hospital stay
Duration of hospital stay
Time frame: 28 days
All-cause day-28 mortality
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Hospital mortality
Time frame: 28 days
Proportion of serious adverse events
Proportion of patients with serious adverse events during hospital stay
Time frame: 28 days
Proportion of bacterial - fungal infections
Proportion of bacterial - fungal infections during hospital stay
Time frame: 28 days