High Flow Nasal Cannula in Severe Sepsis
Atslēgvārdi
Abstrakts
Apraksts
Severe sepsis is a syndrome associated with severe infections with a high morbidity and mortality. In its most severe form, septic shock still leads to an in-hospital mortality of up to 50%. The pathophysiology of severe sepsis / septic shock includes increased work of breathing to compensate for tissue hypoperfusion-induced metabolic acidosis. This exaggerated work of breathing requires increased consumption of oxygen by respiratory muscles, which calls for a greater percentage of the already insufficient cardiac output, which can aggravate tissue hypoperfusion.
In the last decade, high flow nasal cannula (HFNC) appeared as an alternative ventilatory support intermediate between conventional oxygen and mechanical ventilation. Among others (3-7), the investigators have also demonstrated their effectiveness in patients with respiratory failure of different etiologies (8-11). Patients treated with HFNC quickly show a reduction of respiratory rate and respiratory work, associated with an improvement of the functional residual capacity and gas exchange. The absence of significant side effects and low cost makes HFNC especially attractive as adjunctive medical treatment in severe sepsis.
Then, the hypothesis is that in patients with severe sepsis, high flow nasal cannula (HFNC) therapy could reduce work of breathing, which would allow a redistribution of cardiac output from the respiratory muscles to other organs, improving peripheral perfusion with minor injury of organs at distance, less multiorgan failure and improved survival. Therefore, the aim of this study is to evaluate the efficacy of HFNC for improving sixty-day survival in patients with severe sepsis. This study will also provide a detailed evaluation of the HFNC's effects on the need for vital support (mechanical ventilation, dialysis, vasoactive drugs) and physiological parameters (acidosis, clearance of lactate, SvO2 and SOFA).
DESIGN Prospective, multicenter, randomized, controlled trial in 592 patients with severe sepsis admitted into a network of 18 ICUs from university and community hospitals in Spain to define the role of high flow oxygen therapy, with one experimental arm that will receive high flow oxygen therapy and a control arm that will receive conventional oxygen therapy if required.
Patients who consent will be randomized in a 1:1 ratio to receive HFNC or conventional treatment, which consists of adding oxygen on nasal prongs or Venturi mask only if hypoxemia is detected as SpO2 < 92% by pulse oximetry.
STUDY ARMS
1. HFNC therapy (experimental group) Treatment with HFNC (Airvo2® Fisher & Paykel, and AquaNASE® Armstrong Medical) will begin with high flow (50 L/min), high temperature and humidity and oxygen concentration adjusted for SpO2 >92%, even with FiO2 of 0.21, if needed.
The rationale for this HFNC dosage is that minute ventilation can be already reduced with 30 L/min, but functional residual capacity and oxygenation maximally improve at higher flow. On the contrary, flow >50 L/min is uncomfortable for many patients.
In the case of clinical intolerance, flow will be reduced to 40, 30 or 20 L/min. Yet it is not tolerated, HFNC will be stopped and patients will receive conventional oxygen if required, but will be evaluated as in the HFNC group by intention to treat.
In HFNC patients we propose an extra caution to avoid delaying a mechanical ventilation that would be beneficial. To do this, the ROX index (ROX = SpO2/FiO2/respiratory rate) will be calculated and if it is < 5, it is recommended to assess mechanical ventilatory support, either invasive or non-invasive.
2. Conventional therapy (control group) Patients assigned to the conventional treatment will receive the standard care given at hospital which consists of adding oxygen on nasal prongs or Venturi mask only if hypoxemia is suggested by SpO2 < 92% by pulse oximetry.
Target for oxygenation in both arms is SpO2 between 92% and 95%. SpO2 >95% without oxygen supply is acceptable. On the contrary, SpO2 <92% may be acceptable when needed for medical reasons, mainly chronic hypercapnic patients.
Datumi
Pēdējoreiz pārbaudīts: | 10/31/2019 |
Pirmais iesniegtais: | 10/24/2017 |
Paredzētā reģistrācija iesniegta: | 11/05/2017 |
Pirmais izlikts: | 11/06/2017 |
Pēdējais atjauninājums iesniegts: | 11/13/2019 |
Pēdējā atjaunināšana ievietota: | 11/14/2019 |
Faktiskais studiju sākuma datums: | 01/07/2018 |
Paredzamais primārās pabeigšanas datums: | 02/27/2020 |
Paredzamais pētījuma pabeigšanas datums: | 02/27/2020 |
Stāvoklis vai slimība
Iejaukšanās / ārstēšana
Device: High-Flow nasal cannula (HFNC)
Fāze
Roku grupas
Roka | Iejaukšanās / ārstēšana |
---|---|
Experimental: High-Flow nasal cannula (HFNC) Treatment with HFNC will be adjusted for SpO2 >92%, even with FiO2 of 0.21, if needed.
The rationale for this HFNC dosage is that minute ventilation can be already reduced with 30 L/min, but functional residual capacity and oxygenation maximally improve at higher flow. On the contrary, flow >50 L/min is uncomfortable for many patients.
In the case of clinical intolerance, flow will be reduced to 40, 30 or 20 L/min. Yet it is not tolerated, HFNC will be stopped and patients will receive conventional oxygen if required, but will be evaluated as in the HFNC group by intention to treat. | Device: High-Flow nasal cannula (HFNC) The patient will receive HFNC adjusted for SatO2 > 92% and with, at least, 30 liters of total flow. |
No Intervention: Conventional therapy Patients assigned to the conventional treatment will receive the standard care given at hospital which consists of adding oxygen on nasal prongs or Venturi mask only if hypoxemia is suggested by SpO2 < 92% by pulse oximetry.
Target for oxygenation in both arms is SpO2 between 92% and 95%. SpO2 >95% without oxygen supply is acceptable. On the contrary, SpO2 <92% may be acceptable when needed for medical reasons, mainly chronic hypercapnic patients. |
Atbilstības kritēriji
Vecums, kas piemērots studijām | 18 Years Uz 18 Years |
Dzimumi, kas ir piemēroti studijām | All |
Pieņem veselīgus brīvprātīgos | Jā |
Kritēriji | Inclusion Criteria: - Patients > 18 yr. with diagnostic criteria for severe sepsis, within 12 hours of admission in the Emergency Room, defined as hypotension after hemodynamic resuscitation, initial lactate > 4, or persistence of organ dysfunction (oliguria < 0.5 ml/kg/h, cyanosis, or altered consciousness).(qSOFA 1, 2 or 3) Exclusion Criteria: - Patients who require immediate ventilatory support both invasive and non-invasive, defined by severe hypoxemia (PaO2/FiO2 < 150), severe tachypnea (40 x') with signs of respiratory fatigue or low level of consciousness (Glasgow < 8). - Patients with limitation of the therapeutic effort or orders of not CPR. - Patients not susceptible to treatment with HFNC (facial trauma, tracheostomized, rejection of previous treatments with HFNC). - Participation in other clinical trials that may affect survival. - Home treatment with oxygen, CPAP or Non-invasive ventilation. |
Rezultāts
Primārie rezultāti
1. Mortality [60 day]
Sekundārie iznākuma mērījumi
1. Mechanical ventilation support [up to 60-days]
2. Dialysis support [up to 60-days]
3. Vasoactive drugs tappering [up to 60-days]
4. Sequential Organ Failure Assessment [up to 60-days]
5. Acidosis improvement [up to 60-days]
6. Central Venous Oxygen Saturation (SatVO2) [up to 60-days]
7. Lactate clearance [up to 60-days]