Respiratory Insufficiency, Respiratory Failure
Conditions
Keywords
respiratory insufficiency, respiratory failure, non-invasive ventilation, high flow nasal cannula, nasal high flow, trans-nasal insufflation, NIV, HFNC
Brief summary
RENOVATE study aims to investigate if the respiratory support device called High-Flow Nasal Oxygen Cannula (HFNC) acts similarly (non-inferior) to another respiratory support device called Non-Invasive positive-pressure Ventilation (NIPPV) in preventing endotracheal intubation in adult patients with Acute Respiratory Failure (ARF) from different causes. HFNC is a somewhat new method of respiratory support in adults that has been used in neonatal ARF for some years. The reason this study is necessary is that, even though NIPPV has been demonstrated to prevent endotracheal intubation (and its associated complications) in a broad range of ARF patients, HFNC has been proposed to have the same beneficial effect of NIPPV while being easier tolerated, allowing patients to talk, eat and drink through mouth while on HFNC. RENOVATE will recruit between 800 to 2000 patients (adaptive design) with different types of ARF in Brazil. Patients will be randomized to HFNC or NIPPV and the rate of endotracheal intubation will be compared between groups as well as other parameters such as vital status and other health care related complications. \[IMPORTANT NOTE\] On April 13, 2021, on the first interim analysis, the DSMB recommended the interruption of the immunocompromised hypoxemic ARF subgroup.
Detailed description
RENOVATE will investigate if High-Flow Nasal Oxygen Cannula (HFNC) is non-inferior to Non-Invasive positive-pressure Ventilation (NIPPV) in preventing endotracheal intubation or death in adult patients with Acute Respiratory Failure (ARF) from different causes in 7 days. HFNC is a somewhat new method of respiratory support in adults that has been used in neonatal ARF for some years. Even though NIPPV has been demonstrated to prevent endotracheal intubation (and its associated complications) in a broad range of ARF patients, HFNC may have beneficial effect over NIPPV because it is easier to be tolerated, allowing patients to talk, eat and drink through mouth while on therapy. RENOVATE will recruit between 800 to 2000 patients (adaptive design) with different types of ARF in Brazil. The main hypothesis is that HFNC is non inferior to NIPPV in reducing intubation rate or death within 7 days. However, as an adaptive study, this non inferiority hypothesis may change to superiority if gathered data during the study is promissing in the interim analysis. Therefore, sample size may increase to 2000 participants. Patients will be randomized to HFNC or NIPPV and the rate of endotracheal intubation will be compared between groups as well as other parameters such as vital status and other health care related complications. \[IMPORTANT NOTE\] On April 13, 2021, on the first interim analysis, the DSMB recommended the interruption of the immunocompromised hypoxemic ARF subgroup. Trial Update: We have collected Covid 19 information since march 2020 as an added question in the CRF. There are two questions: one in the elegibility criteria form asking if Covid 19 is suspected and another one in the discharge form asking if Covid 19 was laboratory confirmed. Since then, there were considerably change in prevalence of acute respiratory failure subgroups since the beginning of the trial in 2019. Covid 19, nowdays, is responsible for 63% of our sample size, followed by hypoxemic non immunocompromised subgroup with 19%, acute pulmonary edema and hypoxemic immunocompromised with 8% and finally COPD with 2%. These prevalences are completely different from our previous assumptions in 2019 trial simulations as published in our protocol and statistical analysis plan in March 2022 Volume 24 Number 1 at Critical Care Resuscitation journal. Therefore, the Steering Committee decided that all Covid 19 patients, independent of previous subgroup allocation, would be analysed separately in a 5th subgroup. Update in simulations with different scenarios and new statistical models were done by March 13th 2023 to account for the 5th interim analysis which you can access in the document section of ClinicalTrials.gov. No change in inclusion criteria were made. The only change was the introduction of those two questions described before. These updates are aimed at accommodating the presence of COVID-19 patients in the trial as the main subgroup of patients.
Interventions
DEVICEHigh Flow Nasal Catheter
HFNC will deliver through AIRVO2. FiO2 from 21 to 100% and heated humidified gas flow up to 60 l / min with temperature of the circuit maintained at 37 degrees. Oxygen flow will be offered through a humidified nasal catheter. Flow and FiO2 will be titrated according to the protocol to maximize patient´s comfort and SpO2.
DEVICENoninvasive ventilation
NIPPV will be performed using a facial mask (either oronasal or full face). NIPPV will deliver pressures and FiO2 tailored to specific ARF subgroups, according to the protocol. Adjustments of the inspiratory pressure (IPAP) and expiratory pressure (EPAP) and FiO2 according to protocol
Sponsors
Ministry of Health, Brazil
Berry Consultants
Hospital do Coracao
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Adaptive, non-inferiority randomized, open-label, controled clinical trial
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
\[IMPORTANT NOTE\] On April 13th 2021, in the first interim analysis, the DSMB recommended for the interruption of the subgroup Immunocompromised De Novo Hypoxemic ARF due to futility. Sequential adult patients 18 years of age or older admitted to the ICU or emergency department with acute onset respiratory distress suspected of having De Novo hypoxemic ARF (non-immunocompromised) , Immunocompromised De Novo hypoxemic ARF, COPD ARF, Cardiogenic acute pulmonary edema (APE). Inclusion criteria for these 4 ARF subgroups are detailed below: A. Inclusion Criteria for Non-Immunocompromised De Novo Hypoxemic ARF. Patients must meet criteria 1, 2 and 3: 1. Hypoxemia evidenced by SpO2 \<90% or PaO2 \<60 mmHg in room air 2. Use of accessory muscles, paradoxical breathing, and/or thoracoabdominal asynchrony 3. RR\> 25 per minute B. Inclusion Criteria for Immunocompromised De Novo Hypoxemic ARF. Patients must meet criteria 1, 2, 3 and 4: 1. Immunosuppression diagnosis: i. Use of Immunosuppressive drug or long-term \[\>3 months\] or high-dose \[\>0.5 mg/kg/day\] steroids ii. Solid organ transplantation iii. Extensive solid tumor or solid tumor requiring chemotherapy in the last 5 years iv. Hematological malignancy regardless of time since diagnosis and received treatments v. HIV infection vi. Primary immunodefiency 2. Hypoxemia evidenced by SpO2 \<90% or PaO2 \<60 mmHg in room air 3. Use of accessory muscles, paradoxical breathing, and/or thoracoabdominal asynchrony 4. RR\> 25 per minute C. Inclusion Criteria for COPD exacerbation: Patients must meet criteria 1 or 2 and 3 and 4: 1. Previous Diagnosis of COPD based on GOLD guidelines 2. Strong clinical suspicion of COPD i. Smoker or ex-smoker or other CPOD related exposure ii. Presence of chronic dyspnea on exertion or chronic productive cough iii. Excluded other causes for the chronic symptoms (ex. pulmonary fibrosis, heart failure) 3. RR\> 25 per minute or use of accessory muscles, paradoxical breathing, and/or thoracoabdominal asynchrony 4. ABG analysis with pH \< 7,35 , paCO2\> 45 mmHg D. Inclusion Criteria for ARF secondary to Cardiogenic APE. Patients must meet criteria numbers 1, 2 and 3: 1. Diagnosis of Cardiogenic Acute Pulmonary Edema (Nava, 2003): i. Dyspnea of sudden onset ii. Widespread rales with or without third heart sound 1 iii. Absent history of pulmonary aspiration, infection or previous history of pulmonary fibrosis iv. Pulmonary edema as the main clinical hypothesis v. Previous heart failure clinical history or acute coronary syndrome vi. If chest X-ray is already available at randomization, it must be suggestive of bilateral pulmonary edema 2. RR \> 25 per minute 3. SpO2 \< 95%
Exclusion criteria
for all subgroups of ARF 1. Indication of emergency ETI: * Prolonged respiratory pauses * Cardiorespiratory arrest * Glasgow ≤12 * HR \< 50 bpm with decreased level of consciousness * pH \< 7.15 irrespective of the cause 2. Psychomotor agitation that prevents adequate medical / nursing care requiring heavy sedation 3. Persistent hemodynamic instability with MAP \<65 mmHg, SBP \<90 mmHg after adequate volume resuscitation or requiring norepinephrine\> 0.3 microg / kg / min or equivalent. 4. Contraindications to non-invasive ventilation: face deformities or traumas, recent esophageal surgery, hypersecretion, vomiting with aspiration risk 5. Presence of pneumothorax or extensive pleural effusion 6. Severe arrhythmias at risk of hemodynamic instability 7. Thoracic trauma understood as the main cause of ARF 8. Asthma attack 9. Pregnancy 10. Cardiogenic Shock 11. Acute Coronary Syndromes with plans to undergo coronary angiography within 24 hs 12. ARF after orotracheal extubation (up to 72 hours after extubation) 13. Post-surgical ARF (surgery within 72 hours) 14. Hypercapnic ARF due to neuromuscular disease or chest deformities 15. Patients on exclusive palliative care 16. Do Not Intubate order (DNI) 17. Chronic pulmonary disease except COPD 18. Use of more than 6 hours of NIPPV before randomization if hypoxemic ARF in the non-immunosuppressed, in the immunosuppressed hypoxemic, or if exacerbated COPD 19. Use of NIPPV before randomization in the cardiogenic acute pulmonary edema
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Endotracheal intubation rate or death | in 7 days | proportion of endotracheal intubation or death |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Mortality | in 28 days | Death |
| ICU free days | in 28 days | Days out of ICU |
| IMV free days | in 28 days | Days without IMV inside of ICU after 48 hours of being extubated |
Other
| Measure | Time frame | Description |
|---|---|---|
| Length of hospital stay | in 90 days | Time in hospital in days |
| Patient confort score | 7 days | Visual scale varying from 0 (no disconfort) to 100 (maximal disconfort) |
| Length of ICU stay | in 90 days | Time in the ICU in days |
| Vasopressor free days | in 28 days | Days without use of vasopressor inside of ICU |
| Proportion of patients who received do-not-intubate-order | in 7 days | Proportion of patients that received DNI order after randomization was done |
Countries
Brazil
Outcome results
None listed