HiFloWEAN: Weaning Protocol for High-flow Nasal Oxygen Therapy in Intensive Care
Study Details
Study Description
Brief Summary
High-flow nasal oxygen therapy (HFNO) is an oxygenation technique frequently used in intensive care.
The main objective of our study is to show that the use of a protocol for weaning patients off high-flow nasal oxygen therapy (HFNO) in the intensive care unit increases the probability that patients will be weaned from HFNO at Day 7 post-randomisation.
This is a open-label multicentre randomised controlled trial conducted in two parallel groups.
The primary endpoint is the success rate at Day 7, with success defined as "definitive" weaning from HFNO, i.e. patients weaned from HFNO for more than 48 hours without recourse to non-invasive ventilation (NIV) or intubation and still alive at Day 7.
The weaning protocol will be started as soon as the patient meets all the inclusion criteria, considered to be the prerequisites for initiating weaning from HFNO. Patients will be monitored until Day 28 maximum.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Experimental group The flow of the HFNO will remain high (50-60 L/min) guaranteeing the effectiveness of the HFNO on the wash-out of the anatomical space. At the same time, weaning will begin with a gradual reduction in FiO2 of 0.1 every 4 hours. To achieve this reduction, the patient will have to meet the safety targets of a stable respiratory rate at rest (no increase) and pulsed oxygen saturation (SpO2). The SpO2 target will be 92-95%. Once the FiO2 has stabilised at 0.4 for 4 hours, the nurse will initiate a 10 L/min reduction in the flow of HFNO every 4 hours. The oxygen therapy support may be changed for standard oxygen when the HFNO flow rate is 40L/min with an FIO2 of 0.4 for 4 consecutive hours. |
Drug: HFNO weaning protocol
Algorithm based on SpO2 values and respiratory rate: a decrease of FiO2 and of the flow will be done
|
| Active Comparator: Control group Weaning methods will be left to the free choice of the practitioner. Any change in the HFNO setting must be made on medical prescription. A minimum SpO2 objective is required (SpO2 ≥92%). |
Drug: Standard of care
Weaning methods will be left to the free choice of the practitioner.
|
Outcome Measures
Primary Outcome Measures
- The success rate at Day 7 [At day 7]
Success being defined as "definitive" weaning from HFNO, i.e. a patient weaned for more than 48 hours from HFNO without recourse to non-invasive ventilation or intubation and still alive at Day 7.
Secondary Outcome Measures
- High-flow nasal oxygen therapy (HFNO) weaning rate at day 28 [At day 28]
- Time to definitive weaning from HFNO [From randomisation to day 28]
- Cumulative incidence of intubation [From randomisation to day 28]
- Cumulative incidence of use of curative non-invasive ventilation [From randomisation to day 28]
- Mortality rate at day 28 [At Day 28]
- Number of days on HFNO for patients definitively weaned from HFNO [From randomisation to discharge from intensive care or at Day 28]
- Changes in the ROX index during the weaning phase [From randomisation to day 28]
ROX index : [(SpO2/FiO2)/respiratory rate]
- Changes in the use of accessory respiratory muscles [From randomisation to discharge from intensive care or to Day 28]
Using the Patrick score (Score from 0 to 5)
- Progression of dyspnoea [From randomisation to discharge from intensive care or to Day 28]
Assessed by the modified Borg scale (scale from 0 to 10)
- Intensive care unit and/or continuous monitoring unit length of stay [From randomization until the date of discharge, assessed up to 28 days maximum]
- Intensive care unit and/or continuous monitoring unit length of stay or time to ICU discharge readiness [From randomization until the date of discharge OR ability to be discharged from intensive care, assessed up to 28 days maximum]
The ability to go out will be defined by the validation of all the items on the modified ability grid (score modified from Hiller et al. ; 28 items)
Eligibility Criteria
Criteria
Inclusion Criteria:
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Major patient admitted to the intensive care unit or continuous care unit for de novo hypoxaemic acute respiratory failure (with a PaO2/FiO2 ratio <300 mmHg)
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Treated with HFNO with a flow rate ≥ 50L/min and inspired oxygen fraction (FiO2) ≥ 0.5, flow rate and FiO2 having to be stable (i.e. not increased) in the 24 hours prior to inclusion
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With a ROX index (SpO2/FiO2/Respiratory Rate) stable or improving in the 6 hours prior to inclusion and greater than 4.88
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Had a blood gas test under HFNO within 24 hours of inclusion
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Participant covered by or entitled to social security
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Informed consent signed by the patient or its relatives if the patient is incapable; this consent must then be confirmed by the patient as soon as possible
Exclusion Criteria:
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Presence of a patient included in the study and not weaned off HFNO in the sector managed by the nurse of the patient assessed for eligibility
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Concomitant non-invasive ventilation treatment
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Use of HFNO within 7 days of extubation
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Chronic obstructive pulmonary disease (Gold grade 3 or 4)
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Cardiogenic acute pulmonary oedema as the main cause of acute respiratory failure
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Diffuse interstitial lung disease as a medical history
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Patient with long-term non-invasive ventilation with external positive pressure
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Patient on long-term oxygen therapy at home
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Pregnant women, women in labour and breastfeeding mothers
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Persons deprived of their liberty by a judicial or administrative decision, persons hospitalised without consent and persons admitted to a health or social establishment for purposes other than research.
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Minor
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Adult subject to a legal protection measure (guardianship, curators, person under court protection)
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Patient with a medical decision not to intubate
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Patients already included in the study, neither for the same stay if they were to present the inclusion criteria again, nor for subsequent stays
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Intensive care, University Hospital, Blois | Blois | France | ||
| 2 | Intensive care unit, University Hospital, Bourg-en-Bresse | Bourg-en-Bresse | France | ||
| 3 | Intensive care, University Hospital, Bourges | Bourges | France | ||
| 4 | Intensive care, University Hospital, Chartres | Chartres | France | ||
| 5 | Intensive care, University Hospital, Cholet | Cholet | France | ||
| 6 | Intensive care, University Hospital, Dax | Dax | France | ||
| 7 | Intensive care, University Hospital, Le Mans, | Le Mans | France | ||
| 8 | Intensive care, University Hospital, Orléans | Orléans | France | ||
| 9 | Intensive care, University Hospital, Tours | Tours | France | ||
| 10 | Intensive care unit, University Hospital, Vannes | Vannes | France |
Sponsors and Collaborators
- University Hospital, Tours
Investigators
- Principal Investigator: Mai-Anh NAY, MD, CHRU Orléans
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- DR230001