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Clinical Trials/NCT04782817
NCT04782817CompletedNot Applicable

Reducing Reintubation Risk in High-Risk Cardiac Surgery Patients With High-Flow Nasal Cannula

Vanderbilt University Medical Center1 site in 1 country3,568 target enrollmentStarted: November 1, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
3,568
Locations
1
Primary Endpoint
Reintubation within 48 hours of extubation

Study Overview

Brief Summary

The iCAN trial is a pragmatic randomized controlled trial that aims to test the hypothesis that HFNC versus usual care oxygenation strategies applied immediately after initial extubation after cardiac surgery decreases the all-cause 48-hour reintubation rate (extubation failure within 48 hours of initial extubation).

Detailed Description

HFNC may be employed as a strategy to facilitate early extubation and prevent reintubation of patients following cardiac surgery. HFNC is routinely employed by providers in the cardiovascular intensive care unit along with other therapies, including: bi-level positive airway pressure, non-rebreather masks, among others. Currently, no high-quality clinical data exist to demonstrate that HFNC may decrease the risk of reintubation in this critically-ill adult population.

This prospective, randomized, pragmatic clinical trial will compare HFNC to provider choice of usual care in these high-risk patients.

Randomization will occur at the time that the patient is deemed ready for extubation by the attending physician in the cardiovascular intensive care unit. Through randomization, patients will be assigned one of two physician order sets in the electronic medical record system: standard order set with or without recommendation for the use of HFNC. Reintubation and outcome data will be collected until patient discharge.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age ≥18 years
  • Undergoing cardiac surgery, defined as a documented surgical service of "cardiac surgery" in the electronic health record, performed in the main operating rooms at Vanderbilt University Medical Center
  • Admitted to the cardiovascular intensive care unit postoperatively with an endotracheal tube in place and mechanically ventilated
  • Surgery duration (documented time between "Anesthesia start" and "Anesthesia stop" in the EHR) of at least 180 minutes
  • Received an order to be extubated by a treating provider o Patients who meet all other criteria but do not receive an order to extubate will be randomized but not enrolled

Exclusion Criteria

  • Patient does not meet inclusion criteria

Arms & Interventions

High Flow Nasal Canula Oxygen Therapy

Experimental

Participants will be assigned post extubation physician order set which recommends the administration of oxygen therapy via HFNC. HFNC is a heated and humidified system that allows prescribed fraction of inspired oxygen (FIO2) levels to be delivered at very high flow rates.

Intervention: Recommendation for high flow nasal cannula oxygen therapy order set (Other)

Provider Choice Standard Care

Active Comparator

Participants be assigned standard provider choice of standard care therapy physician order set.

Intervention: Provider choice standard care order set (Other)

Outcomes

Primary Outcomes

Reintubation within 48 hours of extubation

Time Frame: 48 hours

Reintubation within 48 hours of initial extubation after cardiac surgery

Secondary Outcomes

  • Reintubation within 72 hours of extubation(72 hours)
  • Reintubation after cardiac surgery(hospital discharge (usually 14 days))
  • All cause mortality(30 days post surgery)
  • Hospital length of stay(8 days)
  • Reintubation within 72 hours of extubation(72 hours)
  • Reintubation after cardiac surgery(hospital discharge (usually 14 days))
  • All cause mortality(30 days post surgery)
  • Hospital length of stay(8 days)
  • In-hospital mortality(Until hospital discharge, which usually occurs in approximately 8 days in the majority of patients)
  • Adjusted reintubation rate(48 hours)
  • Intensive Care Unit length of stay(3 days)
  • Ventilator-free days(1 day)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Robert Freundlich

Assistant Professor of Anesthesiology and Biomedical Informatics

Vanderbilt University Medical Center

Study Sites (1)

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