1 of 3

This document is intended to be educational in nature and is not a substitute for clinical decision making based on the medical condition presented.

This content is a collaborative effort by representatives of multiple institutions, and this document and the information herein are intended and designed for educational purposes only. You should not rely on this information to replace professional medical advice, diagnosis, and/or treatment, nor should this information ever be used as a substitute for either manufacturers’ instructions and guidance or clinical decision-making based on the medical condition presented. It is the responsibility of the user to ensure that all information contained herein is current and accurate, and the creators and hosts of this content make no claims or warranties as to the currency, accuracy, or suitability of this information for any purpose. Any reference to specific equipment, pharmaceuticals, or other medical devices in this document is not meant as an endorsement of such items, and you should consult manufacturers’ documentation prior using any such items that may be referenced here. The use of any information in this document is undertaken solely at your own risk, and the creators and hosts of this content shall not be liable for any damages, losses, or other injury caused by the use of any information in this document, nor for any reliance on the accuracy or reliability of such information.

Disclaimer

This is a living document, created by created by nurses, physicians, respiratory therapists and other healthcare providers from multiple institutions and multiple countries via the OpenCriticalCare.org project.

The goal of this document is to provide tools that can be locally modified to help healthcare providers learning to provide respiratory care for hospitalized patients.

Please copy or download this file and then modify the document to fit your needs, the most current data and local resources. This can be done by going to the “File Menu” at the top left of this window and selecting “File” → “Download” then select the format you prefer. Alternatively you can select “File” → “Make a Copy” then use a copy in Google Slides to make your own edits.

To Print: select “Print” from the file menu at the top left. You may need to scale the size to fit your preferred paper size.

Please check back regularly for updates and send any questions or comments to us here.

Adult Respiratory Care Protocols v1.0

With collaborators & support from multiple institutions, including:

Last updated March 10, 2020

Table of Contents

How to Use This Document

Table of Contents

2 of 3

Strategies for SBT

Adults:

  • Pressure support (PS): Δ 5-7 cmH2O over PEEP 5-8 cmH2O
  • CPAP: 5-8 cm H2O
  • T-piece

Pediatrics:

  • If ETT 3-3.5 mm: PS Δ 10 cmH2O over PEEP 5 cmH2O
  • If ETT 4-4.5 mm: PS Δ 8 cmH2O over PEEP 5 cmH2O
  • If ETT > or = 5 mm: PS Δ 5 cmH2O over PEEP 5 cmH2O
  • T-piece alone is not recommended

Perform SBT

  • Choose appropriate strategy based on patient and ETT size (see box ‘strategies for SBT’)
  • Monitor for signs of failure and intolerance (see box ‘SBT failure’)

SBT Failure

Any sign of respiratory failure:

  • Sustained tachypnea (> 5 min)
  • Hypoventilation or apnea
  • SpO2 < ~90% (except for patients with cyanotic heart lesions)

> Two signs of intolerance:

  • Agitation or diaphoresis
  • Accessory muscle use
  • Hemodynamic instability
  • Tidal volume < 4 cc/kg
  • Significant (> 20%) increase in HR
  • Increased or labile ICP

Sedation Interruption Failure

  • Anxiety, agitation or pain
  • Significant tachypnea
  • SpO2 ~< 90%
  • Respiratory distress
  • Hemodynamic instability

MV = minute ventilation

Sedation Interruption Safety Screen*

  • No active seizures
  • No active withdrawal (e.g. alcohol)
  • No neuromuscular blockade
  • No myocardial ischemia
  • No elevated ICP

Sedation Interruption Safety Screen*

Consider daily if FiO2 < ~50

Discontinue Sedation

or decrease for > 30 min.

Analgesia should be titrated to patient needs.

SBT Readiness Screen

Resume sedatives at ½ dose

  • Treat cause
  • Consider cuff leak test if concern for airway edema (Figure 11.2)
  • Consider tracheostomy

Extubate

Pass

Fail

Fail

Fail

Every 24 hours

Airway ok

Airway not ok

Pass

Pass

Assess Airway Protection

  • Adequate cough and gag
  • No significant secretions or suctioning requirement (<q2-4h)
  • Adequate mental status
  • No risk factors for airway edema (See Figure 11.2)

Fail

Resume assisted ventilation

  • Address reversible processes
  • Avoid muscle fatigue
  • Avoid asynchrony

Repeat** SBT Screen

(Every 24h)

Pass SBT

* Sedation interruptions (i.e. spontaneous awakening trials) may not be suitable or safe for pediatric patients

** Consider repeating SAT and SBT if failure due to easily reversible cause (e.g. oversedation, pain)

*Oxygenation Index (OI) = Fi02 x MAP / Pa02

SBT Readiness Screen

  • Adequate spontaneous breathing effort
  • Disease trajectory: Resolving or stable
  • Oxygenation: SpO2 > 90% & stable FiO2 < 50% & PEEP < 8 cmH20
  • Pediatrics: Oxygenation index*** < 6
  • Ventilation: pH > 7.3 & no significant ↑MV
  • Hemodynamics: No significant vasopressor requirement or myocardial ischemia
  • No elevated intracranial pressure

Spontaneous breathing and awakening trials protocol

3 of 3

Difference between expired TV before and

after cuff deflation is >110 mL

Difference between expired TV before and

after cuff deflation is <110 mL

Cuff leak test necessity screen

Patient meets criteria for SBT* and >1 of the following:

  • Traumatic intubation
  • Intubation more than 6 days
  • Large endotracheal tube (ETT)
  • Female sex
  • Multiple recent intubations
  • Other clinical concern for airway swelling (e.g. prone positioning or anasarca)

Prepare patient for cuff leak test

  • Ensure patient is synchronous with ventilator and adequately sedated (a transient RASS goal of -4 should be considered)
  • Set ventilator to volume control mode with tidal volume (TV) 8-10 ml / kg predicted body weight
  • Suction oropharynx to prevent oral secretions from passing into the trachea with cuff deflation

Perform the cuff leak test

  • Observe and record the measured expired TV
  • Deflate the ETT cuff by attaching syringe to the pilot balloon and pulling back on syringe until the balloon is flat.
  • Observe the measured expired TV on the vent over six breaths

Cuff leak test has been FAILED

  • Address potential causes of failure
  • Consider dexamethasone 5-10 mg IV q6-12h x 2 doses and then reassess for extubation in 12-24h
  • Elevate head of bed

Cuff leak test has been PASSED

  • Proceed to extubation if all other parameters in place as in 11.1

*SBT - Spontaneous breathing trial criteria - See Figure 11.1

Cuff leak protocol