What should the Positive End-Expiratory Pressure (PEEP) be set at for a successful Spontaneous Breathing Trial (SBT)?

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Last updated: December 23, 2025View editorial policy

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PEEP Settings for Spontaneous Breathing Trials

For a successful spontaneous breathing trial (SBT), PEEP should be set at 5 cm H₂O with pressure support of 5-8 cm H₂O, rather than using zero PEEP or T-piece alone. 1

Guideline-Based Recommendations

The American College of Chest Physicians/American Thoracic Society 2017 guidelines provide a conditional recommendation (moderate-quality evidence) that initial SBTs should be conducted with inspiratory pressure augmentation of 5-8 cm H₂O rather than T-piece or CPAP alone. 1 This approach:

  • Increases SBT success rates to 84.6% versus 76.7% with T-piece 1, 2
  • Improves extubation success to 75.4% versus 68.9% with T-piece 1, 2
  • Shows a trend toward lower ICU mortality (8.6% vs 11.6%) 3

Specific PEEP Parameters by Clinical Context

Standard-Risk Patients

  • Use PEEP of 5 cm H₂O with pressure support 5-8 cm H₂O 1, 2
  • Duration: 30 minutes is sufficient for most patients 3, 2
  • This combination reduces work of breathing while still adequately assessing extubation readiness 4

High-Risk Patients

  • Consider CPAP without pressure support augmentation (PEEP alone) for more stringent assessment 3
  • Duration: 60-120 minutes recommended 3, 2
  • High-risk features include: prolonged ventilation >14 days, chronic lung disease, myocardial dysfunction, neurologic impairment, or previous extubation failure 3, 5

Alternative Approach for Difficult-to-Wean Patients

  • Initial trial: Zero PEEP/zero pressure support (ZEEP) 6
  • If ZEEP fails: Immediately perform 5/5 trial (5 cm H₂O PEEP + 5 cm H₂O pressure support) 6
  • This algorithmic approach achieved 96.2% successful liberation (82.4% with ZEEP alone, plus 13.8% who passed subsequent 5/5 trial) 6

Physiological Rationale

PEEP during SBT provides critical physiological support that more accurately reflects post-extubation conditions:

  • Reduces inspiratory muscle effort significantly - esophageal pressure-time product was 128-148 cmH₂O·s/min with pressure support versus 292 cmH₂O·s/min with T-piece 4
  • Prevents left ventricular failure - 11 of 14 difficult-to-wean patients developed LV failure during T-piece but not during pressure-supported trials 4
  • Maintains lower pulmonary artery occlusion pressure - 17 mmHg with PSV-PEEP versus 21 mmHg with T-piece 4
  • Improves breathing pattern - respiratory rate 19 breaths/min with PSV-PEEP versus 27 breaths/min with T-piece 4

Common Pitfalls to Avoid

Do not use T-piece alone as the initial SBT method - this may be overly stringent and delay extubation in patients who could successfully extubate, as T-piece trials underestimate the support provided by maintaining airway patency after extubation 1, 3

Do not assume pressure-supported SBTs guarantee extubation success - approximately 10% of patients who pass an SBT still fail extubation within 48 hours, requiring assessment of upper airway patency, bulbar function, sputum load, and cough effectiveness 3, 5

Avoid same-day repeat SBTs after failure - failed SBTs indicate respiratory muscle fatigue requiring time to resolve before another attempt 3

Post-Extubation Considerations

For high-risk patients who pass the SBT, use prophylactic noninvasive ventilation immediately after extubation rather than standard oxygen therapy (strong recommendation, moderate-quality evidence) 1, 5, 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Spontaneous Breathing Trials in Mechanically Ventilated Patients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

T-Piece Spontaneous Breathing Trial Duration and Criteria for Extubation

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Spontaneous Breathing Trials in Mechanical Ventilation

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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