How do I assess readiness for weaning from mechanical ventilation?

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Last updated: February 8, 2026View editorial policy

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Assessing Readiness for Weaning from Mechanical Ventilation

Use a two-step systematic approach: first perform daily readiness screening, then conduct a spontaneous breathing trial (SBT) with 5-8 cm H₂O pressure support for 30 minutes in standard-risk patients. 1, 2, 3

Step 1: Daily Readiness Screening

Before attempting any weaning trial, verify that all of the following criteria are met:

  • Resolution or significant improvement of the primary condition requiring mechanical ventilation 1, 2
  • Hemodynamic stability without vasopressor support 1, 2
  • Adequate oxygenation: PaO₂/FiO₂ ratio ≥ 200, FiO₂ < 0.50 (ideally ≤ 0.40), PEEP ≤ 5 cm H₂O 1, 2, 3
  • Patient arousable with adequate mental status and absence of heavy sedation 1, 2
  • Intact airway reflexes with effective cough on suctioning and minimal secretions 1, 2
  • Low ventilatory requirements: Rapid Shallow Breathing Index (RSBI or fR/VT ratio) ≤ 105 breaths/min/L 4, 1
  • No new potentially serious conditions 2, 3

Critical Pitfall to Avoid

Do not attempt weaning when PaO₂ < 55 mmHg on FiO₂ ≥ 0.40, as this markedly increases the probability of weaning failure. 1 Similarly, avoid premature weaning in patients still requiring vasopressors or with unresolved primary pathology. 1

Step 2: Measuring the Rapid Shallow Breathing Index (RSBI)

The RSBI (frequency-to-tidal volume ratio, fR/VT) is the most validated predictor of weaning success:

  • Measure after 30-60 minutes of spontaneous breathing, not during the first minute when respiratory drive may still be suppressed 4, 1
  • Use a handheld spirometer attached to the endotracheal tube while the patient breathes spontaneously for 1 minute 4
  • RSBI < 80 breaths/min/L: 7.53 times more likely to predict successful weaning (strong positive predictor) 4
  • RSBI < 105 breaths/min/L: acceptable threshold for proceeding with SBT 4, 1
  • RSBI > 100 breaths/min/L: only 0.04 as likely to occur in patients who will successfully wean (strong negative predictor) 4

The RSBI has superior discriminatory power (area under ROC curve 0.89) compared to traditional indices like minute ventilation (0.40), PaO₂/PAO₂ ratio (0.48), or maximal inspiratory pressure (0.61). 4

Step 3: Conducting the Spontaneous Breathing Trial

Use pressure support ventilation (5-8 cm H₂O) rather than T-piece for the initial SBT, as this achieves significantly higher success rates (84.6% vs 76.7%). 1, 2, 3

SBT Parameters:

  • PEEP: ≤ 5 cm H₂O 1, 3
  • FiO₂: ≤ 0.40 1
  • Duration: 30 minutes for standard-risk patients; 60-120 minutes for high-risk patients 1, 2, 3
  • Most SBT failures occur within the first 30 minutes 1, 2

SBT Failure Criteria - Terminate Immediately if Any Occur:

  • Respiratory distress: Respiratory rate > 35 breaths/min or increasing trend, use of accessory muscles, or abdominal paradox 1, 3
  • Gas exchange deterioration: SpO₂ < 90% 1
  • Hemodynamic instability: Heart rate > 140 bpm or sustained increase > 20%, systolic blood pressure > 180 mmHg or < 90 mmHg 1, 3
  • Altered mental status: Increased anxiety, agitation, or diaphoresis 1, 3

Do not repeat SBTs on the same day after failure, as this leads to respiratory muscle fatigue and worsening outcomes. 3

Step 4: Classification Based on Weaning Difficulty

After the initial SBT, patients fall into three categories:

  • Simple weaning (60-70% of patients): Successfully pass the first SBT and are extubated on the first attempt 1, 5
  • Difficult weaning (15-25% of patients): Require up to three SBTs or up to 7 days from the first SBT to achieve successful weaning 1, 6, 5
  • Prolonged weaning (5-15% of patients): Require more than three SBTs or > 7 days of weaning after the first SBT 1, 6, 5

Implementation Strategy

Use a protocol-driven weaning approach executed by respiratory therapists or nurses, as this reduces mechanical ventilation duration by approximately 25 hours and shortens ICU length of stay by about 1 day compared to physician-judgment-only approaches. 1, 3 The Surviving Sepsis Campaign provides a strong recommendation (high quality evidence) for using weaning protocols with SBTs in mechanically ventilated patients with sepsis. 1, 3

Special Considerations for High-Risk Patients

For patients at high risk of extubation failure (prolonged mechanical ventilation > 14 days, chronic lung disease/COPD, myocardial dysfunction, previously failed extubation), consider:

  • T-piece trials may be more specific (though less sensitive) in identifying true readiness for extubation 1
  • Prophylactic noninvasive ventilation (NIV) immediately after extubation decreases mortality (RR 0.54,95% CI 0.41-0.70) and reduces weaning failure (RR 0.61,95% CI 0.48-0.79) 1, 2, 3

Common Pitfall in Difficult/Prolonged Weaning

Respiratory muscle weakness, including diaphragmatic dysfunction, is a major contributing factor in patients experiencing difficult or prolonged weaning. 1, 5, 7 Early mobilization, well-controlled sedation, and early use of spontaneous breathing may help reduce muscle weakness and hasten the weaning process. 5

References

Guideline

Weaning from Mechanical Ventilation

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Ventilator Sedation and Weaning Criteria

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Weaning Mode of Ventilation

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 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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