Criteria for Initiating a Safe Weaning Trial
Before attempting any spontaneous breathing trial (SBT), the patient must meet all readiness criteria: resolution or marked improvement of the primary respiratory condition, hemodynamic stability without vasopressor support, adequate oxygenation (PaO₂/FiO₂ ≥200, FiO₂ ≤40%, PEEP ≤5 cmH₂O), patient arousable and able to follow simple commands, RSBI ≤105 breaths/min/L, intact cough on suctioning with minimal secretions, and no new serious conditions or planned procedures in the next 12-24 hours. 1, 2, 3
Daily Readiness Screening Checklist
Assess every mechanically ventilated patient daily for the following mandatory criteria:
1. Resolution of Primary Respiratory Failure
- The underlying condition that necessitated intubation must have resolved or shown significant improvement 1, 2
- Examples: pneumonia improving on chest X-ray, ARDS resolving, pulmonary edema controlled
2. Hemodynamic Stability
- No vasopressor support or only minimal doses (e.g., low-dose norepinephrine for blood pressure support, not for shock) 1, 2, 3
- No active myocardial ischemia 1
- Systolic blood pressure stable between 90-180 mmHg without trending 1
- Heart rate <140 bpm without sustained increases >20% 1
3. Adequate Oxygenation Parameters
- PaO₂/FiO₂ ratio ≥200 1, 2, 3
- FiO₂ ≤40% (0.40) 1, 2, 3
- PEEP ≤5 cmH₂O 1, 2, 3
- Do NOT attempt weaning if PaO₂ <55 mmHg on FiO₂ ≥40% 1
4. Ventilatory Requirements
5. Neurological Status
- Patient must be arousable and able to follow simple commands (open eyes, squeeze hand) 1, 2, 3
- Absence of heavy sedation 1, 2
- Light-target sedation that keeps patients awake and cooperative shortens ventilator duration 1
6. Airway Protection
- Intact cough on suctioning 1, 2, 3
- Minimal secretions or effective clearance mechanism 1, 2
- Intact airway reflexes 3
7. Absence of New Complications
- No new potentially serious conditions in the past 24 hours 1, 3
- No planned procedures in the next 12-24 hours 1
Performing the Spontaneous Breathing Trial
Once all readiness criteria are met, proceed with the SBT using the following protocol:
SBT Technique (Standard-Risk Patients)
Use pressure support ventilation (PSV) of 5-8 cmH₂O with PEEP 5 cmH₂O rather than T-piece 1, 2, 3
- This method achieves 84.6% SBT success vs. 76.7% with T-piece 1, 2
- Extubation success increases to 75.4% vs. 68.9% with T-piece 1, 2
- Trend toward lower ICU mortality (8.6% vs. 11.6%) 1
SBT Settings
- Pressure support: 5-8 cmH₂O 1, 2, 3
- PEEP: 5 cmH₂O 1, 2, 3
- FiO₂: ≤40% 1, 2
- Flow trigger: 1-3 L/min (or pressure trigger -0.5 to -2 cmH₂O if flow unavailable) 1
- Expiratory cycling: 25% of peak flow (increase to 40% in COPD) 1
SBT Duration
- Standard-risk patients: 30 minutes 1, 2, 3
- High-risk patients: 60-120 minutes 1, 2, 3
- Most SBT failures occur within the first 30 minutes 1, 2
SBT Failure Criteria—Terminate Immediately If Any Occur
Monitor continuously and stop the trial immediately if the patient develops:
Respiratory Distress
- Respiratory rate >35 breaths/min or increasing trend 1, 2, 3
- Use of accessory muscles or abdominal paradox 1
- Increased anxiety or diaphoresis 1, 2, 3
Gas Exchange Deterioration
Hemodynamic Instability
- Heart rate >140 bpm or sustained increase >20% 1, 2
- Systolic blood pressure >180 mmHg or <90 mmHg 1, 2
Altered Mental Status
High-Risk Patient Identification
Identify patients at high risk for extubation failure before the SBT to plan prophylactic interventions:
High-Risk Criteria (Any One Present)
- Age >65 years with multiple comorbidities 1, 2
- Cardiac failure as primary cause of respiratory failure 1, 2
- Failure of more than one prior SBT 1, 2
- PaCO₂ >45 mmHg after extubation or during SBT 1, 2
- ≥1 comorbid condition (COPD, CHF) 1, 2
- Weak cough or excessive secretions 1, 2
- APACHE II score >12 on day of extubation 1
- Prolonged mechanical ventilation >14 days 1, 3
High-Risk SBT Modification
For high-risk patients, consider T-piece trial (more specific but less sensitive) rather than pressure support 1
Post-SBT Management
If SBT Passes (Standard-Risk)
- Extubate directly to supplemental oxygen via face mask or nasal cannula 1, 2
- Target SpO₂ 88-92% (particularly in chronic hypercapnia) 1, 2
- Monitor continuously for first 24 hours 1
If SBT Passes (High-Risk)
Extubate directly to prophylactic noninvasive ventilation (NIV) within 1 hour 1, 2, 3
- Initial settings: IPAP 10-12 cmH₂O, EPAP 5-10 cmH₂O 1, 2
- This reduces re-intubation risk (RR 0.61) 1, 2, 3
- Reduces mortality (RR 0.54) 1, 2, 3
- Shortens ICU stay by ~2.5 days 1, 2
Cuff-Leak Test (High-Risk for Laryngeal Edema)
Perform in patients with:
- Female sex, nasal intubation, difficult/traumatic intubation, large ETT, high cuff pressures, or intubation >7 days 1
- Positive test: leak volume ≥110 mL or ≥10% of tidal volume 1
- If negative, give systemic corticosteroids (1 mg/kg prednisolone) at least 4-6 hours before extubation 1
Common Pitfalls to Avoid
- Do NOT delay extubation in patients who pass their first SBT, are <65 years, have normal PaCO₂, and lack significant comorbidities 1
- Do NOT use SIMV for weaning—it is inferior to pressure support and T-piece 1, 2
- Do NOT apply pressure support >8 cmH₂O during the final SBT—this masks inadequate respiratory muscle strength 1
- Do NOT attempt weaning in patients still requiring vasopressors or with unresolved primary pathology 1
- An extubation failure rate of 5-10% is acceptable—approximately 10% of patients who pass an SBT will still fail extubation 1, 2