II. Pathophysiology
- Ventilated for less than 2 weeks
- Respiratory Muscles do not decondition significantly
- Exceptions
- Comorbid condition or
- Severe increased VO2 with negative nitrogen balance
- Majority of patients do not need Ventilator Weaning
- Either need the Ventilator or they do not
III. Indications: Weaning
- Prolonged debilitated state, deconditioning or weakness
- Chronic Obstructive Pulmonary Disease
- Severe Congestive Heart Failure
- Catabolic State
- Results from high dose Corticosteroids
- Results in weak chest Muscles
IV. Risk Factors: Reintubation after Extubation
- Age >65 years
- APACHE Score (v2) >12
- BMI >30 kg/m2
- Inadequate clearance of secretions
- Difficult or prolonged Ventilator Weaning
- Intubation indication for CHF or COPD
- Prolonged Mechanical Ventilation
V. Management: Preparation for weaning - Nutritional Status
- Early nutritionist Consultation
- Low Carbohydrate Diet if increased VCo2
- Avoid negative nitrogen balance
- Use a working GI Tract to provide early nutrition
- Place Dobbhoff NG tube (check placement with XRay)
- Select a supplement (e.g. FS Pulmocare)
- Measure q4 hour Residual Volumes
- Consider prokinetic agent for >50 cc residuals
- Metoclopramide (Reglan) 10 mg PO qid
- Erythromycin 250 to 500 mg PO qid
- Consider prokinetic agent for >50 cc residuals
VI. Management: Preparation for weaning - Pulmonary Status
- Maximize bronchodilation if bronchospasm
- Consider Inhaled Corticosteroids over systemic
- Avoid Respiratory Acidosis
- Adjust pCO2 to premorbid level
VII. Management: Preparation for weaning - Psychosocial Status
- Alleviate anxiety
- Reassure of support
- Encourage optimism. and discourage discouragement
- Try not to convey frustration
VIII. Management: Preparation for weaning - Cardiac Status
-
Coronary Artery Disease
- Consider Anti-Anginal medications (Nitroglycerin)
- Check Electrocardiogram
- Baseline
- After a failed weaning trial
-
Congestive Heart Failure
- Maximize volume status
- Reduce Afterload
- Use inotropic agents as needed (Dopamine, Dobutamine)
IX. Management: Preparation for Weaning - Sedation
- Hold benodiazepines (use only prn)
- Decrease Propofol and Fentanyl rates every 4 hours
- Consider Dexmedetomidine (Precedex)
X. Management: Spontaneous Breathing Trial (SBT)
- Assess readiness for Extubation on a daily basis
- Daily interruption of continuous sedation (to RASS of 1)
- "Wake up and breath protocol" for trial of Ventilator Weaning
- Khan (2014) Crit Care Med 42(12):e791-5 +PMID: 25402299 [PubMed]
- Indications: Spontaneous Breathing Trial (SBT) Readiness
- Are there unstable confounding factors that contraindicate a trial?
- Unstable cardiovascular status?
- Unstable medical comorbidity?
- Has the primary indication for Endotracheal Intubation and ventilation resolved?
- Excessive airway secretions?
- Does patient awaken sufficiently?
- Cooperative?
- Able to follow commands?
- Able to initiate breaths?
- Does patient protect their airway?
- Adequate Gag Reflex?
- Good cough?
- Is oxygenation adequate?
- Is Ventilation adequate based on Rapid Shallow Breathing Index (RSBI)
- RSBI calculated on CPAP 5 cmH2O and NO pressure support for 3 minutes
- RSBI = RR/Vt
- Where RR = Respiratory Rate
- Where Vt = Tidal Volume (in Liters)
- RSBI Interpretation
- RSBI <105 suggests adequate ventilation
- Are there unstable confounding factors that contraindicate a trial?
- Technique: Spontaneous Breathing Trial (SBT)
- Perform for 30-60 minutes (with ABG obtained at the end of trial)
- T Piece
- Pressure Support of 6-8 cmH2O
- PEEP 5 cmH2O
- Assessment: Reassuring findings on SBT
- PaO2 >60 mmHg (or O2Sat>90% on FIO2 <0.4)
- PaCO2 <50 mmHg (and increased PaCO2 <10 mmHg during SBT)
- pH decreases <0.10 during SBT
- Respiratory Rate <35
- Heart Rate <120-140 (or increases <20% above baseline Heart Rate during SBT)
- Systolic Blood Pressure 90-180 mmHg (and >20% change from baseline during SBT)
- No significant increased work of breathing during SBT
- Tidal Volume (Vt) >335 ml (or >4 ml/kg Predicted Body Weight)
- Perform for 30-60 minutes (with ABG obtained at the end of trial)
- Failed Spontaneous Breathing Trial approach (15% of cases)
- Attempt to wean to pressure support
- Target comfortable Ventilatory support that does not generate respiratory Fatigue
- Gradually wean Ventilator rate by 2 bpm
- Gradually wean pressure support to 6-8 cmH2O
- Continue daily Spontaneous Breathing Trials
- Consider weaning to BiPAP in COPD exacerbations
- Precautions
- Reintubation is required in 15% of patients even after successful SBT prior to Extubation
- References
- (2025) Introduction of Mechanical Ventilation, Hospital Procedures Course
- McConville (2012) N Engl J Med 367(23):2233-9 +PMID: 23215559 [PubMed]
XI. Management: Concept of Respiratory Muscle training
- Methods
- Pressure Support (favored by some pulmonologists)
- T-Tube trials
- CPAP
- SIMV is no longer recommended for weaning
- Principles
- Give respiratory Muscles a nightly rest
- "Marathon runners do not train around the clock"
- Full Ventilatory support at night
- Maximize sleep at night
- Use Daily standard screening assessment tool
- Completed by Respiratory Therapist
- Reduces intubation time (4.5 versus 6 days)
- Fewer complications (20% versus 41%)
- Ely (1996) N Engl J Med 335:1864-9 [PubMed]
- Give respiratory Muscles a nightly rest
XII. Management: Extubation
- Extubation Criteria
- Are weaning parameters in an acceptable range?
- Respiratory Rate <25 breaths per minute
- Blood Pressure
- Pulse
- FIO2 <0.4 to 0.5
- PEEP <10 cmH2O
- Ventilator Parameters
- Minute Ventilation <10 L/min
- Tidal Volume > 5 ml/kg
- Vital Capacity >10 ml/kg
- Are secretions controlled?
- Can the patient protect their airway?
- Is cough reflex adequate?
- Is the patient alert?
- Are weaning parameters in an acceptable range?
- Extubation Technique
- Patient is placed in reverse Trendelenburg
- Head up
- Legs up
- Monitoring prior to Extubation
- Patient is placed in reverse Trendelenburg
- Consider Prophylactic Corticosteroids for prevention of Post-Extubation Laryngeal Edema (PLE)
- Indications: High Risk for Post-Extubation Laryngeal Edema (PLE)
- Female Gender
- Prolonged Mechanical Ventilation
- Endotracheal Tube (ETT) size >8.0
- High ETT cuff pressure >25 cmH2O
- Failed cuff leak test (cuff leak volume <110 ml or <20% of Tidal Volume)
- Prophylaxis: Dexamethasone Protocol for prophylaxis
- Dexamethasone 0.1 mg/kg (up to 10 mg maximum) IV every 6 hours for 4 doses
- Start at least 4 hours before Extubation
- Management or Post-Extubation Laryngeal Edema (e.g. post-intubation Stridor)
- Nebulized Epinephrine immediately (may repeat every 2 hours)
- Nebulized Budesonide
- Start Dexamethasone protocol if not already initiated
- PLE Prophylaxis Efficacy
- Prophylaxis decreases Post-Extubation Laryngeal Edema (PLE) and reintubation by 50-60%
- References
- Indications: High Risk for Post-Extubation Laryngeal Edema (PLE)
- Post Extubation support
- Consider High Flow Nasal Cannula (or BiPAP) started immediately after Extubation
- Patients transitioned off Ventilator to High Flow Nasal Cannula have lower rates of reintubation
- Start at highest tolerable flow rates 50-60 L/min for the first day post-Extubation
- Pressure Support from 0800 - 2230
- PEEP: 5,
- Pressure support: begin at 15 and wean
- Weaning parameters
- Respiratory Rate <30
- Tidal Volume > 250 cc
- Patient comfortable
- Arterial Blood Gas when Pressure Support 3 for 1h
- AC from 2230-0800
- PEEP: 5
- AC: 12
- Maximize sleep and respiratory rest as above
- Intermittent Rest throughout the day as needed
- PEEP: 5
- AC: 12
- Consider High Flow Nasal Cannula (or BiPAP) started immediately after Extubation
XIII. Reference
- (2025) Introduction of Mechanical Ventilation, Hospital Procedures Course
- Davies (1986) Acute Respiratory Failure, Cyberlog
- Mickman (1995) Lecture, Fairview-Riverside, Minneapolis