Awake ECMO Management
Awake ECMO is a viable strategy for carefully selected patients with severe respiratory failure, allowing spontaneous breathing and early mobilization while on venovenous (VV) ECMO support, though it requires high-volume centers with multidisciplinary expertise and should only be considered when conventional therapies have failed. 1
Patient Selection for Awake ECMO
VV ECMO is indicated for isolated severe respiratory failure when cardiac function remains adequate, specifically when:
- PaO₂/FiO₂ < 80 mmHg for at least 3 hours despite optimal ventilation 1
- PaO₂/FiO₂ < 70 for ≥3 hours or < 100 for ≥6 hours despite optimization of conventional treatments 1
- Plateau pressure > 28 cmH₂O for ≥6 hours despite lung-protective ventilation strategies 1
- Evidence of right ventricular overload with pulmonary artery systolic pressure > 40 mmHg and acute cor pulmonale on echocardiography 1
Critical exclusion criteria include:
- Contraindications to anticoagulation 1
- Prolonged mechanical ventilation (>9.6 days) before ECMO consideration, which is associated with worse outcomes 1
- Cardiac dysfunction requiring hemodynamic support (these patients require VA ECMO instead) 1
Institutional Requirements
ECMO should only be performed at centers meeting strict volume and expertise thresholds:
- Minimum annual volume of 20-25 ECMO cases per year, with significantly better outcomes at higher-volume centers 1, 2
- 24/7 availability of multidisciplinary ECMO team including physicians, nurses, perfusionists, and ECMO specialists 1
- Nurse-to-patient ratio of 1:1 to 1:2 maximum 1, 2
- Quality assurance review procedures and robust expertise in ventilatory management of severe acute respiratory failure 1
- Catchment area of at least 2-3 million population to maintain adequate volume 1
Bedside Management During Awake ECMO
Respiratory Management:
- Avoid arterial hypoxemia (PaO₂ < 70 mmHg) 3
- Avoid severe arterial hyperoxia (PaO₂ > 300 mmHg), especially where reperfusion injury risk is high 3
- For patients with hypercapnia (PaCO₂ > 45 mmHg), avoid rapid change in PaCO₂ within the first 24 hours of ECMO support 3
- Serial arterial blood gas sampling in the first 24 hours of ECMO support is recommended 3
Hemodynamic Targets:
- Maintain mean arterial pressure > 70 mmHg, though individualized BP goals based on patient comorbidities are recommended 3
- Target initial ECMO flow of 3-4 L/min immediately post-cannulation, gradually increasing as tolerated 2
- Maintain arteriovenous oxygen difference between 3-5 cc O₂/100ml blood as the most reliable flow parameter 2
Temperature Management:
- Continuous monitoring of core temperature and active prevention of fever (> 37.7 °C) are recommended 3
- Hypothermia in VV ECMO is not recommended 3
Neurological Monitoring and Complication Management
Acute brain injury (ABI) occurs in 10% of VV-ECMO patients, requiring protocolized monitoring: 2
For suspected stroke:
- Obtain non-contrast head CT immediately to rule out intracranial hemorrhage 3, 2
- Do NOT administer tPA for acute ischemic stroke in ECMO patients due to prohibitively high bleeding risk 3, 2
- Proceed with mechanical thrombectomy for acute large vessel occlusion after CT angiogram confirmation 3, 2
For intracranial hemorrhage:
- Discontinue systemic anticoagulation temporarily 3
- VV ECMO may allow a longer anticoagulation-free period compared to VA ECMO 3
- External ventricular drain insertion is high-risk but may be considered in selected patients at risk of imminent death from intraventricular hemorrhage and hydrocephalus 3
Anticoagulation Balance
Anticoagulation is required for cannulation and circuit/oxygenator clot prevention but must be carefully balanced:
- Recent data shows 42% of VV-ECMO patients experience thrombotic events, 37% experience bleeding events, and 21% experience both 2
- Almost all ECMO patients develop acquired von Willebrand syndrome (AVWS) within hours of device implantation, contributing to bleeding complications 1
Mobilization and Rehabilitation
The awake ECMO strategy specifically allows for:
- Early mobilization while on ECMO support 4
- Spontaneous breathing trials to assess lung recovery 4
- Physical therapy, occupational therapy, and speech therapy as tolerated 2
Weaning Assessment
The possibility of weaning from ECMO should be fully assessed by a multidisciplinary team:
- Futility should not be determined solely by duration of ECMO 4
- Use of prolonged ECMO for lung recovery may be worthwhile 4
- Daily assessment of lung function improvement through imaging and gas exchange parameters 4
Critical Pitfalls to Avoid
Common errors that compromise outcomes:
- Delaying ECMO initiation beyond 7 days of respiratory failure onset reduces optimal outcomes 1
- Failing to optimize conventional treatments (low-volume, low-pressure, lung-protective ventilation or prone positioning) before considering ECMO 1
- Inadequate neurological monitoring leading to delayed detection of acute brain injury 2
- Over-aggressive anticoagulation without considering individual bleeding risk 2