Here is a comprehensive overview of ECMO based on authoritative medical textbooks.
Extracorporeal Membrane Oxygenation (ECMO)
What Is ECMO?
ECMO (also called extracorporeal life support, ECLS) is a form of prolonged cardiopulmonary bypass that provides temporary support to the heart and/or lungs in patients with severe, refractory failure. The concept traces back to Gibbon's cardiopulmonary bypass circuit, first used successfully in 1953. The first successful use for trauma-induced ARDS was reported in 1972.
Basic Circuit Components
Figure: Basic ECMO circuit - Fishman's Pulmonary Diseases and Disorders, p. 2641
An ECMO circuit consists of four main components:
- Inflow (drainage) cannula - drains venous blood from the patient
- Centrifugal pump - magnetically levitated disc that creates a vortex; preload-dependent and afterload-sensitive
- Membrane oxygenator - thousands of hollow-bore microtubules through which oxygen flows; blood oxygenation occurs across a 2 m² surface (vs. 91-118 m² in the human lung)
- Outflow (return) cannula - returns oxygenated blood to the patient
The oxygenator also includes a heat exchanger to compensate for heat loss as blood crosses the membrane.
Types of ECMO
VV ECMO (Veno-Venous)
- Drains blood from a vein and returns it to a vein (typically femoral/internal jugular)
- Provides pulmonary support only - no hemodynamic support
- Primary modality for isolated ARDS and acute respiratory failure
- Requires adequate native cardiac function
VA ECMO (Veno-Arterial)
- Drains venous blood and returns oxygenated blood into the arterial system (usually femoral artery)
- Provides both cardiac and pulmonary support
- Indicated for cardiogenic shock, cardiac arrest, biventricular failure, myocarditis, myocardial stunning
- Can cause left ventricular fluid overload and pulmonary edema because it does not unload the LV - often requires additional LV venting strategies (inotropes, IABP, Impella)
VAV ECMO (Veno-Arterio-Venous)
- Hybrid configuration used when ARF is accompanied by biventricular failure
RVAD-ECMO (Protek Duo)
- Cannula traverses the tricuspid and pulmonic valves; drains from SVC/right atrium and returns blood to the pulmonary artery
- Used for isolated RV failure with ARDS - provides both RV support and oxygenation
Indications
| Category | Examples |
|---|
| Pulmonary (VV ECMO) | Severe ARDS, refractory hypoxemia (PaO2/FiO2 <80 despite optimal vent settings), bridge to lung transplant |
| Cardiac (VA ECMO) | Cardiogenic shock, post-cardiotomy failure, myocarditis, massive PE, cardiac arrest (ECPR) |
| Combined | ARDS with cor pulmonale, sepsis-induced cardiomyopathy with ARDS (occurs in 15-20% of patients) |
| Bridge | Bridge to recovery, bridge to VAD, bridge to transplant |
Criteria for VA ECMO support are still being established and are highly institution-dependent.
ECMO Gas Exchange Physiology
- The oxygenator is very efficient at CO2 removal - complete CO2 removal can be achieved with high sweep gas flows at blood flow rates <1 L/min
- Oxygenation requires higher flows - approximately 4 L/min must be maintained to achieve adequate O2 delivery (~260 mL O2/min), with post-oxygenator PaO2 >300 mmHg
- Pre- and post-membrane pressure sensors monitor oxygenator function; a normal transmembrane pressure drop should not exceed 30 mmHg
Anticoagulation
Anticoagulation is required throughout ECMO to prevent circuit thrombosis:
| Agent | Notes |
|---|
| Unfractionated heparin (UFH) | Most common; easy to monitor (aPTT, ACT); reversible; risk of HIT and variable anticoagulant effect |
| Bivalirudin | Direct thrombin inhibitor; lower HIT risk; independent of antithrombin III; half-life ~25 min; no FDA-approved reversal agent |
| Argatroban | Direct thrombin inhibitor; hepatically cleared; half-life ~45-50 min |
A retrospective study of VV ECMO patients found bivalirudin resulted in decreased circuit thrombosis, decreased transfusion requirements, and significantly fewer major bleeding events (11.7% vs. 40.7% for heparin).
Complications
Bleeding
- Most common complication - caused by anticoagulation, thrombocytopenia, mechanical platelet destruction, loss of clotting factors
- Common sites: epistaxis, GI bleeding
- Rare but severe: intracranial hemorrhage, pulmonary hemorrhage
Thrombotic
- Activation of neutrophils, monocytes, leukocytes in the circuit
- Risk of clot formation in the circuit (oxygenator thrombosis)
- Occasional cytokine storm
Vascular
- Arterial injury, pneumothorax during cannulation
- Mitigated by ultrasound-guided access, TEE guidance, echocardiography
LV-specific (VA ECMO)
- Pulmonary edema and LV fluid overload - because VA ECMO increases afterload on an already impaired LV without providing direct LV unloading
Cannulation and Monitoring
- Ultrasound guidance is mandatory for percutaneous vascular access
- Transesophageal echocardiography (TEE) should be performed before and during cannulation to:
- Assess RV and LV function
- Rule out patent foramen ovale, ASD, VSD (which would cause recirculation)
- Detect pericardial effusion
- Guide cannula tip positioning
- Fluoroscopy is also used, especially for PA cannulas (Protek Duo)
- Transmembrane pressure monitoring and flow monitoring are standard of care
Weaning and Discontinuation
ECMO is used as a bridge to one of three outcomes:
- Bridge to recovery - days to weeks; device removed when native cardiac/pulmonary function recovers
- Bridge to durable device - transition to LVAD or BiVAD
- Bridge to transplant - heart or lung transplant
Note: ECMO is not a sustainable long-term device due to infection risk and ongoing complications. VA ECMO and IABP are acute devices that are replaced by VADs when durable support is needed.
Recent Evidence (2024-2026)
A 2026 systematic review and meta-analysis (
PMID 40920225) examined ECMO cannulation by intensivists, relevant to expanding operator scope in high-acuity settings.
A 2024 Lancet individual patient data meta-analysis (
PMID 39236726) on temporary mechanical circulatory support in infarct-related cardiogenic shock provides updated guidance on device selection including ECMO vs. other support options.
Sources: Fishman's Pulmonary Diseases and Disorders, Chapter 149 (pp. 2641-2703); Fischer's Mastery of Surgery, 8th ed. (pp. 345-346)