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Extracorporeal membrane oxygen
ation
ECMO
Dr Himaaldev
Consultant intensive care
ARDS
1. Lung protective
ventilation
2. Prone ventilation
3. ECMO
Severe ARDS
Pao2/Fio2 ratio <100
PEEP >5cm
Mortality 45%
2
Evolution of ventilators
Negative pressure – positive pressure
NPV
4
PPV
5
PRONING
ECMO
•ECMO-extracorporeal circuit to provide
temporary respiratory or cardiac support to
patients failing conventional therapy
TECHNOLOGY OF CARDIOPULMONARY
BYPASS TO BEDSIDE
Extracorporeal Membrane Oxygenation
(ECMO)
How ECMO works
• External artificial circuit carries venous blood from the patient
to a gas exchange device (oxygenator) where blood becomes
enriched with oxygen and has carbon dioxide removed.
• The blood is then returned to systemic circulation
via another vein (VV ECMO) or artery (VA ECMO).
ECMO Types
Veno-Arterial (V-A) ECMOVeno-Venous (V-V) ECMO
SVC
Return Cannula
IVC
Access Cannula
IVC
Return Cannula
FA Access
Cannula
FV
Veno Venous ECMO Indications
Primary
1. Severe pneumonia
2. ARDS
3. Acute lung (graft) failure following transplant
4. Pulmonary contusion -trauma
Others
1. Smoke inhalation
2. Status asthmaticus
3. Airway obstruction
4. Aspiration
Veno Arterial ECMO Indications
1. Cardiogenic shock: AMI and complications (wall ruptu
re, papillary muscle rupture, refractory VT / VF)
2. Post cardiac surgery: unable to wean safely from cpb
3. Sepsis with profound cardiac depression
4. Drug overdose with profound cardiac depression
5. Myocarditis
6. Chronic cardiomyopathy: as a “bridge” to longer term
ventricular assist device or transplant
Ecmo principle
• Patient care during ECMO has focused on the end organ
perfusion and thus preventing further injury and also
improving or maintaining end organ functions
• Bridge to Decision and to Recovery
HISTORY
• First successful implantation of ECMO dates
from 1972
• 1975 – RH Bartlett - First Successful Neonatal ECMO
ECMO History
ECMO History
From this…
TO THIS!!
Ecmo circuit
18F (6.0mm)
20F (6.7mm)
22F (7.3mm)
24F (8.0mm)
28F (9.3mm)
Cannulation …
55 cm (21.6”)
68 cm (26.8”)
16F (5.3mm)
18F (6.0m
20F (6.7mm)
22F (7.3mm)
ECMO technical advances
A move from roller to centrifugal pumps that do
not damage the red cells
Roller Pump Head
Centrifugal Pump He
ad
Centrifugal Pump Co
nsole
Roller Pump C
onsole
Centrifugal Pum
p Drive Unit
ECMO technical advances
A switch from silicone membrane oxygenators to
polymethylpentene hollow fibre ones
Silicone membrane ox
ygenator unravelled
Oxygenators
Quadrox D – Safeline Coating
Mini Max
Silicones
New Cannula
ECMO technical advances
Miniturisation of circuits - transport on ECMO
run with much less Heparin, thus reducing bleeding risk.
26
Downside
Complications
BLEEDING, COAGULOPATHY AND HAEMOLYSIS
MECHANICAL COMPLICATIONS (e.g. oxygenator failure, circuit disruption,
pump malfunction, problems with cannula placement/removal)
HIT, INFECTION
AIR EMBOLISM, THROMBOEMBOLISM AND NEUROLOGICAL SEQUELAE
COMPARTMENT SYNDROME AND LEG ISCHEMIA
Contraindications
• Irreversible neurological injury
• Malignancy with limited survival
• Multiple trauma/hemorrhage
• Multi organ failure
• Coagulopathy
• Severe aortic valve regurgitation
• Aortic dissection
How do we do it ?
• Ecmo team discussion
• Family counselling
• Cannulation and anticoagulation
• Ecmo circuit establishment and maintainance
• Ventilation and ICU measures
• Daily team discussion and prognostication
• Weaning
THE ECMO TEAM
• CTVS team
• Perfusionist
• Primary care physician
• Intensive care team
• Pulmonologist
• Nursing team
• Respiratory therapist
• Physiotherapist
When to start?
• Severe, life threatening hypoxemia –P/F less than 100
• Lack of recruitment response
inadequate SpO2/PaO2 response to increasing PEEP
• Failure of prone ventilation
• Murray score of more than 2.5 to 3
• Oxygenation index >40 x 2 hours-indicates ecmo
• Ventilator days pre-ECMO
• Compliance < 0.5 ml/cmH2O/kg
Murray Score
Oxygenation Index
OI=
Mean airway pressure x Fi O2 x 100
PaO2
Ecmo pronevs.
Selection of Technique
VA
ECMO
VVvs.
Selection of Technique
“The key to the success of ECMO may be the time
of initiation”
Basic goals:
»
» Decrease further lung damage
»
» Reduce oxygen toxicity
» “Lung Rest”
» Maintain end organ perfusion
»
REST THE LUNG
• Tolerate pCO2 55-65, SpO2 > 88%, Sao2 > 90%
REST LUNG SETTINGS
Limit Plateau pressures <30 cm H2O
Delivered tidal volumes 4 ml/kg
Rate 8-10 breaths/minute
PEEP 12-14 cm H2O
Inspiratory time longer
Goal FiO2 0.4-0.6
Circuit management
• Blood flow litres per minute
• Transmembrane pressure ,Circuit check for clots
• Venous chattering-HYPOVOLEMIA
• Normothermia
• ACT Target 160-200 sec
ECMO maintainance
1. ABG ,ACT– 6hourly
2. Blood Investigations : Complete blood count, RFT,LFT,
LDH and Plasma free HB
3. Doppler examination
4. Antibiotics and septic screening, Sedation holiday
5. Additional procedures
1. Tracheostomy
2. Dialysis on ECMO (CVVHD)
3. Chest physiotherapy
4. Repeated bronchoscopy
Adjunctive therapy
• Fluids/nutrition: Feed ‘em!
• Sedation/analgesia: wake ‘em!
• Antibiotics: Hold ‘em!
• Invasive procedures: Bronch/trach ‘em!
• Weaning: Wean ‘em!
• Decannulation: Cap ‘em!
• Post-ECMO: Rehab ‘em!
Weaning
• Turning off the gas flow to the oxygenator and
simultaneous reestablishing full ventilation is required- VV ECMO
• Circuit flows must be reduced to assess native heart function
(≤ 1.5 LPM) –VA ECMO
• Lower limb arterial /venous Doppler studies
-following decannulation as to prevent distal limb
ischaemia and distal DVT formation
Cost burden
PRONING
THANKYOU

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Ecmo dr himaaldev

  • 1. Extracorporeal membrane oxygen ation ECMO Dr Himaaldev Consultant intensive care
  • 2. ARDS 1. Lung protective ventilation 2. Prone ventilation 3. ECMO Severe ARDS Pao2/Fio2 ratio <100 PEEP >5cm Mortality 45% 2
  • 3. Evolution of ventilators Negative pressure – positive pressure
  • 8. •ECMO-extracorporeal circuit to provide temporary respiratory or cardiac support to patients failing conventional therapy TECHNOLOGY OF CARDIOPULMONARY BYPASS TO BEDSIDE Extracorporeal Membrane Oxygenation (ECMO)
  • 9. How ECMO works • External artificial circuit carries venous blood from the patient to a gas exchange device (oxygenator) where blood becomes enriched with oxygen and has carbon dioxide removed. • The blood is then returned to systemic circulation via another vein (VV ECMO) or artery (VA ECMO).
  • 10. ECMO Types Veno-Arterial (V-A) ECMOVeno-Venous (V-V) ECMO SVC Return Cannula IVC Access Cannula IVC Return Cannula FA Access Cannula FV
  • 11. Veno Venous ECMO Indications Primary 1. Severe pneumonia 2. ARDS 3. Acute lung (graft) failure following transplant 4. Pulmonary contusion -trauma Others 1. Smoke inhalation 2. Status asthmaticus 3. Airway obstruction 4. Aspiration
  • 12. Veno Arterial ECMO Indications 1. Cardiogenic shock: AMI and complications (wall ruptu re, papillary muscle rupture, refractory VT / VF) 2. Post cardiac surgery: unable to wean safely from cpb 3. Sepsis with profound cardiac depression 4. Drug overdose with profound cardiac depression 5. Myocarditis 6. Chronic cardiomyopathy: as a “bridge” to longer term ventricular assist device or transplant
  • 13. Ecmo principle • Patient care during ECMO has focused on the end organ perfusion and thus preventing further injury and also improving or maintaining end organ functions • Bridge to Decision and to Recovery
  • 14. HISTORY • First successful implantation of ECMO dates from 1972 • 1975 – RH Bartlett - First Successful Neonatal ECMO
  • 19. 18F (6.0mm) 20F (6.7mm) 22F (7.3mm) 24F (8.0mm) 28F (9.3mm) Cannulation … 55 cm (21.6”) 68 cm (26.8”) 16F (5.3mm) 18F (6.0m 20F (6.7mm) 22F (7.3mm)
  • 20. ECMO technical advances A move from roller to centrifugal pumps that do not damage the red cells Roller Pump Head Centrifugal Pump He ad Centrifugal Pump Co nsole Roller Pump C onsole Centrifugal Pum p Drive Unit
  • 21. ECMO technical advances A switch from silicone membrane oxygenators to polymethylpentene hollow fibre ones Silicone membrane ox ygenator unravelled
  • 22. Oxygenators Quadrox D – Safeline Coating Mini Max Silicones
  • 24. ECMO technical advances Miniturisation of circuits - transport on ECMO run with much less Heparin, thus reducing bleeding risk.
  • 25. 26 Downside Complications BLEEDING, COAGULOPATHY AND HAEMOLYSIS MECHANICAL COMPLICATIONS (e.g. oxygenator failure, circuit disruption, pump malfunction, problems with cannula placement/removal) HIT, INFECTION AIR EMBOLISM, THROMBOEMBOLISM AND NEUROLOGICAL SEQUELAE COMPARTMENT SYNDROME AND LEG ISCHEMIA
  • 26.
  • 27. Contraindications • Irreversible neurological injury • Malignancy with limited survival • Multiple trauma/hemorrhage • Multi organ failure • Coagulopathy • Severe aortic valve regurgitation • Aortic dissection
  • 28. How do we do it ? • Ecmo team discussion • Family counselling • Cannulation and anticoagulation • Ecmo circuit establishment and maintainance • Ventilation and ICU measures • Daily team discussion and prognostication • Weaning
  • 29. THE ECMO TEAM • CTVS team • Perfusionist • Primary care physician • Intensive care team • Pulmonologist • Nursing team • Respiratory therapist • Physiotherapist
  • 30. When to start? • Severe, life threatening hypoxemia –P/F less than 100 • Lack of recruitment response inadequate SpO2/PaO2 response to increasing PEEP • Failure of prone ventilation • Murray score of more than 2.5 to 3 • Oxygenation index >40 x 2 hours-indicates ecmo • Ventilator days pre-ECMO • Compliance < 0.5 ml/cmH2O/kg
  • 32. Oxygenation Index OI= Mean airway pressure x Fi O2 x 100 PaO2
  • 35. “The key to the success of ECMO may be the time of initiation” Basic goals: » » Decrease further lung damage » » Reduce oxygen toxicity » “Lung Rest” » Maintain end organ perfusion »
  • 36. REST THE LUNG • Tolerate pCO2 55-65, SpO2 > 88%, Sao2 > 90% REST LUNG SETTINGS Limit Plateau pressures <30 cm H2O Delivered tidal volumes 4 ml/kg Rate 8-10 breaths/minute PEEP 12-14 cm H2O Inspiratory time longer Goal FiO2 0.4-0.6
  • 37. Circuit management • Blood flow litres per minute • Transmembrane pressure ,Circuit check for clots • Venous chattering-HYPOVOLEMIA • Normothermia • ACT Target 160-200 sec
  • 38. ECMO maintainance 1. ABG ,ACT– 6hourly 2. Blood Investigations : Complete blood count, RFT,LFT, LDH and Plasma free HB 3. Doppler examination 4. Antibiotics and septic screening, Sedation holiday 5. Additional procedures 1. Tracheostomy 2. Dialysis on ECMO (CVVHD) 3. Chest physiotherapy 4. Repeated bronchoscopy
  • 39. Adjunctive therapy • Fluids/nutrition: Feed ‘em! • Sedation/analgesia: wake ‘em! • Antibiotics: Hold ‘em! • Invasive procedures: Bronch/trach ‘em! • Weaning: Wean ‘em! • Decannulation: Cap ‘em! • Post-ECMO: Rehab ‘em!
  • 40. Weaning • Turning off the gas flow to the oxygenator and simultaneous reestablishing full ventilation is required- VV ECMO • Circuit flows must be reduced to assess native heart function (≤ 1.5 LPM) –VA ECMO • Lower limb arterial /venous Doppler studies -following decannulation as to prevent distal limb ischaemia and distal DVT formation