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What is Perfusion Technology?. Perfusion Technology is the study of physiology, pathology and associated equipment used to support and/or assume the function of the heart and/or lungs during medical procedures.The perfusionist measures various blood and other parameters to identify appropriate mech
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1. EQUIPMENTS FOR EXTRACORPOREAL MEMBRANE OXYGENATION –AN INTRODUCTION TO PERFUSION TECHNOLOGY Dr. Chan King-chung
Pamela Youde Nethersole Eastern Hospital
2. What is Perfusion Technology? Perfusion Technology is the study of physiology, pathology and associated equipment used to support and/or assume the function of the heart and/or lungs during medical procedures.
The perfusionist measures various blood and other parameters to identify appropriate mechanical, pharmacological and thermal manipulation to maintain tissue viability, as directed by physicians.
Operation of cardiopulmonary bypass machine
3. Brief History of Perfusion 1813 – Le Gallois
First proposed extracorporeal circulation to preserve viability of tissue
1858 – Brown-Sequard
Draw his own venous blood
Beating venous blood vigorously
For oxygenation & defibrination
Perfusing an animal limb with syringe
? able to restore local reflexes
1882 – Waldemar von Schroder
Bubbling of blood for oxygenation
Problem with foaming / gas embolism
4. History 1885 – Max von Frey & Max Gruber
“Filming” of blood for oxygenation
Dispersing the blood as a thin film inside a rotating slanted cylinder filled with oxygen
Very limited oxygenating capacity (small animal)
Improved design in 1933 ?
5. History 1895 – Jacobj
Use of animal lung as oxygenator for organ perfusion
6. History 1916 – McLean
Discovery for heparin for anticoagulation
(1870 – Miescher discovered protamine)
1929 – Brukhonenko & Tchetchuline
Perfusion of guillotined head of a dog by cross-perfusion
7. History 1934 – DeBakey
Invented roller pump for transfusion
1935 – Lindbergh & Carrel
Sterile mechanical heart pump
8. History 1944 – Kolff
Extracorporeal circuit for dialysis
1951 – Dennis
First (failed) attempt of CPB for adult heart surgery
1952 – Lewis
First successful ASD closure with open heart under direct vision, with blood inflow stasis and hypothermia only
9. John Gibbon 1937 – First successful CPB on cats
1951 – Screen oxygenator
1953 – First successful CPB for ASD repair
10. Gibbon-IBM Machine
11. History 1955 – Lillehei
Repaired intracardiac defects in 32 infants & young children, using a donor adult to provide oxygenation (with cross circulation)
1955 – Mustard
Animal lungs used as oxygenator
during human cardiac surgery
12. Bubble Oxygenator 1956 – Dewall
Bubbling thought to be dangerous
Overcome by reservoir, bubble traps and defoaming agents coated chamber
Efficient, cheap, easy to assemble, and reusable
Explosive development of cardiac surgery
13. History 1960 – Kay & Cross
Rotating disc oxygenator
1963 – Bodell
Explored use of tubular capillary membrane oxygenator
1965 – Bramson
First commercially available membrane oxygenator (silicone rubber sheets)
14. Components of Perfusion Equipments Pump
Roller
Centrifugal
Oxygenator
Hollow fibre
Silicone membrane
Cannulae
Arterial
Venous
Circuit tubing
Coating
Gas source
Haemofilter
Temperature control
Pressure/Gas Monitors
Filter for emboli
Anticoagulation / Monitor
Priming fluid
16. Much Simpler ECMO Circuit Venous outflow (1x or 2x) ? Pump ? Oxygenator ? Return cannula (± backflow cannula)
Gas blender ? Oxygenator
Water bath ? Oxygenator
17. Roller Pump Positive displacement pump
Commonest pump for CPB
A length of resilient tubing located inside a curved raceway
Rollers mounted on the ends of rotating arms
One roller is compressing the tubing at all times
Blood is pushed ahead of the moving roller, thereby producing continuous blood flow
Flow determined by
Revolutions per minute (rpm) of the pump
Volume displaced with each revolution
Size of tubing
Length of the track
18. Types of Roller Pump Single-roller pump
Used for CPB in the 1950s and early 1960s
Produce more pulsatility
Double-roller pump
Most commonly used pump
210-degree semicircular backing plate
2 rollers with the rotating arms set 180 degrees apart
one of the two rollers is always compressing the tubing
? a relatively nonpulsatile flow
Multiple-roller pump
Not clinically available because it causes more haemolysis
19. Tubing of Roller Pump Polyvinyl chloride (PVC)
Most widely used
Durable
Some spallation (release of plastic microparticles)
Latex rubber
More haemolysis than PVC
Silicone rubber
Less haemolysis than PVC
More spallation then PVC
20. Occlusiveness Adjustable in CPB machine
Excessive occlusion
Haemolysis and tubing wear
Inadequate
Compromises forward flow
Target “barely nonocclusive”
Holding the outflow line with fluid level 60 to 75 cm above the pump
Adjust occlusiveness until the fluid level falls at a rate between 1 and 12 cm/min
Cause less haemolysis than centrifugal pump in some study
21. Complication Malocclusion (over- or under-occlusion)
Miscalibration
Fracture of the tubing
Loss of power
Spallation
Capacity to pump grossly visible air
Tubing or connectors break with outflow obstruction
Microscopic air bubbles ("cavitation") with inflow obstruction
Pinhole leaks from fracture in tubing, leading to microscopic air embolism
22. Centrifugal Pump (Kinetic Pump) Mainstay for ECMO
Impeller with either vanes or a nest of smooth plastic cones inside a plastic housing
Couples magnetically with an electric motor either directly or through a tether
When the impeller rotates rapidly, it generates a pressure differential causing blood flow
23. Characteristics
24. Roller vs. Centrifugal Pump
25. Complications Generally safe
Allows retrograde flow
Exsanguinate a patient by siphon into reservoir
Draw air into the arterial line at the cannulation site
26. Oxygenator Separate blood from gas and allow exchange
2 main types in current use
Hollow Fibre
Silicone membrane (non-porous)
Kolobow spiral coil membrane lung
Medtronic / Avecor
Primarily for ECMO
Ability to maintain stable CO2
& O2 for weeks
27. Membrane Lung vs. Natural Lung
28. Achieving Good Gas Exchange Increasing driving gradient of gas (oxygen)
Increased blood path length
? Increase surface area
? Increase priming volume
Decreasing diffusion path
Minimizing blood path thickness placing membranes as close as possible
? Increase resistance
Secondary flows (induced eddies) to promote mixing
Increasing dwell time of blood in oxygenator
? Increase priming volume
29. Membrane Design Microporous membranes (<1um)
Increases efficiency by enhancing diffusion
Fluid leakage prevented mainly by surface tension
Hydrophobic membrane + coating of pores can produce plasma-proof membrane
30. Other Considerations Blood may flow inside or outside the fiber
Inside: fixed thickness of blood, clotting
Outside: lower resistance, easier de-airing
CO2 transfer depends mainly on membrane material (silicon poorest)
Long duration of use reduce efficiency by
Coating of platelets/fibrin on membrane surface
Water vapour collected in gas pathway
Low priming volume reduce haemodilution
31. Oxygenator Design
32. Medtronic Affinity NT
33. Quadrox PLS
34. Specification of Some Oxygenators
35. Specification of Some Oxygenators
36. Cannulae Peripheral vs. Central ECMO
Wire-reinforced to prevent collapse
Wider, Shorter ? higher flow
Side port available in arterial cannula
For back flow cannula
More side holes preferable for femoral drainage cannula
Appropriate length for femoral vs. jugular placement
Long femoral return cannula without side holes
Coated cannulae available
38. Tubing Standard tubing of 3/8 inch or ½ inch for adult application
3/8 inch was be used mostly in HK for ECMO
Coating available
39. Bioline coating form Maquet Covalently bonded heparin to an albumin layer on PVC surface
Reduced clotting activity
Reduction of platelet adhesion and of thrombi creation
Less complement activation & neutrophil activation
40. Carmeda coating from Medtronic End-point attached heparin
Decreased thrombus formation
Reduced loss of platelets
Attenuated inflammatory response
41. Gas Source Usually a simple oxygen blender for ECMO
O2 flowmeter may suffice during transport
42. Hemofilter Used in operation to remove fluid
CRRT machine for ICU patient on ECMO
Attachment to post-pump, pre-oxygenator preferable
Avoid shunting
Avoid risk of air embolism
Cannot tolerate a positive A-pressure for Prisma machine
(Meaning of A & V are different in CRRT & ECMO circuit)
43. Temperature Control Thermo-controlled water bath necessary
Avoid a high water bath temperature if possible
Bubble formation with heating of blood
Not more than 4C compared with blood
44. Pressure Monitors Venous pressure
Detect insucking
Arterial pressure
Detect obstruction to outflow
Pressure drop across oxygenator
Detect oxygenator clotting
Risk of thrombosis / infection as a segment of stagnant blood is introduced
Integrated senor in the Cardiohelp system (cannot recalibrate)
45. Gas Monitor FiO2 monitor
Detects hypoxic sweep gas
Venous O2 saturation
Detects recirculation
Arterial O2 saturation
Detects failure of oxygenator
Inline pH/pCO2/pO2 monitor
Provide continuous ABG data
Haemoglobin concentration
Detects change in blood volume
Bubble detector
Prevent gas embolism
46. Others Filter / bubble trapper
Anticoagulation / Monitor
Heparin
? Lower dose than recommendation by manufacture
Higher need for anticoagulation when flow is low
Monitor with ACT/APTT/Thromboelastography
Priming fluid
Colloid / Blood prime in children / infants