Haematological effects of bubble oxygenator

 

Bubble oxygenators are intrinsically not biocompatible

 

i) Electrokinetic effects —> Protein denaturation

     There exists a layer of electrokinetic force at the gas-blood interface

     May explain many of the phenomena associated with bubble oxygenators in clinical practice

     The electrokinetic forces at the gas-blood interface tend to orientate the proteins so that their hydrophilic groups are in the blood phase leaving the non-polar groups sticking out into the gaseous phase

     This distortion disrupts the normal configuration of proteins [protein denaturation], alters their biological specificity and causes functional alteration

     Some of the altered proteins acquire increased biological activity (most show a decrease in biological activity)

     Denatured protein aggregates are inherent in bubble oxygenators

 

Protein molecules are large and complex. Their activity depends on their shape and chemical composition. The denaturing or inactivating, of proteins involves the changing of their shape &/or breaking off attached chemical groups. Denatured enzymes may loose their catalytic properties, the anti-body-antigen mechanism may be altered, hormones may loose their function etc.. Surface electrical charges on these molecules are altered, they become sticky and form aggregates. Soluble proteins may become insoluble and precipitate. Denatured globulins may cryoprecipitate (ppt when exposed to hypothermia). Lipid components freed from lipoproteins coalesce to form fat emboli.

 

ii) Platelet activation & aggregation

     Secondary to protein denaturation and gas-blood interface

 

iii) Complement activation

     Secondary to the increased biological activation of some altered proteins

     See resultant kinin release

 

iv) Blood cell damage

     It is well known that bubble oxygenators tend to haemolyse red blood cells

     Mechanism probably due to high shear stresses induced around the bubble

 

v) White blood cell destruction

     Due to activation of complement system