Key result
Vent return to integral cardiotomy reservoirs markedly increases gaseous microemboli transmission past arterial filters.
Why the study?
Previous observations indicated that gaseous microemboli could be detected after the arterial filter when blood/air challenges entered the membrane oxygenator's integral cardiotomy, warranting further study of the oxygenator's integral cardiotomy reservoir.
Does vent return into the oxygenator's integral cardiotomy increase gaseous microemboli activity after the arterial filter in an in vitro cardiopulmonary bypass model?
Does vent return into the oxygenator's integral cardiotomy increase gaseous microemboli activity after the arterial filter in an in vitro cardiopulmonary bypass model?
Vent return into an oxygenator's integral cardiotomy significantly increases gaseous microemboli, and the ability to filter these emboli varies dramatically depending on the specific oxygenator and arterial filter combination used.
May warrant caution with vent return routing in CPB circuits; leaves open clinical relevance pending outcome studies.
During a previously published study on gaseous micro-emboli (GMEs) and perfusionist interventions, it was noted that emboli could be detected after the arterial filter when blood/air challenges entered the membrane oxygenator’s integral cardiotomy. The findings indicated that further study into the oxygenator’s integral cardiotomy reservoir was warranted. This is the first know published report that connects the vent return to GME activity after the arterial filter. To study the air handling ability of the membranes integral cardiotomy, an in vitro study was conducted on five hard shell coated membrane oxygenators (Terumo Capiox SX25, X coated; Sorin Synthesis, phosphorylcholine coated; Gish Vision, GBS coated; Medtronic Affinity NT, trillium coated; Maquet Quadrox, bioline coated). The oxygenators were matched with their own manufacturer’s coated arterial filters (Medtronic 351T Arterial Filter, Sorin Synthesis Integrated Arterial Filter, Terumo CXAF200X Arterial Filter, Gish GAF40GBS-2 Arterial Filter, and Maquet Quart HBF140 Arterial Filter). There were three arms to the study, and three separate oxygenator/filter combinations were used in each arm. The first arm consisted of a pump flow of 4.0 L/min with only the filter purge blood entering the integral cardiotomy. In the second arm, 500 mL/min of simulated vent blood was added to the filter purge blood entering the integral cardiotomy. During the final arm, 200 mL/min of air was added to the vent blood as it entered the integral cardiotomy, to more closely simulate vent return during cardiopulmonary bypass. All GME activity in the oxygenator/filter combinations was examined using the Hatteland CMD20 Microemboli Counter. Placement of the Hatteland probes was 4 in after the hard shell reservoir outlet (PRO) and 12 in after the arterial filter (PAF). When vent blood flow was turned on, there was a significant increase in the PRO microemboli activity detected in all reservoirs. In the PAF position, three of the oxygenator/filter combinations were able to remove 98–99% of the GME, one removed 84.3%, and another removed only 55.5% of the GMEs coming out of the oxygenator’s reservoir. All oxygenators were found to have a dramatic increase in reservoir GME activity when the vent was turned on. Depending on the oxygenator/filter combination, vent return into the oxygenator’s integral cardiotomy resulted in the presence of significant amounts of GMEs after the arterial filter.
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Myers et al. (2009) studied Gaseous microemboli generation during cardiopulmonary bypass (n=15). Vent return and air addition into the integral cardiotomy vs. Control (filter purge blood only) was evaluated on Gaseous microemboli (GME) activity detected after the arterial filter. Introducing vent return into an oxygenator's integral cardiotomy significantly increased gaseous microemboli activity across all tested reservoirs, leading to substantial microemboli transmission past the arterial filter in some devices.
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