Microembolic signals and strategy to prevent gas embolism during extracorporeal membrane oxygenation
© Zanatta et al; licensee BioMed Central Ltd. 2010
Received: 7 October 2009
Accepted: 4 February 2010
Published: 4 February 2010
Extracorporeal membrane oxygenation (ECMO) supplies systemic blood perfusion and gas exchange in patients with cardiopulmonary failure. The current literature lacks of papers reporting the possible risks of microembolism among the complications of this treatment.
In this study we present our preliminary experience on brain blood flow velocity and emboli detection through the transcranial Doppler monitoring during ECMO.
Six patients suffering of heart failure, four after cardiac surgery and two after cardiopulmonary resuscitation were treated with ECMO and submitted to transcranial doppler monitoring to accomplish the neurophysiological evaluation for coma.
Four patients had a full extracorporeal flow supply while in the remaining two patients the support was maintained 50% in respect to normal demand.
All patients had a bilateral transcranial brain blood flow monitoring for 15 minutes during the first clinical evaluation.
Microembolic signals were detected only in patients with the full extracorporeal blood flow supply due to air embolism.
We established that the microembolic load depends on gas embolism from the central venous lines and on the level of blood flow assistance.
The gas microemboli that enter in the blood circulation and in the extracorporeal circuits are not removed by the membrane oxygenator filter.
Maximum care is required in drugs and fluid infusion of this kind of patients as a possible source of microemboli. This harmful phenomenon may be overcome adding an air filter device to the intravenous catheters.
ECMO is a well consolidated method of treatment for patients with heart failure after cardiac surgery besides intraortic balloon pump and pharmacological therapy . Mortality and morbidity of this life saving procedure remain still high . The more frequent complications are bleeding, renal failure, lower limb ischemia and brain iniury like cerebral haemorrhage and oedema.
Our preliminary experience in monitoring ECMO patients sustains the possible role of systemic microembolism in increasing patient morbidity.
ECMO ASSISTANCE 50%
ECMO ASSISTANCE 100%
Body Surface Area (m 2 )
Type of event
Reason for ECMO
Left ventricular failure
Left ventricular failure
Left ventricular failure
Length of ECMO (days)
ECMO flow (l/min)
Weaned from ECMO
ICU Recovery Time (days)
The neurosonology evaluation consists of the standard examination of the brain blood flow velocity of intracranial arteries (first step) and fifteen minutes monitoring with emboli count and differentiation by ultrasound probes placed on the middle cerebral arteries through the transtemporal windows (second step) with Doppler box - DWL.
The ECMO perfusion system consists of a Jostra- Maquet coated minicircuit, a Levitronix centrifugal pump and a Quadrox D oxygenator. Venous drainage was performed with a 21 F Byomedicus Carmeda multistage cannula with the distal portion proximal to the right atrium. Arterial perfusion was maintain with a 17 F Biomedicus Carmeda cannula. Both venous and arterial femoral cannula were inserted percutaneously. A heat exchanger was used to maintain a nasopharyngeal temperature between 34-35°C. All patients were sedated to reduce shivering and excess of oxygen consumption.
The patients received a perfusion assistance according to the heart function monitored by transesophageal echocardiogram and metabolic parameters from blood sampling. Air/oxygen flow was set to maintain a partial oxygen pressure of 150-200 mmHg and a carbon dioxide of 35-40 mmHg. Continuously intravenous infusion of heparin was administered to obtain an activated clotting time between 180-200 seconds.
All patients were assisted with intraortic blood pulsation and with continuous renal replacement therapy.
The standard TCD evaluation showed intracranial brain blood flow velocity in normal range in all patients except the patient 4 in which we found a high brain blood flow velocity because of a non convulsive status epilecticus detected with a subsequent electroencephalogram.
Additional file 1: Movie patient 3. TCD microembolic signals recording from venous gas embolism. (WMV 7 MB)
Additional file 3: Movie patient 1. TCD monitoring during a bubble test in ECMO 50% supply. A double sample TCD recording on the right and left medial cerebral arteries is made. Note also the M-mode and median brain blood flow velocity monitoring. (WMV 3 MB)
Additional file 4: Movie air filter. Efficiency of the SmartSite Extension Set in removing air from crystalloid solution. Methylene blu is added to the solution to better visualize the dearing. (AVI 7 MB)
Patient 3 and 5 treated with the ECMO 100% assistance died because of a multiorgan failure while, the others four patients were successfully weaned from extracorporeal circulation. Only patient 4 had maior neurologic disorders caracterized by a minimal conscious state and a spastic cerebral palsy. The others 3 patient (patient number 1, 2 and 6) had a normal neurological examination. It wasn't possible to perform neurocognitive evaluations in these three patients during the post intensive care recovery time.
Microemboli produced during extracorporeal circulation are a recognised cause of increasing morbidity and mortality in cardiac surgery procedures [3, 4]. We agree that TCD can be helpful in assessing and monitoring the quality of extracorporeal perfusion in regard of blood flow velocity and emboli detection, allowing the best perfusion strategy, not only during cardiopulmonary bypass, but also during ECMO.
In literature there aren't papers about the brain emboli detection monitoring with TCD during ECMO. There are few reports about brain emboli monitoring with TCD on patients treated with left ventricular assist device (LVAD) [5, 6]. One paper reports that in Novacor LVAD patients the amount of MES is directly correlated with clinical thromboembolism ; the pathogenesis of microembolization in LVAD-patients seem to be still unknown.
Our experience sustains the hypothesis that patient treated with high blood flow ECMO can be at high risk for brain and systemic embolization from venous gas embolism. Mini extracorporeal circuits and the membrane oxygenator filters seem to be not efficient enough to remove microemboli. We believe that the 50% ECMO assistance is not associated with microembolic signals because the microemboli enter more easily into the pulmonary circulation. The bubbles test performed with a mixture of 1 ml of air and 9 ml of crystalloid solution, injected into a central venous catheter sustains our hypothesis.
In the last years Doppler technology has made possible to differentiate not only gaseous but also solid microemboli . The solid component of the embolic load that we detected is probably related to platelets aggregation on gas microbubbles, as documented by others papers . The different proportion of solid emboli in four patients treated with ECMO 100%, could be explained with a difference in the coagulation status of the patients, despite activated clotting time was in the same range. Gaseous and solid microemboli can produce tissue ischemia and subsequent tissue damage through the obstruction of the microcirculation. On account of this we hypothesize that the pharmacological anticoagulation requested to maintain the extracorporeal circulation may be a risk factor of subsequent brain haemorrhage .
Our study supports the possible role of microembolization in worsening the patients outcome since the total embolic load can be enormous during several days of ECMO assistance.
Moreover in two of our patients the emboli count is underestimated because they had showers of MES (patient 5 and 6) not countable by the software for the high numbers of microbubbles that occur at once. Some authors recently proposed a radio-frequency based TCD analysis to overcome this limitation and better correlate the neurologic outcome to cerebral embolic load .
To reduce the probability of microembolization on ECMO we tested an air filter device (0.2 micron), high efficient in removing air bubbles from venous infusion lines (Figure 2 and additional file 4). The use of this device has made possible to erase microemboli during crystalloid solution infusion. This investigation is still open during fast infusion of fresh frozen plasma and red packed cells, because a bigger filter capacity is required. Moreover there is evidence, in patients with mechanical heart valves, that gas microbubbles may be reduce by administering 100% oxygen through the mechanism of blood de-nitrogenation . This protective effect could be utilize to reduce number and size of air microbubbles also during extracorporeal perfusion.
Patients treated with high flow ECMO assistance can suffer from microemboli because venous gas embolism. The extracorporeal perfusion system is not enough efficient to remove air microbubbles. During this procedure maximum care is required on setting and managing the infusion lines. The interposition of an air filter device between the intravenous catheter and the infusion lines can prevent air embolization.
Although more studies are required to verify the impact of brain and systemic microembolism during ECMO on patients outcome, we decided that this kind of investigation must not necessarily be submitted to our ethical committee, because the gas embolism can be easily solved with a simple device.
Finally TCD monitoring proved a great utility in verifying the quality of perfusion during ECMO, both for bilateral brain blood flow velocity and emboli detection.
Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
Extracorporeal membrane oxygenation
left ventricular assist device
We thanks Mr Carlo Donà and Mr Dalmazio Vedelago for their help in producing video recordings and all the other Cardiac Surgery Nursing Team involve in a new practice to reduce microembolism during ECMO.
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