Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 2007;116:1888-1895
Published online before print October 8, 2007, doi: 10.1161/CIRCULATIONAHA.107.698001
CLINICAL PERSPECTIVE
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
116/17/1888    most recent
CIRCULATIONAHA.107.698001v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Djaiani, G.
Right arrow Articles by Karski, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Djaiani, G.
Right arrow Articles by Karski, J.
Related Collections
Right arrow Echocardiography
Right arrow CV surgery: coronary artery disease
Right arrow Brain Circulation and Metabolism
Right arrow Doppler ultrasound, Transcranial Doppler etc.
Right arrow Neuroprotectors

(Circulation. 2007;116:1888-1895.)
© 2007 American Heart Association, Inc.


Cardiovascular Surgery

Continuous-Flow Cell Saver Reduces Cognitive Decline in Elderly Patients After Coronary Bypass Surgery

George Djaiani, MD, FRCA; Ludwik Fedorko, MD, PhD; Michael A. Borger, MD, PhD; Robin Green, PhD; Jo Carroll, RN; Michael Marcon, PhD; Jacek Karski, MD

From the Department of Anesthesiology (G.D., L.F., J.C., J.K.), Division of Cardiovascular Surgery (M.A.B.), and Toronto Rehabilitation Institute (R.G.), Toronto General Hospital, University of Toronto, Toronto, Ontario, Canada; and InControl Technologies Inc, Houston, Tex (M.M.).

Correspondence to George Djaiani, MD, Department of Anesthesia and Pain Management, Eaton North 3-410, Toronto General Hospital, University Health Network, 200 Elizabeth St, Toronto, Ontario, M5G 2C4, Canada. E-mail george.djaiani{at}uhn.on.ca

Received February 21, 2007; accepted August 13, 2007.


*    Abstract
up arrowTop
*Abstract
down arrowIntroduction
down arrowMethods
down arrowResults
down arrowDiscussion
down arrowReferences
 
Background— Cerebral microembolization during cardiopulmonary bypass may lead to cognitive decline after cardiac surgery. Transfusion of the unprocessed shed blood (major source of lipid microparticulates) into the patient during cardiopulmonary bypass is common practice to reduce blood loss and blood transfusion. Processing of shed blood with cell saver before transfusion may limit cerebral microembolization and reduce cognitive decline after surgery.

Methods and Results— A total of 226 elderly patients were randomly allocated to either cell saver or control groups. Anesthesia and surgical management were standardized. Epiaortic scanning of the proximal thoracic aorta was performed in all patients. Transcranial Doppler was used to measure cerebral embolic rates. Standardized neuropsychological testing was conducted 1 week before and 6 weeks after surgery. The raw scores for each test were converted to Z scores, and then a combined Z score of 10 main variables was calculated for both study groups. The primary analysis was based on dichotomous composite cognitive outcome with a 1-SD rule. Cognitive dysfunction was present in 6% (95% confidence interval, 1.3% to 10.7%) of patients in the cell saver group and 15% (95% confidence interval, 8% to 22%) of patients in the control group 6 weeks after surgery (P=0.038). The severity of aortic atheroma and cerebral embolic count were similar between the 2 groups.

Conclusions— The present report demonstrates that processing of shed blood with cell saver results in clinically significant reduction in postoperative cognitive dysfunction after cardiac surgery. These findings emphasize the clinical importance of lipid embolization in contributing to postoperative cognitive decline in patients exposed to cardiopulmonary bypass.


Key Words: brain • cardiopulmonary bypass • cognitive symptoms • surgical blood loss


*    Introduction
up arrowTop
up arrowAbstract
*Introduction
down arrowMethods
down arrowResults
down arrowDiscussion
down arrowReferences
 
Recently, cardiopulmonary bypass (CPB) has celebrated its 50th anniversary demonstrating its vital role in the cardiac surgery setting. Although the practice of running CPB has changed over the years, some of the mainstay components of the CPB circuit have remained the same. One of these components is a cardiotomy suction reservoir that is used to return "suctioned" blood from the wound, sternum, and thorax back to the patient to reduce blood loss and blood transfusion. However, the blood collected in cardiotomy suction contains high levels of cellular debris and lipid microparticulates,1,2 which have been shown to cause microembolization to the brain blood vessels.3 One pathology study examined tissue blocks from the brains of patients who died after cardiac surgery from nonneurological causes. The pathological and chemical features of the multiple cerebral microemboli closely resembled the brain microemboli that originated from cardiotomy suction blood in experimental animal studies.4 Cerebral microembolization is considered one of the most likely causal factors leading to cognitive decline after cardiac surgery, which occurs in a considerable number of patients and may result in reduced quality of life during otherwise successful surgery.5,6

Editorial p 1879

Clinical Perspective p 1895

Previous investigators have shown that when shed blood from the cardiotomy reservoir was processed with a cell saver device, it considerably reduced cerebral lipid microembolization.7 Cell savers are commonly used in noncardiac surgery when excessive blood loss is a concern (eg, abdominal aortic aneurysm surgery). Cell savers clean and process shed blood, making it suitable for retransfusion into the patient. In addition to effective removal of fat particles, cell savers appear to be efficient in removing cytokines, S-100β protein, platelet and fibrin aggregates, and complement and coagulation activation products from shed blood.8–11

Removal of these factors from shed blood may reduce the incidence of cognitive decline after cardiac surgery by decreasing the risk of microembolization and/or decreasing the amount of inflammatory activation. However, there have been no human studies investigating a direct link between fat emboli and cognitive dysfunction after cardiac surgery. Consequently, the link between lipid emboli and postoperative cognitive decline is inferential and not definitive because the data are from either animal or human autopsy studies.12 A recent evidence-based review assigned a class IIb, level B evidence for blood cell processing and secondary filtration in decreasing the deleterious effects of reinfused shed blood.13 More studies are required to build up level I clinical evidence.

The objective of this study was to determine whether the replacement of cardiotomy suction with a continuous-flow cell saver device would improve neuroprotection by minimizing cerebral microembolization and reduce cognitive decline in elderly patients after coronary artery bypass graft (CABG) surgery. We therefore performed a randomized, double-blinded trial of cell saver versus cardiotomy suction (ie, control) to test our hypothesis.


*    Methods
up arrowTop
up arrowAbstract
up arrowIntroduction
*Methods
down arrowResults
down arrowDiscussion
down arrowReferences
 
Study Population
After approval by the University Health Network Research Ethics Board, informed consent was obtained from 233 patients older than 60 years who were scheduled for elective CABG surgery. We focused on patients older than 60 years because of their increased risk of postoperative cognitive decline, thereby increasing our ability to detect a clinically significant reduction in cognitive impairment. Patients were excluded if they required redo CABG surgery, emergent surgery, or a surgical procedure in addition to CABG, as well as if they had severe kidney or liver disease (creatinine >133 mg/dL and bilirubin >2 mg/dL), symptomatic cerebrovascular disease, history of stroke, transient ischemic attacks, or atrial fibrillation. We also excluded patients who were unable to complete a preoperative assessment and those who could not speak English. Patients were randomly allocated to either cell saver or control (ie, cardiotomy suction) groups according to a computer-generated randomization code in predetermined size blocks. Patients were unaware of their group assignment.

Anesthetic Management
All patients received premedication with lorazepam 2 mg 1 to 2 hours before surgery. Anesthetic technique was standardized to include fentanyl 10 to 20 µg/kg, midazolam 0.1 mg/kg, pancuronium 0.15 to 0.20 mg/kg, and isoflurane 0.5% to 1.5%. All patients received tranexamic acid 50 mg/kg intravenously after induction of anesthesia. After surgery, patients were transferred to the intensive care unit for postoperative ventilation. Sedation was achieved with propofol infusion 0.5 to 4 mg/kg per hour and morphine boluses. Patients were extubated according to standard criteria.

Operative Technique and Management of CPB
After median sternotomy, patients underwent harvesting of saphenous veins and internal thoracic arteries as conduits. Heparin was given to maintain activated clotting time >400 seconds. Management of CPB included systemic temperature drift to 33°C to 34°C (nasopharyngeal), alpha-stat pH management, mean perfusion pressure between 60 and 80 mm Hg, pump flow rates of 2.0 to 2.4 L/min per square meter, and hematocrit >20%. A single aortic cross-clamp technique was used in all patients. Myocardial protection was achieved with intermittent antegrade and occasionally retrograde cold blood cardioplegia. A 32-µm filter (Avecor Affinity, Minneapolis, Minn) was used in the arterial perfusion line. Before separation from CPB, patients were rewarmed to 36°C to 37°C. During rewarming, the maximal inflow temperature was limited to 37°C. After separation from CPB, heparin was neutralized with protamine.

The continuous-flow cell saver (Fresenius Corporation, Concord, Calif) was used to process shed blood before returning it back to the patient. In control patients, cardiotomy suction was used in a standard closed venous reservoir where cardiotomy blood was collected and reinfused through the arterial circuit back to the patient. Both the cell saver and cardiotomy suction were used during the same time periods, from full heparinization (activated clotting time >400 seconds) to immediately after the initial dose of protamine was given.

Echocardiographic Assessment
A comprehensive transesophageal echocardiography examination with the use of multiplane 4- to 7-MHz probe and Hewlett-Packard Sonos 5500 echocardiograph (Philips Medical Systems, Andover, Mass) was performed after induction of anesthesia to rule out an intracardiac or valvular source of potential emboli. In addition to transesophageal echocardiography, epiaortic scanning was used by the surgeon to scan the ascending aorta from aortic valve to midaortic arch in transverse and longitudinal planes. A 6- to 15-MHz epiaortic probe (Philips Medical Systems, Andover, Mass) covered with ultrasound gel and wrapped in sterile Surgi-Tip transducer cover (CIVCO Medical Instruments, Kalona, Iowa) was utilized. Aortic atheroma was graded on a 4-point scale as previously described.14 The real-time echocardiographic findings were communicated to the operating surgeons who were free to modify the operating technique and apply ultrasound guidance for any intended aortic manipulation to minimize potential embolization.

Transcranial Doppler Measurements
As a secondary outcome, we chose a subset of patients in each group with adequate transcranial Doppler (TCD) signal to determine whether the use of cardiotomy suction reduces the amount of TCD-detected emboli. Difficulty in obtaining an adequate acoustic window for TCD measurements in elderly patients is well recognized and limited the number of patients available for secondary outcome analysis.

TCD monitoring (MultiDop X4, DWL Electronic Systems, Sipplingen, Germany) of the middle cerebral artery was performed continuously from 2 minutes before cannulation of the aorta to 2 minutes after aortic decannulation. The technique of detection and analysis of embolic hits was used, as previously described.15 We calculated a total number of emboli during CPB using a sum from both middle cerebral arteries.

Neuropsychological Testing
The neuropsychological testing was conducted 1 week before (baseline) and 6 weeks after surgery by a trained psychometrist blinded to the treatment arm assignment. The prehospital discharge testing was not conducted because such data are confounded by a variety of factors including medication, fatigue, pain, sleep deprivation, and the traumatic effects of surgery.16 Moreover, the predischarge testing can be frustrating and difficult for some patients, which could compromise compliance on the 6-week follow-up tests.

The proposed battery of tests complied with the international consensus on assessing neuropsychological outcome16 and included tests for learning and memory, attention, concentration, and psychomotor speed, as well as language and higher intellectual functioning. Of the battery of 12 tests, 10 main variables were chosen a priori to be used in the analyses: (1) Rey Auditory Verbal Learning Test, (2) Rey Visual Design Learning Test, (3) Halstead-Reitan Trail-Making Tests Parts A and B (Trails B–Trails A) time, (4) Grooved Pegboard Test time, (5) Wechsler Memory Scale Digit Span Forward, (6) Wechsler Memory Scale Digit Span Backward, (7) Wechsler Memory Scale Spatial Span Forward, (8) Wechsler Memory Scale Spatial Span Backward, (9) Choice and Simple Reaction Time Tests (Choice Reaction Time–Simple Reaction Time), and (10) Verbal Fluency Test.

Parallel versions of the tests were used when available to minimize learning effects between the baseline and 6-week follow-up assessments. If improved performance was reflected by a lower score (Trails A and B, Grooved Pegboard, Simple and Choice Reaction Times tests), the directional data were reversed so that all improvements gave positive change scores. Tests not completed were treated as omissions and not as failures.

To estimate the change in performance from baseline to 6 weeks after surgery, the raw scores for each test were converted to Z scores. A Z score was calculated for each main variable in each patient by subtracting the preoperative score from the postoperative score and dividing the difference by the preoperative SD of that variable.17,18 This standardized score allowed the classification of patients on the basis of the 1-SD rule. Patients with a positive score of >+1 were considered improved, and patients with a negative score of <–1 were considered deteriorated. The primary outcome was the dichotomous cognitive deterioration variable based on the combined cognitive score.

Sample Size Justification and Statistical Analysis
Given that the prevalence of postoperative cognitive dysfunction at 6 weeks after CABG surgery is 36%,5 to see a 50% reduction in cognitive dysfunction from 36% to 18% in patients receiving cell saver management strategy, with {alpha}=0.05 and power 1–β=0.8, a group of 95 patients in each arm of the study is required, for a total of 190 patients in the randomization schedule. We estimated an attrition rate of 10%. The final sample size for randomization purposes therefore was increased to a total of 209 patients.

Comparability of both groups with respect to demographic data and surgical characteristics was tested with the use of {chi}2 statistics on qualitative variables and the t test on quantitative variables. For the primary analysis of composite dichotomous cognitive outcome, the 2 groups were compared with the {chi}2 test for differences in probabilities of a 2x2 contingency table. Confidence intervals (CIs) for proportions were calculated at 95%. Paired t tests were used for the raw cognitive score comparisons between baseline and 6-week follow-up. A 2-tailed t test was used to compare the hematologic and coagulation laboratory parameters between the 2 groups at predetermined time points. The emboli count, extubation time, and hospital length of stay were analyzed with the Mann-Whitney U test. All analyses were performed on an intention-to-treat basis. A probability value <0.05 was considered significant. Statistical analysis was conducted with the use of SPSS computer software.

The authors had full access to and take full responsibility for the integrity of the data. All authors have read and agree to the manuscript as written.


*    Results
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowMethods
*Results
down arrowDiscussion
down arrowReferences
 
Randomization Schematic
Given the planned length of the study, it was decided to add additional test subjects to help ensure that a sufficient sample size was collected to determine a significant difference in cognitive decline if one existed. As a result, a total of 226 patients were randomized to compensate for potentially higher than expected dropout rates. The decision to add subjects was made without breaking the study blind. All randomized patients completed baseline cognitive testing (112 patients in the cell saver group and 114 in the control group). Patients who were not randomized included 5 patients who refused to participate in the study before surgery, 1 patient who sustained cardiac arrest before surgery, and 1 patient whose surgery was cancelled. Cognitive outcome could not be determined at 6-week follow-up in 13 and 15 patients in the cell saver and control groups, respectively (P=0.72). In the cell saver group, the follow-up cognitive testing was not performed in 3 patients because of a change in planned surgical management (1, exploration of the ascending aorta; 1, mitral valve repair; 1, off-pump surgery), and 10 patients refused to participate in the follow-up cognitive testing. In the control group, the follow-up cognitive testing was not performed in 2 patients because of a change in planned surgical management (1, exploration of the ascending aorta; 1, off-pump surgery), 1 patient died, and 12 patients refused to participate in the follow-up cognitive testing.

Demographic Data and Surgical Characteristics
No differences were detected with respect to the baseline demographic data, preoperative variables, and surgical characteristics between the 2 groups (Table 1).


View this table:
[in this window]
[in a new window]

 
Table 1. Demographic Variables and Surgical Characteristics

Neuropsychological Outcomes
Baseline neuropsychological test scores were similar between the 2 groups. The raw neuropsychological test scores are reflected in Table 2.


View this table:
[in this window]
[in a new window]

 
Table 2. Raw Scores of Neuropsychological Tests at Baseline and 6-Week Follow-Up

On the basis of the primary composite outcome, cognitive dysfunction was present in 6% (95% CI, 1.3% to 10.7%) of patients in the cell saver group and 15% (95% CI, 8% to 22%) of patients in the control group (P=0.038). The rates of cognitive improvement were similar between the 2 groups: 19% (95% CI, 11.4% to 26.6%) in the cell saver group versus 17% (95% CI, 9.8% to 24.2%) in the control group (P=0.712) (Figure 1).


Figure 1186885
View larger version (12K):
[in this window]
[in a new window]

 
Figure 1. Rates of improvement (positive bars) and deterioration (negative bars) in neuropsychological test scores 6 weeks after CABG surgery. Values shown are expressed as a percentage of patients outside 1 SD on Z score for each test. CS indicates cell saver group; VF, Verbal Fluency; SSF, Spatial Span Forward; GPB, Grooved Pegboard; RVDLT, Rey Visual Design Learning Test; DSB, Digit Span Backward; RAVLT, Rey Auditory Verbal Learning Test; SSB, Spatial Span Backward; DSF, Digit Span Forward; CRT, Choice Reaction Time; and SRT, Simple Reaction Time. The P value refers to the {chi}2 test for the combined score of the cognitive deterioration variable.

Aortic Atheroma Characteristics
The severity and distribution of atheroma were similar between the 2 groups. A total of 40 (36%) and 42 patients (37%) had atheroma >2 mm present in either the ascending aorta or aortic arch in the cell saver and control groups, respectively (P=0.860).

TCD Findings
Adequate TCD signal was acquired in 43 patients (38%) in the cell saver group and 41 patients (36%) in the control group. Median emboli count was 90 (range, 5 to 1531) in the cell saver and 133 (range, 18 to 1811) in the control group (P=0.31).

Hematologic Parameters and Postoperative Morbidity
The median amount of shed blood recycled via cardiotomy reservoir was 800 mL (range, 175 to 3840 mL). The median amount of red cell concentrate transfused after processing via cell saver was 401 mL (range, 188 to 980 mL).

Patients in the cell saver group had higher hemoglobin levels during the first 24-hour postoperative period. Patients in the control group had higher platelet count and lower international normalized ratio and partial thromboplastin time values at intensive care unit admission. No differences were detected in the discharge hematologic laboratory test values between the 2 groups (Table 3).


View this table:
[in this window]
[in a new window]

 
Table 3. Perioperative Hematologic and Coagulation Laboratory Tests

A total of 28 patients (25%) in the cell saver group and 14 patients (12%) in the control group received fresh frozen plasma (FFP) transfusion at any time during the perioperative period (P=0.018). The FFP transfused group received significantly more cell saver blood then the FFP not transfused group (P<0.0001) (Figure 2). Blood use and postoperative morbidity and mortality are reflected in Table 4.


Figure 2186885
View larger version (11K):
[in this window]
[in a new window]

 
Figure 2. Association between the FFP transfusion rates and the amount of processed cell saver (CS) blood transfusion. The box plot displays the interquartile range representing the 25th (Q1) and 75th (Q3) percentiles. A line across the box is the median. The whiskers represent the lowest and highest observations inside the region. Symbol of plus sign within a circle indicates mean value. The mean amount of the cell saver blood transfused was 632 mL (95% CI, 604 to 660 mL) in the FFP Transfused group and 379 mL (95% CI, 357 to 399 mL) in the FFP Not Transfused group; P=0.0001.


View this table:
[in this window]
[in a new window]

 
Table 4. Comparison of Blood Utilization, Postoperative Complications, and Length of Stay


*    Discussion
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowMethods
up arrowResults
*Discussion
down arrowReferences
 
Replacement of cardiotomy suction with the continuous-flow cell saver is a novel approach to improve neuroprotection and enhance recovery of cognitive function in patients undergoing cardiac surgery. The cell saver separates red cells from plasma and debris by washing and differential centrifugation, providing a high concentration of red blood cells and no or little contaminants.19 The present study demonstrates that "cleansing" of the unprocessed shed blood reduces cognitive decline in elderly patients after CABG surgery. The overall incidence of cognitive dysfunction 6 weeks after surgery was 6% in the cell saver group versus 15% in the cardiotomy suction (control) group. Although our observed rates of cognitive dysfunction are considerably lower than expected at the inception of this study, they are consistent with the recent evidence of cognitive decline after cardiac surgery, ranging from 7.4% to 13.9%.20–22

Cerebral embolization is likely a primary mechanism of central nervous system injury after cardiac surgery.14,23,24 However, the contribution of each type of embolic material (gaseous, solid, or lipid) to the perioperative brain injury is currently unknown. In the present study, the severity and distribution of atheroma (a major contributor to solid particle embolization) were similar between the 2 groups. In addition, no difference existed in the TCD-detected embolic count, predominantly representing larger emboli. Consequently, it is likely that the better cognitive scores in the cell saver group were primarily attributed to the lower lipid cerebral embolic load. This hypothesis is supported by a recent report from Kaza et al,25 who showed that fat particles as small as 10 to 50 µm are effectively removed by the cell saver compared with the cardiotomy suction management strategy. Such microscopic particles of fat would travel through the middle cerebral artery undetected by the TCD devices.

Interestingly, an experimental animal study was performed to determine the brain tolerance to cerebral microemboli, comparing the size versus quantity of the embolic load. The investigators noted that embolic material originating from human carotid atheromatous plaques was composed of various sizes of particles, the smaller particles (20 to 60 µm) being 90 times more common than larger ones (60 to 100 µm). Furthermore, smaller particles were more likely to cause neuronal ischemia and subtle neurological dysfunction, whereas larger particles were more likely to cause brain infarction.26,27 If the same relationship exists during CPB in patients undergoing cardiac surgery, the amount of embolic load to the brain is many-fold greater for smaller emboli. Consequently, one would expect that subtle and diffuse neurological dysfunction would be more common than clinically apparent focal neurological sequelae (ie, stroke). Indeed, this observation has been confirmed by numerous clinical studies.

Recent clinical studies have also emphasized the existence of an association between the cerebral embolic load and the task-orientated reduction in cerebral blood flow in the affected areas of the brain, as identified by functional magnetic resonance imaging.24,28 Furthermore, it is possible that any inflammatory processes that follow an initial embolic insult can considerably modulate the extent of injury resulting in deleterious systemic hemodynamic effects,29 as well as cognitive dysfunction.30,31 In fact, the inflammatory mediators are decreased in cell saver blood,8 and decreased systemic inflammatory response has been observed in patients without cardiotomy suction.32 Therefore, the reduced cognitive decline observed in the cell saver group may also be due to modified systemic inflammatory response with the application of cell saver. However, this hypothesis was not tested directly in our study.

Although the transfusion outcomes were not the primary objective of our study, they deserve some commentary and possibly further prospective evaluation. First, patients in the cell saver group had higher hemoglobin levels during the first 24 hours after surgery; however, the perioperative packed red cell transfusion rates were similar between the 2 groups. Second, patients in the cell saver group had higher international normalized ratio and lower platelet count at the time of intensive care unit admission. These findings are likely a reflection of the principle of the cell saver methodology. Although the cell saver is efficient in removing the detrimental debris from shed blood, it "cleans" the blood from plasma and platelets. The result of this process is a red cell mass with a high hematocrit, which may result in a dilutional coagulopathy if transfused in large quantities. A post hoc analysis showed that the group of patients that received a FFP transfusion had a significant increase in the amount of transfused cell saver blood (Figure 2).

A recent small randomized study by Jewell et al9 showed that postoperative blood loss, hemoglobin concentration, platelet count, and blood product transfusion were similar between the patients managed with either cell saver or cardiotomy suction. Two other studies reported that employment of cell saver was not associated with any adverse impact on coagulation parameters or increased blood product transfusion rates.33,34 However, the extensive use of cell salvage systems to process cardiotomy blood may lead to a critical loss of coagulation factors and platelets, resulting in a bleeding diathesis.35 The findings of our study are in agreement with the latter statement. Recent clinical practice guidelines of perioperative blood transfusion and blood conservation in cardiac surgery prepared by the Society of Thoracic Surgeons and the Society of Cardiovascular Anesthesiologists task forces suggest that on the basis of available evidence, only a weak recommendation for autotransfusion during CPB with a cell-saving device can be made. The authors agreed that most of the studies were too heterogeneous and underpowered to draw firm conclusions.36 A large, prospective, randomized controlled trial with the primary objective concentrating on transfusion outcomes would be required to provide further evidence.

In conclusion, the present report is, to the best of our knowledge, the first randomized controlled trial demonstrating that processing of shed blood with a continuous-flow cell saver results in clinically significant reduction in postoperative cognitive dysfunction after CABG surgery. These findings emphasize the clinical importance of lipid embolization in contributing to postoperative cognitive dysfunction in patients exposed to CPB.


*    Acknowledgments
 
We would like to thank the Fresenius Corporation for making the cell saver device available for the purpose of the study. The authors would like to thank Bobbi Jo Anderson for her assistance in coordinating this project. We would like to acknowledge the support of the Department of Anesthesia, the Division of Cardiac Surgery, and the Perfusionists at Toronto General Hospital, University Health Network and Department of Anesthesia, University of Toronto.

Source of Funding

This study was funded by the Heart and Stroke Foundation of Ontario.

Disclosures

None.


*    References
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowMethods
up arrowResults
up arrowDiscussion
*References
 

  1. Booke M, Fobker M, Fingerhut D, Storm M, Mortlemans Y, Van Aken H. Fat elimination during intraoperative autotransfusion: an in vitro investigation. Anesth Analg. 1997; 85: 959–962.[Abstract]
  2. Booke M, Van Aken H, Storm M, Fritzsche F, Wirtz S, Hinder F. Fat elimination from autologous blood. Anesth Analg. 2001; 92: 341–343.[Abstract/Free Full Text]
  3. Brooker RF, Brown WR, Moody DM, Hammon JW Jr, Reboussin DM, Deal DD, Ghazi-Birry HS, Stump DA. Cardiotomy suction: a major source of brain lipid emboli during cardiopulmonary bypass. Ann Thorac Surg. 1998; 65: 1651–1655.[Abstract/Free Full Text]
  4. Challa VR, Lovell MA, Moody DM, Brown WR, Reboussin DM, Markesbery WR. Laser microprobe mass spectrometric study of aluminium and silicon in brain emboli related to cardiac surgery. J Neuropathol Exp Neurol. 1998; 57: 140–147.[Medline] [Order article via Infotrieve]
  5. Newman MF, Kirchner JL, Phillips-Bute B, Gaver V, Grocott H, Jones RH, Mark DB, Reves JG, Blumenthal JA. Longitudinal assessment of neurocognitive function after coronary-artery bypass surgery. N Engl J Med. 2001; 344: 395–402.[Abstract/Free Full Text]
  6. Newman MF, Grocott HP, Mathew JP, White WD, Landolfo K, Reves JG, Laskowitz DT, Mark DB, Blumenthal JA. Report of the substudy assessing the impact of neurocognitive function on quality of life 5 years after cardiac surgery. Stroke. 2001; 32: 2874–2881.[Abstract/Free Full Text]
  7. Kincaid EH, Jones TJ, Stump DA, Brown WR, Moody DM, Deal DD, Hammon JW Jr. Processing scavenged blood with a cell saver reduces cerebral lipid microembolization. Ann Thorac Surg. 2000; 70: 1296–1300.[Abstract/Free Full Text]
  8. Walpoth BH, Eggensperger N, Hauser SP, Neidhart P, Kurt G, Spaeth PJ, Althaus U. Effects of unprocessed and processed cardiopulmonary bypass blood retransfused into patients after cardiac surgery. Int J Artif Organs. 1999; 22: 210–216.[Medline] [Order article via Infotrieve]
  9. Jewell AE, Akowuah EF, Suvarna SK, Braidley P, Hopkinson D, Cooper G. A prospective randomised comparison of cardiotomy suction and cell saver for recycling shed blood during cardiac surgery. Eur J Cardiothorac Surg. 2003; 23: 633–636.[Abstract/Free Full Text]
  10. Carrier M, Denault A, Lavoie J, Perrault LP. Randomized controlled trial of pericardial blood processing with a cell-saving device on neurologic markers in elderly patients undergoing coronary artery bypass graft surgery. Ann Thorac Surg. 2006; 82: 51–55.[Abstract/Free Full Text]
  11. Ramlawi B, Rudolph JL, Mieno S, Khabbaz K, Sodha NR, Boodhwani M, Levkoff SE, Marcantonio ER, Sellke FW. Serologic markers of brain injury and cognitive function after cardiopulmonary bypass. Ann Surg. 2006; 244: 593–601.[Medline] [Order article via Infotrieve]
  12. Hogue CW Jr, Palin CA, Arrowsmith JE. Cardiopulmonary bypass management and neurologic outcomes: an evidence-based appraisal of current practices. Anesth Analg. 2006; 103: 21–37.[Abstract/Free Full Text]
  13. Shann KG, Likosky DS, Murkin JM, Baker RA, Baribeau YR, DeFoe GR, Dickinson TA, Gardner TJ, Grocott HP, O’Connor GT, Rosinski DJ, Sellke FW, Willcox TW. An evidence-based review of the practice of cardiopulmonary bypass in adults: a focus on neurologic injury, glycemic control, hemodilution, and the inflammatory response. J Thorac Cardiovasc Surg. 2006; 132: 283–290.[Free Full Text]
  14. Djaiani G, Fedorko L, Borger M, Mikulis D, Carroll J, Cheng D, Karkouti K, Beattie S, Karski J. Mild to moderate atheromatous disease of the thoracic aorta and new ischemic brain lesions after conventional coronary artery bypass graft surgery. Stroke. 2004; 35: e356–e358.[Abstract/Free Full Text]
  15. Taylor RL, Borger MA, Weisel RD, Fedorko L, Feindel CM. Cerebral microemboli during cardiopulmonary bypass: increased emboli during perfusionist interventions. Ann Thorac Surg. 1999; 68: 89–93.[Abstract/Free Full Text]
  16. Murkin JM, Newman SP, Stump DA, Blumenthal JA. Statement of consensus on assessment of neurobehavioral outcomes after cardiac surgery. Ann Thorac Surg. 1995; 59: 1289–1295.[Free Full Text]
  17. Rasmussen LS, Larsen K, Houx P, Skovgaard LT, Hanning CD, Moller JT, group TI. The assessment of postoperative cognitive function. Acta Anaesthesiol Scand. 2001; 45: 275–289.[CrossRef][Medline] [Order article via Infotrieve]
  18. Van Dijk D, Jansen EW, Hijman R, Nierich AP, Diephuis JC, Moons KG, Lahpor JR, Borst C, Keizer AM, Nathoe HM, Grobbee DE, De Jaegere PP, Kalkman CJ. Cognitive outcome after off-pump and on-pump coronary artery bypass graft surgery: a randomized trial. JAMA. 2002; 287: 1405–1412.[Abstract/Free Full Text]
  19. Dai B, Wang L, Djaiani G, Mazer CD. Continuous and discontinuous cell-washing autotransfusion systems. J Cardiothorac Vasc Anesth. 2004; 18: 210–217.[CrossRef][Medline] [Order article via Infotrieve]
  20. Keizer AM, Hijman R, Kalkman CJ, Kahn RS, van Dijk D. The incidence of cognitive decline after (not) undergoing coronary artery bypass grafting: the impact of a controlled definition. Acta Anaesthesiol Scand. 2005; 49: 1232–1235.[CrossRef][Medline] [Order article via Infotrieve]
  21. Silbert BS, Scott DA, Evered LA, Lewis MS, Kalpokas M, Maruff P, Myles PS, Jamrozik K. A comparison of the effect of high- and low-dose fentanyl on the incidence of postoperative cognitive dysfunction after coronary artery bypass surgery in the elderly. Anesthesiology. 2006; 104: 1137–1145.[CrossRef][Medline] [Order article via Infotrieve]
  22. Jensen BO, Hughes P, Rasmussen LS, Pedersen PU, Steinbruchel DA. Cognitive outcomes in elderly high-risk patients after off-pump versus conventional coronary artery bypass grafting: a randomized trial. Circulation. 2006; 113: 2790–2795.[Abstract/Free Full Text]
  23. Borger MA, Peniston CM, Weisel RD, Vasiliou M, Green RE, Feindel CM. Neuropsychologic impairment after coronary bypass surgery: effect of gaseous microemboli during perfusionist interventions. J Thorac Cardiovasc Surg. 2001; 121: 743–749.[Abstract/Free Full Text]
  24. Abu-Omar Y, Cader S, Wolf LG, Pigott D, Matthews PM, Taggart DP. Short-term changes in cerebral activity in on-pump and off-pump cardiac surgery defined by functional magnetic resonance imaging and their relationship to microembolization. J Thorac Cardiovasc Surg. 2006; 132: 1119–1125.[Abstract/Free Full Text]
  25. Kaza AK, Cope JT, Fiser SM, Long SM, Kern JA, Kron IL, Tribble CG. Elimination of fat microemboli during cardiopulmonary bypass. Ann Thorac Surg. 2003; 75: 555–559.[Abstract/Free Full Text]
  26. Rapp JH, Pan XM, Sharp FR, Shah DM, Wille GA, Velez PM, Troyer A, Higashida RT, Saloner D. Atheroemboli to the brain: size threshold for causing acute neuronal cell death. J Vasc Surg. 2000; 32: 68–76.[CrossRef][Medline] [Order article via Infotrieve]
  27. Rapp JH, Pan XM, Yu B, Swanson RA, Higashida RT, Simpson P, Saloner D. Cerebral ischemia and infarction from atheroemboli <100 micron in size. Stroke. 2003; 34: 1976–1980.[Abstract/Free Full Text]
  28. Abu-Omar Y, Cifelli A, Matthews PM, Taggart DP. The role of microembolisation in cerebral injury as defined by functional magnetic resonance imaging. Eur J Cardiothorac Surg. 2004; 26: 586–591.[Abstract/Free Full Text]
  29. Westerberg M, Gabel J, Bengtsson A, Sellgren J, Eidem O, Jeppsson A. Hemodynamic effects of cardiotomy suction blood. J Thorac Cardiovasc Surg. 2006; 131: 1352–1357.[Abstract/Free Full Text]
  30. Whitaker D, Stygall J, Harrison M, Newman S. Relationship between white cell count, neuropsychologic outcome, and microemboli in 161 patients undergoing coronary artery bypass surgery. J Thorac Cardiovasc Surg. 2006; 131: 1358–1363.[Abstract/Free Full Text]
  31. Ramlawi B, Rudolph JL, Mieno S, Feng J, Boodhwani M, Khabbaz K, Levkoff SE, Marcantonio ER, Bianchi C, Sellke FW. C-reactive protein and inflammatory response associated to neurocognitive decline following cardiac surgery. Surgery. 2006; 140: 221–226.[CrossRef][Medline] [Order article via Infotrieve]
  32. Westerberg M, Bengtsson A, Jeppsson A. Coronary surgery without cardiotomy suction and autotransfusion reduces the postoperative systemic inflammatory response. Ann Thorac Surg. 2004; 78: 54–59.[Abstract/Free Full Text]
  33. Tempe DK, Banerjee A, Virmani S, Mehta N, Panwar S, Tomar AS, Ghambeer DKS, Nigam M. Comparison of the effects of a cell saver and low-dose aprotinin on blood loss and homologous blood usage in patients undergoing valve surgery. J Cardiothorac Vasc Anesth. 2001; 15: 326–330.[CrossRef][Medline] [Order article via Infotrieve]
  34. Niranjan G, Asimakopoulos G, Karagounis A, Cockerill G, Thompson M, Chandrasekaran V. Effects of cell saver autologous blood transfusion on blood loss and homologous blood transfusion requirements in patients undergoing cardiac surgery on- versus off-cardiopulmonary bypass: a randomised trial. Eur J Cardiothorac Surg. 2006; 30: 271–277.[Abstract/Free Full Text]
  35. Despotis GJ, Filos KS, Zoys TN, Hogue CW Jr, Spitznagel E, Lappas DG. Factors associated with excessive postoperative blood loss and hemostatic transfusion requirements: a multivariate analysis in cardiac surgical patients. Anesth Analg. 1996; 82: 13–21.[Abstract]
  36. Ferraris VA, Ferraris SP, Saha SP, Hessel EA II, Haan CK, Royston BD, Bridges CR, Higgins RS, Despotis G, Brown JR, Spiess BD, Shore-Lesserson L, Stafford-Smith M, Mazer CD, Bennett-Guerrero E, Hill SE, Body S. Perioperative blood transfusion and blood conservation in cardiac surgery: the Society of Thoracic Surgeons and the Society of Cardiovascular Anesthesiologists clinical practice guideline. Ann Thorac Surg. 2007; 83: S27–S86.[Abstract/Free Full Text]

 

CLINICAL PERSPECTIVE

Cerebral microembolization as well as inflammatory response during cardiopulmonary bypass may lead to cognitive decline after cardiac surgery. Currently, transfusion of the unprocessed shed blood (major source of lipid microparticulates and inflammatory mediators) into the patient during cardiopulmonary bypass is common practice to reduce blood loss and blood transfusion. However, processing of shed blood with cell saver before transfusion may reduce the risk of microembolization and/or limit the amount of inflammatory activation. The objective of this study was to determine whether the replacement of cardiotomy suction with a continuous-flow cell saver device would reduce cognitive decline in elderly patients after coronary artery bypass graft surgery. A total of 226 patients were randomly allocated to either cell saver or control groups. Cognitive dysfunction was present in 6% (95% confidence interval, 1.3% to 10.7%) of patients in the cell saver group and 15% (95% confidence interval, 8% to 22%) of patients in the control group 6 weeks after surgery (P=0.038). Whereas the packed red cell and platelet transfusion rates were similar between the 2 groups, the fresh frozen plasma transfusion rates were 25% versus 12% of patients in the cell saver and control groups, respectively (P=0.018). The present report demonstrates that processing of shed blood with a continuous-flow cell saver results in statistically significant reduction in postoperative cognitive dysfunction after coronary artery bypass graft surgery. An association between the fresh frozen plasma transfusion rates and the amount of processed cell saver blood transfusion requires further investigation.


*    Footnotes
 
Clinical trial registration information—URL: http://www.clinicaltrials.gov. Unique identifier: NCT00296985.




This article has been cited by other articles:


Home page
Anesth. Analg.Home page
G. Djaiani, M. Ali, M. A. Borger, A. Woo, J. Carroll, C. Feindel, L. Fedorko, J. Karski, and H. Rakowski
Epiaortic Scanning Modifies Planned Intraoperative Surgical Management But Not Cerebral Embolic Load During Coronary Artery Bypass Surgery
Anesth. Analg., June 1, 2008; 106(6): 1611 - 1618.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
F. D. Rubens, G. A. Wells, and H. J. Nathan
Letter by Rubens et al Regarding Article, "Continuous-Flow Cell Saver Reduces Cognitive Decline in Elderly Patients After Coronary Bypass Surgery"
Circulation, May 27, 2008; 117(21): e348 - e348.
[Full Text] [PDF]


Home page
CirculationHome page
G. Djaiani, L. Fedorko, J. Carroll, J. Karski, M. A. Borger, R. Green, and M. Marcon
Response to Letter Regarding Article, "Continuous-Flow Cell Saver Reduces Cognitive Decline in Elderly Patients After Coronary Bypass Surgery"
Circulation, May 27, 2008; 117(21): e349 - e349.
[Full Text] [PDF]


Home page
Ann. Thorac. Surg.Home page
A. Eyjolfsson, S. Scicluna, P. Johnsson, F. Petersson, and H. Jonsson
Characterization of Lipid Particles in Shed Mediastinal Blood
Ann. Thorac. Surg., March 1, 2008; 85(3): 978 - 981.
[Abstract] [Full Text] [PDF]


Home page
Canadian J. AnesthesiaHome page
H. P. Grocott
Hyperglycemia and postoperative cognitive dysfunction: another call for better glycemic control?/L'hyperglycemie et la dysfonction cognitive postoperatoire : faut-il un meilleur controle de la glycemie?
Can J Anesth, March 1, 2008; 55(3): 140 - 145.
[Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
116/17/1888    most recent
CIRCULATIONAHA.107.698001v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Djaiani, G.
Right arrow Articles by Karski, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Djaiani, G.
Right arrow Articles by Karski, J.
Related Collections
Right arrow Echocardiography
Right arrow CV surgery: coronary artery disease
Right arrow Brain Circulation and Metabolism
Right arrow Doppler ultrasound, Transcranial Doppler etc.
Right arrow Neuroprotectors