Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
Stroke. 2000;31:1817-1823

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
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 arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ackerstaff, R. G. A.
Right arrow Articles by Spencer, M. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ackerstaff, R. G. A.
Right arrow Articles by Spencer, M. P.
Right arrowPubmed/NCBI databases
Medline Plus Health Information
*Stroke

(Stroke. 2000;31:1817.)
© 2000 American Heart Association, Inc.


Original Contributions

Association of Intraoperative Transcranial Doppler Monitoring Variables With Stroke From Carotid Endarterectomy

R. G. A. Ackerstaff, MD; K. G. M. Moons, MD; C. J. W. van de Vlasakker, MD; F. L. Moll, MD; F. E. E. Vermeulen, MD; A. Algra, MD M. P. Spencer, MD

From St. Antonius Hospital (R.G.A.A., K.G.M.M., F.L.M., F.E.E.V.), Nieuwegein; Slingeland Hospital (C.J.W.v.d.V.), Doetinchem; Julius Center for General Practice and Patient Oriented Research (A.A.); and the Department of Neurology (A.A.), University Medical Center Utrecht, Utrecht, the Netherlands; and Spencer Technologies (M.P.S.), Seattle, Wash.

Correspondence to R.G.A. Ackerstaff, MD, St. Antonius Hospital, Nieuwegein, Postbus 2500, 3430 EM Nieuwegein, Utrecht, The Netherlands. E-mail knf{at}antonius.net


*    Abstract
up arrowTop
*Abstract
down arrowIntroduction
down arrowSubjects and Methods
down arrowResults
down arrowDiscussion
down arrowReferences
 
Background and Purpose—The outcomes of carotid endarterectomy (CEA) are, in addition to patient baseline characteristics, highly dependent on the safety of the surgical procedure. During the successive stages of the operation, transcranial Doppler (TCD) monitoring of the middle cerebral artery (MCA) was used to assess the association of cerebral microembolism and hemodynamic changes with stroke and stroke-related death.

Methods—By use of data pooled from 2 hospitals in the United States and the Netherlands, including 1058 patients who underwent CEA, the association of various TCD emboli and velocity variables with operative stroke and stroke-related death was evaluated by univariable and multivariable logistic regression analyses in combination with receiver operating characteristic (ROC) curve analyses. The impact of basic patient characteristics, such as age, sex, preoperative cerebral symptoms, and ipsilateral and contralateral internal carotid artery stenosis, on the prediction of operative stroke was also evaluated.

Results—We observed 31 patients with ischemic and 8 patients with hemorrhagic operative strokes. Four of these patients died. Emboli during dissection (odds ratio [OR] 1.5, 95% CI 0.8 to 2.9) and wound closure (OR 2.3, 95% CI 1.2 to 4.4) as well as >=90% decrease of MCA peak systolic velocity at cross-clamping (OR 3.3, 95% CI 1.3 to 8.5) and >=100% increase of the pulsatility index of the Doppler signal at clamp release (OR 7.1, 95% CI 1.4 to 35.7) were independently associated with stroke. The ROC area of this model was 0.69. Of the patient characteristics, only preoperative cerebral ischemia (OR 1.9, 95% CI 1.0 to 3.7) and >=70% ipsilateral internal carotid artery stenosis (OR 0.5, 95% CI 0.2 to 0.9) were associated with stroke. Adding these patient characteristics to the model, the area under the ROC curve increased to 0.73.

Conclusions—In CEA, TCD-detected microemboli during dissection and wound closure, >=90% MCA velocity decrease at cross-clamping, and >=100% pulsatility index increase at clamp release are associated with operative stroke. In combination with the presence of preoperative cerebral symptoms and >=70% ipsilateral internal carotid artery stenosis, these 4 TCD monitoring variables reasonably discriminate between patients with and without operative stroke. This supports the use of TCD as a potential intraoperative monitoring modality to alter the surgical technique by enhancing a decrease of the risk of stroke during or immediately after the operation.


Key Words: carotid endarterectomy • monitoring, intraoperative • stroke • surgery • ultrasonography, Doppler, transcranial


*    Introduction
up arrowTop
up arrowAbstract
*Introduction
down arrowSubjects and Methods
down arrowResults
down arrowDiscussion
down arrowReferences
 
The beneficial effects of carotid endarterectomy (CEA) in symptomatic and asymptomatic patients with high-grade carotid artery stenosis have been published in detail in 3 previous studies.1 2 3 However, the risk of carotid surgery must be set against its benefits, and unfortunately, the risks are not negligible. In all 3 studies, a small percent (3% to 5%) of the patients who underwent surgery had disabling or nondisabling strokes or died during or just after surgery. Therefore, the safety of the surgical procedure is of paramount importance, and it is essential to place emphasis on the prevention of neurological complications. Many techniques of quality control during CEA have been used to warn the surgeon of the possibility of an adverse outcome. Intraoperative transcranial Doppler (TCD) monitoring provides online surveillance of both hemodynamic changes and cerebral microembolism in the middle cerebral artery (MCA) on the side of surgery.4 5 6 7 8 9

We have previously reported on our separate experience with TCD monitoring and its usefulness with regard to microemboli detection in CEA.4 5 However, these studies were primarily designed to examine the suitability of intraoperative TCD monitoring. Because there were low complication rates and because the clinical relevance of cerebral embolism during CEA still requires further foundation, we performed a pooled data analysis on 2 studies executed in Seattle, Wash, and Nieuwegein, the Netherlands, to increase the number of patients.

In the present study, we analyzed whether intraoperative cerebral embolism as detected by TCD during different stages of CEA was associated with the occurrence of operative stroke (ischemic and hemorrhagic) and stroke-related death within 7 days after surgery. Additionally, we evaluated the association of intraoperative TCD velocity variables with outcome. The identification of emboli and velocity variables as predictors of stroke by TCD monitoring may be useful in stratifying patients during surgery according to their risk of operative stroke and can help the surgeon to improve his or her technique.


*    Subjects and Methods
up arrowTop
up arrowAbstract
up arrowIntroduction
*Subjects and Methods
down arrowResults
down arrowDiscussion
down arrowReferences
 
Patients
The present study is based on individual patient data pooled from the data sets of 2 former studies involving intraoperative TCD monitoring in CEA from 2 major institutes: Spencer Technologies, Seattle, Wash, and St. Antonius Hospital, Nieuwegein, the Netherlands. The methods of both studies are described elsewhere.6 7 8 9 In brief, the Dutch data concern the period from April 1990 until January 1996 and include 602 patients; the American data concern the period between October 1985 and July 1994 and include 456 patients. Only patients with reliable TCD monitoring throughout the entire operation entered the study. No patients who underwent endarterectomy of only the external carotid artery were included, and none had other concurrent surgical procedures. In patients who underwent a second CEA (ipsilaterally or contralaterally), only the first operation was analyzed in the present study. Special efforts were made to conform the definitions of all documented variables used in both countries.

Carotid Endarterectomy
In the vast majority of patients, the operation was performed by general anesthesia with the use of nitrous oxide and halothane or isoflurane. In the American study, in 20 cases, surgery was performed in conscious patients with local-regional anesthetic techniques. In both countries, surgery was executed by an experienced vascular surgeon or by a specialist vascular trainee, and there were no significant differences with respect to specific qualities in the performance of CEA. Before cross-clamping, an intravenous injection of heparin (5000 IU) was administered; protamine reversal was not used. In Nieuwegein, all patients were given a standardized preoperative antiplatelet treatment of 100 mg aspirin daily, whereas in Seattle, aspirin was always canceled before surgery.

TCD Monitoring
The methods of intraoperative TCD monitoring have been described elsewhere.6 7 8 9 Besides hemodynamic changes at cross-clamping and clamp release, in the present study, special interest was paid to the occurrence of embolic transients according to the criteria described by the consensus committee.10 With regard to the criteria for shunting, there were important differences between the Dutch and American studies. In Nieuwegein, a shunt was selectively used on the basis of EEG and TCD criteria, as described in an earlier report.7 In Seattle, some surgeons always shunted regardless of the information provided by TCD, and some surgeons developed in the course of time reliance on TCD data to determine whether or not a shunt was to be placed. In general, in both countries the criteria for shunting based on TCD consisted of a drop in MCA velocity to <30% to 40% of intraoperative pre–cross-clamp value. The Doppler spectra were observed in the operating room by an experienced sonographer, and the audio Doppler signal was made audible throughout the entire operation. Moreover, for offline analysis, the Doppler signals were continuously recorded on video or digital audiotape. In each stage of the operation, microemboli were counted. The identification and counting of microemboli were performed without the use of automatic emboli detection software. On the basis of previous experience,4 5 11 the following TCD emboli and TCD velocity variables that were thought to be associated with adverse outcome were analyzed in the present study.

TCD Emboli Variables
Emboli occurred during (1) dissection (skin preparation to carotid clamping), (2) shunt manipulation (shunt introduction to removal of shunt), (3) clamp release (the first 10 seconds at restoration of flow through the carotid arteries), and (4) wound closure (termination of manipulation to the end of recording, {approx}30 minutes after final restoration of flow). In patients who were not shunted, emboli that occurred during shunting were considered absent. Additionally, a new variable of the number of stages or periods during which emboli occurred was evaluated. This number varied from 0 (no emboli detected) to 4 (emboli occurred during each of the above 4 stages or periods).The possible impact of microemboli during the postoperative stage on clinical outcome was not analyzed.

TCD Velocity Variables
TCD velocity variables were as follows: (1) decrease of peak systolic velocity (PSV) at cross-clamping, (2) increase of PSV, and (3) increase of the Gosling pulsatility index (PI) of the Doppler signal at declamping at the end of the endarterectomy. All 3 velocity variables were computed from the envelope of the Doppler spectrum by the TCD equipment and calculated as the proportional change compared with intraoperative preclamp values.

Preoperative Patient Characteristics
Age, sex, preoperative cerebral symptoms, and ipsilateral and contralateral internal carotid artery stenosis assessed by duplex ultrasonography and digital arteriography were also documented.

Outcome
In both centers, a complete hospital chart review was performed to obtain information about clinical outcome. In patients with possible postoperative cerebral deficit, a neurological consultation was executed by a neurologist. New cerebral deficits persisting for >24 hours were regarded as stroke. Operative stroke was defined per patient and not per operation. In the analyses, we focused on the prediction of ischemic and hemorrhagic stroke and stroke-related death within 7 days after surgery.

Data Analysis
First, within each country, the association between the occurrence of stroke and stroke-related death and each of all above-mentioned TCD variables and preoperative patient characteristics was quantified by use of univariable logistic regression analysis. The odds ratio (OR) and 95% CI were used as measures of association. A variable with a 95% CI that does not include the value 1 can be considered statistically significantly associated with a value of P<0.05. If a test for homogeneity showed no major heterogeneity (P>0.10) of the associations, the ORs were pooled by use of the Mantel-Haenszel method. Continuous variables were initially included without categorization as long as a linear relation was plausible, but various cutoff values and transformations (eg, square root and log) were assessed as well.12 Age showed a linear relation with outcome, but the 3 TCD velocity variables did not. The latter were dichotomized at clinically relevant thresholds on the basis of previous results13 or marked differences in actual stroke incidence. Hence, decrease of PSV at cross-clamping was dichotomized at 90%, and increases of PSV and Gosling PI at clamp release were dichotomized at 100%.

Our aim was not to develop a prediction model primarily based on preoperative clinical and angiographic characteristics but to assess whether and which TCD emboli and velocity variables were associated with adverse outcome. Accordingly, we first estimated which of the 4 TCD emboli variables was independently associated with outcome by use of multivariable logistic regression modeling. Because the aim of these analyses is the prediction of stroke, all variables contributing prognostic information should be included in the model.14 Therefore, as is common in prediction research, we defined an independent association if the OR had a value of P<=0.10. Starting with a model including all 4 TCD emboli variables, the nonsignificant (P>0.10) ones were excluded. This model was extended with the univariate significant (P<=0.10) TCD velocity variables, and the same method of model reduction then was performed. Finally, this last model was extended with the documented preoperative patient characteristics that were significant in the univariate analyses to evaluate whether they additionally contributed to the TCD variables in the prediction of complications, resulting in the final model. Of each model, the ability to discriminate between patients with and without complications was estimated by using the area under the receiver operating characteristic (ROC) curve.14 15 The ROC area is a suitable parameter to summarize the predictive or discriminative ability of a model and can range from 0.5 (useless model, such as a coin flip) to 1.0 (perfect discrimination). A value >0.7 can be interpreted as reasonable, and a value >0.8 can be interpreted as good.16 Differences in discriminative value between models were estimated by differences in ROC area with 95% CI, taking into account the correlation between the models because they were based on the same cases.17 18

Of all 1058 cases, 108 had missing values on >=1 variable (but not on the outcome or TCD emboli variables). To decrease bias and increase statistical efficiency, these missing values were filled in (imputed) by using the expectation maximization method.19 20 Such imputation is based on the correlation between each variable with missing values and all other variables. These correlations were estimated from the 950 complete cases. The results of the analyses based on the complete subject data and on all subject data after imputation were compared. Because this yielded no different results (ie, the same independent predictors were selected with similar regression coefficients), only the latter (imputed) approach is presented.


*    Results
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowSubjects and Methods
*Results
down arrowDiscussion
down arrowReferences
 
Table 1Down shows the distribution of patient characteristics, outcome, and the TCD emboli and velocity variables for both countries separately and in the pooled data set. In all stages of surgery, the number of microemboli assessed by TCD was higher in Seattle than in Nieuwegein. Differences across the countries were also present for the shunt ratio, proportional PSV and PI increase at clamp release, preoperative cerebral ischemia, and >=70% ipsilateral internal carotid artery stenosis. However, the ORs for all variables with the outcome (stroke), except for sex (OR 2.7 and 95% CI 0.6 to 12.1 for the United States versus OR 0.4 and 95% CI 0.2 to 0.8 for the Netherlands) and >=70% contralateral internal carotid artery stenosis (OR 0.4 and 95% CI 0.1 to 1.9 for the United States versus OR 1.9 and 95% CI 0.8 to 4.3 for the Netherlands), were reasonably homogeneous between the 2 countries. In the pooled data set, in 39 (3.7%) of 1058 CEAs, surgery resulted in a stroke. Thirty-one patients developed an ischemic stroke, and 8 patients developed a hemorrhagic stroke. Four patients died from their strokes.


View this table:
[in this window]
[in a new window]
 
Table 1. Patient Characteristics, TCD Emboli and Velocity Variables, and Outcome of Study Population

As shown in Table 2Down, only emboli during dissection (P=0.03) and wound closure (P=0.002) showed a statistically significant association with outcome. Emboli during shunting were also associated with outcome, although only borderline significance (P=0.12) was reached. We also analyzed the impact of the number of embolic periods per operation. Table 2Down delineates that patients with no or only 1 embolic period per operation were less often suffering from stroke than those with >=2 embolic periods. After dichotomization, the TCD emboli variable >=2 embolic periods showed a significant association with stroke (P=0.01). All 3 TCD velocity variables also showed a statistically significant association with outcome. Of the preoperative patient characteristics, only preoperative cerebral ischemia (excluding amaurosis fugax [AFx]) was associated with an increased risk of stroke. For >=70% ipsilateral internal carotid artery stenosis, the association was inverse. Age (whether analyzed as a continuous or as a dichotomous variable with a cutoff of 75 years), sex, and >=70% contralateral internal carotid artery stenosis were not statistically significant.


View this table:
[in this window]
[in a new window]
 
Table 2. Association of Each TCD Variable and Other Patient Characteristics With the Occurrence of Stroke in the Pooled Data Set

After including all 4 TCD emboli variables (dissection, clamp release, wound closure, and shunting) in a multivariable logistic regression model, emboli during dissection and wound closure were independently associated with outcome, whereas emboli during shunting (OR 1.2, 95% CI 0.6 to 2.5) and during clamp release (OR 0.9, 95% CI 0.4 to 1.7) were far from significant. The model including only emboli during dissection and wound closure is given in Table 3Down (model 1). The ROC area of this model was 0.66. The association was weaker for emboli during dissection (P=0.12) than for emboli during wound closure (P=0.007). Inclusion of the number of embolic periods, as 4 indicator variables or dichotomized at a value of >=2 embolic periods, did not improve the model. After adding the 3 TCD velocity variables to model 1, >=90% decrease of PSV at cross-clamping (P=0.02) and >=100% PI increase at clamp release (P=0.02) as well as both embolic variables were associated with outcome (model 2, Table 3Down). However, emboli during dissection became less significant (P=0.18). The ROC area increased to 0.69. Subsequently, model 2 was extended with the 2 univariably significant preoperative patient characteristics. This resulted in an ROC area of 0.73 (model 3, Table 3Down). Of this latter model, all variables were associated with outcome; only emboli during dissection again became less significant (P=0.20).


View this table:
[in this window]
[in a new window]
 
Table 3. Results of Multivariable Logistic Regression Analyses

We also performed the analyses without the 20 patients from the American study who underwent CEA with local-regional anesthesia. However, no differences in the results (ie, the same independent predictors with the same ORs) were found.


*    Discussion
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowSubjects and Methods
up arrowResults
*Discussion
down arrowReferences
 
The present study evaluated which intraoperative TCD emboli and velocity variables were independently associated with operative stroke and stroke-related death from CEA. We found that microemboli that occurred during dissection and wound closure were associated with stroke, whereas microemboli that occurred at clamp release and during shunting were clinically irrelevant. These associations remained after taking into account the TCD velocity variables and various preoperative patient characteristics. Of the TCD velocity variables, >=90% PSV decrease at cross-clamping and >=100% PI increase at clamp release were associated with outcome, independent from the TCD emboli variables and preoperative patient characteristics. The independent patient characteristics were preoperative cerebral ischemia (excluding AFx) and >=70% ipsilateral internal carotid artery stenosis. These results suggest that intraoperative TCD monitoring can be useful in providing an early warning of postoperative complications in patients undergoing CEA.

The results of the present study are consistent with the literature. Previous studies involving cerebral microembolism during CEA have shown that microemboli that occur at clamp release are predominantly gaseous and are not associated with the development of postoperative cerebral deficits.21 During shunting, microemboli are mostly a mixture of air and particulate and are sometimes associated with perioperative complications.4 On the contrary, microemboli that are noticed during dissection and wound closure are particulate and are associated with new mostly transient operative cerebral complications and psychometric deterioration.21 22 Moreover, Jansen et al23 demonstrated an association between multiple microembolism during dissection and new white matter lesions on MRI of the brain made after surgery. However, in the majority of these patients, the new MRI lesions were clinically silent. This finding demonstrates that during CEA the incidence of TCD-detected microemboli far exceeds the morbidity and mortality rates for the operation. However, this does not mean that these phenomena are not clinically important. Strokes that occur during the dissection stage of CEA were reported before the introduction of TCD monitoring, but this was previously thought to be due to the development of one large embolus. Although occlusion of the MCA mainstem by a macroembolus sometimes occurs,24 most research work involving intraoperative TCD monitoring in CEA suggests that multiple microembolization is the more likely mechanism. Microemboli that occur at the end of the operation are possibly a precursor of the well-known phenomenon of postoperative platelet aggregation and thrombus formation at the endarterectomy and clamping sites. This supports the hypothesis that multiple microembolization may result in sustaining postoperative embolization and occlusion.25 26 27 28 29 The latter could not be verified in the present study because postoperative TCD monitoring was not performed in the majority of our patients. The associations we have found between >=90% PSV decrease at cross-clamping and >=100% PI increase at clamp release with postoperative stroke are also supported by earlier evidence.6 13 30 31 32 In a multicenter study of CEA with intraoperative TCD monitoring, Halsey30 showed that severe persisting ischemia without shunting often results in an operative stroke. With respect to a postoperative hyperperfusion syndrome, Dalman et al13 demonstrated that TCD monitoring is a practical and sensitive method to identify intraoperatively the patients who are at risk for this serious postoperative complication. The association of >=70% ipsilateral internal carotid artery stenosis with outcome was inverse, as described previously.33 Although this seems paradoxical, it can be explained from a hemodynamic point of view: cross-clamping of a severely stenosed artery will have less influence on cerebral blood flow than cross-clamping of an artery with a lesser degree of stenosis. It was not our intention to develop a prediction model primarily based on preoperative clinical and angiographic predictors of stroke from CEA, as described elsewhere.34 35 36 Nevertheless, we did evaluate such a model, including all available preoperative patient characteristics. Again, only preoperative cerebral ischemia (excluding AFx) and >=70% ipsilateral internal carotid artery stenosis were associated with outcome with a ROC area of 0.67. Besides preoperative cerebral symptoms, Rothwell et al34 also found age, female sex, hypertension, and peripheral vascular disease as predictors of stroke from CEA. In the present study, age was not associated with outcome. Female sex was very heterogeneously distributed over the 2 countries and could not be analyzed properly, whereas the other 2 variables were not available for our patients. Also, if we repeated the analysis of our data starting with the preoperative patient characteristics, the final model would be the same as model 3 presented in Table 3Up.

Given all available evidence, we believe that intraoperative TCD monitoring is useful for early detection of postoperative complications in patients undergoing CEA. If the Doppler signal is made audible in the operating theater, the acoustic feedback to the surgeon can assist in a more careful dissection of the artery and facilitate an early distal clamping of the internal carotid artery. Sustained embolization during wound closure is probably an indication of a residual luminal thrombus and impending postoperative occlusion. In these cases, quality control with intraoperative duplex37 and completion angioscopy38 can modify the surgical technique and reduce the number of cerebral complications. Although it can be argued that the majority of microemboli during shunting and clamp release are microbubbles and are clinically less important, one must not overlook the fact that lengthy showers of presumed gaseous emboli can contain particulate emboli as well. Therefore, it is preferable to minimize embolization at times of shunt opening and flow restoration. With respect to hemodynamic causes of stroke from CEA, TCD monitoring is a very useful modality for the selective use of a shunt and a sensitive tool for the prediction of postoperative hyperperfusion. When a serious event happens despite all these precautions, the best medical treatment and imaging of the brain and carotid arteries can be started without any delay. In several centers, the operative stroke rate from CEA has declined since the introduction of intraoperative TCD monitoring.4 5 37

To appreciate the present results, a few aspects need to be discussed. First, because we have performed a pooled data analysis over 2 countries, differences in definitions and, therefore, in distributions may have occurred. This was likely for emboli during dissection, clamp release, and shunting, as well as for PI increase at clamp release. This could have biased our findings, although the associations of the investigated factors were not heterogeneous across the countries. Moreover, in daily practice, similar differences between countries and medical institutions will be present, and risk estimates should be sufficiently robust to overcome any heterogeneity. Second, in contrast to other studies33 34 35 that evaluated the association of preoperative patient characteristics with stroke from CEA, we evaluated whether clinically relevant intraoperative TCD emboli and velocity variables were associated with outcome, taking into account some always available basic patient characteristics. Third, in both countries, the data are from the first years of carotid surgery with TCD monitoring; thus, the presence of a learning effect will be likely. Particularly with respect to emboli detection, surgeons developed, in the course of time, an understanding of and reliance on the TCD data.

In conclusion, we have determined that TCD-detected microembolism during dissection and especially during wound closure as well as >=90% MCA velocity decrease at cross-clamping and >=100% PI increase at clamp release were associated with operative stroke and stroke-related death from CEA. To our knowledge, the association with stroke has not been demonstrated before, certainly not by using a multivariable approach that takes into account some basic preoperative patient characteristics. We believe that TCD monitoring is most useful in providing an early warning of unpredictable phenomena. It should be used as a quality control assessment for early detection of microemboli and MCA velocity changes during surgery to modify the surgical technique. This would reduce the number of cerebral complications.

Received March 9, 2000; revision received April 5, 2000; accepted April 18, 2000.


*    References
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowSubjects and Methods
up arrowResults
up arrowDiscussion
*References
 
1. European Carotid Surgery Trialists’ Collaborative Group. Randomised trial of endarterectomy for recently symptomatic carotid stenosis: final results of the MRC European Carotid Surgery Trial (ECST). Lancet. 1988;351:1379–1387.

2. Barnett HJM, Taylor DW, Eliasziw M, Fox AJ, Ferguson GG, Haynes RB, Rankin RN, Clagett GP, Hachinski VC, Sackett DL, Thorpe KE, Meldrum HE, for the North American Symptomatic Carotid Endarterectomy Trial Collaborators. Benefit of carotid endarterectomy in patients with symptomatic moderate or severe stenosis. N Engl J Med. 1998;339:1415–1425.[Abstract/Free Full Text]

3. Executive Committee for the Asymptomatic Carotid Atherosclerosis Study. Endarterectomy for asymptomatic carotid artery stenosis. JAMA. 1995;273:1421–1428.[Abstract/Free Full Text]

4. Ackerstaff RGA, Jansen C, Moll FL, Vermeulen FEE, Hamerlijnck RPHM, Mauser HW. The significance of microemboli detection by means of transcranial Doppler ultrasonography monitoring in carotid endarterectomy. J Vasc Surg. 1995;21:963–969.[Medline] [Order article via Infotrieve]

5. Spencer MP. Transcranial Doppler monitoring and the causes of stroke from carotid endarterectomy. Stroke. 1997;28:685–691.[Abstract/Free Full Text]

6. Jansen C, Vriens EM, Eikelboom BC, Vermeulen FEE, van Gijn J, Ackerstaff RGA. Carotid endarterectomy with transcranial Doppler and electroencephalographic monitoring: a prospective study in 130 operations. Stroke. 1993;24:665–669.[Abstract/Free Full Text]

7. Jansen C, Moll FL, Vermeulen FEE, van Haelst MPI, Ackerstaff RGA. Continuous transcranial Doppler ultrasonography and electroencephalography during carotid endarterectomy: a multimodal monitoring system to detect intraoperative ischemia. Ann Vasc Surg. 1993;7:95–101.[Medline] [Order article via Infotrieve]

8. Spencer MP, Thomas GI, Nicholls SC, Sauvage LR. Detection of middle cerebral artery emboli during carotid endarterectomy using transcranial Doppler ultrasonography. Stroke. 1990;21:415–423.[Abstract/Free Full Text]

9. Ghali R, Palazzo EG, Rodriguez DI, Zammit M, Loudenback DL, DeMuth RP, Spencer MP, Sauvage LR. Transcranial Doppler intraoperative monitoring during carotid endarterectomy: experience with regional or general anesthesia, with and without shunting. Ann Vasc Surg. 1997;11:9–13.[Medline] [Order article via Infotrieve]

10. Basic identification criteria of Doppler microembolic signals: Consensus Committee of the Ninth Cerebral Hemodynamic Symposium. Stroke. 1995;26:1123.[Free Full Text]

11. Jansen C, Ramos LMP, van Heesewijk JPM, Moll FL, van Gijn J, Ackerstaff RGA. Impact of microembolism and hemodynamic changes in the brain during carotid endarterectomy. Stroke. 1994;25:992–997.[Abstract]

12. Harrell FE, Lee KL, Pollock BG. Regression models in clinical studies: determining relationships between predictors and response. J Natl Cancer Inst. 1988;80:1198–1202.[Abstract/Free Full Text]

13. Dalman JE, Beenakkers ICM, Moll FL, Leusink JA, Ackerstaff RGA. Transcranial Doppler monitoring during carotid endarterectomy helps to identify patients at risk of postoperative hyperperfusion. Eur J Vasc Endovasc Surg. 1999;18:222–227.[Medline] [Order article via Infotrieve]

14. Harrell FE, Lee KL, Mark DB. Multivariable prognostic models: issues in developing models, evaluating assumptions and adequacy, and measuring and reducing errors. Stat Med. 1996;15:361–387.[Medline] [Order article via Infotrieve]

15. Hanley JA, McNeil BJ. The meaning and use of the area under a receiver operating characteristic (ROC) curve. Radiology. 1982;143:29–36.[Abstract/Free Full Text]

16. Weinstein MC, Fineberg HV. Clinical Decision Analysis. Philadelphia, Pa: WB Saunders Co; 1980.

17. Hanley JA, McNeil BJ. A method of comparing the areas under receiver operating characteristic curves derived from the same cases. Radiology. 1983;148:839–843.[Abstract/Free Full Text]

18. Delong ER, Delong DM, Clarke-Pearson DL. Comparing the areas under two or more correlated receiver operating characteristic curves: a non parametric approach. Biometrics. 1988;44:817–845.

19. Greenland S, Finkle WD. A critical look at methods for handling missing covariates in epidemiologic regression analyses. Am J Epidemiol. 1995;142:1255–1264.[Abstract/Free Full Text]

20. Little RA. Regression with missing X’s: a review. J Am Stat Assoc. 1992;87:1227–1237.

21. Gaunt ME. Transcranial Doppler: preventing stroke during carotid endarterectomy. Ann R Coll Surg Engl. 1998;80:377–387.[Medline] [Order article via Infotrieve]

22. Gaunt ME, Martin PJ, Smith JL, Rimmer T, Cheerman G, Ratliff DA, Bell PRF, Naylor AR. Clinical relevance of intraoperative embolization detected by transcranial Doppler ultrasonography during carotid endarterectomy: a prospective study of 100 patients. Br J Surg. 1994;81:1435–1439.[Medline] [Order article via Infotrieve]

23. Jansen C, Ramos LMP, van Heesewijk JPM, Moll FL, van Gijn J, Ackerstaff RGA. Impact of microembolism and hemodynamic changes in the brain during carotid endarterectomy. Stroke. 1994;25:992–997.

24. Claus SP, Louwerse ES, Mauser HW, van der Mee M, Moll FL, Mess WH, Ackerstaff RGA. Temporary occlusion of middle cerebral artery by macroembolism in carotid surgery. Cerebrovasc Dis. 1999;9:261–264.[Medline] [Order article via Infotrieve]

25. Stratton JR, Zierler RE, Kazmers A. Platelet deposition at carotid endarterectomy sites in humans. Stroke. 1987;18:722–727.[Abstract/Free Full Text]

26. Lennard N, Smith J, Dumville J, Abbott R, Evans DH, London NJM, Bell PRF, Naylor AR. Prevention of postoperative thrombotic stroke after carotid endarterectomy: the role of transcranial Doppler ultrasound. J Vasc Surg. 1997;26:579–584.[Medline] [Order article via Infotrieve]

27. Levi CR, O’Malley HMO, Fell G, Roberts AK, Hoare MC, Royle JP, Chan A, Beiles BC, Chambers BR, Bladin CF, Donnan GA. Transcranial Doppler detected cerebral microembolism following carotid endarterectomy: high microembolic signal loads predict postoperative cerebral ischaemia. Brain. 1997;120:621–629.[Abstract/Free Full Text]

28. Levi CR, Roberts AK, Fell G, Hoare MC, Royle JP, Chan A, Beiles BC, Last GC, Bladin CF, Donnan GA. Transcranial Doppler microembolus detection in the identification of patients at high risk of perioperative stroke. Eur J Vasc Endovasc Surg. 1997;14:170–176.[Medline] [Order article via Infotrieve]

29. Cantelmo NL, Babikian VL, Samaraweera RN, Gordon JK, Pochay VE, Winter MR. Cerebral microembolism and ischemic changes associated with carotid endarterectomy. J Vasc Surg. 1998;27:1024–1031.[Medline] [Order article via Infotrieve]

30. Halsey JH. Risks and benefits of shunting in carotid endarterectomy. Stroke. 1992;23:1583–1587.[Abstract/Free Full Text]

31. Spencer MP, Thomas GI, Moehring MA. Relation between middle cerebral artery blood flow velocity and stump pressure during carotid endarterectomy. Stroke. 1992;23:1439–1445.[Abstract/Free Full Text]

32. Jansen C, Sprengers AM, Moll FL, Vermeulen FEE, Hamerlijnck RPHM, van Gijn J, Ackerstaff RGA. Prediction of intracerebral haemorrhage after carotid endarterectomy by clinical criteria and intraoperative transcranial Doppler monitoring: results of 233 operations. Eur J Vasc Surg. 1994;8:220–225.[Medline] [Order article via Infotrieve]

33. Jansen C. Static and dynamic risk factors in carotid endarterectomy: results of logistic regression analysis in 301 patients. In: Monitoring of Cerebral Function During Carotid Endarterectomy With Electroencephalography and Transcranial Doppler Ultrasonography [PhD thesis]. Utrecht, the Netherlands: 1994.

34. Rothwell PM, Slattery J, Warlow CP. Clinical and angiographic predictors of stroke and death from carotid endarterectomy: systematic review. BMJ. 1997;315:1571–1577.[Abstract/Free Full Text]

35. Rothwell PM, Slattery J, Warlow CP. A systematic review of the risks of stroke and death due to endarterectomy for symptomatic carotid stenosis. Stroke. 1996;27:260–265.[Abstract/Free Full Text]

36. Rothwell PM, Slattery J, Warlow CP. A systematic comparison of the risks of stroke and death due to carotid endarterectomy for symptomatic and asymptomatic stenosis. Stroke. 1996;27:266–269.[Abstract/Free Full Text]

37. Padayachee TS, Brooks MD, Modaresi KB, Arnold AJ, Self GW, Taylor PR. Intraoperative high resolution duplex imaging during carotid endarterectomy: which abnormalities require surgical correction? Eur J Vasc Endovasc Surg. 1998;15:387–393.[Medline] [Order article via Infotrieve]

38. Lennard N, Smith JL, Gaunt ME, Abbott RJ, London NJM, Bell PRF, Naylor AR. A policy of quality control assessment helps to reduce the risk of intraoperative stroke during carotid endarterectomy. Eur J Vasc Endovasc Surg. 1999;17:234–240.[Medline] [Order article via Infotrieve]




This article has been cited by other articles:


Home page
StrokeHome page
R. E. Latchaw, M. J. Alberts, M. H. Lev, J. J. Connors, R. E. Harbaugh, R. T. Higashida, R. Hobson, C. S. Kidwell, W. J. Koroshetz, V. Mathews, et al.
Recommendations for Imaging of Acute Ischemic Stroke: A Scientific Statement From the American Heart Association
Stroke, November 1, 2009; 40(11): 3646 - 3678.
[Full Text] [PDF]


Home page
StrokeHome page
M. Skjelland, K. Krohg-Sorensen, B. Tennoe, S. J. Bakke, R. Brucher, and D. Russell
Cerebral Microemboli and Brain Injury During Carotid Artery Endarterectomy and Stenting
Stroke, January 1, 2009; 40(1): 230 - 234.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
K. Ogasawara, Y. Suga, M. Sasaki, K. Chida, M. Kobayashi, K. Yoshida, Y. Otawara, and A. Ogawa
Intraoperative Microemboli and Low Middle Cerebral Artery Blood Flow Velocity Are Additive in Predicting Development of Cerebral Ischemic Events After Carotid Endarterectomy
Stroke, November 1, 2008; 39(11): 3088 - 3091.
[Abstract] [Full Text] [PDF]


Home page
PERSPECT VASC SURG ENDOVASC THERHome page
B. G. DeRubertis
Embolization During Carotid Angioplasty and Stenting : What Is the Optimal Method for Detecting Embolic Debris and Its Sequelae?
Perspectives in Vascular Surgery and Endovascular Therapy, September 1, 2008; 20(3): 260 - 269.
[Abstract] [PDF]


Home page
HeartHome page
A. Angelini, M. Della Barbera, and G. Thiene
Interventional procedures for atherothrombosis: pathology of retrieved material
Heart, October 1, 2007; 93(10): 1301 - 1308.
[Full Text] [PDF]


Home page
Br J AnaesthHome page
S. J. Howell
Carotid endarterectomy
Br. J. Anaesth., July 1, 2007; 99(1): 119 - 131.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
M.D. Hill, W. Morrish, G. Soulez, A. Nevelsteen, G. Maleux, C. Rogers, K.E. Hauptmann, A. Bonafe, R. Beyar, L. Gruberg, et al.
Multicenter evaluation of a self-expanding carotid stent system with distal protection in the treatment of carotid stenosis.
AJNR Am. J. Neuroradiol., April 1, 2006; 27(4): 759 - 765.
[Abstract] [Full Text] [PDF]


Home page
ANGIOLOGYHome page
K. I. Paraskevas, S. S. Daskalopoulou, M. E. Daskalopoulos, and C. D. Liapis
Secondary Prevention of Ischemic Cerebrovascular Disease. What Is the Evidence?
Angiology, September 1, 2005; 56(5): 539 - 552.
[Abstract] [PDF]


Home page
StrokeHome page
B.A.N. Verhoeven, J.P.P.M. de Vries, G. Pasterkamp, R.G.A. Ackerstaff, A.H. Schoneveld, E. Velema, D.P.V. de Kleijn, and F.L. Moll
Carotid Atherosclerotic Plaque Characteristics Are Associated With Microembolization During Carotid Endarterectomy and Procedural Outcome
Stroke, August 1, 2005; 36(8): 1735 - 1740.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
E. Furui, Y. Okamoto, S. Kida, J. Yamashita, O. Matsui, and M. Yamada
Transient Occlusion of the Middle Cerebral Artery by Macroembolism During Carotid Stenting for Traumatic Dissection of the Common Carotid Artery
Circulation, July 12, 2005; 112(2): e33 - e34.
[Full Text] [PDF]


Home page
Br J AnaesthHome page
A. Deogaonkar, R. Vivar, R. E. Bullock, K. Price, I. Chambers, and A. D. Mendelow
Bispectral index monitoring may not reliably indicate cerebral ischaemia during awake carotid endarterectomy
Br. J. Anaesth., June 1, 2005; 94(6): 800 - 804.
[Abstract] [Full Text] [PDF]


Home page
Br J AnaesthHome page
I. K. Moppett and R. P. Mahajan
Transcranial Doppler ultrasonography in anaesthesia and intensive care
Br. J. Anaesth., November 1, 2004; 93(5): 710 - 724.
[Full Text] [PDF]


Home page
StrokeHome page
O. Wolf, P. Heider, M. Heinz, H. Poppert, D. Sander, O. Greil, W. Weiss, M. Hanke, and H.-H. Eckstein
Microembolic Signals Detected by Transcranial Doppler Sonography During Carotid Endarterectomy and Correlation With Serial Diffusion-Weighted Imaging
Stroke, November 1, 2004; 35(11): e373 - e375.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
M. A. Sloan, A. V. Alexandrov, C. H. Tegeler, M. P. Spencer, L. R. Caplan, E. Feldmann, L. R. Wechsler, D. W. Newell, C. R. Gomez, V. L. Babikian, et al.
Assessment: Transcranial Doppler ultrasonography: Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
Neurology, May 11, 2004; 62(9): 1468 - 1481.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
A. Cremonesi, R. Manetti, F. Setacci, C. Setacci, and F. Castriota
Protected Carotid Stenting: Clinical Advantages and Complications of Embolic Protection Devices in 442 Consecutive Patients
Stroke, August 1, 2003; 34(8): 1936 - 1941.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
A. Angelini, B. Reimers, M. D. Barbera, S. Sacca, G. Pasquetto, C. Cernetti, M. Valente, P. Pascotto, and G. Thiene
Cerebral Protection During Carotid Artery Stenting: Collection and Histopathologic Analysis of Embolized Debris
Stroke, February 1, 2002; 33(2): 456 - 461.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
G. Devuyst, G.A. Darbellay, J.-M. Vesin, V. Kemeny, M. Ritter, D.W. Droste, C. Molina, J. Serena, R. Sztajzel, P. Ruchat, et al.
Automatic Classification of HITS Into Artifacts or Solid or Gaseous Emboli by a Wavelet Representation Combined With Dual-Gate TCD
Stroke, December 1, 2001; 32(12): 2803 - 2809.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
N. Al-Mubarak, G. S. Roubin, J. J. Vitek, S. S. Iyer, G. New, and M. B. Leon
Effect of the Distal-Balloon Protection System on Microembolization During Carotid Stenting
Circulation, October 23, 2001; 104(17): 1999 - 2002.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
B. Reimers, N. Corvaja, S. Moshiri, S. Sacca, R. Albiero, C. Di Mario, P. Pascotto, and A. Colombo
Cerebral Protection With Filter Devices During Carotid Artery Stenting
Circulation, July 3, 2001; 104(1): 12 - 15.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
C. H. Rabb, K.G.M. Moons, R.G.A. Ackerstaff, F.L. Moll, M.P. Spencer, and A. Algra
Association of Intraoperative Transcranial Doppler Monitoring Variables With Stroke From Carotid Endarterectomy Response
Stroke, March 1, 2001; 32(3): 812 - 813.
[Full Text] [PDF]


Home page
StrokeHome page
V. L. Babikian and N. L. Cantelmo
Cerebrovascular Monitoring During Carotid Endarterectomy
Stroke, August 1, 2000; 31(8): 1799 - 1801.
[Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
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 arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ackerstaff, R. G. A.
Right arrow Articles by Spencer, M. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ackerstaff, R. G. A.
Right arrow Articles by Spencer, M. P.
Right arrowPubmed/NCBI databases
Medline Plus Health Information
*Stroke