|Restenosis after microsurgical non-patch carotid endarterectomy in 586 patients.|
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|PMID: 22113556 Owner: NLM Status: MEDLINE|
|BACKGROUND: Carotid endarterectomy (CEA) reduces the risk of stroke in patients with symptomatic (>50%) and asymptomatic (>60%) carotid artery stenosis. Here we report the midterm results of a microsurgical non-patch technique and compare these findings to those in the literature.
METHODS: From 1998 to 2009 we treated 586 consecutive patients with CEA. CEA was performed, under general anesthesia, with a surgical microscope using a non-patch technique. Somatosensory evoked potential and transcranial Doppler were continuously monitored. Cross-clamping was performed under EEG burst suppression and adaptive blood pressure increase. Follow-up was performed by an independent neurologist. Mortality at 30 days and morbidity such as major and minor stroke, peripheral nerve palsy, hematoma and cardiac complications were recorded. The restenosis rate was assessed using duplex sonography 1 year after surgery.
RESULTS: A total of 439 (75%) patients had symptomatic and 147 (25%) asymptomatic stenosis; 49.7% of the stenoses were on the right-side. Major perioperative strokes occurred in five (0.9%) patients [n = 4 (0.9%) symptomatic; n = 1 (0.7%) asymptomatic patients]. Minor stroke was recorded in six (1%) patients [n = 4 (0.9%) symptomatic; n = 2 (1.3%) asymptomatic patients]. Two patients with symptomatic stenoses died within 1 month after surgery. Nine patients (1.5%) had reversible peripheral nerve palsies, and nine patients (1.5%) suffered a perioperative myocardial infarction. High-grade (>70%) restenosis at 1 year was observed in 19 (3.2%) patients [n = 12 (2.7%) symptomatic; n = 7 (4.7%) asymptomatic patients].
CONCLUSIONS: The midterm rate of restenosis was low when using a microscope-assisted non-patch endarterectomy technique. The 30-day morbidity and mortality rate was comparable or lower than those in recently published surgical series.
|Michael Reinert; Marie-Louise Mono; Dominique Kuhlen; Luigi Mariani; Alain Barth; Jürgen Beck; Robert H Andres; Jan Gralla; Rolf Wymann; Jürgen Schmidt; Christin Kauert; Gerhard Schroth; Marcel Arnold; Heinrich P Mattle; Andreas Raabe; Urs Fischer|
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|Type: Journal Article Date: 2011-11-24|
|Title: Acta neurochirurgica Volume: 154 ISSN: 0942-0940 ISO Abbreviation: Acta Neurochir (Wien) Publication Date: 2012 Mar|
|Created Date: 2012-02-23 Completed Date: 2012-11-06 Revised Date: 2013-06-27|
Medline Journal Info:
|Nlm Unique ID: 0151000 Medline TA: Acta Neurochir (Wien) Country: Austria|
|Languages: eng Pagination: 423-31; discussion 431 Citation Subset: IM|
|Department of Neurosurgery, Inselspital Bern, University of Bern, Switzerland. email@example.com|
|APA/MLA Format Download EndNote Download BibTex|
Carotid Artery, Internal / pathology, surgery*, ultrasonography
Carotid Stenosis / mortality*, physiopathology, surgery*
Endarterectomy, Carotid / methods, mortality*, statistics & numerical data
Microsurgery / methods, mortality*, statistics & numerical data
Postoperative Complications / mortality*, physiopathology, ultrasonography
Recurrence / prevention & control
Journal ID (nlm-ta): Acta Neurochir (Wien)
Publisher: Springer Vienna, Vienna
© The Author(s) 2011
Received Day: 8 Month: 8 Year: 2011
Accepted Day: 9 Month: 11 Year: 2011
Electronic publication date: Day: 24 Month: 11 Year: 2011
pmc-release publication date: Day: 24 Month: 11 Year: 2011
Print publication date: Month: 3 Year: 2012
Volume: 154 Issue: 3
First Page: 423 Last Page: 431
PubMed Id: 22113556
Publisher Id: 1233
|Restenosis after microsurgical non-patch carotid endarterectomy in 586 patients|
Address: +41-31-6322409 +41-31-3822414 firstname.lastname@example.org
|Robert H. Andres1|
|Heinrich P. Mattle2|
1Department of Neurosurgery, Inselspital Bern, University of Bern, 3010 Bern, Switzerland
2Department of Neurology, Inselspital Bern, University of Bern, Bern, Switzerland
3Department of Neuroradiology, Inselspital Bern, University of Bern, Bern, Switzerland
4Department of Anesthesiology, Inselspital Bern, University of Bern, Bern, Switzerland
The aim of treating patients with symptomatic or asymptomatic, middle- to high-grade stenoses of the internal carotid artery (ICA) is to reduce the risk of thromboembolic events [19, 28]. Randomized controlled trials (RCT) and meta-analyses of individual patient data have shown that this goal can be reached both by carotid endarterectomy (CEA) and carotid artery stenting (CAS) [5, 11, 18, 26]. However, there are categories of patients that seem to benefit more from either CEA or CAS ; current ongoing trials aim to answer these questions . Even though the main aim of treatment is the prevention of thromboembolic events, rates of restenosis are an important surrogate marker for recurrent events . In general, restenosis rates are lower in patients after CEA than CAS [9, 21].
Carotid endarterectomy is one of the most thoroughly investigated surgical and neurosurgical procedures. Techniques and results of CEA have evolved over the last decades, partly as a result of the rapidly progressing and challenging endovascular techniques. The superiority of CEA compared with best medical treatment in symptomatic carotid disease is clearly established as long as surgical procedures can be performed with morbidity and mortality rates of less than 6% . Therefore, it is mandatory to analyze institutional results for safety and quality reasons as well as for comparison with published results of RCTs designed to evaluate CEA and CAS. Recently published series have reported lower rates of perioperative stroke and death both for CEA and CAS. In the face of this evolution, analysis of the rate of restenosis also among surgical series is increasingly important.
We therefore prospectively collected data on restenosis and outcome of all patients who underwent CEA at our neurosurgery department from May 1998 to December 2009.
All patients scheduled for CEA because of symptomatic (≥50%) or asymptomatic (≥70%) carotid artery stenosis from May 1998 to December 2009 were prospectively assessed at the Department of Neurosurgery, Bern University Hospital, Bern, Switzerland. Admission of patients and preoperative assessment was performed by the Stroke Unit team of the Department of Neurology, Bern University Hospital, Bern, Switzerland. Patients who were considered symptomatic were those with a new ischemic neurological deficit (transient or permanent) corresponding to lesions identified by diffusion-weighted MRI.
The degree of stenosis was measured according to the North American Symptomatic Carotid Endarterectomy (NASCET) criteria by Doppler/duplex sonography, and magnetic resonance angiography (MRA) or computed tomography angiography (CTA). The percentage of stenosis was calculated using the formula: 100 × [1 - (minimal residual lumen/distal lumen)] . Baseline characteristics such as age, sex, neurological and cardiovascular history as well as vascular risk factors (arterial hypertension, smoking, diabetes mellitus, obesity, positive family history and hyperlipidemia) were collected prior to treatment. This prospective study was approved by the ethics committee of the Canton of Bern, Switzerland (KEK 30/02).
Surgery was performed by three surgeons (A.B., L.M. and M.R.). Patients were placed under general anesthesia. Neuromonitoring was achieved using intraoperative transcranial Doppler (TCD) and somatosensory evoked potentials (SSEP). Before cross-clamping, a burst-suppression EEG pattern was initiated by propofol (AstraZeneca, London, UK) administration. Intravenous heparin (100 U/kg) (Drosspharm Ltd., Basel, Switzerland) was administered prior to exposing the ICA. Patients were treated with anti-platelet agents such as acetyl salicylic acid (ASA;Bayer, Leverkusen, Germany), clopidogrel (Sanofi-Aventis, Paris, France) or both. Patients treated with warfarin were reverted and also received intravenous heparin. Cross-clamping was initiated on the ICA then the common carotid, external carotid and superior thyroid artery. If the mean TCD flow velocity dropped below 50% of the pre-clamping values and could not be restored by increasing blood pressure, or alternatively if SSEP deteriorated, an intraoperative shunt (Integra Lifesciences, Plainsboro, NJ, USA) was inserted. Before the actual endarterectomy, we inserted the shunt after placing a longitudinal incision below and above the plaque. This procedure was followed by a backflow rinse of the ICA. The initial thromboendarterectomy was performed using surgical loupes; the vessel lumen was inspected, cleaned and the arterectomy vessel’s edges sharpened. The thromboendarterectomy was completed under a neurosurgical microscope (Zeiss, Feldbach, Switzerland), and the arteriotomy was closed with a continuous 6–0 monofilament suture (Tyco Healthcare Switzerland Ltd., Wollerau, Switzerland) (Fig. 1). In patients where the distal plaque in the ICA could not be completely or smoothly removed, tacking sutures (6–0 polypropylene sutures, Covidien plc, Dublin, Ireland) were applied. The arteriotomy was closed after reopening the external carotid artery. Thereafter, the clamp on the common carotid artery was released, followed by removal of the clip on the ICA 30 s later. Flow was controlled with a small microdoppler probe (Mizuho Medical Inc., Tokyo, Japan). Hemostatic foam (Nycomed Pharma AG, Dübendorf, Switzerland) was adapted to the arteriotomy. A wound drainage was routinely placed. Closure of the wound was performed only after stopping any visual bleeding using bipolar coagulation and application of a 40°C saline imbued gauze. If diffuse bleeding could not be stopped, half of the infused heparin was antagonized with protamine (Meda Pharmaceuticals, Wangen-Brüttisellen, Switzerland). Six hours after surgery, 300 mg ASA was administered intravenously, followed by oral administration of 100 to 300 mg ASA daily. In patients who were preoperatively on clopidogrel with or without ASA for cardiac reasons, therapy was resumed 1 day after the operation.
Follow-up was performed by an independent neurologist. All neurological and non-neurological complications after CEA were assessed. Vessel patency and rate of restenosis were assessed based on color-coded duplex sonographic findings immediately after the operation and several time points postoperatively: 5 days, 6 weeks and 1 year. Secondary prevention was achieved with administration of ASA or clopidogrel each day. A statin was prescribed in select patients by the treating neurologist until 2006 and to all patients after the publication of the Stroke Prevention by Aggressive Reduction in Cholesterol Levels (SPARCL) study . For classifying the restenosis rate, a postoperative ultrasound 1 year after surgery was performed. In cases of suspected restenosis, either a MRI or CTA was performed.
Patients who died within 30 days after surgery were included in the database and classified as death related to surgery unless another cause was identified. Death from stroke related to a restenosis during the follow-up was recorded as well.
Major stroke was defined as a new neurological deficit lasting more than 3 days or until the clinical follow-up examination performed 30 days after surgery. Minor stroke was defined as a new neurological deficit resolving within 3 days, without causing any transient independency, occurring within 30 days after surgery.
The combined morbidity and mortality rate was defined as all deaths and neurological sequelae, including minor and major strokes, due to the operated carotid artery. Peripheral nerve palsies were assessed separately.
Postoperative hematoma was defined as a swelling due to a local cervical hematoma necessitating a second surgical intervention. Clinically non-relevant postoperative swelling was not recorded.
A peripheral nerve palsy was recorded if a new postoperative palsy for tongue pulling, swallowing or hoarseness was observed (hypoglossal nerve, vagal nerve or ansa cervicalis) and persisted more than 30 days.
Complications other than those mentioned above, such as myocardial infarction (non-ST elevation and ST elevation), were recorded.
Restenosis was assessed 1 year after surgery by color-coded duplex sonography. Restenosis was considered high-grade if peak systolic velocity exceeded 200 cm/s. Moderate stenosis was diagnosed if peak systolic velocity exceeded 120 cm/s. If an increase in the degree of stenosis was detected, additional follow-up visits were required. A second intervention for early redo surgery or stenting was considered only if patients were symptomatic or had stenosis over 70%.
Statistical evaluations were performed using a commercially available software package (GraphPad Software, La Jolla, CA, USA). Data are presented as the mean and standard deviation. Groups were compared using Fisher’s exact test. Significance was set at a p value of 0.05.
From 1998 to 2009, 586 consecutive patients (70% men; mean age 69.4 ± 8.8 years) were treated with microsurgical CEA at our institution. Mean age in symptomatic patients was 69.6 ± 8.8 years, while the age in asymptomatic patients was 68.8 ± 8.5 years (Table 1). Right- and left-sided stenoses were equally distributed (49.7% right, 50.3% left). Four hundred thirty-nine (75%) patients had symptomatic and 147 (25%) asymptomatic stenosis. We had a proportionally higher number of symptomatic patients in our series compared to other series, especially vascular. This can be explained by the standard referral practice used in our hospital, which refers all symptomatic stenosis patients to the neurology department and thereafter to the neurosurgery department, while asymptomatic patients are rather referred directly to vascular surgeons. As a result of this referral practice, the number of symptomatic patients operated on by neurosurgeons is higher.
Four hundred thirty-seven patients with a symptomatic high-grade stenosis completed the 6-week follow-up examination, 397 were seen after 1 year at our institution, and the remaining 40 patients were followed up with duplex sonography in another facility or lost to follow-up. Two patients died within 30 days after surgery. Patients with duplex sonography performed in another hospital were not included into the 1-year follow-up. All 147 patients with asymptomatic high-grade stenosis completed the 6-week clinical follow-up. One hundred thirty-seven patients were seen after 1 year, and the remaining ten patients were either followed up in another facility or lost to follow-up.
The following vascular risk factors did not differ among patients with symptomatic or asymptomatic carotid artery stenosis: arterial hypertension, diabetes, hypercholesterolemia, smoking, peripheral arterial vascular disease, obesity and family history of stroke.
Postoperative death occurred in 2/586 patients (0.34%). Both patients had suffered from a symptomatic carotid stenosis. In one patient there was a fatal intracerebral hemorrhage 72 h (h) after intravenous thrombolysis for middle cerebral artery infarction on the left side and 24 h after CEA. The second fatality was due to a cardiac arrest on postoperative day 2; no autopsy was performed.
The combined mortality and morbidity rate in all patients was 2.2% (13/586), 2.2% (10/439) in symptomatic and 2.0% (3/147) in asymptomatic patients.
Major stroke within 30 days occurred in 5/586 patients (0.85%). Four of these patients (0.9%) were operated on for symptomatic and one patient (0.7%) for asymptomatic high-grade stenosis. Minor stroke within 30 days occurred in six cases (1%); four of these patients had high-grade symptomatic stenosis (Table 2).
Peripheral nerve palsy was observed in 1.53% (9/586) of patients. These deficits resolved rapidly in most of the patients. At 1 year follow-up all patients had normal function of the cranial nerves.
Overall 14 non-neurological complications were observed. Three patients had myocardial infarctions (MI) (n = 2, non-ST elevation MI; n = 1, ST elevation MI), five had angina pectoris, and two had postoperative local infections that were treated with intravenous antibiotics. Additionally, there were two patients with hematomas that required reoperation, one patient with postoperative seizure and one with a newly diagnosed myasthenia gravis
Intraoperative occlusion of the carotid artery during surgery was performed in five (0.8%) patients because of preoperative occlusion and the impossibility of recanalization, and distal extension of the plaques and impossibility of successful recanalization. Three patients were symptomatic and two patients asymptomatic. In addition, one patient had postoperative blood pressure-dependent transient ischemic attacks (TIA), which resolved and did not recur after 30 days.
High-grade restenosis of more than 70% occurred in 3.6% (19/534) of the patients after CEA: 3.0% (12/439) in symptomatic and 4.7% (7/147) in asymptomatic patients. Moderate-grade stenosis of 50 to 70% was observed in 1.2% (7/534) of patients; these seven patients were all symptomatic patients (Table 2, Fig. 2). Of all high- and moderate-grade restenoses, 1.1% (5/439) had symptomatic restenosis, all occurring in the preoperative symptomatic group. Stenting for high-grade restenosis was performed in 1.36% (8/586) of patients: 0.9% (4/439) in symptomatic and 2.7% (4/147) in asymptomatic patients. In one patient (0.2%) with symptomatic carotid artery stenosis reendarterectomy was performed. Restenosis rates did not differ between the pre- and post-statin era; however, the number of patients with restenosis was low in both asymptomatic (0/7) and symptomatic (2/81) patients.
In 11% of all operations, intraoperative shunting was used. The rate of intraoperative shunt placement in patients suffering postoperative minor or major stroke was 23%; however thromboembolic complications were not significantly more common (p = 0.112) when compared to all operated patients.
The NASCET found an absolute risk reduction of ipsilateral stroke of 17% at 2 years in patients with stenosis higher than 70% . Since then, endarterectomy has been recommended for patients with high-grade stenosis. In 1991, the European Carotid Surgery Trial (ECST) demonstrated a significant reduction of the overall stroke risk in operated patients with symptomatic high-grade stenosis (70–99% according to the ECST criteria) compared with best medical treatment . The perioperative risks of stroke and death within 30 days of CEA were 6.8% (95% CI: 5.6–8.0) in the ECST and 6.7% (95% CI: 5.3–8.4%) in the NASCET populations. These risk rates were higher than those reported in many surgical case series as outlined below. The operative risk in the ECST was significantly higher in women (p < 0.0001), although this difference was not seen in the NASCET.
Since these two large multicenter trials demonstrated the benefit of CEA over best medical treatment, two clinically relevant factors have changed, leading to many new RCTs. Firstly CAS has been introduced and equipoise to CEA, defined in specific clinical circumstances. Second, best medical treatment was reinforced with statins , thereby rendering the risk of stroke lower than the stroke risk reduction found in NASCET and ECST. Nevertheless, the data of the NASCET and the ECST trial remain the best available for treatment of carotid artery disease. In the Carotid Revascularization Endarterectomy versus Stenting Trial (CREST), the combined rate of stroke and death was reported in 2.1% asymptomatic and 3.2% symptomatic patients with carotid stenosis having undergone CEA . In a US nationwide inpatient study that included 482,394 patients having undergone CEA, the combined stroke and death rate was reported as 0.9% in the asymptomatic and 5.9% in the symptomatic group overall in high-risk and low-risk patients . A meta-analysis of short-term and long-term outcomes of CAS and CEA trials reported a similar range of rates for stroke and death as previously mentioned . Specifically the rates of periprocedural stroke and death were in favor of CEA compared to CAS.
Over the last decades, the CEA procedure has been constantly critically reviewed in many studies, leading to improvement and standardization. CREST has given us new trends toward the choice of indication for CEA or CAS. However, the question of restenosis is often not taken into account in these studies. Overall, various factors such as usage of surgical microscopes, patch techniques, anesthesia, neuromonitoring, intraoperative shunting and most importantly standardized screening procedures have led to a reduction of mortality and morbidity [13, 31, 32, 37].
Carotid artery stenosis is diagnosed by using color-coded duplex sonography to determine the degree of stenosis. This method also allows accurate assessment of plaque morphology. The exam is completed with TCD sonography of the circle of Willis and the vertebral arteries to assess the flow velocities, the direction of flow and the significance of a collateralization over the anterior and posterior communicating arteries. Intraoperative knowledge about collateral flow lowers the probability of the necessity to place an intraoperative temporary shunt, which is associated with an increased risk of embolism during placement and should thus only be performed when necessary [29, 30, 33].
At our institution, the diagnosis is always confirmed with a second imaging modality, either MRA or CTA. In addition, when determining the anatomical location and extent of the stenosis, MRA allows the visualization of past and present cerebral ischemic areas. This is important in cases of symptomatic carotid artery stenosis with large diffusion-restricted areas since the risk of post-endarterectomy hemorrhagic transformation is increased in these patients [3, 16], especially after intravenous thrombolysis . The previously accepted notion that CEA should be delayed 4 to 6 weeks after stroke is challenged by more recent evidence suggesting that CEA can be safely performed earlier in clinically stable patients who have mild to moderate deficits. This is especially true for patients who have a TIA or minor stroke without or only with minimal imaging evidence of infarction or mass effect, and a stable deficit where there is no reason to empirically delay carotid endarterectomy .
As the reported perioperative risks for the treatment of carotid artery stenosis both for CEA and CAS are lower, the rate of restenosis is increasingly more important. Two to 12% of patients with treated carotid stenosis have recurrent cerebrovascular events due to a high-grade restenosis in CAS as well as CEA [14, 21]. Although CEA has overall a lower rate of restenosis rate than CAS [9, 18], the rates of restenosis of surgical series using different operative techniques also have to be reported. The addition of statins to the medical therapy has without doubt reduced the overall recurrence of restenosis .
The two techniques used in our series, in comparison to other surgical series, were the use of a neurosurgical microscope, resulting in thorough vessel cleaning, and minimal conserving running suture and the waiver of any additional patch. In the literature there are no data supporting the advantages of the use of a microscope over surgical loupes for CEA. Neurosurgeons tend to use the microscope more often than vascular surgeons. The microscope has one advantage over the loupes in that it enables a higher magnification with perfect coaxial illumination. Therefore, a thorough cleaning of the vessel lumen is possible even with microinstruments. Furthermore, the overlay of the running suture for the vessel closure can be kept at a minimum, resulting in no constriction and practically restoring the original size of the vessel. Guzman et al. demonstrated that intraoperatively assessed dimensions of the carotid artery (common, external and internal) after removal of stenosis corresponded to the postoperative 3D-MRA findings that showed an anatomical normalization of the vessel structure . This might be a reason why our results are comparable to other series using a routine patching technique [12, 38].
Recent literature on patching, however, reports a lower restenosis rate when using polytetrafluoroethylene (PTFE) patches, revealing a superiority over Dacron or saphenous vein grafts [1, 10, 12, 32]. In a prospective randomized trial, 1 year restenosis was favorable for Gore-Tex versus Hemashield patching (2% versus 8%, respectively) . In 2005, Bart et al. reported a worsening restenosis rate 400 days after CEA when comparing venous patch, primary closure and Dacron patch (7%, 11% and 16%, respectively). Byrne et al. reviewed the literature in 2007 comparing primary versus venous patching, and venous versus Dacron patching. Dacron patching performed the worst in all studies, and primary was more often worse than venous patching, leading to the conclusion that venous patching appeared to perform superiorly to primary closure . Regarding this evidence, perhaps a new policy with routine use of a roof PTFE patch angioplasty might further improve the restenosis rate in the future. However, a slight increase in postoperative hemorrhage must be considered as well . Less postoperative hemorrhage has been reported when using a pericard patch; in addition, restenosis with a pericard patch has been reported between 2% to 7% [23, 24, 27]. Based on our midterm analysis of restenosis from this series and the reported literature, we conclude that it is essential to continue with primary closure using a microsurgical technique. In our series, a patch enlargement did not seem necessary. However, this will need to be confirmed by long-term analysis.
In our series we did not find a significantly higher rate of postoperative neurological deficits related to intraoperative shunting; however, there was an observable increase in neurological deficits in this group of patients. Although the shunt was immediately placed after opening the vessel below and above the plaque and the backflow of the opened ICA rinsed the vessel, it can be hypothesized that a small amount of debris from the remaining plaque embolized and was responsible for the neurological deficits. Given that we had a higher number of symptomatic patients, an adaptation to our surgical routine may require placing the shunt only after cleaning the internal carotid artery under the microscope or only when the SSEP begins to lower.
A recent Cochrane review compared local versus general anesthesia, where patients and surgeons could choose either anesthetic technique depending on the clinical situation and preferences . It is difficult to ascertain the clinical differences of local anesthesia over general anesthesia. Overall, we can assume that general anesthesia remains the most common practice across all specialties performing CEA. A systematic protocol for the different steps in the endarterectomy procedure is important for the success and reduction of morbidity. Furthermore, the type of anesthesia is also dependent on the clinical condition of the patient.
There are a multitude of different intraoperative techniques for evaluating the necessity for an intraoperative shunt, a topic still much debated in the literature. However, in our study, the stroke risk of distal embolization tended to be higher in shunted than in non-shunted patients, although this was not statistically significant. Visual assessment of back bleeding from the ICA is probably the easiest method for subjective assessment of intracranial collateralization, but at the same time probably also the least significant. Measuring the stump pressure may be more objective, but the literature gives values for a cutoff between 25 to 70 mmHg. Despite stump pressures greater than 50 mmHg, up to 9% of patients lost consciousness and required a temporary shunt in two series of CEA performed under local and general anesthesia [8, 34]. Transcranial Doppler ultrasound is gaining increasing importance for a variety of reasons: first, it gives an objective value of flow velocities that leads to the decision to insert a temporary shunt. Second, the increase of arterial blood pressure during cross-clamping can be directly monitored, in addition to monitoring the correct functioning of a temporary shunt. Although SSEP monitoring is slower in response than TCD, it gives additional security and information, especially when TCD is not possible. The combination of TCD and SSEP monitoring in the setup of general anesthesia with routine burst suppression and adaptive blood pressure control after cross-clamping in our series led to good results also in comparison with the literature. We insert a temporary shunt if pre-cross-clamping TCD flow velocities fall to 50% and a sufficient increase in blood pressure cannot be achieved.
In our series we found non-significantly higher rates of postoperative complications in shunted patients. There are two aspects of this issue to be considered: either there is an inherent higher risk of complications using a shunt or the complication rate is higher because it is not routinely used. This can only be answered by a randomized trial with a long-term follow-up (over several years) .
The recent literature reports that morbidity and mortality need to be lower than 6% in order to perform a CEA, and CAS should also achieve the same rates. It is therefore mandatory to assess results derived from local centers for both CEA and CAS. The recently published results of the CREST study further support a selection of treatment methods according to patient age and presence of symptoms . The findings from our study support the use of CEA both for symptomatic and asymptomatic carotid stenosis using our technical and anesthesiology procedures. The data analysis however does not allow any further specification according to patient age or sex. Furthermore, our study was designed to ascertain the rate of restenosis and the outcome.
Carotid endarterectomy is a safe procedure with an overall low morbidity and mortality in patients with symptomatic and asymptomatic carotid stenosis. Microsurgical techniques using a neurosurgical microscope without patching resulted in a low midterm restenosis rate compared to other surgical series in the literature, especially using patching techniques.
This work has not been previously published or presented.
Carotid endarterectomy still represents a valuable technique in the prevention of major neurologic ischemic events in patients with significant carotid stenosis. The different techniques used for carotid artery closure after this procedure aim to guarantee low restenosis rates, both in terms of early and long-term results. Patch closure has been considered an optimal solution in order to reduce the risk of restenosis related to technical inaccuracies during carotid artery closure. The use of a microsurgical non-patch technique for primary closure compared to the standard primary closure has the appeal of eliminating those technical inadequacies in the suture line; the excellent mid-term results obtained in this series confirm this hypothesis. However, it is important to remember that restenosis could be also and maybe primarily related to miointimal hyperplasia or thrombotic apposition in the endarterectomized carotid wall. Both these events have a long time progression, and restenosis could be identified many years after the procedure. It will be really interesting to have a description of the results presented here in the future for the evaluation of long-term restenosis rates after using the micro-surgical non-patch technique. Another important issue is related to the learning curve needed for this procedure. Neurosurgeons are used to microsurgical procedures, and this represents a great advantage when compared to other specialties involved in the treatment of carotid stenosis, as vascular surgeons are. If microsurgical primary closure demonstrates comparable long-term results to patch closure in terms of reduced restenosis rate, microsurgical techniques should be included in vascular surgery training programs.
The authors here report an institutional series of 586 CEA procedures by three surgeons over 11 years. Follow-up compliance for 1-year ultrasonography was reasonable at about 90%. Surgical skill and technique were excellent, as were the clinical results. The discussion of material issues regarding stent versus CEA and the nuances of the technique is erudite and pertinent.
The main point of this manuscript is to show that microsurgical repair of carotid arteriotomy yields a high-grade restenosis rate of 3.6% at 1 year. This is confounded a bit by the 90% follow-up rate rather than perfect data. However, the conclusion has validity; microsurgical repair with modern techniques yields excellent results.
As I have published many times (1), my preference is for collagen-impregnated Dacron patch repair in every case, no microscope. The high-grade restenosis rate has not yet been published by me, but, simply stated, it is zero at all evaluation time points, many beyond 1 year. So while I accept that these authors are superb technicians—I believe that they have done as well as can possibly be done without patch grafting—yet they still have an honest and valid figure of 3.6% recurrent high-grade stenosis. In my heart, I beleive we can still do better, and in my practice, universal patch grafting is the answer.
I have published many times and completely respect that many techniques can produce good outcomes in CEA. My technique works well for me, and I stand by it. This group shows fine results with a different technique, and I applaud them for their excellent contribution. Christopher M. Loftus
1. Loftus CM: Carotid Artery Surgery: Principles and Technique. 2nd edition. New York, Informa Publishing 2006.
The authors would like to thank Susan Wieting, Bern University Hospital, Department of Neurosurgery, Publications Office, Bern Switzerland for editing the final manuscript.
Conflicts of interest None.
Financial disclosures There are no financial disclosures for any author in this study
Open Access This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
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Mean age of symptomatic and asymptomatic men and women
|Overall age (mean ± years)||Male age (mean ± years)||Female age (mean ± years)||Total n (%)|
|Symptomatic and asymptomatic patients||69.9 ± 8.8||69.0 ± 8.8||70.4 ± 8.9||586 (100%)|
|Symptomatic||69.7 ± 8.8||69.2 ± 8.9||70.6 ± 9.5||439 (75%)|
|Asymptomatic||68.8 ± 8.5||68.5 ± 8.4||69.6 ± 7.1||147 (25%)|
Rate of major/minor stroke and restenosis rate in symptomatic and asymptomatic carotid stenosis
|Overall % (n) (N = 586)||Symptomatic % (n) (N = 439)||Asymptomatic % (n) (N = 147)|
|Minor stroke||1.02% (5)||0.9% (4)||1.4% (2)|
|Major stroke||0.85% (5)||0.9% (4)||0.7% (1)|
|Restenosis (≥70%)||3.2% (19)||2.7% (12)||4.7% (7)|
|Restenosis (≤69%)||1.2% (7)||1.6% (7)||0% (0)|
Keywords: Keywords Carotid Stenosis, Asymptomatic, Symptomatic, Microsurgical, Non-patch, Restenosis.
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