Pricing
Sign Up
Video preload image for Carotid Endarterectomy (Cadaver)
jkl keys enabled
Keyboard Shortcuts:
J - Slow down playback
K - Pause
L - Accelerate playback
  • Title
  • 1. Introduction & Preparation
  • 2. Incision
  • 3. Dissection
  • 4. Review of Anatomy
  • 5. Arteriotomy
  • 6. Placement of Patch
  • 7. Closure

Carotid Endarterectomy (Cadaver)

24779 views

Meghan Robinson1; Laura Boitano, MD2; Samuel Schwartz, MD2
1Lake Erie College of Osteopathic Medicine
2Massachusetts General Hospital

Main Text

Carotid stenosis is one of the leading causes of ischemic stroke worldwide. In the United States, nearly 800,000 strokes are reported each year, with ischemia accounting for 87% of them, and 15% traced to a carotid origin. Carotid endarterectomy represents an effective surgical treatment for carotid stenosis in preventing the risk of future ischemic stroke. In this video-article, we demonstrate the surgical technique for carotid endarterectomy on a cadaver and discuss a typical case presentation of an individual who could potentially benefit from this procedure.

Carotid artery disease; vascular surgical procedures; carotid endarterectomy.

Carotid stenosis occurs when atherosclerotic plaque accumulates within the carotid artery. The risk factors for this condition are similar to those of other atherosclerotic diseases and include hypertension, hyperlipidemia, smoking, obesity, and diabetes.1-4 Carotid stenosis may be discovered following a transient ischemic attack (TIA), ischemic stroke, or incidentally on imaging modalities such as carotid duplex ultrasound, magnetic resonance angiography (MRA), computed tomography angiography (CTA), or conventional angiography. Plaque is usually found in the common and internal carotid arteries within 2 cm of the carotid bulb due to complex flow patterns at that location.5 Carotid endarterectomy (CEA) refers to the surgical removal of atherosclerotic plaque from the carotid for the prevention of future ischemic events in symptomatic patients with significant plaque burden. 

The video demonstrates the surgical procedure on a cadaver, but in this text we will present and discuss the medical and surgical management of a typical patient who might benefit from CEA. The typical patient to be discussed is a 64-year-old male with a past medical history of myocardial infarction status post stenting of the LAD, hypertension, hyperlipidemia, and type 2 diabetes mellitus. He presented to the emergency department with a half-hour history of painless loss of vision in the left eye. He described it as beginning at the top of his visual field and gradually involving the entire field. His vision loss resolved in the emergency department without treatment. He reported two episodes in the past week of muscle weakness in his right leg, each lasting under an hour. Imaging in the emergency department revealed a 90% stenosis of the left carotid artery and a 55% stenosis of the right. He was medically optimized and referred to vascular surgery for evaluation.

The typical patient is of advanced age, has multiple cardiovascular risk factors, and presents with focal neurologic deficits that resolve completely within 24 hours, indicative of a TIA. The episodic painless loss of vision seen in this patient is referred to as a retinal TIA, also known as amaurosis fugax. One sided muscle weakness can be described as a hemispheric TIA. During their workup, they are found to have stenosis of the carotid artery, necessitating referral to vascular surgery.

Physical Exam

A physical exam revealed an overweight man with no focal neurologic deficits. The pupils were equal, round, and reactive to light; acuity was intact. Visual fields were full to confrontation, and ocular movements were intact. A bruit was auscultated bilaterally over the carotid bifurcation, easier to appreciate on the left. Lower extremity pulses were diminished bilaterally.

Physical exam in a patient with carotid artery stenosis may be unremarkable. A bruit may be auscultated over the internal carotid artery; however, this is nonspecific and present in 5% of advanced age patients in absence of significant carotid disease.4 Other signs of arterial disease may be present, such as arterial-based claudication, nonhealing ulcers, and post-prandial abdominal pain.  The presence of coronary artery disease or aneurysmal disease should also be assessed in any vascular evaluation.4

Imaging is not available for this case; however, carotid artery stenosis is typically first identified on imaging during workup for TIA using duplex ultrasound, computed tomography (CT), or magnetic resonance imaging (MRI). For evaluating the extent and severity of extracranial carotid stenoses, it is recommended to use duplex ultrasound as the first-line imaging modality, supplemented by CTA and/or MRA. When considering carotid endarterectomy, it is advised to corroborate duplex ultrasound stenosis estimation with either CTA, MRA, or a repeat duplex ultrasound performed by a second operator. In cases where carotid stenting is being considered, it is recommended that any duplex ultrasound study be followed by CTA or MRA to provide additional information on the aortic arch, as well as the extra- and intracranial circulation. (Class I recommendation, ESVS 2017 guidelines).27

For patients with nondisabling (mRS score 0-2) AIS in the carotid territory, who are candidates for CEA or stenting noninvasive imaging of the cervical carotid arteries should be performed routinely within 24 hours of admission (recommended by guidelines set in 2019 by the American Heart Association/American Stroke Association(AHA/ASA).27 CT is considered suboptimal for the evaluation of cortical injury in this presentation; however, it is recommended if MRI cannot be performed.

Guidelines also recommend routine imaging of the cerebral vasculature as part of the evaluation of patients with suspected TIA.27 It is reasonable to begin this identification with noninvasive methods such as ultrasound, CT angiogram, and/or MRI angiogram; however, if these provide an unclear picture, cerebral angiography may be needed.27

It is important to quantify the degree of stenosis present as this will decide management. There are several comparable methods to do this. The North American Symptomatic Carotid Endarterectomy Trial (NASCET) method compares the lumen at the most stenotic portion of the vessel with the normal lumen distal to the stenosis.3 This method is used to stratify patients in mild (<50%), moderate (50–69%), and severe (70–99%) stenosis.3

Like other atherosclerotic conditions, carotid stenosis is progressive, with a larger atherosclerotic burden presenting higher risk and more severe symptoms. Without treatment, severe narrowing will lead to embolic stroke and decreased survival.4 Nearly one in four strokes are in patients who have had previous strokes.1

Management decisions for carotid stenosis depend on the degree of stenosis, health of the patient, and whether the patient is symptomatic. Medical treatment is recommended for all patients with antiplatelet, antihypertensive, and statin therapy.4 Risk factor management includes quitting smoking, exercise, and weight loss.4

Options for severe carotid artery disease include CEA and carotid artery stenting (CAS). Carotid endarterectomy is currently considered the preferred intervention for most patients. However, selected patients, such as those younger than 70 years with favorable anatomical features or symptomatic patients with severe stenosis who have coexisting conditions that confer a high surgical risk, may benefit more from carotid stenting.4

For symptomatic patients with severe stenosis, endarterectomy is always recommended. Some guidelines recommend CEA over CAS for this patient population, especially if >70 years old.7 Symptomatic patients with moderate stenosis are also generally recommended for endarterectomy, though the benefit is considered less.7 Patients with mild stenosis or complete carotid occlusion have not been shown to benefit and are not recommended for standard internal carotid endarterectomy.7

For asymptomatic disease, there is less consensus on treatment. Guidelines generally recommend endarterectomy for asymptomatic patients with severe stenosis provided the patient is low risk for surgery and has a predicted life expectancy of at least 3–5 years.7

The patient discussed was found to be symptomatic with a 95% stenosis of the left internal carotid, necessitating the need for endarterectomy. His medications and lifestyle recommendations were reviewed and he was scheduled for CEA one week after initial presentation with the goal of preventing future stroke. 

There are some groups for whom CEA is relatively contraindicated. Those are patients with a history of radiation treatment to the head and neck due to the diffuse nature of their plaque, prior neck surgery overlying the carotid artery, and high carotid bifurcation; these patients can benefit from stenting.8 Patients with significant carotid artery stenosis are likely to have other significant risk factors for other cardiovascular disease, which may impact the decision to have surgery. 

CEA is done with an incision along the anterior border of the sternocleidomastoid muscle. After dissection to the carotid sheath, a longitudinal incision is made along the carotid artery, and the plaque is removed. The artery is reconstructed with a patch angioplasty. Patching has shown lower rates of recurrent stenosis and perioperative stroke compared to primary repair;9,10 however, primary repair can also be safe.11 Patches of synthetic material, bovine pericardium, and venous graft have shown similar short- and long-term outcomes.12

The other technique for CEA is eversion carotid endarterectomy (eCEA) involves oblique transection of the ICA and removal of the atheroma by everting the outer layers, followed by reattachment of the ICA to the CCA.28

It is believed that this method reduces ischemia and total operating times with similar outcomes to conventional CEA.13 Shunting can be performed during eversion endarterectomy but it is more technically demanding.

This technique offers several advantages, including the absence of prosthetic infection risk, quicker procedure time compared to patched CEA, preservation of bifurcation geometry, and the ability to shorten the distal ICA if necessary. However, eCEA has limitations, such as delayed shunt insertion until eversion is completed and potential challenges in accessing the upper ICA if distal disease is  underestimated.29 Meta-analyses indicate that eCEA is associated with a higher incidence of post-CEA hypertension but a lower incidence of perioperative hypotension compared to conventional CEA (cCEA). Additionally, eCEA demonstrates significant reductions in perioperative stroke, perioperative death, and late carotid occlusion. Despite these benefits, no significant differences were observed in 30-day death/stroke, perioperative thrombosis, or late stroke between eCEA and cCEA. Notably, eCEA has a lower rate of late restenosis (>50%) compared to cCEA. When compared to patched CEA, eCEA shows no differences in late restenosis rates.28

These findings suggest that eCEA provides outcomes equivalent to cCEA, provided the arteriotomy is closed with a patch.28

Different meta-analysis has shown that routine carotid patching or eversion carotid endarterectomy (eCEA) proved superior to primary closure, supported by level 1 evidence. No significant differences were observed among various patch materials. The incidence of significant post-CEA stenosis was comparable between CEA with patching and eCEA, both outperforming primary closure.29

The choice between eversion or patched endarterectomy should be left to the discretion of the operating surgeon (Class I recommendation).28 
The carotid artery is clamped during surgery, risking intraoperative embolism or cerebral hypoperfusion. To mitigate this, a shunt may be placed routinely or selectively when intraoperative neuromonitoring indicates cerebral hypoperfusion. The neurological status of the patient may be monitored using several methods depending on surgeon preference and capabilities of the facility. The study by Moritz et al. (2007) compares the accuracy of various cerebral monitoring techniques in detecting cerebral ischemia during CEA. Transcranial Doppler sonography (TCD), near-infrared spectroscopy (NIRS), and stump pressure (SP) measurement provided similar accuracy. Somatosensory evoked potentials (SEP) showed lower accuracy compared to TCD, NIRS, and SP. Additionally, TCD monitoring faced a high rate of technical difficulties (21%), making it the least practical method.23

The study by Sef et al. (2018) evaluates the reliability of carotid artery stump pressure (SP) in predicting neurological changes during CEA and its correlation with contralateral internal carotid artery (ICA) occlusion.A mean SP of 31 mmHg is a reliable threshold for predicting the need for shunting during CEA. This research has shown that patients with contralateral ICA occlusion had lower SP and a higher need for shunting.22

Mixed data have not shown a benefit from shunting; however, more powerful studies are warranted.14–16

Longer cross-clamping time is a predictor for delayed neurocognitive recovery following CEA, regardless of shunting.17

The choice of anesthesia for carotid endarterectomy (CEA) remains debated, with no clear consensus on whether regional or general anesthesia is superior. Regional anesthesia offers benefits like improved hemodynamic stability and easier neurological monitoring, while general anesthesia is more commonly used. Both methods show no significant difference in postoperative complications, and the choice should consider clinician preferences, patient comorbidities, and hospital conditions. Further high-quality studies are needed to provide more reliable evidence.24-26

Patients are monitored postoperatively for strict blood pressure control to prevent complications. Low systolic blood pressure may lead to cerebral ischemia, while high blood pressure may cause neck hematoma. A drain may be placed to avoid hematoma. Drain and surgical dressing are removed on postoperative day 1 or 2. In addition to blood pressure, patients are monitored for severe headache, stroke, and myocardial infarction. Outpatient CEA may be safe if the patient is not undergoing general anesthesia,18 but most patients will spend 1–3 days in the hospital. Patients are followed with repeat duplex ultrasound at six weeks following surgery and then at six-month intervals.4

This case illustrates the significance of CEA in the treatment of carotid stenosis. Carotid atherosclerosis is insidious, with stroke symptoms the first indication of occlusive disease.5 In those presenting with symptoms, the risk of recurrent stroke is more than 18% in 30 days, highlighting the importance of treatment in preventing further morbidity and mortality.5

The first known successful attempt at surgical revascularization occurred in 1954, and enthusiasm for the procedure has steadily grown in the decades since then.2 Over time, questions arose over the efficacy and complication rates of the procedure, and which patients would benefit most.

The NASCET established that symptomatic patients with severe stenosis, defined as 70–99%, obtained the greatest benefit to CEA.2,3 These patients saw an absolute risk reduction of 17% compared with medical management alone in the risk of ipsilateral stroke two years following surgery, with statistically significant benefit continuing at 8-year follow-up.2 Those with moderate symptomatic stenosis, 50–69%, saw a decreased but still statistically significant improvement in outcomes, while those with less than 50% stenosis saw no benefit to CEA.3

CEA is of highest benefit when performed after 48 hours but within 14 days of symptom onset.7 There is no consensus on the appropriate interval from thrombolysis to CEA, with some studies showing increased risk of stroke and/or death if CEA is performed within 72 hours of tPA administration.19

Other frontiers in the treatment of carotid stenosis include the use of advanced imaging and big data to identify asymptomatic and symptomatic patients who are at greatest long-term risk of stroke and may benefit from revascularization.7

No special tools.

Nothing to disclose.

Massachusetts General Hospital has given its consent for the cadaver referred to in this video to be used for the education of healthcare professionals and is aware that information will be published online. 

Citations

  1. Virani SS, Alonso A, Benjamin EJ, et al; American Heart Association Council on Epidemiology and Prevention Statistics Committee and Stroke Statistics Subcommittee. Heart Disease and Stroke Statistics-2020 Update: A Report From the American Heart Association. Circulation. 2020 Mar 3;141(9):e139-e596. doi:10.1161/CIR.0000000000000757.
  2. Barnett HJ, Taylor DW, Eliasziw M, et al. Benefit of carotid endarterectomy in patients with symptomatic moderate or severe stenosis. North American Symptomatic Carotid Endarterectomy Trial Collaborators. N Engl J Med. 1998 Nov 12;339(20):1415-25. doi:10.1056/NEJM199811123392002.
  3. North American Symptomatic Carotid Endarterectomy Trial Collaborators; Barnett HJM, Taylor DW, Haynes RB, et al. Beneficial effect of carotid endarterectomy in symptomatic patients with high-grade carotid stenosis. N Engl J Med. 1991 Aug 15;325(7):445-53. doi:10.1056/NEJM199108153250701.
  4. Grotta JC. Carotid stenosis. N Engl J Med. 2013 Dec 12;369(24):2360-1. doi:10.1056/NEJMc1312990.
  5. Gokaldas R, Singh M, Lal S, Benenstein RJ, Sahni R. Carotid stenosis: from diagnosis to management, where do we stand? Curr Atheroscler Rep. 2015;17(2):480. doi:10.1007/s11883-014-0480-7.
  6. Easton JD, Saver JL, Albers GW, et al; American Heart Association; American Stroke Association Stroke Council; Council on Cardiovascular Surgery and Anesthesia; Council on Cardiovascular Radiology and Intervention; Council on Cardiovascular Nursing; Interdisciplinary Council on Peripheral Vascular Disease. Definition and evaluation of transient ischemic attack: a scientific statement for healthcare professionals from the American Heart Association/American Stroke Association Stroke Council; Council on Cardiovascular Surgery and Anesthesia; Council on Cardiovascular Radiology and Intervention; Council on Cardiovascular Nursing; and the Interdisciplinary Council on Peripheral Vascular Disease. The American Academy of Neurology affirms the value of this statement as an educational tool for neurologists. Stroke. 2009 Jun;40(6):2276-93. doi:10.1161/STROKEAHA.108.192218.
  7. Jones DW, Brott TG, Schermerhorn ML. Trials and Frontiers in Carotid Endarterectomy and Stenting. Stroke. 2018 Jul;49(7):1776-1783. doi:10.1161/STROKEAHA.117.019496.
  8. AbuRahma AF, Robinson PA, Saiedy S, Kahn JH, Boland JP. Prospective randomized trial of carotid endarterectomy with primary closure and patch angioplasty with saphenous vein, jugular vein, and polytetrafluoroethylene: long-term follow-up. J Vasc Surg. 1998 Feb;27(2):222-32; discussion 233-4. doi:10.1016/s0741-5214(98)70353-2.
  9. Aburahma AF. Patch closure improves results with carotid endarterectomy. Semin Vasc Surg. 2004 Sep;17(3):243-52. doi:10.1016/s0895-7967(04)00044-4.
  10. Baram A, Majeed G, Subhi Abdel-Majeed A. Carotid endarterectomy: neither shunting nor patching technique. Asian Cardiovasc Thorac Ann. 2018 Jul;26(6):446-450. doi:10.1177/0218492318788777.
  11. Texakalidis P, Giannopoulos S, Charisis N, et al. A meta-analysis of randomized trials comparing bovine pericardium and other patch materials for carotid endarterectomy. J Vasc Surg. 2018;68(4):1241-1256.e1. doi:10.1016/j.jvs.2018.07.023.
  12. Davidovic LB, Tomic IZ. Eversion carotid endarterectomy: a short review. J Korean Neurosurg Soc. 2020;63(3):373-379. doi:10.3340/jkns.2019.0201.
  13. Rocha-Neves JM, Pereira-Macedo J, Dias-Neto MF, Andrade JP, Mansilha AA. Benefit of selective shunt use during carotid endarterectomy under regional anesthesia. Vascular. 2020;28(5):505-512. doi:10.1177/1708538120922098.
  14. Aburahma AF, Mousa AY, Stone PA. Shunting during carotid endarterectomy. J Vasc Surg. 2011;54(5):1502-1510. doi:10.1016/j.jvs.2011.06.020.
  15. Chongruksut W, Vaniyapong T, Rerkasem K. Routine or selective carotid artery shunting for carotid endarterectomy (and different methods of monitoring in selective shunting). Cochrane Database Syst Rev. 2014;(6):CD000190. doi:10.1002/14651858.CD000190.pub3.
  16. Aceto P, Lai C, De Crescenzo F, et al. Cognitive decline after carotid endarterectomy: Systematic review and meta-analysis. Eur J Anaesthesiol. Published online December 12, 2019. doi:10.1097/EJA.0000000000001130.
  17. Doberstein CE, Goldman MA, Grossberg JA, Spader HS. The safety and feasibility of outpatient carotid endarterectomy. Clin Neurol Neurosurg. 2012;114(2):108-111. doi:10.1016/j.clineuro.2011.09.011.
  18. Brinster CJ, Sternbergh WC. Safety of urgent carotid endarterectomy following thrombolysis. J Cardiovasc Surg (Torino). 2020;61(2):149-158. doi:10.23736/S0021-9509.20.11179-0.
  19. Brott TG, Hobson RW, Howard G, et al. Stenting versus endarterectomy for freatment of carotid-artery stenosis. N Engl J Med. 2010;363(1):11-23. doi:10.1056/NEJMoa0912321.
  20. Brahmanandam S, Ding EL, Conte MS, Belkin M, Nguyen LL. Clinical results of carotid artery stenting compared with carotid endarterectomy. J Vasc Surg. 2008;47(2):343-349. doi:10.1016/j.jvs.2007.10.034.
  21. Sef D, Skopljanac-Macina A, Milosevic M, Skrtic A, Vidjak V. Cerebral Neuromonitoring during Carotid Endarterectomy and Impact of Contralateral Internal Carotid Occlusion. J Stroke Cerebrovasc Dis. 2018;27(5):1395-1402. doi:10.1016/j.jstrokecerebrovasdis.2017.12.030.
  22. Moritz S, Kasprzak P, Arlt M, Taeger K, Metz C. Accuracy of cerebral monitoring in detecting cerebral ischemia during carotid endarterectomy: a comparison of transcranial Doppler sonography, near-infrared spectroscopy, stump pressure, and somatosensory evoked potentials. Anesthesiology. 2007;107(4):563-569. doi:10.1097/01.anes.0000281894.69422.ff.
  23. Rerkasem A, Orrapin S, Howard DP, Nantakool S, Rerkasem K. Local versus general anaesthesia for carotid endarterectomy. Cochrane Database Syst Rev. 2021;10(10):CD000126. Published 2021 Oct 13. doi:10.1002/14651858.CD000126.pub5.
  24. Sef D, Skopljanac-Macina A, Milosevic M, Skrtic A, Vidjak V. Cerebral neuromonitoring during carotid endarterectomy and impact of contralateral internal carotid occlusion. Turk J Vasc Surg. 2024;33(2):71-7. doi:10.9739/tjvs.2024.04.017.
  25. Stoneham MD, Stamou D, Mason J. Regional anaesthesia for carotid endarterectomy. Br J Anaesth. 2015;114(3):372-383. doi:10.1093/bja/aeu304.
  26. Powers WJ, Rabinstein AA, Ackerson T, et al. Guidelines for the Early Management of Patients With Acute Ischemic Stroke: 2019 Update to the 2018 Guidelines for the Early Management of Acute Ischemic Stroke: A Guideline for Healthcare Professionals From the American Heart Association/American Stroke Association. Stroke. 2019;50(12):e344-e418. doi:10.1161/STR.0000000000000211.
  27. Aboyans V, Ricco JB, Bartelink ML, et al. 2017 ESC Guidelines on the Diagnosis and Treatment of Peripheral Arterial Diseases, in collaboration with the European Society for Vascular Surgery (ESVS): Document covering atherosclerotic disease of extracranial carotid and vertebral, mesenteric, renal, upper and lower extremity arteries. Eur Heart J. 2018;39(9):763-816. doi:10.1093/eurheartj/ehx0951
  28. AbuRahma AF, Darling RC 3rd. Literature review of primary versus patching versus eversion as carotid endarterectomy closure. J Vasc Surg. 2021;74(2):666-675. doi:10.1016/j.jvs.2021.02.051.

Cite this article

Robinson M, Boitano L, Schwartz S. Carotid endarterectomy (cadaver). J Med Insight. 2024;2024(260.1). doi:10.24296/jomi/260.1.

Share this Article

Authors

Filmed At:

Harvard Medical School

Article Information

Publication Date
Article ID260.1
Production ID0260.1
Volume2024
Issue260.1
DOI
https://doi.org/10.24296/jomi/260.1