Before you go down either route ask your doctor to GUARANTEE NO STROKE from either procedure. If it was me I would ask my doctor to see if the Circle of Willis was complete; if yes, then have the doctor close up the offending artery. My right carotid artery completely closed up for 14 years before collaterals grew around it. I have had no dizziness or cognitive issues with only 3 arteries feeding the Circle of Willis.
Problems to consider:
1. Talk to your doctor about the dangers of stroke due to the endarterectomy procedure and why you would want to put inflexible metal stents in flexible arteries.
2. You might want to prevent stent placement complications per European Society of Cardiology
A - Minor complications
Carotid artery spasm
Sustained hypotension / bradycardia
Carotid artery dissection
Contrast encephalopathy (very rare)
Minor embolic neurological events (TIAs)
B - Major complications
Major embolic stroke
Intracranial hemorrhage
Hyperperfusion syndrome
Carotid perforation (very rare)
Acute stent thrombosis (very rare)
Complications at the site of the vascular access
The latest here:
Carotid Artery Stenting Versus Endarterectomy for Treatment of Carotid Artery Stenosis
Atherosclerotic stenosis of the internal carotid artery is an important cause of stroke. Carotid artery stenting (CAS) is an alternative to carotid endarterectomy (CEA) for the treatment of carotid stenosis. This review updates a previous version last published in 2012 including all randomized clinical trials comparing CAS to CEA for treatment of carotid stenosis.
Objectives
To compare the benefits and risks of CAS and CEA in patients with symptomatic or asymptomatic carotid stenosis.
Methods
We searched the Cochrane Stroke Group Trials Register and the following databases: CENTRAL (Cochrane Central Register of Controlled Trials), MEDLINE (Medical Literature Analysis and Retrieval System Online), Embase, and Science Citation Index (all last searched August 2018). We also searched ongoing trials registers, reference lists, and contacted researchers in the field. All randomized clinical trials comparing CAS with CEA for symptomatic or asymptomatic atherosclerotic carotid stenosis were included.
One review author selected trials for inclusion, assessed trial quality and risk of bias, and extracted data by using Cochrane and GRADE (Grading of Recommendations Assessment, Development and Evaluation Working Group) methodology. A second review author independently validated trial selection and a third review author independently validated data extraction. We calculated treatment effects as odds ratios (OR) and 95% CI, with CEA as the reference group. We quantified heterogeneity using the I2 statistic.
Main Results
Twenty-two trials involving 9753 participants were available to assess the overall certainty of the evidence. We categorized our findings on symptomatic carotid stenosis as high-certainty evidence and on asymptomatic carotid stenosis as medium-certainty evidence.
In symptomatic carotid stenosis, CAS was associated with a higher risk of death or stroke within 30 days of treatment (periprocedural period; OR, 1.70 [95% CI, 1.31–2.19]; P<0.0001, I2=5%; 10 trials, 5396 participants) compared with CEA. Rates of periprocedural death or stroke did not differ significantly in people <70 years (prespecified subgroup analysis; OR, 1.11 [95% CI, 0.74–1.64]) but were significantly increased with CAS compared with CEA in patients ≥70 years (OR, 2.23 [95% CI, 1.61–3.08], interaction P=0.007). CAS was associated with lower risks of myocardial infarction (OR, 0.47 [95% CI, 0.24–0.94]; P=0.03, I2=0%), cranial nerve palsy (OR, 0.09 [95% CI, 0.06–0.16]; P<0.00001, I2=0%), and access site hematoma (OR, 0.32 [95% CI, 0.15–0.68]; P=0.003, I2=27%) than CEA.
CAS was associated with a significantly higher risk of the combination of periprocedural death or stroke or ipsilateral stroke during follow-up compared with CEA (OR, 1.51 [95% CI, 1.24–1.85]; P<0.0001, I2=0%; 8 trials, 5080 participants; Figure). However, the rate of ipsilateral stroke beyond 30 days after treatment alone did not differ between treatments (OR, 1.05 [95% CI, 0.75–1.47]; P=0.77, I2=0%).
Among patients with asymptomatic carotid stenosis, there was a non-significant increase in periprocedural death or stroke with CAS compared with CEA (OR, 1.72 [95% CI, 1.00–2.97]; P=0.05, I2=0%; 7 trials, 3378 participants). The risk of periprocedural death or stroke or ipsilateral stroke during follow-up did not differ significantly between treatments (OR, 1.27 [95% CI, 0.87–1.84]; P=0.22, I2=0%; 6 trials, 3315 participants).
Moderate or higher carotid artery restenosis (≥50%) during follow-up was more common after CAS (OR, 2.00 [95% CI, 1.12–3.60]; P=0.02, I2=44%), but the difference in risk of severe restenosis was not significant (≥70%; OR, 1.26 [95% CI, 0.79–2.00]; P=0.33, I2=58%).
Conclusions
In patients with symptomatic carotid stenosis, CAS is associated with a higher risk of stroke or death within 30 days of treatment than CEA. This extra risk is mostly attributed to an increase in periprocedural stroke occurring in patients ≥70 years. Beyond 30 days after treatment, CAS is as effective in preventing recurrent stroke as CEA. However, combining procedural safety and long-term efficacy in preventing recurrent stroke, CAS is still associated with higher risks than CEA.
In people with asymptomatic carotid stenosis, there may be a small increase in the risk of stroke or death within 30 days of treatment with CAS compared with CEA.
Implications for Practice and Future Research
CAS can be safely(What the fuck is your definition of safety?) offered as an alternative to CEA in patients with symptomatic carotid stenosis <70 years, provided both treatments are technically feasible. Older patients should be treated with CEA. In patients with asymptomatic carotid stenosis, the amount of evidence currently available is limited and further data from randomized trials are needed.
Acknowledgments
This article is based on a Cochrane Review published in The Cochrane Library 2020, Issue 2 (see www.thecochranelibrary.com for information). Cochrane Reviews are regularly updated as new evidence emerges and in response to feedback, and The Cochrane Library should be consulted for the most recent version of the review.
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