Abstract
Background: Carotid endarterectomy is a recognized method for preventing stroke for both symptomatic and asymptomatic hemodynamically carotid artery stenosis. Hemodynamic depression is more frequently associated with carotid artery stenting, while postoperative hypertension and cerebral hyperperfusion syndrome are known frequent complications after carotid endarterectomy. Severe hypotension after carotid revascularization is associated with a higher risk of perioperative stroke, myocardial infarction, and death, with limited data existing regarding risk factors. This study aims to investigate intraoperative risk factors for severe hypotension after carotid endarterectomy. Methods: A total of 160 patients who underwent carotid endarterectomy were included in this study. Patients with other cardiac conditions that required concomitant cardiac surgery, patients with incomplete medical records, and patients considered high risk for surgery were excluded. Results: The incidence of severe hypotension was 30.6%. Patients with severe hypotension after carotid endarterectomy had a higher incidence of diabetes, moderate mitral valve regurgitation, a history of percutaneous coronary intervention, and higher operative times. Using logistic regression, temporary shunt insertion was independently associated with severe postoperative hypotension (OR = 2.26, 95% CI = 1.09–4.71, p = 0.029). Conclusions: This result favors the selective shunting strategy when performing carotid endarterectomies, especially for those patients with comorbidities predisposing to postoperative complications.
1. Introduction
Atherosclerotic extracranial cerebrovascular disease is a major cause of stroke and a leading cause of death [1]. Carotid endarterectomy (CE) was first reported by Eastcott in 1954 in a 66-year-old patient with recurrent transitory ischemic attacks (TIAs) [2]. It was the first time a surgical technique was considered as a treatment for a neurological condition such as cerebral ischemia [3]. The beneficial effect of this surgical technique was confirmed by the North American Symptomatic Carotid Endarterectomy Trial (NASCET) [4] and the European Carotid Surgery Trial (ECST) [5], especially in severe symptomatic carotid artery stenosis, both studies reporting similar rates of periprocedural stroke and in-hospital death.
Guidelines for the treatment of carotid artery disease were elaborated by the American Heart Association [6], the European Society for Vascular Surgery [7], and the European Stroke Organization [8]. CE is indicated in symptomatic (ipsilateral TIA or stroke within the past 6 months) with a 50% to 99% carotid artery stenosis, provided that the perioperative morbidity and mortality risk is low. All the society guidelines recommend that CE should be performed within 14 days from the onset of symptoms to increase the likelihood of a stroke-free outcome. For the asymptomatic 60% to 99% carotid artery stenosis, CE is indicated if there are one or more imaging or clinical signs associated with an increased risk of stroke.
Carotid revascularization is frequently complicated by hemodynamic complications [9]. Hemodynamic depression (HD) (bradycardia, hypotension, or both) occurs more often when carotid artery stenting is performed [10,11,12], while postoperative hypertension and cerebral hyperperfusion syndrome are known frequent complications after CE [13]. The incidence of HD is as high as 54.4% in CAS [14].
Severe hypotension is the consequence of transient baroreceptor dysfunction and carotid sinus manipulation [15,16] and is associated with a higher risk of perioperative stroke, myocardial infarction, and death after carotid artery surgery [14,17]. However, none of the traditional risk indexes encompasses the risk of HD and in particular the risk of severe hypotension [18], especially after CE.
Limited data are available regarding risk factors for severe hypotension after CE, in contrast with postprocedural hypotension in patients with coronary artery stenting (CAS). This study investigates the incidence of severe hypotension post-CE and the risk factors for this complication.
2. Methods
Between January 2020 and December 2023, 172 patients were admitted to our center, proposed for CE. Clinical characteristics and demographic data were collected from medical records and the electronic health system. Local ethics committees approved the protocol, and written informed consent was obtained from each patient.
Indication for surgery was performed after the European Stroke Organization guidelines and after neurological consultation.
The inclusion criteria included patients with symptomatic (ischemic stroke or TIA within 6 months) 50% to 99% carotid artery stenosis or patients with asymptomatic 70% to 99% carotid artery stenosis, assessed by carotid artery angiography or by contrast computed tomography of the cervical region.
The exclusion criteria included (1) patients with severe valvopathies (mitral/aortic or tricuspid valve) that required concomitant surgery; (2) patients with incomplete medical records; (3) patients considered high risk for surgery (symptomatic coronary artery disease, severe coronary artery stenosis diagnosed in the same setting at coronary angiography, NYHA III or IV heart failure); (4) patients with reduced life expectancy due to severe non-cardiac comorbidities like neoplasia; and (5) patients with initial severe carotid artery stenosis based on Doppler Ultrasound, not confirmed by contrast computed tomography of the cervical region or carotid artery angiography.
All patients were evaluated by a cardiology physician before surgery. Patients with a history or risk factors for coronary artery disease, angina or angina equivalent, or signs of coronary artery disease on transthoracic echocardiography were scheduled for coronary angiography before surgery.
The diagnosis of carotid artery stenosis was performed by initial Doppler ultrasound and confirmed by contrast computed tomography of the cervical region or carotid artery angiography.
Stroke was defined as an acute onset neurological deficit corresponding to an ischemic lesion on brain computed tomography or magnetic resonance imaging.
TIA was defined as a transient episode of neurologic dysfunction due to focal brain, spinal cord, or retinal ischemia without acute infarction or tissue injury according to 2009 AHA/ASA guidelines.
Severe hypotension was defined as mean arterial pressure <60 mmHg after volume resuscitation, requiring continuous vasopressor infusion (norepinephrine) in the first 12 h.
2.1. Surgical Technique
Standard and invasive monitoring including continuous blood pressure, central venous pressure, and urine output monitoring were employed through the perioperative setting. After the institution of general anesthesia, the patient is positioned on the operating table with the head extended and rotated to the opposite side of the carotid artery that is to be operated on. Near-infrared spectroscopy (NIRS) is used to monitor cerebral oxygenation. The common, external, and internal arteries are dissected and isolated with arterial loops, via a 10 cm longitudinal incision at the medial border of the sternocleidomastoid muscle. Intravenous heparin is administered before arterial clamping (50 IU/kg, maximum dose of 5000 IU). A longitudinal arteriotomy is made, beginning from the common carotid artery over the carotid bifurcation and extending distally to the internal carotid artery at the level of the normal arterial wall. We usually place a shunt in the following situations: (1) internal carotid artery (ICA) backflow unsatisfactory; (2) retrograde pressure at the level of ICA below 40 mmHg; and (3) a more than 15% drop in NIRS. Continuous transcranial Doppler ultrasonography and EEG monitoring are not available in our institution. Usually, plaque is removed down to the level of the intima, and two 7.0 polypropylene sutures are used to fix the layers at the distal end of the endarterectomy. The endarterectomy is completed using one of the following techniques: direct suture of the artery or a collagen and silver-coated polyester patch, or a saphenous vein patch sutured with a continuous 6.0 polypropylene suture. After completion of the endarterectomy, the temporary shunt is extracted, the arteries are de-aired and declamped, and patency is verified using intraoperative Doppler ultrasound. A surgical drain is inserted via contra incision, hemostasis is achieved, and the surgical wound is closed by suturing the anatomical layers.
2.2. Statistical Analysis
Wizard 2 Statistical Software for Mac OS (Wizard–Statistics & Analysis., Raipur, Chattisgarh, India) was used for statistical analysis. Summary statistics are presented as absolute numbers and percentages for categorical values and as the mean and standard deviation for continuous values.
The incidence of severe postoperative hypotension was investigated.
In order to investigate the association between preoperative and postoperative factors and severe postoperative hypotension, a multivariable analysis was performed using logistic regression, taking into account a model that included variables achieving a p-value < 0.1 in a univariate analysis. A predictive modeling strategy with the backward stepwise method of entering data was then used. Logistic regression results are presented as odds ratios (ORs) with confidence limits and p-values. p < 0.05 was considered statistically significant. Variables included in the univariate analysis were the following: age, history of smoking, chronic kidney disease, lower leg ischemia, hypertension, male sex, hyperlipidemia, diabetes, aortic, mitral, or tricuspid valve moderate or severe stenosis or regurgitation, severe left ventricular dysfunction, myocardial hypokinesia or akinesia, direct carotid artery arteriography, saphenous or silver-coated polyester patch, dual antiplatelet therapy, temporary shunt insertion, maximum levels of cardiac enzymes, left and right non-significant stenosis, 50–69% stenosis, 70–99% stenosis, CA occlusion, preoperative coronary angiography, one/two or three coronary vessels disease, history of PCI, history of stroke or TIA, new postoperative neurological complications, mean duration of surgery, mean duration of intubation, and prolonged ventilation (more than 12 h).
An independent t-test or Chi-square test was used to compare the groups of patients with and without severe postoperative hypotension.
3. Results
3.1. Pre/Intra/Postoperative Characteristics of the Study Population
A total of 172 patients with CE were included in this observational study. Out of these, 12 patients were excluded (9 patients with incomplete medical records, and 3 patients with overestimated carotid artery stenosis based on initial Doppler ultrasound—2 patients had carotid artery angiography in the same setting as coronary angiography and had an initial 70% carotid artery stenosis assessed by DU under 50% and 1 patient had a suboclusive carotid artery stenosis not confirmed by contrast computed tomography of the cervical region).
The general characteristics of the study populations are listed in Table 1. The mean age was 67.64 ± 7.54 years. Almost all patients had hyperlipidemia (93.1%) and arterial hypertension (91.9%), and 63.7% of them were on dual antiplatelet therapy. A history of stroke was present in 52.5% of patients, while 13.2% had a history of transient ischemic attack. Preoperative coronary angiography was performed in 35.7%; 10% had previous coronary artery bypass grafting, 8.8% had a history of percutaneous coronary artery intervention, and three-vessel coronary artery disease was present in 15% of the patients.
Table 1.
General characteristics of patients.
Eight patients (5%) had left ICA occlusion, while six patients (3.8%) had right ICA occlusion. Carotid artery stenosis 70% to 99% was present in 55% of cases on the right side and in 57.2% on the left side. Stenosis between 50% and 69% had an incidence of 11.9% on the left ICA and 12.5% on the right ICA.
Temporary shunt placement was inserted in 50.6% of the cases. CE was most often completed with direct carotid artery arteriography (37.5%), a saphenous vein patch was used in 31.9%, and a silver-coated polyester patch in 30% of the cases. The mean duration of surgery was 3.2 ± 0.71 h.
New neurological complications were encountered in eight patients with delirium, with hypoglossal nerve injury being the most frequent complication (1.9%). One patient developed an ischemic stroke, and another patient developed vagus nerve injury.
Severe hypotension requiring vasopressor support had an incidence of 30.6%. Severe hypertension was seen in 31.9% of the cases.
The mean duration of intubation time was 5.46 ± 3.68 h, with 15.6% of patients requiring more than 12 h of intubation.
3.2. Characteristics of Patients with Severe Hypotension
Table 2 shows the comparison between patients with and without severe hypotension. Regarding preoperative characteristics, patients with severe postoperative hypotension had a higher incidence of diabetes (p = 0.002), moderate mitral valve regurgitation (p = 0.045), and a history of PCI (p = 0.024). Intraoperative temporary shunt placement had a higher incidence in patients with severe hypotension (p = 0.034), and patients with severe postoperative hypotension had longer operative times (p = 0.04).
Table 2.
Comparison between patients with and without severe hypotension.
3.3. Factors Related to Severe Hypotension
The results of the univariate analysis of variables associated with severe postoperative hypotension with a p-value < 0.1 are presented in Table 3. Diabetes (OR = 0.166, 95% CI = 0.06–0.048, p < 0.001) and history of PCI (OR = 6.22, 95% CI = 1.65–23.46, p = 0.007) were included in the final model after backward selection. Temporary shunt placement was the only intraoperative variable associated with severe hypotension in the univariable analysis (OR = 2.1, 95% CI 1.05–4.19, p = 0.035). After model adjustment, shunt placement was independently associated with severe postoperative hypotension (OR = 2.26, 95% CI = 1.09–4.71, p = 0.029).
Table 3.
Factors associated with severe hypotension (multivariable statistics).
4. Discussion
Stroke is the second most common cause of death worldwide. The annual incidence of stroke has increased noticeably in the last decades because of the increase in obesity [19], and it is estimated that 25% of adults will have a stroke in their lifetime [20]. Moreover, half of the surviving patients have severe disability and are a great burden on the public health system [21].
In recent years, stroke prevention measures especially in elderly patients decreased stroke-associated disability, with a decrease in the absolute number of severely disabled (modified Rankin Scale 4–5) stroke patients at discharge [22].
CE has a beneficial effect on stroke prevention in patients with internal carotid artery stenosis. Moreover, in patients with TIA or non-disabling stroke, it is recommended to perform CE within 2 weeks of the index event rather than delay surgery to increase the likelihood of stroke-free outcome [8].
HD such as bradycardia, asystole, and hypotension occur during interventions on the carotid artery, especially in the setting of CAS, and are associated with major adverse cardiovascular events [14].
The incidence of HD after interventions for carotid artery revascularization is variable in different studies, ranging from 7.2% to 70% [14,23]. This non-concordance is probably due to marked heterogeneity in the definitions of HD. Gupta et al. and Bussiere et al. analyzed absolute values (systolic blood pressure < 90 mmHg, and heart rate < 60 bpm) [24,25], Cayne et al. investigated relative values comparing pre- and postoperative parameters [26], while Diehm et al. only investigated the need for treatment [27]. In our study, the incidence of severe postoperative hypotension was 30.6%, defined as mean arterial pressure < 60 mmHg after volume resuscitation, requiring continuous vasopressor infusion.
Bognioti et al. investigated HD after 237 carotid surgeries and included in this category both CE and CAS with an incidence of 54.4% [14]. Both intraoperative and postoperative hypotension had an incidence of 50.2%, and this included both cases with and without vasopressor infusion. The authors found an independent association between hypotension requiring vasopressors and major adverse cardiovascular events. The association between HD and worse outcomes is supported by Park et al. [12] (myocardial infarction, length of stay, and death) and Ullery et al. (stroke) [17].
Limited data are available regarding incidence and risk factors for postoperative hypotensive after CE. Park et al. analyzed 1474 CE and 157 CAS patients and found an incidence of clinically significant hypotension of 12.6% [12], while Altinbas et al. found an incidence of 7.2% [16]. Bogniotti et al. found asymptomatic carotid stenosis, endovascular surgery, and intraoperative hypotension or bradycardia independent predictors for HD in 237 carotid surgeries, including CE and CAS [14]. While we did not investigate intraoperative hypotension or bradycardia, the incidence of asymptomatic carotid artery stenosis was 47.5% (76 patients), and there were no significant differences between patients with and without postoperative severe hypotension. It should be mentioned that, in the Bogniotti study, the hypotension group included both patients with systolic blood pressure below 90 mmHg or mean arterial pressure below 60 mmHg and also the cases requiring vasopressors. In our study, we only included patients with vasopressors, and the smaller number of cases could justify why we could not confirm Bogniotti’s findings. Park et al. found that preoperative nitrate use and a history of tobacco use were correlated with postprocedural hypotension in patients with CE and CAS [12]. Tobacco use had an incidence of 38.1% (61 patients) in our study, with no significant differences. It should be mentioned that because of the retrospective nature of this study, the timing and the magnitude of tobacco use could not be fully characterized, and this is a limitation of our study. Similarly, we did not consider investigating the periprocedural use of nitrates or any other medication because of the inability to fully determine medication compliance and timing before CE. Also, the management of different comorbid conditions is not possible with this type of study. Both studies included patients with CE and CAS, and this could also be a reason why we could not confirm some of the risk factors found for severe postoperative hypotension.
One of the few studies investigating risk factors for postprocedural hypotension in CE was performed by Gibbs et al. [28]. They did not find any demographic or procedural factors associated with postoperative hypotension, and they also concluded that hypotension after CE was transient and not associated with adverse outcomes.
In contrast, in patients with CAS, postprocedural hypotension is well studied, and multiple risk factors have been identified (Table 4).
Table 4.
Main studies investigating risk factors for postprocedural hypotension after CAS.
Temporary shunt placement is a method used for preventing cerebral hypoperfusion during CE [40]. Currently, there are two strategies for shunt placement (routine shunting [41] and selective shunting [42]), with no definitive guidelines. Those who propose selective shunting rely on the fact that most perioperative complications are the result of thrombo-embolic episodes rather than cerebral hypoperfusion and also that mortality and morbidity do not differ significantly when comparing routine vs. selective shunting [43]. Complications associated with shunt insertion such as intimal injury with thrombosis and embolization, pseudoaneurysm, distal embolization at insertion, and rupture of the distal end of the internal carotid artery are well described and have serious adverse effects on the prognostic of the patient [44,45,46].
In our study, the strategy for shunt insertion was selective shunting in the following instances: contralateral carotid artery occlusion, ipsilateral stroke, significant reduction in transcutaneous cerebral oximetry measurement parameters, and inadequate backflow from the ICA after clamping. The incidence of shunt placement was 50.6% of patients. With this strategy, the rate of complication was the following: one patient developed postoperative ischemic stroke with a modified Rankin Scale of 3 at discharge, two patients had cranial nerve injuries, and three patients experienced postoperative delirium.
The association between shunt placement and severe postoperative hypotension has not been communicated so far.
A possible mechanism for this can be a longer duration of surgery because of the technical aspect associated with shunt insertion. Besides the complications listed above, which are time-consuming, the surgical field is reduced, especially the lumen of the internal carotid artery after plaque extraction. In this region, separate 7.0 polypropylene sutures are placed to fixate the remaining intima to the rest of the arterial wall. Placement of these sutures is more time-consuming in the setting of temporary shunting. Also, the entire process of plaque excision is more difficult because of the need to permanently mobilize the shunt for a better visualization of the carotid lumen. Shunt extraction can also be time-consuming and technically difficult, especially when a patch is used to finalize the CE. Loosening the suture used to secure the patch can happen; additionally, sutures are required to achieve hemostasis, prolonging the surgery time. Also, it is more challenging and time-consuming to suture a patch at the native carotid artery wall with a shunt in place.
We investigated intraoperative risk factors for the development of severe postoperative hypotension such as temporary shunt placement, duration of surgery, suture of a patch, or direct arteriography. Unlike preoperative variables, intraoperative variables depend on the surgical team and can be modified. The aim is a surgical technique that can benefit the patient in the intensive care setting, reducing the risk of hemodynamic complications like severe hypotension.
This is an observational study and, as such, is vulnerable to the biases inherent to this type of analysis. Our sample size might still be considered small to have detected significant differences between those with and without severe postoperative hypotension. Further studies are needed to investigate intraoperative risk factors for hemodynamic complications after CE.
5. Conclusions
Data from 160 patients with CE were analyzed. Severe postoperative hypotension had an incidence of 30.6%, and patients with these complications had a higher incidence of diabetes, moderate mitral valve regurgitation, a history of PCI, and longer operative times. Temporary shunt placement was the only intraoperative factor associated with severe postoperative hypotension. This result can be explained by longer operating times because of the technical aspects associated with this method of cerebral protection. Considering this result, the selective shunting strategy could be more beneficial for the patient, especially for those with comorbidities predisposing to postoperative complications. Shunting could be considered only in specific situations such as contralateral subocclusion or occlusion, or severe stenosis on both vertebral arteries. However, further studies are needed to sustain this finding and clarify the need for shunting in CE.
Author Contributions
Conceptualization, M.R., I.-M.M., O.S., H.M., B.R. and V.A.I.; methodology, M.R., O.S., I.-M.M., V.I., G.-P.G. and H.M.; software M.R. and A.R.H.; validation, M.R., V.A.I., H.M. and A.R.H.; formal analysis, M.R., O.S., A.R.H., B.R., M.G., H.M. and V.A.I.; investigation, M.R., C.M., I.-M.M., M.G. and O.S.; resources, M.R., A.R.H., G.-P.G., O.S. and H.M.; data curation, M.R., I.-M.M., V.I., C.M., A.R.H., H.M. and V.A.I.; writing—original draft preparation, M.R., C.M., M.G. and V.A.I.; writing—review and editing, M.R., I.-M.M., G.-P.G., O.S. and H.M.; visualization, M.R., H.M., C.M., V.I., G.-P.G. and V.A.I.; supervision, M.R., H.M., V.I., B.R. and V.A.I.; project administration, B.R., O.S., G.-P.G., B.R. and V.A.I.; funding acquisition, H.M. All authors have read and agreed to the published version of the manuscript.
Funding
The publication of this paper was supported by the University of Medicine and Pharmacy Carol Davila through the institutional program Publish not Perish.
Institutional Review Board Statement
This study was conducted in accordance with the Declaration of Helsinki and approved by the Romanian National Ethics Committee (Approval Code: 197; Approval Date: 24 January 2023).
Informed Consent Statement
Informed consent was obtained from the patients involved in this study.
Data Availability Statement
Data are available upon request.
Conflicts of Interest
The authors declare no conflicts of interest.
References
- Brott, T.G.; Halperin, J.L.; Abbara, S.; Bacharach, J.M.; Barr, J.D.; Bush, R.L.; Cates, C.U.; Creager, M.A.; Fowler, S.B.; Friday, G.; et al. 2011 ASA/ACCF/AHA/AANN/AANS/ACR/ASNR/CNS/SAIP/SCAI/SIR/SNIS/SVM/SVS guideline on the management of patients with extracranial carotid and vertebral artery disease: Executive summary. A report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, and the American Stroke Association, American Association of Neuroscience Nurses, American Association of Neurological Surgeons, American College of Radiology, American Society of Neuroradiology, Congress of Neurological Surgeons, Society of Atherosclerosis Imaging and Prevention, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of NeuroInterventional Surgery, Society for Vascular Medicine, and Society for Vascular Surgery. Circulation 2011, 124, 489–532. [Google Scholar] [CrossRef]
- Eastcott, H.H.; Pickering, G.W.; Rob, C.G. Reconstruction of internal carotid artery in a patient with intermittent attacks of hemiplegia. Lancet 1954, 267, 994–996. [Google Scholar] [CrossRef]
- Riggs, P.N.; DeWeese, J.A. Carotid endarterectomy. Surg. Clin. N. Am. 1998, 78, 881–900. [Google Scholar] [CrossRef]
- North American Symptomatic Carotid Endarterectomy Trial Collaborators; Barnett, H.J.M.; Taylor, D.W.; Haynes, R.B.; Sackett, D.L.; Peerless, S.J.; Ferguson, G.G.; Fox, A.J.; Rankin, R.N.; Hachinski, V.C.; et al. Beneficial effect of carotid endarterectomy in symptomatic patients with high-grade carotid stenosis. N. Engl. J. Med. 1991, 325, 445–453. [Google Scholar] [PubMed]
- Moore, W.S.; Barnett, H.J.; Beebe, H.G.; Bernstein, E.F.; Brener, B.J.; Brott, T.; Caplan, L.R.; Day, A.; Goldstone, J.; Hobson, R.W., 2nd; et al. Guidelines for carotid endarterectomy. A multidisciplinary consensus statement from the ad hoc Committee, American Heart Association. Stroke 1995, 26, 188–201. [Google Scholar] [CrossRef] [PubMed]
- Kleindorfer, D.O.; Towfighi, A.; Chaturvedi, S.; Cockroft, K.M.; Gutierrez, J.; Lombardi-Hill, D.; Kamel, H.; Kernan, W.N.; Kittner, S.J.; Leira, E.C.; et al. 2021 Guideline for the Prevention of Stroke in Patients with Stroke and Transient Ischemic Attack: A Guideline from the American Heart Association/American Stroke Association. Stroke 2021, 52, e364–e467. [Google Scholar] [CrossRef] [PubMed]
- Naylor, R.; Rantner, B.; Ancetti, S.; de Borst, G.J.; De Carlo, M.; Halliday, A.; Kakkos, S.K.; Markus, H.S.; McCabe, D.J.H.; Sillesen, H.; et al. Editor’s Choice—European Society for Vascular Surgery (ESVS) 2023 Clinical Practice Guidelines on the Management of Atherosclerotic Carotid and Vertebral Artery Disease. Eur. J. Vasc. Endovasc. Surg. 2023, 65, 7–111. [Google Scholar] [CrossRef]
- Bonati, L.H.; Kakkos, S.; Berkefeld, J.; de Borst, G.J.; Bulbulia, R.; Halliday, A.; van Herzeele, I.; Koncar, I.; McCabe, D.J.; Lal, A.; et al. European Stroke Organisation guideline on endarterectomy and stenting for carotid artery stenosis. Eur. Stroke J. 2021, 6, 1–47. [Google Scholar] [CrossRef]
- Altinbas, A.; Algra, A.; Brown, M.M.; Featherstone, R.L.; Kappelle, L.J.; Jan de Borst, G.; Mali, W.P.T.M.; van der Worp, H.B.; for the International Carotid Stenting Study Investigators. Effects of carotid endarterectomy or stenting on hemodynamic complications in the International Carotid Stenting Study: A randomized comparison. Int. J. Stroke 2014, 9, 284–290. [Google Scholar] [CrossRef]
- Dangas, G.; Laird, J.R., Jr.; Satler, L.F.; Mehran, R.; Mintz, G.S.; Larrain, G.; Lansky, A.J.; Gruberg, L.; Parsons, E.M.; Laureno, R.; et al. Postprocedural hypotension after carotid artery stent placement: Predictors and short- and long-term clinical outcomes. Radiology 2000, 215, 677–683. [Google Scholar] [CrossRef] [PubMed]
- Howell, M.; Krajcer, Z.; Dougherty, K.; Strickman, N.; Skolkin, M.; Toombs, B.; Paniagua, D. Correlation of periprocedural systolic blood pressure changes with neurological events in high-risk carotid stent patients. J. Endovasc. Ther. 2002, 9, 810–816. [Google Scholar] [CrossRef] [PubMed]
- Park, B.D.; Divinagracia, T.; Madej, O.; McPhelimy, C.; Piccirillo, B.; Dahn, M.S.; Ruby, S.; Menzoian, J.O. Predictors of clinically significant postprocedural hypotension after carotid endarterectomy and carotid angioplasty with stenting. J. Vasc. Surg. 2009, 50, 526–533. [Google Scholar] [CrossRef] [PubMed]
- van Mook, W.N.; Rennenberg, R.J.; Schurink, G.W.; van Oostenbrugge, R.J.; Mess, W.H.; Hofman, P.A.; de Leeuw, P.W. Cerebral hyperperfusion syndrome. Lancet Neurol. 2005, 4, 877–888. [Google Scholar] [CrossRef] [PubMed]
- Bogniotti, L.A.C.; Teivelis, M.P.; Cardozo, F.A.M.; Caramelli, B.; Wolosker, N.; Puech-Leão, P.; De Luccia, N.; Calderaro, D. Hemodynamic depression after carotid surgery: Incidence, risk factors and outcomes. Clinics 2022, 77, 100090. [Google Scholar] [CrossRef] [PubMed]
- Bove, E.L.; Fry, W.J.; Gross, W.S.; Stanley, J.C. Hypotension and hypertension as consequences of baroreceptor dysfunction following carotid endarterectomy. Surgery 1979, 85, 633–637. [Google Scholar]
- Altinbas, A.; Algra, A.; Brown, M.M.; Featherstone, R.L.; Kappelle, L.J.; de Borst, G.J.; Mali, W.P.; van der Worp, H.B. Effects of carotid endarterectomy or stenting on blood pressure in the International Carotid Stenting Study (ICSS). Stroke 2011, 42, 3491–3496. [Google Scholar] [CrossRef] [PubMed]
- Ullery, B.W.; Nathan, D.P.; Shang, E.K.; Wang, G.J.; Jackson, B.M.; Murphy, E.H.; Fairman, R.M.; Woo, E.Y. Incidence, predictors, and outcomes of hemodynamic instability following carotid angioplasty and stenting. J. Vasc. Surg. 2013, 58, 917–925. [Google Scholar] [CrossRef]
- Kristensen, S.D.; Knuuti, J.; Saraste, A.; Anker, S.D.; Bøtker, H.E.; De Hert, S.; Ford, I.; Gonzalez-Juanatey, J.R.; Gorenek, B.; Heyndrickx, G.R.; et al. 2014 ESC/ESA Guidelines on non-cardiac surgery: Cardiovascular assessment and management: The Joint Task Force on non-cardiac surgery: Cardiovascular assessment and management of the European Society of Cardiology (ESC) and the European Society of Anaesthesiology (ESA). Eur. Heart J. 2014, 35, 2383–2431. [Google Scholar] [CrossRef] [PubMed]
- GBD 2019 Stroke Collaborators. Global, regional, and national burden of stroke and its risk factors, 1990–2019: A systematic analysis for the Global Burden of Disease Study 2019. Lancet Neurol. 2021, 20, 795–820. [Google Scholar] [CrossRef] [PubMed]
- Rahman, A.A.; Amruta, N.; Pinteaux, E.; Bix, G.J. Neurogenesis After Stroke: A Therapeutic Perspective. Transl. Stroke Res. 2021, 12, 1–14. [Google Scholar] [CrossRef] [PubMed]
- Bangad, A.; Abbasi, M.; de Havenon, A. Secondary Ischemic Stroke Prevention. Neurotherapeutics 2023, 20, 721–731. [Google Scholar] [CrossRef]
- Foerch, C.; Schaller-Paule, M.A.; Steinmetz, H.; Misselwitz, B.; Bohmann, F.O. Reduction of Ischemic Stroke Associated Disability in the Population: A State-Wide Stroke Registry Analysis over a Decade. J. Clin. Med. 2022, 11, 6942. [Google Scholar] [CrossRef] [PubMed]
- Qazi, U.; Obeid, T.E.; Enwerem, N.; Schneider, E.; White, J.R.; Freischlag, J.A.; Perler, B.A.; Malas, M.B. The effect of ballooning following carotid stent deployment on hemodynamic stability. J. Vasc. Surg. 2014, 59, 756–760. [Google Scholar] [CrossRef] [PubMed][Green Version]
- Gupta, R.; Abou-Chebl, A.; Bajzer, C.T.; Schumacher, H.C.; Yadav, J.S. Rate, predictors, and consequences of hemodynamic depression after carotid artery stenting. J. Am. Coll. Cardiol. 2006, 47, 1538–1543. [Google Scholar] [CrossRef] [PubMed]
- Bussière, M.; Lownie, S.P.; Lee, D.; Gulka, I.; Leung, A.; Pelz, D.M. Hemodynamic instability during carotid artery stenting: The relative contribution of stent deployment versus balloon dilation. J. Neurosurg. 2009, 110, 905–912. [Google Scholar] [CrossRef] [PubMed]
- Cayne, N.S.; Faries, P.L.; Trocciola, S.M.; Saltzberg, S.S.; Dayal, R.D.; Clair, D.; Rockman, C.B.; Jacobowitz, G.R.; Maldonado, T.; Adelman, M.A.; et al. Carotid angioplasty and stent-induced bradycardia and hypotension: Impact of prophylactic atropine administration and prior carotid endarterectomy. J. Vasc. Surg. 2005, 41, 956–961. [Google Scholar] [CrossRef] [PubMed]
- Diehm, N.; Katzen, B.T.; Dick, F.; Kovacs, M.; Zemel, G.; Powell, A.; Samuels, S.; Benenati, J.F. Influence of stent type on hemodynamic depression after carotid artery stent placement. J. Vasc. Interv. Radiol. 2008, 19, 23–30. [Google Scholar] [CrossRef] [PubMed]
- Gibbs, B.F. Temporary hypotension following endarterectomy for severe carotid stenosis: Should we treat it? Vasc. Endovasc. Surg. 2003, 37, 33–38. [Google Scholar] [CrossRef] [PubMed]
- Taha, M.M.; Toma, N.; Sakaida, H.; Hori, K.; Maeda, M.; Asakura, F.; Fujimoto, M.; Matsushima, S.; Taki, W. Periprocedural hemodynamic instability with carotid angioplasty and stenting. Surg. Neurol. 2008, 70, 279–286. [Google Scholar] [CrossRef] [PubMed]
- Lin, P.H.; Zhou, W.; Kougias, P.; El Sayed, H.F.; Barshes, N.R.; Huynh, T.T. Factors associated with hypotension and bradycardia after carotid angioplasty and stenting. J. Vasc. Surg. 2007, 46, 846–854. [Google Scholar] [CrossRef]
- Yang, X.; Liu, Z.; Hu, C.; Li, Y.; Zhang, X.; Wei, L. Incidence and risk factors for hypotension after carotid artery stenting: Systematic review and meta-analysis. Int. J. Stroke 2024, 19, 40–49. [Google Scholar] [CrossRef] [PubMed]
- Rubio, G.; Karwowski, J.K.; DeAmorim, H.; Goldstein, L.J.; Bornak, A. Predicting Factors Associated with Postoperative Hypotension following Carotid Artery Stenting. Ann. Vasc. Surg. 2019, 54, 193–199. [Google Scholar] [CrossRef]
- Choi, J.; Lee, J.Y.; Whang, K.; Cho, S.; Kim, J. Factors associated with hemodynamic instability following carotid artery stenting. Clin. Neurol. Neurosurg. 2021, 203, 106589. [Google Scholar] [CrossRef] [PubMed]
- Pappadà, G.; Beghi, E.; Marina, R.; Agostoni, E.; Cesana, C.; Legnani, F.; Parolin, M.; Petri, D.; Sganzerla, E.P. Hemodynamic instability after extracranial carotid stenting. Acta Neurochir. 2006, 148, 639–645. [Google Scholar] [CrossRef] [PubMed]
- Qureshi, A.I.; Luft, A.R.; Sharma, M.; Janardhan, V.; Lopes, D.K.; Khan, J.; Guterman, L.R.; Hopkins, L.N. Frequency and determinants of postprocedural hemodynamic instability after carotid angioplasty and stenting. Stroke 1999, 30, 2086–2093. [Google Scholar] [CrossRef] [PubMed]
- Wu, T.Y.; Ham, S.W.; Katz, S.G. Predictors and consequences of hemodynamic instability after carotid artery stenting. Ann. Vasc. Surg. 2015, 29, 1281–1285. [Google Scholar] [CrossRef] [PubMed]
- Rhim, J.K.; Jeon, J.P.; Park, J.J.; Choi, H.J.; Cho, Y.D.; Sheen, S.H.; Jang, K.-S. Prediction of Prolonged Hemodynamic Instability During Carotid Angioplasty and Stenting. Neurointervention 2016, 11, 120–126. [Google Scholar] [CrossRef] [PubMed]
- Nonaka, T.; Oka, S.; Miyata, K.; Mikami, T.; Koyanagi, I.; Houkin, K.; Yoshifuji, K.; Imaizumi, T. Prediction of prolonged postprocedural hypotension after carotid artery stenting. Neurosurgery 2005, 57, 472–477. [Google Scholar] [CrossRef]
- Wei, P.; Deng, Q.; Wen, C.; Liu, H. Clinical analysis of patients with hemodynamic depression after carotid artery stenting. Heliyon 2023, 9, e23136. [Google Scholar] [CrossRef] [PubMed]
- Illuminati, G.; Caliò, F.G.; Pizzardi, G.; Vietri, F. Internal carotid artery rupture caused by carotid shunt insertion. Int. J. Surg. Case Rep. 2015, 14, 89–91. [Google Scholar] [CrossRef] [PubMed][Green Version]
- Javid, H.; Julian, O.C.; Dye, W.S.; Hunter, J.A.; Najafi, H.; Goldin, M.D.; Serry, C.; DeLaria, G.A. Seventeen-year experience with routine shunting in carotid artery surgery. World J. Surg. 1979, 3, 167–177. [Google Scholar] [CrossRef] [PubMed]
- Bellosta, R.; Luzzani, L.; Carugati, C.; Talarico, M.; Sarcina, A. Routine shunting is a safe and reliable method of cerebral protection during carotid endarterectomy. Ann. Vasc. Surg. 2006, 20, 482–487. [Google Scholar] [CrossRef] [PubMed]
- Bond, R.; Rerkasem, K.; Rothwell, P.M. Routine or selective carotid artery shunting for carotid endarterectomy (and different methods of monitoring in selective shunting). Cochrane Database Syst. Rev. 2002, CD000190. [Google Scholar] [CrossRef]
- Bandyk, D.F.; Thiele, B.L. Safe intraluminal shunting during carotid endarterectomy. Surgery 1983, 93, 260–263. [Google Scholar] [PubMed]
- Loftus, C.M.; Dyste, G.N.; Reinarz, S.J.; Hingtgen, W.L. Distal cervical carotid dissection after carotid endarterectomy: A complication of indwelling shunt? Neurosurgery 1986, 19, 441–445. [Google Scholar] [CrossRef] [PubMed]
- Filip, C.; Nicolescu, A.; Cinteza, E.; Duica, G.; Nicolae, G.; Safta-Baschieru, D.; Mihalache, I.; Popa, L.; Costin, M.; Matei, G.; et al. Cardiovascular Complications of Hemolytic Uremic Syndrome in Children. Maedica 2020, 15, 305–309. [Google Scholar] [CrossRef] [PubMed]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).