Faculty Bibliography

Objectives: In patients with carotid stenosis, both the severity of the stenosis as well as the plaque morphology influence the likelihood of future transient ischemic attack or stroke. In general, severely stenotic lesions are presumed to have a higher embolic potential than moderately stenotic lesions. Carotid intervention is indicated in patients with both moderate and severe stenosis with related cerebrovascular symptoms. However, the effect of the degree of carotid stenosis in symptomatic patients upon the outcome of carotid intervention has not been extensively studied.
Method(s): The Society for Vascular Surgery Quality Initiative database was queried for all patients undergoing transfemoral carotid stenting (CAS), carotid endarterectomy (CEA), and transcervical carotid stenting (TCAR) between 2003 and 2020. Patients undergoing interventions for symptomatic disease were included in the analysis. Patients were stratified into two cohorts based on the severity of stenosis-moderate (0%-69%) and severe (greater than or equal to 70%). Primary endpoints were perioperative neurologic events (strokes and transient ischemic attacks [TIAs]). Secondary endpoints were perioperative mortality and postoperative complications.
Result(s): Over 50,000 patients were included in the analysis: 5296 patients (8.9%) underwent TCAR, 7844 (13.3%) underwent CAS, and 45,853 (77.8%) underwent CEA for symptomatic carotid artery disease. In the TCAR and CEA cohorts, patients with moderate stenosis had a significantly higher rate of perioperative neurologic events than patients with severe stenosis (TCAR 4.3% vs 3.0%; P =.033; CEA 3.0% vs 2.3%; P <.001). In contrast, in patients undergoing CAS, there was no significant difference noted in the perioperative neurologic event rate (3.5% in moderate stenosis group vs 3.8% in severe stenosis group; P =.518). There were no differences in perioperative myocardial infarction or mortality (Table). On multivariable analysis, moderate stenosis was significantly and independently associated with an increased rate of neurologic events in the TCAR (odds ratio [OR], 0.833; 95% confidence interval, 0.693-1.000; P =.05), and CEA (odds ratio, 0.901; 95% confidence interval, 0.861-0.944; P <.001) cohorts.
Conclusion(s): Moderate carotid stenosis was associated with increased perioperative neurologic events in patients undergoing TCAR and CEA, but not CAS. Therefore, this effect was noted only in the cohorts that require direct open surgical manipulation of the cervical carotid artery (TCAR and CEA). Moderately stenotic lesions that become symptomatic likely have worse intrinsic plaque morphology than severely stenotic lesions, producing cerebrovascular symptoms at a lower degree of stenosis. The mechanism of such events warrants further evaluation with a particular focus on plaque morphology and brain physiology. [Formula presented]
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Objectives: Current guidelines recommend dual antiplatelet therapy (DAPT) in patients undergoing carotid artery stenting. The most common DAPT regimen is aspirin and clopidogrel, a P2Y12 receptor antagonist; however, there is evidence that the prevalence of clopidogrel resistance (CR) in patients undergoing percutaneous coronary interventions may exceed 40%. Few studies have investigated the prevalence and impact of CR in patients undergoing extracranial carotid artery stenting, particularly transcarotid artery revascularization (TCAR).
Method(s): Consecutive patients 18 years and older who underwent TCAR for high grade (>80%) or symptomatic (>50%) carotid stenosis with preoperative P2Y12 testing between January 2018 and January 2021 were identified across six institutions. Preoperative platelet reactivity was measured with the light transmission aggregometry (VerifyNow P2Y12 Reaction Units [PRU] Test; Instrumentation Laboratory, Bedford, MA), with CR defined as PRU >=194 and hyper-responders as PRU <70. Patients without preoperative P2Y12 testing within 30 days prior to TCAR or those on a non-clopidogrel P2Y12 inhibitor preoperatively were excluded. Primary outcome of interest was the prevalence of CR. Secondary outcomes included the incidence of ischemic and hemorrhagic complications.
Result(s): Of the 67 patients identified, 60 met inclusion criteria. The cohort was 63% male (38/60) and 62% (37/60) Caucasian, with mean age of 74 years (+/-8; range, 56-92 years). Preoperatively, 95% of patients were on aspirin, 100% on clopidogrel, and 15% on therapeutic anticoagulation. At presentation, 42% (25) were symptomatic. Mean preoperative P2Y12 was 168 PRU (+/-81; range, 6-349 PRU). In total, 23 patients (38%) met criteria for CR (mean PRU, 249 +/- 43; range, 197-349), and 8 patients (13%) met criteria for hyper-responder (mean PRU, 35 +/- 22; range, 6-64). There was no significant difference between clopidogrel responders and patients with CR in terms of age (P =.1447), gender (P = 1), race (P =.387), or symptomatic presentation (P =.319). Postoperatively, there were no in-hospital transient ischemic attacks, strokes, or myocardial infarctions. Two patients (3%), one CR (PRU, 240) and one responder (PRU, 119), experienced postoperative access site hematomas that required no subsequent intervention; no other index hospitalization hemorrhagic complications occurred.
Conclusion(s): Using preoperative P2Y12 testing with a threshold of PRU >=194 to define CR, we identified a high prevalence of CR in patients undergoing TCAR similar to that in the pre-existing coronary literature. We found no significant differences in postoperative ischemic or hemorrhagic complications by clopidogrel response phenotype, although complication rates in the overall study cohort were low. Further investigation is warranted to determine if a quantitative assessment of CR is sufficient to identify patients at risk of developing secondary cerebrovascular ischemic events in this patient population.
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Objective: Data regarding the effect of bilateral internal iliac artery (IIA) occlusion during endovascular abdominal aortic aneurysm repair (EVAR) are conflicting, with reported varied risks of pelvic and gastrointestinal ischemia. The aim of our study was to report the perioperative and long-term outcomes of IIA occlusion with origin graft coverage in patients undergoing elective EVAR.
Method(s): Using the Vascular Quality Initiative database (2010-2020), we retrospectively identified patients who had undergone EVAR for infrarenal abdominal aortic aneurysms and aortoiliac aneurysms with or without IIA occlusion by graft coverage or coils. The patients were stratified into three groups according to IIA occlusion status (none, unilateral, bilateral). The baseline characteristics, procedural details, in-hospital outcomes, and overall survival at 5 years were reviewed. The primary outcomes were in-hospital mortality and complications. The secondary outcomes included 5-year mortality. Cox proportional hazards models were used to determine the predictive factors of perioperative and 2-year mortality.
Result(s): A total of 26,690 patients were identified (mean age, 73.5 years; 82% male) who had undergone elective EVAR with bifurcated endografts. Of the 26,690 patients, 2195 (8.2%) had undergone adjunctive unilateral IIA origin graft occlusion, 523 (2%) had undergone bilateral IIA origin graft occlusion, and 23,970 (89.8%) had not undergone any IIA graft occlusion. Perioperatively, no statistically significant differences were found in the incidence of death (0.4% vs 0.6% vs 0.4%; P =.2), gastrointestinal ischemia (0.1% vs 0.1% vs 0.2%; P =.888), unplanned reoperation (1.5% vs 1.8% vs 2.3%; P =.181), or cardiopulmonary complications (2.5% vs 2.8% vs 3.4%; P =.247) among those with no, unilateral, and bilateral IIA origin graft occlusion, respectively (Table). The Kaplan-Meier estimate demonstrated comparable overall survival at 5 years (none, 86.7%; unilateral, 85.2%; bilateral, 89.4%; P =.133; Fig). On multivariable analysis, the status of IIA origin graft coverage was not associated with increased perioperative mortality or complications.
Conclusion(s): EVAR with bilateral IIA interruption was associated with favorable perioperative outcomes with a low rate of major complications. At the time of EVAR, unilateral and bilateral IIA occlusion with a stent-graft did not appear to confer additional risks of perioperative complications and mortality. Our results showed the safety of bilateral IIA interruption in patients undergoing elective EVAR for abdominal aortic aneurysms and aortoiliac aneurysms. [Formula presented] [Formula presented]
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Objective: Although beta-blocker (BB) use is routine for type B aortic dissections (TBADs), its effect in patients undergoing thoracic endovascular aortic repair (TEVAR) is unclear. Furthermore, the effect of BB use on the perioperative outcomes after TEVAR has not been evaluated. We evaluated the effect of BB use on the perioperative outcomes in patients with TBAD undergoing TEVAR.
Method(s): The Society for Vascular Surgery Vascular Quality Initiative database was queried for all patients who had undergone TEVAR for TBAD between September 2012 and February 2020. BB use was defined as the use of such medications for >=30 days preoperatively. Patients were dichotomized according to preoperative BB use (no-BB and BB cohorts). The patient characteristics, procedural details, and postoperative outcomes were compared. The primary endpoints were 30-day mortality and overall postoperative complications, including myocardial infarction, new dysrhythmia, congestive heart failure, access site complications, respiratory, cerebrovascular symptoms, and arm, leg, renal, spinal cord, and gastrointestinal ischemia requiring surgical intervention.
Result(s): Of 2283 patients undergoing TEVAR for TBAD, 1130 (49%) were receiving a BB preoperatively. The BB cohort was older with greater proportions of hypertension, coronary artery disease, congestive heart failure, diabetes, chronic kidney disease, and end-stage renal disease (Table I). Additionally, the BB cohort were more likely to be taking aspirin, a P2Y12 antagonist, a statin, or an ACE inhibitor, and/or receiving anticoagulation therapy preoperatively. The non-BB cohort had more nonelective, symptomatic, and acute dissections. The procedural details, including rates of open conversion and general anesthesia, estimated blood loss, transfusion requirements, and operative times were comparable. On univariate analysis, the BB cohort had a lower risk of overall postoperative complications (22% vs 33%; P <.001) and mortality (4.7% vs 7.7%; P =.003) compared with the non-BB cohort. On multivariable analysis, BB use was associated with a 22% reduction in the odds of postoperative complications (odds ratio, 0.78; 95% confidence interval, 0.62-0.99; P =.044) but did not influence mortality (odds ratio, 1.14; 95% confidence interval, 0.73-1.71; P =.562; Table II).
Conclusion(s): BB use was associated with a significant reduction in postoperative complications for patients undergoing TEVAR for TBAD. Therefore, BB use should be strongly encouraged for appropriately selected patients undergoing TEVAR. [Formula presented] [Formula presented]
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Objective: Statins are often used for primary and secondary prevention of cardiovascular events. Multiple studies have demonstrated a significant reduction in perioperative complications after carotid endarterectomy for patients taking statins. However, data for statin use for patients undergoing transcarotid artery revascularization (TCAR) are limited. We evaluated the effects of statin use on the postoperative outcomes after TCAR.
Method(s): The records of the Vascular Quality Initiative carotid artery stenting registry (2012-2020) were reviewed for patients who had undergone TCAR. The patient demographics, perioperative characteristics, and 30-day outcomes were compared between the patients treated with and without statins (statin and no-statin group, respectively). Multivariable logistic regression models were used to estimate the effect of statins on the postoperative outcomes.
Result(s): A total of 15,797 patients had undergone TCAR, of whom, 10,116 (64%) were men. Of the 15,797 patients, 14,152 (89.6%) were taking a statin preoperatively (Table I). The statin group was more likely to have hypertension (91% vs 87%; P <.001), coronary artery disease (26% vs 23%; P =.008), and diabetes mellitus (33% vs 29%; P <.001). The incidence of both prior ipsilateral stroke (17.2% vs 13.5%; P <.001) and recent ipsilateral stroke (<=30 days; 7.1% vs 5.6%; P =.02) was higher in the statin group. No differences were found in the perioperative characteristics, including median operative time, contrast amount used, technical success, and number of stents used. Perioperative stroke and major adverse cardiac events (MACE; myocardial infarction, congestive heart failure, dysrhythmia) occurred in 1.5% and 2.4% of the statin group and 1.4% and 2.3% of the no-statin group, respectively. Controlling for covariates with the logistic regression method, statin use was associated with a 62% reduction in the odds of mortality (odds ratio, 0.38; 95% confidence interval, 0.19-0.99; P =.047; Table II) for patients who had experienced a perioperative stroke or MACE after TCAR.
Conclusion(s): Statin use was associated with a significant reduction in postoperative mortality for patients who had experienced a stroke or MACE after TCAR. Therefore, strict adherence to statin use is strongly recommended, especially for patients who could be at high risk of major postoperative complications. [Formula presented] [Formula presented]
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Objective: Type II endoleaks (T2E), commonly identified after EVAR, are associated with late endograft failure and secondary rupture. Quantity and size of aortic aneurysm sac outflow vessels (AASOV), namely the inferior mesenteric, lumbar, and accessory renal arteries, have been implicated as known risk factors for persistent T2E. Given technical difficulties associated with post-EVAR embolization, prophylactic coil embolization of AASOV-related T2E has been advocated to prevent retrograde T2E; however, current evidence is limited. We sought to examine the effect of concomitant prophylactic AASOV coil embolization in patients undergoing EVAR.
Method(s): Patients 18 and older in the Society for Vascular Surgery Vascular Quality Initiative database who underwent elective EVAR for intact aneurysms between January 2009 and November 2020 were included. Patients with a history of prior aortic repair and those without available follow-up data were excluded. Patient demographics, operative characteristics, and outcomes were analyzed by group: EVAR with or without prophylactic AASOV embolization (emboEVAR). Primary outcomes of interest were rates of in-hospital postoperative complications, incidence of aneurysmal sac regression (>=5 mm), and rates of reintervention in follow-up.
Result(s): A total of 15,060 patients were included: 272 had emboEVAR and 14,788 had EVAR alone. There was no significant difference between groups in terms of age, comorbidities, or anatomic characteristics including mean maximum preoperative aortic diameter (5.5 vs 5.6 cm, P =.48) (Table I). emboEVAR was associated with significantly longer procedural times (148 vs 124 minutes, P <.0001), prolonged fluoroscopy (32 vs 23 minutes, P <.0001), increased contrast use (105 vs 91 mL, P <.0001), without significant reduction in T2E at completion (17.7% vs 16.3%, P =.54). Incidences of postoperative complications (3.7% vs 4.6%, P =.56), index hospitalization reintervention rates (0.7% vs 1.3%, P =.59), length of stay (1.8 vs 2 days, P =.75), and 30-day mortality (0% vs 0%, P = 1) were similar between groups. In mid-term follow-up (14.6 +/- 6.2 months), the emboEVAR group had a significant mean reduction in maximum aortic diameter (0.69 vs 0.54 cm, P =.006) with a higher proportion experiencing sac regression >=5 mm (53.5% vs 48.7%) and reintervention rates were similar between groups. On multivariate analysis, prophylactic AASOV (odds ratio: 1.34, confidence interval: 1.04-1.74, P =.024) was a significant independent predictor of sac regression (Table II).
Conclusion(s): Prophylactic AASOV embolization can be performed safely for patients with intact aortic aneurysms undergoing elective EVAR without significant associated perioperative morbidity or mortality. emboEVAR is associated with significant sac regression compared with EVAR alone in mid-term follow-up. This technique shows promise and future efforts should focus on elucidating the role of concomitant selective vs complete prophylactic AASOV embolization in patients undergoing EVAR. [Formula presented] [Formula presented]
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OBJECTIVE:Contemporary commercially available endovascular devices for the treatment of abdominal aortic aneurysm (AAA) include standard endovascular aortic repair (sEVAR) or fenestrated EVAR (fEVAR) endografts. However, aortic neck dilatation (AND) can occur in nearly 25% of patients following EVAR, resulting in loss of proximal seal with risk of aortic rupture. AND has not been well characterized in fEVAR, and direct comparisons studying AND between fEVAR and sEVAR have not been performed. This study aims to analyze AND in the infrarenal and suprarenal aortic segments, including seal zone, and quantify sac regression following fEVAR implantation compared to sEVAR. METHOD/METHODS:A retrospective review of prospectively collected data on 20 consecutive fEVAR patients (Cook Zenith® Fenestrated) and 20 sEVAR (Cook Zenith®) patients was performed. Demographic data, anatomic characteristics, procedural details, and clinical outcome were analyzed. Pre-operative, post-operative (1 month), and longest follow-up CT scan at an average of 29.3 months for fEVAR and 29.8 months for sEVAR were analyzed using a dedicated 3D workstation (iNtuition, TeraRecon Inc, Foster City, California). Abdominal aortic aneurysm neck diameter was measured in 5 mm increments, ranging from 20 mm above to 20 mm below the lowest renal artery. Sub-analysis comparing the fEVAR to the sEVAR group at 12 months and at greater than 30 months was performed. Standard statistical analysis was done. RESULTS:Demographic characteristics did not differ significantly between the two cohorts. The fEVAR group had a larger mean aortic diameter at the lowest renal artery, shorter infrarenal aortic neck length, increased prevalence of nonparallel neck shape, and longer AAA length. On follow-up imaging, the suprarenal aortic segment dilated significantly more at all locations in the fEVAR cohort, whereas the infrarenal aortic neck segment dilated significantly less compared to the sEVAR group. Compared to the sEVAR cohort, the fEVAR patients demonstrated significantly greater positive sac remodeling as evident by more sac diameter regression, and elongation of distance measured from the celiac axis to the most cephalad margin of the sac. Device migration, endoleak occurrence, re-intervention rate, and mortalities were similar in both groups. CONCLUSION/CONCLUSIONS:Compared to sEVAR, patients undergoing fEVAR had greater extent of suprarenal AND, consistent with a more diseased native proximal aorta. However, the infrarenal neck, which is shorter and also more diseased in fEVAR patients, appears more stable in the post-operative period as compared to sEVAR. Moreover, the fEVAR cohort had significantly greater sac shrinkage and improved aortic remodeling. The suprarenal seal zone in fEVAR may result in a previously undescribed increased level of protection against infrarenal neck dilatation. We hypothesize that the resultant decreased endotension conferred by better seal zone may be responsible for a more dramatic sac shrinkage in fEVAR.

PURPOSE/UNASSIGNED:Acute thromboembolic disease of the innominate artery (IA) poses a unique set of therapeutic challenges, owing to its contribution to both the cerebral and upper extremity circulation, and risks of distal embolization via the carotid and subclavian arteries, respectively. Herein, we present a 74-year-old female who presents with acute IA thrombus treated successfully with right axillary and common carotid exposure and aspiration catheter-directed mechanical thrombectomy (CDT). Furthermore, an emerging use of CDT and its application in acute thromboembolism are outlined. CASE REPORT/UNASSIGNED:A 74-year-old female with history of right lung transplant for pulmonary fibrosis with severe pulmonary hypertension, and stage IIIA left lung adenocarcinoma status post left lower lobectomy undergoing adjuvant chemotherapy presented with acute IA thrombus and right-sided stroke. She was treated successfully with right axillary and common carotid exposure and aspiration CDT. Computed tomography angiography performed 1 month postoperatively confirmed patent IA with no evidence of residual or recurrent thrombus. CONCLUSION/UNASSIGNED:There are currently no standard guidelines on the management of acute IA thromboembolism, with mostly individual cases reported in the literature describing this rare entity. Nevertheless, this unique clinical entity mandates expeditious diagnostic and therapeutic approaches in order to avoid permanent neurologic deficits from distal embolization. Our case demonstrates that aspiration CDT may be an effective treatment modality for patients with acute IA thrombus.

OBJECTIVE:There is a lack of evidence regarding the effect of anticoagulation and antiplatelet medications on aortic remodeling for aortic dissection after endovascular repair. We investigated whether anticoagulation and antiplatelet medications affect aortic remodeling after thoracic endovascular aortic repair (TEVAR) for Type B aortic dissection (TBAD). METHODS:Records of the Vascular Quality Initiative TEVAR registry (2012-2020) were reviewed. Procedures performed for TBAD were included. Aortic reintervention, false lumen thrombosis of the treated aorta and all-cause mortality at follow-up were compared between patients treated with and without anticoagulation medications. A secondary analysis was performed to assess the effect of antiplatelet therapy in patients not on anticoagulation. Cox proportional hazards models were used to estimate the effect of anticoagulation and antiplatelet therapies on outcomes. RESULTS:1,210 patients (mean age, 60.7±12.2 years; 825 (68%) males) were identified with a mean follow-up of 21.2±15.7 months (range 1-94 months). 166 (14%) patients were on anticoagulation medications at discharge and at follow-up. Patients on anticoagulation were more likely to be older (mean age, 65.5 vs 60 years; P<.001) and Caucasian (69% vs 55%; P=.003), with higher proportions of coronary artery disease (10% vs 3%; P<.001), congestive heart failure (10% vs 2%; P<.001) and chronic obstructive pulmonary disease (15% vs 9%; P=.017). There were no differences in the mean preoperative thoracic aortic diameter or the number of endografts used. At 18-month, the rates of aortic reinterventions (8% vs 9% log-rank P=.873), complete false lumen thrombosis (52% vs 45%; P=.175) and mortality (2.5% vs 2.7%; P=.209) were similar in patients with and without anticoagulation, respectively. Controlling for covariates with the Cox regression method, anticoagulation use was not independently associated with a decreased rates of complete false lumen thrombosis (hazard ratio (HR) 0.74; 95% confidence interval (CI), 0.5-1.1; P=.132), increased need for aortic reinterventions (HR 1.02; 95% CI, 0.62-1.68; P=.934), and mortality (HR 1.25; 95% CI, 0.64-2.47; P=.514). On a secondary analysis, antiplatelet medications did not affect the rates of aortic reintervention, complete false lumen thrombosis and mortality. CONCLUSIONS:Anticoagulation and antiplatelet medications do not appear to negatively influence the midterm endpoints of aortic reintervention or death in patients undergoing TEVAR for TBAD. Moreover, it did not impair complete false lumen thrombosis. Anticoagulation and antiplatelet medications do not adversely affect aortic remodeling and survival in this population at midterm.