Key result
Carotid artery stenosis is not linked to increased 30-day neurovascular complications after TAVI.
Why the study?
Stroke is a known complication of both TAVI and carotid artery stenosis, but whether carotid artery stenosis predicts worse prognosis after TAVI remains unclear.
Does carotid artery stenosis increase the risk of 30-day neurovascular complications or mortality in patients undergoing transcatheter aortic valve implantation?
Meta-Analysis (n=30,624)
Does carotid artery stenosis increase the risk of 30-day neurovascular complications or mortality in patients undergoing transcatheter aortic valve implantation?
In patients undergoing TAVI, concurrent carotid artery stenosis is a marker of higher comorbidity burden and increased 30-day mortality, but does not significantly increase the risk of 30-day neurovascular complications.
Stroke is a known complication of both transcatheter aortic valve implantation (TAVI) and carotid artery stenosis (CAS). Whether CAS is a predictor of worse prognosis after TAVI is unclear. We performed a meta-analysis to assess the impact of CAS on the incidence of neurovascular complications and mortality after TAVI. We searched PubMed/MEDLINE and EMBASE databases from inception to January 2023. CAS was defined by ≥50% stenosis of at least 1 carotid artery. Studies comparing CAS versus non-CAS TAVI populations were included. Patients’ baseline characteristics and 30-day clinical outcomes were extracted. End points included the 30-day incidence of neurovascular complications (stroke or transient ischemic attack) and 30-day all-cause mortality. We identified six studies, totaling 6,763 patients in the CAS group and 23,861 patients in the non-CAS group. Patients with CAS had a higher prevalence of hypertension, diabetes mellitus, dyslipidemia, previous myocardial infarction, coronary artery bypass graft, peripheral artery disease, previous neurovascular disease, and chronic kidney disease. There was no significant difference in the rates of 30-day neurovascular complications between CAS and non-CAS groups (relative risk 1.23, 95% confidence interval 0.63 to 2.40, p = 0.54). CAS was associated with a higher risk of 30-day all-cause mortality (relative risk 1.28, 95% confidence interval 1.12 to 1.47, p <0.001), not found in a sensitivity analysis. In conclusion, patients with CAS presented with a significantly higher co-morbidity burden. CAS was not associated with an increased risk of 30-day neurovascular complications. 30-day mortality was higher in the CAS group but that may be a surrogate of the heavy co-morbidity burden of patients with CAS. Stroke is a known complication of both transcatheter aortic valve implantation (TAVI) and carotid artery stenosis (CAS). Whether CAS is a predictor of worse prognosis after TAVI is unclear. We performed a meta-analysis to assess the impact of CAS on the incidence of neurovascular complications and mortality after TAVI. We searched PubMed/MEDLINE and EMBASE databases from inception to January 2023. CAS was defined by ≥50% stenosis of at least 1 carotid artery. Studies comparing CAS versus non-CAS TAVI populations were included. Patients’ baseline characteristics and 30-day clinical outcomes were extracted. End points included the 30-day incidence of neurovascular complications (stroke or transient ischemic attack) and 30-day all-cause mortality. We identified six studies, totaling 6,763 patients in the CAS group and 23,861 patients in the non-CAS group. Patients with CAS had a higher prevalence of hypertension, diabetes mellitus, dyslipidemia, previous myocardial infarction, coronary artery bypass graft, peripheral artery disease, previous neurovascular disease, and chronic kidney disease. There was no significant difference in the rates of 30-day neurovascular complications between CAS and non-CAS groups (relative risk 1.23, 95% confidence interval 0.63 to 2.40, p = 0.54). CAS was associated with a higher risk of 30-day all-cause mortality (relative risk 1.28, 95% confidence interval 1.12 to 1.47, p <0.001), not found in a sensitivity analysis. In conclusion, patients with CAS presented with a significantly higher co-morbidity burden. CAS was not associated with an increased risk of 30-day neurovascular complications. 30-day mortality was higher in the CAS group but that may be a surrogate of the heavy co-morbidity burden of patients with CAS. 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Cerebrovascular events after aortic valve replacement a PubMed Scopus Google Scholar is known impact in patients A Beyersdorf F Praz F Milojevic M Baldus S Bauersachs J Capodanno D Conradi L De Bonis M De Paulis R Delgado V Freemantle N Gilard M Haugaa KH Jeppsson A Jüni P Pierard L Prendergast BD Sádaba JR Tribouilloy C Wojakowski W ESC/EACTS Scientific Document Group2021 ESC/EACTS Guidelines for the management of valvular heart disease.Eur Heart J. 2022; 43: 561-632Crossref PubMed Scopus (1180) Google V M M T JP M De M S C T S L M J M M G M C Scientific Document Guidelines on the and treatment of peripheral in with the for Document of carotid and and the Stroke for the and of of the of and of the for Heart J. 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PubMed Scopus Google Scholar be S F M C M Tarantini G and impact of carotid artery in patients undergoing transcatheter aortic valve 2022; PubMed Scopus Google S R Mehta A J S V L artery and stroke risk after transcatheter aortic valve PubMed Scopus Google Scholar previous that patients with severe carotid have M T M B J severe carotid artery stenosis or and PubMed Scopus Google Scholar may at risk of neurovascular complications after stroke and S A O M E S P O C P P C P outcomes in with carotid artery stenosis in patients undergoing transcatheter aortic valve Cardiol. 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Vella et al. (2023) conducted a meta-analysis in Transcatheter Aortic Valve Implantation (TAVI) (n=30,624). Carotid artery stenosis (CAS) vs. Non-CAS was evaluated on 30-day incidence of neurovascular complications (stroke or transient ischemic attack) (RR 1.23, 95% CI 0.63 to 2.40, p=0.54). Carotid artery stenosis in patients undergoing TAVI was not associated with an increased risk of 30-day neurovascular complications compared to non-CAS patients (RR 1.23; 95% CI 0.63-2.40; p=0.54).
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