# Neurological Complications After Thoracic Endovascular Repair (TEVAR): A Narrative Review of the Incidence, Mechanisms and Strategies for Prevention and Management

**Authors:** Francesca Miceli, Marta Ascione, Rocco Cangiano, Antonio Marzano, Alessia Di Girolamo, Giovanni Gagliardo, Luca di Marzo, Wassim Mansour

PMC · DOI: 10.3390/jpm16020077 · 2026-02-01

## TL;DR

This review discusses neurological complications after TEVAR, focusing on their incidence, causes, and strategies to prevent and manage them.

## Contribution

The paper provides a contemporary narrative review of neurological complications after TEVAR, emphasizing individualized prevention and management strategies.

## Key findings

- Perioperative stroke occurs in ~2–6% of TEVAR cases, with higher rates when the left subclavian artery is covered without revascularization.
- Spinal cord ischemia incidence ranges from ~2–9%, influenced by aortic extent and urgency.
- Postoperative delirium occurs in ~13% of TEVAR-treated type B dissections and correlates with longer hospitalization.

## Abstract

Background: Thoracic endovascular aortic repair (TEVAR) has evolved the management of descending thoracic aortic disease, but neurological complications—particularly spinal cord ischemia (SCI), stroke, and postoperative delirium—remain among the most feared adverse events, adversely affecting survival, quality of life, and functional independence. Objectives: The aim of this study was to provide a contemporary narrative synthesis (2000–2025) of the incidence, mechanisms, risk factors, prevention, and management of neurological complications after TEVAR, emphasizing how current evidence supports individualized and risk-adapted strategies for prevention and management. Methods: A narrative, non-systematic search (PubMed/MEDLINE, Scopus, Cochrane Library; 2000–2025) was conducted using terms related to TEVAR, SCI, cerebrovascular events, delirium, and cognitive dysfunction. Priority was given to large registries, cohort studies, and systematic reviews in adult TEVAR populations. Results: Perioperative stroke occurs in ~2–6% of TEVAR cases, with higher rates in arch/zone 0–2 procedures and when the left subclavian artery (LSA) is covered without revascularization. SCI incidence ranges from ~2–9%, influenced by aortic extent and urgency; Vascular Quality Initiative data report SCI in 3.7% of procedures, with markedly reduced 1-year survival. Major SCI risk factors include extensive thoracic coverage, prior aortic repair, vertebral or hypogastric occlusion, emergency presentation, low perioperative mean arterial pressure, anemia, and chronic kidney disease. Postoperative delirium occurs in ~13% of TEVAR-treated type B dissections and correlates with longer hospitalization and early complications. Emerging nomograms for SCI and delirium enable individualized risk stratification. Conclusions: Neurological complications after TEVAR remain clinically significant. Contemporary evidence supports personalized prevention—selective cerebrospinal fluid (CSF) drainage, LSA revascularization, staging, neuromonitoring, and tailored hemodynamic targets—guided by anatomical complexity, comorbidities, collateral network integrity, and prior aortic history. Further research should refine prediction tools, standardize definitions, and evaluate individualized neuroprotective bundles.

## Linked entities

- **Diseases:** spinal cord ischemia (MONDO:0020688), stroke (MONDO:0005098), chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** anemia (MESH:D000740), thrombosis (MESH:D013927), carotid disease (MESH:D002340), microvascular fragility (MESH:D017566), cortical blindness (MESH:D019575), neurologic damage (MESH:D020196), altered consciousness (MESH:D003244), descending thoracic and thoracoabdominal aneurysms (MESH:D000094627), encephalopathy (MESH:D001927), artery occlusion (MESH:D001157), hypertension (MESH:D006973), atherosclerotic aorta (MESH:D050197), nerve injury (MESH:D000080902), vertebral disease (MESH:C535781), cerebral infarctions (MESH:D002544), SCI (MESH:D020760), cerebral and retinal embolization (MESH:D012173), femoral neuropathy (MESH:D020428), posterior stroke (MESH:D020762), cerebrovascular disease (MESH:D002561), livedo reticularis (MESH:D054068), ulcers (MESH:D014456), embolic (MESH:D004617), renal dysfunction (MESH:D007674), cortical infarcts (MESH:D007238), peripheral neuropathies (MESH:D010523), thromboembolism (MESH:D013923), sensory loss (MESH:C580162), dementia (MESH:D003704), epidural hematoma (MESH:D046748), cognitive decline (MESH:D003072), PRES (MESH:D054038), CES (MESH:D017700), paraparesis (MESH:D020335), inflammatory (MESH:D007249), headache (MESH:D006261), injury to (MESH:D014947), degenerative aneurysm (MESH:D019636), metabolic disturbances (MESH:D024821), hematoma (MESH:D006406), Arterial and Aortic Diseases (MESH:D001018), vertebrobasilar insufficiency (MESH:D014715), visual disturbances (MESH:D014786), pain (MESH:D010146), Peripheral nerve injury (MESH:D059348), aorto-iliac aneurysms (MESH:D017543), aneurysm (MESH:D000783), renal insufficiency (MESH:D051437), thoracoabdominal disease (MESH:D058502), calcification (MESH:D002114), lower-limb weakness (MESH:D018908), cerebral ischemia (MESH:D002545), thoracoabdominal aneurysm (MESH:D000094624), pseudoaneurysm (MESH:D017541), diabetes (MESH:D003920), B aortic dissections (MESH:D000784), TEVAR (MESH:D013896), hyponatremia (MESH:D007010), eosinophilia (MESH:D004802), chronic kidney disease (MESH:D051436)
- **Chemicals:** post (-), benzodiazepine (MESH:D001569), sodium (MESH:D012964), creatinine (MESH:D003404), oxygen (MESH:D010100), cholesterol (MESH:D002784)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12941894/full.md

---
Source: https://tomesphere.com/paper/PMC12941894