# Primary and Secondary Prevention of Ischemic Stroke in Elderly Patients with Cardiovascular Disease: The Role of Frailty and Care Pathways

**Authors:** Fabiana Lucà, Roberto Ceravolo, Michele Massimo Gulizia, Sandro Gelsomino, Carmelo Massimiliano Rao, Nadia Ingianni, Giuseppina Vitale, Giovanna Geraci, Attilio Iacovoni, Pietro Scicchitano, Adriano Murrone, Claudio Bilato, Luigina Guasti, Furio Colivicchi, Fabrizio Oliva, Federico Nardi, Massimo Grimaldi, Iris Parrini

PMC · DOI: 10.3390/neurolint18020036 · Neurology International · 2026-02-14

## TL;DR

This paper reviews how to prevent strokes in elderly patients with heart disease, focusing on managing risk factors and using frailty assessments to guide treatment decisions.

## Contribution

The paper introduces a frailty-informed approach to stroke prevention and emphasizes multidisciplinary care pathways for elderly patients.

## Key findings

- Frailty indices can refine risk–benefit assessments in stroke prevention without leading to therapeutic nihilism.
- Multidisciplinary collaboration improves outcomes in post-discharge stroke prevention for elderly patients.
- Sex- and age-related factors significantly influence treatment effectiveness and safety in stroke prevention.

## Abstract

Stroke is a major global health concern, particularly among the elderly, who frequently present with multiple comorbidities, most notably cardiovascular diseases. Importantly, atrial fibrillation confers a nearly fivefold increase in stroke risk and accounts for up to one-quarter of ischemic strokes in older adults. Stroke is a neurological disease characterised by a strong cardiovascular interplay, and its multifactorial nature requires an integrated preventive approach. This review focuses on primary and secondary prevention in this population, with a frailty-informed perspective. We synthesise evidence on blood pressure control, lipid-lowering (including LDL-C targets), glycemic management, and antithrombotic strategies—particularly oral anticoagulation for atrial fibrillation—as well as the role of frailty indices in guiding individualised risk–benefit decisions. We also discuss practical care pathways, including structured post-discharge programs, continuity of care, and the need for multidisciplinary collaboration involving cardiologists, neurologists, and primary care. We highlight how frailty indices refine risk–benefit assessments without justifying therapeutic nihilism, and how sex- and age-related factors shape treatment effectiveness and safety. By narrowing scope and emphasising practical, multidisciplinary prevention strategies, this review aims to support clinicians in reducing recurrent events, disability, and mortality in very old patients. Future work should prioritise pragmatic trials, including those involving the oldest old and the use of standardised frailty metrics, to inform prevention decisions.

## Linked entities

- **Diseases:** stroke (MONDO:0005098), atrial fibrillation (MONDO:0004981)

## Full-text entities

- **Genes:** PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738] {aka FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1}, COG2 (component of oligomeric golgi complex 2) [NCBI Gene 22796] {aka CDG2Q, LDLC}
- **Diseases:** HF (MESH:D006333), hemorrhagic infarction (MESH:D007238), Depression (MESH:D003866), infective endocarditis (MESH:D004696), Type 2 diabetes mellitus (MESH:D003924), embolic (MESH:D004617), TIA (MESH:D002546), CAD (MESH:D003324), dementia (MESH:D003704), Cardiac comorbidities (MESH:D006331), thromboembolic (MESH:D013923), myopathy (MESH:D009135), migraine (MESH:D008881), sleep apnea (MESH:D012891), Patent foramen ovale (MESH:D054092), Essential thrombocythemia (MESH:D013920), Infectious (MESH:D003141), cognitive decline (MESH:D003072), Carotid Disease (MESH:D002340), left ventricular thrombus (MESH:D013927), pressure ulcers (MESH:D003668), SAH (MESH:D013345), ICH (MESH:D002543), AH (MESH:D000081029), marantic endocarditis (MESH:D059905), atherosclerosis (MESH:D050197), Hypertension (MESH:D006973), Haematological disorders (MESH:D006402), AF (MESH:D001281), ischemic lesion (MESH:D017202), orthostatic hypotension (MESH:D007024), Ischemic Stroke (MESH:D002544), AMI (MESH:D009203), CV symptoms (MESH:D002318), coagulopathies (MESH:D001778), Insulin resistance (MESH:D007333), Antiphospholipid antibody syndrome (MESH:D016736), familial hypercholesterolemia (MESH:D006938), arrhythmia (MESH:D001145), neurological disease (MESH:D020271), obesity (MESH:D009765), bleeding (MESH:D006470), falls (MESH:C537863), left ventricular (LV) dysfunction (MESH:D018487), structural abnormalities (MESH:C566527), cerebral amyloid angiopathy (MESH:D016657), hypercoagulability (MESH:D019851), Stroke (MESH:D020521), inherited thrombophilias (MESH:C540694), aneurysmal rupture (MESH:D017542), confusion (MESH:D003221), fatigue (MESH:D005221), chest pain (MESH:D002637), cardiomyopathies (MESH:D009202), vascular malformations (MESH:D054079), delirium (MESH:D003693), cryptogenic stroke (MESH:D000083242), metabolic dysregulation (MESH:D021081), stenosis (MESH:D003251), metabolic derangements (MESH:D008659)
- **Chemicals:** Lipid (MESH:D008055), simvastatin (MESH:D019821), warfarin (MESH:D014859), glucose (MESH:D005947), rosuvastatin (MESH:D000068718), Antithrombotic (-), clopidogrel (MESH:D000077144), sodium (MESH:D012964), atorvastatin (MESH:D000069059), Aspirin (MESH:D001241), ezetimibe (MESH:D000069438), triglyceride (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942942/full.md

## References

177 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942942/full.md

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Source: https://tomesphere.com/paper/PMC12942942