Drug-eluting stent opening blocked artery in brain

Drug-Eluting Stents: A Promising Solution for Intracranial Atherosclerosis?

"Find out how these innovative stents offer a safer, more effective approach to treating blocked arteries in the brain and preventing stroke."


Intracranial atherosclerotic disease (ICAD), a major cause of stroke worldwide, especially among Asians, Blacks, and Hispanics, involves the narrowing of arteries within the brain. Traditional treatments for symptomatic ICAD (sICAD) have been evolving, but new solutions are needed. The WASID and SAMMPRIS trials highlighted the challenges and limitations of medical management and traditional stenting procedures.

While aggressive medical management and risk factor control are essential, some patients require more. Percutaneous transluminal angioplasty and stenting (PTAS) techniques have been explored; self-expanding stents (SES) and bare metal stents (BMS) were common. However, the SAMMPRIS and VISSIT trials were stopped early because the stent groups showed increased perioperative complications and no long-term benefit.

The problem? In-stent restenosis (ISR), the re-narrowing of the artery after stenting. Drug-eluting stents (DES), widely used in coronary artery disease, slowly release medication to inhibit cell growth and reduce ISR. Now, researchers are exploring DES for ICAD to improve outcomes. This article examines a systematic review and meta-analysis of DES for ICAD, assessing their efficacy and safety compared to other treatments.

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Intracranial DES: Current Evidence

A 2019 source describes drug-eluting stents (DES) as balloon-expandable systems that slowly release paclitaxel or sirolimus into the vessel wall, aiming to inhibit cell proliferation and migration and thereby reduce neointimal hyperplasia and in-stent restenosis (ISR). A 2026 study set out to evaluate intracranial DES for intracranial atherosclerotic stenosis (ICAS)-related emergent large vessel occlusion, including safety and short-term prognosis; the provided summary does not report its results. The listed materials therefore describe the treatment rationale and a research objective, but provide no current population-level impact statistics.

Medical Therapy and Endovascular Questions

A 2026 review reports that international guidelines have recommended drug therapy as first-line treatment for symptomatic intracranial atherosclerotic disease (ICAD) for almost 10 years, citing issues with endovascular treatment. A randomized clinical trial published in 2022 compared DES with standard bare-metal stents (BMS) in patients with symptomatic high-grade intracranial atherosclerotic stenosis, assessing ISR and recurrent stroke. The supplied summaries do not provide the trial’s results, so they establish the comparison being studied rather than showing that either stent type is superior.

The Evolution of Drug-Eluting Stents

A 2022 review examines the history, research hotspots, and emerging trends of drug-eluting stents (DES) over the preceding two decades, using publications retrieved from the Web of Science Core Collection. Another review describes DES as limiting problems associated with uncovered bare-metal stents after coronary interventions, while noting continuing concerns about late stent thrombosis and in-stent restenosis. It also reports that second-generation DES appeared to lessen these concerns compared with first-generation devices. These sources discuss DES history broadly and do not establish a specific milestone in intracranial stenting.

Do Drug-Eluting Stents Reduce Complications and Improve Outcomes?

Drug-eluting stent opening blocked artery in brain

To evaluate the effectiveness of DES for ICAD, researchers conducted a thorough review of medical literature. They analyzed 13 studies involving 336 patients (364 lesions) treated with DES, focusing on key outcomes:

Here's what the analysis revealed about DES:

  • Perioperative Complications: Occurred in 6.0% of patients.
  • Long-Term Complications: Occurred in 2.2% of patients.
  • In-Stent Restenosis (ISR): 4.1% of patients experienced ISR.
  • Symptomatic ISR: Only 0.5% of patients had symptomatic ISR.
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Evidence on DES, Restenosis, and Procedural Risk

A 2025 meta-analysis reported a 4.1% in-stent restenosis rate across 364 ICAS lesions treated with DES, drawing on 13 studies. A separate review of stent-based interventions notes possible higher procedural morbidity from technical challenges, including vessel-wall perforation or distal-branch injury during guidewire exchanges and the stiff profiles of balloon-expandable stents. These findings highlight both a reported restenosis outcome and potential procedural hazards; the supplied summaries do not establish a direct comparison between them.

Persistent Concerns in Endovascular Treatment

A 2026 review states that international guidelines have recommended drug therapy as first-line treatment for symptomatic ICAD for almost 10 years because of issues associated with endovascular treatment. It also reports that endovascular ICAD treatment has progressed and periprocedural complication rates have fallen. However, the excerpt flags early in-stent restenosis as an ongoing concern and does not provide a rate or further outcome details. The source therefore presents both procedural progress and a continuing limitation, without quantifying the balance between them.

DES Compared With Bare-Metal Stents

A meta-analysis published on April 9, 2024, set out to compare the efficacy of drug-eluting stents (DES) and bare-metal stents (BMS) for intracranial atherosclerotic stenosis (ICAS). Its stated background says evidence supports DES efficacy over BMS in the setting of ICAS. The supplied summary does not give comparative effect estimates or specific outcomes, so it supports reporting the review’s stated direction but not quantifying the advantage.

Importantly, a subgroup analysis revealed that patients with severe stenosis (narrowing greater than 70%) before DES implantation had a significantly higher perioperative complication rate (10.6%) compared to those with moderate stenosis (1.0%).

The Future of ICAD Treatment: What Does This Mean for You?

This review suggests that drug-eluting stents are a relatively safe and effective option for treating intracranial atherosclerotic disease, offering improved outcomes compared to older stent designs and medical management alone.

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Stents and Drug-Coated Balloons

A 2026 review describes stent angioplasty as the most common endovascular intervention for intracranial atherosclerotic stenosis (ICAS), particularly when medical therapy has not succeeded, while noting risks including restenosis and thromboembolic events. It presents drug-coated or drug-eluting balloons (DCB/DEBs) as a promising alternative. A separate 2024 review argues that advances in arterial stenting have challenged earlier conclusions favoring medical management and says recent studies suggest DES may be favorable because of their antiproliferative effect. Together, these sources describe evolving options and arguments, but the excerpts do not establish a definitive treatment recommendation.

Recurrent Ischemic Risk and Treatment Constraints

A 2024 report says patients with intracranial in-stent restenosis (ISR) are at high risk of recurrent ischemic events. It reports that the NOVA intracranial drug-eluting stent trial found DES can reduce ISR and stroke recurrence after implantation of an intracranial bare stent. The same source cautions that use of balloon-expanded DES requires specific vascular conditions. The provided summary does not specify those conditions or quantify the reported reductions.

However, the increased risk of perioperative complications in patients with severe stenosis highlights the need for careful patient selection and experienced operators. More research is needed to confirm these findings and optimize the use of DES in ICAD.

If you're at risk for or have been diagnosed with ICAD, talk to your doctor about the best treatment options for you. Drug-eluting stents may offer a promising solution, but the decision should be made in consultation with a qualified medical professional who can assess your individual risk factors and determine the most appropriate course of action.

How other stent evidence compares

Case series of bare-metal stents reported hemodynamically significant ISR rates of 13.8–37% with bare-metal coronary stents and 24.7–31% with self-expanding nitinol stents. These are results from case series, not a direct comparison with the DES estimate.[1]

A network meta-analysis said DES could reduce stroke recurrence compared with BMS by restraining ISR. A clinical-management review likewise characterized the evidence as suggesting relative safety and efficacy against the non-drug-eluting stents used in SAMMPRIS and VISSIT; these are reported interpretations, not a shared effect estimate.[2] [3]

What remains uncertain about intracranial DES

  • Would the lower ISR rate seen in comparisons also translate into fewer recurrent strokes over longer follow-up? The cited comparison reports an early stroke-or-death outcome and a separate ISR outcome, while other evidence proposes a link between ISR and recurrence.[4]
  • Can findings from reported off-label intracranial use establish a general role for DES? The cited source says intracranial use is not generally indicated and mentions reports of off-label use, which limits what those reports alone can establish.[5]

About this Article -

Written with AI assistance from published research, and reviewed by the Mystum team. See our About page for more information.

This article is based on research published under:

DOI-LINK: 10.1016/j.jocn.2018.10.118, Alternate LINK

Title: Efficacy And Safety Of Drug-Eluting Stent For The Intracranial Atherosclerotic Disease: A Systematic Review And Meta-Analysis

Subject: Physiology (medical)

Journal: Journal of Clinical Neuroscience

Publisher: Elsevier BV

Authors: Gengfan Ye, Xiaoliang Yin, Ximeng Yang, Junjie Wang, Peng Qi, Jun Lu, Lijun Wang, Daming Wang

Published: 2019-01-01

Everything You Need To Know

1

What are drug-eluting stents (DES) and how do they work?

Drug-eluting stents (DES) are a type of stent used to treat intracranial atherosclerotic disease (ICAD). Unlike bare metal stents (BMS), DES release medication over time to prevent the re-narrowing of the artery, known as in-stent restenosis (ISR). This is a significant improvement, because ISR was a major issue with earlier stenting methods.

2

What is intracranial atherosclerotic disease (ICAD) and why is treating it important?

Intracranial atherosclerotic disease (ICAD) is a condition where arteries within the brain narrow due to a buildup of plaque, which is a major cause of stroke. Traditional treatments for ICAD have limitations. Drug-eluting stents (DES) offer a potential solution by addressing the problem of in-stent restenosis (ISR) and improving outcomes compared to older methods such as bare metal stents (BMS).

3

What is in-stent restenosis (ISR) and why is it a problem in treating ICAD?

In-stent restenosis (ISR) is the re-narrowing of an artery after a stent has been placed. It occurs because the body's natural healing process can lead to cell growth within the stent. Drug-eluting stents (DES) combat ISR by releasing medication that inhibits this cell growth, thereby keeping the artery open and reducing the risk of future complications.

4

What were the key findings about drug-eluting stents (DES) from the review?

The analysis of drug-eluting stents (DES) found that perioperative complications occurred in 6.0% of patients, long-term complications in 2.2%, and in-stent restenosis (ISR) in 4.1%. Symptomatic ISR was observed in only 0.5% of patients. Patients with severe stenosis had a higher rate of perioperative complications, underscoring the importance of patient selection.

5

Are drug-eluting stents (DES) a good treatment option for ICAD?

Drug-eluting stents (DES) are considered a safer and more effective option compared to earlier stent designs and medical management alone for treating intracranial atherosclerotic disease (ICAD). The review suggests that DES are a promising solution for ICAD, improving patient outcomes and reducing complications such as in-stent restenosis (ISR).

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