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Updated: Aug 18, 2025

Optimized Management of Endovascular Treatment for Acute Ischemic Stroke
Published on: January 18, 2018
Cerebral Small Vessel Diseases and Outcomes for Acute Ischemic Stroke Patients after Endovascular Therapy
Yixin Zhao1, Yuye Ning1, Lei Lei1
1Stroke Centre, Department of Neurology, The First Affiliated Hospital of the Xi'an Jiaotong University, No. 277 Yanta West Road, Xi'an 710061, China.
Insights
Cerebral small vessel disease burden did not significantly impact outcomes for acute ischemic stroke patients undergoing endovascular therapy. However, enlarged perivascular spaces alone increased the risk of early neurological deterioration.
Area of Science:
- Neurology
- Radiology
- Cardiovascular Research
Background:
- Cerebral small vessel disease (CSVD) is common in acute ischemic stroke (AIS) patients.
- The impact of combined white matter hyperintensities (WMH) and enlarged perivascular spaces (EPVS) on AIS outcomes after endovascular therapy (EVT) is not well understood.
Purpose of the Study:
- To investigate the association between baseline CSVD burden (WMH and EPVS) and clinical outcomes in AIS patients treated with EVT.
- To determine if severe CSVD predicts poor outcomes, including neurological function, symptomatic intracerebral hemorrhage, early neurological deterioration, malignant cerebral edema, and hospital death.
Main Methods:
- Retrospective analysis of 100 AIS patients who underwent EVT.
- MRI assessment of WMH and EPVS to quantify CSVD burden (absent-to-moderate vs. severe).
- Clinical outcomes assessed at 90 days using modified Rankin Scale (mRS); secondary outcomes included sICH, END, MCE, and hospital death.
Main Results:
- Severe CSVD burden was not significantly associated with primary or secondary outcomes.
- Patients with AIS undergoing EVT had a higher risk of early neurological deterioration (END) if they had enlarged perivascular spaces (EPVS).
- No correlation was found between severe combined CSVD burden and sICH, END, or MCE after EVT.
Conclusions:
- Baseline CSVD burden, assessed by combined WMH and EPVS, does not appear to significantly influence outcomes in AIS patients treated with EVT.
- Enlarged perivascular spaces (EPVS) alone may be a risk factor for early neurological deterioration in AIS patients undergoing EVT.
- Further research is needed to fully elucidate the complex relationship between CSVD and AIS prognosis.
Abstract:
The correlation between cerebral small vessel disease (CSVD) and the outcomes of acute ischemic stroke (AIS) patients after endovascular therapy (EVT) remains elusive. We aimed to investigate the effect of combined white matter hyperintensities (WMH) and enlarged perivascular spaces (EPVS) as detected in magnetic resonance imaging (MRI) at baseline on clinical outcomes in patients with AIS who underwent EVT. AIS patients that experienced EVT were retrospectively analyzed in this single-center study. Using MRIs taken prior to EVT, we rated WMH and EPVS as the burden of CSVD and dichotomized the population into two groups: absent-to-moderate and severe. Neurological outcome was assessed at day 90 with a modified Rankin Scale (mRS). Symptomatic intracerebral hemorrhage (sICH), early neurological deterioration (END), malignant cerebral edema (MCE), and hospital death were secondary outcomes. Of the 100 patients (64.0% male; mean age 63.71 ± 11.79 years), periventricular WMHs (28%), deep WMHs (41%), EPVS in basal ganglia (53%), and EPVS in centrum semiovale (73%) were observed. In addition, 69% had an absent-to-moderate total CSVD burden and 31.0% had a severe burden. The severe CSVD was not substantially linked to either the primary or secondary outcomes. Patients with AIS who underwent EVT had an elevated risk (OR: 7.89, 95% CI: 1.0, 62.53) of END if they also had EPVS. When considering WMH and EPVS together as a CSVD burden, there seemed to be no correlation between severe CSVD burden and sICH, END, or MCE following EVT for AIS patients. Further studies are warranted to clarify the relationship between CSVD burden and the occurrence, progression, and prognosis of AIS.
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