Circle of Willis Configuration and Thrombus Localization Impact on Ischemic Stroke Patient Outcomes: A Systematic Review
Abstract
:1. What This Research Adds
1.1. What Is Already Known on This Topic
1.2. What This Study Adds
1.3. How This Study might Affect Research, Practice, or Policy
2. Background
3. Methods
- 1.
- Literature search strategy
- 2.
- Selection criteria
Inclusion Criteria |
● publications on the influence of Circle of Willis variants on ischemic stroke outcomes; |
● manuscripts in English, German, and Russian; |
● human studies; |
● available in full text. |
Exclusion criteria |
● hemodynamic model studies; |
● only abstract available; |
● physiology reviews; |
● case-series and case reports. |
- 3.
- Types of studies human studies;
- 4.
- Types of participants: ischemic stroke patients;
- 5.
- Types of outcomes.
- 6.
- Data extraction and critical appraisal
4. Results
5. Discussion
5.1. Importance of Circle of Willis Variants for Stroke Outcomes
5.2. Distal ICA Occlusion
5.3. Fetal Posterior Cerebral Artery
5.4. Circle of Willis Variants Has No Impact in Cases of M1 Occlusion
6. Conclusions
7. Limitations
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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Study | A Clearly Stated Aim | Inclusion of Consecutive Patients | Prospective Collection of Data | Endpoints Appropriate to the Aim of the Study | Unbiased Assessment of the Study Endpoint | Follow-Up Period Appropriate to the Aim of the Study | Loss to Follow Up Less than 5% | Prospective Calculation of the Study Size | An Adequate Control Group | Contemporary Groups | Baseline Equivalence of Groups | Adequate Statistical Analyses | MINORS |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
De Caro et al. [4] | 2 | 2 | 0 | 2 | 2 | n/a | n/a | 0 | 2 | 2 | 2 | 2 | 16 |
Lin et al. [1] | 2 | 2 | 0 | 2 | 2 | 2 | 2 | 0 | 2 | 2 | 2 | 2 | 20 |
Westphal et al. [2] | 2 | 2 | 0 | 2 | 2 | 2 | 0 | 0 | n/a | n/a | n/a | 2 | 12 |
Fischer et al. [12] | 2 | 2 | 0 | 2 | 1 | 2 | 1 | 0 | n/a | n/a | n/a | n/a | 10 |
Seifert-Held et al. [13] | 2 | 0 | 0 | 2 | 2 | 2 | 0 | 0 | n/a | n/a | n/a | 1 | 9 |
Shaban et al. [14] | 2 | 0 | 0 | 2 | 2 | 2 | 0 | 0 | n/a | n/a | n/a | 2 | 10 |
Hong et al. [15] | 2 | 2 | 1 | 2 | 2 | 0 | 0 | 0 | n/a | n/a | n/a | n/a | 9 |
Zhao et al. [5] | 2 | 2 | 0 | 2 | 1 | 2 | 1 | 0 | n/a | n/a | n/a | n/a | 10 |
Lee et al. [11] | 2 | 2 | 0 | 2 | 2 | 2 | 1 | 0 | n/a | n/a | n/a | n/a | 11 |
Zhou et al. [10] | 1 | 2 | 1 | 2 | 2 | 1 | 0 | 0 | n/a | n/a | n/a | n/a | 9 |
Study | Country | Study Design | N | Occlusion Site | NIHSS on Arrival | CoW Variants | Stroke Territory | Treatment | Results | Conclusion | Link | MINORS |
---|---|---|---|---|---|---|---|---|---|---|---|---|
De Caro et al. (2021) [4] | Italy | Cross-sectional study | 1131 + 562 control | Not documented | 11.4 ± 7.1 | 1. No variants 2. Ant. variants 3. Post. Variants 4. Ant. and post. variants | All | MTE ± IVT | Among stroke patients, 702 (62.1%) had one or more vascular variants, compared to 308 (54.8%) of the control group (p < 0.01), 165/702 (23.5%) had an anterior circulation variant only, 384/702 (54.7%) had a posterior circulation variant only, and 153/702 (21.8%) patients had variants in both anterior and posterior circulation. | No statistical significance | https://pubmed.ncbi.nlm.nih.gov/33786665/ (accessed on 11 June 2023) | 16/24 |
Lin et al. (2022) [1] | USA | Cross-sectional study | 297 | 43% had an intracranial occlusion, not detailed | 5.0 ± 7.2 | P1, A1 | N/a | Not documented | The presence of an incomplete circle of Willis decreased the odds of a stroke patient having a good outcome by 47% (p = 0.046, OR 0.53, 95% CI 0.281–0.988), after adjusting for age and severity of stroke at admission. | An incomplete circle of Willis may be associated with a poorer prognosis for stroke patients. | https://pubmed.ncbi.nlm.nih.gov/35661459/ (accessed on 11 June 2023) | 20/24 |
Westphal et al. (2021) [2] | Switzerland | Cross-sectional study | 193 + 73 | M1 | 12 (8–17) | Four flow models (A1/AcomA, P1/PcomA) | M1 | MTE ± IVT | CoW integrity did not differ between groups with favorable (modified Rankin Scale (mRS)): 0–2) and unfavorable (mRS: 3–6) 3-month outcome. However, trends towards a higher mortality in patients with any type of CoW variant (p = 0.08) and a higher frequency of incomplete CoW among patients dying within 3 months after stroke onset (p = 0.119) were found. In a logistic regression analysis adjusted for the potential confounders age, sex, and atrial fibrillation, neither the vascular models nor anterior or posterior variants were independently associated with outcome. | No statistical significance | https://pubmed.ncbi.nlm.nih.gov/34233384/ (accessed on 11 June 2023) | 13/16 |
Seifert-Held et al. (2021) [13] | Austria | Cross-sectional study | 182 | ICA dist., MCA | 16 | Absence of either the iPcomA, iP1 or iA1 were all rated as an incomplete CoW. | Anterior | MTE ± IVT | An incomplete ipsilateral COW was not predictive of the patients’ functional outcome at 90 days. | No statistical significance | https://pubmed.ncbi.nlm.nih.gov/34233384/ (accessed on 11 June 2023) | 9/16 |
Shaban et al. (2013) [14] | USA | Case control | 536 | Not documented | 7 (0–27) 3, 14 | cfPCA/pfPCA/nofPCA | All | Not documented | Patients with complete fPCA had fewer small vessel strokes and more large vessel strokes than patients with no fPCA and partial fPCA. Fetal PCA may predispose an individual toward stroke mechanism, but it is not associated with vascular distribution, stroke severity, or early outcome. | No statistical significance | https://pubmed.ncbi.nlm.nih.gov/23577277/ (accessed on 11 June 2023) | 9/16 |
Hong et al. (2009) [15] | South Korea | Case control | 95 | PA | 10.4 (9.7) | fetal vs. non-fetal PcomA | VB | Natural progression | Among all 95 patients, 58% (n = 55) had good prognosis (mRS (2). Interestingly, 44 patients (46.3%) had at least one fetal-variant PcomA (26 bilateral, 18 unilateral). Through multiple logistic regression analysis, the atherosclerotic mechanism (OR 18.0; 95% CI 3.0 to 107.0) and presence of fetal-variant PcomA (OR 5.1; 95% CI 1.4 to 18.8) were found to be independent predictors for good prognosis and initial NIH stroke scale score (OR 1.24 per one-point increase; 95% CI 1.1 to 1.4) for poor prognosis. | Fetal PcomA appears to be an important factor for positive outcomes in acute stroke victims involving the brainstem with BA occlusive disease | https://pubmed.ncbi.nlm.nih.gov/19917819/ (accessed on 11 June 2023) | 10/16 |
Zhao et al. (2019) [5] | China | Cohort study | 38 | PcomA + T or isolated PcomA | 23 | 1. AcomA (−) 2. AcomA (+); iPcomA (−) 3. AcomA (+); iPcomA (+) | Intracranial ICA | MTE ± IVT | Of 38 iICAO patients, 65.8% (25 in 38) achieved reperfusion. However, only 31.6% (12/38) achieved favorable outcomes at 90 days. With a PCG3, 61.5% of them achieved favorable outcomes, while only 37.5% of those with PCG2 and PCG1 achieved favorable outcomes (p = 0.003). In multivariable logistic regression, PCG was revealed as a predictor for favorable outcomes (OR 5.278, p = 0.019) after adjusting the reperfusion and other factors. | The PCG based on the integrity of Willis’ Circle might be an underlying predictor of the prognosis of AIS in patients with iICAO after MTE. | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908856/ (accessed on 11 June 2023) | 10/16 |
Fischer et al. (2022) [12] | Germany | Case control | 1068 | Intracranial ICA | 17 (13–21) | Normal A1 vs. functional aplasia | Intracranial ICA | MTE ± IVT | Patients with functional contralateral A1 aplasia were more severely affected on admission (median NIHSS 18, IQR 15–23 vs. 17, IQR 13–21; aOR: 0.672, 95% CI: 0.448–1.007, p = 0.054) and post-interventional ischemic damage was larger (median ASPECTS 5, IQR 1–7, vs. 6, IQR 3–8; aOR: 1.817, 95% CI: 1.184–2.789, p = 0.006). Infarction occurred more often within the ipsilateral ACA territory (20/76, 26% vs. 110/961, 11%; aOR: 2.482, 95% CI: 1.389–4.437, p = 0.002) and both ACA territories (8/76, 11% vs. 5/961, 1%; aOR: 17.968, 95% CI: 4.979–64.847, p ≤ 0.001). Functional contralateral A1 aplasia was associated with a lower rate of functional independence at discharge (6/81, 8% vs. 194/965, 20%; aOR: 2.579, 95% CI: 1.086–6.122, p = 0.032) and after 90 days (5/55, 9% vs. 170/723, 24%; aOR: 2.664, 95% CI: 1.031–6.883, p = 0.043). | A functional A1 aplasia contralateral to a distal ICA occlusion associated with a poorer clinical outcome | https://www.mdpi.com/2077-0383/11/5/1293 (accessed on 11 June 2023) | 11/16 |
Lee et al. (2016) [11] | South Korea | Cohort study | 92 | T or L type occlusions | 19 (17–22) | The STO group was classified by acute ICA terminus occlusion and patency of not only the ipsilateral A2 segment via the AcomA but also the ipsilateral PCA via the PcomA or the P1 segment. The CTO group was classified by acute ICA terminus occlusion and had one or more of the following: 1) occlusion of the ipsilateral A2 or more distal segment 2) occlusion of the fetal-type ipsilateral PCA (C6 segment of ICA) 3) insufficient contralateral Willisian collateral blood supply via the AcomA due to contralateral agenesis of A1 (absent or severely hypoplastic) contralateral ICA occlusion. | Anterior | IVT ± MTE, | The STO group (n = 58) showed smaller infarct volumes at 72 h than the CTO group (n = 34) (median, 81 mL (interquartile range, 38–192) vs. (414 mL 193–540, p < 0.001) and more favorable outcomes (3-month modified Rankin Scale 0–3, 44.8% vs. 8.8%, p < 0.001; 3-month mortality, 24.1% vs. 67.6%, p < 0.001). In multivariable analyses, STO remained an independent predictor for favorable outcomes (odds ratio 6.1, p = 0.010). | The acute ICA terminus occlusion outcomes depend on Willisian collateral status. | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4901942/ (accessed on 11 June 2023) | 9/16 |
Zhou et al. (2016) [10] | China | Cohort study | 376 | Not documented | 7.79 ± 5.16 | Four CoW variants: PCG1: complete Circle of Willis; type PCG2: complete anterior half of the circle of Willis and incomplete posterior half of the circle of Willis; PCG3: incomplete anterior half of the circle of Willis and complete posterior half of the circle of Willis; and type PCG4: incomplete anterior and posterior halves of the circle of Willis. | Not documented | Natural progression | Of 38 iICAO patients, 65.8% (25 in 38) achieved reperfusion. However, only 31.6% (12/38) achieved favorable outcomes after 90 days. With a PCG3, 61.5% of them achieved favorable outcomes, while only 37.5% of those with PCG2 and PCG1 achieved favorable outcomes (p = 0.003). In multivariable logistic regression, PCG was revealed as a predictor for favorable outcomes (OR 5.278, p = 0.019) after adjusting the reperfusion and other factors. | Better functional outcomes in patients with complete CoW | https://pubmed.ncbi.nlm.nih.gov/26962785/ (accessed on 11 June 2023) | 10/16 |
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Širvinskas, A.; Lengvenis, G.; Ledas, G.; Mosenko, V.; Lukoševičius, S. Circle of Willis Configuration and Thrombus Localization Impact on Ischemic Stroke Patient Outcomes: A Systematic Review. Medicina 2023, 59, 2115. https://doi.org/10.3390/medicina59122115
Širvinskas A, Lengvenis G, Ledas G, Mosenko V, Lukoševičius S. Circle of Willis Configuration and Thrombus Localization Impact on Ischemic Stroke Patient Outcomes: A Systematic Review. Medicina. 2023; 59(12):2115. https://doi.org/10.3390/medicina59122115
Chicago/Turabian StyleŠirvinskas, Audrius, Givi Lengvenis, Giedrius Ledas, Valerija Mosenko, and Saulius Lukoševičius. 2023. "Circle of Willis Configuration and Thrombus Localization Impact on Ischemic Stroke Patient Outcomes: A Systematic Review" Medicina 59, no. 12: 2115. https://doi.org/10.3390/medicina59122115
APA StyleŠirvinskas, A., Lengvenis, G., Ledas, G., Mosenko, V., & Lukoševičius, S. (2023). Circle of Willis Configuration and Thrombus Localization Impact on Ischemic Stroke Patient Outcomes: A Systematic Review. Medicina, 59(12), 2115. https://doi.org/10.3390/medicina59122115