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. 2021 Dec 23;12:714313. doi: 10.3389/fneur.2021.714313

Preliminary Application of a Quantitative Collateral Assessment Method in Acute Ischemic Stroke Patients With Endovascular Treatments: A Single-Center Study

Ruoyao Cao 1,2, Peng Qi 3, Yun Jiang 4, Shen Hu 3, Gengfan Ye 5, Yaxin Zhu 6, Ling Li 2,7, Zilong You 2, Juan Chen 2,*
PMCID: PMC8732366  PMID: 35002909

Abstract

Objectives: To develop an efficient and quantitative assessment of collateral circulation on time maximum intensity projection CT angiography (tMIP CTA) in patients with acute ischemic stroke (AIS).

Methods: Eighty-one AIS patients who underwent one-stop CTA-CT perfusion (CTP) from February 2016 to October 2020 were retrospectively reviewed. Single-phase CTA (sCTA) and tMIP CTA were developed from CTP data. Ischemic core (IC) volume, ischemic penumbra volume, and mismatch ratio were calculated. The Tan scale was used for the qualitative evaluation of collateral based on sCTA and tMIP CTA. Quantitative collateral circulation (CCq) parameters were calculated semi-automatically with software by the ratio of the vascular volume (V) on both hemispheres, including tMIP CTA VCCq and sCTA VCCq. Spearman correlation analysis was used to analyze the correlation of collateral-related parameters with final infarct volume (FIV). ROC and multivariable regression analysis were calculated to compare the significance of the above parameters in clinical outcome evaluation. The analysis time of the observers was also compared.

Results: tMIP CTA VCCq (r = 0.61, p < 0.01), IC volume (r = 0.66, p < 0.01), Tan score on tMIP CTA (r = 0.52, p < 0.01) and mismatch ratio (r = 0.60, p < 0.01) showed moderate negative correlations with FIV. tMIP CTA VCCq showed the best prognostic value for clinical outcome (AUC = 0.93, p < 0.001), and was an independent predictive factor of clinical outcome (OR = 0.14, p = 0.009). There was no difference in analysis time of tMIP CTA VCCq among observers (p = 0.079).

Conclusion: The quantitative evaluation of collateral circulation on tMIP CTA is associated with clinical outcomes in AIS patients with endovascular treatments.

Keywords: brain ischemia, collateral circulation, computed tomography angiography, CT perfusion, stroke

Introduction

Reperfusion therapies significantly improve the prognosis of patients with acute ischemic stroke (AIS). With the popularization of endovascular treatments (EVTs) in AIS, it is necessary to build an individualized evaluation system, helping physicians make clinical decisions and predict outcomes before invasive intervention (1, 2). Previous studies have indicated that collateral circulation is one of the main factors determining ischemic penumbra (36). Comprehensive and accurate evaluation of collateral circulation is a necessary complement to develop individualized treatments for AIS patients.

The visibility of the collateral circulation on computed tomography angiography (CTA) strongly depends on the acquisition time. The strength of the collateral flow is more important to tissue fate than the velocity of collateral filling (7). Because the interindividual collateral circulation (distribution, filling time, etc.) is highly variable and the optimal acquisition time is individually different, four-dimensional CTA (4D CTA) obtained from the perfusion data (multi-time frame) was applied to evaluate collateral status more accurately (79). Time maximum intensity projection angiography (tMIP CTA), also known as timing-invariant (TI) CTA (10) or temporally fused maximum intensity projection (tMIP) CTA (7), reflects the maximum value on all projection planes scrolling over time, producing a new volume-based data packet that is generated from all phases images of CT perfusion (CTP). tMIP CTA may eliminate the drawback of single-phase CTA (sCTA) wherein collateral vessels are usually displayed incompletely due to delayed pathophysiology status, building a system with high temporal and spatial resolution (7, 8, 1012). Thus, tMIP CTA improves the signal-to-noise ratio (SNR) and contrast-to-noise ratio (CNR) of images and may therefore be an ideal option for assessing collateral circulation (7, 8, 12).

Until now, there has been no unified collateral circulation evaluation system. Several grading scales have been applied in collateral circulation evaluation, including the CTA-based Miteff scale (13), the modified Tan scale (14), and the regional leptomeningeal collateral score (rLMC) (15). It is difficult to verify the predictive value, reliability, and validity of these different scoring systems. Therefore, a standardized evaluation model is needed. Here, we adopted a simple and efficient quantitative assessment based on tMIP CTA to evaluate collateral circulation status.

In this study, we assessed whether this new quantitative assessment system was able to evaluate collateral circulation accurately in comparison with the qualitative collateral score system and CTP. Additionally, the analysis time among observers with different levels of experience was also compared. We aimed to identify an efficient and highly accurate quantitative method for evaluating collateral circulation during the decision-making process.

Methods

This study was approved by our institutional review board. Because patient information was analyzed retrospectively and anonymously, informed consent was waived.

Study Population

The clinical data and imaging data of AIS patients with occlusion of the anterior circulation vessels who had received EVTs from February 2016 to October 2020 were retrospectively analyzed. Inclusion criteria: (1) acute stroke (onset time <24 h); (2) one-stop CT scan indicating occlusion of unilateral anterior circulation vessels [including the internal carotid artery (ICA) and/or the M1 segment of the middle cerebral artery (MCA)]; and (3) integral clinical and imaging data. Exclusion criteria: (1) intracranial hemorrhage; (2) old infarct size ≥ 2/3 of the MCA territory; (3) moderate to severe stenosis of ipsilateral proximal or contralateral arteries; (4) severe dysfunction of the heart, liver, lungs, and kidneys as well as hematological diseases; and (5) history of iodine allergy (16).

The AIS patients' clinical and imaging data were obtained from the medical records, including the National Institutes of Health Stroke Scale (NIHSS) score, Modified Rankin Scale (mRS) score, Alberta Stroke Program Early CT Score (ASPECTS), and related risk factors. The mRS score was used to evaluate the patients' functional outcomes. mRS scores of 0-2 indicate a good outcome, while mRS scores of 3-6 indicate a poor outcome. If patients died during follow-up, the score was recorded as 6. Recanalization was defined as a modified Thrombolysis in Cerebral Infarction grade 2b or 3 (17). The area of low-density on follow-up non-contrast CT (NCCT) images or high signal intensity on MR T2WI or DWI after 3-7 days was considered as the final infarct volume (FIV) (18).

Scanning Protocol

All patients underwent a one-stop CTA-CTP scan on a 320 × 0.5 mm detector row CT scanner (Aquilion ONE, Canon Medical Systems) on admission according to our emergency procedures. An NCCT scan was performed first with the following scan parameters: 120 kV/200 mAs/detector and volume scanning, followed by one-stop dynamic volume 4D CTA-CTP scanning, reconstruction with adaptive iterative dose reduction, and layer thickness 0.5 mm. The contrast agent was injected through the elbow vein with an 18G intravenous catheter, while 40-50 ml of non-ionic contrast agent and 30 ml of saline were sequentially injected through a double-channel high-pressure injector according to the patient's weight (0.6 ml/kg). A CTP scan was performed 7 s after contrast injection with the following scanning parameters: 80 kV, 100 mAs, cover range of 16 cm, reconstruction with adaptive iterative dose reduction, and layer thickness 0.5 mm.

Image Postprocessing

A total of 6,080-frame dynamic volume data in 19 phases of the whole brain were obtained. (1) sCTA: The arterial phase images (the phase with the maximum CT value of the artery) were selected from 19 phases as sCTA images. (2) tMIP CTA: tMIP CTA images were generated from all 19 phases using the analysis software installed in the CT workstation (Aquilion ONE, Canon Medical Systems). tMIP images reflect the maximum value of each matrix in the dynamic data for all phases (12). (3) CTP: Vitrea (Vital Images, Minnetonka, Minnesota) was used to perform all the CTP analyses. The input artery and output vein were obtained from the intracranial segment of the internal carotid artery in the normal side and superior sagittal sinus, respectively, and time-density curves (TDC) were obtained. A 38% reduction in cerebral blood volume (CBV) with a 5.3-s increase in time to peak (TTP) indicated infarct core (IC), and a 5.3-s increase in TTP without CBV reduction indicated ischemic penumbra (IP). The mismatch ratio was the IP volume divided by the IC volume (19).

Colt burden score (CBS) was defined as the extent of thromboembolic vessels of the anterior circulation based on CTA. Occlusions of the supraclinoid ICA, proximal and distal M1 segment were counted as two points, respectively, while each segment of M2 branches, anterior cerebral artery, and infraclinoid ICA occlusion were counted as one point, respectively. If thromboembolism was seen in any segment, the corresponding point was subtracted from 10. The remaining points constituted the final score (20).

Evaluation Methods for the Collateral Status Based on sCTA and tMIP CTA

Quantitative Method

Volume Calc semi-automated volumetric measurement analysis software (Aquilion ONE; Canon Medical Systems Corporation) was used for the quantitative evaluation of collateral circulation. The detailed calculation process of this software was as follows. Step 1: Set thresholds of CT values including the minimum and maximum CT values in the region of interest (ROI) for calculating blood vessel volumes. In this study, the CT values of the intracranial arteries were measured on axial images (0.5-mm layer thickness). The minimum CT value was set as 100 HU (≥CT value of brain tissue and muscle after enhanced scan), and the maximum CT value was defined as the CT value of segment C1 of the internal carotid artery. Step 2: The temporal pole layer, the basal ganglia layer, and the parietal lobe layer were selected as the initial layer, the intermediate layer, and the end layer, respectively. The volume of the blood vessels was calculated automatically by the software. The skull and cerebellar hemispheres were avoided as much as possible when drawing the ROIs (Figure 1). The quantitative measurement of the collateral circulation (CCq) was expressed as a ratio and defined by the following formulas:

Figure 1.

Figure 1

Illustrative example. Baseline one-stop CTA-CTP images and follow-up MRI in a 78-year-old woman with sudden weakness of the left upper limb. The baseline NIHSS score was 5. First, the layers were drawn manually in the right hemisphere on tMIP CTA: the temporal pole layer (A), the basal ganglia layer (B) and the parietal lobe layer (C) were selected as the initial layer, the intermediate layer and the end layer, respectively. The blood vessel volume calculated automatically by the software, which was 36.96 ml in the right hemisphere. Then, the same methods were used to measure the vascular volume in the left hemisphere (normal side). tMIP CTA VCCq was calculated by the ratio the volume of the affected hemisphere to that of the unaffected hemisphere. The (D) image shows the basal ganglia layer on sCTA, and the same method was used to calculate the volume of blood vessels in the right hemisphere as 11.31 ml. And the ratio the volume of the affected hemisphere to that of the unaffected hemisphere was sCTA VCCq. CBV at the affected hemisphere was decreased in the infarction area (E), TTP was obviously prolonged (F). Tissue map shows an IC area (red) of 50.23 ml and IP area (yellow) of 88.78 ml (G). This patient underwent endovascular treatments and had a FIV of 32.86 mL at T2 Flair (H). The 90-day mRS score for this patient was 0.

VCCq=Vaffected/Vunaffected,VCCq 0;

The volume (V) of the collateral vessels on the affected and unaffected sides were calculated automatically on tMIP CTA and sCTA, respectively, yielding the tMIP CTA vascular volume ratio (tMIP CTA VCCq) and the sCTA vascular volume ratio (sCTA VCCq).

Qualitative Method

Collateral vessels were assessed on tMIP CTA (Tan score on tMIP CTA) and sCTA (Tan score on sCTA) by using a four-point Modified Tan grading system. Collaterals were classified as good (2-3 scores) if there were 50% flow or more of the normal side revealed, and as poor (0-1 score) if <50% flow of the normal side was revealed.

Analysis Time

In this study, image postprocessing and diagnosis were performed by three observers. Observer A was a junior radiologist with 2 years of work experience but they had never performed CT image postprocessing. Observer B was an intermediate radiologist who performed imaging diagnoses for approximately 5 years. Observer C was a senior radiologist who performed imaging diagnosis for over 15 years and was well-experienced in CT image postprocessing. The three observers received 20-30 min of basic training about CTP and tMIP image postprocessing.

The analysis time of quantitative collateral assessment on tMIP CTA included the time generating the tMIP CTA images, the time drawing the ROIs, and the time required by the software to calculate the vascular volume automatically. The time spent on quantitative collateral assessment on sCTA was also recorded, including the time selecting the appropriate arterial phase from the 19 phases, the time drawing the ROIs on all three layers, and the time required by the software to calculate the vascular volume automatically. Meanwhile, the analysis time also included the time of selecting the appropriate arterial phase, time generating the tMIP CTA images, and time of evaluation.

The analysis time of CTP included the time of TDC adjustment and the Vitrea software automatic postprocessing.

Statistical Analysis

Normally distributed quantitative data were expressed as the means ± standard errors of the mean (SEMs); non-normally distributed quantitative data were expressed as the medians (Q1, Q3); qualitative data were expressed as the frequencies (percentages). Both parametric and non-parametric statistical tests were used, as the data were skewed. The chi-squared test was performed to test qualitative data. The non-parametric Mann-Whitney U-test was used to test non-normally distributed quantitative data. The unpaired Student's t-test was used to test normally distributed quantitative data. Pairwise comparisons were performed using Fisher's least significant difference (LSD). All patients were assessed twice by each observer independently. Interobserver agreement was described by the intraclass correlation coefficient (ICC), and p < 0.05 was considered statistically significant. Spearman correlation analysis was used to analyze the correlation of collateral-related parameters with FIV. Logistic regression was used to analyze the risk factors of clinical outcomes. The variables in the regression were selected by the Akaike information criterion (AIC). Receiver operating characteristic (ROC) curves were used to evaluate the predictive ability of the above parameters, and the sensitivity, specificity, area under the curve (AUC), and 95% confidence interval (95% CI) were calculated. The results were considered significant for two-tailed p < 0.05. Statistical analysis was performed using Statistical Package for the Social Sciences ver. 25 software (SPSS, Chicago, IL).

Results

Study Population

In total, 81 patients were enrolled in this study, including 41 males (50.6%) and 40 females (49.4%). Compared with those in the poor outcome group, patients with good outcomes showed lower baseline NIHSS scores, younger ages, lower incidences of atrial fibrillation, lower incidences of a previous stroke and/or coronary heart disease, better collateral vessels, less IC volume, and higher mismatch ratio (all, p < 0.05). Detailed information was summarized in Table 1.

Table 1.

Characteristics of patients with good and poor outcome.

Variables Poor outcome n = 36 Good outcome n = 45 U/χ2 P
Age, median [IQR] 81.00(72.25,84.00) 71.00(61.50,81.50) 499.50 0.003
Male, n (%) 15(41.70) 26(57.80) 2.08 0.150
Baseline NIHSS score, median [IQR] 15.50(11.25,21.00) 10.00(6.00,15.00) 421.00 <0.001
IV-tPA, n (%) 8(22.20) 14(31.10) 0.80 0.371
Atrial fibrillation, n (%) 23(63.90) 17(37.80) 5.46 0.020
Hypertension, n (%) 31(86.10) 33(73.30) 1.97 0.161
Diabetes mellitus, n (%) 17(47.20) 12(26.70) 3.68 0.055
Dyslipidemia, n (%) 16(44.40) 15(33.30) 1.05 0.307
Smoking, n (%) 10(27.80) 16(35.60) 0.56 0.456
Previous stroke, n (%) 15(41.70) 9(20.00) 4.50 0.034
Coronary disease, n (%) 19(52.80) 14(31.10) 3.89 0.049
Anticoagulant, n (%) 3(8.30) 5(11.10) 0.17 0.677
ASPECTS,median [IQR] 6.50(3.00,8.00) 8.00(6.00,8.00) 636.00 0.094
Clot burden score, median [IQR] 4.00(0.00,7.00) 6.00(2.00,9.00) 626.50 0.076
Tan score on sCTA, median [IQR] 0.00(0.00,1.75) 1.00(0.00,2.00) 681.00 0.187
Tan score on tMIP CTA, median [IQR] 1.00(1.00,2.00) 3.00(2.00,3.00) 322.00 <0.001
Recanalization, n (%) 28(77.80) 41(91.10) 2.82 0.053
FIV (mL), median [IQR] 98.97(44.37,223.85) 16.25(4.79,46.63) 275.00 <0.001
tMIP CTA VCCq, median [IQR] 0.53(0.34,0.71) 0.97(0.91,1.06) 112.00 <0.001
sCTA VCCq, median [IQR] 0.44(0.33,0.55) 0.63(0.48,0.81) 389.00 <0.001
IC volume (ml), median [IQR] 89.41(52.00,134.06) 90.06(49.07,140.51) 713.00 0.724
IP volume (ml), median [IQR] 26.99(10.41,47.56) 72.58(13.95,145.23) 440.00 0.002
Mismatch ratio, median [IQR] 1.83(0.66,4.44) 3.65(2.01,6.67) 450.50 0.003

IQR, interquartile range; NIHSS, National Institutes of Health Stroke Scale; ASPECTS, Alberta Stroke Program Early CT Score; SD, standard deviation; IV-tPA, intravenous recombinant tissue-type plasminogen activator; FIV, final infarct volume; tMIP CTA, time maximum intensity projection computed tomography angiography; sCTA, single-phase computed tomography angiography; tMIP CTA VCCq, quantitative measurement of vascular volume ratio on tMIP CTA; sCTA VCCq, quantitative measurement of vascular volume ratio on sCTA; IC, ischemic core; IP, ischemic penumbra.

Relationship of Collateral Circulation With FIV

FIV was assessed on NCCT (14 patients) or MRI (67 patients). tMIP CTA VCCq (r = 0.61, p < 0.01), IC volume (r = 0.66, p < 0.01), Tan score on tMIP CTA (r = 0.52, p < 0.01) and Mismatch ratio (r = 0.60, p < 0.01) showed moderate negative correlations with FIV. Patients were further divided into two groups: recanalization group (n = 69) and non-recanalization group (n = 12). In the group of non-recanalization, all of tMIP CTA VCCq (r = 0.63, p < 0.05), sCTA VCCq (r = 0.53, p < 0.05), Tan score on tMIP CTA (r = 0.56, p < 0.05) and IC volume (r = 0.65, p < 0.05) had moderate negative correlations with FIV (Table 2).

Table 2.

Association of collateral-related parameters with FIV in AIS patients after EVTs.

Variables Total
(n = 81)
Recanalization (n = 69) Non-recanalization (n = 12)
tMIP CTA VCCq −0.61** −0.58** −0.63*
sCTA VCCq −0.38* −0.26* −0.53*
Tan score on tMIP CTA −0.52** −0.50** −0.56*
Tan score on sCTA −0.23* −0.31** −0.26
IP volume 0.17 0.17 0.21
IC volume 0.66** 0.66** 0.65*
Mismatch ratio −0.60** −0.63** −0.34

FIV, final infarct volume; tMIP CTA, time maximum intensity projection computed tomography angiography; sCTA, single-phase computed tomography angiography; tMIP CTA VCCq, quantitative measurement of vascular volume ratio on tMIP CTA; sCTA VCCq, quantitative measurement of vascular volume ratio on sCTA; IP, ischemic penumbra; IC, ischemic core.

All correlation coefficients are presented as Spearman r values.

*

P < 0.05.

**

P < 0.01.

Association of Collateral Circulation and Clinical Outcome

In multivariate logistic regression analysis, tMIP CTA VCCq (odds ratio = 0.14; 95%CI, 0.03-0.59; p = 0.009) was an independent predictive factor of outcome (Table 3). The area under the curve (AUC) of indicators for predicting clinical outcome was obtained by receiver operating characteristic (ROC) curve analysis. The results are shown in Table 4: tMIP CTA VCCq had the best value in predicting clinical outcome (AUC, 0.93; sensitivity, 0.88; specificity, 0.80, p < 0.001).

Table 3.

Association between collateral-related parameters and clinical outcome.

Variables β SE Wald χ2 Exp(B) Lower 95% CI Upper 95% CI P
tMIP CTA VCCq −1.96 0.73 6.78 0.14 0.03 0.59 0.009
sCTA VCCq 0.20 4.22 0.00 1.22 0.00 4759.09 0.962
Tan score on tMIP CTA −1.39 1.01 1.89 0.25 0.04 1.81 0.169
Tan score on sCTA 1.66 0.82 0.93 5.25 1.06 26.12 0.336
IP volume −0.01 0.01 1.07 0.99 0.97 1.01 0.300
IC volume 0.01 0.03 0.07 1.01 0.96 1.06 0.798
Mismatch ratio 0.08 0.15 0.28 1.08 0.81 1.46 0.594

FIV, final infarct volume; CI, confidence interval; tMIP CTA, time maximum intensity projection computed tomography angiography; sCTA, single-phase computed tomography angiography; tMIP CTA VCCq, quantitative measurement of vascular volume ratio on tMIP CTA; sCTA VCCq, quantitative measurement of vascular volume ratio on sCTA; IP, ischemic penumbra; IC, ischemic core.

Table 4.

Receiver operating characteristics curves of collateral-related parameters for evaluating clinical outcome.

Variables AUC (95% CI) Sensitivity (95% CI) Specificity (95% CI) Youden index Associated criterion P
tMIP CTA VCCq 0.93(0.85,1.00) 0.88(0.56,0.94) 0.80(0.39,1.00) 0.68 −0.84 <0.001
sCTA VCCq 0.74(0.63,0.85) 0.71(0.38,0.94) 0.66(0.39,0.86) 0.47 0.03 <0.001
Tan score on sCTA 0.56(0.43,0.70) 0.74(0.28,0.99) 0.73(0.19,0.99) 0.47 2.50 0.307
Tan score on tMIP CTA 0.79(0.68,0.89) 0.50(0.07,0.90) 0.98(0.30,1.00) 0.48 −1.00 <0.001
IP volume 0.52(0.39,0.65) 0.50(0.23,0.79) 0.49(0.27,0.75) 0.00 248.96 0.727
IC volume 0.71(0.58,0.83) 0.65(0.47,0.77) 0.60(0.25,0.94) 0.25 52.69 0.002
Mismatch ratio 0.70(0.57,0.82) 0.71(0.44,0.82) 0.61(0.26,0.90) 0.32 9.05 0.002

AUC, area under the curve; CI, confidence interval; tMIP CTA, time maximum intensity projection computed tomography angiography; sCTA, single-phase computed tomography angiography; tMIP CTA VCCq, quantitative measurement of vascular volume ratio on tMIP CTA; sCTA VCCq, quantitative measurement of vascular volume ratio on sCTA.

Analysis Time

For tMIP CTA VCCq, observer A, B, and C had a statistically comparable analysis time (110.43 ± 5.44 s vs. 106.86 ± 6.27 s vs. 101.71 ± 8.31 s, p = 0.079). For CTP, sCTA VCCq, Tan score on tMIP CTA, and Tan score on sCTA, there were significant differences among three observers in analysis time (all, p < 0.001) (Table 5).

Table 5.

Comparison of analysis time of doctors of different grades.

Variables Junior doctor Intermediate doctor Senior doctor F P
Tan score on sCTA (s), mean ± SDab 94.43 ± 7.28 57.57 ± 7.89 20.43 ± 7.89 161.95 <0.001
Tan score on tMIP CTA (s), mean ± SDab 75.43 ± 7.57 44.43 ± 8.06 20.00 ± 4.08 116.67 <0.001
sCTA VCCq (s), mean ± SDab 142.29 ± 14.04 120.86 ± 14.06 115.71 ± 7.27 20.28 <0.001
tMIP CTA VCCq (s), mean ± SD 110.43 ± 5.44 106.86 ± 6.27 101.71 ± 8.31 2.93 0.079
CTP (s), mean ± SDab 152.57 ± 12.22 130.43 ± 8.30 98.43 ± 8.54 53.44 <0.001
a

, The P-value of LSD in Junior Doctor vs. Intermediate Doctor < 0.05.

b

, The P-value of LSD in Junior Doctor vs. Senior Doctor < 0.05.

LSD, least significant difference; tMIP CTA, time maximum intensity projection computed tomography angiography; sCTA, single-phase computed tomography angiography; tMIP CTA VCCq, quantitative measurement of vascular volume ratio on tMIP CTA; sCTA VCCq, quantitative measurement of vascular volume ratio on sCTA; CTP, computed tomography perfusion.

The ICC among the three observers was 0.96 (tMIP CTA VCCq), 0.86 (sCTA VCCq), 0.86 (Tan score on tMIP CTA), 0.67 (Tan score on sCTA), and 0.97 (CTP).

Discussion

Good collateral circulation contributes to maintaining the blood supply around an ischemic lesion for a relatively long time to preserve penumbra tissue (21, 22). Although evaluation of the collateral circulation has not yet been written into current guidelines of treatment for acute ischemic stroke, it is well-known that collateral circulation plays an important role in the development of cerebral infarction. Clinically, the collateral circulation influences the selection of treatment strategies and prognoses of AIS patients.

We found that tMIP CTA VCCq (r = 0.61, p < 0.01), IC volume (r = 0.66, p < 0.01), Tan score on tMIP CTA (r = 0.52, p < 0.01) and the mismatch ratio (r = 0.60, p < 0.01) showed moderate negative correlations with FIV. In the group of non-recanalization, tMIP CTA VCCq (r = 0.63, p < 0.05), sCTA VCCq (r = 0.53, p < 0.05), Tan score on tMIP CTA (r = 0.56, p < 0.05) and IC volume (r = 0.65, p < 0.05) had moderate negative correlations with FIV. Moreover, the tMIP CTA VCCq was an independent predictor of good outcome in AIS patients (OR = 0.14; 95% CI: 0.03, 0.59; p = 0.009), and had the best value in predicting clinical outcome (AUC, 0.93; sensitivity, 0.88; specificity, 0.80, p < 0.001).

Although an increasing number of studies have focused on the role of collateral circulation in clinical treatment decisions, few studies have evaluated intracranial collateral vessels using quantitative analysis (23, 24). Most evaluation methods of the collateral circulation focus on rating scales, where doctors are required to be familiar with the rating rules, and the consistency among observers is low (13, 15). For clinicians, especially junior and intermediate doctors, a reliable quantitative method for evaluating collateral vessels could help them make individualized treatment options more accurately and effectively.

To date, only a few studies have adopted the quantitative evaluation of collateral vessels. Shi et al. reported that measuring the maximum blood flow of the collateral vessels in the Sylvian fissure on CT perfusion images was a feasible method for quantitatively evaluating the collateral circulation, which was related to clinical outcomes in AIS patients (23). Boers et al. proposed that automatic quantitative collateral circulation assessment in AIS patients based on sCTA could be helpful for developing treatment options (24). In our prior study, we reported that tMIP CTA, which integrates the information from multiple CTA phases and displays the maximum CT value of all projection planes, showed higher image quality of intracranial vascularity than sCTA did and then improved the accuracy of collateral circulation evaluation (12). In this study, we performed a further quantitative evaluation of the intracranial collateral circulation based on tMIP CTA.

Previous studies revealed that better collateral status indicates a smaller infarct volume, larger penumbra volume, and decreased infarct growth (21, 25, 26). The results of this study demonstrated that a higher volume ratio of the collateral vessels predicted a better outcome and smaller FIV, and tMIP CTA VCCq had the best predictive value for prognosis. For patients who failed to get successful recanalization, collateral circulation was also an important determinant of FIV, which helped to maintain the blood supply around the FIV for a relatively long period after stroke onset and preserve salvable brain tissue (27). In addition, the above results indicate that sCTA, the most applied technique for AIS patients, may underestimate the status of the collateral circulation due to the lack of time information, whereas tMIP CTA provided more accurate results when evaluating the collateral circulation by integrating the vascular information from multiple phases, including the delayed development of collateral vessels. CTP is also an alternative method for evaluating collateral circulation, however, it is worth noting that CTP parameters may be influenced by variations in postprocessing and algorithms (28, 29). The tMIP CTA VCCq contained complete blood vessel information and was the most accurate parameter for collateral circulation evaluation when compared with the other parameters. Furthermore, it was noticed that 20 patients had better collateral circulation before EVTs (tMIP CTA VCCq > 1) and good clinical outcomes (mRS scores 0-2). Among them, 12 patients had an mRS score of 0 point, 6 patients had 1 point, and 2 patients had 2 points.

It should be mentioned that 40.6% (28/69) of our patients had poor outcomes after vascular recanalization (Table 1). This may be due to their old age and many complications, such as coronary heart disease and atrial fibrillation.

We also recorded the analysis time to investigate whether evaluations with different methods were correlated with diagnostic experience. In this study, the analysis time of Tan score on sCTA, Tan score on tMIP CTA, sCTA VCCq, and CTP were related to the diagnostic experience level, while the analysis time of tMIP CTA VCCq did not. The reason might be that tMIP CTA is a new volume packet where software automatically integrates all phases of CTA information, and the selection time of the optimal arterial phase was not needed. Short-term training (~20-30 min) is enough for the inexperienced doctors to quantitatively evaluate collateral vessel status using the software, and it is possible to obtain reliable results with no increase in evaluating time of tMIP VCCq. Currently, the selection of AIS patients for reperfusion therapy based on a traditional time window is disadvantaged, while tissue window plays a more important role in clinical decision-making (30, 31). However, the tissue window of individual patients is not fixed, depending on several compensation mechanisms, including collateral compensation. Using appropriate imaging modalities before reperfusion therapy in suitable patients, especially mechanical thrombectomy, may benefit patients with AIS. At present, many grading scales are available for collateral status assessment in ischemic stroke (1315). The rLMC score is more comprehensive when evaluating collateral circulation. However, the rLMC score requires evaluation of nine anatomical regions, which is relatively complicated and time-consuming (15, 32). The Miteff score mainly focuses on the surface of the leptomeninges, the sylvian fissure area, and the distal end of the vascular occlusion, so it may ignore other important functional areas for collateral blood flow compensation (13, 22). The Tan score evaluates the collateral circulation based on the range of collateral blood flow after vascular occlusion (14). Although the Tan score is slightly rough, a previous study has shown that the reliability of the Tan score is higher than the Miteff score (22). Meanwhile, the Tan score may be easier for the doctors to assess collateral status. Conversely, a study has shown that the collateral circulation defined by the Tan score is one of the risk factors for patients receiving acute endovascular treatment (21). In general, each of the above methods has respective advantages and disadvantages. In this study we focused on quantitative collateral circulation evaluation methods, so we chose the Tan score to represent the qualitative assessment of collateral circulation. Perfusion parameters were also added to verify the accuracy of the tMIP CTA VCCq.

The limitations of this study are as follows. First, it is a single-center retrospective study, and the sample size is relatively small. Second, the tMIP technique may enhance any artifacts present in the posterior cranial fossa, which is why patients with posterior circulation stroke were not included in this study. Third, tMIP technology includes arterial and venous information. Although most of the current studies focused on arterial collateral circulation studies, there were studies reporting that the venous system has a greater role in assessing ischemia than previously described (33). In the near future, a larger scale prospective trial is needed to further confirm our findings. We did not include multiphase CTA (mCTA) in this study because the evaluation time on mCTA is much more than that on tMIP CTA and sCTA.

Conclusion

Quantitative measurement of tMIP CTA is a reliable and time-saving method for assessing collateral circulation. It may help clinicians develop more precise treatment strategies and can aid in predicting clinical outcomes. In addition, compared with sCTA VCCq, qualitative parameters, and CTP parameters, quantitative measurement on tMIP CTA had the best predictive value for patient outcome. We hope this accurate and effective evaluation of the collateral circulation will provide clinicians with one more option that helps them to choose an appropriate treatment strategy.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The studies involving human participants were reviewed and approved by Beijing Hospital institutional review board. The patients/participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.

Author Contributions

JC conceived and designed the study. PQ, YJ, GY, LL, and ZY collected the data. PQ, YJ, and YZ were responsible for quality control. RC and JC conceived of the project, analyzed the data, and wrote the paper. All authors helped, organized, carried out the research, read, and approved the final manuscript.

Funding

The authors declare that this study received funding from 2020 SKY Imaging Research Fund of the Chinese International Medical Foundation (project No. Z-2014-07-2003-02), 2020 Beijing Hospital National Natural Science Foundation of China Preliminary Research Project (project No. BJ-2020-131).

Conflict of Interest

YZ is employed by Canon Medical System (China) Co., Ltd. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.


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