Skip to main content
Advertisement

Main menu

  • Home
  • Content
    • Current Issue
    • Accepted Manuscripts
    • Article Preview
    • Past Issue Archive
    • AJNR Case Collection
    • Case of the Week Archive
    • Classic Case Archive
    • Case of the Month Archive
  • Special Collections
    • Spinal CSF Leak Articles (Jan 2020-June 2024)
    • 2024 AJNR Journal Awards
    • Most Impactful AJNR Articles
  • Multimedia
    • AJNR Podcast
    • AJNR Scantastics
    • Video Articles
  • For Authors
    • Submit a Manuscript
    • Author Policies
    • Fast publishing of Accepted Manuscripts
    • Graphical Abstract Preparation
    • Manuscript Submission Guidelines
    • Imaging Protocol Submission
    • Submit a Case for the Case Collection
  • About Us
    • About AJNR
    • Editorial Board
  • More
    • Become a Reviewer/Academy of Reviewers
    • Subscribers
    • Permissions
    • Alerts
    • Feedback
    • Advertisers
    • ASNR Home
  • Other Publications
    • ajnr

User menu

  • Alerts
  • Log in

Search

  • Advanced search
American Journal of Neuroradiology
American Journal of Neuroradiology

American Journal of Neuroradiology

ASHNR American Society of Functional Neuroradiology ASHNR American Society of Pediatric Neuroradiology ASSR
  • Alerts
  • Log in

Advanced Search

  • Home
  • Content
    • Current Issue
    • Accepted Manuscripts
    • Article Preview
    • Past Issue Archive
    • AJNR Case Collection
    • Case of the Week Archive
    • Classic Case Archive
    • Case of the Month Archive
  • Special Collections
    • Spinal CSF Leak Articles (Jan 2020-June 2024)
    • 2024 AJNR Journal Awards
    • Most Impactful AJNR Articles
  • Multimedia
    • AJNR Podcast
    • AJNR Scantastics
    • Video Articles
  • For Authors
    • Submit a Manuscript
    • Author Policies
    • Fast publishing of Accepted Manuscripts
    • Graphical Abstract Preparation
    • Manuscript Submission Guidelines
    • Imaging Protocol Submission
    • Submit a Case for the Case Collection
  • About Us
    • About AJNR
    • Editorial Board
  • More
    • Become a Reviewer/Academy of Reviewers
    • Subscribers
    • Permissions
    • Alerts
    • Feedback
    • Advertisers
    • ASNR Home
  • Follow AJNR on Twitter
  • Visit AJNR on Facebook
  • Follow AJNR on Instagram
  • Join AJNR on LinkedIn
  • RSS Feeds

Welcome to the new AJNR, Updated Hall of Fame, and more. Read the full announcements.


AJNR is seeking candidates for the position of Associate Section Editor, AJNR Case Collection. Read the full announcement.

 

Research ArticleExtracranial Vascular

Delayed Contrast-Enhanced MR Angiography for the Assessment of Internal Carotid Bulb Patency in the Context of Acute Ischemic Stroke: An Accuracy, Interrater, and Intrarater Agreement Study

W. Boisseau, A. Benaissa, R. Fahed, J.-L. Amegnizin, S. Smajda, S. Benadjaoud, A.M. Benadjaoud, L. Saint-Val, Q. Alias, P. Iorio, S. Yang, K. Zuber, E. Kalsoum and J. Hodel
American Journal of Neuroradiology June 2021, 42 (6) 1116-1122; DOI: https://doi.org/10.3174/ajnr.A7054
W. Boisseau
aFrom the Department of Neuroradiology (W.B., A.B., J.-L.A., S.B., L.S.-V., Q.A., P.I., S.Y., E.K.), Centre-Hospitalier-Universitaire Henri Mondor, Créteil, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for W. Boisseau
A. Benaissa
aFrom the Department of Neuroradiology (W.B., A.B., J.-L.A., S.B., L.S.-V., Q.A., P.I., S.Y., E.K.), Centre-Hospitalier-Universitaire Henri Mondor, Créteil, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for A. Benaissa
R. Fahed
bDepartment of Interventional Neuroradiology (R.F., S.S.), Fondation Ophtalmologique Adolphe de Rothschild, Paris, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for R. Fahed
J.-L. Amegnizin
aFrom the Department of Neuroradiology (W.B., A.B., J.-L.A., S.B., L.S.-V., Q.A., P.I., S.Y., E.K.), Centre-Hospitalier-Universitaire Henri Mondor, Créteil, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for J.-L. Amegnizin
S. Smajda
bDepartment of Interventional Neuroradiology (R.F., S.S.), Fondation Ophtalmologique Adolphe de Rothschild, Paris, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for S. Smajda
S. Benadjaoud
aFrom the Department of Neuroradiology (W.B., A.B., J.-L.A., S.B., L.S.-V., Q.A., P.I., S.Y., E.K.), Centre-Hospitalier-Universitaire Henri Mondor, Créteil, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for S. Benadjaoud
A.M. Benadjaoud
dDepartment of Radiobiology and Epidemiology (A.M.B.), Institute for Radiological Protection and Nuclear Safety, Fontenay-Aux-Roses, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for A.M. Benadjaoud
L. Saint-Val
aFrom the Department of Neuroradiology (W.B., A.B., J.-L.A., S.B., L.S.-V., Q.A., P.I., S.Y., E.K.), Centre-Hospitalier-Universitaire Henri Mondor, Créteil, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for L. Saint-Val
Q. Alias
aFrom the Department of Neuroradiology (W.B., A.B., J.-L.A., S.B., L.S.-V., Q.A., P.I., S.Y., E.K.), Centre-Hospitalier-Universitaire Henri Mondor, Créteil, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Q. Alias
P. Iorio
aFrom the Department of Neuroradiology (W.B., A.B., J.-L.A., S.B., L.S.-V., Q.A., P.I., S.Y., E.K.), Centre-Hospitalier-Universitaire Henri Mondor, Créteil, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for P. Iorio
S. Yang
aFrom the Department of Neuroradiology (W.B., A.B., J.-L.A., S.B., L.S.-V., Q.A., P.I., S.Y., E.K.), Centre-Hospitalier-Universitaire Henri Mondor, Créteil, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for S. Yang
K. Zuber
eClinical Research Unit (K.Z.), Fondation Ophtalmologique Adolphe de Rothschild, Paris, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for K. Zuber
E. Kalsoum
aFrom the Department of Neuroradiology (W.B., A.B., J.-L.A., S.B., L.S.-V., Q.A., P.I., S.Y., E.K.), Centre-Hospitalier-Universitaire Henri Mondor, Créteil, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for E. Kalsoum
J. Hodel
cDepartment of Radiology, (J.H.), Groupe-Hospitalier-Paris-Saint-Joseph, Paris, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for J. Hodel

Abstract

BACKGROUND AND PURPOSE: CTA has shown limited accuracy and reliability in distinguishing tandem occlusions and pseudo-occlusions on initial acute stroke imaging. The utility of early and delayed contrast-enhanced MRA in this setting is unknown. We aimed to assess the accuracy and reliability of early and delayed contrast-enhanced MRA for carotid bulb patency in patients with acute ischemic stroke.

MATERIALS AND METHODS: We retrospectively reviewed patients who had ICA occlusion and underwent thrombectomy with preprocedural early and delayed contrast-enhanced MRA in a single comprehensive stroke center. During 2 sessions, 10 raters independently assessed 32 cases with early contrast-enhanced MRA (with an additional delayed contrast-enhanced MRA sequence during the second reading session). Their judgments were compared with DSA as a reference standard. Accuracy and interrater agreement were measured. Five raters undertook a third reading session to assess intrarater agreement.

RESULTS: Accuracy for the assessment of carotid bulb patency with early contrast-enhanced MRA was limited (69%; 95% CI, 59%–79%), with moderate interrater agreement (κ = 0.42; 95% CI, 0.27–0.55). The second reading with an additional delayed contrast-enhanced MRA sequence improved both accuracy (82%; 95% CI, 73%–91%; P < .001) (raters corrected 43%–77% of incorrect diagnoses with early contrast-enhanced MRA alone; mean = 59%) and interrater agreement (κ = 0.56; 95% CI, 0.41–0.73; P = .07). Intrarater agreement was almost perfect, substantial, and moderate for 3, 1, and 1 raters.

CONCLUSIONS: Early contrast-enhanced MRA has limited accuracy and repeatability for the evaluation of carotid bulb patency in acute ischemic stroke. The additional delayed contrast-enhanced MRA sequence may improve accuracy and reliability.

ABBREVIATIONS:

AIS
acute ischemic stroke
CE
contrast-enhanced
PO
pseudo-occlusion

Several trials have demonstrated the benefit of mechanical thrombectomy in acute ischemic stroke (AIS) with anterior circulation large-vessel occlusion1 depicted by noninvasive intracranial vascular imaging (CTA or MRA). However, in case of tandem occlusion (ie, an ICA occlusion with an intracranial large-vessel occlusion), there remains uncertainty regarding the optimal management of the carotid bulb lesion,2 and the benefits of acute angioplasty/stent placement are controversial.3,4 Randomized controlled trials are needed to determine the best strategy and will thus require an accurate and repeatable noninvasive imaging method to select patients with an intracranial large-vessel occlusion and an additional carotid bulb occlusion,5 which will typically appear as an absence of visualization of the whole symptomatic carotid artery from the bulb.

However, in AIS, a single, large clot located above the ICA bulb can impede contrast ascension from the common carotid artery, leading to a false image of bulbar occlusion, an entity called ICA pseudo-occlusion (PO).6⇓⇓-9 It can, thus, be challenging to distinguish tandem occlusions and POs on initial acute stroke imaging. A previous study has shown limited accuracy and reliability of CTA for this task.10 CTA might thus be limited for the detection of tandem occlusions, whether in clinical routine (for endovascular management planning) or in research settings (for patient selection in a randomized controlled trial).

MR imaging offers several interesting features for acute stroke imaging and decision-making, including a high sensitivity for the detection of early ischemic lesions11 and the ability to detect stroke mimics12 and identify patients who will benefit from reperfusion therapy in case of unknown onset stroke.13 Noninvasive vascular imaging can then be performed with MRA: The TOF sequence is usually performed for the depiction of intracranial large-vessel occlusion, and early contrast-enhanced MRA (CE-MRA), for the assessment of the complete supra-aortic vasculature. As with CTA, cases with an intraluminal filling defect of the bulb on ICA on the stroke side might correspond to either a tandem occlusion or a PO. Delayed acquisition after gadolinium injection (delayed CE-MRA) might overcome this issue, but CE-MRA performance has not been thoroughly studied in this setting.

In this study, we aimed to assess the accuracy and reliability of early and delayed CE-MRA for the assessment of carotid bulb patency in patients with AIS.

MATERIALS AND METHODS

The local ethics committee (Centre Hospitalo-Univertaire Henri Mondor, Créteil) approved the study protocol and waived written informed consent. This study was prepared in accordance with the Standards for Reporting of Diagnostic Accuracy studies14 and the Guidelines for Reporting Reliability and Agreement Studies.15

Patients

We reviewed a prospectively collected endovascular data base in a single comprehensive stroke center between September 2016 and April 2018. We identified patients who underwent endovascular thrombectomy for AIS of the anterior circulation and in whom DSA showed occlusion of the ICA (at any level) on the symptomatic side. We excluded patients with other occlusion sites (such as isolated middle cerebral artery or posterior circulation occlusions) and patients who did not undergo MR imaging with early and additional delayed CE-MRA. The number of cases in the present study (n = 32) was superior to the recommendations of Donner and Rotondi16 for agreement studies.

Reference Standard

DSA was the reference standard for this study, similar to that in a previous study.10 Two interventional neuroradiologists (with 7 and 10 years of experience in neuroradiology, respectively) reviewed, in consensus, the DSA images obtained during thrombectomy, along with the patient's follow-up imaging and the report from the interventional neuroradiologist who performed the procedure, to determine the location of the occlusion.

DSA was performed with a biplane angiographic system (Axiom Artis dBA; Siemens). Carotid bulb occlusion on DSA was defined as an angiographically viewed obstacle that hindered the passage of contrast agent and/or the guidewire or catheter and the lack of backfilling of the carotid bulb during microcatheter angiography.9

In case of suprabulbar occlusion, 2 interventional neuroradiologists indicated the exact occlusion site based on the classification of Gibo et al,17 dividing the ICA into 4 parts: the cervical, petrous, cavernous, and intracranial portions.

Pseudo-Occlusion

ICA PO was defined as a unilateral intraluminal filling defect from the carotid bulb on the symptomatic side shown on early CE-MRA and in which DSA showed a suprabulbar occlusion.

MR Imaging

For all patients, MR imaging was performed at the same care center as thrombectomy. MRA examinations were performed at 3T (Magnetom Skyra; Siemens), including DWI, T2 FLAIR, SWI, and TOF-MRA.

When required, intravenous thrombolysis was directly initiated in the MR imaging scanner after these 4 sequences and before the acquisition of CE-MRA. Early CE-MRA was acquired after an intravenous injection of gadolinium-based contrast agent. A delayed CE-MRA acquisition was initiated immediately after the early CE-MRA sequence (without further contrast agent administration). This acquisition protocol resulted in fixed amount of time between gadolinium injection and CE-MRA acquisitions. Acquisition parameters of early and delayed CE-MRA are detailed in the Online Supplemental Data.

Raters

All raters were radiologists experienced in neurovascular imaging. Ten raters from 2 institutions, including 5 neuroradiologists and 5 interventional neuroradiologists with various levels of experience (detailed in the Online Supplemental Data) participated in the present study.

Readings

The MR imaging studies were first anonymized and uploaded in the PACS. Raters had no access to other imaging studies or clinical information other than sex, age, symptoms (ie, left or right motor deficit, aphasia), the initial NIHSS score, the time of symptom onset (when available), and the time of the brain MR imaging examination. Each rater performed 2 independent readings as follows: During the first reading, DWI, FLAIR, SWI, TOF-MRA and early CE-MRA were provided; during the second reading (performed 1 month later in a different order), an additional delayed CE-MRA sequence was provided for each patient.

For each case, raters indicated whether there was an occlusion of the ICA at the bulb level. The raters were blinded to the final diagnosis on DSA. Five raters (including 2 neuroradiologists and 3 interventional neuroradiologists) performed a third reading session (similar to the second one), at least 1 month later, to evaluate intrarater agreement.

Statistical Analysis

Mean [SD] was calculated for continuous variables, and frequency was reported for categoric variables. Sensitivity, specificity, and accuracy rates were calculated for each rater using 2 Ă— 2 contingency tables. Group and subgroup validation parameters were calculated using mean sensitivity, specificity, and accuracy.

Interrater and intrarater agreement for the diagnosis of an ICA bulb occlusion was measured using Fleiss Îş statistics with 95% bias-corrected and accelerated confidence intervals obtained by 10,000 bootstrap resampling.18 The Îş comparison inference was conducted according to the method described by Vanbelle and Albert.19

All analyses were performed with R statistical and computing software, Version 3.3.2 (http://www.r-project.org/) and a significance level of 5%. Slight, fair, moderate, and substantial agreement categories were reported according to Landis and Koch.20

RESULTS

Patients

A total of 176 consecutive patients with AIS were treated by mechanical thrombectomy at our institution between September 2016 and April 2018. Among them, 102 patients with an isolated middle cerebral artery occlusion, 21 with vertebrobasilar artery occlusion, and 2 patients who did not receive endovascular treatment (because of catheterization failure) were excluded. Among the 51 remaining patients, 9 patients underwent CTA and 10 patients a early without delayed-phase CE-MRA were also excluded. The remaining 32 patients were thus included in the present study.

Patients' clinical, radiologic, and treatment characteristics are presented in the Online Supplemental Data. On the basis of DSA (reference standard), among the 32 patients, 6 patients had an isolated carotid bulb occlusion and 26 had a suprabulbar occlusion (5 with cervical, 2 with petrous, 3 with cavernous, and 16 with terminus occlusions). Among these same 26 patients, 8 patients had a radiologic pattern of PO (defined as a unilateral intraluminal filling defect from the carotid bulb on the symptomatic side shown with early CE-MRA, while DSA showed a patent bulb with a suprabulbar occlusion).

Illustrative cases of PO on CE-MRA and DSA are shown in Figs 1 and 2. Additional cases are shown in the Online Supplemental Data.

FIG 1.
  • Download figure
  • Open in new tab
  • Download powerpoint
FIG 1.

Case 10. The patient presented 2 hours after acute onset of right-sided hemiparesis and aphasia (NIHSS score of 24). Early CE-MRA (A) shows an intraluminal filling defect of the left proximal bulb ICA. Delayed CE-MRA (B) shows opacification of the left carotid artery up to the terminal ICA. DSA with selective catheterization of the left ICA confirms distal occlusion of the ICA (C, frontal DSA) with slow progression of iodine contrast (PO) (D–F, lateral DSA). White arrows indicates the occlusion site.

FIG 2.
  • Download figure
  • Open in new tab
  • Download powerpoint
FIG 2.

Case 19. This patient with unknown stroke onset presented with left-side hemiplegia and aphasia (NIHSS score of 20). Early CE-MRA (A) shows an intraluminal filling defect of the right proximal bulb ICA. Delayed CE-MRA (B) shows opacification of the right carotid artery up to the terminal ICA. DSA confirms distal occlusion of the right ICA (C, lateral DSA) and the absence of critical stenosis at the proximal ICA (D, lateral DSA). White arrows indicates the occlusion site.

Accuracy Study Results for the Assessment of Internal Carotid Bulb Patency

The assessment of internal carotid bulb patency using early CE-MRA alone (first reading) or with additional delayed CE-MRA (second reading) for all 10 raters is graphically displayed in the Online Supplemental Data. Accuracy parameters (sensitivity, specificity, and accuracy) are detailed in the Table. Graphic representations of the accuracy of each rater for the first, second, and third reading sessions are shown in Fig 3.

FIG 3.
  • Download figure
  • Open in new tab
  • Download powerpoint
FIG 3.

Graphic representation of the accuracy parameters of each rater for the assessment of internal carotid bulb patency for the first, second, and third reading sessions.

View this table:
  • View inline
  • View popup

Diagnostic accuracy parameters and interrater agreement for the presence of carotid bulb occlusiona

During the first reading session, raters' accuracy for the diagnosis of carotid bulb occlusion ranged between 59% and 79% (mean accuracy, 69%; 95% CI, 59%–79%). Sensitivity rates ranged between 33% and 83% (mean sensitivity, 70%; 95% CI, 33%–83%), whereas specificity rates ranged between 50% and 92% (mean specificity, 68%; 95% CI, 50%–92%). No rater achieved 100% sensitivity, ie, no rater correctly identified all patients with a carotid bulb occlusion. The number of erroneous diagnoses (compared with DSA as the reference standard) ranged between 12.5% and 47% among raters (mean, 31%).

The second reading session (with access to an additional delayed CE-MRA sequence) improved accuracy for 9/10 raters (90%), now ranging between 73% and 91% (mean accuracy, 82%; 95% CI, 73%–91%; P < .001). For the last rater (rater 5), accuracy was identical during the first and second readings. Sensitivity was improved for 6/10 raters (including 5 raters with 100% sensitivity) and ranged between 67% and 100% (mean sensitivity, 87%; 95% CI, 67%–100%). Specificity was improved for 7/10 raters and ranged between 65% and 88% (mean specificity, 80%; 95% CI, 65%–88%). During this second reading session with access to delayed CE-MRA, raters corrected 43%–77% of incorrect diagnoses from the previous reading session (mean, 59%), while they erroneously modified 0%–20% of previously correct diagnoses (mean, 8%). Despite the use of additional delayed CE-MRA, most raters (>5/10) continued to provide incorrect diagnoses in 6/32 cases (18.7%) exclusively, by misdiagnosing ICA PO as a bulb occlusion: In 3/6 cases, DSA revealed a preocclusive stenosis of the carotid bulb associated with an intracranial ICA occlusion. In the 3 remaining cases, the quality of delayed CE-MRA was poor due to movement artifacts.

Interrater Agreement

Interrater agreement regarding the diagnosis of carotid bulb patency on early CE-MRA is shown in the Table and Fig 4A. Interrater agreement was moderate for all raters (κ = 0.41; 95% CI, 0.27–0.55), without significant differences between junior and senior raters. In 7/32 cases (22%), all raters agreed on the presence/absence of a carotid bulb occlusion. Interrater agreement during the second reading session (with access to delayed CE-MRA) was improved (κ = 0.56; 95% CI, 0.41–0.73) (Fig 4A) (P = .07): In 17/32 cases (47%), all raters agreed on the presence/absence of a carotid bulb occlusion.

FIG 4.
  • Download figure
  • Open in new tab
  • Download powerpoint
FIG 4.

A, Graphic representation of interrater agreement among all raters for the assessment of internal carotid bulb patency with early CE-MRA (first reading session) and with additional delayed CE-MRA (second reading session) (Fleiss κ). B, Graphic representation of intrarater agreement for 5 raters between the second and third reading session (both with access to delayed CE-MRA) (Cohen κ). κ values >0.6 (dotted line) define a “substantial” agreement.

Intrarater Agreement

Intrarater agreement study results are shown in the Online Supplemental Data and Fig 4B. Intrarater agreement was at least substantial for 4/5 raters, including 2 raters with a perfect intrarater agreement (Îş = 1.0). Compared with the second reading session, accuracy performance during the third reading session was unchanged for 3/5 raters, improved for 1 rater, and decreased for 1 rater (but still improved compared with the first reading session).

DISCUSSION

This is, to our knowledge, the first study addressing the diagnostic accuracy and reliability of CE-MRA for the assessment of carotid bulb patency in patients with acute ischemic stroke. Our study demonstrates a limited accuracy and agreement for the diagnosis of internal carotid bulb occlusion with early CE-MRA compared with the reference DSA. The addition of delayed CE-MRA to our comprehensive MR imaging protocol improved both accuracy and interrater agreement.

ICA PO is a relatively common entity in case of acute terminal ICA occlusion, occurring in about 11%–46% of cases.6⇓⇓-9 The prevalence of ICA PO in our cohort (according to the reference standard DSA) was 8/32 cases (25%), which is in line with results from previous studies.6⇓⇓-9 The lack of differentiation between a “true” bulb carotid occlusion and ICA PO could lead to several issues. First, it may alter the inclusion of patients in future trials focusing on the management of tandem occlusions (for example, the ongoing French multicenter prospective randomized Thrombectomy In TANdem Occlusion [TITAN] trial21), by falsely enrolling patients with an aspect of tandem occlusion on initial noninvasive imaging while showing only an ICA PO on DSA.

Conversely, trials excluding patients with a tandem occlusion might erroneously exclude patients with an isolated intracranial occlusion. This exclusion might have happened in previous mechanical thrombectomy trials: In the Solitaire with the Intention for Thrombectomy as PRIMary Endovascular Treatment (SWIFT PRIME) study,22 for example, patients with a suspicion of extracranial ICA occlusion on initial imaging were excluded. Some of these patients possibly having an ICA PO could explain why the proportion of intracranial ICA occlusions was low in this study (15%)22 compared with other mechanical thrombectomy trials with no such exclusion criterion (for example, 31% in the Endovascular Treatment for Small Core and Proximal Occlusion Ischemic Stroke [ESCAPE] trial23).

Second, the misdiagnosis of a carotid bulb occlusion instead of an isolated intracranial ICA terminus occlusion might alter the preprocedural management of the patient. According to recent studies, carotid stent placement with antiplatelet therapy seems to be the most effective therapeutic approach for tandem occlusion.3,24,25 Moreover, the efficacy of tPA in case of tandem occlusion has been reported to be weak,26 and the association of antiplatelet and tPA in the early phase of AIS is known to increase the risk of hemorrhagic transformation with no additional benefit.27

Given these results, physicians could be tempted to give antithrombotic agents and withhold intravenous thrombolysis because of a suspicion of tandem occlusion while the patients might have a PO. Finally, it may also misguide the operator for procedural planning: Carotid bulb occlusion necessitates specific tools that are not necessary in case of intracranial ICA occlusion such as noncompliant balloons and stents. The optimal management of tandem occlusions for both drugs and devices is still currently unknown, but an accurate and repeatable diagnosis on noninvasive imaging will be necessary in the future to tailor the treatment strategy.

A previous study has shown limited reliability of CTA for the distinction between a tandem occlusion and a PO.10 To overcome this issue, several studies have tested the utility of delayed-phase CTA.7,28⇓-30 Similar to delayed CE-MRA, delayed-phase CTA (with multiphase CTA28,29 or 4D-CTA30) improved the accuracy over arterial phase–only acquisitions. However, regarding 4D-CTA, given the limited coverage length acquisition (about 20 mm in thin-thickness reconstruction modes30), only ICA PO with distal intracranial occlusion might be detected. Moreover, the time necessary for image reconstruction may also restrict its use.30 Finally, these techniques also increase overall patient x-ray exposure.31

Early CE-MRA could be an alternative imaging technique. However, in our study, it showed a limited accuracy and repeatability for the assessment of carotid bulb patency in patients with acute ischemic stroke. Additional delayed CE-MRA improved both the accuracy and interrater agreement and showed strong intrarater agreement. Moreover, delayed CE-MRA does not need further contrast agent administration and requires little extra time: In our protocol, imaging-acquisition delay for delayed CE-MRA was 43 seconds. Otherwise, a range of techniques, such as compressed sensing and/or denoising techniques, could further reduce this delay.32 Other advanced MR imaging sequences such as high-resolution vessel wall imaging have been reported to accurately differentiate true tandem occlusion and ICA PO.33 However, given the acquisition time (7 minutes 43 seconds in the study mentioned above33), this type of sequence does not seem appropriate in the context of acute ischemic stroke. The time spent to perform a brain MR imaging, including postcontrast MRA, is a critical factor for the implementation of this technique in the setting of acute ischemic stroke, which is an absolute emergency. As an example, 8 minutes were necessary for DWI, FLAIR, SWI, and 3D-TOF acquisitions in our protocol. Additional early and delayed CE-MRA requires only 2–3 minutes (including localize sequence acquisitions, bolus-tracking, and the acquisition of the 2 aforementioned sequences). Although this scan duration is slightly longer than CT, a previous study has shown that MR imaging does not significantly change decision-making or impact functional outcome.34

We recognize certain limitations to our study. Our study population included patients scanned with MR imaging, which is not the main imaging technique for the diagnosis of acute ischemic stroke in most centers. Therefore, our findings cannot be extrapolated to centers using CT as first-line imaging. The large number of raters with varying degrees of experience could impact the accuracy of results. However, all raters except one (with identical accuracy during the first and second readings) improved their accuracy with the access to delayed CE-MRA. Greater agreement might have been reached if the readers received standardized training before the reading sessions.

We also cannot exclude the probability that the improved accuracy and interrater agreement during the second reading could be due to a “training effect” from the first reading session; however, the results of each reading session were not disclosed to the readers, so they did not have any feedback to adjust their judgments. Moreover, the second reading session was performed in a different order and at least 1 month later. We also cannot exclude the possibility of cervical clot migration between MRA and DSA in patients treated with intravenous tPA infusion. However, given the low efficacy of tPA in case of tandem occlusion26 and the short time between MRA and DSA (all patients were managed in a mothership paradigm), we can speculate that this phenomenon is very unlikely to occur. We did not assess the accuracy and reliability of the identification of the underlying cause of each tandem occlusion (dissection, atheroma, other). The etiology might modify the endovascular management,35 and the ability of noninvasive imaging to differentiate each cause necessitates further studies.

CONCLUSIONS

Our study demonstrated a limited accuracy and repeatability for the assessment of carotid bulb patency with early CE-MRA compared with the reference DSA in the context of AIS. The addition of delayed CE-MRA to our comprehensive MR imaging protocol improved both accuracy and reliability in this setting.

References

  1. 1.
    1. Goyal M,
    2. Menon BK,
    3. van Zwam WH, et al
    . HERMES Collaborators. Endovascular thrombectomy after large-vessel ischaemic stroke: a meta-analysis of individual patient data from five randomised trials. Lancet 2016;387:1723–31 doi:10.1016/S0140-6736(16)00163-X pmid:26898852
  2. 2.
    1. Jacquin G,
    2. Poppe AY,
    3. Labrie M, et al
    . Lack of consensus among stroke experts on the optimal management of patients with acute tandem occlusion. Stroke 2019;50:1254–56 doi:10.1161/STROKEAHA.118.023758 pmid:30890115
  3. 3.
    1. Papanagiotou P,
    2. Haussen DC,
    3. Turjman F, et al
    . TITAN Investigators. Carotid stenting with antithrombotic agents and intracranial thrombectomy leads to the highest recanalization rate in patients with acute stroke with tandem lesions. JACC Cardiovasc Interv 2018;11:1290–99 doi:10.1016/j.jcin.2018.05.036 pmid:29976365
  4. 4.
    1. Blassiau A,
    2. Gawlitza M,
    3. Manceau PF, et al
    . Mechanical thrombectomy for tandem occlusions of the internal carotid artery-results of a conservative approach for the extracranial lesion. Front Neurol 2018;9:928 doi:10.3389/fneur.2018.00928 pmid:30455664
  5. 5.
    1. Powers WJ,
    2. Rabinstein AA,
    3. Ackerson T, et al
    . American Heart Association Stroke Council. Guidelines for the early management of patients with acute ischemic stroke: a guideline for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 2018;49:e46–110 doi:10.1161/STR.0000000000000158 pmid:29367334
  6. 6.
    1. Chen Z,
    2. Zhang M,
    3. Shi F, et al
    . Pseudo-occlusion of the internal carotid artery predicts poor outcome after reperfusion therapy. Stroke 2018;49:1204–09 doi:10.1161/STROKEAHA.118.021229 pmid:29643257
  7. 7.
    1. Wareham J,
    2. Crossley R,
    3. Barr S, et al
    . Cervical ICA pseudo-occlusion on single phase CTA in patients with acute terminal ICA occlusion: what is the mechanism and can delayed CTA aid diagnosis? J Neurointerv Surg 2018;10:983–87 doi:10.1136/neurintsurg-2017-013708 pmid:29438036
  8. 8.
    1. Grossberg JA,
    2. Haussen DC,
    3. Cardoso FB, et al
    . Cervical carotid pseudo-occlusions and false dissections: intracranial occlusions masquerading as extracranial occlusions. Stroke 2017;48:774–77 doi:10.1161/STROKEAHA.116.015427 pmid:28119435
  9. 9.
    1. Rocha M,
    2. Delfyett WT,
    3. Agarwal V, et al
    . Diagnostic accuracy of emergency CT angiography for presumed tandem internal carotid artery occlusion before acute endovascular therapy. J Neurointerv Surg 2018;10:653–56 doi:10.1136/neurintsurg-2017-013169 pmid:29101306
  10. 10.
    1. Diouf A,
    2. Fahed R,
    3. Gaha M, et al
    . Cervical internal carotid occlusion versus pseudo-occlusion at CT angiography in the context of acute stroke: an accuracy, interobserver, and intraobserver agreement study. Radiology 2018;286:1008–15 doi:10.1148/radiol.2017170681 pmid:29072979
  11. 11.
    1. Fiebach JB,
    2. Schellinger PD,
    3. Jansen O, et al
    . CT and diffusion weighted MR imaging in randomized order: diffusion-weighted imaging results in higher accuracy and lower interrater variability in the diagnosis of hyperacute ischemic stroke. Stroke 2002;33:2206–10 doi:10.1161/01.STR.0000026864.20339.CB pmid:12215588
  12. 12.
    1. Paolini S,
    2. Burdine J,
    3. Verenes M, et al
    . Rapid short MRI sequence useful in eliminating stroke mimics among acute stroke patients considered for intravenous thrombolysis. J Neurol Disord 2013;1:137 doi:10.4172/2329-6895.1000137 pmid:24839612
  13. 13.
    1. Thomalla G,
    2. Simonsen CZ,
    3. Boutitie F, et al
    . WAKE-UP Investigators. MRI-guided thrombolysis for stroke with unknown time of onset. N Engl J Med 2018;379:611–22 doi:10.1056/NEJMoa1804355 pmid:29766770
  14. 14.
    1. Bossuyt PM,
    2. Reitsma JB,
    3. Bruns DE, et al
    . STARD Group. Stard 2015: an updated list of essential items for reporting diagnostic accuracy studies. Radiology 2015;277:826–32 doi:10.1148/radiol.2015151516 pmid:26509226
  15. 15.
    1. Kottner J,
    2. Audigé L,
    3. Brorson S, et al
    . Guidelines for Reporting Reliability and Agreement Studies (GRRAS) were proposed. J Clin Epidemiol 2011;64:96–106 doi:10.1016/j.jclinepi.2010.03.002 pmid:21130355
  16. 16.
    1. Donner A,
    2. Rotondi MA
    . Sample size requirements for interval estimation of the kappa statistic for interobserver agreement studies with a binary outcome and multiple raters. Int J Biostat 2010;6:Article 31 doi:10.2202/1557-4679.1275 pmid:21969984
  17. 17.
    1. Gibo H,
    2. Lenkey C,
    3. Rhoton AL
    . Microsurgical anatomy of the supraclinoid portion of the internal carotid artery. J Neurosurg 1981;55:560–74 doi:10.3171/jns.1981.55.4.0560 pmid:7277004
  18. 18.
    1. DiCiccio TJ,
    2. Efron B,
    3. Hall P, et al
    . Bootstrap confidence intervals. Statistical Science 1996;11:189–212 doi:10.1214/ss/1032280214
  19. 19.
    1. Vanbelle S,
    2. Albert A
    . A bootstrap method for comparing correlated kappa coefficients. Journal of Statistical Computation and Simulation 2008;78:1009–15 doi:10.1080/00949650701410249
  20. 20.
    1. Landis JR,
    2. Koch GG
    . The measurement of observer agreement for categorical data. Biometrics 1977;33:159–74 doi:10.2307/2529310 pmid:843571
  21. 21.
    Thrombectomy In TANdem Occlusion (TITAN). Published June 7, 2019. Updated August 12, 2020. https://clinicaltrials.gov/ct2/show/record/NCT03978988. Accessed February 18, 2021
  22. 22.
    1. Saver JL,
    2. Goyal M,
    3. Bonafe A, et al
    . SWIFT PRIME Investigators. Stent-retriever thrombectomy after intravenous t-PA vs. t-PA alone in stroke. N Engl J Med 2015;372:2285–95 doi:10.1056/NEJMoa1415061 pmid:25882376
  23. 23.
    1. Goyal M,
    2. Demchuk AM,
    3. Menon BK, et al
    . ESCAPE Trial Investigators. Randomized assessment of rapid endovascular treatment of ischemic stroke. N Engl J Med 2015;372:1019–30 doi:10.1056/NEJMoa1414905 pmid:25671798
  24. 24.
    1. Zhu F,
    2. Bracard S,
    3. Anxionnat R, et al
    . Impact of emergent cervical carotid stenting in tandem occlusion strokes treated by thrombectomy: a review of the TITAN Collaboration. Front Neurol 2019;10:206 doi:10.3389/fneur.2019.00206 pmid:30915023
  25. 25.
    1. Sadeh-Gonik U,
    2. Tau N,
    3. Friehmann T, et al
    . Thrombectomy outcomes for acute stroke patients with anterior circulation tandem lesions: a clinical registry and an update of a systematic review with meta-analysis. Eur J Neurol 2018;25:693–700 doi:10.1111/ene.13577 pmid:29350803
  26. 26.
    1. Tsivgoulis G,
    2. Katsanos AH,
    3. Schellinger PD, et al
    . Successful reperfusion with intravenous thrombolysis preceding mechanical thrombectomy in large-vessel occlusions. Stroke 2018;49:232–35 doi:10.1161/STROKEAHA.117.019261 pmid:29212743
  27. 27.
    1. Zinkstok SM,
    2. Roos YB
    ; ARTIS Investigators. Early administration of aspirin in patients treated with alteplase for acute ischaemic stroke: a randomized controlled trial. Lancet 2012;380:731–37 doi:10.1016/S0140-6736(12)60949-0 pmid:22748820
  28. 28.
    1. Chung HJ,
    2. Lee BH,
    3. Hwang YJ, et al
    . Delayed-phase CT angiography is superior to arterial-phase CT angiography at localizing occlusion sites in acute stroke patients eligible for intra-arterial reperfusion therapy. J Clin Neurosci 2014;21:596–600 doi:10.1016/j.jocn.2013.06.021 pmid:24412294
  29. 29.
    1. Choi JH,
    2. Jang J,
    3. Koo J, et al
    . Multiphasic computed tomography angiography findings for identifying pseudo-occlusion of the internal carotid artery. Stroke 2020;51:2558–62 doi:10.1161/STROKEAHA.120.029512 pmid:32586224
  30. 30.
    1. Ng FC,
    2. Choi PM,
    3. Datta M, et al
    . Perfusion-derived dynamic 4D CT angiography identifies carotid pseudo-occlusion in hyperacute stroke. J Neuroimaging 2016;26:588–91 doi:10.1111/jon.12375 pmid:27383381
  31. 31.
    1. Yang CY,
    2. Chen YF,
    3. Lee CW, et al
    . Multiphase CT angiography versus single-phase CT angiography: comparison of image quality and radiation dose. AJNR Am J Neuroradiol 2008;29:1288–95 doi:10.3174/ajnr.A1073 pmid:18403555
  32. 32.
    1. Lustig M,
    2. Donoho D,
    3. Pauly JM
    . Sparse MRI: the application of compressed sensing for rapid MR imaging. Magn Reson Med 2007;58:1182–95 doi:10.1002/mrm.21391 pmid:17969013
  33. 33.
    1. Chai S,
    2. Sheng Z,
    3. Xie W, et al
    . Assessment of apparent internal carotid tandem occlusion on high-resolution vessel wall imaging: comparison with digital subtraction angiography. AJNR Am J Neuroradiol 2020;41:693–99 doi:10.3174/ajnr.A6452 pmid:32115423
  34. 34.
    1. Provost C,
    2. Soudant M,
    3. Legrand L, et al
    . Magnetic resonance imaging or computed tomography before treatment in acute ischemic stroke. Stroke 2019;50:659–64 doi:10.1161/STROKEAHA.118.023882 pmid:30744542
  35. 35.
    1. Eker OF,
    2. BĂĽhlmann M,
    3. Dargazanli C, et al
    . Endovascular treatment of atherosclerotic tandem occlusions in anterior circulation stroke: technical aspects and complications compared to isolated intracranial occlusions. Front Neurol 2018;9:1046 doi:10.3389/fneur.2018.01046] pmid:30619028
  • Received May 21, 2020.
  • Accepted after revision December 21, 2020.
  • © 2021 by American Journal of Neuroradiology
Advertisement

Indexed Content

  • Current Issue
  • Accepted Manuscripts
  • Article Preview
  • Past Issues
  • Editorials
  • Editors Choice
  • Fellow Journal Club
  • Letters to the Editor

Cases

  • Case Collection
  • Archive - Case of the Week
  • Archive - Case of the Month
  • Archive - Classic Case

Special Collections

  • Special Collections

Resources

  • News and Updates
  • Turn around Times
  • Submit a Manuscript
  • Author Policies
  • Manuscript Submission Guidelines
  • Evidence-Based Medicine Level Guide
  • Publishing Checklists
  • Graphical Abstract Preparation
  • Imaging Protocol Submission
  • Submit a Case
  • Become a Reviewer/Academy of Reviewers
  • Get Peer Review Credit from Publons

Multimedia

  • AJNR Podcast
  • AJNR SCANtastic
  • Video Articles

About Us

  • About AJNR
  • Editorial Board
  • Not an AJNR Subscriber? Join Now
  • Alerts
  • Feedback
  • Advertise with us
  • Librarian Resources
  • Permissions
  • Terms and Conditions

American Society of Neuroradiology

  • Not an ASNR Member? Join Now

© 2025 by the American Society of Neuroradiology All rights, including for text and data mining, AI training, and similar technologies, are reserved.
Print ISSN: 0195-6108 Online ISSN: 1936-959X

Powered by HighWire