Skip to main content
Advertisement

Main menu

  • Home
  • Content
    • Current Issue
    • Accepted Manuscripts
    • Article Preview
    • Past Issue Archive
    • Video Articles
    • AJNR Case Collection
    • Case of the Week Archive
    • Case of the Month Archive
    • Classic Case Archive
  • Special Collections
    • AJNR Awards
    • Low-Field MRI
    • Alzheimer Disease
    • ASNR Foundation Special Collection
    • Photon-Counting CT
    • View All
  • Multimedia
    • AJNR Podcasts
    • AJNR SCANtastic
    • Trainee Corner
    • MRI Safety Corner
    • Imaging Protocols
  • For Authors
    • Submit a Manuscript
    • Submit a Video Article
    • Submit an eLetter to the Editor/Response
    • Manuscript Submission Guidelines
    • Statistical Tips
    • Fast Publishing of Accepted Manuscripts
    • Graphical Abstract Preparation
    • Imaging Protocol Submission
    • Author Policies
  • About Us
    • About AJNR
    • Editorial Board
    • Editorial Board Alumni
  • More
    • Become a Reviewer/Academy of Reviewers
    • Subscribers
    • Permissions
    • Alerts
    • Feedback
    • Advertisers
    • ASNR Home

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
    • Video Articles
    • AJNR Case Collection
    • Case of the Week Archive
    • Case of the Month Archive
    • Classic Case Archive
  • Special Collections
    • AJNR Awards
    • Low-Field MRI
    • Alzheimer Disease
    • ASNR Foundation Special Collection
    • Photon-Counting CT
    • View All
  • Multimedia
    • AJNR Podcasts
    • AJNR SCANtastic
    • Trainee Corner
    • MRI Safety Corner
    • Imaging Protocols
  • For Authors
    • Submit a Manuscript
    • Submit a Video Article
    • Submit an eLetter to the Editor/Response
    • Manuscript Submission Guidelines
    • Statistical Tips
    • Fast Publishing of Accepted Manuscripts
    • Graphical Abstract Preparation
    • Imaging Protocol Submission
    • Author Policies
  • About Us
    • About AJNR
    • Editorial Board
    • Editorial Board Alumni
  • 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

AJNR Awards, New Junior Editors, and more. Read the latest AJNR updates

Research ArticleAdult Brain

Reliability of CT Angiography in Cerebral Vasospasm: A Systematic Review of the Literature and an Inter- and Intraobserver Study

L. Letourneau-Guillon, B. Farzin, T.E. Darsaut, M. Kotowski, F. Guilbert, M. Chagnon, A. Diouf, D. Roy, A. Weill, M. Lemus, C. Bard, M. Belair, D. Landry, L. Nico, A. Tellier, R. Jabre, C. Kauffmann and J. Raymond
American Journal of Neuroradiology April 2020, 41 (4) 612-618; DOI: https://doi.org/10.3174/ajnr.A6462
L. Letourneau-Guillon
aFrom the Radiology Department (L.L.-G., B.F., M.K., F.G., A.D., D.R., A.W., M.L., C.B., M.B., D.L., L.N., A.T., J.R.), Centre Hospitalier de l’Universite de Montreal (CHUM), Centre de Recherche du CHUM (CRCHUM), Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for L. Letourneau-Guillon
B. Farzin
aFrom the Radiology Department (L.L.-G., B.F., M.K., F.G., A.D., D.R., A.W., M.L., C.B., M.B., D.L., L.N., A.T., J.R.), Centre Hospitalier de l’Universite de Montreal (CHUM), Centre de Recherche du CHUM (CRCHUM), Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for B. Farzin
T.E. Darsaut
cDepartment of Surgery (T.E.D.), Division of Neurosurgery, University of Alberta Hospital, Edmonton, Alberta, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for T.E. Darsaut
M. Kotowski
aFrom the Radiology Department (L.L.-G., B.F., M.K., F.G., A.D., D.R., A.W., M.L., C.B., M.B., D.L., L.N., A.T., J.R.), Centre Hospitalier de l’Universite de Montreal (CHUM), Centre de Recherche du CHUM (CRCHUM), Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for M. Kotowski
F. Guilbert
aFrom the Radiology Department (L.L.-G., B.F., M.K., F.G., A.D., D.R., A.W., M.L., C.B., M.B., D.L., L.N., A.T., J.R.), Centre Hospitalier de l’Universite de Montreal (CHUM), Centre de Recherche du CHUM (CRCHUM), Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for F. Guilbert
M. Chagnon
dStatistical Consultation Services (M.C.), Department of Mathematics and Statistics, Universite de Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for M. Chagnon
A. Diouf
aFrom the Radiology Department (L.L.-G., B.F., M.K., F.G., A.D., D.R., A.W., M.L., C.B., M.B., D.L., L.N., A.T., J.R.), Centre Hospitalier de l’Universite de Montreal (CHUM), Centre de Recherche du CHUM (CRCHUM), Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for A. Diouf
D. Roy
aFrom the Radiology Department (L.L.-G., B.F., M.K., F.G., A.D., D.R., A.W., M.L., C.B., M.B., D.L., L.N., A.T., J.R.), Centre Hospitalier de l’Universite de Montreal (CHUM), Centre de Recherche du CHUM (CRCHUM), Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for D. Roy
A. Weill
aFrom the Radiology Department (L.L.-G., B.F., M.K., F.G., A.D., D.R., A.W., M.L., C.B., M.B., D.L., L.N., A.T., J.R.), Centre Hospitalier de l’Universite de Montreal (CHUM), Centre de Recherche du CHUM (CRCHUM), Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for A. Weill
M. Lemus
aFrom the Radiology Department (L.L.-G., B.F., M.K., F.G., A.D., D.R., A.W., M.L., C.B., M.B., D.L., L.N., A.T., J.R.), Centre Hospitalier de l’Universite de Montreal (CHUM), Centre de Recherche du CHUM (CRCHUM), Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for M. Lemus
C. Bard
aFrom the Radiology Department (L.L.-G., B.F., M.K., F.G., A.D., D.R., A.W., M.L., C.B., M.B., D.L., L.N., A.T., J.R.), Centre Hospitalier de l’Universite de Montreal (CHUM), Centre de Recherche du CHUM (CRCHUM), Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for C. Bard
M. Belair
aFrom the Radiology Department (L.L.-G., B.F., M.K., F.G., A.D., D.R., A.W., M.L., C.B., M.B., D.L., L.N., A.T., J.R.), Centre Hospitalier de l’Universite de Montreal (CHUM), Centre de Recherche du CHUM (CRCHUM), Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for M. Belair
D. Landry
aFrom the Radiology Department (L.L.-G., B.F., M.K., F.G., A.D., D.R., A.W., M.L., C.B., M.B., D.L., L.N., A.T., J.R.), Centre Hospitalier de l’Universite de Montreal (CHUM), Centre de Recherche du CHUM (CRCHUM), Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for D. Landry
L. Nico
aFrom the Radiology Department (L.L.-G., B.F., M.K., F.G., A.D., D.R., A.W., M.L., C.B., M.B., D.L., L.N., A.T., J.R.), Centre Hospitalier de l’Universite de Montreal (CHUM), Centre de Recherche du CHUM (CRCHUM), Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for L. Nico
A. Tellier
aFrom the Radiology Department (L.L.-G., B.F., M.K., F.G., A.D., D.R., A.W., M.L., C.B., M.B., D.L., L.N., A.T., J.R.), Centre Hospitalier de l’Universite de Montreal (CHUM), Centre de Recherche du CHUM (CRCHUM), Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for A. Tellier
R. Jabre
bNeurosurgery Division, Surgery Department (R.J.), Centre Hospitalier de l’Universite de Montreal, Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for R. Jabre
C. Kauffmann
eLaboratoire Clinique du Traitement de l’Image (C.K.), Centre de Recherche du Centre Hospitalier de l’Universite de Montreal, Universite de Montreal, Montreal, Quebec, Canada.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for C. Kauffmann
J. Raymond
aFrom the Radiology Department (L.L.-G., B.F., M.K., F.G., A.D., D.R., A.W., M.L., C.B., M.B., D.L., L.N., A.T., J.R.), Centre Hospitalier de l’Universite de Montreal (CHUM), Centre de Recherche du CHUM (CRCHUM), Universite de Montreal, Montreal, Quebec, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for J. Raymond
  • Article
  • Figures & Data
  • Supplemental
  • Info & Metrics
  • Responses
  • References
  • PDF
Loading

Abstract

BACKGROUND AND PURPOSE: Computed tomography angiography offers a non-invasive alternative to DSA for the assessment of cerebral vasospasm following subarachnoid hemorrhage but there is limited evidence regarding its reliability. Our aim was to perform a systematic review (Part I) and to assess (Part II) the inter- and intraobserver reliability of CTA in the diagnosis of cerebral vasospasm.

MATERIALS AND METHODS: In Part I, articles reporting the reliability of CTA up to May 2018 were systematically searched and evaluated. In Part II, 11 raters independently graded 17 arterial segments in each of 50 patients with SAH for the presence of vasospasm using a 4-category scale. Raters were additionally asked to judge the presence of any moderate/severe vasospasm (≥ 50% narrowing) and whether findings would justify augmentation of medical treatment or conventional angiography ± balloon angioplasty. Four raters took part in the intraobserver reliability study.

RESULTS: In Part I, the systematic review revealed few studies with heterogeneous vasospasm definitions. In Part II, we found interrater reliability to be moderate at best (κ ≤ 0.6), even when results were stratified according to specialty and experience. Intrarater reliability was substantial (κ > 0.6) in 3/4 readers. In the per arterial segment analysis, substantial agreement was reached only for the middle cerebral arteries, and only when senior raters’ judgments were dichotomized (presence or absence of ≥50% narrowing). Agreement on the medical or angiographic management of vasospasm based on CTA alone was less than substantial (κ ≤ 0.6).

CONCLUSIONS: The diagnosis of vasospasm using CTA alone was not sufficiently repeatable among observers to support its general use to guide decisions in the clinical management of patients with SAH.

ABBREVIATION:

EBM
Evidence-Based Medicine

Cerebral vasospasm is the main cause of delayed cerebral ischemia after rupture of an intracranial aneurysm.1⇓-3 To detect and manage vasospasm, CTA and DSA are commonly used, particularly in comatose or sedated patients, to guide the use of medical and/or endovascular interventions that aim to prevent poor outcomes.3,4 The reliability of CTA in this context has not been rigorously evaluated.5⇓⇓-8

This article is divided in 2 parts. First, we systematically reviewed the literature on the CTA evaluation of vasospasm with emphasis on grading classifications and interobserver reliability. Second, we performed a local reliability study to assess whether clinicians agreed in making the diagnosis of moderate or severe vasospasm using CTA and in recommending further investigations or treatments based on CTA results in a series of 50 patients.

MATERIALS AND METHODS

Part I: Systematic Review

Classification systems used to quantify the degree of vasospasm with DSA and/or CTA and intra-/interobserver agreement studies on the diagnosis of vasospasm using CTA were systematically reviewed. A detailed protocol for the search strategy was prepared according to the Preferred Reported Items for Systematic Reviews and Meta-Analysis statement.9 The EMBASE, CINAHL, Evidence-Based Medicine (EBM), Cochrane, and MEDLINE databases were searched with no starting date specification, capturing English and French publications up to May 3, 2018. The search strategy is available in On-line Tables 1–5. One author (B.F.) tested the search strategy for its ability to recover pertinent articles. The data were collected and reviewed in detail by 2 authors with 5 and 6 years of experience, respectively (B.F. and L.L.-G.). Discrepancies were resolved by consensus.

Part II: Reliability Study

The Guidelines for Reporting Reliability and Agreement Studies were followed.10 The Centre de Recherche du Centre Hospitalier Universitaire de Montreal review board waived informed consent to access the patients’ clinical and radiologic data. Written informed consent was obtained from all raters participating in the study.

Patients.

We assembled a portfolio of 50 patients. The number of patients was predefined using the method of Donner and Rotondi11 and the kappaSize package12 in R, Version 3.4.4 (https://www.r-project.org/),13 taking into account pragmatic factors such as the willingness of observers to complete segment-by-segment evaluations.

All consecutive patients presenting to our institution from January 2005 to May 2017 with nontraumatic nonperimesencephalic SAH14 and who had undergone at least 2 CTAs (one on admission, the other follow-up CTA performed 2–21 days later to assess the presence of vasospasm) were retrospectively recovered from our radiology information system. The 2- to 21-day interval was chosen to cover the typical vasospasm window, assuming that the initial CTA could potentially be delayed by up to 24 hours since the onset of symptoms.4,15,16 The admission CTA was used as a reference when evaluating vasospasm on follow-up CTA.7,8 To minimize the issue of the κ paradox, CTAs were chosen in approximately equal proportions of vasospasm severity with reference to the official radiology report.17⇓-19 We did not exclude examinations degraded by coil or clip artifacts unless the study was rendered nondiagnostic (1 patient with 3 coiled aneurysms). All radiologic studies were de-identified and sent to the PACS for this study. The retrieved clinical information included demographic data (age, sex) and initial SAH-related patient characteristics (Hunt and Hess scale,20 hydrocephalus, ventricular drainage, craniectomy, anatomic location of the culprit vascular lesion causing the SAH, type of treatment of the vascular lesion) as well as the reason for performing the follow-up CTA in search of vasospasm and the time delay between the initial and follow-up CTA. One author (L.L.-G.) retrospectively graded each admission noncontrast head CT for SAH using the modified Fisher scale.21

Readers.

Eleven clinicians involved in the diagnosis and management of vasospasm, from different specialties (radiology, neurosurgery) and with different levels of experience in the management of vasospasm from our institution participated in the study. Readers were stratified by experience as junior (residents and fellows) or senior (attending physicians with ≥5 years of experience; range, 5–35 years).

Evaluations and Categories.

For each case, readers were asked to grade the degree of vasospasm of 17 arterial segments on a 4-category scale (none, mild [<50%], moderate [50%–74%], and severe [≥75% narrowing]) compared with the initial CTA.8,22 Arterial segments were predefined as proximal (intracranial internal carotid arteries, A1, M1, and P1 segments, basilar and vertebral arteries) or distal (A2–3, M2–3, P2–3 segments), as previously reported.7 For each patient, there were 3 additional questions (yes/no): 1) Is there moderate-severe vasospasm at any location? 2) Presuming the presence of a new neurologic deficit corresponding to the territory of the artery affected by vasospasm, would you recommend a change in medical management? 3) Would you recommend DSA with or without balloon angioplasty? The latter 2 clinical decisions were based on the readers’ clinical experience.

All the aforementioned readings were performed using only the pair of de-identified admission and follow-up CTAs, with the reader blinded to the initial report, other clinical information, or follow-up imaging as well as other reader assessments. For the intrarater portion of the study, all cases were read a second time by 4 raters. The second set of readings was permutated and performed at least 4 weeks following the initial readings to minimize recall bias.

CTAs.

All CTAs were performed on a 64-section Somatom Sensation scanner (Siemens, Erlangen, Germany), using 60-mL injections of iohexol (350 mg iodine per millimeter, Omnipaque; GE Healthcare, Piscataway, New Jersey), followed by a 30-mL saline bolus at 5 mL/s. Scanning parameters were 120-kV tube voltage, 250 mAs, pitch of 0.6, section thickness of 0.6 with 0.4-mm intervals from C2 to the vertex, matrix of 512 × 512, FOV of 30–32 cm. Minimal reformations were (section thickness/increments): 1/1-mm axial MPR images, 3/1-mm coronal and sagittal MIP images, as well as 30/3-mm axial MIP images.

Data Analyses.

Intra- and interobserver reliability statistics were computed using STATA/IC, Version 14.2 (StataCorp, College Station, Texas) and R13 using the irr package23 under the supervision of a statistician (M.C.). Cohen and Fleiss κ reliability coefficients were calculated for intraobserver and multirater interobserver analyses, respectively, using 1000 bootstrap samples (bias-corrected) to obtain 95% confidence intervals. In the per-patient analysis, the 3 main questions generated dichotomous results (yes/no). In the per-segment analysis, the 4-point grading system for vasospasm (none, mild, moderate, severe) generated an ordinal scale (0–3). We did not add weightings to the κ calculation for the latter data. This scale was then dichotomized (none-mild versus moderate-severe, corresponding to <50 versus ≥50% arterial narrowing) for a secondary analysis. An exploratory analysis was also performed, removing all arterial segments obscured by clip or coil artifacts. All κ coefficients were stratified according to experience (junior versus senior) and specialty among senior readers (diagnostic versus interventional neuroradiology). κ coefficients were interpreted using Landis and Koch guidelines,24 predefining κ > 0.6 as “substantial agreement.”

RESULTS

Part I: Systematic Review

A total of 5761 titles were reviewed, 2780 abstracts were examined, and 304 full-text articles were read in detail, leaving 14 articles for the systematic review (On-line Fig 1). In these studies, 8 different classification systems were used (with 3–5 categories) with various arbitrary cutoffs (On-line Table 6). All 14 were diagnostic accuracy studies, but 3 also assessed interobserver agreement on cerebral vasospasm using CTA. One of the interobserver variability studies had 3 raters, while the other 2 studies had 2. No study assessed intraobserver reliability. Results are summarized in On-line Table 7. The degree of blinding of the raters was not reliably reported. The paucity of data and the heterogeneity of methods and end points precluded the performance of a meta-analysis.

Part II: Reliability Study

Patients and their characteristics are summarized in Table 1 and On-line Fig 2, respectively. The CTAs were performed between March 27, 2008, and April 6, 2017. The mean time interval between the initial and follow-up CTA was 7.1 days (range, 2–15 days). Characteristics related to follow-up CTAs as well as subsequent vasospasm management are summarized in Table 2.

View this table:
  • View inline
  • View popup
Table 1:

Baseline demographics, clinical, and radiologic characteristics of the patientsa

View this table:
  • View inline
  • View popup
Table 2:

Vasospasm-related characteristicsa

The 11 readers were 3 interventional neuroradiologists (>15 years of experience each in evaluating CTAs for vasospasm), 3 diagnostic neuroradiologists (15, 12, and 5 years of experience), 2 interventional neuroradiology fellows, 2 senior diagnostic radiology residents, and 1 senior neurosurgery resident.

The interobserver agreement for the detection of moderate-to-severe vasospasm (≥50% narrowing in any segment) was only fair (κ = 0.340; 95% CI, 0.232−0.462) for all raters (Fig 1, data in On-line Table 8). Agreement between senior raters improved to moderate (κ = 0.433; 95% CI, 0.266–0.582). Perfect agreement was found for few patients: Six of 50 (12%) patients were judged by all raters to have moderate-severe vasospasm, while 3/50 (6%) were judged by all raters not to have any vasospasm. These proportions improved slightly when only senior readers were considered, reaching 7/50 (14%) and 16/50 (32%), respectively. There were significant differences (p < .001) in the proportions of patients judged to have moderate-to-severe vasospasm between junior and senior raters, as well as between diagnostic and interventional neuroradiologists (On-line Table 9 and On-line Fig 3A).

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

Interreader reliability coefficients (95% confidence intervals) including all subgroups (senior, junior, interventional, and diagnostic neuroradiologists) for the 3 main questions: detection of moderate-severe vasospasm in any arterial segment (≥ 50% narrowing), recommendations of medical treatment augmentation, and DSA ± angioplasty based on imaging findings. The horizontal dashed line indicates the threshold for substantial agreement (κ > 0.6). INR indicates interventional neuroradiology; DNR, diagnostic neuroradiology.

Interobserver agreement regarding augmentation of medical treatment based on CTA alone was fair (κ = 0.245; 95% CI, 0.179–0.336) (Fig 1, data in On-line Table 8). Interobserver agreement on recommending DSA ± balloon angioplasty based on CTA alone was also fair (κ = 0.272; 95% CI, 0.159–0.415) (Fig 1, data in On-line Table 8). There were only 2/50 (4%) cases in which all raters agreed that DSA ± angioplasty should be performed (On-line Fig 3C).

The segment-by-segment analysis evaluating the presence of moderate-severe vasospasm did not reach substantial agreement for any arterial segment when considering all raters (On-line Fig 4, full data in On-line Tables 11 and 12). Judgments regarding proximal segments (M1, A1, vertebral and basilar arteries) were, in general, more repeatable than judgments regarding distal segments, with the exception of the internal carotid artery, for which agreement remained only slight. When only senior raters were considered, agreement for the presence of moderate-severe vasospasm (dichotomous scale) in the M1 segments improved to substantial (On-line Fig 4D). Examples of maximal agreement and maximal disagreement for the M1 segments are illustrated in On-line Fig 5.

An exploratory analysis was conducted to examine the role of metal artifacts from endovascular coils or surgical clips in affecting the repeatability of diagnoses. Thirty-six A1, 13 A2–A3, 11 ICA, and 7 M1 segments were excluded from this analysis, retaining only arterial segments that were not obscured by artifacts (On-line Fig 6, full data in On-line Table 13). κ coefficients remained below the 0.6 threshold, except for the left M1 segment, which reached the substantial agreement threshold among all observers.

Four observers completed the intraobserver study (3 interventional neuroradiologists and 1 radiology resident). Intraobserver reliability was “substantial” (κ > 0.6) in 3/4 readers (Fig 2, data in On-line Table 10) for the detection of moderate-to-severe vasospasm. For the management recommendations based on imaging findings, intraobserver reliability was substantial for 3 readers for medical management and for 2 readers for the decision to perform DSA.

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

Intrareader reliability coefficients for the 3 main questions (95% confidence intervals) among 4 observers: detection of moderate-severe vasospasm in any arterial segment (≥ 50% narrowing), recommendations for medical treatment augmentation, and DSA ± angioplasty based on imaging findings. The horizontal dashed line indicates the threshold for substantial agreement (κ > 0.6).

DISCUSSION

The systematic review revealed a wide variation in grading systems of vasospasm. In addition, few studies evaluated the reliability of CTA for the diagnosis of vasospasm. Most reports were primarily diagnostic accuracy studies, dedicated to a comparison with DSA, while agreement studies were limited to 2–3 raters. The relatively good agreement between readers in these studies could not be confirmed in our center.

The main finding of our reliability study, which included a higher number of observers and wider range of experience compared with prior reports, is that the reliability of CTA alone in the diagnosis of moderate-to-severe cerebral vasospasm was not substantially repeatable between observers, even when verdicts were dichotomized and even when analyses were restricted to experienced raters.

This problem has previously been identified.25 When a noninvasive imaging test is proposed to replace a more invasive one (here conventional angiography), the emphasis is usually placed on diagnostic accuracy, rather than on studying the repeatability of judgments made with the new imaging technique by multiple observers.10,25 A major difficulty is the shift in the clinical spectrum of patients who are undergoing the test, which naturally occurs as the imaging test becomes widely accepted in routine clinical applications. Initially, for the diagnostic accuracy studies, the new test is likely to be compared with DSA for patients on the “severe” end of the spectrum (patients for whom DSA is judged to be indicated). Later on, at the time of clinical usage, the less invasive test is increasingly used in patients who have less severe disease, for whom DSA would not necessarily be performed. The consequence is that the relatively good interobserver agreement typically found between 2 or 3 expert raters in early diagnostic accuracy studies cannot be reproduced in real-world practice.

The poor repeatability of CTA judgments on vasospasm may not be surprising when one considers a number of unresolved problems. Despite the fact that CTA has been used for decades in the diagnosis of post-SAH cerebral vasospasm, there is no consensus on diagnostic criteria and our systematic review revealed a wide range of grading scales with various arbitrary cutoff values. Whether observers can reliably differentiate 25% or 30% luminal narrowing is questionable, given the small caliber of arteries and the limited spatial resolution of CTA. Even if precise and reliable measurements were possible, there is no agreement on which baseline reference value should be used. Some authors, similar to our study, use the baseline examination (when available) as a reference while others use the ipsilateral or contralateral “uninvolved” arteries. Various methods (eyeballing versus measuring with a caliper, for example) are commonly used. The rationale for various grading scales and the exact procedural methodology have not been clearly stated or validated.

In general, scales should be valid, reliable, and clinically relevant.26 A scale that is too complex or that introduces too many categories is less repeatable, leaving too much room for variations in interpretation by different observers. There is also no standardized way to summarize the findings of each arterial segment in 1 global verdict that concerns the individual patient. We chose a grading system that had been used previously.8,22 We also predefined a 50% diameter narrowing cutoff to explore whether better agreement could be achieved by simplifying responses through dichotomization and also because the 50% threshold has been suggested to correlate with decreased cerebral perfusion in the setting of cerebral vasospasm.2,27⇓-29 Further exploration of the diagnostic value of other threshold values may be warranted, given the low reliability found in the current study as well as possible lack of specificity of the 50% narrowing cutoff to predict ischemia.15,28,30

The primary end point of the study was the identification of moderate-to-severe vasospasm in any arterial segment for a given patient. If agreement between observers failed to reach the substantial (κ > 0.6) threshold, even for experienced raters, at least the intrarater agreement was better for most readers. There remains hope that better interobserver agreement could be attained, at least for major proximal arterial segments (excluding the carotid arteries), with more precise definitions and standardized procedures.

No matter how vasospasm is interpreted, the most important questions concern the clinical relevance of the CTA verdict. We were interested in exploring whether agreement existed, if not for the grade of vasospasm, at least for the clinical significance of the CTA findings in terms of whether medical treatment should be increased or whether DSA ± balloon angioplasty should be performed. We were careful not to provide clinical information that could bias the interpretation of the clinical history by different observers.31 Despite this effort and contrary to a previous report,7 interrater agreement remained below the substantial level.

A striking finding was the difference in the severity of vasospasm adjudicated by readers of different experiences and specialties. Diagnostic radiologists had a higher proportion of moderate-to-severe vasospasm diagnoses compared with interventional neuroradiologists. Junior readers had a higher proportion of positive answers to the 3 main questions, compared with more experienced readers. Interventional neuroradiologists, who are exposed to the most severe end of the disease spectrum because they may be required to treat these patients, may have a higher threshold for diagnosing severe vasospasm than other clinicians.

Segment-by-segment analyses were performed to explore potential ways to improve the reliability of CTA. This analysis also showed lower agreement than previously reported.7 However, the relatively low reliability of the assessment of the carotid arteries and the relatively better agreement found in the evaluation of middle cerebral arteries have previously been noted.6 These observations suggest that readers looking for vasospasm on CTA should perhaps focus on more reliable segments such as the M1 segments and basilar artery and not on less reliable segments such as carotid arteries or distal vessels.

The present study did not select the best cases or exclude patients with clip or coil artifacts, to reflect real-life clinical conditions. Including mainly patients without metal artifacts, as in a previous report,6 would hardly have reflected normal clinical usage, for most patients at risk of vasospasm have already undergone endovascular or surgical treatment of the aneurysm at the time of the CTA assessment. Metal artifacts remain a limitation of CTA, a problem that could perhaps be mitigated by specific algorithms and/or dual-energy CT.32 However, agreement improved only minimally when a second analysis excluding arterial segments obscured by beam-hardening artifacts was performed.

Several factors may explain the lower reliability we found compared with previous reports. Reliability is the complex product of interactions among the test, subjects, raters, and the context of assessment.33,34 κ coefficients based on a limited number of subjects and raters can result in overestimates.35 Our study included a larger number of readers and index cases than in previous reports. The spectrum of patients included in our study also differed, as we discussed previously. Grading scales, exact methods of measurement, and statistical analyses also differed. One frequent source of artificial inflation of agreement is the lack of blinding of raters to other raters’ observations, to the reference test, or to clinical information or clues.31 In our study, observers independently analyzed anonymized images; they could not access the clinical or radiologic file of patients.

CTA is performed at our institution in patients with severe SAH grades in whom neurologic monitoring is difficult or impossible and/or when transcranial Doppler sonography findings are concerning for cerebral vasospasm. Angiography was performed in only 8% of studied patients; only 1 patient received intra-arterial milrinone. This is in contrast to almost 50% of patients undergoing angioplasty in the study by Shankar et al.7 A retrospective review at our institution during the same period revealed that most patients with vasospasm treated with angioplasty had lateralizing neurologic symptoms despite maximal medical treatment. They were directly referred to the angiography suite without CTA. In such patients, the addition of CTA in the investigation of vasospasm may be superfluous. It seems that in our institution, CTA is most often used as a screening test for patients in intensive care, who are difficult to monitor clinically. Unfortunately, our study suggests that in this context, CTA interpretations are not repeatable enough to guide management decisions. If CTA is to be used as a screening test in patients with a low prior probability of symptomatic vasospasm, our study suggests that interpretations should be cautious, perhaps using a diagnostic threshold at a higher level than 50% narrowing, limited to more reliable proximal arterial segments.

Our study had several limitations. The portfolio of cases was artificially constructed, and raters were self-selected. A different set of cases and observers could have produced different results. Given our low prevalence of severe vasospasm in individual arterial segments, our κ coefficients could potentially be underestimated due to a skewed rating distribution in the per-segment analysis.19 We did not try to differentiate focal-versus-diffuse vasospasm when a narrowing was present.30 The experimental setup and the use of a portfolio differ from the case-by-case evaluation of real patients, and we can only surmise that responders took the time and care to respond as if they were evaluating real patients.

CONCLUSIONS

The systematic review found few reliability studies, limited to 2–3 readers. Our agreement study, which included a larger number of observers, revealed that the diagnosis of moderate-severe vasospasm was not sufficiently repeatable to support the use of CTA alone to guide decisions in the clinical management of patients with SAH. The repeatability of verdicts could potentially be improved by raising the diagnostic threshold above 50% narrowing for substantial vasospasm, by focusing on proximal arterial segments such as the M1 and basilar arteries, and by standardizing interpretation protocols.

Acknowledgment

We thank Guylaine Gevry for support during manuscript writing, editing, and submission as well as Daniela Ziegler, MSI (librarian) for support during the systematic review.

Footnotes

  • Preliminary results previously presented at: Annual Meeting of the Eastern Neuroradiological Society, August 22–25, 2019; Brooklyn, New York.

  • Laurent Letourneau-Guillon received Can $1125.00 from the ninth competition of the Program de Support Professoral du département de radiologie, radio-oncologie et médecine nucléaire de l’Université de Montréal to cover statistical analysis fees (internal funding program).

  • Disclosures: Laurent Letourneau-Guillon—RELATED: Grant: Laurent Letourneau-Guillon received Can $1125.00 from the ninth competition of the Program de Support Professoral du département de radiologie, radio-oncologie et médecine nucléaire de l’Université de Montréal to cover statistical analysis fees (internal funding program). The full amount was transferred to the statistician.* Miguel Chagnon—RELATED: Consulting Fee or Honorarium: University of Montreal.* Daniel Roy—UNRELATED: Payment for Lectures Including Service on Speakers Bureaus: Société des sciences vasculaires du Québec (Can $500); Payment for Development of Educational Presentations: Société des Radiologues du Québec (Can $5000); Travel/Accommodations/Meeting Expenses Unrelated to Activities Listed: ABC Win 2019, WFITN 2019, Comments: ABC Win, guest speaker (travel and accommodations), WFITN 2019, faculty (accommodations). *Money paid to institution.

References

  1. 1.↵
    1. Macdonald RL
    . Origins of the concept of vasospasm. Stroke 2016;47:e11–15 doi:10.1161/STROKEAHA.114.006498 pmid:26337970
    FREE Full Text
  2. 2.↵
    1. Budohoski KP,
    2. Guilfoyle M,
    3. Helmy A, et al
    . The pathophysiology and treatment of delayed cerebral ischaemia following subarachnoid haemorrhage. J Neurol Neurosurg Psychiatry 2014;85:1343–53 doi:10.1136/jnnp-2014-307711 pmid:24847164
    Abstract/FREE Full Text
  3. 3.↵
    1. Findlay JM,
    2. Nisar J,
    3. Darsaut T
    . Cerebral vasospasm: a review. Can J Neurol Sci 2016;43:15–32 doi:10.1017/cjn.2015.288 pmid:26332908
    CrossRefPubMed
  4. 4.↵
    1. Francoeur CL,
    2. Mayer SA
    . Management of delayed cerebral ischemia after subarachnoid hemorrhage. Crit Care 2016;20:277 doi:10.1186/s13054-016-1447-6 pmid:27737684
    CrossRefPubMed
  5. 5.↵
    1. Greenberg ED,
    2. Gold R,
    3. Reichman M, et al
    . Diagnostic accuracy of CT angiography and CT perfusion for cerebral vasospasm: a meta-analysis. AJNR Am J Neuroradiol 2010;31:1853–60 doi:10.3174/ajnr.A2246 pmid:20884748
    Abstract/FREE Full Text
  6. 6.↵
    1. Chaudhary SR,
    2. Ko N,
    3. Dillon WP, et al
    . Prospective evaluation of multidetector-row CT angiography for the diagnosis of vasospasm following subarachnoid hemorrhage: a comparison with digital subtraction angiography. Cerebrovasc Dis 2008;25:144–50 doi:10.1159/000112325 pmid:18073468
    CrossRefPubMed
  7. 7.↵
    1. Shankar JJ,
    2. Tan IY,
    3. Krings T, et al
    . CT angiography for evaluation of cerebral vasospasm following acute subarachnoid haemorrhage. Neuroradiology 2012;54:197–203 doi:10.1007/s00234-011-0876-9 pmid:21541687
    CrossRefPubMed
  8. 8.↵
    1. Binaghi S,
    2. Colleoni ML,
    3. Maeder P, et al
    . CT angiography and perfusion CT in cerebral vasospasm after subarachnoid hemorrhage. AJNR Am J Neuroradiol 2007;28:750–58 pmid:17416833
    Abstract/FREE Full Text
  9. 9.↵
    1. Moher D,
    2. Liberati A,
    3. Tetzlaff J, et al
    ; PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. J Clin Epidemiol 2009;62:1006–12 doi:10.1016/j.jclinepi.2009.06.005 pmid:19631508
    CrossRefPubMed
  10. 10.↵
    1. Kottner J,
    2. Audige 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
    CrossRefPubMed
  11. 11.↵
    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
    CrossRefPubMed
  12. 12.↵
    1. Rotondi M
    . kappaSize: sample size estimation functions for studies of interobserver agreement. R package version 1.1 2013. https://CRAN.R-project.org/package=kappaSize. Accessed January 10, 2018
  13. 13.↵
    R Core Team. R: A language and environment for statistical computing. Version 3.4.4. R Foundation for Statistical Computing 2018. https://www.R-project.org. Accessed April 2, 2018
  14. 14.↵
    1. Cruz JP,
    2. Sarma D,
    3. Noel de Tilly L
    . Perimesencephalic subarachnoid hemorrhage: when to stop imaging? Emerg Radiol 2011;18:197–202 doi:10.1007/s10140-011-0939-6 pmid:21360167
    CrossRefPubMed
  15. 15.↵
    1. Budohoski KP,
    2. Czosnyka M,
    3. Kirkpatrick PJ, et al
    . Clinical relevance of cerebral autoregulation following subarachnoid haemorrhage. Nat Rev Neurol 2013;9:152–63 doi:10.1038/nrneurol.2013.11 pmid:23419369
    CrossRefPubMed
  16. 16.↵
    1. Lazaridis C,
    2. Naval N
    . Risk factors and medical management of vasospasm after subarachnoid hemorrhage. Neurosurg Clin N Am 2010;21:353–64 doi:10.1016/j.nec.2009.10.006 pmid:20380975
    CrossRefPubMed
  17. 17.↵
    1. Feinstein AR,
    2. Cicchetti DV
    . High agreement but low kappa, I: the problems of two paradoxes. J Clin Epidemiol 1990;43:543–49 doi:10.1016/0895-4356(90)90158-L pmid:2348207
    CrossRefPubMed
  18. 18.↵
    1. Cicchetti DV,
    2. Feinstein AR
    . High agreement but low kappa, II: resolving the paradoxes. J Clin Epidemiol 1990;43:551–58 doi:10.1016/0895-4356(90)90159-m pmid:2189948
    CrossRefPubMed
  19. 19.↵
    1. Quarfoot D,
    2. Levine RA
    . How robust are multirater interrater reliability indices to changes in frequency distribution? The American Statistician 2016;70:373–84 doi:10.1080/00031305.2016.1141708
    CrossRef
  20. 20.↵
    1. Hunt WE,
    2. Hess RM
    . Surgical risk as related to time of intervention in the repair of intracranial aneurysms. J Neurosurg 1968;28:14–20 doi:10.3171/jns.1968.28.1.0014 pmid:5635959
    CrossRefPubMed
  21. 21.↵
    1. Frontera JA,
    2. Claassen J,
    3. Schmidt JM, et al
    . Prediction of symptomatic vasospasm after subarachnoid hemorrhage: the modified Fisher scale. Neurosurgery 2006;59:21–27; discussion 21–27 doi:10.1227/01.NEU.0000218821.34014.1B pmid:16823296
    CrossRefPubMed
  22. 22.↵
    1. Takagi R,
    2. Hayashi H,
    3. Kobayashi H, et al
    . Three-dimensional CT angiography of intracranial vasospasm following subarachnoid haemorrhage. Neuroradiology 1998;40:631–35 doi:10.1007/s002340050654 pmid:9833891
    CrossRefPubMed
  23. 23.↵
    1. Gamer M,
    2. Lemon J,
    3. Fellows I, et al
    . irr: Various coefficients of interrater reliability and agreement. R package version 0.84. https://CRAN.R-project.org/package=irr. Accessed June 1, 2018
  24. 24.↵
    1. Landis JR,
    2. Koch GG
    . The measurement of observer agreement for categorical data. Biometrics 1977;33:159–74 pmid:843571
    CrossRefPubMed
  25. 25.↵
    1. Farzin B,
    2. Gentric JC,
    3. Pham M, et al
    . Agreement studies in radiology research. Diagn Interv Imaging 2017;98:227–33 doi:10.1016/j.diii.2016.05.014 pmid:27473190
    CrossRefPubMed
  26. 26.↵
    1. Cloft HJ,
    2. Kallmes DF
    . Scaling back on scales with a scale of scales. AJNR Am J Neuroradiol 2011;32:219–20 doi:10.3174/ajnr.A2432 pmid:21183620
    FREE Full Text
  27. 27.↵
    1. Kelly PJ,
    2. Gorten RJ,
    3. Grossman RG, et al
    . Cerebral perfusion, vascular spasm, and outcome in patients with ruptured intracranial aneurysms. J Neurosurg 1977;47:44–49 doi:10.3171/jns.1977.47.1.0044 pmid:864506
    CrossRefPubMed
  28. 28.↵
    1. Ohkuma H,
    2. Manabe H,
    3. Tanaka M, et al
    . Impact of cerebral microcirculatory changes on cerebral blood flow during cerebral vasospasm after aneurysmal subarachnoid hemorrhage. Stroke 2000;31:1621–27 doi:10.1161/01.str.31.7.1621 pmid:10884463
    Abstract/FREE Full Text
  29. 29.↵
    1. Voldby B,
    2. Enevoldsen EM,
    3. Jensen FT
    . Regional CBF, intraventricular pressure, and cerebral metabolism in patients with ruptured intracranial aneurysms. J Neurosurg 1985;62:48–58 doi:10.3171/jns.1985.62.1.0048 pmid:3964855
    CrossRefPubMed
  30. 30.↵
    1. Lodi CA,
    2. Ursino M
    . Hemodynamic effect of cerebral vasospasm in humans: a modeling study. Ann Biomed Eng 1999;27:257–73 doi:10.1114/1.168 pmid:10199702
    CrossRefPubMed
  31. 31.↵
    1. Lucas NP,
    2. Macaskill P,
    3. Irwig L, et al
    . The development of a quality appraisal tool for studies of diagnostic reliability (QAREL). J Clin Epidemiol 2010;63:854–61 doi:10.1016/j.jclinepi.2009.10.002 pmid:20056381
    CrossRefPubMed
  32. 32.↵
    1. Winklhofer S,
    2. Hinzpeter R,
    3. Stocker D, et al
    . Combining monoenergetic extrapolations from dual-energy CT with iterative reconstructions: reduction of coil and clip artifacts from intracranial aneurysm therapy. Neuroradiology 2018;60:281–91 doi:10.1007/s00234-018-1981-9 pmid:29356855
    CrossRefPubMed
  33. 33.↵
    1. Barth J,
    2. de Boer WE,
    3. Busse JW, et al
    . Inter-rater agreement in evaluation of disability: systematic review of reproducibility studies. BMJ 2017;356:14 doi:10.1136/bmj.j14 pmid:28122727
    CrossRefPubMed
  34. 34.↵
    1. Spanjer J,
    2. Krol B,
    3. Brouwer S, et al
    . Sources of variation in work disability assessment. Work 2010;37:405–11 doi:10.3233/WOR-2010-1094 pmid:21099015
    CrossRefPubMed
  35. 35.↵
    1. Gwet KL
    . Handbook of Inter-Rater Reliability: The Definitive Guide to Measuring the Extent of Agreement Among Raters. Gaithersburg: Advanced Analytics; 2014
  36. 36.
    1. Schneck SA,
    2. Kricheff, II.
    . Intracranial Aneurysm Rupture, Vasospasm, and Infarction. Arch Neurol 1964;11:668–80 doi:10.1001/archneur.1964.00460240100013 pmid:14202184
    CrossRefPubMed
  37. 37.
    1. Kassell NF,
    2. Helm G,
    3. Simmons N, et al
    . Treatment of cerebral vasospasm with intra-arterial papaverine. J Neurosurg 1992;77:848–52 doi:10.3171/jns.1992.77.6.0848 pmid:1432125
    CrossRefPubMed
  38. 38.
    1. Anderson GB,
    2. Ashforth R,
    3. Steinke DE, et al
    . CT angiography for the detection of cerebral vasospasm in patients with acute subarachnoid hemorrhage. AJNR American journal of neuroradiology 2000;21:1011–15 pmid:10871004
    Abstract/FREE Full Text
  39. 39.
    1. Otawara Y,
    2. Ogasawara K,
    3. Ogawa A, et al
    . Evaluation of Vasospasm after Subarachnoid Hemorrhage by Use of Multislice Computed Tomographic Angiography. Neurosurgery 2002;51:939–43 doi:10.1097/00006123-200210000-00015 pmid:12234400
    CrossRefPubMed
  40. 40.
    1. Yoon DY,
    2. Choi CS,
    3. Kim KH, et al
    . Multidetector-Row CT Angiography of Cerebral Vasospasm after Aneurysmal Subarachnoid Hemorrhage: Comparison of Volume-Rendered Images and Digital Subtraction Angiography. American Journal of Neuroradiology 2006;27:370–77 pmid:16484413
    Abstract/FREE Full Text
  41. 41.
    1. Joo SP,
    2. Kim TS,
    3. Kim YS, et al
    . Clinical utility of multislice computed tomographic angiography for detection of cerebral vasospasm in acute subarachnoid hemorrhage. Minim Invasive Neurosurg 2006;49:286–90 doi:10.1055/s-2006-954826 pmid:17163342
    CrossRefPubMed
  42. 42.
    1. Aralasmak A,
    2. Akyuz M,
    3. Ozkaynak C, et al
    . CT angiography and perfusion imaging in patients with subarachnoid hemorrhage: correlation of vasospasm to perfusion abnormality. Neuroradiology 2009;51:85–93 doi:10.1007/s00234-008-0466-7 pmid:18850093
    CrossRefPubMed
  43. 43.
    1. Zhang H,
    2. Zhang B,
    3. Li S, et al
    . Whole brain CT perfusion combined with CT angiography in patients with subarachnoid hemorrhage and cerebral vasospasm. Clinical neurology and neurosurgery 2013;115:2496–501 doi:10.1016/j.clineuro.2013.10.004 pmid:24210268
    CrossRefPubMed
  44. 44.
    1. Danura H,
    2. Schatlo B,
    3. Marbacher S, et al
    . Acute angiographic vasospasm and the incidence of delayed cerebral vasospasm: preliminary results. Acta neurochirurgica Supplement 2015;120:187–90 doi:10.1007/978-3-319-04981-6_32 pmid:25366622
    CrossRefPubMed
  45. 45.
    1. Stecco A,
    2. Fabbiano F,
    3. Amatuzzo P, et al
    . Computed tomography perfusion and computed tomography angiography in vasospasm after subarachnoid hemorrhage. Journal of neurosurgical sciences 2018;62:397–405 doi:10.23736/S0390-5616.16.03622-5 pmid:27124176
    CrossRefPubMed
  • Received October 18, 2019.
  • Accepted after revision January 27, 2020.
  • © 2020 by American Journal of Neuroradiology
View Abstract
PreviousNext
Back to top

In this issue

American Journal of Neuroradiology: 41 (4)
American Journal of Neuroradiology
Vol. 41, Issue 4
1 Apr 2020
  • Table of Contents
  • Index by author
  • Complete Issue (PDF)
Advertisement
Print
Download PDF
Email Article

Thank you for your interest in spreading the word on American Journal of Neuroradiology.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Reliability of CT Angiography in Cerebral Vasospasm: A Systematic Review of the Literature and an Inter- and Intraobserver Study
(Your Name) has sent you a message from American Journal of Neuroradiology
(Your Name) thought you would like to see the American Journal of Neuroradiology web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Cite this article
L. Letourneau-Guillon, B. Farzin, T.E. Darsaut, M. Kotowski, F. Guilbert, M. Chagnon, A. Diouf, D. Roy, A. Weill, M. Lemus, C. Bard, M. Belair, D. Landry, L. Nico, A. Tellier, R. Jabre, C. Kauffmann, J. Raymond
Reliability of CT Angiography in Cerebral Vasospasm: A Systematic Review of the Literature and an Inter- and Intraobserver Study
American Journal of Neuroradiology Apr 2020, 41 (4) 612-618; DOI: 10.3174/ajnr.A6462

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
0 Responses
Respond to this article
Share
Bookmark this article
Reliability of CT Angiography in Cerebral Vasospasm: A Systematic Review of the Literature and an Inter- and Intraobserver Study
L. Letourneau-Guillon, B. Farzin, T.E. Darsaut, M. Kotowski, F. Guilbert, M. Chagnon, A. Diouf, D. Roy, A. Weill, M. Lemus, C. Bard, M. Belair, D. Landry, L. Nico, A. Tellier, R. Jabre, C. Kauffmann, J. Raymond
American Journal of Neuroradiology Apr 2020, 41 (4) 612-618; DOI: 10.3174/ajnr.A6462
del.icio.us logo Twitter logo Facebook logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One
Purchase

Jump to section

  • Article
    • Abstract
    • ABBREVIATION:
    • MATERIALS AND METHODS
    • RESULTS
    • DISCUSSION
    • CONCLUSIONS
    • Acknowledgment
    • Footnotes
    • References
  • Figures & Data
  • Supplemental
  • Info & Metrics
  • Responses
  • References
  • PDF

Related Articles

  • PubMed
  • Google Scholar

Cited By...

  • Reply:
  • CTA Supplemented by CTP Increases Interrater Reliability and Endovascular Treatment Use in Patients with Aneurysmal SAH
  • Reply:
  • Transcranial Doppler Velocities and Angiographic Vasospasm after SAH: A Diagnostic Accuracy Study
  • Development and external validation of a dynamic nomogram for delayed cerebral ischaemia after aneurysmal subarachnoid hemorrhage: a study protocol for a multicentre retrospective cohort study
  • Reliability of the Diagnosis of Cerebral Vasospasm Using Catheter Cerebral Angiography: A Systematic Review and Inter- and Intraobserver Study
  • Crossref (25)
  • Google Scholar

This article has been cited by the following articles in journals that are participating in Crossref Cited-by Linking.

  • Spontaneous subarachnoid haemorrhage
    Jan Claassen, Soojin Park
    The Lancet 2022 400 10355
  • Reliability of the Diagnosis of Cerebral Vasospasm Using Catheter Cerebral Angiography: A Systematic Review and Inter- and Intraobserver Study
    T.E. Darsaut, C. Derksen, B. Farzin, M.B. Keough, R. Fahed, W. Boisseau, L. Letourneau-Guillon, A.-C. Januel, A. Weill, D. Roy, T.N. Nguyen, S. Finitsis, J.-C. Gentric, D. Volders, A. Carlson, M.M. Chow, C. O’Kelly, J.L. Rempel, R.A. Ashforth, M. Chagnon, J. Zehr, J.M. Findlay, G. Gevry, J. Raymond
    American Journal of Neuroradiology 2021 42 3
  • Transcranial Doppler Velocities and Angiographic Vasospasm after SAH: A Diagnostic Accuracy Study
    T.E. Darsaut, M.B. Keough, A.M. Chan, B. Farzin, J.M. Findlay, M.M. Chow, M. Chagnon, J. Zehr, G. Gevry, J. Raymond
    American Journal of Neuroradiology 2022 43 1
  • Standardized Classification of Cerebral Vasospasm after Subarachnoid Hemorrhage by Digital Subtraction Angiography
    Helena Merkel, Dirk Lindner, Khaled Gaber, Svitlana Ziganshyna, Jennifer Jentzsch, Simone Mucha, Thilo Gerhards, Sabine Sari, Annika Stock, Felicitas Vothel, Lea Falter, Ulf Quäschling, Karl-Titus Hoffmann, Jürgen Meixensberger, Dirk Halama, Cindy Richter
    Journal of Clinical Medicine 2022 11 7
  • Vasospasm
    Jana Ivanidze, Pina C. Sanelli
    Neuroimaging Clinics of North America 2021 31 2
  • Angiographic vasospasm and delayed cerebral ischemia after subarachnoid hemorrhage: Moving from theoretical to practical research pertinent to neurosurgical care
    J. Raymond, L. Létourneau-Guillon, T.E. Darsaut
    Neurochirurgie 2022 68 4
  • Interleukin-6 in Cerebrospinal Fluid Small Extracellular Vesicles as a Potential Biomarker for Prognosis of Aneurysmal Subarachnoid Haemorrhage
    Yang Yao, Xinggen Fang, Jinlong Yuan, Feiyun Qin, Tao Yu, Dayong Xia, Zhenbao Li, Niansheng Lai
    Neuropsychiatric Disease and Treatment 2021 Volume 17
  • Modern Imaging of Aneurysmal Subarachnoid Hemorrhage
    Simon Levinson, Arjun V. Pendharkar, Andrew J. Gauden, Jeremy J. Heit
    Radiologic Clinics of North America 2023 61 3
  • CTA Supplemented by CTP Increases Interrater Reliability and Endovascular Treatment Use in Patients with Aneurysmal SAH
    Christian Heitkamp, Vincent Geest, Bogdana Tokareva, Laurens Winkelmeier, Tobias D. Faizy, Lukas Meyer, Anna A. Kyselyova, Hanno S. Meyer, Rabea Wentz, Jens Fiehler, Maxim Bester, Christian Thaler
    American Journal of Neuroradiology 2024 45 3
  • Imaging Predictors of Vasospasm and Delayed Cerebral Ischaemia After Subarachnoid Haemorrhage
    Isabel Fragata, Bruno Cunha, Patrícia Canhão
    Current Treatment Options in Neurology 2020 22 12

More in this TOC Section

Adult Brain

  • Diagnostic Neuroradiology of Monoclonal Antibodies
  • NCCT vs. MRI for Brain Atrophy in Acute Stroke
  • Clinical Outcomes After Chiari I Decompression
Show more Adult Brain

Neurointervention

  • Contour Neurovascular System: Five Year Follow Up
  • Effect of SARS-CoV2 on Endovascular Thrombectomy
  • Optimizing Voxel Size in 3D Rotational Angiography
Show more Neurointervention

Similar Articles

Advertisement

Indexed Content

  • Current Issue
  • Accepted Manuscripts
  • Article Preview
  • Past Issues
  • Editorials
  • Editor's Choice
  • Fellows' Journal Club
  • Letters to the Editor
  • Video Articles

Cases

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

More from AJNR

  • Trainee Corner
  • Imaging Protocols
  • MRI Safety Corner
  • Book Reviews

Multimedia

  • AJNR Podcasts
  • AJNR Scantastics

Resources

  • Turnaround Time
  • Submit a Manuscript
  • Submit a Video Article
  • Submit an eLetter to the Editor/Response
  • Manuscript Submission Guidelines
  • Statistical Tips
  • Fast Publishing of Accepted Manuscripts
  • Graphical Abstract Preparation
  • Imaging Protocol Submission
  • Evidence-Based Medicine Level Guide
  • Publishing Checklists
  • Author Policies
  • Become a Reviewer/Academy of Reviewers
  • News and Updates

About Us

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

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