Treatment of the extracranial carotid artery in tandem lesions during endovascular treatment of acute ischemic stroke: a systematic review and meta-analysis
Introduction
In 20–30% of patients with acute ischemic stroke (AIS) caused by an intracranial large vessel occlusion (LVO) there is a concomitant high-grade stenosis or occlusion of the ipsilateral extracranial internal carotid artery (EICA). For decades, these tandem lesions (TL) had a poor prognosis due to a poor response on intravenous thrombolysis (IVT) alone, with a favorable outcome of only 30% and mortality rates up to 50% (1,2).
Recently, endovascular therapy (EVT), where the clot is mechanically extracted through endovascular access, has been proven effective and safe in patients with a LVO of the anterior circulation. EVT results in a higher recanalization rate and better functional outcomes than IVT alone and has been rapidly implemented in to national stroke guidelines and standard clinical care (3-5). For patients with a concomitant EICA lesion, EVT has also been shown to contribute to good functional outcome (6,7). In those patients with a significant EICA stenosis, a balloon angioplasty (BA) is performed in order gain access to the intracerebral vessels for thrombectomy. The BA does however not lead to a definitive treatment of the lesion as there is often a recoil or residual-stenosis of the EICA (8).
Current literature does not provide a clear answer on whether the EICA lesion should also be stented in the acute setting. Guidelines recommend carotid endarterectomy (CEA) within 2 weeks after the first event in order to prevent a second event, however this is based on trials comparing CEA and stenting in a different population of patients with a subacute TIA or non-disabling stroke (5,9-12). Acute patients may potentially benefit from early treatment as it further reduces the risk of recurrent stroke and the potential complication risks may be lower as endovascular access has already been obtained and the lesion has yet been passed with guidewires. The safety of immediate carotid artery stenting (iCAS) in the EVT group has not been fully elucidated. Since dual antiplatelet therapy (DAPT) is required after stenting, it may potentially lead to an increase in hemorrhagic complications in these patients with an acute stroke. Furthermore, it is unclear whether the EICA should be stented before or after recanalization of the occluded cerebral artery (13-17).
The aim of this review is to compare two treatment strategies, immediate CAS and BA, for tandem lesions during EVT and assess good functional outcome, efficacy and safety of external carotid artery treatment during EVT.
Methods
This systematic review was conducted in accordance to the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) statement and Cochrane guideline of systematic reviews of interventions (18,19).
Data sources
Databases of PubMed, Embase and Cochrane were searched till June 1st 2019 for eligible studies. Medical subject headings, terms and additional free entry terms for patient groups (patients with a tandem lesion, high-grade stenosis or occlusion, during acute ischemic stroke) and the treatment (BA, carotid artery stent) were used. The search strategy was formulated with the aid of a clinical librarian (Supplement file). The references of the selected papers were reviewed for the completion of the list of articles eligible for full text assessment.
Study selection
Two investigators (JH and ML) individually reviewed eligible titles and abstracts. Conflicts in inclusion were resolved through consensus. In case of disagreement a consensus was reached by consultation of a third reviewer (RB). Prespecified inclusion and exclusion criteria in our research protocol were used to select potentially eligible studies for full text analysis. Inclusion of a study followed if the study described the type of treatment of the EICA in TL during MT or delayed treatment after MT with separately reported outcomes. Prospective and retrospective observational studies, case series and randomized controlled trials were eligible for inclusion. Studies describing less than 10 patients were excluded from this review. The year of publication was no restriction on inclusion. Only full-text articles in English were included.
Data extraction and quality assessment
One investigator (JH) extracted necessary information from the eligible articles. The data extracted was checked by sampling (RB, ML). Discrepancies were resolved by discussion between the investigators. If any of the main variables were missing or not reported separately, they were reported as missing data.
Data on the year of publication and year of last inclusion, number of included patients and type of procedure were extracted. Patient, procedural and outcome characteristics were recorded for all included articles.
All studies were non-randomized trials. Therefore, the methodological quality of the included studies was evaluated by the ‘Methodological Index for Non-Randomized Studies’ (MINORS) (20). Quality was categorized as: very low (0 to 6), low (7 to 10), fair (10 to 14) and good (>14).
Outcome measures
The primary goal of this review and meta-analysis was to estimate the incidence of good functional outcome at 90 days by means of modified Rankin Scale (mRS) score ≤2 (21).
Secondary outcomes for this review were mortality at 90 days, defined as a mRS score of 6 or otherwise noted in the articles 90 days after intervention, symptomatic intracerebral hemorrhage (sICH) defined as any extravascular blood in the cranium or brain associated with neurological deterioration by means of NIHSS of ≥4 points (22), successful reperfusion, defined as TICI 2b or higher (23), (in-stent) re-stenosis or occlusion and cerebral hyperperfusion syndrome (CHS). We registered the preferable approach for recanalization (intracranial treatment versus extracranial treatment first respectively). One study defined sICH as any PH on following imaging (24) and one study only reported in-hospital mortality (25).
In addition, odds ratio’s (ORs) were calculated to evaluate the association between type of intervention and the outcomes of favorable neurological outcome, sICH and mortality.
Statistical analysis
A logit transformation was used to calculate an overall estimate from studies reporting single proportions. After back transformation, pooled incidences with their 95% confidence intervals (95% CIs) were reported and illustrated in forest plots. Odds ratios with their 95% CIs were calculated and displayed for the comparative studies. All analyses were carried out using a random effects model.
To quantify heterogeneity, the Q-statistic, the between-study variance [T2, and standard deviation (T)] and the ratio of true heterogeneity to total observed variation (I2) were computed. The between-study variance was estimated using the restricted maximum-likelihood estimator (REML). An I2 of >50% represented a large degree of inconsistency across the studies.
In addition to funnel plots, both the Egger’s test and Begg’s rank test were used to detect publication bias when the number of included studies was at least 20 (26). A P values of <0.05 were considered statistically significant. All statistical analyses were performed using R 3.6.1 software using the meta package (27,28).
Results
The search resulted in 391 records of which 319 were duplicates or irrelevant to the topic. After evaluation of the titles and abstracts, 72 articles were selected for full-text assessment. Twenty-one studies met our inclusion criteria for this literature review (7,14-17,24,25,29-42). Most frequent reason for exclusion (n=37) of an article was that data was not presented separately on outcome for the different treatment options or insufficiently reported. The review process is summarized in detail in Figure 1.
Fourteen of the 21 studies were retrospective cohort studies, six were comparative and one study was a prospective non-randomized observational study. The quality assessment of all 21 included studies is shown in Table 1. The methodological quality of the papers was low to fair. The MINORS score averaged 9.9 (9 to 11, SD 0.7) out of 16 for non-comparative studies and 16.8 (15 to 18, SD 1.1) out of 24 for comparative studies.
Full table
Study characteristics
The included studies enrolled a total of 1,758 patients (mean sample size, 84; range, 10–482). Of all included patients, 1,476 received iCAS (84%) during EVT and 149 underwent BA (8.4%). An extracranial first approach was favorable in 15 out of the 21 included studies. In total 7.6% was not treated during EVT. Because of the unclear method of how they were treated during EVT, we performed no further analysis within this subgroup.
Immediate carotid artery stent placement for extracranial lesions during EVT
Twenty-one of the 21 studies reported neurological outcome and safety for iCAS in patients undergoing EVT. Sixteen studies described only iCAS during EVT, of which only one study prospectively collected data. Table 1 shows the study characteristics in detail.
The pooled incidences are depicted in Figure 2. Good neurological outcome was seen in 53% (95% CI, 46–59%). The proportion of good neurological outcome varied largely across the studies (Q =116.52, d.f. =20, P<0.0001; T2=0.29; I2=82.8%). Mortality at 90 days was 16% (95% CI, 13–19%). Heterogeneity was low in these studies (Q =35.29, d.f. =20, P=0.02; T2=0.092; I2=43.3%). Mortality was mostly related to sICH (17,29,38,40) and pneumonia or sepsis (30,40). Age, duration of treatment and time to recanalization were independently associated for all-cause mortality (7). In addition, prior IVT and the severity of the stroke was also correlated to all-cause mortality (16).
The incidence of sICH was 8% (95% CI, 6–10%). No substantial heterogeneity was seen in the studies (Q =30.01, d.f. =20, P=0.07; T2=0.15; I2=33.4%). Successful cerebral reperfusion was reported in 19 studies and achieved in 79% (95% CI, 74–84%). There was a significant heterogeneity in this subgroup (Q =51.88, d.f. =18, P<0.0001; T2=0.25; I2=65.3%). In-stent occlusion or stenosis on follow up imaging was documented in ten studies with an absolute incidence of 7.6% (n=39). In total, 25 asymptomatic in-stent restenosis or occlusions, two symptomatic in-stent occlusions after 24–48 hours and 12 acute in-stent occlusions were reported (17,24,29,31,32,34,35,40-42). Only two studies reported on CHS, with an incidence of 2.4% (n=1) and 4.5% (n=1) (35,37).
Visual inspection of the funnel plots shown in Figure 3 indicate no presence of publication bias for favorable outcome, mortality and sICH. Using both the Egger’s test and Begg’s rank test, no statistically significant presence of publication bias was found (all P values >0.4). Due to missing data of two studies for successful reperfusion, there were not enough studies to perform a funnel plot for this outcome.
BA for extracranial lesions during EVT
Five of the 21 studies reported neurological outcome and safety for iCAS in patients undergoing EVT. All studies were retrospectively comparative studies for iCAS (14-16,31,41). In all studies, the choice for BA was made by the discretion of the treating physicians, taking the access for distal treatment of the intracranial lesion into consideration.
Figure 4 shows the pooled incidence of endpoints in the BA group. Favorable outcome was seen in 46% (95% CI, 36–55%). No substantial heterogeneity was seen in the studies (Q =4.89, d.f. =4, P=0.30; T2=0.04; I2=18.2%). Overall mortality at 90 days was 14.7%. Mortality at 90 days was equal to the iCAS group with 16% (95% CI, 10–23%). No significant heterogeneity was found (Q =3.71, d.f. = 4, P=0.45; T2<0.0001; I2=0.0%). Three cases of sICH, 4% (95% CI, 1–9%), were reported. No substantial heterogeneity was seen in the studies (Q =2.35, d.f. =4, P=0.67; T2=0.0; I2=0.0%). Reperfusion was only reported in four articles, with a successful reperfusion rate of 71% (95% CI, 37–91%) (15,31,36,41). Heterogeneity was low in these studies (Q =9.82, d.f. =2, P=0.01, T2=1.22; I2=79.6%). Asymptomatic post procedural EICA re-occlusion was described in 8% (n=8) on ultrasound (15,31,41). Nor acute nor symptomatic occlusions were reported. Of the two studies who reported CHS, no CHS occurred in the BA group.
iCAS versus BA alone during EVT
Five studies compared the iCAS to BA alone. All studies were nonrandomized observational studies. In the five included comparative studies for iCAS or BA, iCAS during EVT was associated with better functional outcome at 90 days than BA only (OR 1.99, 95% CI: 1.35–2.93%). Heterogeneity was low in these studies (Q =2.5, d.f. =4, P=0.64; T2=0.00; I2=0.0%). No association was found between iCAS and BA related to 90-day mortality (OR 1.27, 95% CI: 0.73–2.19) and sICH (OR 0.48, 95% CI: 0.16–1.45) (Figure 5A,B,C). There was no significant heterogeneity in these subgroups (Q =3.26, d.f. =4, P=0.52; T2=0.0; I2=0.0% and Q =2.00, d.f. =4, P=0.74; T2=0.0; I2=0.0% for mortality and sICH respectively). These findings follow the trend of the separately performed pooled incidence analysis.
Extracranial treatment versus intracranial treatment first
In most studies approach considerations of the TL was reported, favoring extracranial approach first. Successful reperfusion in this group was seen in 84.7% with a 90-day good functional outcome of 47.2%. sICH was reported in 4.5% and 90-day mortality of 18.1% (7,17,24,30,32-34,37,38,42).
In case of intracranial treatment first, successful reperfusion was seen in 80.3% and 90-day good functional outcome of 51.8% with 17.8% mortality rate and an incidence of 12.5% for sICH (15,32).
Only three studies reported outcomes of intracranial treatment first of which two discuss their motive for intracranial treatment first in more detail. Lockau et al. (32) found that the mean times from first puncture of the groin till reperfusion of intracranial occlusion and overall perfusion, including the ipsilateral EICA, were significantly shorter when the intracranial thrombectomy was performed prior to iCAS (43.1±30.8 vs. 110.8±43.0 min, P<0.001, 58.6± 26.1 vs. 130.2±45.1 min, P<0.01 intracranial treatment vs. extracranial treatment first respectively).
Another study (34) also compared both approaches. However, there was no significant difference in time from groin puncture till reperfusion [110 minutes (range, 15–208 minutes) vs. 125 minutes (range, 45–212 minutes), P=0.42, intracranial treatment vs. extracranial treatment first respectively]. The authors also referred to an incidental finding with a potential benefit for extracranial approach first of spontaneous distal, e.g., intracranial, thrombus dissolution in 24% (n=4/17), without seeing this observation in the intracranial approach first.
Discussion
This systematic review and meta-analysis evaluate the safety and efficacy of treatment of EICA lesion in combination with an intracranial lesion during EVT by means of iCAS or BA. The current evaluation shows that despite the fact of having a tandem lesion, iCAS during EVT was associated with a good 90-day functional outcome, without significant differences in mortality or bleeding complications in comparison to BA alone.
In 2016, the HERMES collective published the first meta-analysis on EVT for LVO. This study was focused on the intracranial LVO and confirmed the efficacy of EVT in this subgroup with a favorable functional outcome in 46.0% (3). The current review shows a comparable or better functional outcome at 90 days for EICA lesions treated with iCAS with similar incidence of mortality, with a slightly higher incidence of sICH.
Bleeding complications like sICH due to DAPT are feared after treatment with stents in the acute phase, mainly because of the associated high morbidity and mortality afterwards. A few of the included studies showed a high incidence of sICH. A possible explanation for these high rates is the use of a strict and alternate high dosed antiplatelet regime. In up to 31% of a treated subgroup with Glycoprotein IIb/IIIA inhibitors (Abciximab, Eptifibatide respectively), sICH was reported (29,38). Treatment protocols of both studies were changed after these findings. Unfortunately, literature is ambiguous about the impact and effects of DAPT during CAS, nor is there consensus on a standardized antiplatelet regime for (immediate) CAS. As an example, none of the included studies in this review have applied the same antiplatelet protocol with a high heterogeneity among the studies. A meta-analysis in 2016 evaluated the evidence for DAPT after elective endovascular arterial procedures, with primary endpoint restenosis and stent thrombosis, with secondary endpoint bleeding complications (43). Most studies involved coronary literature, two studies involved CAS. They found no significant evidence for superiority for DAPT over monotherapy for neither restenosis nor for stent thrombosis. The two included carotid studies (44,45) both stopped prematurely because of the large differences in outcome between monotherapy and DAPT, in favor of DAPT with less neurological complications (stroke, transient ischemic attacks or intracerebral bleedings). However, none of latter studies looked at functional outcome nor mortality.
Despite most studies did not report CHS, hyperperfusion after CAS is an infamous complication. Huibers et al. (46) investigated in their meta-analysis if CHS in clinically relevant in relation to procedural stroke rate following elective CAS. A pooled estimate for CHS of 3.5% was found, not associated with the type of anesthesia. Approximately 8% of CHS occurred after hospital discharge. However, the authors expect an underreporting due to a majority of the studies only report in hospital outcomes.
Little is known about the long-term outcomes for TL treated with EVT. Ten included studies reported on acute stent occlusions and in-stent stenosis during follow up. Only one study documented the need for delayed treatment in both groups (15). In 22 cases of BA, delayed carotid revascularization was required by form of delayed iCAS (n=1) or carotid endarterectomy (CEA) (n=7). No additional treatment after iCAS were reported in this cohort.
Long-term results of the EVA-3S, CREST and ICSS suggest a benefit-risk balance in favor of CEA over CAS on short term results after treatment. This difference is mainly driven by a lower risk of AIS during the intervention. Both techniques were associated with similar long-term risks of recurrent mainly non-disabling stroke, myocardial infarction and death up to 10 years after intervention (10-12). In case of EVT in the presence of a tandem lesion, a larger chance on disrupting the plaque and creating micro-emboli stroke due to passing of the carotid lesion is inherent to the executed EVT. Earlier drawn conclusions may therefore not be applicable for patient with TL undergoing EVT. However, insufficient data is available to make any statements on long-term results in this specific population.
Several included studies described predictors for good functional outcome. A TICI score of 3 and early neurological improvement are factors for a favorable outcome at 90 days (35). Other predictors of good functional outcome months are age (7,15,16,34,41), low NIHSS score at baseline (14,16) and procedure time to recanalization (7,15,41). An additional hour between arrival at the emergency department and puncture of the femoral artery was associated with a 22% reduction of TICI 2b/3 reperfusion (47). In addition, in procedures ranging from 20 to 60 min the functional outcome was good in 79% of patients (41). In procedures lasting more than 60min, only 50% of the patients had a mRS 0–2 at long-term follow-up. According to the adagium “time is brain”, a fast passage of the EICA and intracranial recanalization may further improve functional outcomes. It is possible to conclude that an intracranial first approach may be beneficial (48).
This review holds some inherent limitations. Firstly, the quality of this systematic review and meta-analysis is directly related to the quality of the predominantly uncontrolled studies included. All but one study were retrospective series and therefore subjected to a marked risk of selection bias. Most studies did not meet an adequate score on the MINORS tool. None of the studies prospectively randomized their study size nor was there mention of an unbiased assessment of the study endpoints. Secondly, there is a considerable heterogeneity among the studies due to different treatment plans, different primary outcomes and different antiplatelet regimes. As already discussed earlier on, the difference in antiplatelet regime may affect the neurological outcomes and complication rates. Thirdly, most studies depicted poorly the type of lesions found during EVT in the ipsilateral EICA. These different presentations may require different approaches with possible effect on outcome. Fourthly, only ten studies noted the presence of potential in-stent stenosis and re-occlusions of the EICA after treatment. It is not sufficiently clear what the implications are on 90-day good functional outcome nor mortality nor the long-term outcome with BA of iCAS. Lastly, hemorrhagic complications were reported variously in the included studies. Several studies also reported parenchymal hemorrhages (subdivided or as one), asymptomatic ICH or even by any hemorrhage. Due to the lacking synchronicity of definitions, it is possible that an underestimation of relevant bleeding complications is represented in this review.
Conclusions
In conclusion, this systematic review shows that treatment with iCAS of a simultaneously ipsilateral EICA lesion during EVT is associated with a favorable functional outcome at 90 days compared to BA only with no significant increase in mortality or sICH. No conclusion could be drawn about the intracranial or extracranial first approach due to scarce of data. More studies are needed to determine long-term neurological outcomes, the necessity of re-interventions and optimal technical approach (intracranial or extracranial first). Prospective randomized control trials are mandatory, as selection or publication bias, may have influenced the results.
Supplementary
Search strategies
PubMed
("Stroke"[Mesh] OR stroke[tiab] OR CVA[tiab] OR cerebrovascular accident*[tiab]) AND ("Thrombolytic Therapy"[Mesh] OR "Mechanical Thrombolysis"[Mesh] OR "Infusions, Intra-Arterial"[Mesh] OR "Endovascular Procedures"[Mesh:NoExp] OR intraarterial[tiab] OR intra-arterial[tiab] OR thromboly*[tiab]) AND ("Carotid Arteries"[Mesh] OR "Carotid Stenosis"[Mesh] OR caroti*[tiab] OR extracranial occlus*[tiab]) AND tandem*[tiab]
Embase
('cerebrovascular accident'/exp OR (stroke OR CVA OR ‘cerebrovascular accident*’):ab,ti) AND ('fibrinolytic therapy'/exp OR 'mechanical thrombectomy'/exp OR 'intraarterial drug administration'/de OR 'intracarotid drug administration'/exp OR 'endovascular surgery'/de OR (intraarterial OR ‘intra-arterial’ OR thromboly* OR ‘acute ischemic stroke’ OR ‘acute ischaemic stroke’ OR (acute AND (‘ischemic stroke’ OR ‘ischaemic stroke’))):ab,ti) AND ('carotid artery'/de OR 'carotid artery bifurcation'/exp OR 'common carotid artery'/exp OR 'external carotid artery'/exp OR 'internal carotid artery'/exp OR 'carotid artery obstruction'/exp OR caroti*:ab,ti) NOT (('animal'/exp OR 'nonhuman'/exp) NOT 'human'/exp) NOT 'conference abstract'/it AND tandem
Cochrane
(stroke OR CVA OR cerebrovascular accident*) AND (intraarterial OR “intra-arterial” OR thromboly* OR thrombectom* OR (acute AND (“ischemic stroke” OR “ischaemic stroke”)) OR “fibrinolytic therapy” OR intracaroti* OR endovascular*) AND (caroti*) AND tandem*
Acknowledgments
Funding: None.
Footnote
Provenance and Peer Review: This article was commissioned by the Guest Editor (Dr. Kosmas I. Paraskevas) for the series “Carotid Artery Stenosis and Stroke: Prevention and Treatment Part I” published in Annals of Translational Medicine. The article was sent for external peer review organized by the Guest Editor and the editorial office.
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/atm-2020-cass-17). The series “Carotid Artery Stenosis and Stroke: Prevention and Treatment Part I” was commissioned by the editorial office without any funding or sponsorship. The authors have no other conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
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