Abstract
BACKGROUND AND PURPOSE: Patients with acute ischemic stroke in the anterior circulation are at risk for either primary or, following mechanical thrombectomy, secondary occlusion of the anterior cerebral artery. Because previous studies had only a limited informative value, we report our data concerning the frequency and location of distal anterior cerebral artery occlusions, recanalization rates, periprocedural complications, and clinical outcome.
MATERIALS AND METHODS: We performed a retrospective analysis of prospectively collected data of patients with acute ischemic stroke undergoing mechanical thrombectomy in the anterior circulation between June 2010 and April 2015.
RESULTS: Of 368 patients included in this analysis, we identified 30 (8.1%) with either primary (n = 17, 4.6%) or secondary (n = 13, 3.5%) embolic occlusion of the distal anterior cerebral artery. The recanalization rate after placement of a stent retriever was 88%. Periprocedural complications were rare and included vasospasms (n = 3, 10%) and dissection (n = 1, 3.3%). However, 16 (53.5%) patients sustained an (at least partial) infarction of the anterior cerebral artery territory. Ninety days after the ictus, clinical outcome according to the modified Rankin Scale score was the following: 0–2, n = 11 (36.6%); 3–4, n = 9 (30%); 5–6, n = 10 (33.3%).
CONCLUSIONS: Occlusions of the distal anterior cerebral artery affect approximately 8% of patients with acute ischemic stroke in the anterior circulation receiving mechanical thrombectomy. Despite a high recanalization rate and a low complication rate, subsequent (partial) infarction in the anterior cerebral artery territory occurs in approximately half of patients. Fortunately, clinical outcome appears not to be predominately unfavorable.
ABBREVIATIONS:
- ACA
- anterior cerebral artery
- MT
- mechanical thrombectomy
Mechanical thrombectomy (MT) is an effective treatment in acute ischemic stroke secondary to a large-vessel occlusion.1⇓⇓–4 Patients with acute ischemic stroke secondary to an occlusion of the internal carotid artery–T, middle cerebral artery trunk (M1), or MCA secondary division (M2) have relatively high rates of revascularization and favorable clinical outcomes after MT.5,6 Unfortunately, for patients with ICA-T occlusions and MCA occlusions, there is a risk of approximately 8.6%–11.4% for secondary emboli into the anterior cerebral artery (ACA), especially the distal branches such as the pericallosal artery, during MT.2,7,8 Although various technical possibilities, such as proximal flow control or combined aspiration, have been recommended to reduce the risk of secondary emboli9⇓⇓⇓–13, occlusions of the distal ACA occur.
Regardless of the cause of the occlusion (primary occlusion or secondary emboli during MT), cerebral infarctions in the ACA territory may cause relevant clinical deficits by affecting the primary or supplementary motor areas.14 In a previous, relatively small patient cohort (n = 6), treatment of secondary ACA occlusions was technically successful in 80% of the cases and uneventful in all instances.7
We present data on the frequency and location of distal ACA occlusions, recanalization rates, periprocedural complications, and clinical outcome.
Materials and Methods
Patient Selection
On the basis of a prospectively collected patient cohort with acute ischemic stroke undergoing MT in the anterior circulation at our institution between June 2010 and April 2015, we selected patients with a primary or secondary embolic occlusion of the distal ACA for this retrospective analysis. We excluded patients with an absent or severely hypoplastic ipsilateral A1 segment and those with proximal occlusions of the A1 segment from this analysis.
Stroke Therapy
Our institution provides neurologic, neuroradiologic, and neurointerventional services within a maximum-care university hospital center serving more than 500,000 individuals within its county limits and nearly 2.3 million within a greater metropolitan area. For each patient, a stroke neurologist performed physical neurologic examinations and detailed assessment of the NIHSS score in the emergency department on admission. Patients with suspected acute ischemic stroke received a standardized stroke imaging protocol: either MR imaging (including axial DWI, axial FLAIR, axial SWI, TOF-MRA, contrast-enhanced MRA of the aortic arch and cervical arteries, and axial PWI) or CT (including a non-contrast-enhanced CT, CT angiography, and perfusion CT) for assessment of their eligibility for intravenous rtPA and MT. The decision between MR imaging and CT was made individually on the basis of the patient's condition, known or unknown time of symptom onset, MR imaging eligibility, and immediate availability of the MR imaging and CT scanners.
Administration and dosing of intravenous rtPA followed national and international guidelines and an institutional standard operating procedure. Patients were considered eligible for MT by the treating neurointerventionalist if an occlusion of a major intracranial artery was detected by CTA or MRA, therapy could be accomplished within 8 hours of onset, the NIHSS score was ≥8 on evaluation, and the initial imaging excluded hemorrhage or a large infarct core of more than one-third of the middle cerebral artery territory or an ASPECTS of <6. In case of unknown onset of symptoms, patients were considered eligible for MT if stroke imaging ruled out a large infarct core and revealed a relevant, salvageable penumbra. No age limit was used as an inclusion or exclusion criterion for eligibility for MT, and the decision to perform MT was made individually on the basis of the patient's comorbidities, prestroke mRS, and the assumed choice of the patient. In case of fluctuating or progressive neurologic deficits, patients with minor symptoms (NIHSS score of <8) were treated as well.
Intraprocedural use of mechanical and/or pharmacologic treatments remained at the discretion of the treating neurointerventionalist. Microcatheters and stent retrievers used for MT in this patient cohort were subject to change due to technical development during the observation period. Between June 2010 and July 2013, general anesthesia, performed by experienced neurointensivists, was routinely administered during MT. Starting in August 2013, procedures were performed with the patient under conscious sedation as well. Independent of the performed management of sedation, patients received standardized peri-interventional management and monitoring of physiologic target values according to our in-house standard operating procedure at the discretion of the neurointensivist adapted to the patient and situation.
Postinterventional Management
All patients were observed in a neurologic intensive care unit after MT. The aim was transfer to the stroke unit as soon as possible, depending on the condition of the patient. Follow-up imaging (either CT or MR imaging) was routinely performed at 20–36 hours after treatment, or earlier if neurologic deterioration occurred. Postinterventional NIHSS and mRS were assessed by detailed physical examinations performed by an independent stroke neurologist at discharge. Follow-up data after 3 months were obtained by an in-patient visit or a telephone call by a neurologist not blinded to the type of treatment. The modified Rankin Scale was used to measure the severity of the disability.
Data Collection
Data collection included baseline demographics (age and sex) and medical history (eg, hypertension, coronary artery disease, congestive heart failure, atrial fibrillation, diabetes mellitus, hypercholesterolemia, history of smoking, and previous stroke) and symptom onset time and stroke severity as measured by the NIHSS. The time of initiation of stroke imaging and the time of start of angiography were captured automatically by the CT scanner and angiography system. The onset and duration of occlusion (secondary emboli) and time of recanalization were evaluated according to the timestamp of the referring angiographic image. Vessel diameter and location of the occlusion were assessed on angiographic images as well. The location of the occlusion was categorized following the segmentation of the ACA with regard to its anatomic position relative to the corpus callosum and the origin of the frontopolar artery, orbitofrontal artery, callosomarginal artery, and distal branches as characterized by Lehecka et al.15 Devices and medication used during the interventional procedures, number of thrombectomy maneuvers, and intraprocedural complications were evaluated according to the treatment protocols. Angiographic outcome by TICI and complications (eg, vessel perforation, dissection of the anterior cerebral artery) were assessed by a senior neurointerventionalist. The incidences of cerebral infarction, parenchymal hemorrhage (by criteria of the second European-Australasian Acute Stroke Study [ECASS II])16), or subarachnoid hemorrhage were assessed by using routinely performed follow-up imaging. Clinical outcome was evaluated according to the modified Rankin Scale.
Statistical Analysis
We compared data by using the χ2 test for categoric variables. P < .05 was considered significant in the final model. All statistical analyses were performed by using SPSS 21.0.0.0 (IBM, Armonk, New York).
Ethics Approval
The study was approved by our local ethics committee.
Results
Between June 2010 and April 2015, 388 patients underwent MT due to an acute ischemic stroke in the anterior circulation at our institution. Twenty of 388 (5.2%) patients were excluded because of an absent or severely hypoplastic ipsilateral A1 segment. Among the remaining 368 patients, we identified 30 (8.1%) with a distal ACA occlusion (for patient baseline characteristics, see Table 1). The distal ACA occlusion was, according to initial angiographic imaging, preexisting in 17/368 (4.6%) cases and occurred in 13/368 (3.5%) patients secondary to a recanalization maneuver (for distal ACA occlusion sites, see Table 2).
Mechanical thrombectomy with a stent retriever was intended for all patients, but a stent retriever could not be deployed in 5/30 (16.6%) because placement of a guidewire (n = 1, 3.3%; occlusion in the middle pericallosal artery [superior segment]), or placement of a microcatheter behind the thrombus was not possible (n = 4, 13.3%; occlusion in the middle pericallosal artery [inferior segment, n = 1], distal pericallosal artery [n = 2], and callosomarginal artery [n = 1]). In 2 of these cases (6.6%), intra-arterial rtPA (5 mg and 2 mg, respectively) was administered immediately at the occlusion via a microcatheter. In consideration of the time window and possible risks, there was no further treatment in the other 3 (10%) cases. Deployment of a stent retriever was achieved and MT was performed in 25/30 (83.3%) patients (for type and manufacturer of the devices used as well as the number of MT maneuvers performed, see Table 3).
Angiographic Outcome
Recanalization of the distal ACA occlusion (TICI 2b/3) was achieved in 22/30 (73.3%) patients. However, in each of these 22 patients, at least 1 stent-retrieval maneuver was performed. With regard to all patients in whom placement of a stent retriever was possible (n = 25), the accumulated recanalization rate (TICI 2b/3) was 88% (Fig 1). Recanalization after a single retrieval maneuver occurred in 17/30 (56.6%) cases with a distal ACA occlusion, and in 68% (17/25) of all patients in whom placement of a stent retriever was possible. None of the patients in whom a stent retriever could not be properly placed achieved TICI 2b/3 (5/30, 16.6%). In 3 cases in which stent retrievers were used (Aperio; Acandis, Pforzheim, Germany; Revive; Codman Neurovascular, Raynham, Massachusetts; and Solitaire FR; Covidien, Irvine, California, respectively), recanalization could not be achieved. With regard to the possible risk of vessel injury and/or rupture, no other devices were used, and no further recanalization maneuvers were performed in these patients.
Intraprocedural Complications and Frequency of Infarction and Hemorrhage in the ACA Territory
There were 3 cases of vasospasms in the distal ACA following a retrieval maneuver in the superior A3 segment (n = 2) and the callosomarginal artery (n = 1). In 2 cases, the vasospasms resolved completely after intra-arterial administration of nimodipine into the affected segment via a microcatheter. The third case of vasospasm was self-limiting within 5 minutes without further treatment.
A dissection of the distal ACA (A4/A5 segment) with minimal distal flow impairment occurred in 1 patient after thrombectomy. Considering the risk of further manipulation and the location of the dissected vessel, no further treatment was considered. According to the imaging data and treatment protocols, there was no vessel perforation with secondary hemorrhage. We did not observe secondary emboli from the ACA into a new vascular territory. Furthermore, no air emboli or device detachment was observed.
Follow-up imaging revealed partial or complete ACA infarction in 16/30 (53.3%) patients, 11 of whom had a primary and 5 of whom had a secondary occlusion. The frequency of infarction between both groups was, however, not significantly different in this small patient cohort (P = .153). There was only 1 case (3.3%) with hemorrhagic transformation in the ACA territory (superior frontal gyrus) with confluent petechiae within the infarcted area, but without space-occupying effect (HI2, according to ECASS II criteria). Four of 30 (13.3%) patients exhibited angiographically occult, self-limiting, minimal SAH in the ipsilateral Sylvian fissure detected on follow-up CT imaging. SAHs were estimated to be caused by recanalization maneuvers in the distal MCA (M2 segment) in these patients. None of the patients experienced SAH in the anterior cerebral artery territory.
Clinical Outcome
Ninety days after the ictus, clinical outcome according to the modified Rankin Scale score was the following: 0–2, n = 11 (36.6%); 3–4, n = 9 (30%); 5–6, n = 10 (33.3%).
Discussion
ACA emboli may occur before or during intra-arterial treatment of an ICA or MCA occlusion. The frequency of new emboli during IV, intra-arterial, or combined IV–intra-arterial treatment of a large-vessel occlusion in the anterior circulation has been reported to be between 1.7% and 15%.7,8,17 In our patient cohort, the rate of new distal ACA emboli secondary to a recanalization maneuver was lower (3.5%). Similar to secondary emboli, a relatively low frequency of primary distal ACA occlusions (4.6%) occurred. However, in combination, about 8% of all patients with a large-vessel occlusion of the anterior circulation receiving MT had a distal ACA occlusion, which is consistent with the results from the Multicenter Randomized Clinical Trial of Endovascular Treatment for Acute Ischemic Stroke in the Netherlands (MR CLEAN) trial.2 If one assumes that following the publication of recent study data on thrombectomy1⇓–3,18 the frequency of patients receiving MT will increase, distal ACA occlusions and the corresponding prevention and treatment options will become an even more relevant topic than they are today.
Because recanalization is a predictor of good clinical outcome,19 high recanalization rates should be achieved. Considering the risk of an infarction and possible neurologic deficits following an ACA occlusion14 and against the background of positive experience in the treatment of distal M2 occlusions,20 interventional neuroradiologists are urged to consider treatment of distal ACA occlusions to achieve high recanalization rates. In our patient cohort, the recanalization rate was 73.3% of all distal ACA occlusions, respectively, 88% after successful placement of a stent retriever. This is comparable with recanalization rates of M1 or M2 occlusions after MT.20⇓–22 In 4 (13.3%) patients, placement of a microcatheter behind the thrombus was not possible. However, these cases were in 2010 and early 2012 when only “large” microcatheters (Rebar-18 and Rebar-27; Covidien) were available at our site. With the introduction of smaller microcatheters and stent retrievers, successful retrieval maneuvers in small and/or tortuous distal intracranial vessels will probably be easier.23 For example, the outside diameter of the device-delivering microcatheter could be reduced by 29% by using a Headway 17 microcatheter (1.7F; MicroVention, Tustin, California) instead of a Rebar-18 microcatheter (2.4F). Thus, our department started using microcatheters with a 0.017-inch inner diameter in selected cases in the second quarter of 2012, when placement of our standard microcatheter (0.021-inch inner diameter) was not possible. So far, virtually every distal occlusion could be reached successfully.
The risk of periprocedural complications with MT in distal ACA occlusions does not seem be higher than that in the MCA. We experienced 1 case of dissection (3.3%) and 3 cases of vasospasm (10%) but no case of symptomatic intracranial hemorrhage into the ACA territory. In comparison, the frequency of dissection (1.8%–4.5%), vasospasm (3%–22.5%, including asymptomatic vasospasm), and symptomatic intracranial hemorrhage (5%–10.9%) was reported within the same range or even higher during endovascular treatment of MCA occlusions.21,24,25
Independent of the underlying cause of the occlusion, primary occlusion or thrombus fragmentation and secondary emboli as a by-product of recanalization maneuvers, occlusions of the ACA may cause infarction and significant neurologic deficits.14 Despite a high recanalization rate, ipsilateral infarction (at least partial) in the ACA territory occurred in 53.5% of our cases. This relatively high rate of ACA territory infarction might be secondary to insufficiency or absences of collaterals in the setting of concurrent or preceding ICA or MCA occlusion.26,27 With a frequency of 38.5% of ACA infarction in patients with secondary emboli, our data are comparable with those in previous studies, in which the frequency was reported to be 32% and 40%, respectively.7,8 Because primary occlusions are present longer than secondary occlusions before recanalization, the frequency of ACA infarction in patients with primary occlusions was higher (64.7%). However, our analysis did not reach statistical significance for this matter (P = .153). This finding should be viewed cautiously. A larger patient population might demonstrate a significant difference and, following the law of stroke (time is brain28), probably with a disadvantage for primary occlusions.
Compared with outcomes in recent clinical trials, clinical outcomes after 90 days were not predominately1⇓–3 unfavorable in this patient cohort. This outcome might be because of the following: a possible MCA and ACA territory infarction, due to a larger infarct volume and/or the involvement of the supplementary motor cortex.14,29
Limitations
This analysis has several limitations. First, because this article focusses on occlusions of the distal ACA, the overall occurrence of occlusions of the ACA (including the A1 segment) is likely to be higher. Under this premise, our data might underestimate the frequency of occlusions and infarctions in the ACA territory.
Second, allocation of clinical deficits to the ACA territory is, especially in patients with concurrent MCA infarction, not always possible. Therefore, comparison of clinical outcome of these patients with those of patients with isolated MCA territory infarction needs to be viewed cautiously.
Third, because occlusions were treated with different revascularization devices, a recommendation of a specific device for treatment of distal ACA occlusions is not possible and was not the aim of the study. In this patient cohort and in the large interventional stroke trials, the standard approach for treatment of an intracranial vessel occlusion was MT by using a stent retriever. However, MT in distal cerebrovascular occlusions appears to be feasible even with a direct-aspiration first-pass technique.30 The smaller diameter and pronounced kinking of a vessel should be taken into account when choosing catheters and devices to minimize alteration of the vessel wall.
Conclusions
Occlusions of the distal ACA affect approximately 8% of patients with acute ischemic stroke in the anterior circulation undergoing MT. Despite a high recanalization rate and a low complication rate, subsequent (partial) infarction in the ACA territory occurred in approximately half of patients. Fortunately, clinical outcome appears not to be predominately unfavorable.
Footnotes
Disclosures: Christian Herweh—UNRELATED: Travel/Accommodations/Meeting Expenses Unrelated to Activities Listed: Travel accommodations and registration for the Live Interventional Neuroradiology & Neurosurgery Course, 2015, paid by Covidien. Mirko Pham—UNRELATED: Grants/Grants Pending: M.P. is supported by a Memorial Stipend from Else Kröner-Fresenius-Stiftung*; Payment for Lectures (including service on Speakers Bureaus): M.P. received speaker honorarium from Penumbra Europe GmbH; Travel/Accommodations/Meeting Expenses Unrelated to Activities Listed: Travel expenses from Covidien. Peter A. Ringleb—UNRELATED: Consultancy: Advisory Boards for Boehringer Ingelheim, Daiichi Sankyo, and Covidien; Payment for Lectures (including service on Speakers Bureaus): Bayer, Daiichi Sankyo, Boehringer Ingelheim, Comments: Lectures; Travel/Accommodations/Meeting Expenses Unrelated to Activities Listed: Boehringer Ingelheim, Bayer, Comments: travel support. Martin Bendszus—UNRELATED: Board Membership: Data Safety Monitoring Board Vascular Dynamics; Consultancy: Roche, Guerbet; Grants/Grants Pending: Deutsche Forschungsgemeinschaft,* Hopp Foundation,* Novartis,* Codman,* Guerbet,* Siemens*; Payment for Lectures (including service on Speakers Bureaus): Guerbet, Novartis, Codman, Roche. Markus Möhlenbruch—UNRELATED: Board Membership: Codman Neurovascular; Consultancy: Acandis, MicroVention; Payment for Lectures (including service on Speakers Bureaus): Codman Neurovascular. *Money paid to the institution.
Mirko Pham, Christian Herweh, Simon Schieber, and Peter Arthur Ringleb contributed in data collection and reporting of this study. Johannes Pfaff, Martin Bendszus, and Markus Möhlenbruch had access to all data and supervised data collection and analysis, writing, and editing of article.
This work received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.
REFERENCES
- Received July 27, 2015.
- Accepted after revision August 29, 2015.
- © 2016 by American Journal of Neuroradiology