Brain arteriovenous malformations (AVM) are connections between cerebral arteries and veins by way of an interposing nidus. AVMs may become symptomatic by hemorrhage, seizure, headache, or cause focal neurological deficits without evidence of hemorrhage. Treatment modalities for AVMs are aimed at their angiographic eradication. This is accomplished by sole implementation or a combination of microsurgery, radiation therapy, and embolization [24].

Embolization involves endovascular administration of materials into feeding arteries, the nidus, and/or draining veins. The embolic material of choice has evolved from polyvinyl alcohol particles to cyanoacrylate liquid embolic agents including n-butyl cyanoacrylate (n-BCA), (Trufill, Johnson and Johnson, New Brunswick, NJ, USA) to ethylene vinyl alcohol copolymer liquid embolic (Onyx, Medtronic, Minneapolis, MN, USA) [16,18]. The goal of embolization can be categorized as curative, adjuvant (pre-surgical, pre-radiosurgery), targeted (e.g. occluding a ruptured perinidal aneurysm), or palliative (e.g. reducing flow in patients with cerebral ischemia due to vascular steal).

Metrics for successful embolization vary based on the initial goal of embolization [22]. For curative treatment, the metric is permanent angiographic eradication of the lesion. For adjuvant and palliative treatment, the most accepted metric is a percentage reduction of AVM volume [25]. Contrarily, a successful targeted embolization may only occlude a perinidal aneurysm or ruptured portion of the nidus with less focus on reducing the volume of the nidus [2].

Due to the rarity of AVMs, heterogeneity in endovascular technique, and rapid evolution of endovascular technology, consistent practices regarding AVM embolization have been hard to define [4,6,11,13,22,25,26]. Retrospective analysis of AVM embolization results remains invaluable to our development of safe and effective embolization practices. In this study, we retrospectively evaluate the AVM embolization experience at a single center over 18 years with specific focus on the goals of intervention, embolic agent used (n-BCA vs Onyx), and AVM volume reduction.

The Loyola Health electronic health records were accessed to obtain adult patients who were diagnosed with brain AVMs from the date imaging was still available within our electronic medical records (2002-2019). Loyola University Medical Center electronic medical record was queried for ICD-9 (747.81) and ICD-10 (Q28.2 and Q28.3) codes corresponding to vascular malformations and CPT codes for AVM treatment (61680, 61682, 61684, 61686, 61690, and 61692). Individual patient charts were then reviewed to confirm an AVM diagnosis by angiographic or pathologic criteria. Patients with insufficient information in their medical record regarding their AVM diagnosis were excluded. Only patients who received an embolization treatment with reviewable angiograms were selected. Interventions were provided by 1 interventional neurologists, 3 interventional neuroradiologists, and 4 endovascular neurosurgeons over this time period. Over the 18-year period from 2002-2019, 92 AVMs were treated by surgery, radiosurgery, embolization, or a combination of these modalities at our institution. In this cohort, 30 AVM patients were treated with embolization as either a primary or adjunctive method and were included in the study.

Variables extracted from the medical record included patient demographics of age at diagnosis, sex, and race. Presentations were recorded as hemorrhage, headache, seizure, incidental, and other (including focal neurological deficit without hemorrhage). AVM characteristics included nidus appearance (diffuse versus compact), eloquence, deep venous drainage, size, location (cerebellar, deep cerebral, frontal, temporal, and parieto-occipital), nidal volume, AVM rupture status, eloquence, and Spetzler-Martin grade. Embolization variables including embolic agent, number of sessions, numbers of arterial pedicles treated, relative volume of AVM embolized ([pre-embolization AVM volume - post-embolization AVM volume]/[pre-embolization AVM volume]), embolization 30-day complication outcomes, and status of cure were collected through a comprehensive chart review [3]. The volume of the AVM was calculated with (A+B+C)/2 methodology. The height and width of the AVM was taken from the anteroposterior (AP) angiogram and the depth was measured from the orthogonal lateral angiogram on the baseline and post-treatment studies [8,15,19,21]. Successful embolization was defined as ≥50% devascularization after the final embolization [16]. Complications were categorized into three groups of minor (transient or non-disabling fixed deficit), major (disabling non-fatal), and death. AVMs embolized for cure were only defined as cured if a delayed (>6 months) angiogram confirmed angiographic eradication [14].

The intention of treatment was categorized based on retrospective review on the interventionalists’ clinical and procedural notes into 5 categories: curative, palliative, pre-radiotherapy, pre-surgical, or targeted. The latter 4 categories were then combined to make a non-curative embolization cohort. Embolization outcomes based on intention of treatment was evaluated.

Over an 18-year period, 30 AVMs were embolized at our institution. Patient and AVM characteristics are listed in Table 1. The average age at diagnosis was 36±16 years, and 17 patients (57%) were male. Fifteen (50%) of the AVMs were Spetzler Martin (SM) Grade 1-2, 9 (30%) were SM Grade 3, and 6 (20%) were SM Grade 4-5. The AVM locations was cerebellar (10%), frontal (43%), temporal (10%), and parieto-occipital (30%). AVMs presented with hemorrhage, seizure, headache, neurological deficit without hemorrhage, and other in 6 (20%), 6 (20%), 12 (40%), 2 (6.7%), and 4 (17%) cases, respectively.

These 30 patients underwent 47 embolization sessions (median 1, interquartile range (IQR) 1-2 sessions per patient) and had 87 pedicles embolized (median 2 IQR 1-2.3 pedicles per session and median 2 IQR 2-3 pedicles embolized per patient). The embolic agent used was n-BCA in 12 (40%) patients and 42 (48%) of the pedicles treated and Onyx in 18 (60%) patients and 45 (52%) of the pedicles treated. There were no complications associated with AVMs embolized with Onyx, and one minor complication (quadrantanopia) and one major complication (anterior choroidal artery stroke) were associated with the AVMs embolized with n-BCA. The overall complications rate was 6.7% per AVM, 4.3% per session, and 2.3% pedicle. Ultimately, 8 patients (27%) only had embolization, 12 patients (40%) had surgery in addition to embolization, 9 patients (30%) had radiosurgery in addition to embolization, and 1 patient (3%) had all three modalities of treatment (Table 1). Clinical follow-up for these patients was 39 months±42 months. Angiographic follow-up for these patients was 19 months±26 months.

The median size of the AVMs treated with n-BCA was 3.5 mL (IQR 1.1-9.9 mL) compared to 4.4 mL (IQR 1.9-11 mL) in those that were embolized with Onyx. The median total percent volume reduction (percent devascularization) in the AVMs that were embolized with n-BCA was 52% (IQR 31-67%) compared to 51% (IQR 27-86%) in those that were embolized with Onyx (Table 2). Successful embolization (≥50% devascularization) occurred in 58% of n-BCA embolized versus 56% of Onyx embolized AVMs (Fig. 1). After the initial embolization, n-BCA AVMs had a median percent devascularization of 30% (IQR 0-52) compared to 43% (IQR 15-86) in the Onyx AVMs. The total number of pedicles embolized in the first embolization was 1.8 per patient in n-BCA AVMs compared to 2.2 per patient in the Onyx AVMs. Six (50%) of n-BCA embolized AVMs underwent more than one embolization session compared to 4 (22%) of the Onyx AVMs (Table 2).

The total number of sessions per person was 1.8±1.0 in n-BCA and 1.4±0.8 in Onyx. The total number of pedicles per session was 2.1±0.9 in n-BCA and 1.9±1.1 in Onyx. The percent devascularization per pedicle was 16% ±14 in n-BCA and 34% ±29 in Onyx with a p-value of 0.032 (Fig. 2). Additionally, the correlation of percent devascularization with initial AVM volume and number of pedicles are presented in Fig. 3 and 4 respectively. Lastly, the percent devascularization based on the objective of embolization was 61% ±34 in cure attempt, 79% in palliative, 54% ±36 in targeted, 47% ±29 in pre-surgery, and 48% ±19 in pre-radiosurgery (Table 2). This further summarizes into 61% ±34 in the cure attempt group versus 50% ±28 in the non-curative group.

This single center retrospective analysis of AVM embolization demonstrates similar final nidal reduction results whether using n-BCA or Onyx liquid embolic agents. However, more pedicles and more sessions were required to achieve similar embolization results with n-BCA. Additionally, it does appear that even though achieving the benchmark embolization result of 50% is the same for both groups, achieving a >75% embolization result may slightly favor Onyx. Most importantly, with the caveat of including patients over a 18-year period amongst 8 interventionalists, the use of both agents appears relatively safe and effective.

Trans-arterial embolization of AVMs warrants continued study given the high complications seen in the ARUBA (a randomised trial of unruptured brain arteriovenous malformations) trial amongst AVMs receiving embolization. Of the 3 arms of intervention (microsurgery, stereotactic radiotherapy, and embolization), embolization was used the most commonly (62% of cases) and had the highest occurrence of a primary event (50% of cases) [17]. During the ARUBA enrollment years, 2007-2013, all practitioners would have had substantial experience with n-BCA and/or Onyx. Little granular data is available from the trial about the embolizations, but overall, the results were disparaging and suggests the field needs improvement.

Continued analysis of AVM embolization experience is needed to identify risk factors for complications and improved embolization results. In this small retrospective series, Onyx and n-BCA achieved similar occlusion results although n-BCA required more session and pedicles embolized to do so. Both agents had low complications which may be related to less aggressive embolization strategies.