Background and objective To date, there have been few published studies examining the relationship between arteriovenous malformation (AVM) angioarchitecture and hemorrhagic presentation among children with cerebral AVMs. This study examines this relationship in this unique population, in whom symptomatic presentation of cerebral AVM is the norm rather than the exception.
Methods A cohort of children with AVMs from 2000 to 2011 were included. Predictors studied included patient age, gender and angioarchitectural features, including AVM location, nidus size and morphology, venous drainage, presence of venous outflow lesions and associated aneurysms. Predictors of hemorrhagic presentation were assessed using multivariate logistic regression.
Results 135 children (70 males, mean age 10.1 years) were included. 86/135 (63.7%) children presented with hemorrhage, 18 (13.3%) with seizures, 17 (12.6%) with headaches or neurological deficits and 14 (10.4%) were asymptomatic. AVM location, morphology and the presence of associated aneurysm, venous ectasia, draining vein stenosis and single draining vein were not significantly associated factors. After multivariate analysis, AVM size (OR 0.57, 95% CI 0.43 to 0.77; p<0.01), exclusive deep venous drainage (OR 4.94, 95% CI 1.30 to 18.8; p=0.02) and infratentorial location (OR 9.94, 95% CI 1.71 to 51.76; p=0.01) were independently associated with hemorrhagic presentation.
Conclusion Smaller AVM size, exclusive deep venous drainage and infratentorial location are specific angioarchitectural factors independently associated with initial hemorrhagic presentation in children with AVMs.
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Management of cerebral arteriovenous malformations (AVMs) in children requires careful consideration of treatment related risks weighed against the natural history of the lesion, including the risk of intracranial hemorrhage. While the past few decades have brought remarkable improvements in neuroimaging and the therapeutic armamentarium with which we approach these lesions, few advances have been made in our understanding of the natural history and clinical behavior of pediatric AVMs.
Studies in adults have identified specific angioarchitectural features of AVMs that are associated with hemorrhagic presentation and future hemorrhage. Small size, deep location, deep venous drainage, single draining vein, intranidal aneurysms and associated venous abnormalities such as ectasia and stenosis have all been implicated as morphological risk factors of hemorrhage.1–11 Similar studies in children are lacking and treatment decision making is therefore often extrapolated from adult data.
This study aims to associate the presence of specific angioarchitectural features with hemorrhagic presentation among a cohort of children with AVMs managed at two pediatric neurosurgery referral centers.
We retrospectively reviewed the demographic, clinical and radiological characteristics of all patients (≤19 years of age) with an AVM who were referred to us between January 2000 and March 2011. Only patients who underwent cerebral angiography and cross sectional imaging prior to AVM directed treatment were included. All patients with spinal AVMs, vein of Galen aneurysmal malformations, dural arteriovenous fistulae or single hole pial arteriovenous fistulae were excluded from the study. Research ethics boards at both institutions approved the protocol for this study.
Patient age at presentation, gender, past medical history and clinical presentation were recorded. Angioarchitectural features were analyzed using the methodology established by the Joint Writing Group of the Technology Assessment Committee, 2001.12 AVM characteristics, including location, diameter and venous drainage, were recorded and graded using the Spetzler–Martin grading scale.13 AVM size was classified as: small (<3 cm), medium (3–6 cm) and large (>6 cm) for the purpose of descriptive statistics but was analyzed as a continuous variable for the purpose of univariate and multivariate analysis. AVM location, based on nidus location, was classified in two different ways: deep (located in the basal ganglia, thalamus, brainstem or corpus callosum) versus superficial (all other locations) and supratentorial versus infratentorial. AVM nidus morphology was subjectively classified as compact (presence of little or no intervening brain within the AVM nidus), diffuse (presence of significant intervening brain within the AVM nidus) or fistulous (predominant AV shunting with little intervening nidus). Venous drainage was classified as superficial, deep or both, and lesions were evaluated for the presence of single or multiple draining veins. Venous pouches were defined as focal aneurysmal dilatations of the proximal draining vein. Venous ectasia was defined as a greater than twofold increase in a segment of the draining vein along its course from the nidus to its venous collector. Venous stenosis was defined in two ways: angiographic venous stenosis (defined as >50% narrowing of the draining vein or venous system) and functional venous stenosis (defined as the persistence of contrast within the AVM nidus and draining vein at the time of visualization of the normal cortical or cerebellar venous drainage). Venous sinus abnormalities that contributed to venous outflow obstruction (ie, sinus thrombosis) were also characterized. Associated aneurysms were described based on their relationship to the AVM nidus (prenidal, intranidal or remote).
Descriptive statistics were used to characterize the study population. The Student's t test was used to compare means between groups, and Pearson's χ2 and Fisher's exact tests were used for comparisons of categorical variables where appropriate. Univariate logistic regression analysis was used to identify potential independent predictors of hemorrhagic presentation. Variables previously examined in the adult literature were initially chosen for an exploratory univariate analysis of potential features associated with hemorrhagic presentation in children. The Harrell method14 was subsequently used to build a multivariate logistic regression model. Statistical significance was set at p<0.05. All statistics were performed using SAS V.9.2 for Windows.
The study included 135 children (70 males and 65 females): 89 (66%) from the Hospital for Sick Children, Toronto, and 46 (34%) from the Children's Hospital Boston. Twenty-one children were excluded from the study based on incomplete neuroimaging or previous AVM directed therapy. Mean age at presentation was 10.1 years (range 0–19 years). There was no significant difference in the mean age of those presenting with and without hemorrhage (10.3 vs 9.7 years; p=0.42). Eighty-six of 135 (63.7%) children presented with hemorrhage, 18 (13.3%) with seizures, 17 (12.6%) with headaches or neurological deficits and 14 (10.4%) were asymptomatic. Seven (5.2%) patients had a documented diagnosis of hereditary hemorrhagic telangiectasia but none presented with hemorrhage. The frequency of hemorrhage among those patients with specific angioarchitectural features is summarized in table 1. One patient demonstrated AVM venous drainage into a thrombosed venous sinus.
Factors not significantly associated with hemorrhagic presentation included patient age, gender, AVM location, morphology and the presence of venous ectasia or pouch, associated aneurysm, angiographic and functional venous stenosis, and single draining vein. Univariate analysis revealed four features to be significantly associated with initial hemorrhagic presentation: smaller AVM size, exclusive deep venous drainage, infratentorial location and venous obstruction (the composite presence of any of venous ectasia, functional venous stenosis, single draining vein and draining venous sinus thrombosis). Only smaller AVM size, exclusive deep venous drainage and infratentorial location were independently associated with hemorrhagic presentation in multivariate analysis (table 2).
Studies aimed at identifying angioarchitectural features associated with hemorrhagic presentation and with risk of future hemorrhage in patients with AVMs have been largely limited to single institution studies involving predominantly adult patients. As a result, little is known about such relationships in children with AVMs. To date, only one published abstract has addressed this issue in an exclusive pediatric cohort. Kellner et al 15 studied the morphology of AVMs in 77 children referred to Columbia University Medical Center (CUMC), 62% of whom presented with hemorrhage. Small AVM size, eloquent location and deep venous drainage were independently associated with AVM hemorrhage.
To fully characterize this relationship, we evaluated the clinical and angioarchitectural features in a combined exclusively pediatric cohort with AVMs referred to two high volume pediatric neurosurgery centers over the past 11 years. Our multivariate analysis yielded smaller AVM size, exclusive deep venous drainage and infratentorial location as being independently associated with initial hemorrhagic presentation.
Smaller AVM size
Several adult studies have identified small AVM size (≤3 cm) as a risk factor for hemorrhage. Guidetti and Delitala,16 Itoyama et al,17 Graf et al 18 and Crawford et al 19 all observed a higher rate of hemorrhagic presentation among smaller versus larger AVMs. Although the pathophysiological mechanisms underlying this association remain unclear, some authors have postulated a relationship between AVM size and feeding artery pressures. Spetzler et al 20 found a higher rate of hemorrhagic presentation among smaller AVMs and noted that smaller AVMs were associated with higher feeding artery pressures at the time of surgical management as well as larger hematoma sizes. Despite the high rates of hemorrhagic presentation observed among small AVMs, several prospective studies have failed to find an association between AVM size and future hemorrhage.2 ,3 ,7 ,9
In the present study, we found a higher rate of hemorrhagic presentation among small AVMs (72.7%) compared with medium sized (48.8%) and large AVMs (25%), and smaller AVM size was independently associated on multivariate analysis. These results corroborate those of the CUMC study and suggest that smaller AVM size is a potentially important risk factor for hemorrhagic presentation in children with AVMs.
Deep venous drainage
The presence of deep venous drainage is among the most consistently reported features associated with hemorrhage in adult AVMs. Marks et al 6 found hemorrhagic presentation more frequently in patients with central venous drainage (94%) over cortical (37%) or mixed drainage (50%). Miyasaka et al 21 found a similar relationship, with 94% of AVMs with exclusive deep drainage presenting with hemorrhage. Because deep seated AVMs are more likely to have a component of deep venous drainage, previous studies have pointed out that the relationship between deep venous drainage and hemorrhage may be influenced by AVM location. Although one study identified deep location and not deep venous drainage as a significant factor at presentation,10 others have identified both deep drainage4 ,22 and exclusive deep drainage23 as independent predictors of hemorrhagic presentation. Prospective studies have also identified deep venous drainage2 ,7 and exclusive deep venous drainage9 as important risk factors for future AVM hemorrhage.
In this study, hemorrhagic presentation was observed in 87% of children with exclusive deep venous drainage, 56.7% with superficial and deep venous drainage, and 59.8% with superficial drainage alone. Moreover, exclusive deep venous drainage was independently associated with hemorrhagic presentation. We did not observe a relationship between deep location and hemorrhagic presentation in this study. Therefore, these findings, and those of the CUMC study, suggest that deep venous drainage is an important independent risk factor of hemorrhage in pediatric AVMs.
The role of location in AVM hemorrhage is unclear. Although comprising only 7–15% of intracranial AVMs, hemorrhage rates of infratentorial AVMs among adult surgical series range from 72% to 92%,24 and studies have identified infratentorial location as independently associated with both initial5 and future3 AVM hemorrhage. This high hemorrhage rate has been explained by several factors, including the high frequency of perforator supply and exclusive deep venous drainage,3 as well as ‘kinking’ of the venous system at the level of the tentorium.11 Because infratentorial AVMs are less likely to present with seizures, some authors have suggested that this may contribute to the higher rates of hemorrhage observed among reported series.
Our study included 16 children with infratentorial AVMs, 14 (87.5%) of whom presented with hemorrhage. Infratentorial location was found to be independently associated with hemorrhagic presentation. The true impact of this finding is difficult to determine, however, as this is the only study to implicate infratentorial location as an independent risk factor in children and has a sample size too small to make definitive conclusions.
Associated aneurysms and venous pouches
The incidence of arterial aneurysms associated with adult AVMs varies in the literature from 10% to 58% and is complicated by inconsistent definitions and variations in imaging techniques.1 ,2 ,8 ,25 Multiple adult studies have established associated aneurysms as a risk factor for both initial hemorrhagic presentation and future hemorrhage.1 ,2 ,6 ,8 ,25 Our study included only 11 (8%) children with associated aneurysms (seven patients with intranidal, four patients with proximal flow related aneurysms), nine (81.8%) of whom presented with hemorrhage. Despite this high rate of hemorrhage, this feature was not significantly associated even on univariate analysis, likely due to the small number of children with associated aneurysms. Importantly, arterial aneurysms can be difficult to discern from venous pouches which, although less studied, have also been implicated as a predisposing factor to AVM hemorrhage. In this study, 8/15 (53.3%) children with associated venous pouches presented with hemorrhage although this feature was not independently predictive of hemorrhage.
Venous drainage anatomy
Several AVM features that either promote or reflect the development of venous outflow restriction and subsequent disruption of the transmural pressure gradient across AVMs have been studied. Specifically, studies among adults have noted higher rates of hemorrhage among AVMs with deep venous drainage obstruction, draining vein stenosis, a small number of draining veins and venous ectasias.3 ,21 ,26–28 On univariate analysis, the presence of venous obstruction (the presence of a single draining vein, venous ectasia or functional venous stenosis) was associated with a higher likelihood of hemorrhagic presentation. However, on multivariate analysis, no individual feature of the venous system (other than exclusive deep venous drainage) was found to be significant.
AVMs display wide variability in their overall angiographic morphology and flow characteristics, and represent a continuum from high flow fistulous lesions to linear cylindrical lesions extending from the cortex towards the ventricle,29 to compact or glomerular-type lesions, to diffuse or proliferative lesions. In this study, we did not observe an association between nidus morphology and hemorrhagic presentation in children with AVMs.
Study limitations and clinical implications
Despite providing important insight into the natural history of pediatric AVMs, this study has several limitations. The most important of these is selection bias, which is common to all of the discussed studies and is impacted by both the study population and the referral center. Among adult neurosurgical centers, major differences in the demographic, clinical and morphological features of AVM patient populations have been observed.30 These differences may, in part, explain the wide variability in which AVM features are identified as risk factors of hemorrhage among reported studies. Although differences in the institutional populations were not formally assessed, certain referral biases were evident in this study. For instance, the greater proportion of hemorrhagic AVMs among the Hospital for Sick Children cohort (73% vs 45%) and higher rates of non-hemorrhagic AVMs among the Children's Hospital Boston cohort (54% vs 27%) may reflect differences in referral patterns between pediatric institutions.
A second important limitation of this study that is also common to the other discussed studies is sample size. While the present study analyzed angioarchitectural features in an 11 year combined cohort from two high volume pediatric neurosurgery centers, the relatively small sample size may be underpowered to assess the true impact of certain angioarchitectural features on AVM hemorrhage and may also not be able to fully control for the interaction between specific variables and the risk of false positive results in the setting of multiple comparisons.
A third important limitation to this study concerns the use of superselective angiography. Despite tremendous advances in conventional and three-dimensional rotational angiography, these techniques are still limited in their ability to characterize intranidal abnormalities such as arterial aneurysms and venous pouches. Because we did not exclude the small proportion of children that underwent superselective angiography for pretreatment planning of endovascular embolization, we may have overestimated the frequency of these features in this patient population. By the same token, we may have also failed to detect important intranidal pathology in those children that were not considered for endovascular therapy.
The final limitation concerns the clinical implications of this study. The true value of AVM natural history studies resides in their ability to discriminate between AVMs that carry a high risk of hemorrhage versus those with a lower risk of hemorrhage on the basis of AVM angioarchitecture. Future risk of hemorrhage can then be weighed against the risk of treatment to help guide therapeutic decision making. The extent to which the presence of certain morphological risk factors present at the time of hemorrhagic presentation can be extrapolated as predictors of future hemorrhage in AVMs is controversial. Although smaller AVM size, exclusive deep drainage and infratentorial location were found to be independently associated with hemorrhage in pediatric AVMs, this analysis represents only those factors significant at presentation and not necessarily those that predict future hemorrhage. While further prospective studies, as well as the ongoing ARUBA trial (A Randomized Trial of Unruptured Brain Arteriovenous Malformations, NCT00389181) will help clarify those features that are predictive of future hemorrhage in adults with AVMs, similar studies are unlikely to be completed among children where very few are treated conservatively. In our opinion, ruptured AVMs in children carry a significant risk of recurrent hemorrhage and associated morbidity and mortality and, as such, should be treated aggressively with the goal of complete AVM obliteration with minimal neurological morbidity. Although the management of unruptured AVMs remains controversial, we believe the presence of high risk angioarchitectural features should be strongly considered when weighing treatment related risks against the natural history of AVMs in children.
Despite these limitations, the present study provides important insight into the angioarchitectural features that are associated with hemorrhagic presentation in a large combined cohort of pediatric AVMs. If the morphological risks of future AVM hemorrhage are to be determined in the future, they will undoubtedly require the collaborative efforts of multiple pediatric neurosurgical centers.
In this combined cohort of 135 children with AVMs, smaller AVM size, exclusive deep venous drainage and infratentorial location were independently associated with initial hemorrhagic presentation on multivariate analysis. Future prospective collaborative studies are needed to confirm these findings and identify factors predictive of future hemorrhage in children with AVMs.
Funding Partial support for some of the Canadian investigators was provided by the Ontario Stroke System Research Program.
Competing interests None.
Ethics approval Ethics approval was provided by the institutional review board of the Hospital for Sick Children Toronto and the Children's Hospital Boston.
Provenance and peer review Not commissioned; externally peer reviewed.
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