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Surgical Treatment vs Nonsurgical Treatment for Brain Arteriovenous Malformations in Patients with Hereditary Hemorrhagic Telangiectasia: A Retrospective Multicenter Consortium Study
Journal article   Peer reviewed

Surgical Treatment vs Nonsurgical Treatment for Brain Arteriovenous Malformations in Patients with Hereditary Hemorrhagic Telangiectasia: A Retrospective Multicenter Consortium Study

Ali Tayebi Meybodi, Helen Kim, Jeffrey Nelson, Steven W Hetts, Timo Krings, Karel G terBrugge, Marie E Faughnan, Michael T Lawton and Brain Vascular Malformation Consortium HHT Investigator Group
Neurosurgery, Vol.82(1), pp.35-47
01/2018
PMID: 28973426

Abstract

Adolescent Adult Aged Brain - blood supply Brain - diagnostic imaging Brain - surgery Central Nervous System Vascular Malformations - diagnostic imaging Central Nervous System Vascular Malformations - surgery Central Nervous System Vascular Malformations - therapy Child Child, Preschool Databases, Factual - trends Female Humans Infant Intracranial Arteriovenous Malformations - diagnostic imaging Intracranial Arteriovenous Malformations - surgery Intracranial Arteriovenous Malformations - therapy Male Middle Aged Retrospective Studies Telangiectasia, Hereditary Hemorrhagic - diagnostic imaging Telangiectasia, Hereditary Hemorrhagic - surgery Telangiectasia, Hereditary Hemorrhagic - therapy Treatment Outcome Young Adult
Cerebral arteriovenous malformations (AVMs) are common in patients with hereditary hemorrhagic telangiectasia (HHT). However, due to the rarity of HHT and little published evidence of outcomes from management of brain AVMs in this disease, current international HHT guidelines recommend an individualized approach. Specifically, the outcomes for surgical vs nonsurgical management of these lesions have not been reported to date. To report long-term outcomes of surgical resection of brain AVMs in HHT patients compared to outcomes in nonsurgically treated patients. From the database of the Brain Vascular Malformation Consortium HHT project, 19 patients with 20 resected AVMs (group 1) and 22 patients with 33 AVMs who received nonsurgical treatment (group 2) were studied. The groups were retrospectively reviewed for changes in functional status (modified Rankin Scale score) during the follow-up period. During the follow-up period, 9% of patients in group 1 suffered from worsening of functional status, whereas this figure was 16% for group 2 (P > .05). Functional outcomes were not statistically different between the 2 groups at the latest follow-up (P > .05). HHT patients treated surgically for brain AVMs appear to have long-term functional outcomes comparable to nonsurgical (including observational) therapy with fewer unfavorable outcomes. It is therefore reasonable to consider surgical resection as a management option in the multidisciplinary team's individualized treatment strategy for HHT patients with brain AVMs.

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