| Literature DB >> 26277650 |
F J Arroyo-Fernández1, E Calderón-Seoane2, F Rodríguez-Peña3, L M Torres-Morera2.
Abstract
Pial arteriovenous fistula is a rare intracranial congenital malformation (0.1-1: 100,000). It has a high blood flow between one or more pial arteries and drains into the venous circulation. It is usually diagnosed during the childhood by triggering an intracranial hypertension and/or congestive heart failure due to left-right systemic shunt. It is a rare malformation with a complex pathophysiology. The perioperative anaesthetic management is not well established. We present a 6-month-old infant diagnosed with pial arteriovenous fistula with hypertension and congestive heart failure due to left-right shunt. He required a craniotomy and clipping of vascular malformation. Anaesthetic considerations in patients with this condition are a great challenge. It must be performed by multidisciplinary teams with experience in paediatrics. The maintenance of blood volume during the intraoperative course is very important. Excessive fluid therapy can precipitate a congestive heart failure or intracranial hypertension, and a lower fluid therapy may cause a tissue hypoxia due to the bleeding.Entities:
Keywords: Congestive heart failure; Fístula arteriovenosa pial; Insuficiencia cardiaca congestiva; Neuroanaesthesia; Neuroanestesia; Paediatric; Pediátrica; Pial arteriovenous fistula
Mesh:
Year: 2015 PMID: 26277650 DOI: 10.1016/j.redar.2015.07.002
Source DB: PubMed Journal: Rev Esp Anestesiol Reanim ISSN: 0034-9356