Loading…

Treatment of traumatic acute posterior fossa subdural hematoma: report of four cases with systematic review and management algorithm

Background Traumatic posterior fossa subdural hematomas (SDHs) are rare lesions. Despite improvements in intensive care and surgical management of traumatic brain injuries over the last decades, the outcome for posterior fossa subdural hematomas remains poor. Methods We conduct a retrospective study...

Full description

Saved in:
Bibliographic Details
Published in:Acta neurochirurgica 2014, Vol.156 (1), p.199-206
Main Authors: de Amorim, Robson Luis Oliveira, Stiver, Shirley I., Paiva, Wellingson Silva, Bor-Seng-Shu, Edson, Sterman-Neto, Hugo, de Andrade, Almir Ferreira, Teixeira, Manoel Jacobsen
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Background Traumatic posterior fossa subdural hematomas (SDHs) are rare lesions. Despite improvements in intensive care and surgical management of traumatic brain injuries over the last decades, the outcome for posterior fossa subdural hematomas remains poor. Methods We conduct a retrospective study over a 2-year period of patients sustaining traumatic brain injury and posterior fossa SDH. Additionally, a systematic review of case series published to date was performed. Results The incidence of posterior fossa SDH was 0,01 % (4/326). All patients in this current series had poor prognosis. Three out of four exhibited ischemic/edema lesions in postoperative CT scans leading to fourth ventricle effacement and persistent brainstem compression. Our literature review retrieved 57 patients from only seven case series. Unfavorable outcomes were seen in 63 % of patients. Conclusions Our data and data from the literature do not provide sufficient evidence to establish an optimal treatment strategy for posterior fossa SDH. However, based on lessons learned with these four cases, together with results from review of the literature, we propose an algorithm for the management of this rare condition.
ISSN:0001-6268
0942-0940
DOI:10.1007/s00701-013-1850-6