Brain Advance Access published online on October 25, 2006
Brain, doi:10.1093/brain/awl297
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1 Department of Experimental Neurology and Neurology, Charité University Medicine Berlin, Berlin, Germany
* To whom correspondence should be addressed. Progressive ischaemic damage in animals is associated with spreading mass depolarizations of neurons and astrocytes, detected as spreading negative slow voltage variations. Speculation on whether spreading depolarizations occur in human ischaemic stroke has continued for the past 60 years. Therefore, we performed a prospective multicentre study assessing incidence and timing of spreading depolarizations and delayed ischaemic neurological deficit (DIND) in patients with major subarachnoid haemorrhage (SAH) requiring aneurysm surgery. Spreading depolarizations were recorded by electrocorticography with a subdural electrode strip placed on cerebral cortex for up to 10 days. A total of 2110 h recording time was analysed. The clinical state was monitored every 6 h. Delayed infarcts after SAH were verified by serial CT scans and/or MRI. Electrocorticography revealed 298 spreading depolarizations in 13 of the 18 patients (72%). A clinical DIND was observed in seven patients 7.8 days (7.3, 8.2) after SAH. DIND was time-locked to a sequence of recurrent spreading depolarizations in every single case (positive and negative predictive values: 86 and 100%, respectively). In four patients delayed infarcts developed in the recording area. As in the ischaemic penumbra of animals, delayed infarction was preceded by progressive prolongation of the electrocorticographic depression periods associated with spreading depolarizations to >60 min in each case. This study demonstrates that spreading depolarizations have a high incidence in major SAH and occur in ischaemic stroke. Repeated spreading depolarizations with prolonged depression periods are an early indicator of delayed ischaemic brain damage after SAH. In view of experimental evidence and the present clinical results, we suggest that spreading depolarizations with prolonged depressions are a promising target for treatment development in SAH and ischaemic stroke.
Received April 8, 2006
Revised September 14, 2006
Accepted September 15, 2006
Article
Delayed ischaemic neurological deficits after subarachnoid haemorrhage are associated with clusters of spreading depolarizations
Jens P. Dreier 1 * *, Johannes Woitzik 2 *, Martin Fabricius 3 *, Robin Bhatia 4, Sebastian Major 1, Chistoph Drenckhahn 1, Thomas-Nicolas Lehmann 5, Asita Sarrafzadeh 5, Lisette Willumsen 6, Jed A. Hartings 7, Oliver W. Sakowitz 8, Jörg H. Seemann 9, Anja Thieme 10, Martin Lauritzen 3, and Anthony J. Strong 4
2 Department of Neurosurgery, University Hospital Mannheim, Faculty for Clinical Medicine of the University of Heidelberg, Mannheim, Germany
3 Department of Clinical Neurophysiology, University of Copenhagen, Glostrup Hospital, Copenhagen, Denmark
4 Department of Neurosurgery, King's College, London, UK
5 Department of Neurosurgery, Charité University Medicine Berlin, Berlin, Germany
6 Department of Neurosurgery, University of Copenhagen, Glostrup Hospital, Copenhagen, Denmark
7 The Division of Psychiatry and Neuroscience, Walter Reed Army Institute of Research, Silver Spring, MD, USA
8 Department of Neurosurgery, University of Heidelberg, Heidelberg, Germany
9 Department of Neuroradiology, Charité University Medicine Berlin, Berlin, Germany
10 Department of Anaesthesiology, Charité University Medicine Berlin, Berlin, Germany
Jens P. Dreier, E-mail: jens.dreier{at}charite.de
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Abstract
*These authors contributed equally to this work.
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