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Electroencephalographic response to sodium nitrite may predict delayed cerebral ischemia after severe subarachnoid hemorrhage.

Abstract:

Objective

Aneurysmal subarachnoid haemorrhage (SAH) often leads to death and poor clinical outcome. Injury occurring during the first 72 hours is termed early brain injury (EBI), with disruption of the nitric oxide (NO) pathway playing an important pathophysiological role in its development. Quantitative electroencephalography (qEEG) parameters such as alpha/delta frequency ratio (ADR) are surrogate markers of cerebral ischaemia. This study assessed the qEEG response to a cerebral NO donor (intravenous sodium nitrite) to explore whether this correlates with the eventual development of delayed cerebral ischaemia (DCI).

Design

Unblinded pilot study testing response to drug intervention.

Setting

Neurosciences Intensive Care Unit (NICU), John Radcliffe Hospital, Oxford, UK

Patients

14 World Federation of Neurosurgeons grades 3, 4 and 5 patients (mean age 52.8; range 41-69; 11 female).

Interventions

IV sodium nitrite 10 mcg/kg/min for one hour.

Measurements and Main Results

Continuous EEG recording for two hours. The ADR was measured before and during intravenous sodium nitrite infusion. Seven out of fourteen patients developed DCI. There was a +30% to +118% (range) increase in ADR in patients who did not develop DCI (p <0.0001) but an overall decrease in ADR in those patients who did develop DCI (range +11% to -31%) (p=0.006, multivariate analysis accounting for major confounds).

Conclusions

Administration of sodium nitrite after severe SAH differentially influences qEEG parameters depending on the patient’s susceptibility to development of DCI. With further validation in a larger sample size, this response may be developed as a tool for risk stratification after aneurysmal SAH.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1097/CCM.0000000000001950

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author


Publisher:
Lippincott, Williams & Wilkins
Journal:
Critical Care Medicine More from this journal
Volume:
44
Issue:
11
Pages:
e1067–e1073
Publication date:
2016-08-09
Acceptance date:
2016-03-25
DOI:
EISSN:
1530-0293
ISSN:
0090-3493
Pmid:
27441898


Language:
English
Keywords:
Pubs id:
pubs:636651
UUID:
uuid:f5de637a-7b36-464a-8cc4-1b2882037ac8
Local pid:
pubs:636651
Source identifiers:
636651
Deposit date:
2016-09-23

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