Cerebral perfusion pressure thresholds for brain tissue hypoxia and metabolic crisis after poor-grade subarachnoid hemorrhage

Stroke. 2011 May;42(5):1351-6. doi: 10.1161/STROKEAHA.110.596874. Epub 2011 Mar 24.

Abstract

Background and purpose: To identify a minimally acceptable cerebral perfusion pressure threshold above which the risks of brain tissue hypoxia (BTH) and oxidative metabolic crisis are reduced for patients with subarachnoid hemorrhage (SAH).

Methods: We studied 30 poor-grade SAH patients who underwent brain multimodality monitoring (3042 hours). Physiological measures were averaged over 60 minutes for each collected microdialysis sample. Metabolic crisis was defined as a lactate/pyruvate ratio>40 with a brain glucose concentration≤0.7 mmol/L. BTH was defined as PbtO2<20 mm Hg. Outcome was assessed at 3 months with the Modified Rankin Scale.

Results: Multivariable analyses adjusting for admission Hunt-Hess grade, intraventricular hemorrhage, systemic glucose, and end-tidal CO2 revealed that cerebral perfusion pressure≤70 mm Hg was significantly associated with an increased risk of BTH (OR, 2.0; 95% CI, 1.2-3.3; P=0.007) and metabolic crisis (OR, 2.1; 95% CI, 1.2-3.7; P=0.007). Death or severe disability at 3 months was significantly associated with metabolic crisis (OR, 5.4; 95% CI, 1.8-16; P=0.002) and BTH (OR, 5.1; 95% CI, 1.2-23; P=0.03) after adjusting for admission Hunt-Hess grade.

Conclusions: Metabolic crisis and BTH are associated with mortality and poor functional recovery after SAH. Cerebral perfusion pressure levels<70 mm Hg was associated with metabolic crisis and BTH, and may increase the risk of secondary brain injury in poor-grade SAH patients.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Energy Metabolism / physiology
  • Female
  • Glucose / metabolism
  • Humans
  • Hypoxia, Brain / epidemiology*
  • Hypoxia, Brain / physiopathology*
  • Lactates / metabolism
  • Logistic Models
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Oxidative Stress / physiology*
  • Perfusion
  • Pyruvates / metabolism
  • Retrospective Studies
  • Risk Factors
  • Subarachnoid Hemorrhage / metabolism*
  • Subarachnoid Hemorrhage / physiopathology*

Substances

  • Lactates
  • Pyruvates
  • Glucose