Dynamics of cerebral metabolism in patients with chronic subdural hematoma evaluated with phosphorous 31 MR spectroscopy before and after surgery.

PURPOSE To determine whether the depression of cerebral bioenergetic metabolism caused by chronic subdural hematomas can account for neurologic dysfunction and whether the degree of metabolic depression may be useful for clinical assessment and therapy. METHODS Sixteen patients who had chronic subdural hematomas with hemiparesis and/or mental disturbances underwent phosphorous 31 MR spectroscopy before and 10 to 14 days after surgery. Phosphorous 31 MR spectroscopy was also performed on 5 patients who had chronic subdural hematomas with only slight headaches who were treated by conservative therapy and on 10 healthy volunteers. RESULTS The peroperative phosphocreatine-to-inorganic phosphate ratio (2.10 +/- 0.36) improved to normal values (2.69 +/- 0.44) after evacuation of hematomas. This improvement was accompanied by complete disappearance of hemiparesis and/or mental disturbance. Brain tissue pH also improved from 7.07 +/- 0.11 to 7.205 +/- 0.13 after surgery. On the other hand, patients who had chronic subdural hematomas with only slight headaches had the same phosphocreatine-to-inorganic phosphate ratio and brain intracellular pH as healthy volunteers. CONCLUSION The phosphocreatine-to-inorganic phosphate ratio may be useful for determining when to operate on patients with chronic subdural hematomas and to assess the efficacy of treatment.

[1]  A. Tanaka,et al.  Computed tomography and cerebral blood flow correlations of mental changes in chronic subdural hematoma. , 1992, Neurosurgery.

[2]  S. Price Effects of tromethamine and hyperventilation on brain injury in the cat: Yoshida K, Marmarou A J Neurosurg 74: 87–96 Jan 1991 , 1991 .

[3]  A. Tanaka,et al.  Xenon-enhanced computed tomographic measurement of cerebral blood flow in patients with chronic subdural hematomas. , 1990, Neurosurgery.

[4]  J. Yamashita,et al.  Relation of regional cerebral blood flow to hemiparesis in chronic subdural hematoma. , 1990, Surgical neurology.

[5]  R. Ordidge,et al.  A general approach to selection of multiple cubic volume elements using the ISIS technique , 1988, Magnetic resonance in medicine.

[6]  L. Pitts,et al.  High Energy Phosphate Metabolism in Experimental Permanent Focal Cerebral Ischemia: An in vivo 31P Magnetic Resonance Spectroscopy Study , 1988, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[7]  M. Schnall,et al.  Triple nuclear NMR studies of cerebral metabolism during generalized seizure , 1988, Magnetic resonance in medicine.

[8]  M. Weiner,et al.  Effects of Traumatic Brain Injury on Cerebral High-Energy Phosphates and pH: A 31P Magnetic Resonance Spectroscopy Study , 1987, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[9]  L. Pitts,et al.  Effect of hypoxia on traumatic brain injury in rats: Part 2. Changes in high energy phosphate metabolism. , 1987, Neurosurgery.

[10]  B. Drayer,et al.  Chronic adult cerebral infarction studied by phosphorus NMR spectroscopy. , 1986, Radiology.

[11]  Roger J. Ordidge,et al.  Image-selected in Vivo spectroscopy (ISIS). A new technique for spatially selective nmr spectroscopy , 1986 .

[12]  R. Hayes,et al.  Regional brain metabolite levels following mild experimental head injury in the cat. , 1985, Journal of neurosurgery.

[13]  R G Shulman,et al.  Cerebral intracellular pH by 31P nuclear magnetic resonance spectroscopy , 1985, Neurology.

[14]  J. Haselgrove,et al.  In vivo Time-Resolved Brain Phosphorus Nuclear Magnetic Resonance , 1984, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[15]  R. Shulman,et al.  In vivo phosphorus nuclear magnetic resonance spectroscopy in status epilepticus , 1984, Annals of neurology.

[16]  A. Koretsky,et al.  Comparison of 31P NMR spectra of in Vivo rat brain using convolution difference and saturation with a surface coil. Source of the broad component in the brain spectrum , 1984 .

[17]  C. Tanaka,et al.  In vivo measurement of energy metabolism and the concomitant monitoring of electroencephalogram in experimental cerebral ischemia , 1984, Brain Research.

[18]  R G Shulman,et al.  Cerebral metabolic studies in vivo by 31P NMR. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[19]  G. Radda,et al.  A 31P Nuclear Magnetic Resonance in vivo Study of Cerebral Ischaemia in the Gerbil , 1982, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[20]  D. Delpy,et al.  Noninvasive investigation of cerebral ischemia by phosphorus nuclear magnetic resonance. , 1982, Pediatrics.

[21]  R. Duckrow,et al.  Oxidative metabolic activity of cerebral cortex after fluid-percussion head injury in the cat. , 1981, Journal of neurosurgery.

[22]  F. Gjerris,et al.  REGIONAL CEREBRAL BLOOD FLOW IN PATIENTS WITH CHRONIC SUBDURAL HEMATOMAS , 1975, Acta neurologica Scandinavica.

[23]  D. I. Hoult,et al.  Observation of tissue metabolites using 31P nuclear magnetic resonance , 1974, Nature.

[24]  H. Zaren,et al.  Experimental study of patterns of brain distortion and ischemia produced by an intracranial mass. , 1968, Journal of neurosurgery.

[25]  A. Marmarou,et al.  Effects of tromethamine and hyperventilation on brain injury in the cat. , 1991, Journal of neurosurgery.

[26]  F. Gjerris,et al.  Proceedings: Regional cerebral blood flow in patients with chronic subdural haematoma before and after operation. , 1975, Acta neurochirurgica.