L. Philip Carter

Long-term Surface Cortical Cerebral Blood Flow Monitoring in Temporal Lobe Epilepsy

Long-term subdural surface cortical cerebral blood flow (CBF) and electrocorticographic monitoring was performed in 12 patients with complex partial seizures. A total of 40 seizures were analyzed. Baseline CBF values from nonepileptic and epileptic temporal lobe (mean +/- standard error) were 60.0 +/- 1.0 and 50.2 +/- 1.8 ml/100 g per minute, respectively (P < 0.05). In general, clinical seizure onset was preceded by a 20-minute preictal CBF increase from baseline in the epileptic temporal lobe. Peak early postictal CBF values of nonepileptic and epileptic temporal lobes were 57.7 +/- 13.3 and 89.0 +/- 21.7 ml/100 g per minute (P > 0.05) at 5.2 +/- 2.2 and 2.4 +/- 1.0 minutes (P > 0.05) after clinical seizure onset, respectively. Statistically significant differences between nonepileptic and epileptic temporal lobe CBF were detected at 50 minutes (74.0 +/- 14.2 and 37.5 +/- 9.2 ml/100 g per minute, respectively; P < 0.05) and 60 minutes (75.6 +/- 13.6 and 36.1 +/- 8.5 ml/100 g per minute, respectively; P < 0.05) postictal. The data suggest that the optimal times for CBF analysis to differentiate epileptic from nonepileptic temporal lobe are 1) during the interictal period and 2) late (50 to 60 minutes) postictal. The results of this study should improve the understanding of the dynamic cerebral perfusion patterns in the epileptic human brain.

Surface cortical cerebral blood flow monitoring and single photon emission computed tomography: prognostic factors for selecting temporal lobectomy candidates

A series of 23 patients with medically intractable temporal lobe epilepsy was studied with surface cortical cerebral blood flow monitoring, single photon emission computed tomography (SPECT) and subdural strip electrocorticographic (ECoG) monitoring for localization of the seizure focus. All patients underwent anterior temporal lobectomy and seizure outcome was determined after a mean of 9 months (range: 3-17 months). Invasive and non-invasive cerebral blood flow (CBF) parameters with prognostic value for seizure-free outcome were: (a) inter-ictal seizure focus with CBF < 65 ml/100 gm-min; (b) inter-ictal seizure focus CBF < or = normal temporal lobe CBF; and (c) concordance of inter-ictal and/or early post-ictal SPECT and ictal ECoG for seizure focus localization. These results should improve prognostic value of invasive and non-invasive cerebral blood flow data for selection of temporal lobectomy candidates.

Continuous postoperative monitoring of cortical blood flow and intracranial pressure

A new technique to continuously monitor cortical blood flow and intracranial pressure in postoperative patients is described. A thermal diffusion flow probe with a pressure port is left in contact with the cortex at craniotomy. Postoperative intracranial pressure--cortical blood flow can be monitored and acute changes or trends are readily detected. The thermal flow probe has been previously compared with radioactive xenon (133Xe) clearance and hydrogen clearance methods of measuring cortical blood flow in animals. The technique gives a real-time quantitative indication of flow. Changes in cortical blood flow can be observed within a few seconds and the effects of treatment can be readily observed. Changes in flow due to vasospasm have been demonstrated in subarachnoid hemorrhage. It is anticipated that information learned from this method will aid in the management of patients with head trauma, tumors, and subarachnoid hemorrhage.

Postoperative monitoring of cerebral blood flow in patients harboring intracranial aneurysms

Fifteen patients harbouring intracranial aneurysms were monitored postoperatively. A thermal diffusion flow probe was placed on the cortex, in an area of interest, and continuous recording of cerebral blood flow (CBF) was carried out for 1-4 days. Vasospasm can also be detected by clinical deterioration, increased velocity by transcranial Doppler, and by angiographical evidence of decrease in vessel calibre. A comparison was made between these methods of determining vasospasm and changes in CBF. Three patients had unruptured aneurysms and no evidence of vasospasm. These patients had a range of CBF from 44 to 100 cc 100 g-1 min-1 with a daily mean of 78 cc 100 g-1 min-1. One patient was operated on, in a delayed fashion, after a period of vasospasm on post-subarachnoid haemorrhage (SAH) Day 18 and was found to have a CBF of 40 cc 100 g-1 min-1 when the pCO2 was 21 Torr and the mean blood pressure (BP) was 99 Torr. The development of vasospasm was correlated with a CBF of less than 40 cc 100 g-1 min-1. Some patients with vasospasm also develop a significant drop in CBF during the period of monitoring. Using these criteria, CBF monitoring predicted the development of vasospasm in seven patients, was compatible with the clinical course in three patients and was misleading in two patients. In the seven patients in which CBF predicted vasospasm, changes were seen in CBF prior to changes observed by clinical examination, transcranial Doppler, and/or angiography.(ABSTRACT TRUNCATED AT 250 WORDS)

Response of human epileptic temporal lobe cortical blood flow to hyperventilation

Bilateral long-term surface cortical cerebral blood flow (CBF) and electrocorticographic (ECoG) monitoring were performed in eight patients with complex partial seizures. In each patient, the epileptic temporal lobe was localized using ictal ECoG. Mean seizure interval (frequency-1) off anticonvulsant medication, a clinical measure of epileptogenicity, was 1.0 +/- 0.3 h (range: 0.4 to 2.5 h). During 13 interictal hyperventilation periods, 3.6 +/- 0.6 min in duration, the mean decrease in epileptic and nonepileptic temporal cortical CBF was 13.7 +/- 2.3 versus 6.4 +/- 1.9 ml/(100 g min) (t = 2.230, d.f. = 16, P < 0.05), representing 20.9% and 10.8% reduction from baseline CBF during hyperventilation, respectively. Seizure interval decreased (i.e. frequency increased) with increasing magnitude of seizure focus CBF reduction during hyperventilation. Seizure interval was significantly correlated with epileptic temporal lobe CBF decrease during hyperventilation (R = 0.763, d.f. = 5, P < 0.05). The data suggest that, compared to nonepileptic brain, epileptic temporal lobe is particularly prone to hypoperfusion during hyperventilation. Epileptogenicity is a function of this seizure focus susceptibility to ischemia. The finding of abnormal seizure focus autoregulation during hyperventilation has implication for epileptic focus localization with cerebral blood flow analysis.

Abnormal vasomotor response of human epileptogenic cortex to reversal of hyperventilation A long-term surface cerebral blood flow monitoring study

Abstract Human epileptogenic and nonepileptogenic surface cerebral blood flow (CBF) was studied during hyperventilation (HV) recovery. Bilateral subdural temporal lobe CBF probes were placed for long-term monitoring. Epileptic cortex became ischemic as an inverse linear function of HV duration ( r = 0.923, df=9, P P r = 0.890, df=9, P r = 0.784, df=5, P r = 0.782, df=9, P