PHYSIOLOGICAL DETERMINATION OF CEREBROVASCULAR RESERVES AND ITS USE IN CLINICAL MANAGEMENT

Citation
H. Yonas et Rr. Pindzola, PHYSIOLOGICAL DETERMINATION OF CEREBROVASCULAR RESERVES AND ITS USE IN CLINICAL MANAGEMENT, Cerebrovascular and brain metabolism reviews, 6(4), 1994, pp. 325-340
Citations number
105
Categorie Soggetti
Neurosciences
ISSN journal
10408827
Volume
6
Issue
4
Year of publication
1994
Pages
325 - 340
Database
ISI
SICI code
1040-8827(1994)6:4<325:PDOCRA>2.0.ZU;2-8
Abstract
Cerebrovascular reserve (CVR) can be assessed by measuring the hemodyn amic response to a physiological stress such as alteration of blood pr essure, increase in tissue acidosis, lowered oxygen supply, increase i n metabolic demand, or occlusion of an artery. Failure of the cerebrov ascular system to maintain function or normative values of several int errelated hemodynamic variables-cerebral blood flow (CBF), oxygen extr action fraction (OEF), cerebral blood volume (CBV), and cerebral metab olic rate of oxygen (CMRO(2)),-in response to a stress implies a compr omise of the normally robust compensatory mechanisms. The conclusions that are possible from this information depend on the type of stress i nduced and the technology used to measure the response. Technologies t hat permit a rapid test-retest format coupled with a physiological str ess provide the most direct information about the hemodynamics of cere brovascular territories. Patients whose cerebral vasculature becomes c ompromised by any of a broad range of disorders and who, thus, are at increased risk for stroke now can be readily identified based upon evi dence of exhausted CVR. Strategies for treating hemodynamically driven disorders also can now be designed based upon such patient-specific C VR information. It is hoped that integration of CVR into the standard clinical assessment of patients with occlusive vascular disorders (OVD ) will lead to treatments that focus not only on the previously unders tood embolic causes of stroke, but also on the often interrelated hemo dynamic factors.