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Rev Esp Anestesiol Reanim · Dec 2006
Clinical Trial[Behaviour of near-infrared cerebral oximetry readings during percutaneous carotid angioplasty].
- L Rodríguez, L Salvador, R Valero, E Carrero, J Fontanals, and N Fàbregas.
- Servicio de Anestesiología, Reanimación y Tratamiento del Dolor, Hospital Clinic i Provincial, Universitat de Barcelona. lrodri@clinic.ub.es
- Rev Esp Anestesiol Reanim. 2006 Dec 1;53(10):633-8.
BackgroundTransluminal percutaneous carotid angioplasty and stenting (CAS) carries a risk of cerebral ischemia, hemorrhage, or edema due to relative hyperemia and hemodynamic instability during and after the procedure. Noninvasive monitoring of near-infrared regional cerebral oxygen saturation (SrO2) offers an indirect way to estimate cerebral blood flow.ObjectiveTo evaluate the behaviour of SrO2 during CAS and the usefulness of this variable for continuous monitoring of cerebral blood flow variation and neurological status.Material And MethodsProspective study of 25 patients scheduled for unilateral CAS under monitored anesthesia care. SrO, and other hemodynamic and clinical data were recorded. A change in SrO2 (deltaSrO2) of 15% or more in comparison with the baseline value and lasting more than 30 seconds was considered clinically significant. Neurological complications in the first 24 hours were also registered.ResultsBaseline SrO, ranged from 51% to 75%. With administration of papaverine SrO2 values increased by a mean (SD) of 5.6% (6%) (P<.05 vs baseline). They decreased during angioplasty, -2.5% (5.7%) (P<.05 vs baseline), increased after 5 minutes, and fell again at 30 minutes to a level 3% (6.54%) above baseline. Two patients showed signs of elevated intracranial pressure after the procedures and also had ASrO2 readings exceeding 15%; measures to lower arterial hypertension reduced SrO2 in these patients.ConclusionHigh interindividual variability of absolute SrO2 values has been confirmed. SrO, fluctuates with maneuvers that change cerebral blood flow in the same way. Changes can precede the onset of other clinical signs.
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