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Info RESEARCH GRANTS AND AWARDS
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Resident
Travel Awards
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TOP Outcomes
Research Award
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TOP 2004 - Winner of the Outcomes Research Award - TOP
Principal Investigator:
In spite of its high prevalence, causal mechanisms are poorly understood, and few (if any) preventive therapies are available. POCD has been previously postulated to result from the inflammatory or metabolic stress response associated with surgery.4 This association leads to a hypothesis that a decrease in stress response would lead to a decrease in the incidence of POCD, a phenomenon that can be accomplished by preoperative steroids.5-6 The same rationale can be applied to other causes of POCD, including postoperative pain and postoperative fatigue.7 In addition, preoperative steroids reduce the duration of convalescence leading to early mobilization and potentially fewer incidences of POCD.7 In relation to monitoring of anesthesia depth, previous studies have pointed to anesthesia duration and continued exposure of the central nervous system to anesthetic drugs3 as a direct cause of short-term POCD.4 Although no previous study has been conducted to evaluate the role of anesthesia depth on POCD, it is plausible that keeping patients at a higher consciousness level and less exposed to anesthetic drugs would potentially decrease the incidence of POCD. Although the use of preoperative steroids and monitoring of anesthesia depth (determined by the bispectral index monitor, or BIS) during anesthesia have been previously shown to reduce adverse outcomes that are commonly associated with POCD, the direct effect of these interventions in the reduction of POCD has not been evaluated. Therefore the aim of this multicenter factorial randomized controlled trial is to determine whether combinations of two different levels of depth of consciousness during anesthesia and preoperative intravenous dexamethasone can decrease the incidence of POCD. Three hundred people above the age of 60 undergoing ambulatory surgery under general anesthesia will be enrolled in this study. The incidence of POCD in young patients is not significant, and they will not be studied. Participants will be randomized to one of four arms: light anesthesia (BIS 50-60) plus dexamethasone (8 mg I.V. two hours prior to surgery), deep anesthesia (BIS 30-40) plus dexamethasone, light anesthesia plus placebo or deep anesthesia plus placebo. Anesthetic management will be standardized. Prior to surgery, baseline cognitive function will be evaluated using validated tests (Telephone Cognitive Assessment Battery, Blessed Telephone Information- Memory-Concentration Test). Participants also will be evaluated using a battery of validated cognitive tests measured by telephone and/or the Internet applied at baseline and closely monitored at postoperative 1, 3, 7, 21, 60 and 180 days. Extensive information on potential confounders will be obtained. Additional patient outcomes will be collected, including postoperative pain (Visual Analogue Scale), postoperative nausea and vomiting (Visual Analogue Scale), postoperative fatigue (The Fatigue Self Rating Scale), depression (Center for Epidemiological Studies Depression Scale-CES-D), quality of life (Sabin-Feldman-36), and social support given by family, friends or significant other (Multidimensional Scale of Perceived Social Support). Evaluation of the role of dexamethasone and level of consciousness during anesthesia on POCD will allow for the assessment of factors that can potentially increase the safety of ambulatory anesthesia improving patient outcomes. References
are available on the SAMBA Web site. TOP
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