Optimization of Desflurane in Elderly Patients
- Conditions
- Postoperative Cognitive Dysfunction
- Interventions
- Registration Number
- NCT01700907
- Lead Sponsor
- Sapporo Medical University
- Brief Summary
Various issues had been pointed out when undergoing the anesthesia for elderly patients with sevoflurane, such as delayed emergence, post-operative trouble with swallowing.
Desflurane, which has a lower blood/gas partition coefficient, is expected to contribute the better emergence, along with the recent progress on optimization of delivered amount of anesthesia.
The purpose of this study is to compare the time to emergence in long elderly patient cases with desflurane or sevoflurane, with the recently developed drug-delivery optimization system "Aisys®" (GE Healthcare Japan).
- Detailed Description
The objectives of this study is to compare the time to emergence and quality of recovery in long elderly patient cases with desflurane or sevoflurane, with the recently developed drug-delivery optimization system "Aisys®" (GE Healthcare Japan).
Inclusion Criteria:
- Elderly patients (\>= 65 yr-old), long operation (\> 4hours), abdominal surgery patients
Exclusion Criteria:
- Liver dysfunction, Renal dysfunction, preoperative dementia Neurosurgery patients, Cardiac surgery patients, obese patients(BMI\>35)
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 20
- Elderly patients (>= 65 yr-old), long operation (> 4hours), abdominal surgery patients
- Liver dysfunction, Renal dysfunction, preoperative dementia Neurosurgery patients, Cardiac surgery patients, obese patients(BMI>35)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description group DES Desflurane The patients in this arm will be given the general anesthesia with desflurane and be used the Aysis as the anesthetic machine. group SEVO Sevoflurane The patients in this arm will be given the general anesthesia with sevoflurane and be used the Aysis as the anesthetic machine.
- Primary Outcome Measures
Name Time Method The Time From the End of Anesthesia to Extubation Within 60 minutes after the end of anesthesia When surgery ends, the fresh gas flow rate will be increased to 6L/min (100% oxygen). Patients will be asked to open eyes by touching the shoulder, calling the name every 15 seconds. Patients will be applied stimulus every 15 seconds until following commands. Extubation will be performed when the patient is judged to be awake and spontaneous breathing recovery substantially.
- Secondary Outcome Measures
Name Time Method The Incidence of Postoperative Delirium from 15 minutes to 48 hrs postoperatively The incidence of post operative delirium will be measured by Confusion Assessment Method (CAM) at baseline, 15mins, 3hrs, 6hrs, 12hrs, 24hrs, 48hrs postoperatively.
The Time From the End of Anesthesia to Following Commands Within 60 minutes after the end of anesthesia When surgery ends, the fresh gas flow rate will be increased to 6L/min (100% oxygen). Patients will be asked to open eyes by touching the shoulder, calling the name every 15 seconds. Patients will be applied stimulus every 15 seconds until following commands. Extubation will be performed when the patient is judged to be awake and spontaneous breathing recovery substantially.
Cognitive Function 24 hrs pre and postoperatively Cognitive function will be measured by MMSE (Mini-Mental State Examination) at 24hrs pre and postoperatively. Total MMSE score is recorded by interview ranging from 0 (minimum) to 30 (maximum). MMSE score is consisted on 11 subscales, and total MMSE score is simply summation of all the subscale scores. Maximum MMSE score indicates that the patient is excellent for cognitive function. MMSE score under 26 indicated the cognitive dysfunction.
The Time From the End of Anesthesia to Eye Opening Within 60 minutes after the end of anesthesia When surgery ends, the fresh gas flow rate will be increased to 6L/min (100% oxygen). Patients will be asked to open eyes by touching the shoulder, calling the name every 15 seconds. Patients will be applied stimulus every 15 seconds until following commands. Extubation will be performed when the patient is judged to be awake and spontaneous breathing recovery substantially.
Trial Locations
- Locations (1)
Sapporo Medical University, School of Medicine
🇯🇵Sappro, Hokkaido, Japan