How Are Cognitive Functions Affected by Different Sedation Methods in Geriatric Endoscopic Retrograde Cholangiopancreatography Patients?
Overview
- Phase
- Not Applicable
- Intervention
- Propofol group
- Conditions
- Cognition
- Sponsor
- Ankara City Hospital Bilkent
- Enrollment
- 184
- Locations
- 1
- Primary Endpoint
- Assesment of cognitive function
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
The investigators wanted to observe the change in the level of consciousness of patients undergoing ERCP after anesthesia. For this, the investigators evaluated the patients with the mini mental state examination test and the frail scale.
Detailed Description
Background and Aim: For patients, endoscopic retrograde cholangiopancreatography (ERCP) is a painful procedure and requires deeper sedation and less body movement than routine gastrointestinal endoscopy. Different sedation methods can be used during the ERCP procedure, which is increasingly used in elderly patients, but their effects on cognitive functions are not clearly known. The main aim of our study was to observe the effect of different sedation methods routinely used in geriatric ERCP patients on cognitive functions. Methods: Our observational prospective study included 184 inpatients aged 65 years and older who received propofol or propofol + dexmedetomidine for sedation during ERCP. To evaluate cognitive function, Mini Mental State Examination (MMSE) was administered 3 times before the procedure and 2 hours and 24 hours after the procedure. Frailty level of the patient was determined using the frail frailty questionnaire. Each patient received 0.5µg/kg fentanyl (iv). In the propofol group, propofol loading dose: 0.2-0.5mg/kg, maintenance infusion dose: 0.5-4mg/kg/h was continued. In the dexmedetomidine group, in addition to propofol infusion at the same doses, dexmedetomidine 0.5 μg/kg-1 loading dose was administered within 10 minutes and then continued as infusion at a dose of 0.2-0.7 μg/kg/h. Ramsey score was kept at 3-4. ERCP procedure time, total amount of propofol and dexmedetomidine used, atropine and ephedrine administered additionally were recorded.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients aged 65 years older and who underwent ERCP and were hospitalized were included in the study.
Exclusion Criteria
- •Patients with 2nd and 3rd degree Atrioventricular Block,
- •Recent history of stroke
- •Severe hypotensive
- •Cardiorespiratory instability
- •Substance abuse
- •Psychotic illness
- •Severe dementia
Arms & Interventions
Propofol
aged 65 years and older who received propofol
Intervention: Propofol group
Dexmedetomidine
aged 65 years and older who received propofol + dexmedetomidine
Intervention: Dexmedetomidine group
Outcomes
Primary Outcomes
Assesment of cognitive function
Time Frame: Maximum 1 day (Mini Mental State Examination scores can be between 0-30. Less than 10 is considered severe impairment, 10-19 is considered moderate dementia, 19-24 is considered early dementia and 25 and above is considered normal)
Evaluating patients with Mini Mental State Examination (MMSE). Cognitive disfunctions are recorded