Postoperative Delirium Clinical Trial
Official title:
Manual vs Automated Optimization of Anesthesia, Analgesia, Fluid Management and Ventilation Using Closed-loop Systems: Impact On The Incidence Of POCD In Elderly Patients Undergoing Moderate to High Risk Surgery
Verified date | January 2020 |
Source | Erasme University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will be the first study to report the combined use of three independent
closed-loop systems together to assist clinicians in titrating anesthesia, analgesia, fluid
and optimize ventilation in frailty old patients undergoing moderate to high risk surgery.
The potential benefits of optimizing the control of these variables by advanced closed loop
systems are two-fold. Firstly, this will likely decrease the variance of delivered care and
reduce deviation from the established standards, resulting in improved post operative
cognitive outcomes in elderly patients. Secondly, this would establish a precedent that
automated intraoperative systems have strong clinical significance and are more than
"complicated toys", which is unfortunately how they are perceived now.
Hypothesis: Automated control of anesthetic depth (minimal episodes of overly deep or light
anesthesia) and hemodynamics (via improved volume administration) can decrease the occurrence
of postoperative cognitive dysfunction in elderly patients undergoing moderate to high risk
surgery (Better MOCA test in the postoperative period compared to the manual group [+ two
points in average])
Status | Completed |
Enrollment | 90 |
Est. completion date | November 21, 2017 |
Est. primary completion date | November 21, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 60 Years and older |
Eligibility |
Inclusion Criteria: - Adult patients > or equal 60 years old - ASA score I-III - Scheduled for non cardiac surgery under total intravenous anesthesia - Self sufficient (living at home or in non medical institution) - MOCA test preop > 23/30 - No Stroke, alzeihmer, Parkinson disease - Written informed consent signed Exclusion Criteria: - Allergy to propofol or remifentanil - MOCA test < 23/30 - Visual or hearing deficiency - Atrial fibrillation, or other Contra indication to the use of dynamic parameters of fluid responsiveness. - Chronic renal failure ( creatinin level maximum at 2 mg/ml; no dialysis) - Large liver resection : our center has a strict fluid /CVP fluid restriction in place |
Country | Name | City | State |
---|---|---|---|
Belgium | Erasme | Brussels |
Lead Sponsor | Collaborator |
---|---|
Erasme University Hospital |
Belgium,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Incidence of postoperative cognitive dysfunction (POCD) | assessment of the POCD using the MOCA test ( done by a psychiatrist and a psychologist). This will be done preoperatively, at postoperative day 3-5 for moderate risk surgery and postoperative day 7-10 for high risk surgery | first month | |
Secondary | Assesment of the incidence of POCD using different others tests: | 1) assessment of verbal episodic memory (van der linden et al, 2004: RL/RI-16 2) Digit Span (assessment of short term memory: in order and reverse order (assessment of working memory) 3) Stroop test: assessment of inhibition (Chatelois, 1993). This will be done day the before surgery | Before Surgery | |
Secondary | Assesment of the incidence of POCD using different others tests: | 1) assessment of verbal episodic memory (van der linden et al, 2004: RL/RI-16 2) Digit Span (assessment of short term memory: in order and reverse order (assessment of working memory) 3) Stroop test: assessment of inhibition (Chatelois, 1993). This will be done on postoperative day 3-5 (for moderate risk surgery) | day 5 after surgery | |
Secondary | Assesment of the incidence of POCD using different others tests: | 1) assessment of verbal episodic memory (van der linden et al, 2004: RL/RI-16 2) Digit Span (assessment of short term memory: in order and reverse order (assessment of working memory) 3) Stroop test: assessment of inhibition (Chatelois, 1993). This will be done on postoperative day 7-10 for high risk surgery | day 10 after surgery | |
Secondary | Long term incidence of POCD | results of the MOCA test | month 3 post surgery | |
Secondary | Assessment of the Quality of life EQ-5D-5L | self assessment by the patient: done the day before surgery and at month 3 post surgery | 3 months | |
Secondary | Assessment of Quality of recovery (QoR) | self assessment by the patient: QoR-15 items: questionnaire done before surgery to provide baseline data and then repeated after surgery (post operative day 3 for moderate risk surgery and postoperative day 7for high risk surgery). | first month | |
Secondary | Amount of i.v drugs used ( propofol, remifentanil, vasopressors) | amount of iv drugs used during the surgery | first 24 hours | |
Secondary | Amount of total fluid infused to the patient | comparison of the amount of fluid administered to the patients between groups | first 24 hours | |
Secondary | Mean BIS values and Burst suppression ratio (BSR) incidence defined as a period of isoelectric cortical signal with a treshold at 10% for > 1 minutes. | comparison of the mean BIS values and occurrence of BSR between groups | first 24 hours | |
Secondary | mean arterial pressure (MAP) during surgery | comparison of the mean values of these variables between both groups | first 24 hours | |
Secondary | Mean : mean stroke volume, stroke volume variation and cardiac output and cardiac index | comparison of the mean values of these variables between both groups | first 24 hours | |
Secondary | Incidence of postoperative complications (major and minor) | comparison of the incidence of postoperative complications between both groups | From date of surgery until day 30 after surgery | |
Secondary | Length of stay in the intensive care unit (ICU) and/or postanesthesia care unit (PACU) | comparison of the length of stay between both groups | From date of surgery until the date of Postanesthesia or intensive care setting discharge or date of death from any cause assessed up to 100 weeks after surgery | |
Secondary | Length of stay in the hospital ( | comparison of the hospital length of stay between both groups | From date of surgery until the date of hopital discharge or date of death from any cause assessed up to 100 weeks after surgery | |
Secondary | Mortality at day 30 | death at 1 month | 30 days | |
Secondary | Mortality at month 3 | death at 3 months | 3 months | |
Secondary | Comparison of performance of the automated system vs the manual group | defined as the time of the surgery spent with a BIS values [40-60] and a SVV <13% and/or a CI > 2.5 l/min/m2 for | first 24 hours | |
Secondary | Occurrence of arterial hypotension (mean arterial pressure (MAP) < 65 mmHg) | MAP < 65 mmHg | first 24 hours | |
Secondary | Occurrence of awarness | questionnaire | first 24 hours |
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