Different Frailty Scores to Incidence of Post-operative Delirium and Cognitive Dysfunction
NCT ID: NCT04056871
Last Updated: 2020-04-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
400 participants
OBSERVATIONAL
2019-08-20
2020-02-20
Brief Summary
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So, it is crucial to find a suitable frailty assessment tool that can be incorporated into a guideline and reference for our local setting in geriatric peri-operative management. In the mean time, create awareness regarding the frailty elderly population with POD, POCD and other associated poor outcomes among our clinicians.
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Detailed Description
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So, it is crucial to identify the risk factors pre-operatively to minimize the risk of POD and POCD. The frail patients are more likely to have pre-existing cognitive impairment with reduced cognitive reserve, hence, they are the most vulnerable to POCD and POD. One of the most commonly used frailty screening tools is Fried Frailty criteria which is an easily accessible tool that mainly screens and scores the patients physically. However, the investigators propose to use the Groningen Frailty scale as it can assess the patients in a more holistic approach, not only in physical, but also vision, heating, nutritional, co-morbidities, cognition, psychosocial and mobility of the patients.
Method:
Elderly patients \>65 years old undergoing elective surgery under general or local anaesthesia in University Malaya Medical Centre will be recruited for this study, over a 6 months period from August 2019 to January 2020. Patients will be assessed with baseline cognitive assessment, nutritional status, psychological status, and frailty scores prior to the surgery. After the operation, patients will be assessed using 4AT and CAM for at least 5 days or until patients discharged. Cognitive functions will be assessed on post-operative 7th day, 1 month and 3 months with T-MOCA via phone.
All data will be analyzed using SPSS.
Impact of research:
A suitable frailty assessment tool will be identified to be used pre-operatively for elderly patients undergoing elective surgery. This tool will then be incorporated into a guideline and reference in our local setting for geriatric peri-operative management protocol.
Moreover, with the results, investigators hope to create awareness within our multidisciplinary care of elderly surgical population on frailty assessment and its correlation to post-operative delirium, cognitive dysfunction and associated poor outcomes.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Fried Frailty Phenotype
This group of patients will be assess by using 5 characteristics of Frailty which are weight loss, weakness, exhaustion, low activity and physical fitness of the patients. Patients classify as frail will have more than 3 criteria, intermediate or pre-frail will be 1 or 2 criteria present and robust will not have criteria.
Frailty Screening Tools
This is an observational and prospective study of patients who are going for elective surgery, thus no intervention will be given.
Groningen Frailty Index
GFI is a simple questionnaire consisting of 15 items which are classified into 8 groups, consistent of 4 domains of functioning. A score of 4 or more indicates a higher risk for frailty and possible delirium.
Frailty Screening Tools
This is an observational and prospective study of patients who are going for elective surgery, thus no intervention will be given.
Interventions
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Frailty Screening Tools
This is an observational and prospective study of patients who are going for elective surgery, thus no intervention will be given.
Eligibility Criteria
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Inclusion Criteria
* ASA 1 - 3
* Full GCS
* Elective surgery
* Able to communicate well
* Consented
* Extubated at the end of surgery
Exclusion Criteria
* On drugs affecting the central nervous system
* Admission to ICU intubated to continue ventilation.
* Refusal of consent
* Severe hearing loss
* Unable to use telephone/ mobile phone for communication
65 Years
ALL
No
Sponsors
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University of Malaya
OTHER
Responsible Party
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Dr Loh Pui San
Consultant Anaesthesiologist
Principal Investigators
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Pui San Loh
Role: PRINCIPAL_INVESTIGATOR
University of Malaya
Locations
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University Malaya
Kuala Lumpur, Kuala Lumpur, Malaysia
Countries
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References
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Other Identifiers
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U1111-1237-9788
Identifier Type: -
Identifier Source: org_study_id
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