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Clinical Trials/NCT02820831
NCT02820831
Terminated
Not Applicable

Anesthesia Geriatric Evaluation and the Prediction of Quality of Life in Elderly Peripheral Vascular Surgery Patients

St. Antonius Hospital1 site in 1 country88 target enrollmentJune 9, 2016
ConditionsQuality of Life

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Quality of Life
Sponsor
St. Antonius Hospital
Enrollment
88
Locations
1
Primary Endpoint
Quality of Life
Status
Terminated
Last Updated
4 years ago

Overview

Brief Summary

A prospective observational cohort study to assess the predictive value of preoperative frailty on postoperative quality of life in peripheral vascular surgery patients.

Detailed Description

Introduction: The percentage of elderly in the general population is increasing rapidly. Currently, the Dutch population comprises for one fifth of persons aged 65 years or older and recent estimates show this will increase to roughly a quarter in the next 20 years. Since th incidence of peripheral arterial disease increases with age, this rise in elderly will also reflect on the population of patients being referred for vascular surgery. Elderly patients are at higher risk for postoperative complications, mortality or functional decline than younger patients. In frail elderly this effect might be more pronounced. Frailty is an umbrella term that encompasses patient related factors such as weight loss, muscle wasting, inactivity, comorbidities and polypharmacy. Current scoring systems that are used to predict postoperative mortality and complications following vascular surgery perform poorly in the elderly population and do not take into account frailty. Moreover they are designed to predict mortality and complications and are not validated to predict patient reported outcome measures such as quality of life or functional status. The aim of the AGE VASC study is assess the value of frailty factors in predicting an improvement in quality of life one year after peripheral vascular surgery. Methods: The AGE VASC study is a prospective observational cohort study. All patients aged 70 years or older, scheduled for peripheral vascular surgery of the lower limb, mentally competent and have signed informed consent are eligible for the study. Before surgery patients will be screened for frailty using different questionnaires and physical tests. The battery of tests exists of Short Form 36 (SF36), Walking Impairment Questionnaire (WIQ), Multi Nutritional Assessment (MNA), Montreal Cognitive Assessment (MoCA), Nagi's scale for disability, Geriatric Depression Scale -8 (GDS8), three physical tests: five meter walking speed, timed get up and go test and hand grip strength. And a non-invasive measurement of Advanced Glycation Endproducts (AGEs). A blood sample will be taken to determine vitamin status, immune status and iron deficiency. After surgery, electronic patients charts will be studied to score postoperative complications or mortality. Three and twelve months after surgery patients will receive SF-36, WIQ, and World Health Organization Disability Assessment Schedule (WHODAS) 2.0 questionnaires to determine quality of life and functional status.

Registry
clinicaltrials.gov
Start Date
June 9, 2016
End Date
February 2, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

dr. P. Noordzij

dr. P.G. Noordzij

St. Antonius Hospital

Eligibility Criteria

Inclusion Criteria

  • Aged 70 years or older
  • Mentally competent
  • Planned peripheral vascular surgery of the lower limb (femoral artery desobstruction, bypass surgery, amputation), possibly combined with endovascular procedure
  • Signed informed consent

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Quality of Life

Time Frame: 12 months after surgery

Assessed by Medical Outcomes Study Short Form-36 (SF-36)

Secondary Outcomes

  • Quality of Life(3 months after surgery)
  • Walking Impairment(3 and 12 months after surgery)
  • Psychosocial or physical functioning(3 and 12 months after surgery)
  • Incidence of postoperative complications and mortality(30 days after surgery)
  • Length of in-hospital stay(Post-surgical. The expected length of stay is 5-7 days)

Study Sites (1)

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