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Interprofessional Preoperative Geriatric Assessment for Older Arthroplasty Patients With Multimorbidity

Not Applicable
Not yet recruiting
Conditions
Knee Arthrosis
Multimorbidity
Hip Arthrosis
Interventions
Other: Preoperative geriatric assessment
Registration Number
NCT04001699
Lead Sponsor
University of Eastern Finland
Brief Summary

The objective of this randomized control trial is to investigate effects and cost effectiveness of interprofessional preoperative assessment among older knee or hip arthroplasty patients. The main hypothesis is that preoperative assessment and optimization have a positive impact on the patents' quality of life and expenditure of social and health care services.

Detailed Description

Knee and hip arthrosis are common conditions among older adults. Progression of arthrosis often leads to worsening of symptoms and decreased mobility, daily functioning and quality of life. Total joint arthroplasty improves pain in end-stage arthrosis but accustomed postoperative care and rehabilitation alone may not guarantee optimal regain of functioning for frail and vulnerable older arthroplasty patients. Preoperative optimization of older patients with multimorbidity and functional limitations may improve benefits of the arthroplasty even at lower costs. Patients randomized into intervention arm of the present study receive preoperative assessment with treatment and prehabilitation plan. The focuses of the intervention are patient's chronic conditions, nutritional status, medication and physical activity. The intervention is delivered by multiprofessional team (geriatrician, registered nurse, physiotherapist and pharmacist).

Older adults undergoing surgery are a rapidly growing but vulnerable patient group. Knowledge on effects of preoperative evaluation and optimization is sparse, especially on the effects of multi-domain interventions.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
140
Inclusion Criteria
  • Place of residence: Kuopio or Vesanto municipality
  • Age ≥ 65 years
  • Clinical decision for knee or hip arthroplasty, elective operation with more than one month waiting time, primary arthroplasty of the index joint.
  • Multimorbidity: the patient has at least two chronic diseases with potential to affect functioning, diseases are defined according to the Function Comorbidity Index (FCI)

Additional inclusion criteria, at least two of the following:

  • 5 or more medicines taken regularly (polypharmacy)
  • continuous walking distance less than 500 m
  • needs help in dressing and/or washing oneself
  • needs help when visiting or taking care of businesses outside home
  • body mass index ≤ 23 or ≥ 34
Exclusion Criteria
  • does not meet the above inclusion criteria

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionPreoperative geriatric assessmentPreoperative assessment conducted by an interprofessional team
Usual carePreoperative geriatric assessmentUsual care
Primary Outcome Measures
NameTimeMethod
Health-related quality of life (15-D)Preoperative measurement at baseline, postoperative measurements 3 and 9 months after the arthroplasty.

Change in quality of life is measured using the 15-dimensions health-related quality of life questionnaire (15-D) in three time points

Costs of social and health care servicesChanges in costs of care are evaluated for a period starting from one year before and ending two years after the baseline examinations.

Data on the use and costs of social and health care services are obtained from the national and local care registers. The costs of the intervention are evaluated by measuring working time of the inter-professional team members (used per every study patient).

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Eastern Finland

🇫🇮

Kuopio, Finland

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