Out Patient Surgery for Total Knee and Hip Replacement and Unicompartmental Knee Replacement - a Feasibility Study

Sponsor
Kirill Gromov (Other)
Overall Status
Completed
CT.gov ID
NCT02544620
Collaborator
Rigshospitalet, Denmark (Other), Vejle Hospital (Other), Holsterbro Sygehus, DK (Other)
1,000
1
40
25

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate feasibly of outpatient Total Knee Replacement, Total Hip Replacement and Unicompartmental Knee Replacement in a modern fast-track setup. The design is as an observational prospective study, evaluating patients that fulfil discharge criteria on the day of the surgery. The investigators will further evaluate safety aspects, such a early morbidity and mortality, as well as patient satisfaction.

Condition or Disease Intervention/Treatment Phase
  • Other: Does fulfil of discharge criteria on the day of the surgery
  • Other: Does not fulfil of discharge criteria on the day of the surgery

Detailed Description

Fast-track total hip arthroplasty (THA), total knee arthroplasty (TKA) and Unicompartmental Knee arthroplasty (UKA) with length of stay (LOS) of 1-3 is a well established concept for treating hip and knee osteoarthritis, resulting in short reconvalescence, high patient satisfaction, and an excellent safety profile (lower or similar mortality / morbidity compared to conventional pathways with longer LOS). LOS have been significantly reduced during the past decade, and several centers have published even shorter hospitals stays: <24 hours, with patients staying the night at the hospital but also outpatient surgery, with patients being discharged on the day of surgery.

However, these proposed pathways with extremely short LOS, are performed on very selected patients, with few details on patient satisfaction, outcome and most important patient safety. Therefore, it is not possible to draw conclusions on feasibility of outpatient THA, TKA and UKA surgery in a general and unselected population. Further on, there is a need for investigation of safety aspects of outpatient surgery in respect to mortality, morbidity, patient satisfaction and patient reported outcomes. As some, most likely healthy and younger, patients might benefit from outpatient surgery - eg discharge on the day of surgery, while others might not; the first step is to identify the patients that are suitable for outpatient THA and TKA surgery and investigate the safety aspects in respect to mortality, morbidity, patient satisfaction and patient reported outcomes.

Aim:

The aim of this study is to investigate "feasibility" and "safety" of outpatient THA, TKA and

UKA surgery, respectively as follows:

Feasibility

  • Proportion of patients, that can be included in the study according to inclusion criteria stated below, and be evaluated for potential same-day discharge (I) (I = included)

  • Proportion of included patients (I), that are discharged on the day of surgery (U) and those who are not discharged and stay for >1 day (B)

  • Identify reasons for patients not being able to be discharged on the day of surgery (B)

Safety

  • risk for complications (morbidity) in group (U) compared to group (B) (are there complications that potentially could have been avoided is the patient was not discharged)

  • readmissions in group (U ) compared to group (B) within 90 days

  • mortality in group (U ) compared to group (B) within 90 days

  • patient satisfaction in group (U ) compared to group (B)

  • Patient reported outcome (Oxford knee score + range of motion for TKA and UKA group, and Oxford hip score for THA group) in group (U) compared to group (B)

  • contacts to primary sector in group (U ) compared to group (B) within 7 days.

  • use of rescue morphine (pain journal) for 7 days post op in group (U ) compared to group (B)

Study Design

Study Type:
Observational
Actual Enrollment :
1000 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Study Start Date :
Sep 1, 2015
Actual Primary Completion Date :
Aug 31, 2018
Actual Study Completion Date :
Dec 31, 2018

Arms and Interventions

Arm Intervention/Treatment
Total Hip arthroplasty

Unselected primary THA American Society of Anesthesiologists (ASA) score I/II Can be operated as #1 or #2 No sleep apnea treated with Continuous positive airway pressure (CPAP)

Other: Does fulfil of discharge criteria on the day of the surgery

Other: Does not fulfil of discharge criteria on the day of the surgery

Total Knee arthroplasty

Unselected primary TKA American Society of Anesthesiologists (ASA) score I/II Can be operated as #1 or #2 No sleep apnea treated with Continuous positive airway pressure (CPAP)

Other: Does fulfil of discharge criteria on the day of the surgery

Other: Does not fulfil of discharge criteria on the day of the surgery

unicompartmental knee arthroplasty

Unselected primary UKA American Society of Anesthesiologists (ASA) score I/II Can be operated as #1 or #2 No sleep apnea treated with Continuous positive airway pressure (CPAP)

Other: Does fulfil of discharge criteria on the day of the surgery

Other: Does not fulfil of discharge criteria on the day of the surgery

Outcome Measures

Primary Outcome Measures

  1. Fulfilment of same day discharge criteria [12 hours]

    On the days of surgery following discharge criteria are continuously evaluated: < 500 ml intraoperative blood loss Back in patient ward <15.00 Received instruction from physiotherapist and is safely mobilized No clinical symptoms of anemia Pain <3 while resting, <5 during exercise. Spontaneous urination Post op x-ray is performed and approved Relatives or friends with patient for >24 hours Motivated and accepts same day discharge Standard discharge criteria fulfilled Can be discharged before 20.00 If all of the above criteria are fulfilled, the patient can be discharged

Secondary Outcome Measures

  1. Readmissions [3 months]

  2. Patient reported satisfaction [3 months]

    OKS (Oxford Knee score) and ROM (Range og motion) for TKA and UKA, OHS for THA

  3. Use of rescue morphine [7 days]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Unselected primary THA/TKA

  • ASA score I/II

  • Can be operated as #1 or #2

  • No sleep apnea treated with CPAP

Exclusion Criteria:
  • Selected primary THA/TKA

  • ASA score > 2

  • Cannot be operated as #1 or #2

  • Sleep apnea treated with CPAP

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hvidovre Hospital Hvidovre Denmark 2650

Sponsors and Collaborators

  • Kirill Gromov
  • Rigshospitalet, Denmark
  • Vejle Hospital
  • Holsterbro Sygehus, DK

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Kirill Gromov, MD, PhD, Hvidovre University Hospital
ClinicalTrials.gov Identifier:
NCT02544620
Other Study ID Numbers:
  • HVH-SK-TKA-THA-UKA
First Posted:
Sep 9, 2015
Last Update Posted:
Mar 28, 2019
Last Verified:
Mar 1, 2019
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 28, 2019