Tissue Adhesive in Hip and Knee Arthroplasty, A Cost -Effectiveness Analysis

Prolonged wound drainage after total hip or knee arthroplasty is a very undesirable complication, both from medical as patients view. Wound drainage prolongs hospital admission and is associated with an increased risk of infection (1) post-operative wound drainage of more than 48 hours is associated with an increased infection risk of 42 percent a day in hip arthroplasty and 27 percent a day in knee arthroplasty. (2) Patient organizations report that wound drainage is considered as one of the most undesirable complications.

In our hospital, patients undergoing hip or knee arthroplasty are treated according to a "fast track" protocol, in most cases resulting in a hospital admission of only two days. This increases the chance that patient's release from hospital will be delayed due to wound drainage. The fact that our department recently started to perform hip and knee arthroplasty in a daycare setting increases this chance substantially.

In hemiarthroplasty of the knee, tissue adhesive was used in addition to conventional wound closure techniques with monocryl sutures. Resorbable monocryl sutures were used so that the usual visit to our outpatient department to remove the sutures was no longer necessary. However, we experienced an increase in wound drainage and complications using only monocryl. The addition of a tissue adhesive decreased the post-operative wound complication drastically. This in mind, we started to use tissue adhesive in regular hip and knee arthroplasty as well. With tissue adhesive in addition to conventional staples, we noticed good results. These results however, were subjective and not officially recorded.

In a previous study, good results are reported in decreasing wound drainage with the use of a tissue adhesive in addition to staples. Clinical relevance was not reported and the study design lacked a cost-effectiveness analysis (3) The increase in cost for the use of the tissue adhesive involved was noted by our board of directors. Because lack of a clear medical of financial benefit, we were asked to minimize the use of tissue adhesive, resulting in usage of tissue adhesive solely in a day care setting, which comprises only 5 to 10 percent of our treated population. Previous study reported a decrease in post-operative wound drainage when tissue adhesive was used in addition to staples in knee arthroplasty. However, no financial benefit is known, therefore this treatment has not been accepted into daily practice. In our department, prolonged hospital admission due to wound drainage is not found to be uncommon. Our hypothesis is that the addition of tissue adhesive in wound closure after hip and knee arthroplasty will significantly decrease post-operative wound drainage, leading to a reduced number of admission days. In addition, we expect less patients to return to our outpatient clinic for non-regular visits due to wound complications. Expensive bandages are used in our standard treatment protocol. Less wound drainage would mean less bandages. All these things combined will lead to a reduction in overall health care costs

Study Overview

• Status: Unknown
• Conditions: Knee Osteoarthritis; Hip Osteoarthritis
• Intervention / Treatment: Procedure: Tissue adhesive in primary Total Hip and Total Knee arthroplasty

• Study Type: Observational
• Enrollment (Anticipated): 980

Contacts and Locations

• Study Contact: Name: Koen Koenraadt, PhD; Phone Number: +31765955000; Email: kkoenraadt@amphia.nl
• Study Contact Backup: Name: Rutger van Geenen; Phone Number: +31765955000; Email: orthopedie@amphia.nl

Study Locations

• Netherlands
  • Noord-Brabant
    • Breda, Noord-Brabant, Netherlands, 4818CK
      • Recruiting
      • Amphia Hospital
      • Contact: RCI van Geenen, MD, PhD

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

• Sampling Method: Probability Sample

Study Population

THA and TKA patients

Description

Inclusion Criteria:

• primary total hip or knee arthroplasty

Exclusion Criteria:

• revision surgery

Study Plan

How is the study designed?

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Admission days	30 days

Collaborators and Investigators

• Sponsor: Amphia Hospital
• Collaborators: Ethicon, Inc.; R.C.I. van Geenen, orthopedic surgeon, Amphia, Breda, The Netherlands
• Investigators: Principal Investigator: Rutger van Geenen, MD, PhD, Amphia Hospital, Breda, The Netherlands

Study record dates

Study Major Dates

• Study Start (Actual): January 23, 2017
• Primary Completion (Anticipated): January 23, 2018
• Study Completion (Anticipated): June 1, 2018

Study Registration Dates

• First Submitted: June 8, 2017
• First Submitted That Met QC Criteria: June 8, 2017
• First Posted (Actual): June 12, 2017

Study Record Updates

• Last Update Posted (Actual): June 12, 2017
• Last Update Submitted That Met QC Criteria: June 8, 2017
• Last Verified: June 1, 2017

More Information

Terms related to this study

• Keywords: Tissue Adhesive
• Additional Relevant MeSH Terms: Joint Diseases; Musculoskeletal Diseases; Rheumatic Diseases; Arthritis; Osteoarthritis; Osteoarthritis, Knee; Osteoarthritis, Hip
• Other Study ID Numbers: IIS 15-212

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO