A Randomized Trial Investigating the Cost-Utility of Patient-Specific Instrumentation in Total Knee Arthroplasty in an Obese Population.


Journal

The Journal of arthroplasty
ISSN: 1532-8406
Titre abrégé: J Arthroplasty
Pays: United States
ID NLM: 8703515

Informations de publication

Date de publication:
09 2021
Historique:
received: 08 02 2021
revised: 22 04 2021
accepted: 23 04 2021
pubmed: 1 6 2021
medline: 26 10 2021
entrez: 31 5 2021
Statut: ppublish

Résumé

Patient-specific instrumentation (PSI) has been introduced in total knee arthroplasty (TKA) with the goal of increased accuracy of component positioning by custom fitting cutting guides to the patient's bony anatomy. A criticism of this technology is the associated cost. The purpose of this randomized controlled trial was to determine the cost-utility of PSI compared with standard of care (SOC) instrumentation for TKA in an obese population. Patients with body mass index greater than 30 with osteoarthritis and undergoing primary TKA were randomized to SOC or PSI. Patients completed a health care resource use diary and the EuroQol-5D at three, six, nine, and 12 months and the Western Ontario and McMaster Universities Osteoarthritis Index at three and 12 months postsurgery. We performed cost-utility and cost-effectiveness analyses from public health care payer and societal perspectives. One hundred seventy-three patients were included in the analysis with 86 patients randomized to PSI and 87 to SOC. PSI was dominated (more costly and less effective) by SOC from a health care payer perspective. From a societal perspective, an incremental cost-utility ratio was calculated at $11,230.00 per quality-adjusted life year gained, which is cost-effective at a willingness to pay threshold of $50,000. Net benefit analyses found PSI was not significantly cost-effective at any willingness to pay value from either perspective. Our results suggest that widespread adoption of PSI may not be economically attractive or clinically indicated. Future considerations are to compare long-term clinical outcomes and radiographic alignment between the groups.

Sections du résumé

BACKGROUND
Patient-specific instrumentation (PSI) has been introduced in total knee arthroplasty (TKA) with the goal of increased accuracy of component positioning by custom fitting cutting guides to the patient's bony anatomy. A criticism of this technology is the associated cost. The purpose of this randomized controlled trial was to determine the cost-utility of PSI compared with standard of care (SOC) instrumentation for TKA in an obese population.
METHODS
Patients with body mass index greater than 30 with osteoarthritis and undergoing primary TKA were randomized to SOC or PSI. Patients completed a health care resource use diary and the EuroQol-5D at three, six, nine, and 12 months and the Western Ontario and McMaster Universities Osteoarthritis Index at three and 12 months postsurgery. We performed cost-utility and cost-effectiveness analyses from public health care payer and societal perspectives.
RESULTS
One hundred seventy-three patients were included in the analysis with 86 patients randomized to PSI and 87 to SOC. PSI was dominated (more costly and less effective) by SOC from a health care payer perspective. From a societal perspective, an incremental cost-utility ratio was calculated at $11,230.00 per quality-adjusted life year gained, which is cost-effective at a willingness to pay threshold of $50,000. Net benefit analyses found PSI was not significantly cost-effective at any willingness to pay value from either perspective.
CONCLUSION
Our results suggest that widespread adoption of PSI may not be economically attractive or clinically indicated. Future considerations are to compare long-term clinical outcomes and radiographic alignment between the groups.

Identifiants

pubmed: 34053752
pii: S0883-5403(21)00401-0
doi: 10.1016/j.arth.2021.04.029
pii:
doi:

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3078-3088

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Bryn O Zomar (BO)

Health and Rehabilitation Sciences, Faculty of Health Sciences, Western University, London, Ontario, Canada; Bone and Joint Institute, Western University, London, Ontario, Canada.

Edward M Vasarhelyi (EM)

Bone and Joint Institute, Western University, London, Ontario, Canada; Division of Orthopaedic Surgery, London Health Sciences Centre, London, Ontario, Canada; Department of Surgery, Schulich School of Medicine & Dentistry, Western University, London, Ontario, Canada.

Lyndsay E Somerville (LE)

Health and Rehabilitation Sciences, Faculty of Health Sciences, Western University, London, Ontario, Canada; Division of Orthopaedic Surgery, London Health Sciences Centre, London, Ontario, Canada.

Brent A Lanting (BA)

Bone and Joint Institute, Western University, London, Ontario, Canada; Division of Orthopaedic Surgery, London Health Sciences Centre, London, Ontario, Canada; Department of Surgery, Schulich School of Medicine & Dentistry, Western University, London, Ontario, Canada.

James L Howard (JL)

Bone and Joint Institute, Western University, London, Ontario, Canada; Division of Orthopaedic Surgery, London Health Sciences Centre, London, Ontario, Canada; Department of Surgery, Schulich School of Medicine & Dentistry, Western University, London, Ontario, Canada.

Jacquelyn D Marsh (JD)

Health and Rehabilitation Sciences, Faculty of Health Sciences, Western University, London, Ontario, Canada; Bone and Joint Institute, Western University, London, Ontario, Canada.

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