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Bisphosphonates Use After Total Joint Arthroplasty

Postoperative Use of Bisphosphonates Reduces Adverse Outcome After Primary Total Joint Arthroplasty: A Nationwide Population-based Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05623540
Enrollment
27405
Registered
2022-11-21
Start date
2000-01-01
Completion date
2022-11-02
Last updated
2022-11-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diphosphonates

Keywords

Bisphosphonates, Total joint arthroplasty, Revision surgery, Periprosthetic fracture

Brief summary

Background Bisphosphonates has been associated with a decreased risk of revision total joint replacements because of its effects on decreased periprosthetic bone loss and prosthetic migration. However, the results in the early literature are inconsistent and the influence of bisphosphonates on associated complications and subsequent total joint arthroplasty (TJA) remains unknown. This study is to investigate the association between the use of bisphosphonates and risk of adverse outcomes after primary TJA. Materials and Methods This matched cohort study utilized National Health Insurance Research Database in Taiwan to identify patients who underwent primary TJA over a 15-year period (January 2000- December 2015 inclusive). Study participants were further categorized into two groups: bisphosphonates users and nonusers, using propensity score matching. The Kaplan-Meier curve analysis and adjusted hazard ratios (aHR) of revision surgery, adverse outcomes of primary surgery and undergoing subsequent TJA were calculated using Cox regression analysis.

Interventions

DRUGBisphosphonates, Combinations

Sponsors

National Defense Medical Center, Taiwan
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum

Inclusion criteria

1. Patients who underwent primary total joint arthroplasty during the study period (January 1, 2000 to December 31, 2015).

Exclusion criteria

1. Patients with total joint arthroplasty before the index date, 2. Patients with existing pathologic fracture, nonunion of fracture and partial joint replacement, 3. Patients who were lost to follow-up 4. Patients \< 40 years old

Design outcomes

Primary

MeasureTime frameDescription
revision rate of joint arthroplastya 15-year period (January 2000- December 2015 inclusive)revision rate of joint arthroplasty after primary surgery

Secondary

MeasureTime frameDescription
The rate of secondary total joint arthroplastya 15-year period (January 2000- December 2015 inclusive)The rate of secondary total joint arthroplasty
The rate of periprosthetic joint infectiona 15-year period (January 2000- December 2015 inclusive)The rate of periprosthetic joint infection
The rate of periprosthetic fracturea 15-year period (January 2000- December 2015 inclusive)The rate of periprosthetic fracture
Mortality ratea 15-year period (January 2000- December 2015 inclusive)Mortality rate

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026