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Single bisphosphonate infusion does not speed up fracture healing in high tibial osteotomy
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OSTEOARTHRITIS
Single bisphosphonate infusion does not speed up fracture healing in high tibial osteotomy .
High Impact
This study has been identified as potentially high impact. OE's AI-driven High Impact metric estimates the influence a paper is likely to have by integrating signals from both the journal in which it is published and the scientific content of the article itself. Developed using state-of-the-art natural language processing, the OE High Impact model more accurately predicts a study's future citation performance than journal impact factor alone. This enables earlier recognition of clinically meaningful research and helps readers focus on articles most likely to shape future practice.

OrthoEvidence Journal (OE Journal) - ACE Report

OE Journal. 2013;1(11):170 Acta Orthop. 2011 Aug;82(4):465-70. Epub 2011 Jun 21

46 patients with knee osteoarthritis undergoing high tibial osteotomies were randomized 4 weeks postoperatively to receive a single bisphosphonate infusion of zoledronic acid or a sodium chloride placebo. The primary outcome was reduction in healing time. Other outcomes included hip knee ankle (HKA) angle and patient-relevant outcome measures (Knee injury and osteoarthritis outcomes score (KOOS)). Results indicated that a single bisphosphonate infusion intervention does not accelerate healing in high tibial osteotomies.


Publication Funding Details +
Funding:
Non-Industry funded
Sponsor:
Region Skane, Lund University Hospital, the Swedish Medical Research Council, the Thure Carlsson, Alfred Osterlund, Greta and Johan Kock, and Maggie Stephens Foundations, and by the Faculty of Medicine, Lund University
Conflicts:
None disclosed

Risk of Bias

6.5/10

Reporting Criteria

19/20

Fragility Index

N/A

Was the allocation sequence adequately generated?

Was allocation adequately concealed?

Blinding Treatment Providers: Was knowledge of the allocated interventions adequately prevented?

Blinding Outcome Assessors: Was knowledge of the allocated interventions adequately prevented?

Blinding Patients: Was knowledge of the allocated interventions adequately prevented?

Was loss to follow-up (missing outcome data) infrequent?

Are reports of the study free of suggestion of selective outcome reporting?

Were outcomes objective, patient-important and assessed in a manner to limit bias (ie. duplicate assessors, Independent assessors)?

Was the sample size sufficiently large to assure a balance of prognosis and sufficiently large number of outcome events?

Was investigator expertise/experience with both treatment and control techniques likely the same (ie.were criteria for surgeon participation/expertise provided)?

Yes = 1

Uncertain = 0.5

Not Relevant = 0

No = 0

The Reporting Criteria Assessment evaluates the transparency with which authors report the methodological and trial characteristics of the trial within the publication. The assessment is divided into five categories which are presented below.

3/4

Randomization

4/4

Outcome Measurements

4/4

Inclusion / Exclusion

4/4

Therapy Description

4/4

Statistics

Detsky AS, Naylor CD, O'Rourke K, McGeer AJ, L'Abbé KA. J Clin Epidemiol. 1992;45:255-65

The Fragility Index is a tool that aids in the interpretation of significant findings, providing a measure of strength for a result. The Fragility Index represents the number of consecutive events that need to be added to a dichotomous outcome to make the finding no longer significant. A small number represents a weaker finding and a large number represents a stronger finding.

Why was this study needed now?

Strength of a healing fracture has been known to increase with the use of anti-catabolic drugs, such as bisphosphonates. A human pilot study examined high tibial osteotomies in knee osteoarthritis, which indicated healing time was shortened with the use of bisphosphonates. The current study examines the effect of a bisphosphonate (zoledronic acid) infusion on reducing healing time after high tibial osteotomies.

What was the principal research question?

What are the outcomes in rate of fracture healing, hip-knee-ankle (HKA) angle, and patient-relevant outcome measures when a single bisphosphonate (zoledronic acid) infusion is intravenously administered, compared to a sodium chloride placebo in patients with knee osteoarthritis after undergoing a high tibial osteotomy?

Study Characteristics +
Population:
46 patients with knee osteoarthritis undergoing high tibial osteotomies, using the hemicallotasis technique (HCO). (Age: 35-65 years) (Male: 36, Female: 10)
Intervention:
Intravenous infusion of 4 mg zoledronic Acid (A bisphosphonate) (Mean age: 48 (7 SD) years) (n=25)
Comparison:
Placebo: Intravenous infusion of sodium chloride (9 mg/mL) (Mean age: 50 (5 SD) years) (n=21)
Outcomes:
Rate of fracture healing, hip-knee-ankle (HKA) angle (Assessment using dual-energy X-ray absorptiometry (DEXA) and radiographic analysis), patient-relevant outcome measure (Knee injury and osteoarthritis outcomes score(KOOS))
Methods:
RCT
Time:
1.5 years (Evaluation at 10, 12, 14, and 16 weeks)
What were the important findings?
  • All osteotomies healed in both the zoledronic acid (intervention) and sodium chloride (control) groups.
  • No difference was seen in the rate of healing between the intervention and control group. Zoledronic group: 77 days (95% CI: 75-80); Sodium chloride group: 77 days (95%CI: 74-81). However, pin fixation of the external frame increased with the intervention of a single zoledronic acid infusion.
  • The DEXA analysis indicated similar outcomes in bone mineral density and bone mineral content between the two groups.
  • Both groups showed an improvement in KOOS scores. Small but non-statistically significant differences were seen between the groups.
  • For the hip, knee, ankle (HKA) angles, no change was seen between the two groups. The zoledronic group had a mean change of 0.3 (SD 3.3) degrees compared to -1.0 (SD 3.3) degrees in the control group (p=0.2)
  • 13/25 patients from the zoledronic group reported muscle pain and influenza-like symptoms compared to 2/21 patients from the placebo group (RR=5, CI: 1.3-20; p=0.004).
  • According to the radiographic results, both the intervention and control group retained correction when examined at the 1.5-year follow-up.
What should I remember most?

The single zoledronic acid (bisphosphonate) infusion intervention did not accelerate healing in high tibial osteotomies when compared to the sodium chloride placebo. However, there was an increase in pin fixation of the external frame in the zoledronic acid group.

How will this affect the care of my patients?

The use of a single dose of zoledronic acid after undergoing a knee osteotomy does not appear to provide patients with an increased rate of fracture healing. Further examination is required to identify if single dose zoledronic acid treatment provides improved healing rates or superior bone mineral density for different orthopaedic procedures.

DISCLAIMER

This content found on this page is for informational purposes only and is not intended to be a substitute for professional medical advice, diagnosis, or treatment. If you require medical treatment, always seek the advice of your physician or go to your nearest emergency department. The opinions, beliefs, and viewpoints expressed by the individuals on the content found on this page do not reflect the opinions, beliefs, and viewpoints of OrthoEvidence.

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How to cite this ACE Report

OrthoEvidence. Single bisphosphonate infusion does not speed up fracture healing in high tibial osteotomy. OE Journal. 2013;1(11):170. Available from: https://myorthoevidence.com/AceReport/Show/single-bisphosphonate-infusion-does-not-speed-up-fracture-healing-in-high-tibial-osteotomy

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