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The Efficacy and Safety of Vertebral Augmentation : A Second ASBMR Task Force Report

Ebeling, Peter R. (author)
Monash University
Akesson, Kristina (author)
Lund University,Lunds universitet,Ortopedi - klinisk och molekylär osteoporosforskning,Forskargrupper vid Lunds universitet,Orthopedics - Clinical and Molecular Osteoporosis Research,Lund University Research Groups
Bauer, Douglas C. (author)
University of California, San Francisco
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Buchbinder, Rachelle (author)
Monash University
Eastell, Richard (author)
University of Sheffield
Fink, Howard A. (author)
University of Minnesota
Giangregorio, Lora (author)
University of Waterloo
Guanabens, Nuria (author)
University of Barcelona
Kado, Deborah (author)
University of California, San Diego
Kallmes, David (author)
Mayo Clinic Minnesota
Katzman, Wendy (author)
University of California, San Francisco
Rodriguez, Alexander (author)
Monash University
Wermers, Robert (author)
Mayo Clinic Minnesota
Wilson, H. Alexander (author)
No affiliation available (private)
Bouxsein, Mary L. (author)
Beth Israel Deaconess Medical Center
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 (creator_code:org_t)
2019-01-24
2019
English 19 s.
In: Journal of Bone and Mineral Research. - : Wiley. - 0884-0431 .- 1523-4681. ; 34:1, s. 3-21
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Vertebral augmentation is among the current standards of care to reduce pain in patients with vertebral fractures (VF), yet a lack of consensus regarding efficacy and safety of percutaneous vertebroplasty and kyphoplasty raises questions on what basis clinicians should choose one therapy over another. Given the lack of consensus in the field, the American Society for Bone and Mineral Research (ASBMR) leadership charged this Task Force to address key questions on the efficacy and safety of vertebral augmentation and other nonpharmacological approaches for the treatment of pain after VF. This report details the findings and recommendations of this Task Force. For patients with acutely painful VF, percutaneous vertebroplasty provides no demonstrable clinically significant benefit over placebo. Results did not differ according to duration of pain. There is also insufficient evidence to support kyphoplasty over nonsurgical management, percutaneous vertebroplasty, vertebral body stenting, or KIVA®. There is limited evidence to determine the risk of incident VF or serious adverse effects (AE) related to either percutaneous vertebroplasty or kyphoplasty. No recommendation can be made about harms, but they cannot be excluded. For patients with painful VF, it is unclear whether spinal bracing improves physical function, disability, or quality of life. Exercise may improve mobility and may reduce pain and fear of falling but does not reduce falls or fractures in individuals with VF. General and intervention-specific research recommendations stress the need to reduce study bias and address methodological flaws in study design and data collection. This includes the need for larger sample sizes, inclusion of a placebo control, more data on serious AE, and more research on nonpharmacologic interventions. Routine use of vertebral augmentation is not supported by current evidence. When it is offered, patients should be fully informed about the evidence. Anti-osteoporotic medications reduce the risk of subsequent vertebral fractures by 40–70%.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Ortopedi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Orthopaedics (hsv//eng)

Keyword

KYPHOPLASTY
OSTEOPOROSIS
VERTEBRAL AUGMENTATION
VERTEBRAL FRACTURE
VERTEBROPLASTY

Publication and Content Type

art (subject category)
ref (subject category)

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