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Recommendations of the OARSI FDA Osteoarthritis Devices Working Group.

Publication ,  Journal Article
Goldberg, VM; Buckwalter, J; Halpin, M; Jiranek, W; Mihalko, W; Pinzur, M; Rohan, B; Vail, T; Walker, P; Windsor, R; Wright, T
Published in: Osteoarthritis Cartilage
May 2011

Osteoarthritis (OA) is the most common type of arthritis and a major cause of chronic musculoskeletal pain and functional disability. While both pharmacologic and non-pharmacologic modalities are recommended in the management of OA, when patients with hip or knee OA do not obtain adequate pain relief and/or functional improvement, joint replacement surgery or other surgical interventions should be considered. Total joint arthroplasties are reliable and cost-effective treatments for patients with significant OA of the hip and knee. Evidence from cohort and observational studies has confirmed substantial improvements in pain relief with cumulative revision rates at 10 years following total hip (THA) and total knee arthroplasties (TKA) at 7% and 10%, respectively. Joint replacements have been used in most every synovial joint, although results for joints other than hip and knee replacement have not been as successful. The evolution of new device designs and surgical techniques highlights the need to better understand the risk to benefit ratio for different joint replacements and to identify the appropriate methodology for evaluating the efficacy and optimal outcomes of these new devices, designed to treat OA joints.

Duke Scholars

Published In

Osteoarthritis Cartilage

DOI

EISSN

1522-9653

Publication Date

May 2011

Volume

19

Issue

5

Start / End Page

509 / 514

Location

England

Related Subject Headings

  • Treatment Outcome
  • Risk Assessment
  • Osteoarthritis
  • Joint Prosthesis
  • Humans
  • Device Approval
  • Arthroplasty, Replacement
  • Arthritis & Rheumatology
  • 4207 Sports science and exercise
  • 3202 Clinical sciences
 

Citation

APA
Chicago
ICMJE
MLA
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Goldberg, V. M., Buckwalter, J., Halpin, M., Jiranek, W., Mihalko, W., Pinzur, M., … Wright, T. (2011). Recommendations of the OARSI FDA Osteoarthritis Devices Working Group. Osteoarthritis Cartilage, 19(5), 509–514. https://doi.org/10.1016/j.joca.2011.02.017
Goldberg, V. M., J. Buckwalter, M. Halpin, W. Jiranek, W. Mihalko, M. Pinzur, B. Rohan, et al. “Recommendations of the OARSI FDA Osteoarthritis Devices Working Group.Osteoarthritis Cartilage 19, no. 5 (May 2011): 509–14. https://doi.org/10.1016/j.joca.2011.02.017.
Goldberg VM, Buckwalter J, Halpin M, Jiranek W, Mihalko W, Pinzur M, et al. Recommendations of the OARSI FDA Osteoarthritis Devices Working Group. Osteoarthritis Cartilage. 2011 May;19(5):509–14.
Goldberg, V. M., et al. “Recommendations of the OARSI FDA Osteoarthritis Devices Working Group.Osteoarthritis Cartilage, vol. 19, no. 5, May 2011, pp. 509–14. Pubmed, doi:10.1016/j.joca.2011.02.017.
Goldberg VM, Buckwalter J, Halpin M, Jiranek W, Mihalko W, Pinzur M, Rohan B, Vail T, Walker P, Windsor R, Wright T. Recommendations of the OARSI FDA Osteoarthritis Devices Working Group. Osteoarthritis Cartilage. 2011 May;19(5):509–514.
Journal cover image

Published In

Osteoarthritis Cartilage

DOI

EISSN

1522-9653

Publication Date

May 2011

Volume

19

Issue

5

Start / End Page

509 / 514

Location

England

Related Subject Headings

  • Treatment Outcome
  • Risk Assessment
  • Osteoarthritis
  • Joint Prosthesis
  • Humans
  • Device Approval
  • Arthroplasty, Replacement
  • Arthritis & Rheumatology
  • 4207 Sports science and exercise
  • 3202 Clinical sciences