PM&R
Volume 2, Issue 4 , Pages 259-267, April 2010

Efficacy and Safety of Hylan G-F 20 for Symptomatic Glenohumeral Osteoarthritis: A Prospective, Pilot Study

  • Victoria Anne Brander, MD

      Affiliations

    • Physical Medicine and Rehabilitation, Northwestern University Feinberg School of Medicine, Northwestern Orthopedic Institute, 680 North Lake Shore Drive, Suite 1028, Chicago, IL 60611
    • Corresponding Author InformationAddress correspondence to: V.A.B.
  • ,
  • Ameer Gomberawalla, MS

      Affiliations

    • Northwestern University Feinberg School of Medicine, Chicago, IL
  • ,
  • Michelle Chambers, MS, PA

      Affiliations

    • Northwestern Memorial Hospital, Northwestern Orthopedic Institute, Chicago, IL§
  • ,
  • Mark Bowen, MD

      Affiliations

    • Orthopedic Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL
  • ,
  • Gordon Nuber, MD

      Affiliations

    • Orthopedic Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL

Received 9 June 2009; accepted 24 February 2010.

Objective

To determine the safety and efficacy of 2 intra-articular, fluoroscopically guided hylan G-F 20 injections for painful glenohumeral osteoarthritis.

Design

This study was a prospective open-label pilot investigation with both U.S. Food and Drug Administration and institutional review board approval.

Setting

Private, outpatient practice within a tertiary care, university medical school.

Participants

Thirty-six subjects with moderate to severe glenohumeral osteoarthritis, with pain (visual analog scale [VAS] 40 mm or greater) despite following a 3-month standard, nonsurgical treatment program.

Interventions

Two injections of 2 mL hylan G-F 20, under fluoroscopic guidance confirmed by arthrography, 2 weeks apart. No new treatments were allowed during the course of the study. Analgesics were discontinued 24 hours before visits.

Main Outcome Measurements

Data collected were radiographs; rotator cuff integrity as determined with magnetic resonance imaging; VAS for pain at rest, at night, and with activity; and shoulder-related quality of life (Western Ontario Rotator Cuff Index [WORC]). Subjects were re-evaluated after each injection and at 6 weeks, 3 months, and 6 months. Changes from baseline for VAS and WORC were recorded in Excel and analyzed using SPSS. Intent-to-treat analysis was performed. The type and severity of adverse events were recorded.

Results

Mean VAS at baseline was 63 mm (SD 14.5). Clinically (≥20% improvement) and statistically significant improvements (P < .001) in VAS pain were seen at 6 weeks, 3 months, and 6 months. Mean improvement in WORC at 6 months was 16.5 (P < .01), with most gains in “lifestyle” and “emotion” questions. Age, gender, body mass index, and rotator cuff pathology did not correlate with response. Three subjects described heightened pain for a few days after injections. Three subjects reported greater pain at 6 months and were unsatisfied. Four experienced no effect of treatment. There were no inflammatory reactions.

Conclusion

Two hylan G-F 20 injections improved pain and function, and should be considered as part of a multimodal shoulder osteoarthritis treatment program.

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  •  Disclosure: 2A, Genzyme; 3A, Genzyme; 7B, Genzyme Biosurgery
  •  Disclosure: nothing to disclose
  • § Disclosure: nothing to disclose
  •  Disclosure: nothing to disclose
  •  Disclosure: nothing to disclose

 Disclosure Key can be found on the Table of Contents and at www.pmrjournal.org

 This study was funded, in part, by an investigator-initiated grant from Genzyme Biosurgery, who also provided partial support to a medical writer for assistance in manuscript preparation.

PII: S1934-1482(10)00135-8

doi:10.1016/j.pmrj.2010.02.010

PM&R
Volume 2, Issue 4 , Pages 259-267, April 2010