Key result
The presence of an effusion requiring aspiration at the onset of hylan G-F 20 viscosupplementation did not negatively impact efficacy, with 0 adverse events occurring in either group.
Why the study?
Does the presence of an effusion requiring aspiration diminish the efficacy of hylan G-F 20 in patients with knee osteoarthritis?
Cohort (n=100)
Does the presence of an effusion requiring aspiration diminish the efficacy of hylan G-F 20 in patients with knee osteoarthritis?
The presence of an effusion requiring aspiration does not negatively impact the efficacy or safety of hylan G-F 20 injections for knee osteoarthritis.
An effusion at the onset of viscosupplementation has been thought to diminish the efficacy and increase adverse event rates. This study compares efficacy of hylan G-F 20 in patients with and without an effusion. Patients with knee osteoarthritis (OA) received three weekly injections of hylan G-F 20. A total of 50 patients with an effusion requiring aspiration were compared with 50 matched patients without an effusion. Outcome measurements included Western Ontario and McMaster's Universities Osteoarthritis index (WOMAC) and visual analog scale (VAS). Patients were followed for 26 weeks. Both effusion and control group VAS was significantly lowered at all time points. WOMAC scores improved (p < 0.025) at all visits in the effusion group except for WOMAC A-1 week 14. Control WOMAC scores also significantly improved at all visits (p < 0.027), except for full WOMAC and WOMAC A-1 at week 1. Neither group experienced an adverse event. Presence of an effusion at onset of viscosupplementation requiring aspiration does not negatively impact efficacy of hylan G-F 20 or increase adverse event rates.
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Waddell et al. (2014) conducted a cohort in Knee osteoarthritis (n=100). Presence of an effusion requiring aspiration vs. Matched patients without an effusion was evaluated on Western Ontario and McMaster's Universities Osteoarthritis index (WOMAC) and visual analog scale (VAS). The presence of an effusion requiring aspiration at the onset of hylan G-F 20 viscosupplementation did not negatively impact efficacy, with 0 adverse events occurring in either group.
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