2008
DOI: 10.1185/030079908x291930
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Intra-articular administration of hylan G-F 20 in patients with symptomatic hip osteoarthritis: tolerability and effectiveness in a large cohort study in clinical practice

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Cited by 35 publications
(25 citation statements)
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“…There is good evidence that BMI does not predict response to COX-2 inhibitors for hip and knee OA management (20,21). The evidence is weak that BMI is not predictive of treatment response to either a multi-modal stepped-care pain management model (18,19), hip CSI (22) hip IA Hylan G-F20 (27), or glucosamine for chronic knee pain (28). The evidence for BMI as a predictor of response to knee IA Hylan G-F is weak and conflicting (23)(24)(25)(26).…”
Section: Body Mass Indexmentioning
confidence: 99%
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“…There is good evidence that BMI does not predict response to COX-2 inhibitors for hip and knee OA management (20,21). The evidence is weak that BMI is not predictive of treatment response to either a multi-modal stepped-care pain management model (18,19), hip CSI (22) hip IA Hylan G-F20 (27), or glucosamine for chronic knee pain (28). The evidence for BMI as a predictor of response to knee IA Hylan G-F is weak and conflicting (23)(24)(25)(26).…”
Section: Body Mass Indexmentioning
confidence: 99%
“…Treatment response was defined as a ≥30% improvement in baseline Lequesne scores or NSAID usage at 6 months, the number of participants classified as responders was unclear. Ten possible predictors of treatment response were analysed, BMI was not a significant predictor of response to hip IA Hylan G-F 20 (27). The large number of drop-outs (42%) affected the validity of this study.…”
Section: Body Mass Indexmentioning
confidence: 99%
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