Etoricoxib improves pain, function and quality of life: results of a real-world effectiveness trial

Objective:  To evaluate the effectiveness and tolerability of etoricoxib in patients with osteoarthritis (OA) with suboptimal response to existing pain regimens. Methods:  A multicenter, prospective, open‐label, single‐arm study. OA patients (n = 500) taking nonsteroidal anti‐inflammatory drugs (NSA...

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Veröffentlicht in:International journal of rheumatic diseases 2010-05, Vol.13 (2), p.144-150
Hauptverfasser: LIN, Hsiao-Yi, CHENG, Tien-Tsai, WANG, Jyh-Horng, LEE, Chyou-Shen, CHEN, Ming-Han, LEI, Vanessa, LAC, Christina, GAMMAITONI, Arnold R., SMUGAR, Steven S., CHEN, Wen-Jer
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Sprache:eng
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Zusammenfassung:Objective:  To evaluate the effectiveness and tolerability of etoricoxib in patients with osteoarthritis (OA) with suboptimal response to existing pain regimens. Methods:  A multicenter, prospective, open‐label, single‐arm study. OA patients (n = 500) taking nonsteroidal anti‐inflammatory drugs (NSAIDs) or other analgesics who had inadequate response as determined by their physicians (≥ 40 mm on a 0–100 mm pain scale) were switched directly to etoricoxib 60 mg once daily for 4 weeks without prior medication washout. The primary endpoint was the percentage of patients with ≥ 30% improvement in Western Ontario McMaster Universities Osteoarthritis Index (WOMAC) pain walking on a flat surface after 4 weeks of treatment. Other endpoints included WOMAC Pain, Stiffness, and Physical Function subscales, Brief Pain Inventory (BPI), investigator’s global assessment of response to therapy (IGART), the Treatment Satisfaction Questionnaire for Medication (TSQM) and Short Form 36 (SF36). Safety and tolerability were assessed by collecting adverse events. Results:  After switching to etoricoxib, 52% (95% confidence interval: 47%, 57%) of patients reported a clinically meaningful reduction (≥ 30%) for WOMAC pain walking on a flat surface. Disability in daily activities and pain interference were significantly improved (P 
ISSN:1756-1841
1756-185X
DOI:10.1111/j.1756-185X.2010.01468.x