2008
DOI: 10.3310/hta12110
|View full text |Cite
|
Sign up to set email alerts
|

Cyclooxygenase-2 selective non-steroidal anti-inflammatory drugs (etodolac, meloxicam, celecoxib, rofecoxib, etoricoxib, valdecoxib and lumiracoxib) for osteoarthritis and rheumatoid arthritis: a systematic review and economic evaluation

Abstract: Non-UK purchasers will have to pay a small fee for post and packing. For European countries the cost is £2 per monograph and for the rest of the world £3 per monograph.You can order HTA monographs from our Despatch Agents:-fax (with credit card or official purchase order) -post (with credit card or official purchase order or cheque) -phone during office hours (credit card only).Additionally the HTA website allows you either to pay securely by credit card or to print out your order and then post or fax it. NHS … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

3
178
1
31

Year Published

2008
2008
2017
2017

Publication Types

Select...
7
3

Relationship

0
10

Authors

Journals

citations
Cited by 271 publications
(213 citation statements)
references
References 106 publications
(144 reference statements)
3
178
1
31
Order By: Relevance
“…Studies comparing nSAIds with COX-2 inhibitors in patients without underlying liver disease have demonstrated similar effectiveness in the treatment of musculoskeletal pain. 32,33 Although some COX-2 inhibitors may protect against gastrointestinal hemorrhage compared with nSAIds, an increased risk of cardiovascular adverse events has been observed. Cyclooxygenases are highly regulated in response to changes in intravascular volume, and COX-2 is implicated in the mediation of renin release, sodium regulation, and the maintenance of renal blood flow.…”
Section: Acetaminophenmentioning
confidence: 99%
“…Studies comparing nSAIds with COX-2 inhibitors in patients without underlying liver disease have demonstrated similar effectiveness in the treatment of musculoskeletal pain. 32,33 Although some COX-2 inhibitors may protect against gastrointestinal hemorrhage compared with nSAIds, an increased risk of cardiovascular adverse events has been observed. Cyclooxygenases are highly regulated in response to changes in intravascular volume, and COX-2 is implicated in the mediation of renin release, sodium regulation, and the maintenance of renal blood flow.…”
Section: Acetaminophenmentioning
confidence: 99%
“…However, treatment from the post-discontinuation therapy continued for life. Also, several other models, including those by Bessette et al (44), Chen et al (45), and Maetzel et al (21), have used similar maximum treatment lengths. The NICE model (20) utilized a base-case treatment duration of 3 months, but in sensitivity analysis allowed for lifetime treatment.…”
Section: Discussionmentioning
confidence: 99%
“…NICE failed to update this guidance in 2004, when it was due, after rofecoxib was withdrawn; an independent review completed at that time has only recently been published. 3 The current guideline recommends that a traditional NSAID or a COX-2 inhibitor may be offered if a topical NSAID and/or paracetamol are ineffective, but that both standard NSAIDs and COX 2 inhibitors, at the lowest effective dose and for the shortest time necessar y, should be given with a proton pump inhibitor (PPI). A decision to recommend more liberal use of PPIs is surprising and justified by an economic analysis 4 that depends on a number of questionable assumptions and disregards possible differences in cardiovascular risk between different NSAIDs.…”
Section: Cox-2 Inhibitor Technology Appraisalmentioning
confidence: 99%