Cardiovascular safety of non-steroidal anti-inflammatory drugs among healthy individuals

被引:34
作者
Fosbol, Emil Loldrup [1 ]
Kober, Lars [2 ]
Torp-Pedersen, Christian
Gislason, Gunnar H.
机构
[1] Copenhagen Univ Hosp Gentofte, Dept Cardiol, Hellerup, Denmark
[2] Rigshosp, Copenhagen Univ Hosp, Ctr Heart, Copenhagen, Denmark
关键词
cancer bleeding complications; cardiovascular death; cause-specific mortality; myocardial infarction; NSAIDs; selective COX-2 inhibitors; stroke; ACUTE MYOCARDIAL-INFARCTION; CONGESTIVE-HEART-FAILURE; LOW-DOSE ASPIRIN; SERIOUS GASTROINTESTINAL COMPLICATIONS; SELECTIVE CYCLO-OXYGENASE-2 INHIBITORS; ADENOMA CHEMOPREVENTION TRIAL; CYCLOOXYGENASE-2; INHIBITORS; BLOOD-PRESSURE; RHEUMATOID-ARTHRITIS; COX-2;
D O I
10.1517/14740338.2010.501331
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Importance of the field: Studies have raised concern on the cardiovascular safety of NSAIDs. We studied safety of NSAID therapy in a nationwide cohort of healthy individuals. Areas covered in this review: This is a review of the literature regarding cardiovascular safety of NSAIDs with special focus on the few studies investigating healthy individuals. What the reader will gain: Due to a high frequency of gastrointestinal complications related to NSAID treatment a new generation of NSAID, called the selective COX-2 inhibitors, were developed in order to use the beneficial pain-relieving effect of NSAIDs without the COX-1 related risk of gastrointestinal bleeding. However, the selective COX-2 inhibitor rofecoxib was withdrawn from the market in 2004 after studies had documented an increased risk of myocardial infarction related to this drug. Focus also turned to the traditional NSAIDs and found similar results for some of the older drugs, especially diclofenac and high-dose ibuprofen. Most interventional studies have not been designed specifically to evaluate the cardiovascular safety of NSAIDs and no studies have previously investigated the relationship between NSAID treatment and cardiovascular risk in healthy individuals. Overall, evidence regarding the selective COX-2 inhibitors' cardiovascular risk profile ( mostly thrombo-embolic events) is derived from the clinical trials whereas results on the traditional NSAIDs are based on observational studies and meta-analyses. Importantly, some of the randomized trials comparing COX-2 inhibitors with traditional NSAIDs did not show a difference in cardiovascular risk and it cannot be denied that the traditional NSAIDs are characterized by a different cardiovascular risk-profile than the COX-2 inhibitors. A recent cohort study among one million healthy people showed that the selective COX-2 inhibitors as well as diclofenac are associated with an increased risk of death or myocardial infarction. This was further underlined by a dose-response relationship. Take home message: Individual NSAIDs have different cardiovascular safety that needs to be considered when choosing appropriate treatment. In particular, rofecoxib and diclofenac were associated with increased cardiovascular mortality and morbidity and should be used with caution in most individuals. This notion is also valid for healthy individuals and underlines the importance of critical use of NSAID therapy in the general population and also that over-the-counter retail of NSAIDs should be reassessed.
引用
收藏
页码:893 / 903
页数:11
相关论文
共 88 条
[1]
Use of first- and second-generation cyclooxygenase-2 selective nonsteroidal antiinflammatory drugs and risk of acute myocardial infarction [J].
Andersohn, F ;
Suissa, S ;
Garbe, E .
CIRCULATION, 2006, 113 (16) :1950-1957
[2]
[Anonymous], PLOS CLIN TRIALS
[3]
Use of nonsteroidal Antiinflammatory drugs an update for clinicians - A scientific statement from the American Heart Association [J].
Antman, Elliott M. ;
Bennett, Joel S. ;
Daugherty, Alan ;
Furberg, Curt ;
Roberts, Harold ;
Taubert, Kathryn A. .
CIRCULATION, 2007, 115 (12) :1634-1642
[4]
Cyclooxygenase inhibition and cardiovascular risk [J].
Antman, EM ;
DeMets, D ;
Loscalzo, J .
CIRCULATION, 2005, 112 (05) :759-770
[5]
Use of cyclo-oxygenase 2 inhibitors (COX-2) and prescription non-steroidal anti-inflammatory drugs (NSAIDS) in UK and USA populations. Implications for COX-2 cardiovascular profile [J].
Arellano, Felix M. ;
Yood, Marianne Ulcickas ;
Wentworth, Charles E. ;
Oliveria, Susan A. ;
Rivero, Elena ;
Verma, Anila ;
Rothman, Kenneth J. .
PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2006, 15 (12) :861-872
[6]
Meta-analysis of cyclooxygenase-2 inhibitors and their effects on blood pressure [J].
Aw, TJ ;
Haas, SJ ;
Liew, D ;
Krum, H .
ARCHIVES OF INTERNAL MEDICINE, 2005, 165 (05) :490-496
[7]
Cardiovascular events associated with rofecoxib: final analysis of the APPROVe trial [J].
Baron, John A. ;
Sandler, Robert S. ;
Bresalier, Robert S. ;
Lanas, Angel ;
Morton, Dion G. ;
Riddell, Robert ;
Iverson, Erik R. ;
DeMets, David L. .
LANCET, 2008, 372 (9651) :1756-1764
[8]
A randomized trial of rofecoxib for the chemoprevention of colorectal adenomas [J].
Baron, John A. ;
Sandler, Robert S. ;
Bresalier, Robert S. ;
Quan, Hui ;
Riddell, Robert ;
Lanas, Angel ;
Bolognese, James A. ;
Oxenius, Bettina ;
Horgan, Kevin ;
Loftus, Susan ;
Morton, Dion G. .
GASTROENTEROLOGY, 2006, 131 (06) :1674-1682
[9]
Intestinal permeability in the pathogenesis of NSAID-induced enteropathy [J].
Bjarnason, Ingvar ;
Takeuchi, Ken .
JOURNAL OF GASTROENTEROLOGY, 2009, 44 :23-29
[10]
Critical role of COX-1 in prostacyclin production by human endothelial cells under modification of hydroperoxide tone [J].
Bolego, Chiara ;
Buccellati, Carola ;
Prada, Alberto ;
Gaion, Rosa Maria ;
Folco, Giancarlo ;
Sala, Angelo .
FASEB JOURNAL, 2009, 23 (02) :605-612