选择性非甾体抗炎药物的安全性:最近几年的数据分析

N. Shostak, A. Klimenko, N. Demidova, D. A. Anichkov
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引用次数: 2

摘要

非甾体抗炎药(NSAIDs)是最常用的止痛药。然而,非甾体抗炎药的使用往往会带来严重的不良反应,主要是对心血管系统(CVS)、胃肠道、肾脏和肝脏造成损害。非甾体抗炎药处方的禁忌症有明确的规定,在考虑到心血管和胃肠道不良事件的风险因素后,确定了个性化用药的算法。非甾体抗炎药副作用的严重程度主要取决于对环氧化酶-2(COX-2)的选择性以及各种药物的理化性质。各种非甾体抗炎药的心血管不良反应各不相同,既有常用药物之间的差异,也有 COX-2 抑制剂之间的差异。众所周知,就对胃肠道的影响而言,选择性 COX-2 非甾体抗炎药比非选择性药物更安全。一项荟萃分析表明,相对选择性的 COX-2 抑制剂(美洛昔康、依托度酸)发生症状性溃疡和内镜检查发现的溃疡的风险相当,而且药物的安全性和耐受性相似。非甾体抗炎药的心血管不良反应机制与血压升高、钠潴留、血管收缩、血小板活化和促血栓形成状态有关。研究表明,服用 COX-2 抑制剂(塞来昔布、依托昔布)会显著增加心血管不良事件的风险。一项对 800 多万人进行的研究发现,服用酮咯酸的患者发生心肌梗死的风险增加。此外,风险从高到低的作者还列出了吲哚美辛、依托考昔、罗非昔布(目前未使用)、双氯芬酸、双氯芬酸与米索前列醇的固定组合、吡罗昔康、布洛芬、萘普生、塞来昔布、美洛昔康、尼美舒利和酮洛芬。服用非甾体抗炎药时,心衰失代偿的风险会增加,其中以酮咯酸、依托考昔和吲哚美辛的风险最大。美洛昔康、醋氯芬酸、酮洛芬几乎不会增加心衰风险。值得注意的是,在使用这些药物(吲哚美辛和美洛昔康除外)时,随着剂量的增加,心血管和肾脏的总风险有增加的趋势。因此,在选择非甾体抗炎药时显然需要非常谨慎。如果非甾体抗炎药会增加胃肠道并发症的风险,那么选择性非甾体抗炎药是首选,在研究中,coxibs 和传统选择性非甾体抗炎药的安全性最好。为了最大限度地减少心血管副作用,专科医生应考虑心血管并发症的风险水平,以及对特定非甾体抗炎药进行比较的大型临床研究结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety of selective non-steroidal anti-inflammatory drugs: analysis of the last years data
Nonsteroidal anti-inflammatory drugs (NSAIDs) are the most commonly used pain relievers. However, their use often threatens with serious undesirable effects, associated mainly with damage to cardiovascular system (CVS), gastrointestinal tract, kidneys and liver. Contraindications to NSAIDs prescription are clearly regulated, algorithms for their personalized appointment are determined taking into account risk factors for cardiovascular and gastrointestinal adverse events. The severity of NSAIDs side effects is mainly due to the selectivity to cyclooxygenase-2 (COX-2), as well as the physicochemical properties of various drugs. Cardiovascular adverse events differ among various NSAIDs both within commonly used drugs and among COX-2 inhibitors. It is well known that NSAIDs selective for COX-2 are safer in terms of the effect on the gastrointestinal tract than non-selective drugs. A meta-analysis showed that relatively selective COX-2 inhibitors (meloxicam, etodolac) were associated with a comparable risk of developing symptomatic ulcers and ulcers identified by endoscopy, and safety and tolerability profiles of the drugs were similar.All NSAIDs are associated with cardiovascular toxicity, however, different drugs have significant risk differences. The mechanism of NSAIDs cardiovascular adverse effects is associated with an increase of blood pressure, sodium retention, vasoconstriction, platelet activation, and prothrombotic state. It has been shown that the risk of cardiovascular adverse events when taking COX-2 inhibitors (celecoxib, etoricoxib) significantly increases. According to a study of more than 8 million people, it was found that the risk of myocardial infarction was increased in patients taking ketorolac. Further, highest to lowest risk authors list indomethacin, etoricoxib, rofecoxib (not currently used), diclofenac, a fixed combination of diclofenac with misoprostol, piroxicam, ibuprofen, naproxen, celecoxib, meloxicam, nimesulide and ketoprofen. When taking NSAIDs, the risk of heart failure decompensation increases, and it turned out to be the greatest for ketorolac, etoricoxib, and indomethacin. Meloxicam, aceclofenac, ketoprofen almost did not increase heart failure risk. It should be noted that when using the drugs (except for indomethacin and meloxicam), there is a tendency to increase the total cardiovascular and renal risks with increasing doses. Thus, it is obvious that a very careful approach is required when choosing NSAIDs. If there is an increased risk of gastrointestinal complications associated with NSAIDs, selective NSAIDs are preferred, with both coxibs and traditional selective NSAIDs showing the best safety profile in the studies. To minimize cardiovascular side effects specialists should consider the risk level of cardiovascular complications, as well as results of large clinical studies where particular NSAIDs are compared.
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