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首页> 外文期刊>The New England journal of medicine >Cardiovascular events associated with rofecoxib in a colorectal adenoma chemoprevention trial.
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Cardiovascular events associated with rofecoxib in a colorectal adenoma chemoprevention trial.

机译:在结肠直肠腺瘤化学预防试验中与罗非昔布相关的心血管事件。

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BACKGROUND: Selective inhibition of cyclooxygenase-2 (COX-2) may be associated with an increased risk of thrombotic events, but only limited long-term data have been available for analysis. We report on the cardiovascular outcomes associated with the use of the selective COX-2 inhibitor rofecoxib in a long-term, multicenter, randomized, placebo-controlled, double-blind trial designed to determine the effect of three years of treatment with rofecoxib on the risk of recurrent neoplastic polyps of the large bowel in patients with a history of colorectal adenomas. METHODS: A total of 2586 patients with a history of colorectal adenomas underwent randomization: 1287 were assigned to receive 25 mg of rofecoxib daily, and 1299 to receive placebo. All investigator-reported serious adverse events that represented potential thrombotic cardiovascular events were adjudicated in a blinded fashion by an external committee. RESULTS: A total of 46 patients in the rofecoxib group had a confirmed thrombotic event during 3059 patient-years of follow-up (1.50 events per 100 patient-years), as compared with 26 patients in the placebo group during 3327 patient-years of follow-up (0.78 event per 100 patient-years); the corresponding relative risk was 1.92 (95 percent confidence interval, 1.19 to 3.11; P=0.008). The increased relative risk became apparent after 18 months of treatment; during the first 18 months, the event rates were similar in the two groups. The results primarily reflect a greater number of myocardial infarctions and ischemic cerebrovascular events in the rofecoxib group. There was earlier separation (at approximately five months) between groups in the incidence of nonadjudicated investigator-reported congestive heart failure, pulmonary edema, or cardiac failure (hazard ratio for the comparison of the rofecoxib group with the placebo group, 4.61; 95 percent confidence interval, 1.50 to 18.83). Overall and cardiovascular mortality was similar in the two groups. CONCLUSIONS: Among patients with a history of colorectal adenomas, the use of rofecoxib was associated with an increased cardiovascular risk.
机译:背景:选择性抑制环氧合酶2(COX-2)可能与血栓形成事件的风险增加有关,但只有有限的长期数据可用于分析。我们在一项长期,多中心,随机,安慰剂对照,双盲试验中报告了与使用选择性COX-2抑制剂罗非考昔相关的心血管结局,该试验旨在确定罗非考昔三年治疗对罗非考昔的影响。有结直肠腺瘤病史的大肠复发性肿瘤性息肉的风险。方法:共有2586名具有大肠腺瘤病史的患者接受了随机分组:1287名患者每天接受25 mg罗非考昔治疗,1299名患者接受安慰剂治疗。所有由研究者报告的代表潜在血栓性心血管事件的严重不良事件均由外部委员会以盲目方式裁决。结果:罗非昔布组中共有46例患者在3059病人-年的随访期间确认了血栓事件(每100病人-年1.50例事件),而安慰剂组的26例在3327病人-年期间发生了血栓事件。随访(每100个病人年0.78个事件);相应的相对风险为1.92(95%置信区间为1.19至3.11; P = 0.008)。在治疗18个月后,相对危险度明显增加;在最初的18个月中,两组的事件发生率相似。结果主要反映了罗非昔布组中更多的心肌梗塞和缺血性脑血管事件。在非陪审员报告的充血性心力衰竭,肺水肿或心力衰竭的发生率方面,各组之间有较早的分离(大约五个月)(罗非考昔组与安慰剂组比较的危险比为4.61; 95%的置信度区间1.50至18.83)。两组的总体死亡率和心血管死亡率相似。结论:在有结直肠腺瘤病史的患者中,使用罗非昔布与心血管风险增加有关。

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