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Benefits of nifedipine GITS in stable coronary artery disease: Further analysis of the 'ACTION' database.

机译:硝苯地平GITS在稳定冠状动脉疾病中的益处:“ ACTION”数据库的进一步分析。

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INTRODUCTION: Retrospective analyses of specific subgroups of patients from the database of the ACTION study have evaluated the effectiveness of a nifedipine gastrointestinal therapeutic system (GITS) on clinical outcomes. These subgroups included those patients receiving: 1) full "optimal" therapy at baseline; 2) full optimal (RAS)-blocking drugs; 3) treatment with nifedipine GITS who were not treated with RAS blockers versus those treated with RAS blockers but not nifedipine GITS. METHODS: Analyses were performed on an intention-to-treat basis. Treatment groups were compared by log-rank test without adjustment for covariates. Hazard ratios with 95% confidence intervals were obtained using Cox proportional hazards models with treatment allocation as the only covariate. RESULTS: 2461 patients randomized in ACTION were receiving optimal therapy (beta blockers, nitrates, aspirin, statins) excluding RAS blockers at baseline. There were reductions associated with nifedipine GITS compared with placebo in all prespecified endpoints but statistical significance was only achieved for debilitating stroke (48%; P<0.02) and coronary angiography (14%; P<0.05). These benefits were paralleled by a -4.1 and -2.8 mmHg difference between the groups for systolic and diastolic blood pressure, respectively. Patients randomized to nifedipine GITS but no RAS blockers (n=2966) when compared to those receiving RAS blockers but no nifedipine GITS (n=880) had highly statistically significant reductions in cardiovascular events (22%), new-onset heart failure (53%), and debilitating stroke (45%). However, the groups differed in their baseline characteristics. CONCLUSION: Addition of nifedipine GITS to the treatment regimen of selected patient groups with symptomatic coronary artery disease results in a significant reduction of cardiovascular morbidity. While the interpretation of these subgroup analyses must obviously be cautious, there is a clear message relating to "best practice" treatment of angina, which suggests that "reliance" on RAS blockade may be misplaced and greater attention should be directed towards control of blood pressure.
机译:引言:对来自ACTION研究数据库的特定患者亚组的回顾性分析评估了硝苯地平胃肠治疗系统(GITS)对临床结局的有效性。这些亚组包括接受以下治疗的患者:1)基线时完全“最佳”治疗; 2)完全最佳(RAS)阻断药物; 3)与未使用RAS阻断剂治疗但未使用硝苯地平GITS的硝苯地平GITS相比,未使用RAS阻断剂治疗的硝苯地平GITS的治疗。方法:在意向性治疗的基础上进行分析。通过对数秩检验比较治疗组,但不调整协变量。使用Cox比例风险模型(唯一分配为治疗分配)获得具有95%置信区间的风险比率。结果:2461例随机接受ACTION治疗的患者接受了最佳治疗(β受体阻滞剂,硝酸盐,阿司匹林,他汀类药物),基线时不包括RAS阻滞剂。与所有安慰剂相比,硝苯地平GITS均较安慰剂减少,但统计学意义仅在使中风虚弱的中风(48%; P <0.02)和冠状动脉造影(14%; P <0.05)上达到。这些益处与两组的收缩压和舒张压分别相差-4.1和-2.8 mmHg相平行。随机接受硝苯地平GITS但无RAS阻滞剂的患者(n = 2966)与接受RAS阻滞剂但无硝苯地平GITS的患者(n = 880)相比,心血管事件(22%),新发心力衰竭的减少具有统计学意义%)和使人衰弱的中风(45%)。但是,各组的基线特征有所不同。结论:在选定的有症状冠心病患者组中,加用硝苯地平GITS可显着降低心血管疾病的发病率。尽管对这些亚组分析的解释显然必须谨慎,但有一个明确的信息涉及心绞痛的“最佳实践”治疗,这表明对RAS阻滞的“依赖”可能放错了位置,应将更多的注意力转向控制血压。

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