Kenchaiah Satish, Davis Barry R, Braunwald Eugene, Rouleau Jean-Lucien, Dagenais Gilles R, Sussex Bruce, Steingart Richard M, Brown Edward J, Lamas Gervasio A, Gordon David, Bernstein Victoria, Pfeffer Marc A
Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Am Heart J. 2004 Aug;148(2):356-64. doi: 10.1016/j.ahj.2004.02.011.
Hypertension is a well-established risk factor for myocardial infarction (MI), but its prognostic importance in survivors of an acute MI is less clear.
We used Cox proportional hazards models to examine the risk of any major cardiovascular event (cardiovascular death, heart failure, recurrent MI, or stroke)-combined or individual components-and all-cause death and evaluate the efficacy of captopril in 906 patients with hypertension and 1325 patients without hypertension in the Survival and Ventricular Enlargement (SAVE) clinical trial. All patients had survived an acute MI with resultant left ventricular (LV) systolic dysfunction, but without overt heart failure, and were randomized within 3 to 16 days after the index MI to receive either captopril or placebo. The mean (+/- SD) follow-up period was 42 +/- 10 months.
After adjustment for known risk factors, medication use at enrollment, and baseline systolic blood pressure, patients with hypertension had a significant increase in the risk of experiencing a combined cardiovascular event (47.7% vs 31.3%; hazard ratio [HR], 1.49; 95% CI, 1.28-1.74), cardiovascular death (23.4% vs 15.9%; HR, 1.40; 95% CI, 1.12-1.74), heart failure (27.7% vs 15.5%; HR, 1.64; 95% CI, 1.34-2.02), and all-cause death (27.4 vs 19.3%; HR, 1.25; 95% CI, 1.02-1.53), and a similar but statistically non-significant increase in the risk of non-fatal or fatal recurrent MI (17.4% vs 10.9%; HR, 1.27; 95% CI, 0.98-1.65), and non-fatal or fatal stroke (5.0% vs 3.6%; HR, 1.31; 95% CI, 0.81-2.09). Captopril resulted in similar benefits for both patients with and patients without hypertension. The number of combined cardiovascular events prevented for every 100 patients treated with captopril was 7.0 (95% CI, 0.5-13.5) in patients with hypertension and 7.5 (95% CI, 2.6-12.5) in patients without hypertension.
In survivors of an acute MI with LV systolic dysfunction, antecedent hypertension was associated with a greater risk of subsequent adverse cardiovascular events, not directly explained by elevated blood pressure levels. Captopril use was beneficial in both patients with and patients without hypertension.
高血压是心肌梗死(MI)公认的危险因素,但其在急性心肌梗死幸存者中的预后重要性尚不清楚。
我们使用Cox比例风险模型,在生存与心室扩大(SAVE)临床试验中,研究了906例高血压患者和1325例非高血压患者发生任何主要心血管事件(心血管死亡、心力衰竭、复发性心肌梗死或中风)——合并或单独成分——以及全因死亡的风险,并评估卡托普利的疗效。所有患者均在急性心肌梗死后存活,伴有左心室(LV)收缩功能障碍,但无明显心力衰竭,并在索引心肌梗死后3至16天内随机接受卡托普利或安慰剂治疗。平均(±标准差)随访期为42±10个月。
在对已知危险因素、入组时的用药情况和基线收缩压进行调整后,高血压患者发生合并心血管事件的风险显著增加(47.7%对31.3%;风险比[HR],1.49;95%可信区间[CI],1.28 - 1.74)、心血管死亡(23.4%对15.9%;HR,1.40;95%CI,1.12 - 1.74)、心力衰竭(27.7%对15.5%;HR,1.64;95%CI,1.34 - 2.02)和全因死亡(27.4%对19.3%;HR,1.25;95%CI,1.02 - 1.53),非致命或致命复发性心肌梗死(17.4%对10.9%;HR,1.27;95%CI,0.98 - 1.65)和非致命或致命中风(5.0%对3.6%;HR,1.31;95%CI,0.81 - 2.09)的风险有类似但无统计学意义的增加。卡托普利对高血压患者和非高血压患者均产生了类似的益处。每100例接受卡托普利治疗的高血压患者预防的合并心血管事件数量为7.0(95%CI,0.5 - 13.5),非高血压患者为7.5(95%CI,2.6 - 12.5)。
在伴有左心室收缩功能障碍的急性心肌梗死幸存者中,既往高血压与随后发生不良心血管事件的风险更高相关,这不能直接由血压升高水平解释。使用卡托普利对高血压患者和非高血压患者均有益。