Garzillo Cibele Larrosa, Hueb Whady, Gersh Bernard, Rezende Paulo Cury, Lima Eduardo Gomes, Favarato Desiderio, Franchini Ramires José Antônio, Kalil Filho Roberto
Instituto do Coração (InCor), Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Department of Medicine, Mayo Clinic College of Medicine, Rochester, Minnesota.
JAMA Intern Med. 2019 Oct 1;179(10):1345-1351. doi: 10.1001/jamainternmed.2019.2227.
The long-term prognostic implications of myocardial ischemia documented during stress testing in patients with multivessel coronary artery disease (CAD) are unclear.
To assess whether documented stress testing-induced myocardial ischemia is associated with major adverse cardiovascular events or ventricular function changes in patients with stable multivessel CAD.
DESIGN, SETTING, AND PARTICIPANTS: A prospective cohort study was conducted using data from a single-center randomized clinical trial (Medicine, Angioplasty, or Surgery Study [MASS] II) to examine the association of myocardial ischemia documented during stress testing at baseline with cardiovascular events and ventricular function changes during follow-up. Participants were previously randomized (May 1, 1995, to May 31, 2000) to medical therapy, percutaneous coronary intervention with bare metal stents, or coronary artery bypass grafting. Event-free survival was estimated by the Kaplan-Meier method, and multivariable Cox regression models were calculated to assess the association between ischemia and the primary composite end point. The vital status was determined on February 28, 2011. Data were analyzed from February 1, 2016, to April 1, 2017.
Cardiovascular events (overall mortality, myocardial infarction, and revascularization for refractory angina) were tracked from the time of randomization to the end of the 10-year follow-up (mean [SD] duration, 11.4 [4.3] years). Myocardial ischemia was assessed at baseline and at 1-year intervals by exercise stress testing, and ventricular function (left ventricular ejection fraction) was assessed by echocardiography at baseline and after 10 years. Patients with documented ischemia were compared with those without ischemia regarding the outcomes and changes in ventricular function.
Of 611 participants, 535 underwent exercise stress testing at baseline: 270 with documented ischemia and 265 without. Of these 535 patients, 373 (69.7%) were men, and the mean (SD) age for the entire cohort was 59.7 (9.2) years. No association was found between the presence of ischemia at baseline and survival free of combined cardiovascular events (hazard ratio, 1.00; 95% CI, 0.80-1.27; P = .95) after multivariable adjustment that included CAD initial randomized treatments. In addition, among 320 patients who underwent echocardiographic evaluation, the slight decline in left ventricular ejection fraction after 10 years was similar in both groups (median [SD] difference, -4.9% [18.7%] vs -6.6% [20.0%], respectively, for groups with and without ischemia; P = .97).
In this study, regardless of the therapeutic strategy applied, the presence of documented myocardial ischemia did not appear to be associated with an increased occurrence of major adverse cardiovascular events or changes in ventricular function in patients with multivessel CAD during a long-term follow-up.
在多支冠状动脉疾病(CAD)患者的负荷试验中记录到的心肌缺血的长期预后影响尚不清楚。
评估在稳定的多支CAD患者中,记录到的负荷试验诱发的心肌缺血是否与主要不良心血管事件或心室功能变化相关。
设计、设置和参与者:一项前瞻性队列研究,使用来自单中心随机临床试验(药物、血管成形术或手术研究[MASS]II)的数据,以检查基线时负荷试验中记录到的心肌缺血与随访期间心血管事件和心室功能变化之间的关联。参与者先前于1995年5月1日至2000年5月31日被随机分配接受药物治疗、裸金属支架经皮冠状动脉介入治疗或冠状动脉旁路移植术。采用Kaplan-Meier方法估计无事件生存期,并计算多变量Cox回归模型以评估缺血与主要复合终点之间的关联。于2011年2月28日确定生命状态。数据分析时间为2016年2月1日至2017年4月1日。
从随机分组时间到10年随访结束(平均[标准差]持续时间,11.4[4.3]年)跟踪心血管事件(全因死亡率、心肌梗死和难治性心绞痛的血运重建)。通过运动负荷试验在基线和每年间隔评估心肌缺血,并通过超声心动图在基线和10年后评估心室功能(左心室射血分数)。比较有记录缺血的患者和无缺血的患者在结局和心室功能变化方面的情况。
611名参与者中,535人在基线时接受了运动负荷试验:270人有记录的缺血,265人无缺血。在这535名患者中,373名(69.7%)为男性,整个队列的平均(标准差)年龄为59.7(9.2)岁。在包括CAD初始随机治疗的多变量调整后,未发现基线时存在缺血与无合并心血管事件的生存期之间存在关联(风险比,1.00;95%CI,0.80-1.27;P = 0.95)。此外,在320名接受超声心动图评估的患者中,两组在10年后左心室射血分数的轻微下降相似(有缺血组和无缺血组的中位数[标准差]差异分别为-4.9%[18.7%]和-6.6%[20.0%];P = 0.97)。
在本研究中,无论应用何种治疗策略,在长期随访中,多支CAD患者中记录到的心肌缺血的存在似乎与主要不良心血管事件的发生率增加或心室功能变化无关。