...
首页> 外文期刊>Open Heart >Original research: Cardiogenic shock after ST elevation myocardial infarction and IABP-SHOCK II risk score validation in a cohort treated with pharmacoinvasive strategy
【24h】

Original research: Cardiogenic shock after ST elevation myocardial infarction and IABP-SHOCK II risk score validation in a cohort treated with pharmacoinvasive strategy

机译:原始研究:在以药物侵入性疗法治疗的队列中,ST抬高型心肌梗死后的心源性休克和IABP-SHOCK II风险评分验证

获取原文

摘要

Objective To validate the Intra-aortic Balloon Pump in Cardiogenic Shock II (IABP-SHOCK II) score in patients with cardiogenic shock after ST elevation myocardial infarction (STEMI) treated with pharmacoinvasive strategy (PhIS) and to analyse the influence of ischaemia time on different risk strata.Methods We analysed 2143 patients with STEMI who underwent reperfusion with tenecteplase in primary health services between May 2010 and April 2017 and were transferred to a tertiary hospital for cardiac catheterisation and continuity of care. Those who evolved to cardiogenic shock were scored as low (0–2), moderate (3–4) or high (5–9) risk of death in 30 days and pairwise-log-rank test was used to compare strata. Time intervals between symptoms onset and lytic (pain-to-needle) and fibrinolytic-catheterisation were also compared.Results Cardiogenic shock occurred in 212 (9.9%) individuals. The 30-day mortality using the IABP-SHOCK II score was 26.6% for low-risk (n=94), 53.2% for moderate-risk (n=62) and 76% for high-risk (n=25) analysed patients (p0.001). Validation of the score showed good discrimination for death, area under the curve of 0.73 (CI: 0.66 to 0.81;?p0.001). The median intervals of pain-to-needle and fibrinolytic-catheterisation showed no association with the group stratification (220 vs 251 vs 200?min; p=0.22?and 390 vs 435 vs 315?min; p=0.18, respectively).Conclusions In patients with cardiogenic shock after STEMI treated with PhIS, risk stratification using IABP-SHOCK II score was adequate. There was no influence of pain-to-needle and fibrinolytic-catheterisation times on the ability to the score model stratification.
机译:目的验证药物侵入性策略(PhIS)治疗ST段抬高型心肌梗死(STEMI)后心源性休克患者的主动脉内球囊泵性心源性休克II(IABP-SHOCK II)评分,并分析缺血时间对不同时间的影响方法我们分析了2010年5月至2017年4月之间在初级卫生服务中接受替奈普酶再灌注的2143例STEMI患者,并将其转移到三级医院进行心脏导管插入术和连续治疗。那些演变为心源性休克的患者在30天内被分为低(0–2),中度(3–4)或高(5–9)死亡风险,并使用成对对数秩检验进行分层比较。还比较了症状发作与溶栓(针刺)和纤维蛋白溶导管插入之间的时间间隔。结果心源性休克发生在212位(9.9%)个体中。使用IABP-SHOCK II评分的30天死亡率,低危(n = 94)为26.6%,中危(n = 62)为53.2%,高危(n = 25)患者为76% (p <0.001)。得分的验证显示出对死亡的良好辨别力,曲线下面积为0.73(CI:0.66至0.81;Δp<0.001)。针刺和纤溶导管插入术的中位间隔与组分层无关(分别为220 vs 251 vs 200?min; p = 0.22?和390 vs 435 vs 315?min; p = 0.18)。在用PhIS治疗STEMI后发生心源性休克的患者中,使用IABP-SHOCK II评分进行危险分层是足够的。针刺时间和纤溶导尿时间对评分模型分层的能力没有影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号