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直接经皮冠状动脉介入治疗延迟对死亡率的影响:急性心肌梗死试验中佩昔单抗评估的见解

Mortality implications of primary percutaneous coronary intervention treatment delays: insights from the Assessment of Pexelizumab in Acute Myocardial Infarction trial.

作者信息

Hudson Michael P, Armstrong Paul W, O'Neil William W, Stebbins Amanda L, Weaver W Douglas, Widimsky Petr, Aylward Philip E, Ruzyllo Witold, Holmes David, Mahaffey Kenneth W, Granger Christopher B

机构信息

Henry Ford Heart & Vascular Institute, Detroit, MI 48202, USA.

出版信息

Circ Cardiovasc Qual Outcomes. 2011 Mar;4(2):183-92. doi: 10.1161/CIRCOUTCOMES.110.945311. Epub 2011 Feb 8.

Abstract

BACKGROUND

Prior studies demonstrate a direct relationship between treatment delays to primary percutaneous intervention and mortality in patients with ST-segment elevation myocardial infarction (STEMI). This analysis compared the relationship of symptom onset-to-balloon time and door-to-balloon time on mortality in patients with STEMI.

METHODS AND RESULTS

We analyzed different treatment delays (symptom onset-to-balloon time, door-to-balloon time) and mortality in 5745 STEMI patients. Baseline characteristics, flow grade, 90-day mortality, and clinical outcomes were compared in patients stratified by treatment delay. Multivariable logistic regression modeling was performed to assess the independent and relative effect of each treatment delay on 90-day mortality. Female sex, increased age, and worse thrombolysis in myocardial infarction flow grade were significantly associated with longer symptom onset-to-balloon times and door-to-balloon times. Longer symptom onset-to-balloon time was significantly associated with worse 90-day mortality (3.7%, 4.2%, and 6.5% for time delays <3 hours, 3 to 5 hours, and >5 hours, respectively, P<0.0001). Similarly, longer door-to-balloon times were significantly associated with worse 90-day mortality (3.2%, 4.0%, 4.6%, and 5.3% for delays <60 minutes, 60 to 90 minutes, 90 to 120 minutes, and ≥120 minutes respectively, P<0.0001). In a multivariate model of 90-day mortality, door-to-balloon time (χ(2) 6.0, P<0.014), and symptom onset-to-hospital arrival (χ(2) 9.8, P<0.007) remained independent determinants.

CONCLUSIONS

Both symptom onset-to-balloon time and hospital door-to-balloon time are strongly associated with 90-day mortality following STEMI. Clinical Trial Registration- URL: http://www.clinicaltrials.gov. Unique identifier: NCT00091637.

摘要

背景

既往研究表明,ST段抬高型心肌梗死(STEMI)患者接受直接经皮冠状动脉介入治疗的延迟时间与死亡率之间存在直接关系。本分析比较了STEMI患者症状发作至球囊扩张时间和门至球囊扩张时间与死亡率的关系。

方法与结果

我们分析了5745例STEMI患者的不同治疗延迟时间(症状发作至球囊扩张时间、门至球囊扩张时间)及死亡率。对按治疗延迟时间分层的患者的基线特征、血流分级、90天死亡率及临床结局进行了比较。进行多变量逻辑回归建模,以评估每种治疗延迟时间对90天死亡率的独立及相对影响。女性、年龄增加及心肌梗死血流分级较差与较长的症状发作至球囊扩张时间和门至球囊扩张时间显著相关。较长的症状发作至球囊扩张时间与较差的90天死亡率显著相关(延迟时间<3小时、3至5小时及>5小时的死亡率分别为3.7%、4.2%及6.5%,P<0.0001)。同样,较长的门至球囊扩张时间与较差的90天死亡率显著相关(延迟时间<60分钟、60至90分钟、90至120分钟及≥120分钟的死亡率分别为3.2%、4.0%、4.6%及5.3%,P<0.0001)。在90天死亡率的多变量模型中,门至球囊扩张时间(χ(2) 6.0,P<0.014)及症状发作至入院时间(χ(2) 9.8,P<0.007)仍是独立的决定因素。

结论

症状发作至球囊扩张时间及医院门至球囊扩张时间均与STEMI后的90天死亡率密切相关。临床试验注册-网址:http://www.clinicaltrials.gov。唯一标识符:NCT00091637。

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