The effect of tirofiban on ST segment resolution in patients with non-ST elevated myocardial infarction.

Ozgür Bayturan, Ali Riza Bilge, Cevad Seküri, Ozan Utük, Hakan Tikiz, Erhan Eser, Ugur Kemal Tezcan
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引用次数: 2

Abstract

ST segment resolution in ST elevated myocardial infarction has independent predictive value for congestive heart failure and death at 30 days. ST segment depression in unstable angina pectoris (UAP) and non-ST elevated myocardial infarction (NSTEMI) predicts high risk of MI and death and may discriminate patients likely to have greater benefit from aggressive antithrombotic and interventional therapy. This study assessed the effect of tirofiban added to conventional treatment on ST segment resolution in NSTEMI patients. Sixty-four patients were randomized to one of the two groups: 32 patients received conventional treatment while tirofiban was added in the second group of 32 patients. In the first group, 6 patients refused to participate further after giving initial informed consent while 1 patient in the tirofiban group dropped out. We had 26 patients (mean age, 59 years) in the conventional treatment group and 31 patients (mean age, 59 years) received also tirofiban. Tirofiban was administered by intravenous infusion over a 72 hour period. More than 50% regression of depression was considered to be ST segment resolution. The characteristics of the two groups were comparable (Table I). The ST segment resolution evolution did not differ at the 4th and 24th hours between the two groups. Significant differences occurred in the 72nd hour ECG (Table III). ST resolution was present in 67.9% of the tirofiban patients and in 32.1% of the conventional treatment group (P < 0.05). Tirofiban treatment was not associated with an increase in major bleeding even though there was a trend toward an increase in minor bleeding cases and did not influence the occurrence of refractory angina pectoris.

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替罗非班对非ST段升高型心肌梗死患者ST段溶解的影响。
ST段升高的心肌梗死ST段分辨率对30天内充血性心力衰竭和死亡有独立的预测价值。不稳定心绞痛(UAP)和非ST段升高型心肌梗死(NSTEMI)的ST段下降预示着心肌梗死和死亡的高风险,并可能区分出可能从积极抗栓和介入治疗中获益更多的患者。本研究评估了替罗非班在常规治疗基础上对非stemi患者ST段溶解的影响。64名患者被随机分为两组:32名患者接受常规治疗,而在第二组32名患者中加入替罗非班。第一组有6例患者在初步知情同意后拒绝进一步参与,替罗非班组有1例患者退出。26例患者(平均年龄59岁)为常规治疗组,31例患者(平均年龄59岁)同时接受替罗非班治疗。替罗非班在72小时内静脉输注。50%以上的抑郁回归被认为是ST段的消退。两组的特征具有可比性(表1)。两组在第4和24小时的ST段分辨率演变无差异。第72小时心电图差异有统计学意义(表III)。替罗非班组67.9%的患者ST消退,常规治疗组32.1% ST消退(P < 0.05)。替罗非班治疗与大出血的增加无关,即使有轻微出血病例增加的趋势,也不影响难治性心绞痛的发生。
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