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非糖尿病患者 C 反应蛋白水平升高行冠状动脉成形术后口服免疫抑制剂泼尼松的长期结果。

Long-term results of immunosuppressive oral prednisone after coronary angioplasty in non-diabetic patients with elevated C-reactive protein levels.

机构信息

Division of Cardiology of the Università di Verona, Verona, Italy.

出版信息

EuroIntervention. 2009 Jun;5(2):250-4. doi: 10.4244/eijv5i2a39.

Abstract

AIMS

To present the long-term results of prednisone-treated patients enrolled in the IMPRESS studies. Such studies demonstrated the efficacy of a short course of immunosuppression with oral prednisone after percutaneous coronary intervention (PCI) with bare metal stent (BMS) implantation compared to BMS alone at one year.

METHODS AND RESULTS

Eighty-four non-diabetic patients with elevated C-reactive protein after PCI treated with BMS and prednisone, were followed clinically for a minimum of five years. Event-free survival was defined as freedom from death, myocardial infarction, and need for target vessel revascularisation. Event-free survival rate at a mean of 6.5 +/- 1.4 years was significantly better in prednisone-treated patients of the IMPRESS and IMPRESS-2/MVD respectively compared to their original control arms: 87.8 versus 47.6%, relative risk: 7.9; 95%CI: 2.6-24.1, p<0.0001, log-rank=13.06, p=0.0003; and 93 versus 60.5%, relative risk: 8.7; 95%CI: 2.3-32.7, p=0.0004, log-rank=13,18, p=0.0003, respectively. The event-free survival was 54.1% in controls and 90.5% in the prednisone group; relative risk: 8.1; 95%CI: 3.5-18.7, p<0.0001, log-rank= 26.33, p<0.0001.

CONCLUSIONS

The clinical benefits of oral treatment with prednisone after conventional PCI in non-diabetic patients with evidence of systemic inflammation after stenting are maintained at long-term follow-up, either in patients with single or multivessel coronary artery disease.

摘要

目的

介绍接受 IMPRESS 研究中泼尼松治疗的患者的长期结果。这些研究表明,与单独使用裸金属支架(BMS)相比,在经皮冠状动脉介入治疗(PCI)后使用 BMS 联合口服泼尼松进行短期免疫抑制治疗在一年时具有疗效。

方法和结果

84 名接受 PCI 治疗的非糖尿病患者,在 PCI 后 BMS 联合泼尼松治疗后,C 反应蛋白升高,这些患者在临床随访至少 5 年。无事件生存定义为无死亡、心肌梗死和需要靶血管血运重建。在平均 6.5±1.4 年时,IMPRESS 和 IMPRESS-2/MVD 中接受泼尼松治疗的患者的无事件生存率明显优于各自的原始对照组:分别为 87.8%和 47.6%,相对风险:7.9;95%CI:2.6-24.1,p<0.0001,对数秩检验=13.06,p=0.0003;和 93%和 60.5%,相对风险:8.7;95%CI:2.3-32.7,p=0.0004,对数秩检验=13,18,p=0.0003。对照组的无事件生存率为 54.1%,泼尼松组为 90.5%;相对风险:8.1;95%CI:3.5-18.7,p<0.0001,对数秩检验=26.33,p<0.0001。

结论

在有支架后全身炎症证据的非糖尿病患者中,常规 PCI 后接受口服泼尼松治疗的临床获益在长期随访中得到维持,无论是在单支血管还是多支血管冠状动脉疾病患者中。

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