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首页> 外文期刊>Pakistan Heart Journal >THREE MONTHS CLINICAL OUTCOMES OF DRUG ELUTING STENTS IN PATIENTS WITH STABLE ANGINA PECTORIS
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THREE MONTHS CLINICAL OUTCOMES OF DRUG ELUTING STENTS IN PATIENTS WITH STABLE ANGINA PECTORIS

机译:稳定型心绞痛患者的药物洗脱期三个月临床结果

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Objective: The objective of this study was to determine the frequency of three months clinical outcomes of Drug Eluting Stents in patients with stable angina pectoris. Methodology: This was a cross sectional descriptive study. Patients who were admitted to Cardiology unit Lady Reading Hospital through OPD or casualty department were included in the study. Our study included all the patients with stable coronary artery disease who had received Drug eluting stents from April 01 2011 to July 31 2012. The total study duration was 15 months. The primary end points were, rate of Myocardial infarction (MI), unstable angina(UA) and positive ETT at three months. All patients who underwent Percutaneous coronary intervention with Drug eluting stent for stable angina pectoris were followed and reassessed after 3 months from the index procedure. Exercise Tolerance Test (ETT) was performed on every patient and recorded on proforma. Data analysis was done using SPSS version 16. Results: A total of 376 patients were included in this study. The mean age was 57±9.313 years. Males were 271(72.1%). Majority of the patients got stented to Left anterior descending and left circumflex arteries. Mean length of drug eluting stent was 27.313±7.235 mm while mean diameter of stent was 2.90±0.2483 mm. About 11 (2.9%) patients suffered from MI. About 26 (6.9%) patients had unstable angina and 37 (9.8%) patients had positive ETT at three months followup post PCI. Conclusion: Short-term results from this study suggest that real-world outcomes among 376 patients are comparable to those reported across other registries and trials, and safety outcomes as measured by rates of MI, UA and positive ETT were low. The long-term safety of drug-eluting stents needs to be ascertained in larger randomized trials.
机译:目的:本研究的目的是确定稳定型心绞痛患者三个月药物洗脱支架临床疗效的频率。方法:这是一项横断面描述性研究。通过OPD或伤亡部门被录入心脏病部门Lady Reading医院的患者纳入研究。我们的研究包括所有从2011年4月1日至2012年7月31日接受药物洗脱支架的稳定冠状动脉疾病患者。研究总时间为15个月。主要终点为三个月时的心肌梗死(MI),不稳定型心绞痛(UA)和ETT阳性。随访所有从药物洗脱支架经皮冠状动脉介入治疗稳定型心绞痛的患者,并在索引程序后3个月进行重新评估。对每位患者进行运动耐受力测试(ETT),并记录在形式上。使用SPSS 16版进行数据分析。结果:本研究共纳入376名患者。平均年龄为57±9.313岁。男性为271(72.1%)。多数患者被固定在左前降支和左旋支动脉上。药物洗脱支架的平均长度为27.313±7.235 mm,而支架的平均直径为2.90±0.2483 mm。大约11名(2.9%)患者患有MI。 PCI术后三个月随访时,约有26名患者(6.9%)患有不稳定型心绞痛,而有37名患者(9.8%)ETT呈阳性。结论:这项研究的短期结果表明,在376名患者中的实际结果与在其他注册和试验中报告的结果相当,并且以MI,UA和ETT阳性率衡量的安全性结果较低。在较大的随机试验中需要确定药物洗脱支架的长期安全性。

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