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艾司洛尔在接受溶栓治疗且对β受体阻滞剂治疗有相对禁忌证的急性心肌梗死患者中的安全性。

Safety of esmolol in patients with acute myocardial infarction treated with thrombolytic therapy who had relative contraindications to beta-blocker therapy.

作者信息

Mooss A N, Hilleman D E, Mohiuddin S M, Hunter C B

机构信息

Coronary Care Unit, Creighton University Medical Center, Omaha, NE.

出版信息

Ann Pharmacother. 1994 Jun;28(6):701-3. doi: 10.1177/106002809402800601.

Abstract

OBJECTIVE

This study was conducted to evaluate the safety of esmolol in 114 patients treated with thrombolytic therapy for acute myocardial infarction who also had relative contraindications to beta-blockade, and the predictive value of patient tolerance to esmolol and subsequent patient tolerance of oral beta-blocker therapy.

PATIENTS

One hundred and fourteen patients with myocardial infarction documented by enzyme concentrations and electrocardiographic changes who also had relative contraindications to beta-blockade.

METHODS

Esmolol was initiated during acute myocardial infarction for myocardial ischemia (n = 88), hypertension (n = 13), or supraventricular tachycardia (n = 13). Relative contraindications to beta-blocker therapy included either active signs/symptoms of left ventricular dysfunction or a history of congestive heart failure (n = 40), a history of chronic obstructive pulmonary disease or asthma (n = 31), bradycardia (HR < 60 beats/min; n = 18), peripheral vascular disease (n = 15), or hypotension (systolic BP < 100 mm Hg; n = 14).

RESULTS

During initial esmolol dose titration, 69 patients tolerated 300 micrograms/kg/min, 12 patients tolerated 200 micrograms/kg/min, 17 patients tolerated 100 micrograms/kg/min, and 16 patients tolerated 50 micrograms/kg/min. Twenty-eight patients (25 percent) developed dose-limiting adverse effects during esmolol maintenance infusions. Sixteen patients required esmolol dose reduction and 12 required esmolol discontinuation. Adverse effects reversed within 30-45 minutes following dose reduction or discontinuation. The 86 patients who tolerated esmolol infusions without dose reduction or drug discontinuation were subsequently treated with oral beta-blockers. Eleven of these patients (13 percent) developed adverse effects requiring oral beta-blocker discontinuation. Nine of these patients had tolerated only 50 micrograms/kg/min of esmolol, and the other 2 patients had tolerated only 100 micrograms/kg/min.

CONCLUSIONS

Esmolol can be used safely in most patients treated with thrombolytic therapy for acute myocardial infarction who have relative contraindications to beta-blockers. Tolerance to higher maintenance doses of esmolol is a good predictor of subsequent outcome with oral beta-blocker therapy.

摘要

目的

本研究旨在评估艾司洛尔在114例接受急性心肌梗死溶栓治疗且有β受体阻滞剂相对禁忌证患者中的安全性,以及患者对艾司洛尔的耐受性和随后对口服β受体阻滞剂治疗的耐受性的预测价值。

患者

114例经酶浓度和心电图变化证实为心肌梗死且有β受体阻滞剂相对禁忌证的患者。

方法

在急性心肌梗死期间,因心肌缺血(n = 88)、高血压(n = 13)或室上性心动过速(n = 13)开始使用艾司洛尔。β受体阻滞剂治疗的相对禁忌证包括左心室功能障碍的活动体征/症状或充血性心力衰竭病史(n = 40)、慢性阻塞性肺疾病或哮喘病史(n = 31)、心动过缓(心率<60次/分钟;n = 18)、外周血管疾病(n = 15)或低血压(收缩压<100 mmHg;n = 14)。

结果

在初始艾司洛尔剂量滴定期间,69例患者耐受300微克/千克/分钟,12例患者耐受200微克/千克/分钟,17例患者耐受100微克/千克/分钟,16例患者耐受50微克/千克/分钟。28例患者(25%)在艾司洛尔维持输注期间出现剂量限制性不良反应。16例患者需要降低艾司洛尔剂量,12例患者需要停用艾司洛尔。不良反应在剂量降低或停药后30 - 45分钟内逆转。86例耐受艾司洛尔输注且未降低剂量或停药的患者随后接受口服β受体阻滞剂治疗。其中11例患者(13%)出现需要停用口服β受体阻滞剂的不良反应。这些患者中有9例仅耐受50微克/千克/分钟的艾司洛尔,另外2例仅耐受100微克/千克/分钟。

结论

艾司洛尔可安全用于大多数接受急性心肌梗死溶栓治疗且有β受体阻滞剂相对禁忌证的患者。对较高维持剂量艾司洛尔的耐受性是随后口服β受体阻滞剂治疗结果的良好预测指标。

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