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首页> 外文期刊>Circulation journal >Multicenter Prospective Investigation on Efficacy and Safety of Garperitide as a First-Line Drug for Acute Heart Failure Syndrome With Preserved Blood Pressure COMPASS: Carperitide Effects Observed Through Monitoring Dyspnea in Acute Decompensated He
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Multicenter Prospective Investigation on Efficacy and Safety of Garperitide as a First-Line Drug for Acute Heart Failure Syndrome With Preserved Blood Pressure COMPASS: Carperitide Effects Observed Through Monitoring Dyspnea in Acute Decompensated He

机译:保留加仑帕比作为急性心衰综合征一线药物的一抗的疗效和安全性的多中心前瞻性研究:通过监测急性代偿失调的呼吸困难观察到的卡培肽作用

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Background Recently, vasodilators have been increasingly being recognized as useful for the treatment of acute heart failure syndromes (AHFS). Although carperitide (a-human atrial natriuretic peptide) has vasodilatory, diuretic and organ-protective effects, its efficacy and safety for the first-line drug treatment of AHFS have not been reported.Methods and Results A prospective observational study was performed in AHFS patients with preserved systolic blood pressure (SBP >120mmHg), pulmonary congestion and dyspnea who were receiving carperitide monotherapy. The analysis was conducted in 1,832 patients (male: 52.7%; mean age: 75.1+-12.7 years). The initial SBP was 151.1+-25.7mmHg; 62.0% were diagnosed as having acutely decompensated chronic heart failure and 78.8% were assessed as functional class III-IV according to New York Heart Association classification. Carperitide was administered at an initial dosage of 0.025-0.05mug~(-1)min~(-1) in 50.4% of patients. In 1,524 patients (83.2%), carperitide monotherapy restored the acute phase and improved the degree of dyspnea as assessed using the modified Borg scale. The incidence of adverse drug reactions was 4.64%; the most frequently reported adverse reaction was hypotension (3.55%).Conclusion In the present study, following carperitide monotherapy, 83.2% of AHFS patients recovered from the acute phase. Based on these findings, carperitide seems useful for the first-line drug treatment of AHFS in patients with pulmonary congestion and preserved blood pressure.
机译:背景技术近来,血管扩张剂已被越来越多地认为可用于治疗急性心力衰竭综合征(AHFS)。尽管卡培肽(a-人心钠素)具有血管舒张,利尿和器官保护作用,但尚未报道其在AHFS一线药物治疗中的疗效和安全性。方法和结果在AHFS患者中进行了前瞻性观察性研究。接受卡培肽单药治疗的患者,其收缩压保持稳定(SBP> 120mmHg),肺充血和呼吸困难。在1,832例患者中进行了分析(男性:52.7%;平均年龄:75.1 + -12.7岁)。初始SBP为151.1 + -25.7mmHg;根据纽约心脏协会的分类,诊断为急性失代偿性慢性心力衰竭的占62.0%,功能性III-IV级的占78.8%。在50.4%的患者中,以0.025-0.05mug〜(-1)min〜(-1)的初始剂量给予卡哌肽。使用改良的Borg量表评估,在1,524例患者(占83.2%)中,卡培肽单药治疗恢复了急性期并改善了呼吸困难的程度。药物不良反应发生率为4.64%。最常见的不良反应是低血压(3.55%)。结论在本研究中,卡培利肽单药治疗后,有83.2%的AHFS患者从急性期康复。基于这些发现,卡培利肽似乎可用于肺充血和血压保持正常的AHFS的一线药物治疗。

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