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卡维地洛用于儿童及先天性心脏病患者心力衰竭的疗效与安全性。

Efficacy and safety of carvedilol for heart failure in children and patients with congenital heart disease.

作者信息

Nishiyama Mitsunori, Park In-Sam, Yoshikawa Tadahiro, Hatai Yoshiho, Ando Makoto, Takahashi Yukihiro, Mori Katsuhiko, Murakami Yasuo

机构信息

Department of Pediatrics and Cardiovascular Surgery, Sakakibara Heart Institute, 3-16-1 Asahi-cho Fuchu, Tokyo 183-0003, Japan.

出版信息

Heart Vessels. 2009 May;24(3):187-92. doi: 10.1007/s00380-008-1102-5. Epub 2009 May 24.

Abstract

There have been few reports describing the use of carvedilol in children or patients with congenital heart disease. Therefore, its optimal regimen, efficacy, and safety in these patients have not been adequately investigated. Subjects were 27 patients with two functioning ventricles, for whom carvedilol was initiated (from December 2001 to December 2005) to treat heart failure. All patients had failed to respond to conventional cardiac medication. They consisted of 12 males and 15 females, aged 23 days to 47 years (median age: 2 years). Heart failure due to ischemia (myocardial infarction, intraoperative ischemic event) or due to myocardial disease (cardiomyopathy, myocarditis), and heart failure with atrial or ventricular tachyarrhythmia represented 70% of all cases. Carvedilol was initiated at a dose of 0.02-0.05 mg/kg/day, which was increased by 0.05-0.1 mg/kg/day after 2 days, 0.1 mg/kg/day after 5 days, and 0.05-0.1 mg/kg/day every month thereafter with a target dose of 0.8 mg/kg/day. This study retrospectively assessed the efficacy and adverse reactions based on changes of symptoms, cardiothoracic ratio (CTR), left ventricular ejection fraction (LVEF), and human atrial natriuretic peptide (hANP)/b-type natriuretic peptide (BNP) blood levels. The mean follow-up period was 10.2 months (range: 1-46 months). Twenty-six (96.3%) patients showed improvement in symptoms and were discharged from the hospital. However, the remaining one patient failed to respond and died. Significant cardiovascular adverse reaction was seen in none of the patients. The mean CTR decreased from 61.8% +/- 5.3% before treatment to 57.6% +/- 7.4% after treatment (P < 0.05, n = 25), and the mean LVEF improved from 41.4% +/- 23.1% to 61.1% +/- 10.1% (P < 0.05, n = 10), respectively. Mean hANP and BNP levels showed a decrease from 239.1 pg/ml to 118.3 pg/ml and a significant decrease from 437.9 pg/ml to 120.5 pg/ml, respectively (P < 0.05, n = 10). Improvements in these data were also demonstrated when analyzed individually among the pediatric group (aged younger than 18) and the congenital heart disease group. Initiation of carvedilol at a lower dose with more gradual dose escalation, compared with previously reported regimens, might have efficacy with low incidence of adverse effects in pediatric patients and patients with congenital heart disease. Carvedilol may be effective in treating heart failure in children due to ischemia, myocardial disease, and complicated by tachyarrhythmia.

摘要

鲜有报告描述卡维地洛在儿童或先天性心脏病患者中的应用情况。因此,其在这些患者中的最佳用药方案、疗效及安全性尚未得到充分研究。研究对象为27例具有双心室功能的患者,于2001年12月至2005年12月开始使用卡维地洛治疗心力衰竭。所有患者对传统心脏药物治疗均无反应。其中男性12例,女性15例,年龄23天至47岁(中位年龄:2岁)。因缺血(心肌梗死、术中缺血事件)或心肌疾病(心肌病、心肌炎)导致的心力衰竭,以及伴有房性或室性快速心律失常的心力衰竭占所有病例的70%。卡维地洛起始剂量为0.02 - 0.05 mg/kg/天,2天后剂量增加0.05 - 0.1 mg/kg/天,5天后增加0.1 mg/kg/天,此后每月增加0.05 - 0.1 mg/kg/天,目标剂量为0.8 mg/kg/天。本研究基于症状变化、心胸比率(CTR)、左心室射血分数(LVEF)以及人心房利钠肽(hANP)/B型利钠肽(BNP)血药浓度,对疗效和不良反应进行了回顾性评估。平均随访期为10.2个月(范围:1 - 46个月)。26例(96.3%)患者症状改善并出院。然而,其余1例患者无反应并死亡。所有患者均未出现明显的心血管不良反应。平均CTR从治疗前的61.8%±5.3%降至治疗后的57.6%±7.4%(P < 0.05,n = 25),平均LVEF分别从41.4%±23.1%提高至61.1%±10.1%(P < 0.05,n = 10)。平均hANP和BNP水平分别从239.1 pg/ml降至118.3 pg/ml以及从437.9 pg/ml显著降至120.5 pg/ml(P < 0.05,n = 10)。在儿科组(年龄小于18岁)和先天性心脏病组中单独分析时,这些数据也显示出改善。与先前报道的用药方案相比,以较低剂量起始并更缓慢地增加剂量使用卡维地洛,可能在儿科患者和先天性心脏病患者中具有疗效且不良反应发生率较低。卡维地洛可能对因缺血、心肌疾病以及并发快速心律失常导致的儿童心力衰竭有效。

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