课题基金 / 基金详情

ACE INHIBITION IN SINGLE VENTRICLE/PULMON. HYPERTENSION

ACE INHIBITION IN SINGLE VENTRICLE/PULMON. HYPERTENSION
单心室/肺动脉的 ACE 抑制。
批准号:
6652128
负责人:
WELTON M GERSONY
金额:
$47.55万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-09-05 至 2006-08-31

项目摘要

项目成果

WELTON M GERSONY的其他基金

相关文献

中文摘要
翻译
描述(由申请人提供) 本应用程序的总体目标是检查以下治疗方式 可提高两组先天性心脏病患者的临床护理水平 疾病:婴儿出生时只有一个脑室向 肺与身体和儿童的肺动脉高压相关 先天性心脏病。单纯性结肠炎患儿的基本假设 心室是慢性血管紧张素转换酶(ACE)的抑制 有利地改变对容量超负荷的心室重塑反应和 在生命的第一年改善心脏功能。中的系列更改 将使用磁共振成像和 与收缩和舒张期功能的测量相比较,包括 压力/体积关系和Tei指数,以及临床结果测量 包括手术后的进程和罗斯的变化?心力衰竭 分类。血管紧张素转换酶抑制的有益效果有望出现 双向Glenn减容手术前后的对比研究 分流或半方坦。先天性心脏病研究的基本假设 与肺动脉高压相关的疾病是远期疗效 口服前列环素类似物或口服内皮素受体治疗 阻滞剂对运动能力、寿命和运动质量有有益的作用 生活。还将确定这些患者中是否有任何人带有缺陷 原发性肺动脉高压-1基因的突变。这些研究中的每一个都可以 潜在地导致预后的显著改善:在单一 防止脑室长期恶化的脑室组 功能和在肺动脉高压患者中通过提高质量 不需要移植的生命和生存。
英文摘要
DESCRIPTION (provided by applicant) The overall goal of this application is to examine treatment modalities which may improve the clinical care of two groups of patients with congenital heart disease: infants born with a single ventricle supplying blood flow to the lungs and body and children with pulmonary hypertension associated with congenital heart disease. The primary hypothesis in infants with single ventricle is that chronic angiotensin converting enzyme (ACE) inhibition favorably modifies the ventricular remodeling response to volume overload and improves ventricular function over the first year of life. Serial changes in ventricular geometry will be assessed using magnetic resonance imaging and compared with measurements of systolic and diastolic function, including the pressure/volume relation and the Tei index, and clinical outcome measures including post-operative course and changes in the Ross? heart failure classification. The beneficial effect of ACE inhibition is expected to occur prior to and following volume unloading surgery with the bidirectional Glenn shunt or hemi-Fontan. The primary hypothesis of the study in congenital heart disease associated with pulmonary hypertension is that the effect of long-term treatment with an oral prostacyclin analogue or an oral endothelin receptor blocker has a salutory effect on exercise capacity, longevity, and quality of life. It will also be determined whether any of these patients carry a defect of the primary pulmonary hypertension-1 gene. Each of these studies could potentially lead to a significant improvement in prognosis: in the single ventricle group by preventing a long-term deterioration in ventricular function and in the pulmonary hypertension patients by improving quality of life and survival without transplantation.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
KAWASAKI DISEASE STUDY
Trial of Pulse Steroid Therapy in Kawaski Disease
ACE INHIBITION IN SINGLE VENTRICLE/PULMON. HYPERTENSION
ACE INHIBITION IN SINGLE VENTRICLE/PULMON. HYPERTENSION