利用心内膜入路给药治疗血管生成:技术和结果。

Garcia, Baim, Post, Simons, Laham
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引用次数: 0

摘要

各种血管生成生长因子和基因治疗载体的可用性,以及它们在慢性心肌缺血动物模型中血管生成潜力的证明,推动了它们在缺血性心脏病患者血管生成治疗性临床试验中的研究。尽管大多数临床前研究采用了延长给药时间和局部治疗的方法,但重复给药和侵入性通路的需要限制了这些给药策略的临床实用性。冠状动脉内和静脉内给药,由于其潜在的广泛适用性,促进了它们在大多数治疗性血管生成的临床试验中的应用;然而,显著的全身再循环、有限的心肌保留和潜在的严重全身不良事件是其临床应用的主要限制。心外膜手术入路已在若干临床研究中使用,但手术入路和全身麻醉的需要可能限制了该技术的有效性。使用透视引导或Biosense NOGA (Biosense Laboratories, Haifa, Israel)电磁三维导航系统的经皮心内膜输送导管的发展已经引起了人们对在治疗性心肌血管生成研究中使用这种输送策略的极大兴趣。这些策略正在临床前研究中进行深入研究,随后将进行临床研究。我们描述了这些给药装置的有限经验。
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Therapeutic Angiogenesis Using Endocardial Approach to Administration: Techniques and Results.

The availability of various angiogenic growth factors and gene therapy vectors, and the demonstration of their angiogenic potential in animal models of chronic myocardial ischemia, has propelled their investigation in clinical trials of therapeutic angiogenesis in patients with ischemic heart disease. Although most preclinical studies have employed methods of prolonged drug delivery and local therapy, the need for repeated administration and invasive access has limited the clinical usefulness of these delivery strategies. Intracoronary and intravenous delivery, with their potential widespread applicability, has fueled their use in most clinical trials of therapeutic angiogenesis; however, the significant systemic recirculation, limited myocardial retention, and potential for serious systemic adverse events are major limitations to their clinical use. Epicardial delivery using surgical access has been used in several clinical studies, but the need for surgical access and general anesthesia may limit the usefulness of this technique. The development of percutaneous endocardial delivery catheters using fluoroscopic guidance or Biosense NOGA (Biosense Laboratories, Haifa, Israel) electromagnetic three- dimensional navigation system has generated significant interest in the use of this delivery strategy in therapeutic myocardial angiogenesis studies. These strategies are being intensively investigated in preclinical studies with clinical studies soon to follow. We describe the limited experience with these drug delivery devices.

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