"Pathophysiologic mapping" of venous thromboembolism: opportunities for radiolabeled peptides.

M P Bernarducci
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Abstract

The serious clinical and economic impact of venous thromboembolic (VTE) disease is undisputed. What concerns practitioners and researchers alike is the seeming inability to truly mitigate the ramifications of VTE. Ironically, the current approaches to the diagnostic evaluation of suspected VTE patients tends to favor the application of anatomic modalities, which by virtue of their principles of detection, seemingly ignore the extensive knowledge base of VTE pathophysiology and natural history. In other words, are we seeking the appropriate types of information in patients with suspected VTE? Research in nuclear medicine techniques for detecting VTE began approximately 25 years ago. Recently, the emergence of the radiolabeled peptides as a clinically applicable technology platform has encouraged a different way of evaluating VTE. Many radiolabeled peptide candidates are undergoing preclinical and clinical research. Currently, only one, (99m)Tc-apcitide (AcuTect), has been approved (since 1998) for clinical use, specifically in the United States. Its availability this time has fueled ongoing clinical research to further elucidate the benefits of this unique peptide technology. Consequently, significant insight has been gained from large prospective clinical trials. Furthermore, this insight has kindled increasing interest in (99m)Tc-apcitide and potential new entrants into this special "diagnostic class". Unlike the more popular modalities, radiolabeled peptides circumvent many of the clinical and anatomic challenges to objectively and accurately diagnosing VTE. The importance of an objective and accurate diagnosis is understood, because it is paramount to a cost-effective treatment strategy. In addition to describing the current activities concerning the development for and use of radiolabeled peptides for clinical practice, this manuscript is intended to promulgate a thought-provoking argument for changing our current approach to the diagnostic evaluation of VTE. Despite technological and medical advances, we continue to debate controversial issues in VTE, which seemingly and arguably disproportionately, focus on treatment (i.e., who?, when?, how much? and for how long?). Should we not adopt a more robust approach to VTE problem-solving, which would logically start with the diagnosis? Perhaps the validated and perceived advantages of the radiolabeled peptides are all the rationale we need to advance beyond the status quo? Only time and continued research will tell.

静脉血栓栓塞的“病理生理制图”:放射性标记肽的机会。
静脉血栓栓塞(VTE)疾病的严重临床和经济影响是无可争议的。从业人员和研究人员同样关心的是,似乎无法真正减轻静脉血栓栓塞的后果。具有讽刺意味的是,目前对疑似静脉血栓栓塞患者的诊断评估方法往往倾向于应用解剖模式,由于其检测原理,似乎忽略了静脉血栓栓塞病理生理学和自然史的广泛知识基础。换句话说,我们是否在寻找可疑静脉血栓栓塞患者的适当类型的信息?检测静脉血栓栓塞的核医学技术研究大约始于25年前。最近,放射性标记肽作为一种临床应用的技术平台的出现,鼓励了一种评估静脉血栓栓塞的不同方法。许多放射性标记的候选肽正在进行临床前和临床研究。目前,只有一种(99m)Tc-apcitide (AcuTect)被批准(自1998年以来)用于临床使用,特别是在美国。它的可用性这次推动了正在进行的临床研究,以进一步阐明这种独特的肽技术的好处。因此,从大型前瞻性临床试验中获得了重要的见解。此外,这一发现还激发了人们对(99m)Tc-apcitide的兴趣,以及这一特殊“诊断类”的潜在新进入者。与更流行的方式不同,放射性标记肽绕过了客观准确诊断静脉血栓栓塞的许多临床和解剖学挑战。客观和准确诊断的重要性是可以理解的,因为它对于具有成本效益的治疗策略至关重要。除了描述目前有关临床实践中放射性标记肽的开发和使用的活动外,本文还旨在为改变我们目前对静脉血栓栓塞的诊断评估方法提出一个发人深省的论点。尽管技术和医学取得了进步,但我们仍在继续争论静脉血栓栓塞的争议性问题,这些问题似乎不成比例地关注于治疗(即谁?,更待何时?多少钱?能维持多久?)我们是否应该采用一种更可靠的方法来解决静脉血栓栓塞问题,从逻辑上讲,这种方法应该从诊断开始?也许放射性标记肽的验证和感知优势是我们需要超越现状的所有理由?只有时间和持续的研究才能告诉我们答案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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