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VALIDATION OF HEARTSBREATH TEST FOR HEART TRANSPLANT REJECTION

VALIDATION OF HEARTSBREATH TEST FOR HEART TRANSPLANT REJECTION
心跳呼吸测试对心脏移植排斥的验证
批准号:
8284347
负责人:
Michael Phillips
金额:
$98.51万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-03-01 至 2013-05-31

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项目成果

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中文摘要
翻译
临床问题:全球每年约有3500人接受心脏移植手术。大多数心脏移植受者在手术后的头12个月内通过一系列心内膜活检来监测器官排斥反应的发展。这个过程是侵入性的,痛苦的,并且有潜在的危险。临床需要一种检测方法来提供与心内膜心肌活检相同的关于心脏移植排斥反应的信息,但没有其侵入性、疼痛性或危害。临床问题的解决方案:心脏呼吸测试是一种本质上安全、无痛、无创的心脏移植排斥呼吸测试,使用挥发性氧化应激生物标志物。在多中心临床研究中,心脏呼吸试验对3级心脏移植排斥反应(现在称为2R级)具有敏感性和特异性。美国食品和药物管理局(FDA)批准了心脏呼吸测试在人道主义设备豁免(HDE)下的临床应用。营销问题:尽管FDA已经批准了该测试的临床应用,但心脏呼吸测试还没有在临床实践中使用,因为它还没有得到保险公司的报销。由于心脏呼吸测试的HDE状态,医疗保险尚未批准心脏呼吸测试的全国覆盖范围确定(NCD)。营销问题的解决方案:医疗保险现在通过其“以数据收集为覆盖条件的全国覆盖范围确定:证据开发的覆盖范围”计划,为心脏呼吸测试提供了保险报销途径。该计划通过开发和捕获额外的患者数据,为心脏呼吸测试提供了一条通往非传染性疾病的途径。实验计划:我们将验证心脏呼吸试验作为预测2R级(以前称为3级)心脏移植排斥反应的准确性,以满足医疗保险非传染性疾病的要求。我们将对1000名在过去12个月内接受过心脏移植的匿名患者进行横断面多中心研究。作为常规临床护理的一部分,我们将在对这些患者进行心肌膜活检之前对其进行心脏呼吸测试,并比较两种测试的结果。该研究的长期目标是:科学:验证心脏呼吸测试作为心脏移植排斥反应呼吸测试的准确性;商业:获得医疗保险非传染性疾病(Medicare NCD)对心脏呼吸测试的报销,并在国内和国际上推广该测试。研究的重要性:在临床实践中,心脏呼吸试验可以为心脏移植排斥反应提供一种完全安全、无创的辅助试验,这将减少与心内膜心肌活检相关的疼痛和发病率,同时也降低了临床护理的成本
英文摘要
DESCRIPTION (provided by applicant): The clinical problem: Approximately 3,500 people worldwide now undergo heart transplantation every year. Most heart transplant recipients are monitored for the development of organ rejection with a series of endomyocardial biopsies during the first twelve months after operation. This procedure is invasive, painful, and potentially hazardous. There is a clinical need for a test to provide the same information about heart transplant rejection as an endomyocardial biopsy, but without its invasiveness, pain, or hazards. A solution to the clinical problem: The Heartsbreath test is an intrinsically safe, painless, and non-invasive breath test for heart transplant rejection that employs volatile biomarkers of oxidative stress. In multicenter clinical studies, the Heartsbreath test was sensitive and specific for Grade 3 heart transplant rejection (now known as Grade 2R). The Food & Drug Administration (FDA) approved the Heartsbreath test for clinical use with a Humanitarian Device Exemption (HDE). The marketing problem: Even though FDA has approved the test for clinical use, the Heartsbreath test is not yet employed in clinical practice because it is not yet reimbursed by insurers. Medicare has not approved a National Coverage Determination (NCD) of the Heartsbreath test because of its HDE status. A solution to the marketing problem: Medicare now offers a pathway to insurance reimbursement of the Heartsbreath test through its program "National Coverage Determinations with Data Collection as a Condition of Coverage: Coverage with Evidence Development". This program offers a pathway to an NCD for the Heartsbreath test by developing and capturing additional patient data. Experimental plans: We will validate the accuracy of the Heartsbreath test as a predictor of Grade 2R (formerly known as Grade 3) heart transplant rejection, in order to fulfill Medicare NCD requirements. We will perform a cross-sectional multicenter study of 1,000 anonymized patients who have received a heart transplant during the preceding 12 months. We will perform a Heartsbreath test on these patients prior to an endomyocardial biopsy performed as part of their regular clinical care, and compare the results of the two tests. The long-term aims of the research are a. Scientific: To validate the accuracy of the Heartsbreath test as a breath test for heart transplant rejection b. Commercial: To obtain Medicare NCD for reimbursement of the Heartsbreath test, and market the test nationally and internationally. The importance of the research: In clinical practice, the Heartsbreath test could provide a completely safe and non-invasive ancillary test for heart transplant rejection that would reduce the pain and morbidity associated with endomyocardial biopsy, while also reducing the costs of clinical care PUBLIC HEALTH RELEVANCE: The Heartsbreath test is an FDA-approved breath test for heart transplant rejection that employs breath biomarkers of oxidative stress. It could provide a safe and non-invasive ancillary test for heart transplant rejection that would reduce the pain and morbidity associated with endomyocardial biopsy, and also reduce the costs of clinical care. We will validate the Heartsbreath test as a predictor of Grade 2R heart transplant rejection in order to fulfill Medicare requirements for reimbursement.
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    2015
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    2014
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海外基金