Development of a POC device to guide efficient use of blood products

开发POC装置以指导血液制品的有效使用

• 批准号: 8885338
• 负责人: FRANCESCO VIOLA
• 金额: $ 99.97万
• 依托单位: HEMOSONICS
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-08-06 至 2017-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8885338
• 关键词: Baltimore; Biomedical Engineering; Blood; Blood Banks; Blood Coagulation Factor; Blood Platelets; Bypass; Cardiac; Clinical; Clinical Research; Coagulation Process; Controlled Environment; Cost Savings; Data; Defect; Development; Devices; Diagnosis; Diagnostic tests; Dose; Europe; European; Evaluation; Fibrinogen; Fibrinolysis; Fresh Frozen Plasmas; Funding Agency; Goals; Hemorrhage; Hemostatic Agents; Hemostatic function; Hospital Mortality; Hospitals; Infection; Legal patent; Length of Stay; Literature; Lung; Military Personnel; Morbidity - disease rate; Neurologic; Operative Surgical Procedures; Outcome; Patient Care; Patients; Performance; Phase; Plasma; Postoperative Period; Procedures; Process; Proteins; Quality Control; Research; Risk; Savings; Series; Small Business Innovation Research Grant; Solutions; Source; System; Technology; Testing; Time; Transfusion; United States; Universities; Virginia; Work; base; blood product; clinical practice; cost; design; experience; high risk; improved; instrument; medical schools; mortality; novel; point of care; point-of-care diagnostics; programs; prototype; public health relevance; trauma care; verification and validation

 DESCRIPTION (provided by applicant): The Problem: The inability of blood to coagulate properly represents a major source of preventable morbidity, mortality, and unnecessary costs. For example, over 60% of the 600,000 patients undergoing cardio- pulmonary bypass (CPB) procedures in the US each year experience excessive bleeding, which requires transfusions of blood products. There are four treatment options available, each corresponding to a specific hemostatic defect: (a) fresh frozen plasma (FFP) to correct the plasma coagulation factors, (b) platelet concentrate to restore platelets, (c) cryoprecipitate to restore fibrinogen, and (d) anti-fibrinolytics to slow the activity of the clot-dissolving proteins. However, clinical literature stongly indicates that morbidity and mortality risks, as well as post-operative length of stay, increase in a dose-dependent way with increased use of blood products. Meanwhile, targeted use of these products can produce savings of up to $4m/year per hospital. Similar reasoning can be extended to any surgical procedure at high risk for major bleeding as well as civilian/military trauma care. Unfortunately, there is no global test of hemostasis available at the point of care (POC), which is able to provide rapid results about the best treatment option. The tests that are available at POC can't provide the required information, even if used in combination. Thus, current clinical practice is iterative transfusion of blood products and subjective evaluation of bleeding. This process is slow and prone to over transfusions, resulting in increased risk of worsened outcomes and unnecessary expenses. HemoSonics' Solution: HemoSonics LLC is developing a novel POC platform device, the Global Hemostasis Analyzer (GHA), to diagnose and guide the treatment of excessive bleeding and overactive clotting in a variety of clinical settings. The GHA is based on a patented technology able to characterize the key components of hemostasis for which a treatment is readily available: coagulation factors, fibrinogen, platelets, and fibrinolysis. We believe the GHA will help: (i) the surgical team administer the correct treatment, (ii) the hospital save costs by reducing unnecessary transfusions, (iii) the blood bank save valuable blood products, and, most importantly, (iv) improve patient care. Proposed SBIR Work: With support from this SBIR program and other sources of funds (including angel investors), we have proven the feasibility of the technology, developed and tested a fully integrated prototype of the GHA. In Phase IIB, we intend to complete design for manufacturing under a quality control environment, complete verification and validation, and submit all the necessary documents required for US and European regulatory approval. This research is a collaborative effort between HemoSonics, the University of Virginia Department of Biomedical Engineering and School of Medicine, and Key Tech Inc (Baltimore, MD).