Venous Thrombosis After Traumatic Injury
外伤后静脉血栓形成
基本信息
- 批准号:10655727
- 负责人:
- 金额:$ 68.5万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-08-15 至 2027-07-31
- 项目状态:未结题
- 来源:
- 关键词:ADAMTSAccelerationAddressAdhesivesArtificial IntelligenceBindingBiological AssayBiological MarkersBloodBlood Coagulation DisordersBlood Coagulation FactorBlood PlateletsBlood VesselsBlood specimenBody mass indexCalibrationCategoriesCessation of lifeCharacteristicsChemoprophylaxisClinicalClinical DataCoagulation ProcessCollaborationsComplexComplicationConsumptionDataDeep Vein ThrombosisDeoxyribonuclease IDepositionDevelopmentDisciplineElementsEndothelial CellsEndotheliumEtiologyEventFactor VIII-Related AntigenFibrinFibrinogenFosteringFoundationsFunctional disorderFutureGenerationsGoalsHealthHealthcare SystemsHemorrhageHemostatic functionHospitalizationHyperactivityIncidenceIndividualInjuryInterventionJointsKineticsKnowledgeLaboratoriesLigandsMachine LearningModelingMolecular ConformationMonitorMultiple TraumaMusOutcomePathogenesisPatientsPlasmaPlayProcessProtein-arginine deiminasePulmonary EmbolismQuality of CareRNARecommendationResearch PersonnelRiskRisk AssessmentRisk FactorsRoleSamplingScienceScientific InquirySensitivity and SpecificitySiteSmokingSurgeonTestingTherapeuticThrombinThrombophiliaThrombosisTimeTissue SampleTraumaTrauma patientTraumatic injuryUnited StatesUnited States National Institutes of HealthVenous Thrombosisaptamerarmcleavage factorclinically significantcostdiagnostic strategydiverse dataexperienceextracellularhigh riskimprovedimproved outcomeinjuredinsightmouse modelneutrophilnew therapeutic targetnovelpatient populationpredictive markerpreventsexstatisticssyndecantherapeutic targettissue injurytreatment strategyvenous thromboembolismvon Willebrand Factor
项目摘要
PROJECT SUMMARY
Venous thromboembolism (VTE) continues to be a major health problem with over 500,000 VTE events in the
US annually. Venous thromboembolism costs more than $8 billion per year to our health care system and causes
more than 100,000 deaths per year in the US alone. Venous thromboembolism is particularly problematic in
patients who experience trauma. Despite administration of chemoprophylaxis to trauma patients during
hospitalization, about 5% of patients still develop symptomatic VTE prior to discharge, and, more alarmingly, 40
- 60% of patients who develop symptomatic VTE, do so after discharge. An accurate assessment of traumatic-
injury based coagulopathies remains dependent on unavailable basic scientific knowledge needed to address
the National Institutes of Health (NIH) initiative of defining the “role of laboratory monitoring…to help better define
those at risk of bleeding and thrombosis.” To understand the etiologies of trauma-induced venous
thromboembolism, a comprehensive approach that assesses plasma coagulation factor activities, platelet
reactivity, and endothelial function within the context of pre-trauma patient characteristics (sex, BMI, smoking
etc.) and “real-time” blood studies at the time of trauma is required”. Obtaining integrated lab and clinical data
from a diverse trauma patient population is not readily feasible in a single investigator’s laboratory or site. The
long-term goal is to develop novel predictive, diagnostic and treatment strategies that identify “at risk” individuals
for VTE or bleeding soon after trauma. Our Central Hypothesis is that clinically significant thrombosis requires
the integrated dysregulation of NETosis, thrombin generation, endothelial injury, and von Willebrand factor-
platelet dysfunction. Our collaboration embodies all of the elements needed to improve the quality of care of
trauma patients. The investigators are from multiple health-related professions and this leverages experiences
and knowledge from different, but related disciplines. Our collaboration also encourages and fosters scientific
inquiry with the scientific expertise that will create and disseminate new knowledge and applications. Finally, the
team science approach that we have culminated is expected to provide for the highest quality of care and
improvement of trauma health outcomes.
项目摘要
静脉血栓栓塞(VTE)仍然是一个主要的健康问题,其中超过500,000个VTE事件
我们每年。我们的医疗保健系统每年的静脉血栓栓塞费用超过80亿美元
仅在美国,每年就有100,000多人死亡。静脉血栓主义在
经历创伤的患者。尽管在创伤患者中施用了化学预防
住院,约有5%的患者在出院前仍会出现症状性VTE,更令人震惊的是40
-60%发生症状性VTE的患者,出院后这样做。对创伤的准确评估
基于伤害的凝血病仍然取决于无法解决的基本科学知识
国家卫生研究院(NIH)定义“实验室监测的作用……帮助更好地定义
那些有出血和血栓形成的风险。”
血栓栓塞,一种评估血浆凝血因子活动的综合方法,血小板
在创伤前患者特征(性,BMI,吸烟)的背景下,反应性和内皮功能
等等)和“实时”血液研究需要在创伤时”。获得综合实验室和临床数据
在单个研究者的实验室或现场,来自潜水员创伤的患者人群不容易可行。这
长期目标是制定新颖的预测性,诊断和治疗策略,以识别“处于危险”的个人
在创伤后不久进行VTE或出血。我们的中心假设是临床意义的血栓形成需要
Netosis,凝血酶产生,内皮损伤和von Willebrand因子的综合失调 -
血小板功能障碍。我们的合作体现了提高护理质量所需的所有要素
创伤患者。调查人员来自多个与健康相关的专业人员,并利用经验
以及来自不同但相关学科的知识。我们的合作也鼓励并培养科学
询问将创建和传播新知识和应用的科学专业知识。最后,
我们达到高潮的团队科学方法将提供最高质量的护理和
改善创伤健康结果。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Matthew Auton其他文献
Matthew Auton的其他文献
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{{ truncateString('Matthew Auton', 18)}}的其他基金
Structure-Resolved Mechanistic Phenotyping of Von Willebrand Disease
冯维勒布兰德病的结构解析机制表型
- 批准号:
10188620 - 财政年份:2020
- 资助金额:
$ 68.5万 - 项目类别:
Structure-Resolved Mechanistic Phenotyping of Von Willebrand Disease
冯维勒布兰德病的结构解析机制表型
- 批准号:
10440371 - 财政年份:2020
- 资助金额:
$ 68.5万 - 项目类别:
Structure-Resolved Mechanistic Phenotyping of Von Willebrand Disease
冯维勒布兰德病的结构解析机制表型
- 批准号:
10677858 - 财政年份:2020
- 资助金额:
$ 68.5万 - 项目类别:
Thermodynamics of the Conformational Activation of Von Willebrand Factor
冯维勒布兰德因子构象激活的热力学
- 批准号:
8683219 - 财政年份:2011
- 资助金额:
$ 68.5万 - 项目类别:
Thermodynamics of the Conformational Activation of Von Willebrand Factor
冯维勒布兰德因子构象激活的热力学
- 批准号:
8302350 - 财政年份:2011
- 资助金额:
$ 68.5万 - 项目类别:
Thermodynamics of the Conformational Activation of Von Willebrand Factor
冯维勒布兰德因子构象激活的热力学
- 批准号:
8497717 - 财政年份:2011
- 资助金额:
$ 68.5万 - 项目类别:
Thermodynamics of the Conformational Activation of Von Willebrand Factor
冯维勒布兰德因子构象激活的热力学
- 批准号:
8155294 - 财政年份:2011
- 资助金额:
$ 68.5万 - 项目类别:
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