Point-of-care system to assess the risk of trauma-induced acute respiratory distress syndrome
Point-of-care system to assess the risk of trauma-induced acute respiratory distress syndrome
批准号:
10594793
负责人:
Ian M White
金额:
$39.28万
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
未结题
起止时间:
2023-03-01 至 2025-01-31
关键词:
Accident and Emergency departmentAcuteAcute Respiratory Distress SyndromeAdmission activityAlkanesAnti-Inflammatory AgentsAntibodiesAutomationBenchmarkingBindingBiological AssayBloodBlood VesselsBlood capillariesBlood specimenBody partCell DeathCellsCirculationClinicalCytolysisDNADataDeath RateDetectionDiagnosticEarly DiagnosisEdemaEnvironmentEnzyme-Linked Immunosorbent AssayFingersFreeze DryingGoalsHemorrhageHeparinHistonesImmuneIncidenceInfectionInflammatory ResponseInjuryIntellectual PropertyInvestmentsLabelLifeLinkLungManualsMeasurementMeasuresMorbidity - disease rateOperating RoomsOpticsOrganOutcomePatient riskPatientsPerformancePhasePoint-of-Care SystemsPreventive treatmentReagentRefrigerationReportingResearchRespiration DisordersRiskRisk AssessmentSamplingSecureShockSyndromeSystemTechnologyTemperatureThrombosisTraumaTrauma patientTraumatic injuryTubeVacuumValidationVenousWhole Bloodcommercializationdesigndiagnostic technologiesdiagnostic toolimprovedinnovationinstrumentinventionlung failurelung injurymeetingsmortalityneutrophilpoint of carepoint of injuryportabilitypreservationpreventprototypesample collectiontrauma centers
中文摘要
项目概要/摘要
创伤引起的急性呼吸功能障碍综合征 (ARDS) 是一种致命疾病,导致肺衰竭
由身体另一部位遭受外伤所致。最近,多项研究建立了联系
循环组蛋白和肺衰竭之间的关系。外伤导致大量细胞死亡,
导致高浓度的组蛋白释放到循环中,这可以直接导致 ARDS,如
组蛋白会损害肺部。此外,循环组蛋白加剧了夸大的亲和抗-
炎症反应也会导致肺部和其他器官受损。识别和
创伤触发的循环组蛋白的量化将提供一种评估 ARDS 风险的方法,
这可以在患者出现 ARDS 之前进行挽救生命的治疗。提供早期诊断解决方案
创伤后组蛋白的检测应该是便携式且快速的,以便在创伤后不久对患者进行评估
发生伤害。然而,目前还没有可移植且快速的方法来检测
循环组蛋白来评估创伤患者发生 ARDS 的风险。我们的目标是开发一种诊断方法
能够在护理时定量评估创伤引起的 ARDS 风险的工具。这可能
包括在受伤时、在前往创伤中心的运输车辆中、在急诊室 (ED) 中,或
在手术室(OR)。我们发明了一种便携式组蛋白检测技术 (PHAST),可以
在 30 分钟内直接对全血中的循环组蛋白进行定量。
。
英文摘要
PROJECT SUMMARY/ABSTRACT
Trauma-induced acute respiratory dysfunction syndrome (ARDS) is a deadly condition in which lung failure
results from a traumatic injury to another part of the body. Recently, several studies have established a link
between circulating histones and lung failure. Traumatic injuries cause a massive amount of cell death,
resulting in the release of high concentrations of histones into circulation, which can directly lead to ARDS, as
histones damage the lungs. In addition, circulating histones exacerbate exaggerated pro- and anti-
inflammatory responses that also result in damage to the lungs and other organs. Identification and
quantification of trauma-triggered circulating histones would provide an approach to assess the risk of ARDS,
which could enable life-saving therapies before a patient develops ARDS. Diagnostic solutions to provide early
detection of histones following trauma should be portable and rapid in order to assess the patient soon after
the injury occurs. Currently, however, there are no portable and rapid approaches that enable detection of
circulating histones to assess a trauma patient’s risk of developing ARDS. Our goal is to develop a diagnostic
tool that is capable of quantitatively assessing the risk of trauma-induced ARDS at the point of care. This may
include at the point of injury, in the transport vehicle to a trauma center, in the Emergency Department (ED), or
in the operating room (OR). We have invented a Portable Histone Assay Technology (PHAST) that can
quantify circulating histones directly from whole blood within 30 minutes.
.
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会议论文
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依托单位:
海外基金