Siglec 9 for the diagnosis of ARDS
Siglec 9 for the diagnosis of ARDS
批准号:
9810521
负责人:
Sajid Shahul
金额:
$12.15万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-07-04 至 2021-06-30
关键词:
AcuteAcute respiratory failureAddressAdmission activityAdult Respiratory Distress SyndromeAldosterone AntagonistsAspirinAttenuatedBasic ScienceBinding ProteinsBiological MarkersBloodCathetersChestClinicalClinical ResearchCongestive Heart FailureDataDevelopmentDiagnosisDiagnosticDiseaseEFRACEarly DiagnosisEarly InterventionEndotheliumEpithelialGoalsHeart failureHeterogeneityHospital MortalityIncidenceInduction of neuromuscular blockadeInflammationInflammatoryInjuryIntensive Care UnitsLeadLeukocytesLigand BindingLiquid substanceLungLung InflammationNeutrophil ActivationNeutrophil InfiltrationOutcomePatient-Focused OutcomesPatientsPermeabilityPharmacologic SubstancePlasmaProne PositionPulmonary EdemaRandomized Controlled TrialsRiskRisk stratificationSample SizeSamplingSerumSeveritiesSialic AcidsSourceSpironolactoneSurfaceTestingUncertaintyValidationVentilator-induced lung injuryWorkbaseclinical practicecohorteffective therapyexperimental studyheart functionheart preservationimmune activationimprovedinjury preventionlung injurymortalitymortality riskmouse modelneutrophilnew therapeutic targetnon cardiogenic pulmonary edemaoutcome forecastpredictive toolspreservationprognosticrandomized trialreceptor functionsialic acid binding Ig-like lectintreatment trialvalidation studies
中文摘要
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英文摘要
Project Summary/Abstract
Acute respiratory distress syndrome (ARDS) accounts for 10% of admissions and 30% of mortality in intensive
care units. Despite extensive basic and clinical research, hospital mortality for patients with ARDS remains as
high as 45%. Major reasons for the lack of effective therapies include the lack of tools for predicting which
patients will develop ARDS and the difficulty of differentiating ARDS from other causes of pulmonary edema
like congestive heart failure (CHF). Because of such diagnostic uncertainty, fewer than half of ARDS cases are
recognized, and ARDS-specific therapies are underutilized by 25% worldwide. Using plasma samples from the
Fluid and Catheter Treatment Trial (a randomized controlled trial of liberal versus conservative fluid
management) in patients with ARDS, and the Treatment of Preserved Cardiac Function Heart Failure with an
Aldosterone Antagonist trial (a randomized trial of spironolactone in patients with heart failure with preserved
ejection fraction), we will in AIM 1 determine how well serum Siglec-9 distinguishes between ARDS and CHF
and in AIM 2 Correlate Siglec-9 levels with ARDS severity and clinical outcomes. The results of this work have
tremendous potential to enable earlier diagnosis, treatment, and prognostic assessment of patients with ARDS.
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