P01 Administrative Core
P01 行政核心
基本信息
- 批准号:10024957
- 负责人:
- 金额:$ 16.95万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2020
- 资助国家:美国
- 起止时间:2020-08-01 至 2025-07-31
- 项目状态:未结题
- 来源:
- 关键词:AccountabilityAddressAdvisory CommitteesAgricultureAntibiotic ResistanceAntibioticsAntimicrobial ResistanceBenchmarkingBudgetsClinicalClinical DataClostridium difficileCollaborationsCombating Antibiotic Resistant BacteriaCommunicationCritical IllnessDataDecision MakingDevelopmentDiagnosticDisease ProgressionDisputesEffectivenessEnsureEnterobacteriaceaeExtended-spectrum β-lactamaseGenomicsGoalsGovernmentHome environmentHuman ResourcesImmunocompromised HostIndustrializationInfectionIntensive Care UnitsLeadershipLifeLiquid substanceLogisticsMediatingMedicalMedical centerMinorModern MedicineMonitorOnline SystemsOperations ResearchOrganismPathogenicityPatientsPersonsPhenotypePositioning AttributeProcessProductivityProgram ReviewsProgress ReportsProteomicsPublic HealthQuality ControlRegimenResearchResearch ActivityResearch PersonnelResearch Project GrantsResolutionSamplingSystemTechniquesTexasTherapeuticTranslatingUnited NationsUnited States National Institutes of HealthVancomycin resistant enterococcusWorkcarbapenemaseclinical practicecommensal microbesconflict resolutiondata managementdata sharingfunctional genomicsgastrointestinalgut colonizationgut microbiotahigh riskimproved outcomeinsightmeetingsmetabolomicsmicrobiotamicroorganismmortalitymulti-drug resistant pathogennoveloutcome predictionpathogenprogramssample collectionsuccesssynergismtreatment strategy
项目摘要
ABSTRACT (Administrative Core)
The clinical introduction of antibiotics in 1930s-40s represented a major medical breakthrough enabling many
advances in modern medicine, agriculture and industrial practice. Unfortunately, the rise of antibiotic-resistant
microorganisms globally is now considered one of the most challenging public health threats of the 21st century.
The call for action against the threat of antibiotic resistance has now reached the highest level of government
including the Office of the US President (with the creation of the Presidential Advisory Council on Combating
Antibiotic-Resistant Bacteria) and the initiative for global action by the United Nations, among others.
Vancomycin-resistant enterococci (VRE), Enterobacteriaceae carrying extended spectrum β-lactamases and
carbapenemases (ESBL-E/CRE), and Clostridiodes difficile are particularly concerning for high-risk patients
who are immunocompromised and/or admitted to intensive care units (ICUs). Having the potential to cause life-
threatening infections, particularly in those patients who have already been subjected to multiple antibiotic
regimens, each of these organisms colonize the intestines, and their presence impacts subsequent colonization
by other pathogens further contributing to serious disease progression and even mortality in these high-risk
patients. Although these pathogens have been studied in isolation, elucidation of the dynamic interactions
between pathogens and commensal gut microbiota and their implication for predicting outcomes and,
thus, treatment strategies is more urgent than ever and requires a strategic, coordinated effort. The Texas
Medical Center in Houston, Texas is home to several world leaders in antimicrobial resistance research and
clinical practice with patient access and tremendous expertise in the cutting-edge genomic and phenotypic
techniques who are uniquely positioned to perform concerted and synergistic systems-level studies of the
multiple players that must be understood to address this challenge. These experts have recognized this
exceptional opportunity and the strength of addressing the critical and unmet challenge through the formation of
a multi-institutional collaborative research program Dynamics of Colonization and Infection by Multidrug-
Resistant Pathogens in Immunocompromised and Critically Ill Patients (DYNAMITE). Crucial for the
effectiveness of this multi-institutional research effort, is dedicated centralized administrative oversight and
support. The Administrative Core will serve as the central “hub” for program oversight, accountability,
communication, and project/process coordination for the three Projects and the Functional Genomics Core. To
achieve these goals, the Administrative Core will provide integrative accountability and oversight through the
Executive Leadership Team and the Internal and External Advisory Committees, and administrative support for
all project leaders, research personnel, key collaborators and advisors, and institutional administrative liaisons.
摘要(管理核心)
20 世纪 30 年代至 40 年代抗生素的临床应用代表了一项重大的医学突破,使许多人受益匪浅。
现代医学、农业和工业实践的进步不幸的是抗生素耐药性的增加。
全球微生物现在被认为是 21 世纪最具挑战性的公共卫生威胁之一。
政府最高层已呼吁采取行动应对抗生素耐药性的威胁
包括美国总统办公室(成立了总统抗疫咨询委员会)
抗生素耐药细菌)和联合国全球行动倡议等。
耐万古霉素肠球菌 (VRE)、携带广谱 β-内酰胺酶的肠杆菌科细菌和
碳青霉烯酶 (ESBL-E/CRE) 和艰难梭菌对高危患者尤其重要
免疫功能低下和/或住进重症监护病房 (ICU) 的人 有可能导致生命危险。
威胁感染,尤其是那些已经接受过多种抗生素治疗的患者
方案中,这些微生物中的每一种都会在肠道中定殖,它们的存在会影响随后的定殖
其他病原体进一步导致这些高危人群的严重疾病进展甚至死亡
尽管这些病原体已被单独研究,但仍需阐明其动态相互作用。
病原体和常见肠道微生物群之间的关系及其对预测结果的影响,
因此,治疗策略比以往任何时候都更加紧迫,需要战略性的、协调一致的努力。
德克萨斯州休斯顿的医疗中心是抗菌素耐药性研究和治疗方面几位世界领先者的所在地。
与患者接触的临床实践以及尖端基因组和表型方面的丰富专业知识
具有独特定位的技术,可以对系统进行协调一致和协同的系统级研究
这些专家已经认识到这一点。
通过组建
多机构合作研究项目“多种药物的定植和感染动态”
免疫功能低下和危重患者中的耐药病原体(DYNAMITE)对于患者至关重要。
这项多机构研究工作的有效性在于专门的集中行政监督和
行政核心将作为项目监督、问责、支持的中心“枢纽”。
三个项目和功能基因组核心的沟通和项目/流程协调。
为了实现这些目标,行政核心将通过
执行领导团队和内部和外部咨询委员会,以及行政支持
所有项目负责人、研究人员、主要合作者和顾问以及机构行政联络人。
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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Cesar Augusto Arias其他文献
Cesar Augusto Arias的其他文献
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{{ truncateString('Cesar Augusto Arias', 18)}}的其他基金
Clinical Impact of the Cefazolin Inoculum Effect
头孢唑啉接种效果的临床影响
- 批准号:
10735541 - 财政年份:2023
- 资助金额:
$ 16.95万 - 项目类别:
The LiaFSR system and antimicrobial peptide resistance in enterococci
LiaFSR 系统和肠球菌抗菌肽耐药性
- 批准号:
10553808 - 财政年份:2022
- 资助金额:
$ 16.95万 - 项目类别:
VENOUS: A translational study of enterococcal bacteremia
静脉:肠球菌菌血症的转化研究
- 批准号:
10197036 - 财政年份:2020
- 资助金额:
$ 16.95万 - 项目类别:
Project 1: Genomics of Pathobionts and Transition From Colonization to Infection
项目 1:病原体基因组学和从定植到感染的转变
- 批准号:
10614693 - 财政年份:2020
- 资助金额:
$ 16.95万 - 项目类别:
VENOUS: A translational study of enterococcal bacteremia
静脉:肠球菌菌血症的转化研究
- 批准号:
10624439 - 财政年份:2020
- 资助金额:
$ 16.95万 - 项目类别:
Project 1: Genomics of Pathobionts and Transition From Colonization to Infection
项目 1:病原体基因组学和从定植到感染的转变
- 批准号:
10226287 - 财政年份:2020
- 资助金额:
$ 16.95万 - 项目类别:
Project 1: Genomics of Pathobionts and Transition From Colonization to Infection
项目 1:病原体基因组学和从定植到感染的转变
- 批准号:
10024959 - 财政年份:2020
- 资助金额:
$ 16.95万 - 项目类别:
VENOUS: A translational study of enterococcal bacteremia
静脉:肠球菌菌血症的转化研究
- 批准号:
10593508 - 财政年份:2020
- 资助金额:
$ 16.95万 - 项目类别:
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