Lidocaine for Neuroprotection During Cardiac Surgery

利多卡因在心脏手术期间的神经保护作用

基本信息

  • 批准号:
    7915376
  • 负责人:
  • 金额:
    $ 35.88万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2009
  • 资助国家:
    美国
  • 起止时间:
    2009-08-20 至 2014-05-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Cognitive impairment after surgery occurs frequently in the large number of increasingly elderly patients undergoing cardiac surgery every year. Postoperative cognitive deficit (POCD) is present in 36-50% of patients in the early phases after surgery and has been shown to adversely impact quality of life as much as one year after surgery. Despite substantial advancement in technology, pharmacology, and perioperative organ protection leading to reductions in mortality associated with cardiac surgery, the incidence of POCD has changed little over the last ten years. While multiple etiologic factors have been proposed for this neurological injury including cerebral embolic processes and hypoperfusion, it is likely that the degree of dysfunction is significantly modulated by the inflammatory responses that define ischemia and reperfusion. The objective of our multidisciplinary Neurological Outcome Research Group (NORG) is to understand the mechanisms underlying neurologic and neurocognitive dysfunction after cardiac surgery and to reduce the incidence of these devastating outcomes. Recently we administered lidocaine as an infusion during and after cardiac surgery and found preliminary data for a protective effect of lidocaine against POCD in non-diabetic subjects. We believe that intravenous lidocaine at antiarrhythmic doses offers neuroprotection by membrane stabilization and prevention of ion flux during initial vessel occlusion, followed by amelioration of the secondary inflammatory changes. Thus the primary aim of our prospective, randomized, double-blind interventional clinical trial is to determine the effectiveness of lidocaine in reducing postoperative cognitive decline. Secondarily, we will determine the effect of lidocaine upon the inflammatory response across the cerebral vasculature by measuring the jugular-arterial monocyte, polymorphonuclear, and platelet activation gradients. Little is more devastating to a patient or the patient's family than to have a successful operation that prolongs life but diminishes the quality of that life. Nothing is more likely to adversely impact quality of life than deterioration in a patient's neurocognitive status with resultant loss of independence. With the large number of patients still undergoing cardiac surgery, a simple and inexpensive intervention such as intravenous lidocaine holds the potential of dramatically increasing the quality of life for hundreds of thousands of patients world- wide. PUBLIC HEALTH RELEVANCE: Cognitive impairment is a common complication of cardiac surgery. In this research proposal, we plan to use lidocaine, an inexpensive and commonly available drug, to reduce postoperative cognitive dysfunction. The use of lidocaine therapy holds great promise for improving cognitive function and as a consequence, quality of life and functional independence for the large number of our increasingly elderly patients.
描述(申请人提供):每年大量接受心脏手术的老年患者经常出现术后认知障碍。 36-50% 的患者在术后早期阶段会出现术后认知缺陷 (POCD),并且已被证明会对术后一年内的生活质量产生不利影响。尽管技术、药理学和围手术期器官保护方面的重大进步导致与心脏手术相关的死亡率降低,但 POCD 的发病率在过去十年中几乎没有变化。虽然这种神经损伤有多种病因,包括脑栓塞过程和灌注不足,但功能障碍的程度很可能受到定义缺血和再灌注的炎症反应的显着调节。我们的多学科神经结果研究小组 (NORG) 的目标是了解心脏手术后神经系统和神经认知功能障碍的机制,并减少这些破坏性结果的发生率。最近,我们在心脏手术期间和术后输注利多卡因,并发现了利多卡因对非糖尿病受试者对 POCD 的保护作用的初步数据。我们认为,抗心律失常剂量的静脉注射利多卡因通过膜稳定和防止初始血管闭塞期间的离子通量提供神经保护,随后改善继发性炎症变化。因此,我们的前瞻性、随机、双盲介入临床试验的主要目的是确定利多卡因在减少术后认知能力下降方面的有效性。其次,我们将通过测量颈动脉单核细胞、多形核细胞和血小板活化梯度来确定利多卡因对整个脑血管系统炎症反应的影响。对于患者或患者家属来说,没有什么比成功延长生命但降低生活质量的手术更具破坏性的了。没有什么比患者神经认知状态恶化并导致独立性丧失更可能对生活质量产生不利影响的了。由于大量患者仍在接受心脏手术,静脉注射利多卡因等简单且廉价的干预措施有可能显着提高全世界数十万患者的生活质量。公共卫生相关性:认知障碍是心脏手术的常见并发症。在本研究提案中,我们计划使用利多卡因(一种廉价且常用的药物)来减少术后认知功能障碍。利多卡因疗法的使用对于改善认知功能具有巨大的希望,从而提高我们大量老年患者的生活质量和功能独立性。

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)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

Joseph P Mathew其他文献

Association of Early Beta-Blocker Exposure and Functional Outcomes in Critically Ill Patients With Moderate to Severe Traumatic Brain Injury: A Transforming Clinical Research and Knowledge in Traumatic Brain Injury Study
中度至重度创伤性脑损伤危重患者的早期 β 受体阻滞剂暴露与功能结果的关联:创伤性脑损伤研究中临床研究和知识的变革
  • DOI:
  • 发表时间:
    2023
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Margot Kelly;Sunny Yang Liu;N. Temkin;Jason Barber;Jordan M. Komisarow;Geoffrey Manley;T. Ohnuma;Katharine Colton;Miriam M. Treggiari;Eric E. Monson;M. Vavilala;R. Grandhi;D. Laskowitz;Joseph P Mathew;Adrian Hernandez;Michael L James;K. Raghunathan;Ben Goldstein;A. Markowitz;V. Krishnamoorthy
  • 通讯作者:
    V. Krishnamoorthy
Association of Early Dexmedetomidine Utilization With Clinical Outcomes After Moderate-Severe Traumatic Brain Injury: A Retrospective Cohort Study.
早期使用右美托咪定与中度至重度创伤性脑损伤后临床结果的关联:一项回顾性队列研究。
  • DOI:
  • 发表时间:
    2024
  • 期刊:
  • 影响因子:
    5.7
  • 作者:
    Sunny Yang Liu;Margot Kelly;Jordan M. Komisarow;J. Hatfield;T. Ohnuma;Miriam M. Treggiari;Katharine Colton;Evangeline Arulraja;Monica S Vavilala;Daniel T. Laskowitz;Joseph P Mathew;Adrian Hernandez;Michael L James;K. Raghunathan;Vijay Krishnamoorthy
  • 通讯作者:
    Vijay Krishnamoorthy

Joseph P Mathew的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('Joseph P Mathew', 18)}}的其他基金

Neurocognition and Greater Maintenance of Sinus Rhythm in AF (NOGGIN AF)
AF 中的神经认知和窦性心律的更好维持 (NOGGIN AF)
  • 批准号:
    10632044
  • 财政年份:
    2021
  • 资助金额:
    $ 35.88万
  • 项目类别:
Neurocognition and Greater Maintenance of Sinus Rhythm in AF (NOGGIN AF)
AF 中的神经认知和窦性心律的更好维持 (NOGGIN AF)
  • 批准号:
    10299458
  • 财政年份:
    2021
  • 资助金额:
    $ 35.88万
  • 项目类别:
Neurocognition and Greater Maintenance of Sinus Rhythm in AF (NOGGIN AF)
AF 中的神经认知和窦性心律的更好维持 (NOGGIN AF)
  • 批准号:
    10475214
  • 财政年份:
    2021
  • 资助金额:
    $ 35.88万
  • 项目类别:
Identification and Validation of a Novel Central Analgesia Circuit
新型中枢镇痛回路的识别和验证
  • 批准号:
    10362236
  • 财政年份:
    2021
  • 资助金额:
    $ 35.88万
  • 项目类别:
Resolution of Neuroinflammation and Persistent Pain by Complementary Approaches
通过补充方法解决神经炎症和持续性疼痛
  • 批准号:
    9703529
  • 财政年份:
    2020
  • 资助金额:
    $ 35.88万
  • 项目类别:
Cortical Beta-amyloid Levels and Neurocognitive Performance After Cardiac Surgery
心脏手术后皮质 β-淀粉样蛋白水平和神经认知功能
  • 批准号:
    8095975
  • 财政年份:
    2011
  • 资助金额:
    $ 35.88万
  • 项目类别:
Cortical Beta-amyloid Levels and Neurocognitive Performance After Cardiac Surgery
心脏手术后皮质 β-淀粉样蛋白水平和神经认知功能
  • 批准号:
    8306387
  • 财政年份:
    2011
  • 资助金额:
    $ 35.88万
  • 项目类别:
Lidocaine for Neuroprotection During Cardiac Surgery
利多卡因在心脏手术期间的神经保护作用
  • 批准号:
    8277106
  • 财政年份:
    2009
  • 资助金额:
    $ 35.88万
  • 项目类别:
Lidocaine for Neuroprotection During Cardiac Surgery
利多卡因在心脏手术期间的神经保护作用
  • 批准号:
    7698221
  • 财政年份:
    2009
  • 资助金额:
    $ 35.88万
  • 项目类别:
Lidocaine for Neuroprotection During Cardiac Surgery
利多卡因在心脏手术期间的神经保护作用
  • 批准号:
    8475499
  • 财政年份:
    2009
  • 资助金额:
    $ 35.88万
  • 项目类别:

相似国自然基金

Kallistatin抑制管周脂肪细胞线粒体裂变拮抗动脉粥样硬化的作用及机制研究
  • 批准号:
    82370443
  • 批准年份:
    2023
  • 资助金额:
    49 万元
  • 项目类别:
    面上项目
蛋白激酶D(PKD)抑制剂CRT0066101通过囊泡转运蛋白/TGN/NLRP3途径抗动脉粥样硬化炎症的作用及机制
  • 批准号:
    82304489
  • 批准年份:
    2023
  • 资助金额:
    30 万元
  • 项目类别:
    青年科学基金项目
NPTX1促进血管内皮细胞衰老在动脉粥样硬化中的作用机制及临床价值研究
  • 批准号:
    82372302
  • 批准年份:
    2023
  • 资助金额:
    49 万元
  • 项目类别:
    面上项目
SAH水解酶缺乏通过表观遗传调控KLF4促进动脉粥样硬化易损斑块形成的作用机制研究
  • 批准号:
    82373553
  • 批准年份:
    2023
  • 资助金额:
    49 万元
  • 项目类别:
    面上项目
二肽基肽酶在免疫-菌群失衡促动脉粥样硬化中的作用及机制研究
  • 批准号:
    82370465
  • 批准年份:
    2023
  • 资助金额:
    49 万元
  • 项目类别:
    面上项目

相似海外基金

Coronary plaque changes with statin and colchicine among people with high polygenic risk- a mechanistic pilot study
他汀类药物和秋水仙碱对高多基因风险人群的冠状动脉斑块变化——一项机制试点研究
  • 批准号:
    10736120
  • 财政年份:
    2023
  • 资助金额:
    $ 35.88万
  • 项目类别:
Cystathionine Gamma Lyase (CSE) and Hydrogen Sulfide Regulation of Vascular Aging
胱硫醚γ裂解酶 (CSE) 和硫化氢对血管老化的调节
  • 批准号:
    10715408
  • 财政年份:
    2023
  • 资助金额:
    $ 35.88万
  • 项目类别:
Contribution of Vitamin D Deficiency to Pathological Progression in Models of Cerebral Hypoperfusion
维生素 D 缺乏对脑低灌注模型病理进展的影响
  • 批准号:
    10725358
  • 财政年份:
    2023
  • 资助金额:
    $ 35.88万
  • 项目类别:
Microvascular Neuroimaging in Age-related Alzheimer's Disease and Tauopathies
年龄相关性阿尔茨海默病和 Tau蛋白病的微血管神经影像学
  • 批准号:
    10738372
  • 财政年份:
    2023
  • 资助金额:
    $ 35.88万
  • 项目类别:
Identification of plasma lipoprotein proteins and lipids as biomarkers of innate-immunity and vascular contributions to Alzheimer's disease and Alzheimer's disease-related dementias in older adults
鉴定血浆脂蛋白和脂质作为老年人阿尔茨海默病和阿尔茨海默病相关痴呆的先天免疫和血管贡献的生物标志物
  • 批准号:
    10660037
  • 财政年份:
    2023
  • 资助金额:
    $ 35.88万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了