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Survival and Comorbidities after Dementia

Survival and Comorbidities after Dementia
痴呆症后的生存和合并症
批准号:
6522207
负责人:
ANNETTE L. FITZPATRICK
金额:
$6.15万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-09-01 至 2004-08-31

项目摘要

项目成果

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中文摘要
翻译
描述(由申请人提供)随着美国的老龄化,痴呆症发作后的生存率估计是一个极其重要的公共卫生问题。最近的一项研究报告痴呆症后的中位生存期为3.3年,比以前估计的要短得多。同样,随着认知能力下降而发生的疾病数量也给家庭和医疗资源带来了巨大的负担。这两个措施的准确估计,需要预测照顾者和卫生资源的负担。最近,心血管健康研究(CHS),一个多中心观察队列,旨在调查老年人心脏病和中风的危险因素,完成了一项辅助研究(由NIA资助),以评估3602名参与者的痴呆症。共480例痴呆患者,其中阿尔茨海默病(AD)330例(68.8%),血管性痴呆52例(10.8%),AD和血管性痴呆76例(15.8%),其他类型22例(4.6%)。我们建议利用这些数据沿着CHS队列的广泛临床和监测数据来回答以下问题:(1)参与心血管健康研究(CHS)的被归类为偶发性痴呆的个体的生存期是多长?(2)痴呆症发作后的住院率和疗养院入院率是多少?(3)这些比率是否因痴呆类型、年龄、性别、种族或ApoE状态而异?(4)这些比率在患有痴呆症的个体和参加CHS的年龄和性别相似的其他人之间是否有差异?(5)痴呆症患者生存的预测因素是什么?我们将合并以下来源的数据以实现我们的目标:(1)CHS记忆研究数据库中的痴呆分类、痴呆类型、患病率/发病率状态和发病日期;(2)所有人口统计学、风险因素数据(包括MRI和神经系统症状)和认知评分;(3)死亡日期和原因、随访结束时的状态以及来自CHS事件数据库的所有住院数据;以及(4)来自HCFA MEDPAR文件的疗养院信息。将对死亡原因和住院诊断进行编码,以满足分析需求。将根据需要访问和提取已收集的住院和死亡记录,以获取更多信息。分析将包括计算长度偏倚(如果存在)、估计中位生存期以及根据选定的人口统计学和痴呆类型进行的住院和入住疗养院的诊断特异性比率。考克斯比例风险回归将用于确定痴呆发作后生存的预测因子。我们还将继续汇编数据集,并支持研究合作者使用该数据。该应用程序的优势包括CHS队列已有数据的广度,包括记录良好的痴呆症事件病例和最新的监测。该应用程序将支持对一个重要数据库的持续分析,该数据库旨在为该国痴呆症的预防和影响提供有价值的研究。
英文摘要
DESCRIPTION (provided by applicant) Estimation of survival following the onset of dementia is an extremely important public health issue as America ages. A recent study reported median survival after dementia to be 3.3 years, much shorter than previously estimated. Likewise, the amount of illness that occurs as cognition declines presents a huge burden on family and health care resources alike. Accurate estimation of both of these measures is needed to predict burden for caregivers and on health resources. Recently, the Cardiovascular Health Study (CHS), a multi-site observational cohort established to investigate risk factors for heart disease and stroke in the elderly, completed an ancillary study (funded by NIA) to evaluate dementia in a subset of 3602 of its participants. A total of 480 cases of incident dementia resulted, 330 (68.8 percent) Alzheimer's disease (AD), 52 (10.8 percent) vascular dementia, 76 (15.8 percent) both AD and vascular dementia and 22 (4.6 percent) other types. We propose to utilize these data along with the extensive clinical and surveillance data of the CHS cohort to answer the following questions: (1) What is the duration of survival for individuals classified with incident dementia participating in the Cardiovascular Health Study (CHS)? (2) What are the rates of hospitalization and nursing home admission following onset of dementia? (3) Do these rates differ by type of dementia, age, gender, race or ApoE status? (4) Do these rates differ between individuals evaluated with incident dementia and others of similar age and gender enrolled in CHS? (5) What are the predictors of survival for individuals with incident dementia? We will merge together data from the following sources to achieve our goals: (1) dementia classification, type of dementia, prevalence/incidence status, and date of onset from the CHS Memory Study database; (2) all demographics, risk factor data (including MRI and neurologic symptoms) and cognition scores from the CHS clinic database; (3) date and cause of death, status at end of follow-up, and all hospitalization data from the CHS Events database; and (4) nursing home information from HCFA MEDPAR files. Cause of death and hospitalization diagnoses will be coded to meet analytic needs. Hospital and death records already collected, will be accessed and abstracted for additional information as needed. Analyses will include calculation of length bias (if present), estimation of median survival and diagnosis-specific rates of hospitalization and nursing home admission by selected demographics and type of dementia. Cox proportional hazards regression will be used to identify predictors of survival after onset of dementia. We will also continue to compile datasets and support use of the date for study collaborators. The strengths of this application include the breadth of data already available for the CHS cohort, the inclusion of well-documented incident cases of dementia, and up-to-date surveillance. This application will support continued analyses of an important database designed to provide valuable research for the prevention and impact of dementia in this country.
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Building Capacity to Address the Burden of Cardiometabolic Risk Factors and Diseases in LMICs
  • 批准号:
    10634663
  • 项目类别:
  • 资助金额:
    $23.65万
  • 财政年份:
    2020
  • 负责人:
    ANNETTE L. FITZPATRICK
  • 依托单位:
Building Capacity to Address the Burden of Cardiometabolic Risk Factors and Diseases in LMICs
  • 批准号:
    10054300
  • 项目类别:
  • 资助金额:
    $23.94万
  • 财政年份:
    2020
  • 负责人:
    ANNETTE L. FITZPATRICK
  • 依托单位:
Building Capacity to Address the Burden of Cardiometabolic Risk Factors and Diseases in LMICs
  • 批准号:
    10256077
  • 项目类别:
  • 资助金额:
    $23.92万
  • 财政年份:
    2020
  • 负责人:
    ANNETTE L. FITZPATRICK
  • 依托单位:
Building Capacity to Address the Burden of Cardiometabolic Risk Factors and Diseases in LMICs
  • 批准号:
    10435535
  • 项目类别:
  • 资助金额:
    $23.83万
  • 财政年份:
    2020
  • 负责人:
    ANNETTE L. FITZPATRICK
  • 依托单位:
海外基金