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Pulmonary Disease in Patients Referred for Coronary CT

2014年12月2日 更新者:University of Sao Paulo General Hospital

Pulmonary Disease in Patients Referred for Coronary CT and Association Between Spirometric Abnormalities and Coronary Calcium Score.

Several studies show an association between chronic obstructive pulmonary disease (COPD) and coronary artery disease (CAD). Besides risk factors such as smoking, both are associated with physical inactivity, advanced age and systemic inflammation The use of coronary computed tomography (CCT) with multiple detectors is a diagnostic method for coronary disease, describing the anatomy and severity of arterial obstruction. One way of estimating the cardiovascular risk is coronary calcium score (CCS). Due to the association between COPD and CAD, it is likely that many patients with IHD diagnosed by CT have reduced lung function.

The aim of this observational study is to establish the correlation between the CCS and lung function. It will also correlate the presence of irreversible airway obstruction with significant coronary lesions.

Patients over 40 years referred to CCT who agree to participate in the study will perform a spirometry with bronchodilator and collect a blood sample to measure serum markers of inflammation and cardiovascular risk (glycemia, lipid profile, C reactive protein (CRP), tumor necrosis factor-alpha (TNF-Alpha) and fibrinogen). The data will be compared in the general population and in subgroups: smokers, former smokers and nonsmokers.

One year after the CCT patients will be contacted by the investigators and accessed for emergency room visits, hospital admissions and fatal or nonfatal coronary or respiratory events.

The investigators hypothesis is that reduced lung function is independently associated with elevated CCS and is, also a risk factor for increased hospital admission and coronary events.

The concomitant assessment of lung function and CCS can contribute knowledge about the epidemiological association between pulmonary disease and CAD. This can also add to evidence for the use of spirometry as a marker of cardiovascular risk.

研究概览

研究类型

观察性的

注册 (实际的)

205

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • SP
      • Sao Paulo、SP、巴西、05403-000
        • Heart Institute (InCor) do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

40年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Patients over 40 years old refereed to coronary CT in the investigator´s institution.

描述

Inclusion Criteria:

  • Patients referred for coronary CT.
  • Age greater than 40 years

Exclusion Criteria:

  • History of myocardial revascularization (surgical or percutaneous)
  • Cognitive-functional incapacity to perform spirometry
  • Contraindication for administration of 400 mcg of albuterol
  • Acute myocardial infarction or unstable angina within 2 weeks
  • Angina pectoris class III or IV according to the Canadian Cardiovascular Society
  • Heart failure New York Heart Association class III or IV

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
Coronary CT Spirometry Cohort
Patients refereed to coronary CT enrolled in the study.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Coronary Calcium Score
大体时间:Baseline
Coronary calcium score is a measurement obtained in coronary computer tomography. The results will be compared between group with and without spirometric abnormalities.
Baseline

次要结果测量

结果测量
措施说明
大体时间
Coronary obstruction on CT
大体时间:Baseline
Presence or absence of coronary obstruction and it´s quantification by Duke score will be compared between group with and without spirometric abnormality.
Baseline
Hospital Admissions
大体时间:1 year
Hospital admissions will be accessed after one year from enrollment and compared between groups
1 year
ER visits
大体时间:1 year
ER visits will be accessed after one year from enrollment and compared between groups
1 year
Fatal and non fatal cardiac or respiratory events
大体时间:1 year
Fatal and non fatal cardiac or respiratory events will be accessed after one year from enrollment and compared between groups
1 year

其他结果措施

结果测量
措施说明
大体时间
Smoking Status
大体时间:1 year
All endpoints will be evaluated in smoking and nonsmoking subgroups.
1 year

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Alberto Cukier, MD PHD、InCor - HCFMUSP

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2011年4月1日

初级完成 (实际的)

2013年12月1日

研究完成 (实际的)

2014年12月1日

研究注册日期

首次提交

2012年11月21日

首先提交符合 QC 标准的

2012年11月26日

首次发布 (估计)

2012年11月27日

研究记录更新

最后更新发布 (估计)

2014年12月3日

上次提交的符合 QC 标准的更新

2014年12月2日

最后验证

2013年11月1日

更多信息

与本研究相关的术语

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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