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单光子发射计算机断层扫描用于冠状动脉疾病的诊断:一项基于证据的分析。

Single photon emission computed tomography for the diagnosis of coronary artery disease: an evidence-based analysis.

出版信息

Ont Health Technol Assess Ser. 2010;10(8):1-64. Epub 2010 Jun 1.

Abstract

UNLABELLED

In July 2009, the Medical Advisory Secretariat (MAS) began work on Non-Invasive Cardiac Imaging Technologies for the Diagnosis of Coronary Artery Disease (CAD), an evidence-based review of the literature surrounding different cardiac imaging modalities to ensure that appropriate technologies are accessed by patients suspected of having CAD. This project came about when the Health Services Branch at the Ministry of Health and Long-Term Care asked MAS to provide an evidentiary platform on effectiveness and cost-effectiveness of non-invasive cardiac imaging modalities.After an initial review of the strategy and consultation with experts, MAS identified five key non-invasive cardiac imaging technologies for the diagnosis of CAD. Evidence-based analyses have been prepared for each of these five imaging modalities: cardiac magnetic resonance imaging, single photon emission computed tomography, 64-slice computed tomographic angiography, stress echocardiography, and stress echocardiography with contrast. For each technology, an economic analysis was also completed (where appropriate). A summary decision analytic model was then developed to encapsulate the data from each of these reports (available on the OHTAC and MAS website).The Non-Invasive Cardiac Imaging Technologies for the Diagnosis of Coronary Artery Disease series is made up of the following reports, which can be publicly accessed at the MAS website at: www.health.gov.on.ca/mas or at www.health.gov.on.ca/english/providers/program/mas/mas_about.htmlSINGLE PHOTON EMISSION COMPUTED TOMOGRAPHY FOR THE DIAGNOSIS OF CORONARY ARTERY DISEASE: An Evidence-Based AnalysisSTRESS ECHOCARDIOGRAPHY FOR THE DIAGNOSIS OF CORONARY ARTERY DISEASE: An Evidence-Based AnalysisSTRESS ECHOCARDIOGRAPHY WITH CONTRAST FOR THE DIAGNOSIS OF CORONARY ARTERY DISEASE: An Evidence-Based Analysis64-Slice Computed Tomographic Angiography for the Diagnosis of Coronary Artery Disease: An Evidence-Based AnalysisCARDIAC MAGNETIC RESONANCE IMAGING FOR THE DIAGNOSIS OF CORONARY ARTERY DISEASE: An Evidence-Based AnalysisPease note that two related evidence-based analyses of non-invasive cardiac imaging technologies for the assessment of myocardial viability are also available on the MAS website:POSITRON EMISSION TOMOGRAPHY FOR THE ASSESSMENT OF MYOCARDIAL VIABILITY: An Evidence-Based AnalysisMAGNETIC RESONANCE IMAGING FOR THE ASSESSMENT OF MYOCARDIAL VIABILITY: an Evidence-Based AnalysisThe Toronto Health Economics and Technology Assessment Collaborative has also produced an associated economic report entitled:The Relative Cost-effectiveness of Five Non-invasive Cardiac Imaging Technologies for Diagnosing Coronary Artery Disease in Ontario [Internet]. Available from: http://theta.utoronto.ca/reports/?id=7

OBJECTIVE

The objective of the analysis is to determine the diagnostic accuracy of single photon emission tomography (SPECT) in the diagnosis of coronary artery disease (CAD) compared to the reference standard of coronary angiography (CA). The analysis is primarily meant to allow for indirect comparisons between non-invasive strategies for the diagnosis of CAD, using CA as a reference standard. SPECT: Cardiac SPECT, or myocardial perfusion scintigraphy (MPS), is a widely used nuclear, non-invasive image acquisition technique for investigating ischemic heart disease. SPECT is currently appropriate for all aspects of detecting and managing ischemic heart disease including diagnosis, risk assessment/stratification, assessment of myocardial viability, and the evaluation of left ventricular function. Myocardial perfusion scintigraphy was originally developed as a two-dimensional planar imaging technique, but SPECT acquisition has since become the clinical standard in current practice. Cardiac SPECT for the diagnosis of CAD uses an intravenously administered radiopharmaceutical tracer to evaluate regional coronary blood flow usually at rest and after stress. The radioactive tracers thallium (201Tl) or technetium-99m (99mTc), or both, may be used to visualize the SPECT acquisition. Exercise or a pharmacologic agent is used to achieve stress. After the administration of the tracer, its distribution within the myocardium (which is dependent on myocardial blood flow) is imaged using a gamma camera. In SPECT imaging, the gamma camera rotates around the patients for 10 to 20 minutes so that multiple two-dimensional projections are acquired from various angles. The raw data are then processed using computational algorithms to obtain three-dimensional tomographic images. Since its inception, SPECT has evolved and its techniques/applications have become increasingly more complex and numerous. Accordingly, new techniques such as attenuation correction and ECG gating have been developed to correct for attenuation due to motion or soft-tissue artifact and to improve overall image clarity.

RESEARCH QUESTIONS

What is the diagnostic accuracy of SPECT for the diagnosis of CAD compared to the reference standard of CA?Is SPECT cost-effective compared to other non-invasive cardiac imaging modalities for the diagnosis of CAD?What are the major safety concerns with SPECT when used for the diagnosis of CAD?

METHODS

A preliminary literature search was performed across OVID MEDLINE, MEDLINE In-Process and Other Non-Indexed Citations, EMBASE, the Cochrane Library, and the International Agency for Health Technology Assessment (INAHTA) for all systematic reviews/meta-analysis published between January 1, 2004 and August 22, 2009. A comprehensive systematic review was identified from this search and used as a basis for an updated search. A second comprehensive literature search was then performed on October 30, 2009 across the same databases for studies published between January 1, 2002 and October 30, 2009. Abstracts were reviewed by a single reviewer and, for those studies meeting the eligibility criteria, full-text articles were obtained. Reference lists were also hand-searched for any additional studies. Inclusion CriteriaExclusion CriteriaSystematic reviews, meta-analyses, controlled clinical trials, and observational studiesMinimum sample size of 20 patients who completed coronary angiographyUse of CA as a reference standard for the diagnosis of CADData available to calculate true positives (TP), false positives (FP), false negatives (FN) and true negatives (TN)Accuracy data reported by patient not by segmentEnglish languageNon-systematic reviews, case reportsGrey literature and abstractsTrials using planar imaging onlyTrials conducted in patients with non-ischemic heart diseaseStudies done exclusively in special populations (e.g., patients with left branch bundle block, diabetics, minority populations) unless insufficient data available

SUMMARY OF FINDINGS

Eighty-four observational studies, one non-randomized, single arm controlled clinical trial, and one poorly reported trial that appeared to be a randomized controlled trial (RCT) met the inclusion criteria for this review. All studies assessed the diagnostic accuracy of myocardial perfusion SPECT for the diagnosis of CAD using CA as a reference standard. Based on the results of these studies the following conclusions were made: According to very low quality evidence, the addition of attenuation correction to traditional or ECG-gated SPECT greatly improves the specificity of SPECT for the diagnosis of CAD although this improvement is not statistically significant. A trend towards improvement of specificity was also observed with the addition of ECG gating to traditional SPECT.According to very low quality evidence, neither the choice of stress agent (exercise or pharmacologic) nor the choice of radioactive tracer (technetium vs. thallium) significantly affect the diagnostic accuracy of SPECT for the diagnosis of CAD although a trend towards accuracy improvement was observed with the use of pharmacologic stress over exercise stress and technetium over thallium.Considerably heterogeneity was observed both within and between trials. This heterogeneity may explain why some of the differences observed between accuracy estimates for various subgroups were not statistically significant.More complex analytic techniques such as meta-regression may help to better understand which study characteristics significantly influence the diagnostic accuracy of SPECT.

摘要

未标注

2009年7月,医学咨询秘书处(MAS)开始了关于用于诊断冠状动脉疾病(CAD)的非侵入性心脏成像技术的工作,这是一项对围绕不同心脏成像方式的文献进行的循证综述,以确保疑似患有CAD的患者能够使用适当的技术。该项目是在卫生与长期护理部的卫生服务处要求MAS提供关于非侵入性心脏成像方式的有效性和成本效益的证据平台后开展的。在对策略进行初步审查并与专家协商后,MAS确定了用于诊断CAD的五种关键非侵入性心脏成像技术。已针对这五种成像方式中的每一种进行了循证分析:心脏磁共振成像、单光子发射计算机断层扫描、64层计算机断层血管造影、负荷超声心动图以及负荷超声心动图造影。对于每种技术,还完成了经济分析(如适用)。然后开发了一个汇总决策分析模型,以汇总这些报告中的数据(可在安大略卫生技术评估中心和MAS网站上获取)。

用于诊断冠状动脉疾病的非侵入性心脏成像技术系列由以下报告组成,可在MAS网站上公开获取:www.health.gov.on.ca/mas或www.health.gov.on.ca/english/providers/program/mas/mas_about.html

用于诊断冠状动脉疾病的单光子发射计算机断层扫描

循证分析

用于诊断冠状动脉疾病的负荷超声心动图

循证分析

用于诊断冠状动脉疾病的负荷超声心动图造影

循证分析

用于诊断冠状动脉疾病的64层计算机断层血管造影:循证分析

用于诊断冠状动脉疾病的心脏磁共振成像

循证分析

请注意,MAS网站上也提供了两项关于用于评估心肌活力的非侵入性心脏成像技术的相关循证分析:

用于评估心肌活力的正电子发射断层扫描

循证分析

用于评估心肌活力的磁共振成像

循证分析

多伦多卫生经济与技术评估协作组织还编制了一份相关的经济报告,题为:

安大略省用于诊断冠状动脉疾病的五种非侵入性心脏成像技术的相对成本效益[互联网]。可从:http://theta.utoronto.ca/reports/?id=7获取

目的

本分析的目的是确定与冠状动脉造影(CA)这一参考标准相比,单光子发射断层扫描(SPECT)在诊断冠状动脉疾病(CAD)方面的诊断准确性。该分析主要旨在允许以CA作为参考标准,对CAD诊断的非侵入性策略进行间接比较。

SPECT

心脏SPECT,即心肌灌注闪烁显像(MPS),是一种广泛使用的核医学非侵入性图像采集技术,用于研究缺血性心脏病。SPECT目前适用于检测和管理缺血性心脏病的各个方面,包括诊断、风险评估/分层、心肌活力评估以及左心室功能评估。心肌灌注闪烁显像最初是作为一种二维平面成像技术开发的,但自那时以来,SPECT采集已成为当前临床实践中的标准方法。用于诊断CAD的心脏SPECT使用静脉注射放射性药物示踪剂,通常在静息和负荷后评估局部冠状动脉血流。放射性示踪剂铊(201Tl)或锝 - 99m(99mTc),或两者均可用于可视化SPECT采集。使用运动或药物制剂来实现负荷状态。注射示踪剂后,使用伽马相机对其在心肌内的分布(取决于心肌血流)进行成像。在SPECT成像中,伽马相机围绕患者旋转10至20分钟,以便从各个角度获取多个二维投影。然后使用计算算法对原始数据进行处理,以获得三维断层图像。自其诞生以来,SPECT不断发展,其技术/应用变得越来越复杂和多样。因此,已经开发了诸如衰减校正和心电图门控等新技术,以校正由于运动或软组织伪影引起的衰减,并提高整体图像清晰度。

研究问题

与CA参考标准相比,SPECT诊断CAD的诊断准确性如何?

与其他用于诊断CAD的非侵入性心脏成像方式相比,SPECT是否具有成本效益?

SPECT用于诊断CAD时的主要安全问题有哪些?

方法

在OVID MEDLINE、MEDLINE在研及其他未索引引文、EMBASE、Cochrane图书馆和国际卫生技术评估机构(INAHTA)中对2004年1月1日至2009年8月22日期间发表的所有系统评价/荟萃分析进行了初步文献检索。从该检索中确定了一项全面的系统评价,并将其用作更新检索的基础。然后于2009年10月30日在相同数据库中对2002年1月1日至2009年10月30日期间发表的研究进行了第二次全面文献检索。由一名评审员对摘要进行评审,对于符合纳入标准的研究,获取全文文章。还手动检索参考文献列表以查找任何其他研究。

纳入标准

排除标准

系统评价、荟萃分析、对照临床试验和观察性研究

完成冠状动脉造影的患者最小样本量为20例

使用CA作为CAD诊断的参考标准

可获得计算真阳性(TP)、假阳性(FP)、假阴性(FN)和真阴性(TN)的数据

按患者而非节段报告的准确性数据

英语语言

非系统评价、病例报告

灰色文献和摘要

仅使用平面成像的试验

在非缺血性心脏病患者中进行的试验

专门在特殊人群(如左束支传导阻滞患者、糖尿病患者、少数族裔人群)中进行的研究,除非数据不足

研究结果总结

84项观察性研究、1项非随机单臂对照临床试验以及1项报告不佳似乎为随机对照试验(RCT)的试验符合本综述的纳入标准。所有研究均以CA作为参考标准评估心肌灌注SPECT诊断CAD的诊断准确性。基于这些研究的结果得出以下结论:

根据极低质量的证据,在传统或心电图门控SPECT中添加衰减校正可显著提高SPECT诊断CAD的特异性,尽管这种提高在统计学上不显著。在传统SPECT中添加心电图门控也观察到特异性有改善趋势。

根据极低质量的证据(证据质量极低),负荷剂(运动或药物)的选择以及放射性示踪剂(锝与铊)的选择均未显著影响SPECT诊断CAD的诊断准确性,尽管使用药物负荷比运动负荷以及使用锝比铊观察到有准确性提高的趋势。

在试验内部和试验之间均观察到相当大的异质性。这种异质性可能解释了为什么在各个亚组的准确性估计之间观察到的一些差异在统计学上不显著。

更复杂的分析技术,如荟萃回归,可能有助于更好地理解哪些研究特征显著影响SPECT的诊断准确性。

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