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2
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JAMA. 2016 Sep 13;316(10):1051-60. doi: 10.1001/jama.2016.12680.
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Sex Differences in Functional and CT Angiography Testing in Patients With Suspected Coronary Artery Disease.疑似冠状动脉疾病患者功能和CT血管造影检查中的性别差异
J Am Coll Cardiol. 2016 Jun 7;67(22):2607-16. doi: 10.1016/j.jacc.2016.03.523. Epub 2016 Apr 4.
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J Am Coll Radiol. 2016 Apr;13(4):381-6. doi: 10.1016/j.jacr.2015.11.015. Epub 2016 Jan 14.
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Comparison of Radiation Doses and Best-Practice Use for Myocardial Perfusion Imaging in US and Non-US Laboratories: Findings From the IAEA (International Atomic Energy Agency) Nuclear Cardiology Protocols Study.美国与非美国实验室心肌灌注成像辐射剂量及最佳实践使用情况比较:国际原子能机构(IAEA)核心脏病学协议研究结果
JAMA Intern Med. 2016 Feb;176(2):266-9. doi: 10.1001/jamainternmed.2015.7102.
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Diagnostic and Therapeutic Usefulness of Coronary Computed Tomography Angiography in Out-Clinic Patients Referred for Chest Pain.冠状动脉计算机断层扫描血管造影术在因胸痛转诊的门诊患者中的诊断和治疗价值
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在 PROMISE 试验中,对于稳定型胸痛患者,冠状动脉 CT 血管造影和功能检测的安全性:检测并发症、偶然发现和辐射剂量的随机比较。

Safety of coronary CT angiography and functional testing for stable chest pain in the PROMISE trial: A randomized comparison of test complications, incidental findings, and radiation dose.

机构信息

Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.

出版信息

J Cardiovasc Comput Tomogr. 2017 Sep-Oct;11(5):373-382. doi: 10.1016/j.jcct.2017.08.005. Epub 2017 Aug 15.

DOI:10.1016/j.jcct.2017.08.005
PMID:28838846
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6201309/
Abstract

BACKGROUND

Coronary computed tomography angiography (CTA) and functional testing strategies for stable chest pain yield similar outcomes; one aspect that may guide test choice is safety.

METHODS

We compared test safety (test complications, incidental findings, and effective radiation dose) between CTA and functional testing as-tested in PROMISE (PROspective Multicenter Imaging Study for Evaluation of Chest Pain). In the subgroup whose physicians intended nuclear stress over other functional tests if randomized to the functional arm, we compared radiation dose of CTA versus nuclear stress and identified characteristics associated with dose.

RESULTS

Of 9470 patients, none had major and <1% had minor complications (CTA: 0.8% [37/4633] vs. functional: 0.6% [27/4837]). CTA identified more incidental findings (11.6% [539/4633] vs. 0.7% [34/4837], p < 0.001), most commonly pulmonary nodules (9.4%, 437/4633). CTA had similar 90-day cumulative radiation dose to functional testing. However, in the subgroup whose physicians intended nuclear stress (CTA 3147; nuclear 3203), CTA had lower median index test (8.8 vs. 12.6 mSv, p < 0.001) and 90-day cumulative (11.6 vs. 13.1 mSv, p < 0.001) dose, independent of patient characteristics. The lowest nuclear doses employed 1-day Tc-99m protocols (12.2 mSv). The lowest CTA doses were at sites performing ≥500 CTAs/year (6.9 mSv) and with advanced (latest available) CT scanners (5.5 mSv).

CONCLUSION

Complications were negligibly rare for both CTA and functional testing. CTA detects more incidental findings. Compared to nuclear stress testing, CTA's lower radiation dose, independent of patient characteristics, makes it an attractive test choice. Radiation dose varies with imaging protocol, indicating opportunities to further reduce dose. (ClinicalTrials.gov number, NCT01174550).

摘要

背景

对于稳定性胸痛,冠状动脉计算机断层血管造影(CTA)和功能检测策略的结果相似;一个可能指导测试选择的方面是安全性。

方法

我们比较了 PROMISE(前瞻性多中心成像研究评估胸痛)中 CTA 和功能测试的测试安全性(测试并发症、偶然发现和有效辐射剂量)。在亚组中,如果随机分配到功能组,医生打算进行核应激而不是其他功能测试,我们比较了 CTA 与核应激的辐射剂量,并确定了与剂量相关的特征。

结果

在 9470 名患者中,均无重大并发症(CTA:0.8%[37/4633] vs. 功能:0.6%[27/4837]),<1%有轻微并发症。CTA 发现更多偶然发现(11.6%[539/4633] vs. 0.7%[34/4837],p<0.001),最常见的是肺结节(9.4%,437/4633)。CTA 与功能检测的 90 天累积辐射剂量相似。然而,在亚组中,医生打算进行核应激(CTA 3147;核 3203),CTA 的中位数指标检测(8.8 比 12.6 mSv,p<0.001)和 90 天累积剂量(11.6 比 13.1 mSv,p<0.001)较低,与患者特征无关。最低的核剂量采用 1 天 Tc-99m 方案(12.2 mSv)。最低的 CTA 剂量是在每年进行≥500 次 CTA 的地点(6.9 mSv)和使用先进(最新可用)CT 扫描仪(5.5 mSv)。

结论

CTA 和功能检测的并发症都很少见。CTA 检测到更多的偶然发现。与核应激检测相比,CTA 的辐射剂量较低,与患者特征无关,使其成为一个有吸引力的测试选择。辐射剂量随成像方案而变化,表明有进一步降低剂量的机会。(临床试验编号,NCT01174550)。