Shujaat Adil, Bajwa Abubakr A, Al-Saffar Farah, Bellardini Jason, Jones Lisa, Cury James D
Division of Pulmonary, Critical Care and Sleep Medicine, University at Buffalo, SUNY, Buffalo, NY, USA.
Division of Pulmonary, Critical Care and Sleep Medicine, University of Florida at Jacksonville, Jacksonville, FL, USA.
Clin Respir J. 2018 Mar;12(3):948-952. doi: 10.1111/crj.12610. Epub 2017 Feb 3.
Transthoracic echocardiography (TTE) and computerized axial tomography (CT) are complementary imaging techniques. It is possible that a combination of the two may offer a better way of identifying pulmonary hypertension (PH) than either one alone.
To determine the diagnostic accuracy of TTE combined with chest CT in pulmonary hypertension.
We performed a retrospective review of consecutive patients who had undergone TTE, CT and right heart catheterization (RHC) between 7/1/2008 and 6/30/2012. PH was defined as systolic pulmonary artery pressure >40 mm Hg or tricuspid regurgitant (TR) jet velocity >2.8m/s on TTE, ratio of diameter of pulmonary artery to ascending aorta (rPA) >1 or diameter of PA (dPA) >30 mm on CT, and mean PAP (mPAP) >25 mm Hg on RHC.
There was a total of 87 patients. The mean ± SD age was 54.3 ± 15.9 years and 69 (79%) were female. The prevalence of PH was 75%. The mean ± SD mPAP was 35.8 ± 14.2 mm Hg. The majority of the patients belonged to World Health Organization group I PH. Fifty per cent of the CT scans were done with intravenous contrast dye. The combination of TR jet velocity and rPA provided the best combination of sensitivity (98%) and specificity (70%) with an ROC area under the curve of 0.84.
The combination of TTE and chest CT is better than either imaging technique alone in identifying patients with PH in a heterogeneous population and may exclude PH.
经胸超声心动图(TTE)和计算机断层扫描(CT)是互补的成像技术。两者结合可能比单独使用任何一种技术都能提供更好的识别肺动脉高压(PH)的方法。
确定TTE联合胸部CT对肺动脉高压的诊断准确性。
我们对2008年7月1日至2012年6月30日期间连续接受TTE、CT和右心导管检查(RHC)的患者进行了回顾性研究。PH的定义为:TTE显示收缩期肺动脉压>40 mmHg或三尖瓣反流(TR)射流速度>2.8m/s;CT显示肺动脉直径与升主动脉直径之比(rPA)>1或肺动脉直径(dPA)>30 mm;RHC显示平均肺动脉压(mPAP)>25 mmHg。
共有87例患者。平均年龄±标准差为54.3±15.9岁,69例(79%)为女性。PH的患病率为75%。平均±标准差mPAP为35.8±14.2 mmHg。大多数患者属于世界卫生组织I组PH。50%的CT扫描使用了静脉造影剂。TR射流速度和rPA的组合提供了最佳的敏感性(98%)和特异性(70%)组合,曲线下面积为0.84。
在识别异质性人群中的PH患者方面,TTE和胸部CT联合使用比单独使用任何一种成像技术更好,并且可能排除PH。