Tan R T, Kuzo R, Goodman L R, Siegel R, Haasler G B, Presberg K W
Division of Pulmonary and Critical Care Medicine, Medical College of Wisconsin and Zablocki VA Medical Center, Milwaukee, USA.
Chest. 1998 May;113(5):1250-6. doi: 10.1378/chest.113.5.1250.
To determine the utility of CT-determined main pulmonary artery diameter (MPAD) for predicting pulmonary hypertension (PH) in patients with parenchymal lung disease.
Retrospective review of right-heart hemodynamic data and chest CT scans in 45 patients.
Tertiary-referral teaching hospital and VA hospital.
Between October 1990 and December 1995, 36 patients referred for evaluation of parenchymal lung disease or possible pulmonary vascular disease were found to have PH, as defined by mean pulmonary artery pressure (mPAP) > or =20 mm Hg. Nine control patients (mPAP <20 mm Hg) were also identified (4 from hospital records search, 5 after evaluation for possible PH).
CT-determined MPAD was 35+/-6 mm in patients with PH and 27+/-2 mm in control subjects. In our group of patients, MPAD > or =29 mm had a sensitivity of 87%, specificity of 89%, positive predictive value (PPV) of 0.97, and positive likelihood ratio (LR) of 7.91 for predicting PH; in the subgroup of patients with parenchymal lung disease (n=28, PH and control subjects), MPAD > or =29 mm had a sensitivity of 84%, specificity of 75%, PPV of 0.95, and positive LR of 3.36 for predicting PH. The most specific findings for the presence of PH were both MPAD > or =29 mm and segmental artery-to-bronchus ratio > 1:1 in three or four lobes (specificity, 100%). There was no linear correlation between the degree of PH and MPAD (r=0.124).
CT-determined MPAD has excellent diagnostic value for detection of PH in patients with advanced lung disease. Therefore, standard chest CT scans can be used to screen for PH as a cause of exertional limitation in patients with parenchymal lung disease. Because CT is commonly used to evaluate parenchymal lung disease, this information is readily available.
确定计算机断层扫描(CT)测定的主肺动脉直径(MPAD)对预测实质性肺疾病患者肺动脉高压(PH)的效用。
对45例患者的右心血流动力学数据和胸部CT扫描进行回顾性研究。
三级转诊教学医院和退伍军人管理局医院。
在1990年10月至1995年12月期间,36例因实质性肺疾病或可能的肺血管疾病接受评估的患者被发现患有PH,定义为平均肺动脉压(mPAP)≥20 mmHg。还确定了9例对照患者(mPAP <20 mmHg)(4例通过医院记录搜索,5例在评估可能的PH后确定)。
PH患者CT测定的MPAD为35±6 mm,对照受试者为27±2 mm。在我们的患者组中,MPAD≥29 mm对预测PH的敏感性为87%,特异性为89%,阳性预测值(PPV)为0.97,阳性似然比(LR)为7.91;在实质性肺疾病患者亚组(n = 28,PH和对照受试者)中,MPAD≥29 mm对预测PH的敏感性为84%,特异性为75%,PPV为0.95,阳性LR为3.36。PH存在的最具特异性的发现是MPAD≥29 mm且在三个或四个肺叶中节段性动脉与支气管比率>1:1(特异性,100%)。PH程度与MPAD之间无线性相关性(r = 0.124)。
CT测定的MPAD对检测晚期肺病患者的PH具有优异的诊断价值。因此,标准胸部CT扫描可用于筛查PH,作为实质性肺疾病患者运动受限的原因。由于CT常用于评估实质性肺疾病,该信息很容易获得。