Chen Yingming Amy, Prabhudesai Vikramaditya, Castel Helene, Gupta Samir
Department of Medical Imaging, St. Michael's Hospital, University of Toronto, Toronto, Canada.
Département de Medecine, Université de Montréal, Montreal, Canada.
PLoS One. 2016 Jul 6;11(7):e0158637. doi: 10.1371/journal.pone.0158637. eCollection 2016.
Hepatopulmonary syndrome (HPS) is defined by liver dysfunction, intrapulmonary vascular dilatations, and impaired oxygenation. The gold standard for detection of intrapulmonary vascular dilatations in HPS is contrast echocardiography. However, two small studies have suggested that patients with HPS have larger segmental pulmonary arterial diameters than both normal subjects and normoxemic subjects with cirrhosis, when measured by CT. We sought to compare CT imaging-based pulmonary vasodilatation in patients with HPS, patients with liver dysfunction without HPS, and matching controls on CT imaging.
We performed a retrospective cohort study at two quaternary care Canadian HPS centers. We analyzed CT thorax scans in 23 patients with HPS, 29 patients with liver dysfunction without HPS, and 52 gender- and age-matched controls. We measured the artery-bronchus ratios (ABRs) in upper and lower lung zones, calculated the "delta ABR" by subtracting the upper from the lower ABR, compared these measurements between groups, and correlated them with clinically relevant parameters (partial pressure of arterial oxygen, alveolar-arterial oxygen gradient, macroaggregated albumin shunt fraction, and diffusion capacity). We repeated measurements in patients with post-transplant CTs.
Patients had significantly larger lower zone ABRs and delta ABRs than controls (1.20 +/- 0.19 versus 0.98 +/- 0.10, p<0.01; and 0.12 +/- 0.17 versus -0.06 +/- 0.10, p<0.01, respectively). However, there were no significant differences between liver disease patients with and without HPS, nor any significant correlations between CT measurements and clinically relevant parameters. There were no significant changes in ABRs after liver transplantation (14 patients).
Basilar segmental artery-bronchus ratios are larger in patients with liver disease than in normal controls, but this vasodilatation is no more severe in patients with HPS. CT does not distinguish patients with HPS from those with uncomplicated liver disease.
肝肺综合征(HPS)的定义为肝功能障碍、肺内血管扩张和氧合受损。检测HPS中肺内血管扩张的金标准是对比超声心动图。然而,两项小型研究表明,通过CT测量,HPS患者的节段性肺动脉直径大于正常受试者和无低氧血症的肝硬化患者。我们试图比较基于CT成像的HPS患者、无HPS的肝功能障碍患者以及匹配对照组的肺血管扩张情况。
我们在加拿大的两个四级医疗HPS中心进行了一项回顾性队列研究。我们分析了23例HPS患者、29例无HPS的肝功能障碍患者以及52例性别和年龄匹配的对照组的胸部CT扫描。我们测量了上下肺区的动脉-支气管比值(ABR),通过下肺区ABR减去上肺区ABR计算“delta ABR”,比较了各组之间的这些测量值,并将它们与临床相关参数(动脉血氧分压、肺泡-动脉血氧梯度、大颗粒白蛋白分流分数和弥散能力)进行关联。我们对移植后进行CT检查的患者重复进行了测量。
患者的下肺区ABR和delta ABR显著大于对照组(分别为1.20±0.19对0.98±0.10,p<0.01;以及0.12±0.17对-0.06±0.10,p<0.01)。然而,有HPS和无HPS的肝病患者之间没有显著差异,CT测量值与临床相关参数之间也没有显著相关性。肝移植后(14例患者)ABR没有显著变化。
肝病患者的基底节段动脉-支气管比值大于正常对照组,但这种血管扩张在HPS患者中并不更严重。CT无法区分HPS患者和无并发症的肝病患者。