TY - T1的血液动力学预测的结果pulmonary hypertension due to left heart disease: a meta-analysis JF - European Respiratory Journal JO - Eur Respir J DO - 10.1183/13993003.02427-2017 VL - 51 IS - 4 SP - 1702427 AU - Caravita, Sergio AU - Dewachter, Céline AU - Soranna, Davide AU - D'Araujo, Sandy Carolino AU - Khaldi, Amina AU - Zambon, Antonella AU - Parati, Gianfranco AU - Bondue, Antoine AU - Vachiéry, Jean-Luc Y1 - 2018/04/01 UR - //www.qdcxjkg.com/content/51/4/1702427.abstract N2 - Pulmonary hypertension (PH) is a common complication of left heart disease (LHD), as the result of a “passive” increase of left atrial pressure (LAP), leading to isolated post-capillary PH [1–3]. Several haemodynamic parameters have been proposed to identify a more severe phenotype of PH-LHD, for which the increase in pulmonary artery pressure cannot be accounted for by the increase in LAP, and described as combined post-capillary PH with a pre-capillary component, or CpcPH [1–3]. The latter haemodynamic phenotype may potentially expose patients to a higher risk of right ventricular failure and a poorer outcome [4, 5]. However, since the last World Symposium in 2013, how to define the pre-capillary component in PH-LHD has been a matter of debate, as pathophysiological arguments have been suggested to potentially contrast with clinical and prognostic evidences [1].PVR, DPG, PAC are all associated with survival in pulmonary hypertension due to left heart disease http://ow.ly/R8sF30ieHSQThe authors would like to thank Irene Lang, Christian Gerges and Mario Gerges (Division of Cardiology, Department of Internal Medicine II, General Hospital Vienna (AKH-Wien), Medical University of Vienna, Vienna, Austria) for having provided their own data, otherwise not available for this meta-analysis. ER -