Article
Idiopathic pulmonary arterial hypertension phenotypes determined by cluster analysis from the COMPERA registry.
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation - 1 Dec 2020
Hoeper Marius M, Pausch Christine, Grünig Ekkehard, Klose Hans, Staehler Gerd, Huscher Doerte, Pittrow David, Olsson Karen M, Vizza Carmine Dario, Gall Henning, Benjamin Nicola, Distler Oliver, Opitz Christian, Gibbs J Simon R, Delcroix Marion, Ghofrani H Ardeschir, Rosenkranz Stephan, Ewert Ralf, Kaemmerer Harald, Lange Tobias J, Kabitz Hans-Joachim, Skowasch Dirk, Skride Andris, Jureviciene Elena, Paleviciute Egle, Miliauskas Skaidrius, Claussen Martin, Behr Juergen, Milger Katrin, Halank Michael, Wilkens Heinrike, Wirtz Hubert, Pfeuffer-Jovic Elena, Harbaum Lars, Scholtz Werner, Dumitrescu Daniel, Bruch Leonhard, Coghlan Gerry, Neurohr Claus, Tsangaris Iraklis, Gorenflo Matthias, Scelsi Laura, Vonk-Noordegraaf Anton, Ulrich Silvia, Held Matthias
Abstract excerpt
The term idiopathic pulmonary arterial hypertension (IPAH) is used to categorize patients with pre-capillary pulmonary hypertension of unknown origin. There is considerable variability in the clinical presentation of these patients. Using data from the Comparative, Prospective Registry of Newly Initiated Therapies for Pulmonary Hypertension, we performed a cluster analysis of 841 patients with IPAH based on age,...
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