6.
Rosenkranz S, Pausch C, Coghlan J, Huscher D, Pittrow D, Grunig E
. Risk stratification and response to therapy in patients with pulmonary arterial hypertension and comorbidities: A COMPERA analysis. J Heart Lung Transplant. 2022; 42(1):102-114.
DOI: 10.1016/j.healun.2022.10.003.
View
7.
Ling Y, Johnson M, Kiely D, Condliffe R, Elliot C, Gibbs J
. Changing demographics, epidemiology, and survival of incident pulmonary arterial hypertension: results from the pulmonary hypertension registry of the United Kingdom and Ireland. Am J Respir Crit Care Med. 2012; 186(8):790-6.
DOI: 10.1164/rccm.201203-0383OC.
View
8.
Kylhammar D, Kjellstrom B, Hjalmarsson C, Jansson K, Nisell M, Soderberg S
. A comprehensive risk stratification at early follow-up determines prognosis in pulmonary arterial hypertension. Eur Heart J. 2017; 39(47):4175-4181.
DOI: 10.1093/eurheartj/ehx257.
View
9.
Galie N, Barbera J, Frost A, Ghofrani H, Hoeper M, McLaughlin V
. Initial Use of Ambrisentan plus Tadalafil in Pulmonary Arterial Hypertension. N Engl J Med. 2015; 373(9):834-44.
DOI: 10.1056/NEJMoa1413687.
View
10.
Frost A, Badesch D, Barst R, Benza R, Elliott C, Farber H
. The changing picture of patients with pulmonary arterial hypertension in the United States: how REVEAL differs from historic and non-US Contemporary Registries. Chest. 2010; 139(1):128-37.
DOI: 10.1378/chest.10-0075.
View
11.
Hoeper M, Kramer T, Pan Z, Eichstaedt C, Spiesshoefer J, Benjamin N
. Mortality in pulmonary arterial hypertension: prediction by the 2015 European pulmonary hypertension guidelines risk stratification model. Eur Respir J. 2017; 50(2).
DOI: 10.1183/13993003.00740-2017.
View
12.
Boucly A, Weatherald J, Savale L, de Groote P, Cottin V, Prevot G
. External validation of a refined four-stratum risk assessment score from the French pulmonary hypertension registry. Eur Respir J. 2021; 59(6).
PMC: 9245192.
DOI: 10.1183/13993003.02419-2021.
View
13.
Hoeper M, Pausch C, Grunig E, Klose H, Staehler G, Huscher D
. Idiopathic pulmonary arterial hypertension phenotypes determined by cluster analysis from the COMPERA registry. J Heart Lung Transplant. 2020; 39(12):1435-1444.
DOI: 10.1016/j.healun.2020.09.011.
View
14.
Benza R, Kanwar M, Raina A, Scott J, Zhao C, Selej M
. Development and Validation of an Abridged Version of the REVEAL 2.0 Risk Score Calculator, REVEAL Lite 2, for Use in Patients With Pulmonary Arterial Hypertension. Chest. 2020; 159(1):337-346.
PMC: 7462639.
DOI: 10.1016/j.chest.2020.08.2069.
View
15.
Hjalmarsson C, Radegran G, Kylhammar D, Rundqvist B, Multing J, Nisell M
. Impact of age and comorbidity on risk stratification in idiopathic pulmonary arterial hypertension. Eur Respir J. 2018; 51(5).
DOI: 10.1183/13993003.02310-2017.
View
16.
Hoeper M, McLaughlin V, Barbera J, Frost A, Ghofrani H, Peacock A
. Initial combination therapy with ambrisentan and tadalafil and mortality in patients with pulmonary arterial hypertension: a secondary analysis of the results from the randomised, controlled AMBITION study. Lancet Respir Med. 2016; 4(11):894-901.
DOI: 10.1016/S2213-2600(16)30307-1.
View
17.
Wissmuller M, Xanthouli P, Benjamin N, Grunig E, Richter M, Gall H
. Profiles and treatment patterns of patients with pulmonary arterial hypertension on monotherapy at experienced centres. ESC Heart Fail. 2022; 9(5):2873-2885.
PMC: 9715885.
DOI: 10.1002/ehf2.13804.
View
18.
Rosenkranz S, Channick R, Chin K, Jenner B, Gaine S, Galie N
. The impact of comorbidities on selexipag treatment effect in patients with pulmonary arterial hypertension: insights from the GRIPHON study. Eur J Heart Fail. 2021; 24(1):205-214.
PMC: 9298818.
DOI: 10.1002/ejhf.2369.
View
19.
Humbert M, Kovacs G, Hoeper M, Badagliacca R, Berger R, Brida M
. 2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension. Eur Respir J. 2022; 61(1).
DOI: 10.1183/13993003.00879-2022.
View
20.
Badagliacca R, DAlto M, Ghio S, Argiento P, Brunetti N, Casu G
. Relevance of comorbidities on initial combination therapy in pulmonary arterial hypertension. ERJ Open Res. 2022; 8(4).
PMC: 9638831.
DOI: 10.1183/23120541.00298-2022.
View