The DOI matches its Crossref record; 471 of the 471 references it cites were found in a registry or an index.
2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension
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national Society for Heart and Lung Transplantation; d Representing the European League Against Rheumatism; and e Representing the European Society of Radiology.ESC entities having participated in the development of this document: ESC Associations: Acute Cardiovascular Care Association (ACCA), European Association for Cardiovascular Prevention & Rehabilitation (EACPR), European Association of Cardiovascular Imaging (EACVI), European Association of Percutaneous Cardiovascular Interventions (EAPCI), European Heart Rhythm Association (EHRA), Heart Failure Association (HFA).ESC Councils: Council for Cardiology Practice (CCP), Council on Cardiovascular Nursing and Allied Professions (CCNAP), Council on Cardiovascular Primary Care (CCPC).ESC Working Groups: Cardiovascular Pharmacotherapy, Cardiovascular Surgery, Grown-up Congenital Heart Disease, Pulmonary Circulation and Right Ventricular Function, Valvular Heart Disease.The content of these European Society of Cardiology (ESC) and European Respiratory Society (ERS) Guidelines has been published for personal and educational use only.
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“In the World Symposium of Pulmonary Hypertension classification of PAH, group 1 is the most common indication.”
From Indications for Lung Transplantation and Patient Selection (2022) · cites this paper as [61]
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In the citing paper
“The ESC/ERS model also employs the assessment of risk using a multi-parametric comprehensive analysis of clinical variables.(284) Unlike REVEAL, this model avoids use of any non-modifiable criteria, and does not “weight” the variables according to their relative importance.”
From Consensus document for the selection of lung transplant candidates: An update from the International Society for Heart and Lung Transplantation. (2021) · cites this paper as [284]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Unlike REVEAL, this model avoids use of any non-modifiable criteria, and does not “weight” the variables according to their relative importance.”
From Consensus document for the selection of lung transplant candidates: An update from the International Society for Heart and Lung Transplantation. (2021) · cites this paper as [284]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“transplantation may be necessary if prostacyclin treatment is required for an appropriate intervention, there is accompanying liver or renal failure, or severe hemoptysis is present [3,59-62]”
From Indications for Lung Transplantation and Patient Selection (2022) · cites this paper as [61]
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“group 3 with PAH and accompanying pathological changes in the lung parenchyma can be considered for transplantation.”
From Indications for Lung Transplantation and Patient Selection (2022) · cites this paper as [61]
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“Group 2, with decreased left ventricular function, is not an indication for transplantation”
From Indications for Lung Transplantation and Patient Selection (2022) · cites this paper as [61]
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“The two most frequently used risk assessment models are the Registry to Evaluate Early and Long-term Pulmonary Arterial Hypertension Disease Management (REVEAL) 2.0 and the 2015 European Society of Cardiology/European Respiratory Society (ESC/ERS) model.(283, 284)”
From Consensus document for the selection of lung transplant candidates: An update from the International Society for Heart and Lung Transplantation. (2021) · cites this paper as [284]
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“The ESC/ERS model also employs the assessment of risk using a multi-parametric comprehensive analysis of clinical variables.(284)”
From Consensus document for the selection of lung transplant candidates: An update from the International Society for Heart and Lung Transplantation. (2021) · cites this paper as [284]
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“The current consensus is based on 2 tools for referral and listing: the REVEAL Registry 2.2 (Registry to Evaluate Early and Long-term Pulmonary Arterial Hypertension Disease Management 2.0) and 2015 European Society of Cardiology/European Respiratory Society.”
From Indications for Lung Transplantation and Patient Selection (2022) · cites this paper as [61]
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Research works printed but not linked: 2
- Galiè, 2014, Anticoagulant therapy does not influence long-term outcomes in patients with pulmonary arterial hypertension (PAH): insights from the randomised controlled SERAPHIN trial of macitentan, Eur Heart J, 35, 10
- Galiè, 2013, New treatment strategies for pulmonary arterial hypertension: hopes or hypes, J Am Coll Cardiol, 62, 1101, 10.1016/j.jacc.2013.06.032 · DOI
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Metadata
- Authors
- Galiè, N., Humbert, M., Vachiery, J.-L., Gibbs, S., Lang, I., Torbicki, A., Simonneau, G., Peacock, A., Vonk Noordegraaf, A., Beghetti, M., Ghofrani, A., Gomez Sanchez, M. A., Hansmann, G., Klepetko, W., Lancellotti, P., Matucci, M., McDonagh, T., Pierard, L. A., Trindade, P. T., Zompatori, M., Hoeper, M., ESC Scientific Document Group, Aboyans, V., Vaz Carneiro, A., Achenbach, S., Agewall, S., Allanore, Y., Asteggiano, R., Badano, L. P., Barberá, J. A., Bouvaist, H., Bueno, H., Byrne, R. A., Carerj, S., Castro, G., Erol, Ç., Falk, V., Funck-Brentano, C., Gorenflo, M., Granton, J., Iung, B., Kiely, D. G., Kirchhof, P., Kjellstrom, B., Landmesser, U., Lekakis, J., Lionis, C., Lip, G. Y. H., Orfanos, S. E., Park, M. H., Piepoli, M. F., Ponikowski, P., Revel, M.-P., Rigau, D., Rosenkranz, S., Völler, H., Zamorano, J. L., Zamorano, J. L., Aboyans, V., Achenbach, S., Agewall, S., Badimon, L., Barón-Esquivias, G., Baumgartner, H., Bax, J. J., Bueno, H., Carerj, S., Dean, V., Erol, Ç., Fitzsimons, D., Gaemperli, O., Kirchhof, P., Kolh, P., Lancellotti, P., Lip, G. Y., Nihoyannopoulos, P., Piepoli, M. F., Ponikowski, P., Roffi, M., Torbicki, A., Vaz Carneiro, A., Windecker, S., Myftiu, S., Bonderman, D., Firdovsi, I., Lazareva, I., De Pauw, M., Sokolovic, Š., Velchev, V., Cikeš, M., Moutiris, J. A., Jansa, P., Nielsen-Kudsk, J. E., Anton, L., Jääskeläinen, P., Bauer, F., Chukhrukidze, A., Opitz, C., Giannakoulas, G., Karlócai, K., Oddsson, H., Gaine, S., Menachemi, D., Emdin, M., Sooronbaev, T., Rudzitis, T. A., Gumbiene, L., Lebrun, F., Micallef, J., Botnaru, V., Oukerraj, L., Andreassen, A. K., Kurzyna, M., Leite Baptista, M. J. R., Coman, I. M., Moiseeva, O., Stefanovic, B. S., Šimková, I., Wikström, G., Schwerzmann, M., Srbinovska-Kostovska, E., van Dijk, A. P. J., Mahdhaoui, A., Kaymaz, C., Coghlan, G., & Sirenko, Y.
- Affiliations
- University of Bologna (IT)
- Université Paris-Sud (FR)
- ORCID
- Galiè, Nazzareno
- Humbert, Marc
- Lang, Irene
- Simonneau, Gérald
- Beghetti, Maurice
- Hansmann, Georg
- Klepetko, Walter
- Trindade, Pedro T.
- Hoeper, Marius
- Asteggiano, Riccardo
- Badano, Luigi Paolo
- Falk, Volkmar
- Iung, Bernard
- Kiely, David G
- Landmesser, Ulf
- Lionis, Christos
- Park, Myung H
- Revel, Marie-Pierre
- Bax, Jeroen J
- Kolh, Philippe
- Windecker, Stephan
- Giannakoulas, George
- Botnaru, Victor
- Kurzyna, Marcin
- Šimková, Iveta
- Coghlan, Gerry
- Sirenko, Yuriy
- Venue
- European Heart Journal
- Publisher
- Oxford University Press (OUP)
- Published
- 2015-08-29
- Volume
- 37
- Issue
- 1
- Pages
- 67-119
- ISSN
- 0195-668X (ISSN-L)
- 1522-9645
- OpenAlex
- W2161370807
- Cited by
- 6,931
- References
- 471
- Citations by year
- 2026: 174 · 2025: 297 · 2024: 408 · 2023: 560 · 2022: 778 · 2021: 953 · 2020: 930 · 2019: 794 · 2018: 801 · 2017: 659 · 2016: 461 · 2015: 65
- FWCI
- 524.32
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- European Heart Journal (publishedVersion)
- PubMed (publishedVersion)
- Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion)
- Open Repository and Bibliography (University of Liège) (submittedVersion, other-oa)
- Pure Amsterdam UMC (submittedVersion, other-oa)
- BOA (University of Milano-Bicocca) (submittedVersion)
- Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) (submittedVersion)
- IRIS (submittedVersion)
- University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
- SERVAL (Université de Lausanne) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Funders
- European Respiratory Society
- European Society of Cardiology
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Pulmonary Hypertension Research and Treatments
- Health Sciences › Medicine › Genetics (clinical) › Vascular Anomalies and Treatments
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Congenital Heart Disease Studies
- Keywords
- pulmonary hypertension, diagnosis, treatment, right ventricular function, pulmonary circulation, congenital heart disease, valvular heart disease, heart failure, pharmacotherapy, cardiovascular surgery
- MeSH terms
- Adult, Algorithms, Antihypertensive Agents, Arrhythmias, Cardiac, Child, Combined Modality Therapy, Connective Tissue Diseases, Cross Infection, Drug Interactions, Echocardiography, Electrocardiography, Exercise Test, Exercise Therapy, Female, Genetic Counseling, Genetic Testing, Health Status, Cardiac Catheterization, Heart Defects, Congenital, Hemangioma, Hemoptysis, Humans, Hypertension, Portal, Hypertension, Pulmonary, Patient Compliance, Pregnancy, Pregnancy Complications, Cardiovascular, Referral and Consultation, Respiratory Function Tests, Risk Factors, Social Support, Terminal Care, Thromboembolism, Tomography, X-Ray Computed, Biomarkers, HIV Infections, Lung Transplantation, Treatment Outcome, Elective Surgical Procedures, Ventricular Dysfunction, Right, Risk Assessment, Magnetic Resonance Angiography, Therapies, Investigational, Travel Medicine, Balloon Embolectomy, Multimodal Imaging
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