Prognostic Implications of the Novel Pulmonary Hypertension Definition in Patients with Aortic Stenosis after Transcatheter Valve Replacement.

aortic stenosis pulmonary hypertension transcatheter aortic valve replacement

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
22 Jul 2022
Historique:
received: 16 05 2022
revised: 08 07 2022
accepted: 15 07 2022
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 28 7 2022
Statut: epublish

Résumé

Introduction: Pulmonary hypertension (PH), traditionally defined as a mean pulmonary artery pressure (PAP) ≥ 25 mmHg, is associated with poor outcomes in patients undergoing a transcatheter aortic valve replacement (TAVR) for severe aortic stenosis (AS). Recently, a novel definition for PH has been proposed, placing the cut-off value of mean PAP at 20 mmHg, and introducing pulmonary vascular resistance as an exclusive indicator for the pre-capillary involvement. In light of the novel criteria, whether PH still preserves its prognostic significance remains unknown. Methods: The study population consisted of 380 patients with AS, who underwent a right heart catheterization before TAVR. The cohort was divided according to the presence of PH (n = 174, 45.7%) or not. Patients with PH were further divided into the following groups: (1) Pre-capillary PH ((Pre-capPH), n = 46, 12.1%); (2) Isolated post-capillary PH ((IpcPH), n = 78, 20.5%); (3) Combined pre and post-capillary PH ((CpcPH), n = 82, 21.6%). The primary endpoint was all-cause mortality at 1 year. Results: A total of 246 patients (64.7%) exhibited mean PAP > 20 mmHg. Overall, the presence of PH was associated with higher 1-year mortality rates (hazard ratio (HR) 2.8, 95% CI: 1.4−5.8, p = 0.004). Compared to patients with no PH, Pre-capPH and CpcPH (but not IpcPH) were related to higher 1-year mortality (HR 2.7, 95% CI: 1.0−7.2, p = 0.041 and HR 3.9, 95% CI: 1.8−8.5, p = 0.001, respectively). This remained significant even after the adjustment for baseline comorbidities. Conclusions: Pre-interventional PH according to the novel hemodynamic criteria, is linked with poor outcomes in patients undergoing TAVR for severe AS. However, this is mainly driven by patients with mean PAP ≥ 25 mmHg. Patients with a pre-capillary PH component as defined by increased PVR present an even worse prognosis as compared to patients with isolated post-capillary or no PH who present comparable 1-year mortality rates.

Identifiants

pubmed: 35893367
pii: jcm11154279
doi: 10.3390/jcm11154279
pmc: PMC9332728
pii:
doi:

Types de publication

Journal Article

Langues

eng

Déclaration de conflit d'intérêts

Noble Stephane has financial relations with industry (proctor for Medtronic) and has received institutional grants from Edwards Sapien, Medtronic and Abbott Vascular. The authors declare no conflict of interest.

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Auteurs

Dionysios Adamopoulos (D)

Faculty of Medicine, Department of Medicine, Geneva University, 1206 Geneva, Switzerland.
Department of Internal Medicine, Division of Cardiology, Hôpitaux Universitaires de Genève (HUG), 1205 Geneva, Switzerland.

Stamatia Pagoulatou (S)

Laboratory of Hemodynamics and Cardiovascular Technology, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland.

Georgios Rovas (G)

Laboratory of Hemodynamics and Cardiovascular Technology, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland.

Vasiliki Bikia (V)

Laboratory of Hemodynamics and Cardiovascular Technology, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland.

Hajo Müller (H)

Department of Internal Medicine, Division of Cardiology, Hôpitaux Universitaires de Genève (HUG), 1205 Geneva, Switzerland.

Georgios Giannakopoulos (G)

Department of Internal Medicine, Division of Cardiology, Hôpitaux Universitaires de Genève (HUG), 1205 Geneva, Switzerland.

Sarah Mauler-Wittwer (S)

Department of Internal Medicine, Division of Cardiology, Hôpitaux Universitaires de Genève (HUG), 1205 Geneva, Switzerland.

Marc-Joseph Licker (MJ)

Faculty of Medicine, Department of Medicine, Geneva University, 1206 Geneva, Switzerland.
Department of Acute Medicine, Division of Anaesthesiology, Hôpitaux Universitaires de Genève (HUG), 1205 Geneva, Switzerland.

Nikolaos Stergiopulos (N)

Laboratory of Hemodynamics and Cardiovascular Technology, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland.

Frédéric Lador (F)

Faculty of Medicine, Department of Medicine, Geneva University, 1206 Geneva, Switzerland.
Department of Internal Medicine, Division of Pneumology, Hôpitaux Universitaires de Genève (HUG), 1205 Geneva, Switzerland.
Pulmonary Hypertension Program, Hôpitaux Universitaires de Genève (HUG), 1205 Geneva, Switzerland.

Stéphane Noble (S)

Faculty of Medicine, Department of Medicine, Geneva University, 1206 Geneva, Switzerland.
Department of Internal Medicine, Division of Cardiology, Hôpitaux Universitaires de Genève (HUG), 1205 Geneva, Switzerland.
Pulmonary Hypertension Program, Hôpitaux Universitaires de Genève (HUG), 1205 Geneva, Switzerland.

Classifications MeSH