Isoproterenol Improves Hemodynamics And Right Ventricle-Pulmonary Artery Coupling After Heart Transplantation.

Heart transplantation Hemodynamics Isoproterenol RV-PA coupling right ventricular failure

Journal

American journal of physiology. Heart and circulatory physiology
ISSN: 1522-1539
Titre abrégé: Am J Physiol Heart Circ Physiol
Pays: United States
ID NLM: 100901228

Informations de publication

Date de publication:
03 May 2024
Historique:
medline: 3 5 2024
pubmed: 3 5 2024
entrez: 3 5 2024
Statut: aheadofprint

Résumé

Right ventricular failure (RVF) is a major cause of early mortality after heart transplantation (HT). Isoproterenol has chronotropic, inotropic, and vasodilatory properties which might improve right ventricle function in this setting. We aimed to investigate the hemodynamic effects of isoproterenol on patients with post-HT RVF. We conducted a one-year retrospective observational study including patients receiving isoproterenol and dobutamine for early RVF after HT. A comprehensive multiparametric hemodynamic evaluation was performed successively at three times: no isoproterenol, low doses: 0.025 µg/kg/min and high doses: 0.05 µg/kg/min (henceforth respectively called no-iso, low-iso and high-iso). From June 2022 to June 2023, 25 patients, median [IQR25-75] age 54 [38-61] years, were included. Before isoproterenol introduction, all patients received dobutamine and 15 (60%) were on veno-arterial extracorporeal membrane oxygenation. Isoproterenol significantly increased heart rate from 84 [77-99] (no-iso) to 91 [88-106] (low-iso) and 102 [90-122] bpm (high-iso, p<0.001). Similarly, cardiac index raised from 2.3 [1.4-3.1] to 2.7 [1.8-3.4] and 3 [1.9-3.7] l/min/m In post-HT RVF, isoproterenol exhibits chronotropic and inotropic effects, thereby improving RV-PA coupling and resulting in a clinically relevant increase in the cardiac index.

Sections du résumé

BACKGROUND BACKGROUND
Right ventricular failure (RVF) is a major cause of early mortality after heart transplantation (HT). Isoproterenol has chronotropic, inotropic, and vasodilatory properties which might improve right ventricle function in this setting. We aimed to investigate the hemodynamic effects of isoproterenol on patients with post-HT RVF.
METHODS METHODS
We conducted a one-year retrospective observational study including patients receiving isoproterenol and dobutamine for early RVF after HT. A comprehensive multiparametric hemodynamic evaluation was performed successively at three times: no isoproterenol, low doses: 0.025 µg/kg/min and high doses: 0.05 µg/kg/min (henceforth respectively called no-iso, low-iso and high-iso).
RESULTS RESULTS
From June 2022 to June 2023, 25 patients, median [IQR25-75] age 54 [38-61] years, were included. Before isoproterenol introduction, all patients received dobutamine and 15 (60%) were on veno-arterial extracorporeal membrane oxygenation. Isoproterenol significantly increased heart rate from 84 [77-99] (no-iso) to 91 [88-106] (low-iso) and 102 [90-122] bpm (high-iso, p<0.001). Similarly, cardiac index raised from 2.3 [1.4-3.1] to 2.7 [1.8-3.4] and 3 [1.9-3.7] l/min/m
CONCLUSIONS CONCLUSIONS
In post-HT RVF, isoproterenol exhibits chronotropic and inotropic effects, thereby improving RV-PA coupling and resulting in a clinically relevant increase in the cardiac index.

Identifiants

pubmed: 38700470
doi: 10.1152/ajpheart.00200.2024
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

David Levy (D)

Médecine intensive-Réanimation, Pitié-Salpêtrière Hospital, Paris, France.

Ouriel Saura (O)

Pitié-Salpêtrière Hospital, France.

Manuela Lucenteforte (M)

Pitié-Salpêtrière Hospital, France.

Elena Collado Lledó (E)

PitiÃ{copyright, serif}-Salpêtrière Hospital, Paris, France.

Pierre Demondion (P)

Pitié-Salpêtrière Hospital, France.

Nadjib Hammoudi (N)

Pitié-Salpêtrière Hospital, France.

Benjamin Assouline (B)

Pitié-Salpêtrière Hospital, France.

Matthieu Petit (M)

Pitié-Salpêtrière Hospital, France.

Melchior Gautier (M)

Pitié-Salpêtrière Hospital, France.

Lucie Le Fevre (L)

Pitié-Salpêtrière Hospital, France.

Marc Pineton de Chambrun (M)

Pitié-Salpêtrière Hospital, France.

Guillaume Coutance (G)

Pitié-Salpêtrière Hospital, France.

Elodie Berg (E)

Pitié-Salpêtrière Hospital, France.

Juliette Chommeloux (J)

Pitié-Salpêtrière Hospital, France.

Matthieu Schmidt (M)

Pitié-Salpêtrière Hospital, France.

Charles-Edouard Luyt (CE)

Pitié-Salpêtrière Hospital, France.

Guillaume Lebreton (G)

Pitié-Salpêtrière Hospital, France.

Pascal Leprince (P)

Pitié-Salpêtrière Hospital, France.

Guillaume Hekimian (G)

Pitié-Salpêtrière Hospital, France.

Alain Combes (A)

Pitié-Salpêtrière Hospital, France.

Classifications MeSH