Almitrine Infusion in Severe Acute Respiratory Syndrome Coronavirus 2-Induced Acute Respiratory Distress Syndrome: A Single-Center Observational Study.


Journal

Critical care medicine
ISSN: 1530-0293
Titre abrégé: Crit Care Med
Pays: United States
ID NLM: 0355501

Informations de publication

Date de publication:
01 02 2021
Historique:
pubmed: 24 10 2020
medline: 26 1 2021
entrez: 23 10 2020
Statut: ppublish

Résumé

Treating acute respiratory failure in patients with coronavirus disease 2019 is challenging due to the lack of knowledge of the underlying pathophysiology. Hypoxemia may be explained in part by the loss of hypoxic pulmonary vasoconstriction. The present study assessed the effect of almitrine, a selective pulmonary vasoconstrictor, on arterial oxygenation in severe acute respiratory syndrome coronavirus 2-induced acute respiratory distress syndrome. Single-center retrospective observational study. ICU of Lille Teaching Hospital, France, from February 27, 2020, to April 14, 2020. Patients with coronavirus disease 2019 pneumonia confirmed by positive reverse transcriptase-polymerase chain reaction for severe acute respiratory syndrome-coronavirus 2 and acute respiratory distress syndrome according to Berlin definition. Data focused on clinicobiological features, ventilator settings, therapeutics, outcomes, and almitrine-related adverse events. Almitrine was considered in patients with severe hypoxemia (Pao2/Fio2 ratio < 150 mm Hg) in addition to the recommended therapies, at an hourly IV delivery of 10 μg/kg/min. Comparative blood gases were done before starting almitrine trial and immediately after the end of the infusion. A positive response to almitrine was defined by an increase of Pao2/Fio2 ratio greater than or equal to 20% at the end of the infusion. A total of 169 patients were enrolled. Thirty-two patients with acute respiratory distress syndrome received an almitrine infusion trial. In most cases, almitrine was infused in combination with inhaled nitric oxide (75%). Twenty-one patients (66%) were responders. The median Pao2/Fio2 ratio improvement was 39% (9-93%) and differs significantly between the responders and nonresponders (67% [39-131%] vs 6% [9-16%], respectively; p < 0.0001). The 28-day mortality rates were 47.6% and 63.6% (p = 0.39) for the responders and nonresponders, respectively. Hemodynamic parameters remained similar before and after the trial, not suggesting acute cor pulmonale. Almitrine infusion improved oxygenation in severe acute respiratory syndrome coronavirus 2-induced acute respiratory distress syndrome without adverse effects. In a multistep clinical approach to manage severe hypoxemia in this population, almitrine could be an interesting therapeutic option to counteract the loss of hypoxic pulmonary vasoconstriction and redistribute blood flow away from shunting zones.

Identifiants

pubmed: 33093279
pii: 00003246-202102000-00038
doi: 10.1097/CCM.0000000000004711
doi:

Substances chimiques

Respiratory System Agents 0
Almitrine 9A1222NBG4

Types de publication

Clinical Trial Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e191-e198

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 by the Society of Critical Care Medicine and Wolters Kluwer Health, Inc. All Rights Reserved.

Déclaration de conflit d'intérêts

This work was supported by the French government through the Programme Investissement d’Avenir (I-SITE ULNE/ANR-16-IDEX-0004 ULNE) managed by the Agence Nationale de la Recherche ("PHYSIO COVID" and "PREDICT" projects) The authors have disclosed that they do not have any potential conflicts of interest.

Références

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Auteurs

Morgan Caplan (M)

Pôle de Réanimation, CHU Lille, University of Lille, Lille, France.

Julien Goutay (J)

Pôle de Réanimation, CHU Lille, University of Lille, Lille, France.

Anne Bignon (A)

Réanimation Chirurgicale, CHU Lille, University of Lille, Lille, France.

Emmanuelle Jaillette (E)

Pôle de Réanimation, CHU Lille, University of Lille, Lille, France.

Raphael Favory (R)

Pôle de réanimation, Lille Inflammation Research International Center (LIRIC), CHU Lille, Inserm U995, University of Lille, Lille, France.

Daniel Mathieu (D)

Pôle de Réanimation, CHU Lille, University of Lille, Lille, France.

Erika Parmentier-Decrucq (E)

Pôle de Réanimation, CHU Lille, University of Lille, Lille, France.

Julien Poissy (J)

Pôle de réanimation, CNRS, UMR 8576 - Unité de Glycobiologie Structurale et Fonctionnelle, CHU Lille, Inserm U1285, University of Lille, Lille, France.

Thibault Duburcq (T)

Pôle de Réanimation, CHU Lille, University of Lille, Lille, France.

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