Prognostic value of right ventricular dilatation on computed tomography pulmonary angiogram for predicting adverse clinical events in severe COVID-19 pneumonia.

ARDS AVDS COVID-19 angiogram computed tomography pneumonia right ventricle dilatation

Journal

Frontiers in medicine
ISSN: 2296-858X
Titre abrégé: Front Med (Lausanne)
Pays: Switzerland
ID NLM: 101648047

Informations de publication

Date de publication:
2023
Historique:
received: 28 04 2023
accepted: 03 07 2023
medline: 16 8 2023
pubmed: 16 8 2023
entrez: 16 8 2023
Statut: epublish

Résumé

Right ventricle dilatation (RVD) is a common complication of non-intubated COVID-19 pneumonia caused by pro-thrombotic pneumonitis, intra-pulmonary shunting, and pulmonary vascular dysfunction. In several pulmonary diseases, RVD is routinely measured on computed tomography pulmonary angiogram (CTPA) by the right ventricle-to-left ventricle (LV) diameter ratio > 1 for predicting adverse events. The aim of the study was to evaluate the association between RVD and the occurrence of adverse events in a cohort of critically ill non-intubated COVID-19 patients. Between February 2020 and February 2022, non-intubated patients admitted to the Amiens University Hospital intensive care unit for COVID-19 pneumonia with CTPA performed within 48 h of admission were included. RVD was defined by an RV/LV diameter ratio greater than one measured on CTPA. The primary outcome was the occurrence of an adverse event (renal replacement therapy, extracorporeal membrane oxygenation, 30-day mortality after ICU admission). Among 181 patients, 62% ( Right ventricle (RV) dilatation assessed by RV/LV ratio was a common CTPA finding in non-intubated critical patients with COVID-19 pneumonia and was not associated with the occurrence of clinical adverse events.

Sections du résumé

Background UNASSIGNED
Right ventricle dilatation (RVD) is a common complication of non-intubated COVID-19 pneumonia caused by pro-thrombotic pneumonitis, intra-pulmonary shunting, and pulmonary vascular dysfunction. In several pulmonary diseases, RVD is routinely measured on computed tomography pulmonary angiogram (CTPA) by the right ventricle-to-left ventricle (LV) diameter ratio > 1 for predicting adverse events.
Objective UNASSIGNED
The aim of the study was to evaluate the association between RVD and the occurrence of adverse events in a cohort of critically ill non-intubated COVID-19 patients.
Methods UNASSIGNED
Between February 2020 and February 2022, non-intubated patients admitted to the Amiens University Hospital intensive care unit for COVID-19 pneumonia with CTPA performed within 48 h of admission were included. RVD was defined by an RV/LV diameter ratio greater than one measured on CTPA. The primary outcome was the occurrence of an adverse event (renal replacement therapy, extracorporeal membrane oxygenation, 30-day mortality after ICU admission).
Results UNASSIGNED
Among 181 patients, 62% (
Conclusion UNASSIGNED
Right ventricle (RV) dilatation assessed by RV/LV ratio was a common CTPA finding in non-intubated critical patients with COVID-19 pneumonia and was not associated with the occurrence of clinical adverse events.

Identifiants

pubmed: 37583421
doi: 10.3389/fmed.2023.1213775
pmc: PMC10425267
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1213775

Informations de copyright

Copyright © 2023 Beyls, Vial, Lefebvre, Muller, Hanquiez, Besserve, Guilbart, Haye, Bernasinski, Huette, Dupont, Abou-Arab, Jounieaux and Mahjoub.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Christophe Beyls (C)

Department of Anesthesiology and Critical Care Medicine, Amiens University Hospital, Amiens, France.

Jeremie Vial (J)

Department of Radiology, Amiens University Hospital, Amiens, France.

Thomas Lefebvre (T)

Department of Anesthesiology and Critical Care Medicine, Amiens University Hospital, Amiens, France.

Charlotte Muller (C)

Department of Anesthesiology and Critical Care Medicine, Amiens University Hospital, Amiens, France.

Thomas Hanquiez (T)

Department of Anesthesiology and Critical Care Medicine, Amiens University Hospital, Amiens, France.

Patricia Besserve (P)

Department of Anesthesiology and Critical Care Medicine, Amiens University Hospital, Amiens, France.

Mathieu Guilbart (M)

Department of Anesthesiology and Critical Care Medicine, Amiens University Hospital, Amiens, France.

Guillaume Haye (G)

Department of Anesthesiology and Critical Care Medicine, Amiens University Hospital, Amiens, France.

Michael Bernasinski (M)

Department of Anesthesiology and Critical Care Medicine, Amiens University Hospital, Amiens, France.

Pierre Huette (P)

Department of Anesthesiology and Critical Care Medicine, Amiens University Hospital, Amiens, France.

Hervé Dupont (H)

Department of Anesthesiology and Critical Care Medicine, Amiens University Hospital, Amiens, France.

Osama Abou-Arab (O)

Department of Anesthesiology and Critical Care Medicine, Amiens University Hospital, Amiens, France.

Vincent Jounieaux (V)

Department of Pneumology, Amiens University Hospital, Amiens, France.

Yazine Mahjoub (Y)

Department of Anesthesiology and Critical Care Medicine, Amiens University Hospital, Amiens, France.

Classifications MeSH