High prevalence of pre-existing sarcopenia in critically ill patients with hematologic malignancies admitted to the intensive care unit for sepsis or septic shock.


Journal

Clinical nutrition ESPEN
ISSN: 2405-4577
Titre abrégé: Clin Nutr ESPEN
Pays: England
ID NLM: 101654592

Informations de publication

Date de publication:
06 2023
Historique:
received: 22 12 2022
revised: 31 03 2023
accepted: 09 04 2023
medline: 22 5 2023
pubmed: 19 5 2023
entrez: 18 5 2023
Statut: ppublish

Résumé

We aimed to evaluate body composition (BC) by computed tomography (CT) in hematologic malignancy (HM) patients admitted to the intensive care unit (ICU) for sepsis or septic shock. We retrospectively assessed BC and its impact on outcome of 186 patients at the 3rd lumbar (L3) and 12th thoracic vertebral levels (T12) using CT-scan performed before ICU admission. The median patient age was 58.0 [47; 69] years. Patients displayed adverse clinical characteristics at admission with median [q1; q3] SAPS II and SOFA scores of 52 [40; 66] and 8 [5; 12], respectively. The mortality rate in the ICU was 45.7%. Overall survival rates at 1 month after admission in the pre-existing sarcopenic vs. non pre-existing sarcopenic patients were 47.9% (95% CI [37.6; 61.0]) and 55.0% (95% CI [41.6; 72.8]), p = 0.99), respectively, at the L3 level and 48.4% (95% CI [40.4; 58.0]) vs. 66.7% (95% CI [51.1; 87.0]), p = 0.062), respectively, at the T12 level. Sarcopenia is assessable by CT scan at both the T12 and L3 levels and is highly prevalent in HM patients admitted to the ICU for severe infections. Sarcopenia may contribute to the high mortality rate in the ICU in this population.

Sections du résumé

BACKGROUND & AIMS
We aimed to evaluate body composition (BC) by computed tomography (CT) in hematologic malignancy (HM) patients admitted to the intensive care unit (ICU) for sepsis or septic shock.
METHODS
We retrospectively assessed BC and its impact on outcome of 186 patients at the 3rd lumbar (L3) and 12th thoracic vertebral levels (T12) using CT-scan performed before ICU admission.
RESULTS
The median patient age was 58.0 [47; 69] years. Patients displayed adverse clinical characteristics at admission with median [q1; q3] SAPS II and SOFA scores of 52 [40; 66] and 8 [5; 12], respectively. The mortality rate in the ICU was 45.7%. Overall survival rates at 1 month after admission in the pre-existing sarcopenic vs. non pre-existing sarcopenic patients were 47.9% (95% CI [37.6; 61.0]) and 55.0% (95% CI [41.6; 72.8]), p = 0.99), respectively, at the L3 level and 48.4% (95% CI [40.4; 58.0]) vs. 66.7% (95% CI [51.1; 87.0]), p = 0.062), respectively, at the T12 level.
CONCLUSIONS
Sarcopenia is assessable by CT scan at both the T12 and L3 levels and is highly prevalent in HM patients admitted to the ICU for severe infections. Sarcopenia may contribute to the high mortality rate in the ICU in this population.

Identifiants

pubmed: 37202070
pii: S2405-4577(23)00100-6
doi: 10.1016/j.clnesp.2023.04.007
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

373-383

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest No conflicts of interest.

Auteurs

Antoine Herault (A)

Intensive Care Unit, Charles Nicolle University Hospital, Rouen, France; Department of Hematology and INSERM U1245, Centre Henri Becquerel, Rouen, France.

Emilie Lévêque (E)

Clinical Research Unit, Centre Henri Becquerel, Rouen, France.

Simon Draye-Carbonnier (S)

Department of Nuclear Medicine, Centre Henri Becquerel, Rouen, France.

Pierre Decazes (P)

Department of Nuclear Medicine, Centre Henri Becquerel, Rouen, France; Unité QuantIF LITIS EA 4108, Université de Rouen, Normandie, France; Département D'imagerie, Centre Henri-Becquerel, Rouen, France.

Alexandra Zduniak (A)

Department of Hematology and INSERM U1245, Centre Henri Becquerel, Rouen, France.

Romain Modzelewski (R)

Unité QuantIF LITIS EA 4108, Université de Rouen, Normandie, France; Département D'imagerie, Centre Henri-Becquerel, Rouen, France.

Julie Libraire (J)

Clinical Research Unit, Centre Henri Becquerel, Rouen, France.

Najate Achamrah (N)

Department of Nutrition, Charles Nicolle University Hospital, Rouen, France.

Anne-Lise Ménard (AL)

Department of Hematology and INSERM U1245, Centre Henri Becquerel, Rouen, France.

Pascal Lenain (P)

Department of Hematology and INSERM U1245, Centre Henri Becquerel, Rouen, France.

Nathalie Contentin (N)

Department of Hematology and INSERM U1245, Centre Henri Becquerel, Rouen, France.

Maximilien Grall (M)

Intensive Care Unit, Charles Nicolle University Hospital, Rouen, France.

Stéphane Leprêtre (S)

Department of Hematology and INSERM U1245, Centre Henri Becquerel, Rouen, France.

Emilie Lemasle (E)

Department of Hematology and INSERM U1245, Centre Henri Becquerel, Rouen, France.

Hélène Lanic (H)

Department of Hematology and INSERM U1245, Centre Henri Becquerel, Rouen, France.

Mustafa Alani (M)

Department of Hematology and INSERM U1245, Centre Henri Becquerel, Rouen, France.

Aspasia Stamatoullas-Bastard (A)

Department of Hematology and INSERM U1245, Centre Henri Becquerel, Rouen, France.

Hervé Tilly (H)

Department of Hematology and INSERM U1245, Centre Henri Becquerel, Rouen, France.

Fabrice Jardin (F)

Department of Hematology and INSERM U1245, Centre Henri Becquerel, Rouen, France.

Fabienne Tamion (F)

Intensive Care Unit, Charles Nicolle University Hospital, Rouen, France; Normandie Univ, UNIROUEN, INSERM U1096, CHU Rouen, France.

Vincent Camus (V)

Department of Hematology and INSERM U1245, Centre Henri Becquerel, Rouen, France. Electronic address: vincent.camus@chb.unicancer.fr.

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