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Multicentric Standardized Flow Cytometry Routine Assessment of Patients With Sepsis to Predict Clinical Worsening.

Authors :
Daix, Thomas
Guerin, Estelle
Tavernier, Elsa
Mercier, Emmanuelle
Gissot, Valérie
Hérault, Olivier
Mira, Jean-Paul
Dumas, Florence
Chapuis, Nicolas
Guitton, Christophe
Béné, Marie C.
Quenot, Jean-Pierre
Tissier, Cindy
Guy, Julien
Piton, Gaël
Roggy, Anne
Muller, Grégoire
Legac, Éric
De Prost, Nicolas
Khellaf, Mehdi
Source :
CHEST. Sep2018, Vol. 154 Issue 3, p617-627. 11p.
Publication Year :
2018

Abstract

<bold>Background: </bold>In this study, we primarily sought to assess the ability of flow cytometry to predict early clinical deterioration and overall survival in patients with sepsis admitted in the ED and ICU.<bold>Methods: </bold>Patients admitted for community-acquired acute sepsis from 11 hospital centers were eligible. Early (day 7) and late (day 28) deaths were notified. Levels of CD64pos granulocytes, CD16pos monocytes, CD16dim immature granulocytes (IGs), and T and B lymphocytes were assessed by flow cytometry using an identical, cross-validated, robust, and simple consensus standardized protocol in each center.<bold>Results: </bold>Among 1,062 patients screened, 781 patients with confirmed sepsis were studied (age, 67 ± 48 years; Simplified Acute Physiology Score II, 36 ± 17; Sequential Organ Failure Assessment, 5 ± 4). Patients were divided into three groups (sepsis, severe sepsis, and septic shock) on day 0 and on day 2. On day 0, patients with sepsis exhibited increased levels of CD64pos granulocytes, CD16pos monocytes, and IGs with T-cell lymphopenia. Clinical severity was associated with higher percentages of IGs and deeper T-cell lymphopenia. IG percentages tended to be higher in patients whose clinical status worsened on day 2 (35.1 ± 35.6 vs 43.5 ± 35.2, P = .07). Increased IG percentages were also related to occurrence of new organ failures on day 2. Increased IG percentages, especially when associated with T-cell lymphopenia, were independently associated with early (P < .01) and late (P < .01) death.<bold>Conclusions: </bold>Increased circulating IGs at the acute phase of sepsis are linked to clinical worsening, especially when associated with T-cell lymphopenia. Early flow cytometry could help clinicians to target patients at high risk of clinical deterioration.<bold>Trial Registry: </bold>ClinicalTrials.gov; No.: NCT01995448; URL: www.clinicaltrials.gov. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00123692
Volume :
154
Issue :
3
Database :
Academic Search Index
Journal :
CHEST
Publication Type :
Academic Journal
Accession number :
131468815
Full Text :
https://doi.org/10.1016/j.chest.2018.03.058