| Title |
Multicentric Standardized Flow Cytometry Routine Assessment of Patients With Sepsis to Predict Clinical Worsening
|
|---|---|
| Published in |
CHEST, April 2018
|
| DOI | 10.1016/j.chest.2018.03.058 |
| Pubmed ID | |
| Authors |
Thomas Daix, Estelle Guerin, Elsa Tavernier, Emmanuelle Mercier, Valérie Gissot, Olivier Hérault, Jean-Paul Mira, Florence Dumas, Nicolas Chapuis, Christophe Guitton, Marie C. Béné, Jean-Pierre Quenot, Cindy Tissier, Julien Guy, Gaël Piton, Anne Roggy, Grégoire Muller, Éric Legac, Nicolas de Prost, Mehdi Khellaf, Orianne Wagner-Ballon, Rémi Coudroy, Elodie Dindinaud, Fabrice Uhel, Mikaël Roussel, Thomas Lafon, Robin Jeannet, Frédéric Vargas, Catherine Fleureau, Mickaël Roux, Kaoutar Allou, Philippe Vignon, Jean Feuillard, Bruno François, Septiflux Trial Group, Adollës Di Vittorio, Sébastien Lachot, Marie-Thérèse Georget, Joelle Hanna, Cédric Bretonnière, Olivier Zambon, Laurent Nicolet, Noëlle Brule, Camille Debord, Yannick Le Bris, Nelly Robillard, Auguste Dargent, Anne Bretagnol, Armelle Mathonnet, Thierry Boulain, François Barbier, Dalila Benzekri, Isabelle Runge, Toufik Kamel, Jérôme Cecchini, Sabrina Bouyer, René Robert, Alexandre Ouattara |
| Abstract |
In this study, we primarily sought to assess the ability of flow cytometry to predict early clinical deterioration and overall survival in septic patients admitted in the emergency department and intensive care unit. 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 (IG), T and B lymphocytes were assessed by flow cytometry, using an identical, cross-validated, robust and simple consensus standardized protocol in each center. Among 1062 patients screened, 781 patients with confirmed sepsis were studied (age: 67±48 years, SAPS II: 36±17, SOFA: 5±4). Patients were divided into three groups (sepsis, severe sepsis and septic shock) on Day 0 and on Day 2. On Day 0, septic patients exhibited increased level of CD64pos granulocytes, CD16pos monocytes and IG with T-cell lymphopenia. Clinical severity was associated with higher percentages of IG 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=0.07). 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<0.01) and late (p<0.01) death. Increased circulating IG 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. |
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X Demographics
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| United States | 1 | 14% |
| Colombia | 1 | 14% |
| United Kingdom | 1 | 14% |
| Unknown | 4 | 57% |
Demographic breakdown
| Type | Count | As % |
|---|---|---|
| Members of the public | 4 | 57% |
| Practitioners (doctors, other healthcare professionals) | 2 | 29% |
| Scientists | 1 | 14% |
Mendeley demographics
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 88 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Student > Master | 10 | 11% |
| Student > Bachelor | 9 | 10% |
| Student > Ph. D. Student | 9 | 10% |
| Student > Doctoral Student | 8 | 9% |
| Student > Postgraduate | 4 | 5% |
| Other | 10 | 11% |
| Unknown | 38 | 43% |
| Readers by discipline | Count | As % |
|---|---|---|
| Medicine and Dentistry | 26 | 30% |
| Immunology and Microbiology | 7 | 8% |
| Biochemistry, Genetics and Molecular Biology | 6 | 7% |
| Nursing and Health Professions | 4 | 5% |
| Pharmacology, Toxicology and Pharmaceutical Science | 2 | 2% |
| Other | 7 | 8% |
| Unknown | 36 | 41% |