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Enteral citrulline supplementation versus placebo on SOFA score on day 7 in mechanically ventilated critically ill patients: the IMMUNOCITRE randomized clinical trial.
Tadié, Jean-Marc; Locher, Clara; Maamar, Adel; Reignier, Jean; Asfar, Pierre; Commereuc, Morgane; Lesouhaitier, Mathieu; Gregoire, Murielle; Le Pabic, Estelle; Bendavid, Claude; Moreau, Caroline; Diehl, Jean-Luc; Gey, Alain; Tartour, Eric; Le Tulzo, Yves; Thibault, Ronan; Terzi, Nicolas; Gacouin, Arnaud; Roussel, Mikael; Delclaux, Christophe; Tarte, Karin; Cynober, Luc.
Afiliação
  • Tadié JM; UMR 1236, Univ Rennes, INSERM, Établissement Français du Sang, LabexIGO, Rennes, France. jeanmarc.tadie@chu-rennes.fr.
  • Locher C; SITI Laboratory, CHU Rennes, Rennes, France. jeanmarc.tadie@chu-rennes.fr.
  • Maamar A; Réanimation Médicale, CHU Rennes, Rennes, France. jeanmarc.tadie@chu-rennes.fr.
  • Reignier J; Centre d'investigation clinique de Rennes (CIC1414), CHU Rennes, Rennes, France. jeanmarc.tadie@chu-rennes.fr.
  • Asfar P; Centre Hospitalier Universitaire, Université de Rennes 1, Rennes, France. jeanmarc.tadie@chu-rennes.fr.
  • Commereuc M; Hôpital Pontchaillou, CHU Rennes, 2 rue Henri Le Guillloux, 35033, Rennes Cedex, France. jeanmarc.tadie@chu-rennes.fr.
  • Lesouhaitier M; Inserm, Centre d'investigation clinique de Rennes (CIC1414), service de pharmacologie clinique, Institut de recherche en santé, environnement et travail (Irset), UMR S 1085, EHESP, Univ Rennes, CHU Rennes, 35000, Rennes, France.
  • Gregoire M; UMR 1236, Univ Rennes, INSERM, Établissement Français du Sang, LabexIGO, Rennes, France.
  • Le Pabic E; MIP, UR 4334, Médecine Intensive Réanimation, Nantes Université, CHU Nantes, 44000, Nantes, France.
  • Bendavid C; Département de Médecine Intensive - Réanimation et Médecine Hyperbare, Centre Hospitalier Universitaire, Angers, France.
  • Moreau C; Service de Réanimation Médicale, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Européen Georges Pompidou, Paris, France.
  • Diehl JL; UMR 1236, Univ Rennes, INSERM, Établissement Français du Sang, LabexIGO, Rennes, France.
  • Gey A; SITI Laboratory, CHU Rennes, Rennes, France.
  • Tartour E; Réanimation Médicale, CHU Rennes, Rennes, France.
  • Le Tulzo Y; Centre d'investigation clinique de Rennes (CIC1414), CHU Rennes, Rennes, France.
  • Thibault R; UMR 1236, Univ Rennes, INSERM, Établissement Français du Sang, LabexIGO, Rennes, France.
  • Terzi N; SITI Laboratory, CHU Rennes, Rennes, France.
  • Gacouin A; Inserm, Centre d'investigation clinique de Rennes (CIC1414), service de pharmacologie clinique, Institut de recherche en santé, environnement et travail (Irset), UMR S 1085, EHESP, Univ Rennes, CHU Rennes, 35000, Rennes, France.
  • Roussel M; Laboratoire de Biochimie-Métabolique, CHU Rennes, Rennes, France.
  • Delclaux C; Laboratoire de Biochimie-Métabolique, CHU Rennes, Rennes, France.
  • Tarte K; Service de Réanimation Médicale, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Européen Georges Pompidou, Paris, France.
  • Cynober L; INSERM U970, Université Paris Cité, Paris, France.
Crit Care ; 27(1): 381, 2023 10 03.
Article em En | MEDLINE | ID: mdl-37784110
ABSTRACT

BACKGROUND:

Restoring plasma arginine levels through enteral administration of L-citrulline in critically ill patients may improve outcomes. We aimed to evaluate whether enteral L-citrulline administration reduced organ dysfunction based on the Sequential Organ Failure Assessment (SOFA) score and affected selected immune parameters in mechanically ventilated medical intensive care unit (ICU) patients.

METHODS:

A randomized, double-blind, multicenter clinical trial of enteral administration of L-citrulline versus placebo for critically ill adult patients under invasive mechanical ventilation without sepsis or septic shock was conducted in four ICUs in France between September 2016 and February 2019. Patients were randomly assigned to receive enteral L-citrulline (5 g) every 12 h for 5 days or isonitrogenous, isocaloric placebo. The primary outcome was the SOFA score on day 7. Secondary outcomes included SOFA score improvement (defined as a decrease in total SOFA score by 2 points or more between day 1 and day 7), secondary infection acquisition, ICU length of stay, plasma amino acid levels, and immune biomarkers on day 3 and day 7 (HLA-DR expression on monocytes and interleukin-6).

RESULTS:

Of 120 randomized patients (mean age, 60 ± 17 years; 44 [36.7%] women; ICU stay 10 days [IQR, 7-16]; incidence of secondary infections 25 patients (20.8%)), 60 were allocated to L-citrulline and 60 were allocated to placebo. Overall, there was no significant difference in organ dysfunction as assessed by the SOFA score on day 7 after enrollment (4 [IQR, 2-6] in the L-citrulline group vs. 4 [IQR, 2-7] in the placebo group; Mann‒Whitney U test, p = 0.9). Plasma arginine was significantly increased on day 3 in the treatment group, while immune parameters remained unaffected.

CONCLUSION:

Among mechanically ventilated ICU patients without sepsis or septic shock, enteral L-citrulline administration did not result in a significant difference in SOFA score on day 7 compared to placebo. TRIAL REGISTRATION ClinicalTrials.gov Identifier NCT02864017 (date of registration 11 August 2016).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Choque Séptico / Sepse Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Choque Séptico / Sepse Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article