Early decreased neutrophil responsiveness is related to late onset sepsis in multitrauma patients: An international cohort study

• Published in: PloS one 2017-06, Vol.12 (6), p.e0180145-e0180145
• Main Authors: Groeneveld, Kathelijne M, Koenderman, Leo, Warren, Brian L, Jol, Saskia, Leenen, Luke P H, Hietbrink, Falco
• Format: Article
• Language: English
• Subjects: Adult; Age; Aged; Analysis; Biology and Life Sciences; Cohort analysis; Cohort Studies; Complications; Female; Flow Cytometry; Health aspects; Health care; Hospitals; Humans; Immune response; Immune system; Immunology; Inflammation; Inflammatory response; Injuries; Intensive care; Laboratories; Leukocytes (neutrophilic); Male; Medicine and Health Sciences; Middle Aged; Morbidity; Mortality; Multiple Trauma - immunology; Neutrophils; Neutrophils - immunology; Patient outcomes; Patients; People and Places; Risk factors; Sepsis; Sepsis - immunology; Septic shock; Shock; Studies; Surgery; Trauma
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0180145

Severe trauma can lead to the development of infectious complications after several days, such as sepsis. Early identification of patients at risk will aid anticipating these complications. The aim of this study was to test the relation between the acute (5 days) development of septic complications and validate this in different trauma populations. Two prospective, observational, cohort series in the Netherlands and South Africa, consisting of severely injured trauma patients. Neutrophil responsiveness by fMLF-induced active FcγRII was measured in whole blood flowcytometry, as read out for the systemic immune response within hours after trauma. Sepsis was scored daily. Ten of the 36 included Dutch patients developed septic shock. In patients with septic shock, neutrophils showed a lower expression of fMLF-induced active FcγRII immediately after trauma when compared to patients without septic shock (P = 0.001). In South Africa 11 of 73 included patients developed septic shock. Again neutrophils showed lower expression of fMLF induced active FcγRII (P = 0.001). In the combined cohort, all patients who developed septic shock demonstrated a decreased neutrophil responsiveness. Low responsiveness of neutrophils for the innate stimulus fMLF immediately after trauma preceded the development of septic shock during admission by almost a week and did not depend on a geographical/racial background, hospital protocols and health care facilities. Decreased neutrophil responsiveness appears to be a prerequisite for septic shock after trauma. This might enable anticipation of this severe complication in trauma patients.