4.2 Article

Dexmedetomidine protects against acute kidney injury in patients with septic shock

Journal

ANNALS OF PALLIATIVE MEDICINE
Volume 9, Issue 2, Pages 224-230

Publisher

AME PUBL CO
DOI: 10.21037/apm.2020.02.08

Keywords

Acute kidney injury (AKI); multiple organ dysfunction syndrome (MODS); mechanical ventilation; dexmedetomidine

Funding

  1. Health Department of Zhejiang Province [2019KY012, 2018KY219, 2018KY210, 2018KY248, 2015KYA018]
  2. Chinese Medical Association [13091470532]

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Background: This study aimed to assess the relationship between the use of dexmedetomidine and the incidence of acute kidney injury (AKI) in septic shock patients undergoing mechanical ventilation and reveal the potential mechanism. Methods: Septic shock patients undergoing mechanical ventilation were included. Patients were randomized into two groups including propofol group and dexmedetomidine group. Plasma samples were obtained from veins at 0, 12, 24, 72 and 120 h after receiving mechanical ventilation in ICU. Results: Cohorts with septic shock after mechanical ventilation in ICU had similar baseline and demographic characteristics. Serum creatinine (SCr) and blood urea nitrogen (BUN) was lower in dexmedetomidine group (P<0.05) and also lower renal injury markers were detected in the dexmedetomidine group, compared with propofol group (P<0.05). Dexmedetomidine infusion reduced the TNF-alpha, IL-1 level in blood samples and maintained the balance of proportion of CD4+ and CD8+ T-lymphocytes. Patients receiving dexmedetomidine were less likely to develop AKI. The median ICU stay was decreased in dexmedetomidine group (P<0.05). Moreover, the case and duration of CRRT was also decreased by using dexmedetomidine (P<0.05). There was no significant difference between the cohorts with respect to the duration of mechanical ventilation. Conclusions: The use of dexmedetomidine infusion in ICU patients was associated with a decreased incidence of AKI and reduced ICU stay and CRRT performance. The mechanism may be related to anti-inflammatory reaction and immunoregulation.

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