Introduction: Septic shock leads to high morbidity and mortality in critically ill patients. Several lower-case scientific studies have supported the synergistic positive effect of vitamin C, thiamine, and hydrocortisone on sepsis-induced organ dysfunction. Aim: Our aim was to investigate the effect of vitamin complex on organ failure, laboratory parameters, respiratory and antibiotic treatment, intensive care time, and mortality in septic shock patients. Material and methods: In our retrospective and prospective analysis, we collected parameters from 43 (23 vitamin-treated, 20 control) septic shock patients. Patients treated with vitamin, they received vitamin C (4x1500 mg), thiamine (2x200 mg) for three days (2). In other respects, and for hydrocortisone (200 mg / 24h), both groups of patients received treatment according to the European Sepsis Recommendation. SPSS (V-21) data were used for data collection, Kolmogorov-Smirnov, Wilcoxon, Mann-Whitney U tests were used for statistical analysis. Ethical license: 7849-PTE 2019.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
43
Patients in the intervention group (G1) (n=23) received the combined vitamin therapy: IV vitamin C (1.5 g every 6 hours administered as an infusion over 30 to 60 minutes and mixed in a 100- mL solution of normal saline), hydrocortisone (100 mg in bolus-100 mg in perfusor up to 60 min (200mg 24h),), and thiamine (200 mg every 12 hours administered as an infusion over 30 to 60 minutes and mixed in a 100-mL solution of normal saline) for 3 days.
Department of Anaesthesia and Intensive Therapy University of Pecs
Pécs, Baranya, Hungary
ventilation
duration of mechanical ventilation (days)
Time frame: intensive care unit discharge (up to 90 days)
vasopressors
length of circulatory support (days)
Time frame: intensive care unit discharge (up to 90 days)
Length of stay
length of Intensive care unit staying (days)
Time frame: intensive care unit discharge (up to 90 days)
main mortality
all-cause mortality (dead/survived) in the intensive care unit
Time frame: intensive care unit discharge (up to 90 days)
secondary outcomes
development of inflammatory laboratory parameters: \- se-carbamide (mg/dl)
Time frame: up to 5 days after admission to intensive care
secondary outcomes
development of inflammatory laboratory parameters: \- se-creatinine (µmol/L)
Time frame: up to 5 days after admission to intensive care
secondary outcomes
development of inflammatory laboratory parameters: \- plateletes (G/L),
Time frame: up to 5 days after admission to intensive care
secondary outcomes
development of inflammatory laboratory parameters: \- procalcitonin (ng/ml),
Time frame: up to 5 days after admission to intensive care
secondary outcomes
development of inflammatory laboratory parameters: \- white blood cells (G/L)
Time frame: up to 5 days after admission to intensive care
secondary outcomes
development of inflammatory laboratory parameters: \- heat shock C-reactive protein (mg/L)
Time frame: up to 5 days after admission to intensive care
secondary outcomes
development of inflammatory laboratory parameters: \- se-lactate (mmol/L)
Time frame: up to 5 days after admission to intensive care
antibiotics
the length of antibiotic treatment (days)
Time frame: intensive care unit discharge (up to 90 days)
PiCCO parameters
changes in invasive hemodynamic parameters-PiCCO ®: \- cardiac index (l/min/m2)
Time frame: up to 5 days after admission to intensive care
PiCCO parameters
changes in invasive hemodynamic parameters-PiCCO ®: \- extravascular lung water (ml/kg)
Time frame: up to 5 days after admission to intensive care
PiCCO parameters
changes in invasive hemodynamic parameters-PiCCO ®: \- intrathoracic body water (ml/m2)
Time frame: up to 5 days after admission to intensive care
PiCCO parameters
changes in invasive hemodynamic parameters-PiCCO ®: \- myocardial contractility (dP/dTmax- (mm hg/s)
Time frame: up to 5 days after admission to intensive care
other mortality's
in-hospital, 30- and 60-day mortality (dead/survived)
Time frame: up to 60 days after admission to intensive care
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