Acute kidney injury (AKI) is a frequent complication that occurs in 15 to 25% of patients after vascular surgery, and up to 40% of patients after cardiac surgery. AKI compromises seriously short and long-term prognosis of critically ill patients. Several AKI risk factors have been identified including a chronic pathology of the patient such as kidney failure or diabetes, acute kidney injury related to hemodynamic disorders during surgery, including cardiopulmonary bypass, or sepsis, and the use of nephrotoxic agents such as some antibiotics, colloids or iodine contrast agents. Avoiding nephrotoxic agents is therefore strongly recommended in ICU patients, to reduce the incidence of AKI, or to reduce its severity. The aim of this cohort study was to assess whether the use of daptomycin, was associated to a lower incidence of AKI than vancomycin in cardiovascular ICU patients, with similar efficacy. This is a retrospective observational study with a propensity score adjustment to reduce the bias of selection for a comparative analysis between two antibacterial treatments used in routine care. Since treatments were not randomized, the investigators used the propensity score method for primary endpoint analysis. For this, the investigators included the covariates potentially related to treatment and outcome in a multivariate logistic model explaining the choice of treatment. This propensity score was used in the second model as an adjustment covariate included in the multivariate analysis to determine factors independently associated with the primary endpoint (AKI within 7 days). The main hypothesis is the first line antibiotic treatment with daptomycin leads to less nephrotoxicity than vancomycin in a population known at high risk for AKI and with at least a similar efficacy on clinical success rate.
Study Type
OBSERVATIONAL
Enrollment
72
Group DAP : Daptomycin was administered at a dose of 8 mg/kg in thirty-minutes intravenous infusion every 24 hours in patients without severe impairment of kidney function or every 48 hours in case of GFR below 30 ml/min/m2. The creatine-kinase (CK) level was measured before the initiation of DAP and at least once a week to assess the occurrence of muscular toxicity defined by an increase of CK up to 3-fold the upper superior limit without any evidence of member ischaemia.
Group VAN : Vancomycin intravenous treatment was initiated by a loading dose of 30 mg/kg in 1 hour and followed by a continuous maintenance infusion dosing between 15 and 30 mg/kg/d. The VAN dose was adapted to achieve a target serum vancomycin steady-state concentration of 20-30 mg/L assessed by a daily pharmacologic monitoring (therapeutic drug monitoring).
Uh Montpellier
Montpellier, France
Incidence of Acute Kidney Injury (AKI)
AKI stade 1, 2 or 3 according to KDIGO definition with baseline creatinine given by the last creatinine value before the start of treatment
Time frame: 7 days after the treatment initiation
Incidence of Acute Kidney Injury (AKI)
AKI stade 1, 2 or 3 according to KDIGO definition with baseline creatinine given by the last creatinine value before the start of treatment
Time frame: 14 days after the treatment initiation
Maximal decrease of glomerular filtration rate (GFR)
Decrease of GFR, estimated by CKD-EPI formula, from baseline as measured by all serum creatinine determinations during treatment
Time frame: Through study treatment completion, an average of 2 weeks
Incidence of severe renal failure
AKI stade 2 or 3 according to KDIGO definition or decrease of GFR more than 50% from baseline
Time frame: Through study treatment completion, an average of 2 weeks
Incidence of renal replacement therapy (RRT)
RRT initiated between the first and the last treatment administrations
Time frame: Through study treatment completion, an average of 2 weeks
Duration of RRT
Number of days between the first RRT initiation and the end of the last RRT during the ICU stay (excluding RRT performed in a dialysis center for chronic renal failure)
Time frame: Through study completion limited to ICU stay, an average of 2 weeks
Incidence of clinical treatment failure
defined by either persistent positive cultures, worsening of clinical status, death due to initial infection, or relapse after the end of treatment. It was assessed in case of documented GPC infection
Time frame: 15 days after the end of treatment
Incidence of premature discontinuation of treatment
defined as a treatment stopped because of adverse event or clinical failure except death
Time frame: Through study treatment completion, an average of 2 weeks
Mortality
all cause mortality
Time frame: 28 days after treatment initiation
Mortality
all cause mortality
Time frame: 6 months (180 days) after treatment initiation
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