Infection Related to Vascular Prothesis, Infection Related to Ventricular Assist Device, Infective Endocarditis, Mediastinitis, Surgical Site Infection
Conditions
Keywords
Vancomycin, Daptomycin, Acute Kidney Injury, Nephrotoxicity, Infective Endocarditis, Foreign Body Associated Infection, Cardiovascular surgery
Brief summary
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.
Interventions
DRUGDaptomycin (DAP) treatment
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).
Sponsors
University Hospital, Montpellier
Study design
Observational model
COHORT
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patient older than 18 years * Admitted in ICU from January 2010 to December 2012 * Suspected or proven cardiac, vascular or profound surgical site infection with Gram-positive cocci (GPC) methicillin-resistant (MR) strains (including probabilistic treatment for patients with acquisition of MR risk factors) * Treatment duration greater than or equal to 48 hours (at least 2 doses of daptomycin administered or 2 days of vancomycin infusion) * Antibiotic treatment started in peri-operative (from 48 hours before the onset of surgery) or in postoperative period (during ICU stay)
Exclusion criteria
* Prophylaxis indication of antibiotics * Kidney disease on chronic dialysis * Acute onset of RRT before initiation of DAP or VAN treatment * Staphylococcus pneumonia
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of Acute Kidney Injury (AKI) | 7 days after the treatment initiation | AKI stade 1, 2 or 3 according to KDIGO definition with baseline creatinine given by the last creatinine value before the start of treatment |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Duration of RRT | Through study completion limited to ICU stay, an average of 2 weeks | 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) |
| Incidence of clinical treatment failure | 15 days after the end of treatment | 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 |
| Incidence of Acute Kidney Injury (AKI) | 14 days after the treatment initiation | AKI stade 1, 2 or 3 according to KDIGO definition with baseline creatinine given by the last creatinine value before the start of treatment |
| Incidence of renal replacement therapy (RRT) | Through study treatment completion, an average of 2 weeks | RRT initiated between the first and the last treatment administrations |
| Incidence of severe renal failure | Through study treatment completion, an average of 2 weeks | AKI stade 2 or 3 according to KDIGO definition or decrease of GFR more than 50% from baseline |
| Incidence of premature discontinuation of treatment | Through study treatment completion, an average of 2 weeks | defined as a treatment stopped because of adverse event or clinical failure except death |
| Mortality | 28 days after treatment initiation | all cause mortality |
| Maximal decrease of glomerular filtration rate (GFR) | Through study treatment completion, an average of 2 weeks | Decrease of GFR, estimated by CKD-EPI formula, from baseline as measured by all serum creatinine determinations during treatment |
Countries
France
Outcome results
None listed