Burns, Infection
Conditions
Keywords
Aminoglycoside, Pharmacokinetics, Once daily dosing
Brief summary
Effective antimicrobial use in the burn population is important since this population is at an increased risk for infections during their stay in hospital as a result of their burn injury. Tobramycin is an antibiotic that has activity against common burn wound associated pathogens, such as Pseudomonas Aeruginosa, and its use is becoming increasingly relevant due to the increased incidence of bacterial resistance to currently utilized antibiotics. Once daily dosing of tobramycin has been safely and effectively used in the majority of infected patients for many years with the proposed benefits of optimized antibacterial activity and reduced nephrotoxicity compared to traditional dosing. But, the once daily dosing regimen has yet to be validated in the burn population. The purpose of this study is to validate the plausibility of once daily tobramycin dosing in the burn population with intent to determine a safe, effective, and efficient dosing regimen for this population.
Interventions
DRUGTobramycin
Sponsors
Sandra Walker
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Adult burn patient (≥ 18 years old) * Total burn surface area less than 20% * At least 48 hours after the time of the initial burn injury event * Has a suspected or confirmed infection * Has been receiving antibiotic therapy for at least 24 hours
Exclusion criteria
* Pediatric patients (\< 18 years old); * Pregnant * Documented history of cochlear or vestibular injury * Creatinine clearance \< 50 ml/min * Requiring any modality of dialysis * Has been receiving antibiotic therapy for longer than 72 hours * Known allergy or adverse reaction to aminoglycoside antibiotics * Known allergy or adverse reaction to sulfites * Diagnosis of Parkinson's disease or myasthenia gravis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Proportion of patients able to achieve therapeutic target | 24 hours |
| Clearance of tobramycin in the burn population | 24 hours |
| Volume of distribution of tobramycin in the burn population | 24 hours |
| Breakpoint in tobramycin clearance based on time post-burn, body burn surface area, inhalation injury score, or percentage of open wounds | 24 hours |
| Breakpoint in tobramycin volume of distribution based on time post-burn, body burn surface area, inhalation injury score, or percentage of open wounds | 24 hours |
Countries
Canada
Outcome results
None listed