Antimicrobial Resistance, Bacterial Infections, Hemodynamic Instability, Sepsis, Therapeutic Drug Monitoring
Conditions
Keywords
Sepsis, Hemodynamic Instability, Therapeutic Drug Monitoring, Gram-negative Bacteria, Beta-Lactams, Fosfomycin, Fluoroquinolone, Glycylcycline, Dialysis
Brief summary
A prospective, open-label, randomized controlled trial will be conducted to evaluate a novel TDM-guided therapy in management of DT-GNB infections. We hypothesize that TDM-guided antibiotic therapy will reduce 14-day all-cause mortality by 6% (absolute risk reduction) in septic patients with DT-GNB infections, when compared to standard therapy. TDM for 11 antibiotics will be performed for all trial patients although test information will be withheld for the standard therapy arm. The primary aim is to compare the 14-day all-cause mortality rates of novel TDM-guided antibiotic dosing versus standard therapy.
Detailed description
Sepsis remains a major cause of morbidity and mortality worldwide in the face of antimicrobial resistance especially in patients with Gram-negative bacteria (GNB) infections. Limited new antibiotics for GNB infections pose a severe threat to clinical management of these patients and thus call for old antibiotics to be repurposed. Dosing regimens of old antibiotics often fail to achieve therapeutic drug concentrations in some septic patients. Septic patients commonly have significant hemodynamic changes and/or undergo extracorporeal interventions that may increase patients' susceptibility to treatment failure and increase the chance of more resistant bacteria emergence, or toxicity from the antibiotic. Hence, the one size fits all dosing principle for antimicrobial treatments of suspect sepsis due to infection by antibiotic-resistant- or less susceptible-GNB \[collectively known as difficult-to-treat (DT)-GNB infections\] is no longer viable. This will require therapeutic drug monitoring (TDM) to inform if the dosing is adequate to treat such infections. This study seeks to provide evidence supporting the application of TDM-guided antibiotic therapy on reducing mortality and morbidity among septic patients with DT-GNB infections and significant hemodynamic changes, which can potentially shift current practice paradigms.
Interventions
Upon randomization and before the bacterial culture results are known, blood sampling will be obtained from the patient during the morning round of initial empiric antibiotic administration. PK/PD target analysis based on the clinical susceptibility breakpoints of Enterobacterales (the most prevalent organism family of DT-GNB infections in our setting) will be performed and a dosage recommendation will be communicated to the primary ID clinician. Antibiotic dosing adjustments (if any) will be made within 8 - 24 hours of the blood sampling by the Primary / Infectious Diseases clinician. In case of inappropriate dosing, where the PK/PD target is not achieved or exceeded with antibiotic side effects observed, the dosage will be increased or decreased, respectively.
Sponsors
Singapore General Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
16 Years to 99 Years
Healthy volunteers
No
Inclusion criteria
* 16 years or older * Receive intravenous therapy of the study antibiotics * Antibiotic treatment should be aimed for at least 3 days at time of inclusion
Exclusion criteria
* Pregnancy * Antibiotics cessation before first blood sample collection * Receiving antibiotics only as prophylaxis * On palliative care or with less than 48 hours of life expectancy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 14-day All-Cause Mortality Rate | 14 Days | This is defined as death of any cause. Study aims to compare the difference in 14-day all-cause mortality rates from the day of randomization between both arms. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Fever Resolution | 14 Days | This is defined as the days to defervescence. Study aims to compare the difference in the days to defervescence after initiation of targeted antibiotic therapy between both arms. |
| Microbiological Treatment Cure of Difficult to Treat Gram-Negative Bacteria (DT-GNB) | 14 Days | This is defined as presence of sterile site culture or absence of intended bacterial growth in culture of infection site. Study aims to compare microbiological cure of difficult to treat GNB between both arms. |
| Improved or Stabilized Sequential Organ Failure Assessment (SOFA) | 14 Days | This is defined as delta SOFA or change in SOFA score between day 1 (randomization) to day 14. Study aims to compare the changes in SOFA scores between the two arms. |
| Incidences of Adverse Drug Reactions | Start to End of Antibiotic Therapy (Up to 90 days from randomization, discharge or demise, whichever comes earliest) | Adverse Drug Reactions (ADRs) are defined as renal failure (defined using RIFLE criteria), Neurologic disorders (defined as altered mental status, peripheral neuropathy, or seizures in the absence of preexisting neurologic conditions, substance-related toxic effects, or infectious syndromes) and hematological disorders (defined as anemia (hemoglobin level \<10 g/dL), leukopenia (white blood cell count \<4500 cells/μL), or thrombocytopenia (platelet count \<150 × 103/μL) with levels below patient's baseline and in the absence of bleeding or myelosuppressive therapies). Study aims to compare the incidences of ADRs between the two arms. |
Countries
Singapore
Contacts
Primary ContactTze Peng Lim, PhD
Outcome results
None listed