A Platform Trial for Gram Negative Bloodstream Infections
Gram-negative BacteremiaBALANCE+ is a perpetual multiple domain randomized controlled platform trial to evaluate various treatment strategies for Gram-negative bloodstream infections (GN BSIs). Each domain addresses critical questions in the management of GN BSIs, aiming to refine treatment strategies, enhance patient outcomes, and reduce antimicrobial resistance.
The initial vanguard pilot RCT (NCT05893147) started on 29 August 2023 and has successfully completed the pilot phase on 24-Apr-2024. All patients enrolled in the vanguard phase are part of the main platform trial.
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Conditions de participation
-
Sexe:
ALL -
Âges admissibles:
0 and up
Critères de participation
PLATFORM INCLUSION CRITERIA
Platform Inclusion Criteria:
* admitted to a participating hospital
* positive blood culture with Gram negative (GN) bacterium
Platform Exclusion Criteria:
* patient's goals of care are for palliation with no active treatment
* moribund patient, not expected to survive \> 72 hours
* previously enrolled in the platform trial
* not eligible for any domain at the time of screening
DOMAIN SPECIFIC INCLUSION AND EXCLUSION CRITERIA
1. De-escalation versus no de-escalation domain
Inclusion Criteria
- included in BALANCE+ platform
Exclusion Criteria
* receiving an empiric antibiotic regimen at the time of blood culture finalization to which the GN pathogen(s) are not sensitive
* arbapenem-non-susceptible
* no de-escalation option due to any or all of:
* antimicrobial resistance
* allergies
* medical contraindications
* drug-drug interaction risk
* other relevant reason
* patients with a suspected or proven polymicrobial source of infection
* \> 24 hours since index blood culture susceptibility results finalization
2. Beta-lactam versus non-beta-lactam oral/enteral treatment domain
Inclusion Criteria
* included in BALANCE+ platform
* initially treated with intravenous antibiotics, but clinical team transitioning patient to oral/enteral antibiotic within 7 days of starting treatment
Exclusion Criteria
* enrolled in an arm of another BALANCE+ platform domain which limits the use of oral/enteral therapy:
* no-de-escalation arm (patients in the no de-escalation arm cannot be randomized into this domain unless they are ready for discharge home, in which case de-escalation is allowable to oral agents at discharge)
* no non-beta-lactam options due to any or all of:
* resistance
* allergies
* medical contraindications
* drug-interaction risk
* other relevant reason
* no beta-lactam options due to any or all of:
* resistance
* allergies
* medical contraindications
* drug-interaction risk
* other relevant reason
* pregnancy
* already received \>24 hours of oral antibiotics after index blood culture finalization
3. Central vascular catheter replacement domain
Inclusion Criteria
* included in BALANCE+ platform
* has an indwelling central vascular catheter that was already in place within the 48-hour period before the onset of bloodstream infection (i.e. is not a new catheter placed within 48 hours of the onset of infection)
Exclusion Criteria
* patient has no ongoing need for a central vascular catheter
* patient has definite indication for central vascular catheter removal
* ongoing septic shock with definite/probable line source
* concomitant S. aureus bacteremia
* concomitant candidemia
* local suppurative signs (severe redness, warmth, pain, swelling or fluctuance/collection) necessitating catheter removal, or other clinical evidence of infected line (e.g. imaging/echocardiographic findings)
4. Low-risk AmpC domain
Inclusion Criteria
* included in BALANCE+ platform
* positive blood culture with GN bacterium, of the following species: i. Serratia spp. ii Morganella spp. iii Providencia spp. iv Proteus spp. other than P.mirabilis
* organism is susceptible to ceftriaxone
Exclusion Criteria
* severe allergy to beta-lactams (e.g., type 4 hypersensitivity reaction or DRESS)
* baseline phenotypic non-susceptiblity to ceftriaxone
* more than 1 calendar day beyond availability of susceptibility results
5. Follow up blood culture domain
Inclusion Criteria
- included in BALANCE+ platform
Exclusion Criteria
* patient died or discharged from hospital prior to day 4
* blood culture already collected by the treating team at day 4±1
* \>5 days since index positive blood culture collection
* definite indication for repeat blood culture testing
* concomitant S. aureus bacteremia
* concomitant Candidemia
* clinical suspicion for infective endocarditis
Lieu de l'étude
Eastern Regional Health Authority
Eastern Regional Health AuthoritySaint John's, Newfoundland and Labrador
Canada
Contactez l'équipe d'étude
Peter Daley, MD
Michael Garron Hospital
Michael Garron HospitalToronto, Ontario
Canada
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Christopher Kandel, MD
Foothills Hospital
Foothills HospitalCalgary, Alberta
Canada
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Ranjani Somayaji, MD
Sunnybrook Health Sciences Centre
Sunnybrook Health Sciences CentreToronto, Ontario
Canada
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Université de Sherbrooke
Université de SherbrookeSherbrooke, Quebec
Canada
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François Lamontagne, MD
The Ottawa Hospital
The Ottawa HospitalOttawa, Ontario
Canada
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Derek McFadden, MD
Mount Sinai Hospital
Mount Sinai HospitalToronto, Ontario
Canada
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Michael Fralick, PhD
Niagara Health System
Niagara Health SystemSt. Catharines, Ontario
Canada
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Aidan Findlater, MD
University Health Network
University Health NetworkToronto, Ontario
Canada
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Bryan Coburn, MD
- Étude parrainée par
- Sunnybrook Health Sciences Centre
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT06537609