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A number of rapid panel-based molecular assays for direct organism identification and resistance characterization in positive blood culture bottles are now commercially available. They have been shown to improve accuracy and decrease the time-to-result, allowing targeted treatment in hospitalized patients with bacteraemia, in high-income countries (HICs). However, these molecular assays are add-on tests performed in addition to conventional testing, increasing the complexity of diagnostic algorithms and costs of patient care. Conventional organism identification includes performing a Gram stain, biochemical identification and phenotypic drug susceptibility testing. The FilmArray Blood Culture Identification (BioFire, USA) is an example of a rapid panel-based molecular assay that combines nesting and multiplexing of PCR (nested multiplex PCR) to detect multiple pathogens simultaneously. There are limited data on how such tests impact patient management, health care costs and how they can better be incorporated into diagnostic algorithms.
The aim of this study is to assess the added value and acceptability of a multiplexed molecular diagnostic assay in the identification of pathogens in patients presenting with bacteremia at hospitals in LMICs, and to assess health care providers' satisfaction with the assay.
The study will address the following questions:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Molecular dx arm | Active Comparator | Positive blood cultures are tested using a molecular ID system in addition to the standard of care (biochemical identification) |
|
| Standard of care arm | No Intervention | Positive blood cultures are treated as per normal lab protocol (biochemical identification) |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Multiplex molecular diagnostic assay | Diagnostic Test | To assess the added value and acceptability of a multiplexed molecular diagnostic assay in the identification of pathogens in patients presenting with bacteremia at hospitals in LMICs, and to assess health care providers' satisfaction with the assay. |
| Measure | Description | Time Frame |
|---|---|---|
| Time from blood collection to definitive treatment initiation (optimal treatment defined as time from blood culture collection to the initiation of a predetermined pathogen-specific antimicrobial therapy) | The judgment as to whether antimicrobial treatment was effective or optimal will be assessed by two members of the study team (infectious disease specialists and/or microbiologists) blinded to treatment group. A third, blinded, party member will be available to adjudicate unresolved disagreements. The Principal Investigators will not be involved in outcome classification. | 1year |
| Measure | Description | Time Frame |
|---|---|---|
| Time from blood collection to initiation of effective antimicrobial therapy (initiation of antimicrobials active against the identified causative pathogen) | The aim is to understand the reduction in time it takes clinical staff to act upon the result. Faster treatment is associated with reduced mortality. | 1year |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jeffrey Pernica, MD, FRCPC | McMaster University | Principal Investigator |
| David Goldfarb, MD, FRCPC | University of British Columbia | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Princess Marina Hospital | Gaborone | Botswana |
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| ID | Term |
|---|---|
| D018805 | Sepsis |
| ID | Term |
|---|---|
| D007239 | Infections |
| D018746 | Systemic Inflammatory Response Syndrome |
| D007249 | Inflammation |
| D010335 | Pathologic Processes |
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|
| Time from blood collection to pathogen identification |
The hypothesis is that faster identification will lead to faster action. |
| 1year |
| Proportion of patients with a confirmed diagnosis of bloodstream infection who are started on optimal antimicrobial therapy in the intervention compared to control arm. | This outcome will inform how the inclusion of a faster diagnosis can support antibiotic stewardship efforts. | 1year |
| Frequency of discrepant results between molecular identification vs standard of care. | Current panels are design for common pathogens in the USA and Europe and given that this is the first evaluation in Africa it will advice on the suitability. | 1year |
| Clinicians' satisfaction with the assay, predominantly in terms of time-to-result and actionable results. | To inform future projects and help guide implementation efforts. | 2month |
| Laboratory professional satisfaction with the assay, predominantly in terms of ease of use and workflow. | To inform future projects and help guide implementation efforts. | 2month |
| In-hospital mortality. | Faster treatment is associated with reduced mortaltity and as a secondary outcome we want to assess the difference between standard of care and diagnostic intervention. | 1year |
| 30-day mortality. | Faster treatment is associated with reduced mortaltity and as a secondary outcome we want to assess the difference between standard of care and diagnostic intervention. | 1year |
| D013568 |
| Pathological Conditions, Signs and Symptoms |