Endocarditis, Febrile Neutropenia, Severe Sepsis
Conditions
Keywords
bacteria, fungi, real time PCR, adequate antimicrobial therapy, microbial DNA, microbial diagnosis
Brief summary
The primary purpose is to improve and quicken the microbial diagnosis in severe infections, since only one third of the cases are documented by blood cultures and adequate anti-infective therapy in the 48 hours reduced mortality and morbidity. Our hypothesis is that detection of microbial DNA in blood by real time PCR may increase the number of cases diagnosed for bacteraemia or fungemia and shorten the time to positive results, which will provide information for an adequate anti-infectious therapy.
Detailed description
We will evaluate the advantage of adding the molecular test to the microbial investigations usually done (blood cultures and others) in cases of febrile neutropenia, suspicion of infective endocarditis and severe sepsis in intensive care units. This is a prospective study conducted in 18 sites (7 in the Paris area and 11 all over France) which will enrolled about 2000 patients over 18 years. Sites are randomized for starting with a 6-month period performing the test or 6-month period without the test (control time with the standard of care). Primary outcome are the number of patients with documented bacteraemia or fungemia. Secondary outcome are (1) the number of patients with an adequate anti-infective therapy and how long it happens after the diagnosis, (2) mortality, (3) new complicated infection, (4) number of investigations (microbial and non microbial) done for the etiological diagnosis, and global hospitalization costs. The advantage of the new test will be evaluated per protocol and with an intend to treat analyses. We hypothesized that the new test will bring 15% more microbial diagnosis than the standard of care. Consequently, and according to the number of sites interested in the study, 166 to 2500 patients will be enrolled with 480 to 750 patients with febrile neutropenia, 1000 to 1500 patients with severe sepsis in Intensive Care Units (ICU). Patients with suspicion of infective endocarditis will be evaluated for the number of diagnosis of true endocarditis according to Duke Criteria, and the time to diagnosis. Health economic evaluation will compare the costs of hospitalization, microbial investigations including the new test, other non clinical investigations and consequences on the organization.
Interventions
OTHERDetection of microbial DNA in blood by SeptiFast®
The LightCycler® SeptiFast Test, the innovative real-time PCR test from Roche Diagnostics, is designed to detect and identify the 25 most important bacterial and fungal species causing bloodstream infections within just a few hours. The LightCycler® SeptiFast Test detects the pathogenic bacteria and fungi directly from whole blood without the need for prior incubation or culture steps. Rapid detection and identification of bacterial and fungal DNA, directly from a 1.5 ml whole blood sample, without prior incubation or culture steps in less than 6 hours.
OTHERdetection of microbial DNA in blood by blood culture
A blood culture is a test to find an infection in the blood. Most bacteria can be seen in the culture in 2 to 3 days, but some types can take 10 days or longer to show up. Fungus can take up to 30 days to show up in the culture.
Sponsors
Hoffmann-La Roche
Assistance Publique - Hôpitaux de Paris
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age≥ 18 years * Written signed and dated inform consent * First time with fever observed in a neutropenic patient * Severe sepsis in a patient hospitalized in ICU * Suspicion of infective endocarditis * Microbial investigation from Monday to Friday
Exclusion criteria
* Not affiliated to Health Insurance (social security) * Included in another interventional trial testing microbial DNA detection during the time without Septifast® * Included in another clinical trial for which the clinician assumes that it will not be possible to prescribe an anti-infectious therapy adequately to microbial detection in the blood * Patient previously included in the protocol * Sepsis with a microbial diagnosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of bacteraemia and of fungemia - overall - each condition | max Day 30 |
Secondary
| Measure | Time frame |
|---|---|
| Adequate anti-infective therapy | at 24h, 48h, > 48h |
| Time between sampling for microbial investigation and positive results relevant for the diagnosis | between sampling for microbial investigation and positive results |
| Mortality | at Day 30 |
| Sepsis chock, secondary infectious focus | at Day 30 |
| Number of patients with adequate anti-infective therapy | at day 30 |
| Diagnosis of endocarditis | at Day 45 |
| Number of non clinical investigations (microbial and non microbial) | at day 30 |
| Length of hospital stay | at day 30 |
| For neutropenia cases, number of patients who evaluated with a clinical focus of infection | at day 30 |
Countries
France
Outcome results
None listed