Sepsis
Conditions
Keywords
next- generation sequencing; blood culture;IDSeqTM Ultra
Brief summary
mNGS is popular in research and recently it has been used clinically to detect microbes in the blood or other secretion in infected patients for quicker ,broad and accurate detection of microbes. In ICU ,patients are critically ill and need quicker and accurate antibiotics use to stop the pathologic process. The purpose of this study was to determine whether the positive detection rate of pathogens in patients with sepsis by metagenomic full-targeted detection technology was higher than that in blood culture, and to determine whether the pathogens found in patients with sepsis by metagenomic full-targeted detection technology were important for clinical development. Anti-infective regimens can help.
Detailed description
Sepsis patients in ICU were took blood culture sample and blood sample for mNGS test (IDSeqTM Ultra, Combing with Metagenomics and Pathogen/AMR/VF Probe Enrichment). Clinicians use their knowledge and experience to decide antibiotics use with the guide of Culture results or mNGS results. Validation with digital droplet PCR assays when metagenomic full-targeted assays identify pathogens not identified in conventional blood cultures The difference between the positive rate of mNGS and the positive rate of blood culture were recorded. Patient were followed at least 28 days after enrollment or an outcome indicator. Possible scenarios for detecting clinical impact were detected. Etiology, biochemical indicators, immune function, infection indicator, secondary infection, SOFA score and length of stay,outcome were recorded.
Interventions
take blood samples for mNGS and Culture at the same time in sepsis patients. No intervention on the treatment of the patients.
Sponsors
Study design
Eligibility
Inclusion criteria
Age \> 18years admit to ICU Meet the Sepsis 3.0 diagnostic criteria and suspected bloodstream infection, and the diagnosis of Sepsis ≤ 24 hours; Estimated ICU stay ≥ 24 hours; Informed consent;
Exclusion criteria
Severe organ dysfunction, expected death within 72 hours; Receive palliative care; Refuse to participate;
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| difference of positive rate between mNGS and Culture | 28 day | The difference between the positive rate of mNGS and the positive rate of blood culture. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The difference between the positive rate of metagenomic full capture technology and the Category of Clinical Impact | 28 day | Positive, Negative,None and Indeterminate |
| Change of SOFA | 7 day | change of SOFA score (include each organ) at baseline, day 3 and day 7 clinical improvement :Improvement in 2 or more clinical signs and symptoms no requirement for additional antibacterial treatment Clinical failure:Persistence or progression of baseline signs and symptoms |
| Mortality | During hospitalization | 28 day,ICU and hospital mortality Documented microbiologic eradication:Absence of primary microbe from infection site Presumed microbiologic eradication:Clinical cure without available microbiologic culture data Presumed microbiologic persistence:Clinical failure in the absence of any microbiologic data Documented microbiologic persistence:Continued presence of MRSA based on microbiologic culture Superinfection: Clinical failure and isolation of a pathogen not present at baseline at the original infection site |
| Length of stay | During hospitalization | ICU and hospital length of stay |
| Anti-infective treatment adjustment | 28 day | each Anti-infective treatment adjustment |
Other
| Measure | Time frame | Description |
|---|---|---|
| pathogen | 28 day | all the detect pathogens from mNGS and blood culture |
| secondary infection | 28 day | infection secondary to the primary infection |
Countries
China