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Rapid identification of pathogens and early warning of host response are key to improve the prognosis of sepsis. Establishing a comprehensive identification system based on pathogen identification and host immune status is an effective way to achieve early warning stratification of patients with infections in the emergency department. This prospective multicenter clinical study will combine droplet digital PCR (ddPCR) and transcriptomic molecular target assay for validation in patients with suspected sepsis in the emergency department. The purpose is to (1) compare the efficacy of ddPCR with blood culture for early diagnosis and prognosis; (2) assess the diagnostic value of transcriptomic molecular targets based on 29 messenger RNA for the presence or absence of infection as well as infectious agents, and to evaluate their efficacy for prognosis; and (3) assess the diagnostic and therapeutic monitoring value of ddPCR combined with transcriptome analysis methods.
Rapid identification of pathogens and early warning of host response are key to improve the prognosis of sepsis. Establishing a comprehensive identification system based on pathogen identification and host immune status is an effective way to achieve early warning stratification of patients with infections in the emergency department. Therefore, based on our preliminary single-center study, this prospective multicenter clinical study will combine droplet digital PCR (ddPCR) and transcriptomic molecular target assay for validation in patients with suspected sepsis in the emergency department. The purpose is to (1) compare the efficacy of ddPCR with blood culture for early diagnosis and prognosis; (2) assess the diagnostic value of transcriptomic molecular targets based on 29 messenger RNA for the presence or absence of infection as well as infectious agents, and to evaluate their efficacy for prognosis; and (3) assess the diagnostic and therapeutic monitoring value of ddPCR combined with transcriptome analysis methods. In a word, this study will be undertaken to assess the diagnostic and therapeutic monitoring value of early warning models for sepsis in emergency department and to promote them to improve the identification ability of emergency infections.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Experimental group | The experimental group will recruit 300 participants undergoing blood culture, droplet digital PCR and transcriptome analysis. |
| |
| Control group | The control group will recruit 60 participants undergoing blood culture only. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Droplet digital PCR | Diagnostic Test | Droplet digital PCR has potential in resolving polymicrobial infection because it simultaneously achieves unprecedented high sensitivity , high specificity, and absolute quantification without the need for a standard curve. |
| Measure | Description | Time Frame |
|---|---|---|
| Diagnostic efficiency of ddPCR combined with transcriptomic analysis in suspected sepsis | Diagnostic efficiency of ddPCR combined with transcriptomic analysis for suspected sepsis in the emergency medicine | 7days |
| Prognostic value of ddPCR combined with transcriptomic analysis in suspected sepsis | Prognostic value of ddPCR combined with transcriptomic analysis for suspected sepsis in the emergency medicine | 28 days |
| Measure | Description | Time Frame |
|---|---|---|
| 7-day all-cause mortality rate | Evaluation of combined examination by ddPCR and transcriptomic analysis for the evaluation of the prognosis of the sepsis. | 7 days |
| 28-day all-cause mortality rate |
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Inclusion Criteria:
Exclusion Criteria:
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Prospective inclusion of patients with suspected sepsis with MSS ≥ 2 in the emergency department of Shanghai East Hospital, Shanghai Pudong New District Zhoupu Hospital, Shanghai Pudong New District Gongli Hospital, Shanghai Pudong Hospital and Shanghai Punan Hospital Hospital, Shanghai Pudong Hospital, Shanghai Pudong New Area Hospital and Shanghai Pudong New Area Punan Hospital. The patients will be randomized by stratified grouping and assigned to two parallel groups in the ratio of 5:1.
All individual participant data that underlie results in a publication
3 years
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| ID | Term |
|---|---|
| D018805 | Sepsis |
| D000093742 | Breakthrough Infections |
| ID | Term |
|---|---|
| D007239 | Infections |
| D018746 | Systemic Inflammatory Response Syndrome |
| D007249 | Inflammation |
| D010335 | Pathologic Processes |
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Evaluation of combined examination by ddPCR and transcriptomic analysis for the evaluation of the prognosis of the sepsis.
| 28 days |
| 90-day all-cause mortality rate | Evaluation of combined examination by ddPCR and transcriptomic analysis for the evaluation of the prognosis of the sepsis. | 90 days |
| Antimicrobial Resistance and antibiotic application | Evaluation of combined examination by ddPCR and transcriptomic analysis for the the value of guiding clinical drug therapy. | 7 days |
| D013568 |
| Pathological Conditions, Signs and Symptoms |
| D020969 | Disease Attributes |