Gene Expression-Based Diagnosis of Infections in Critically Ill Patients-Prospective Validation of the SepsisMetaScore in a Longitudinal Severe Trauma Cohort.

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Gene Expression-Based Diagnosis of Infections in Critically Ill Patients-Prospective Validation of the SepsisMetaScore in a Longitudinal Severe Trauma Cohort. / Thair, S; Mewes, C; Hinz, J; Bergmann, I; Büttner, B; Sehmisch, S; Meissner, K; Quintel, M; Sweeney, TE; Khatri, P; Mansur, A.

In: CRIT CARE MED, Vol. 49, No. 8, 01.08.2021, p. e751-e760.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Thair, S, Mewes, C, Hinz, J, Bergmann, I, Büttner, B, Sehmisch, S, Meissner, K, Quintel, M, Sweeney, TE, Khatri, P & Mansur, A 2021, 'Gene Expression-Based Diagnosis of Infections in Critically Ill Patients-Prospective Validation of the SepsisMetaScore in a Longitudinal Severe Trauma Cohort.', CRIT CARE MED, vol. 49, no. 8, pp. e751-e760. https://doi.org/10.1097/ccm.0000000000005027

APA

Thair, S., Mewes, C., Hinz, J., Bergmann, I., Büttner, B., Sehmisch, S., Meissner, K., Quintel, M., Sweeney, TE., Khatri, P., & Mansur, A. (2021). Gene Expression-Based Diagnosis of Infections in Critically Ill Patients-Prospective Validation of the SepsisMetaScore in a Longitudinal Severe Trauma Cohort. CRIT CARE MED, 49(8), e751-e760. https://doi.org/10.1097/ccm.0000000000005027

Vancouver

Bibtex

@article{9a283e4c8b674fe499a358cd5d6b239d,
title = "Gene Expression-Based Diagnosis of Infections in Critically Ill Patients-Prospective Validation of the SepsisMetaScore in a Longitudinal Severe Trauma Cohort.",
abstract = "OBJECTIVES: Early diagnosis of infections is pivotal in critically ill patients. Innovative gene expression-based approaches promise to deliver precise, fast, and clinically practicable diagnostic tools to bedside. This study aimed to validate the SepsisMetaScore, an 11-gene signature previously reported by our study group, in a representative longitudinal cohort of trauma patients.DESIGN: Prospective observational cohort study.SETTING: Surgical ICUs of the University Medical Center Goettingen, Germany.PATIENTS: Critically ill patients with severe traumatic injuries.INTERVENTIONS: None.MEASUREMENTS AND MAIN RESULTS: Paired box gene (PAXgene) RNA blood tubes were drawn at predefined time points over the course of disease. The performance of the SepsisMetaScore was tested using targeted polymerase chain reaction and compared with Procalcitonin using area under the receiver operating characteristics analyses. The SepsisMetaScore showed significant differences between infected and noninfected patients (n = 52). It was able to accurately discriminate infectious from noninfectious acute inflammation with an area under the receiver operating characteristics of 0.92 (95% CI, 0.85-0.99) and significantly outperformed Procalcitonin (area under the receiver operating characteristics curve = 0.53; 95% CI, 0.42-0.64) early in the course of infection (p = 0.014).CONCLUSIONS: We demonstrated the clinical utility for diagnosis of infections with higher accuracy using the SepsisMetaScore compared with Procalcitonin in a prospective cohort of severe trauma patients. Future studies should assess whether the SepsisMetaScore may substantially improve clinical practice by accurate differentiation of infections from sterile inflammation and identification of patients at risk for sepsis. Our results support further investigation of the SepsisMetaScore for the development of tailored precision treatment of critically ill patients.",
author = "S Thair and C Mewes and J Hinz and I Bergmann and B B{\"u}ttner and S Sehmisch and K Meissner and M Quintel and TE Sweeney and P Khatri and A Mansur",
year = "2021",
month = aug,
day = "1",
doi = "10.1097/ccm.0000000000005027",
language = "English",
volume = "49",
pages = "e751--e760",
journal = "CRIT CARE MED",
issn = "0090-3493",
publisher = "Lippincott Williams and Wilkins",
number = "8",

}

RIS

TY - JOUR

T1 - Gene Expression-Based Diagnosis of Infections in Critically Ill Patients-Prospective Validation of the SepsisMetaScore in a Longitudinal Severe Trauma Cohort.

AU - Thair, S

AU - Mewes, C

AU - Hinz, J

AU - Bergmann, I

AU - Büttner, B

AU - Sehmisch, S

AU - Meissner, K

AU - Quintel, M

AU - Sweeney, TE

AU - Khatri, P

AU - Mansur, A

PY - 2021/8/1

Y1 - 2021/8/1

N2 - OBJECTIVES: Early diagnosis of infections is pivotal in critically ill patients. Innovative gene expression-based approaches promise to deliver precise, fast, and clinically practicable diagnostic tools to bedside. This study aimed to validate the SepsisMetaScore, an 11-gene signature previously reported by our study group, in a representative longitudinal cohort of trauma patients.DESIGN: Prospective observational cohort study.SETTING: Surgical ICUs of the University Medical Center Goettingen, Germany.PATIENTS: Critically ill patients with severe traumatic injuries.INTERVENTIONS: None.MEASUREMENTS AND MAIN RESULTS: Paired box gene (PAXgene) RNA blood tubes were drawn at predefined time points over the course of disease. The performance of the SepsisMetaScore was tested using targeted polymerase chain reaction and compared with Procalcitonin using area under the receiver operating characteristics analyses. The SepsisMetaScore showed significant differences between infected and noninfected patients (n = 52). It was able to accurately discriminate infectious from noninfectious acute inflammation with an area under the receiver operating characteristics of 0.92 (95% CI, 0.85-0.99) and significantly outperformed Procalcitonin (area under the receiver operating characteristics curve = 0.53; 95% CI, 0.42-0.64) early in the course of infection (p = 0.014).CONCLUSIONS: We demonstrated the clinical utility for diagnosis of infections with higher accuracy using the SepsisMetaScore compared with Procalcitonin in a prospective cohort of severe trauma patients. Future studies should assess whether the SepsisMetaScore may substantially improve clinical practice by accurate differentiation of infections from sterile inflammation and identification of patients at risk for sepsis. Our results support further investigation of the SepsisMetaScore for the development of tailored precision treatment of critically ill patients.

AB - OBJECTIVES: Early diagnosis of infections is pivotal in critically ill patients. Innovative gene expression-based approaches promise to deliver precise, fast, and clinically practicable diagnostic tools to bedside. This study aimed to validate the SepsisMetaScore, an 11-gene signature previously reported by our study group, in a representative longitudinal cohort of trauma patients.DESIGN: Prospective observational cohort study.SETTING: Surgical ICUs of the University Medical Center Goettingen, Germany.PATIENTS: Critically ill patients with severe traumatic injuries.INTERVENTIONS: None.MEASUREMENTS AND MAIN RESULTS: Paired box gene (PAXgene) RNA blood tubes were drawn at predefined time points over the course of disease. The performance of the SepsisMetaScore was tested using targeted polymerase chain reaction and compared with Procalcitonin using area under the receiver operating characteristics analyses. The SepsisMetaScore showed significant differences between infected and noninfected patients (n = 52). It was able to accurately discriminate infectious from noninfectious acute inflammation with an area under the receiver operating characteristics of 0.92 (95% CI, 0.85-0.99) and significantly outperformed Procalcitonin (area under the receiver operating characteristics curve = 0.53; 95% CI, 0.42-0.64) early in the course of infection (p = 0.014).CONCLUSIONS: We demonstrated the clinical utility for diagnosis of infections with higher accuracy using the SepsisMetaScore compared with Procalcitonin in a prospective cohort of severe trauma patients. Future studies should assess whether the SepsisMetaScore may substantially improve clinical practice by accurate differentiation of infections from sterile inflammation and identification of patients at risk for sepsis. Our results support further investigation of the SepsisMetaScore for the development of tailored precision treatment of critically ill patients.

UR - http://europepmc.org/abstract/med/33883455

U2 - 10.1097/ccm.0000000000005027

DO - 10.1097/ccm.0000000000005027

M3 - SCORING: Journal article

C2 - 33883455

VL - 49

SP - e751-e760

JO - CRIT CARE MED

JF - CRIT CARE MED

SN - 0090-3493

IS - 8

ER -