Clinical evaluation of droplet digital PCR in the early identification of suspected sepsis patients in the emergency department: A prospective observational study

Author:

Jiang Sen1,Zhao Dongyang1,Wang Chunxue1,Liu Xiandong1,Yang Qian1,Bao Xiaowei1,Dong Tiancao1,Li Gen2,Gu Yi1,Ye Yangqin2,Sun Bingke1,Xu Shumin1,Zhou Xiaohui2,Fan Lieying2,Tang Lunxian1

Affiliation:

1. Tongji University School of Medicine

2. Tongji University

Abstract

Abstract Background Rapid and accurate diagnosis of the causative agents is essential for clinical management of bloodstream infections (BSIs) that might induce sepsis/septic shock. A considerable number of suspected sepsis patients initially enter the health-care system through an emergency department (ED), hence it is vital to establish an early strategy to recognize sepsis and initiate prompt care in ED. This study aimed to evaluate the diagnostic performance and clinical value of droplet digital PCR (ddPCR) assay in suspected sepsis patients in the ED. Methods This was a prospective single-centered observational study including patients admitted to the ED from 25 October 2022 to 3 June 2023 with suspected BSIs screened by Modified Shapiro Score (MSS) score. The comparison between ddPCR and blood culture (BC) was performed to evaluate the diagnostic performance of ddPCR for BSIs. Meanwhile, correlative analysis between ddPCR and the inflammatory and prognostic-related biomarkers were conducted to explore the relevance. Further, the health economic evaluation of the ddPCR was analyzed. Results 258 samples from 228 patients, with BC and ddPCR performed simultaneously, were included in this study. The etiological diagnosis revealed that the ddPCR yielded 147 positive results, with a positive rate of 56.98%. In contrast, BC only detected 18 positives, 88.8% of which were identified by ddPCR. When considering BSIs with comprehensive microbiological testing, ddPCR shows an overall sensitivity of 91.73% and specificity of 81.6%, the optimal diagnostic power for quantifying BSI through ddPCR is achieved with a copy cutoff of 166. We further found that ddPCR exhibited a high accuracy especially in liver abscess patients. Among all the identified virus by ddPCR, EBV has a substantially higher positive rate with a link to immunosuppression. Moreover, the copies of pathogens in ddPCR were positively correlated with various markers of inflammation, coagulation, immunity as well as prognosis. With high sensitivity and specificity, ddPCR facilitates precision antimicrobial stewardship and reduces health care costs. Conclusions The multiplexed ddPCR delivers precise and quantitative load data on the causal pathogen, offers the ability to monitor the patient's condition and may serve as early warning of sepsis in time-urgent clinical situations as ED.

Publisher

Research Square Platform LLC

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