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Performance Characteristics of Sepsis Screening Tools During Delivery Admissions.
Elliott K Main1, Matt Fuller, Vesela P Kovacheva
1Department of Obstetrics and Gynecology, Stanford University, Palo Alto, the Sutter Health Institute for Advancing Health Equity and the Center for Health Systems Research, Sutter Health, Sacramento, Common Spirit Health, the Department of Systems Clinical Informatics, Common Spirit Health, and the Department of Obstetrics, Gynecology, and Reproductive Sciences, University of California, San Francisco, San Francisco, California; the Department of Anesthesiology and the Department of Obstetrics and Gynecology, Duke University, Durham, North Carolina; the Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, Boston, Massachusetts; the Department of Anesthesiology, University of Arkansas for Medical Sciences, Little Rock, Arkansas; the Department of Obstetrics and Gynecology and the Department of Anesthesiology, Baylor College of Medicine, Houston, Texas; Wayne State University School of Medicine, Wayne, and the Department of Obstetrics and Gynecology, Oakland University William Beaumont School of Medicine, Royal Oak, Michigan; and the Department of Anesthesiology, Perioperative Medicine and Pain Management, University of Miami Miller School of Medicine, Miami, Florida.
The California Maternal Quality Care Collaborative (CMQCC) and United Kingdom Obstetric Surveillance System (UKOSS) screening tools demonstrate superior performance for diagnosing sepsis during delivery admissions. These tools offer the lowest false-positive rates while maintaining high sensitivity for sepsis detection.
Area of Science:
- Obstetrics and Gynecology
- Infectious Disease
- Critical Care Medicine
Background:
- Sepsis is a life-threatening condition that can occur during delivery admissions.
- Accurate and timely diagnosis of sepsis is crucial for effective treatment and improved patient outcomes.
- Existing sepsis screening tools require evaluation for their performance in the obstetric population.
Purpose of the Study:
- To evaluate the screening performance characteristics of existing tools for the diagnosis of sepsis during delivery admissions.
- To compare the sensitivity and false-positive rates of multiple sepsis screening criteria.
Main Methods:
- A case-control study utilizing electronic health record data from 59 hospitals.
- Patients with sepsis during delivery admissions were matched with controls.
- Evaluated screening criteria included CMQCC, SIRS, MEWC, UKOSS, and MEWT.
- Analyses were stratified into cohorts with and without chorioamnionitis-endometritis.
Main Results:
- In the absence of chorioamnionitis-endometritis, CMQCC and UKOSS demonstrated the lowest false-positive rates (6.9% and 9.6%) and highest C-statistics (0.92 and 0.91).
- SIRS and MEWC showed similar sensitivities but significantly higher false-positive rates.
- In the presence of chorioamnionitis-endometritis, CMQCC and UKOSS still yielded the highest C-statistics (0.67 and 0.64).
Conclusions:
- CMQCC and UKOSS pregnancy-adjusted criteria are effective for sepsis screening during delivery admissions, offering low false-positive rates and high sensitivity.
- The performance of all evaluated sepsis screening tools is diminished in the presence of chorioamnionitis-endometritis.
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