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Hospital-onset bacteremia in the neonatal intensive care unit: strategies for risk adjustment

Published online by Cambridge University Press:  17 February 2025

Erica C. Prochaska*
Affiliation:
Division of Pediatric Infectious Diseases, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA Department of Hospital Epidemiology and Infection Control, Johns Hopkins Health System, Baltimore, MD, USA
Shaoming Xiao
Affiliation:
Department of Epidemiology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA
Elizabeth Colantuoni
Affiliation:
Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA
Nora Elhaissouni
Affiliation:
Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA
Reese H. Clark
Affiliation:
Pediatrix Medical Group, Sunrise, FL, USA
Julia Johnson
Affiliation:
Division of Neonatology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA Department of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
Sagori Mukhopadhyay
Affiliation:
Division of Neonatology, Department of Pediatrics, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
Ibukunoluwa C. Kalu
Affiliation:
Division of Pediatric Infectious Diseases, Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA
Danielle M. Zerr
Affiliation:
Division of Infectious Diseases, Department of Pediatrics, University of Washington and Seattle Children’s Hospital, Seattle, WA, USA
Patrick J. Reich
Affiliation:
Division of Pediatric Infectious Diseases, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, USA
Jessica Roberts
Affiliation:
Division of Neonatology, Department of Pediatrics, Emory University School of Medicine & Children’s Healthcare of Atlanta, Atlanta, GA, USA
Dustin D. Flannery
Affiliation:
Division of Neonatology, Department of Pediatrics, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
Aaron M. Milstone
Affiliation:
Division of Pediatric Infectious Diseases, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA Department of Hospital Epidemiology and Infection Control, Johns Hopkins Health System, Baltimore, MD, USA
*
Corresponding author: Erica C. Prochaska; Email: eprocha1@jhmi.edu
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Abstract

Objective:

To quantify the impact of patient- and unit-level risk adjustment on infant hospital-onset bacteremia (HOB) standardized infection ratio (SIR) ranking.

Design:

A retrospective, multicenter cohort study.

Setting and participants:

Infants admitted to 284 neonatal intensive care units (NICUs) in the United States between 2016 and 2021.

Methods:

Expected HOB rates and SIRs were calculated using four adjustment strategies: birthweight (model 1), birthweight and postnatal age (model 2), birthweight and NICU complexity (model 3), and birthweight, postnatal age, and NICU complexity (model 4). Sites were ranked according to the unadjusted HOB rate, and these rankings were compared to rankings based on the four adjusted SIR models.

Results:

Compared to unadjusted HOB rate ranking (smallest to largest), the number and proportion of NICUs that left the fourth quartile (worst-performing) following adjustments were as follows: adjusted for birthweight (16, 22.5%), birthweight and postnatal age (19, 26.8%), birthweight and NICU complexity (22, 31.0%), birthweight, postnatal age and NICU complexity (23, 32.4%). Comparing NICUs that moved into the better-performing quartiles after birthweight adjustment to those that remained in the better-performing quartiles regardless of adjustment, the median percentage of low birthweight infants was 17.1% (Interquartile Range (IQR): 15.8, 19.2) vs 8.7% (IQR: 4.8, 12.6); and the median percentage of infants who died was 2.2% (IQR: 1.8, 3.1) vs 0.5% (IQR: 0.01, 12.0), respectively.

Conclusion:

Adjusting for patient and unit-level complexity moved one-third of NICUs in the worst-performing quartile into a better-performing quartile. Risk adjustment may allow for a more accurate comparison across units with varying levels of patient acuity and complexity.

Information

Type
Original Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2025. Published by Cambridge University Press on behalf of The Society for Healthcare Epidemiology of America
Figure 0

Figure 1. Scatter Plots of Neonatal Intensive Care Unit-level Characteristics with Site Hospital-Onset Bacteremia Rates. Correlation coefficients are shown as rs.

Figure 1

Figure 2. Alluvial plot of neonatal intensive care unit (NICU) rankings based upon the unadjusted HOB rate and standardized infection ratios (SIR) calculated from four adjusted models: birthweight (model 1), birthweight and postnatal age (model 2), birthweight and NICU complexity (model 3), and all variables (model 4). Based upon unadjusted HOB rate, the sites in the fourth quartile (worst-performing) are shown in dark gray and first-third quartiles (better-performing) are shown in light gray. Forty-four sites remained in the fourth quartile and 185 sites remained in the first-third quartiles regardless of adjustment. Across all adjustment strategies, 55 sites experienced a change into or out of the fourth quartile. The plot is truncated to show the 55 sites that experienced a change in performance quartiles and is not to scale.

Figure 2

Figure 3. Scatterplots, with Spearman correlation coefficients, of HOB Standardized Infection Ratio (SIR) rank (ordered smallest to largest) derived from adjusted SIR model 1 compared to adjusted SIR model 2–4 (Panels A through C) for 284 neonatal intensive care units (NICUs) in the analysis. Risk adjustments include: birthweight (model 1), birthweight and postnatal age (model 2), birthweight and NICU complexity (model 3), and birthweight, postnatal age, and NICU complexity (model 4). Panel D displays adjusted SIR model 4 based on all HOB to the corresponding SIR rank using only non-commensal and treated commensal HOB events based on 277 NICUs that provided antibiotic data.

Figure 3

Table 1. Characteristics of NICUs included in the analysis, grouped by change in standardized infection ratio (SIR) rank after changes in the risk adjustment strategy