Estimating the Probability of Neonatal Early-Onset Infection on the Basis of Maternal Risk Factors

Author:

Puopolo Karen M.1234,Draper David5,Wi Soora6,Newman Thomas B.67,Zupancic John348,Lieberman Ellice49,Smith Myesha6,Escobar Gabriel J.610

Affiliation:

1. Department of Newborn Medicine and

2. Channing Laboratory, Brigham and Women's Hospital, Boston, Massachusetts;

3. Division of Newborn Medicine, Children's Hospital Boston, Boston, Massachusetts;

4. Harvard Medical School, Boston, Massachusetts;

5. Department of Applied Mathematics and Statistics, University of California, Santa Cruz, California;

6. Division of Research, Kaiser Permanente Medical Care Program, Oakland, California;

7. Departments of Epidemiology and Biostatistics and Pediatrics, University of California, San Francisco, California;

8. Department of Neonatology, Beth Israel-Deaconess Medical Center, Boston, Massachusetts;

9. Department of Obstetrics, Gynecology and Reproductive Biology, Brigham and Women's Hospital, Boston, Massachusetts; and

10. Department of Pediatrics, Kaiser Permanente Medical Center, Walnut Creek, California

Abstract

OBJECTIVE: To develop a quantitative model to estimate the probability of neonatal early-onset bacterial infection on the basis of maternal intrapartum risk factors. METHODS: This was a nested case-control study of infants born at ≥34 weeks' gestation at 14 California and Massachusetts hospitals from 1993 to 2007. Case-subjects had culture-confirmed bacterial infection at <72 hours; controls were randomly selected, frequency-matched 3:1 according to year and birth hospital. We performed multivariate analyses and split validation to define a predictive model based only on information available in the immediate perinatal period. RESULTS: We identified 350 case-subjects from a cohort of 608 014 live births. Highest intrapartum maternal temperature revealed a linear relationship with risk of infection below 100.5°F, above which the risk rose rapidly. Duration of rupture of membranes revealed a steadily increasing relationship with infection risk. Increased risk was associated with both late-preterm and postterm delivery. Risk associated with maternal group B Streptococcus colonization is diminished in the era of group B Streptococcus prophylaxis. Any form of intrapartum antibiotic given >4 hours before delivery was associated with decreased risk. Our model showed good discrimination and calibration (c statistic = 0.800 and Hosmer-Lemeshow P = .142 in the entire data set). CONCLUSIONS: A predictive model based on information available in the immediate perinatal period performs better than algorithms based on risk-factor threshold values. This model establishes a prior probability for newborn sepsis, which could be combined with neonatal physical examination and laboratory values to establish a posterior probability to guide treatment decisions.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

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