Predictive Models of Neurodevelopmental Outcomes After Neonatal Hypoxic-Ischemic Encephalopathy

Author:

Peeples Eric S.1,Rao Rakesh2,Dizon Maria L.V.3,Johnson Yvette R.45,Joe Priscilla6,Flibotte John7,Hossain Tanzeema8,Smith Danielle9,Hamrick Shannon10,DiGeronimo Robert11,Natarajan Girija12,Lee Kyong-Soon13,Yanowitz Toby D.14,Mietzsch Ulrike11,Wu Tai-Wei15,Maitre Nathalie L.16,Pallotto Eugenia K.17,Speziale Mark18,Mathur Amit M.19,Zaniletti Isabella20,Massaro An21,

Affiliation:

1. Department of Pediatrics, University of Nebraska Medical Center, Omaha, Nebraska;

2. Department of Pediatrics, School of Medicine, Washington University in St Louis, St Louis, Missouri;

3. Department of Pediatrics, Ann & Robert H. Lurie Children’s Hospital of Chicago and Northwestern University, Chicago, Illinois;

4. Department of Pediatrics, Cook Children’s Medical Center, Fort Worth, Texas;

5. Department of Pediatrics, Texas Christian University and University of North Texas Health Science Center, Fort Worth, Texas;

6. Department of Pediatrics, University of California, San Francisco Benioff Children’s Hospital, Oakland, California;

7. Department of Pediatrics, Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania;

8. Department of Pediatrics, Boston Children’s Hospital, Boston, Massachusetts;

9. Department of Pediatrics, University of Colorado Denver, Denver, Colorado;

10. Department of Pediatrics, Emory University and Children’s Healthcare of Atlanta, Atlanta, Georgia;

11. Department of Pediatrics, University of Washington, Seattle, Washington;

12. Department of Pediatrics, Children’s Hospital of Michigan, Detroit, Michigan;

13. Department of Pediatrics, Hospital for Sick Children, Toronto, Ontario, Canada;

14. Department of Pediatrics, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania;

15. Department of Pediatrics, Keck School of Medicine, University of Southern California and Children’s Hospital Los Angeles, Los Angeles, California;

16. Department of Pediatrics, Nationwide Children’s Hospital, Columbus, Ohio;

17. Department of Pediatrics, Children’s Mercy Hospital, Kansas City, Missouri;

18. Department of Pediatrics, Rady Children’s Hospital–San Diego and University of California, San Diego, San Diego, California;

19. Department of Pediatrics, Saint Louis University, St Louis, Missouri;

20. Department of Pediatrics, Children’s Hospital Association, Lenexa, Kansas; and

21. Department of Pediatrics, Children’s National Health System, Washington, District of Columbia

Abstract

OBJECTIVES: To develop predictive models for death or neurodevelopmental impairment (NDI) after neonatal hypoxic-ischemic encephalopathy (HIE) from data readily available at the time of NICU admission (“early”) or discharge (“cumulative”). METHODS: In this retrospective cohort analysis, we used data from the Children’s Hospitals Neonatal Consortium Database (2010–2016). Infants born at ≥35 weeks’ gestation and treated with therapeutic hypothermia for HIE at 11 participating sites were included; infants without Bayley Scales of Infant Development scores documented after 11 months of age were excluded. The primary outcome was death or NDI. Multivariable models were generated with 80% of the cohort; validation was performed in the remaining 20%. RESULTS: The primary outcome occurred in 242 of 486 infants; 180 died and 62 infants surviving to follow-up had NDI. HIE severity, epinephrine administration in the delivery room, and respiratory support and fraction of inspired oxygen of 0.21 at admission were significant in the early model. Severity of EEG findings was combined with HIE severity for the cumulative model, and additional significant variables included the use of steroids for blood pressure management and significant brain injury on MRI. Discovery models revealed areas under the curve of 0.852 for the early model and of 0.861 for the cumulative model, and both models performed well in the validation cohort (goodness-of-fit χ2: P = .24 and .06, respectively). CONCLUSIONS: Establishing reliable predictive models will enable clinicians to more accurately evaluate HIE severity and may allow for more targeted early therapies for those at highest risk of death or NDI.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

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