Neonatal Follow-up
NICU Follow Up and Neurodevelopment 5: Impact of Parents and Social Determinants of Health
Molly F. Lazarus (she/her/hers)
Clinical Research Coordinator
Stanford University School of Medicine
Menlo Park, California, United States
We performed a retrospective cohort study of VPT infants (6-month N=77, 12-month N=37, Table 1). Daily minutes of family-administered KC and visitation were derived from the electronic medical record (EMR) and frequencies during hospitalization (instances/days of hospitalization) were computed. Early cognitive development, expressed as age-adjusted 6- and 12-month Cognitive-Adaptive Test (CAT) scores from the Capute Scales, were collected as part of routine High-Risk Infant Follow Up visits.
Results: Hierarchical linear regression modeling showed that KC uniquely predicted 6-month CAT scores over and above GA, SES, health acuity, and visitation (full model: F=2.44, p</em>=0.042, r2=0.15; KC r2 change=0.07, p=0.017, Figure 1). KC also predicted CAT scores at 12 months over and above birth GA, SES, health acuity, and 6-month CAT score (full model: F=4.77, p=0.002, r2=0.44; KC r2 change=0.09, p=0.030, Figure 2). Health acuity score moderated the relation between KC and CAT at 6 months (full model: F=3.79, p=0.004, r2=0.21; interaction r2 change=0.07, p=0.016) but not 12 months (full model: F=3.85, p=0.006, r2=0.44; interaction r2 change< 0.001, p=0.979); associations at 6 months were significant only among sicker children but were present across the entire sample by 12 months.
Conclusion(s): VPT infants who experienced more KC during hospitalization demonstrated higher scores on 6- and 12-month assessments of cognitive development. These positive associations demonstrate that KC uniquely contributes to neurodevelopmental outcomes in VPT infants over and above other common sociodemographic and clinical factors. Critically, KC was beneficial independent of infants’ health acuity at 12 months. Together, these results provide strong evident that KC has significant potential as a long-term neuroprotective clinical strategy for all VPT infants.