The Infant High-Risk Follow-Up™ (HRF™) is a clinical database solution developed with the help of physicians, nurses and administrators. Designed specifically for high-risk infants, the HRF™ allows you to track outcomes and development through infancy and childhood.

The system encompasses the scope of high-risk infant follow-up medicine including the NICHD guidelines for follow-up assessment at 18 - 22 months corrected age. Demographic, perinatal, hospital stay and discharge data is automatically linked to the HRF™ saving time and avoiding double data entry. Alternatively, new patient data for patients not cared for in your hospital can also be entered into the HRF™ clinical database.

Data is captured from each HRF™ visit including, but not limited to, the physical and neurological exam, the Bayley Scales of Infant Development- III and the Brief Infant-Toddler Social Emotional Assessment (BITSAE).