Neonatal General
Neonatal General 8: NICU Practices 2
Raman Singla, Doctor of Medicine (Paediatrics) (he/him/his)
Senior Resident
All India Institute of Medical Sciences, New Delhi
New Delhi, Delhi, India
This descriptive study was conducted on inborn preterm neonates undergoing their first ROP screening in a level III NICU in India.
The primary outcome was to assess the magnitude of pain within 48 hours after screening by using the revised premature infant pain profile (PIPP-R) score. The score was measured at 5 minutes before the procedure (baseline), 5 min (immediately) post-procedure, 30 minutes, 6, 24 and 48 hours. Non-pharmacological (nesting, swaddling, 25% oral dextrose solution) and pharmacological (0.5% topical proparacaine) measures were used to reduce pain during the screening. Secondary outcomes were to measure the incidence of apneas, increased baseline oxygen requirement (FiO2) ≥ 5%, additional respiratory support requirement, and feed intolerance following the screening.