Table 2

Overview of long-term outcome in relation to Sarnat stage of HIE in all children for whom outcome was known (overlap between diagnoses is possible)

HIE stage II (n=45)HIE stage III (n=11)HIE stage I
(n=2)
GA <36 weeks
(n=3)
Start of active TH>6 hours postpartum
(n=3)
Favourable outcome22 (49%)1 (9%)1 (50%)1 (33%)
Adverse outcome (combined)23 (51%)10 (91%)1 (50%)3 (100%)2 (67%)
 Death2 (4%)6 (55%)1 (33%)
 CP7 (16%)2 (18%)1 (33%)1 (33%)
 Epilepsy4 (9%)1 (9%)1 (33%)
 Intellectual disability3 (7%)1 (33%)
 BIF6 (13%)1 (50%)1 (33%)1 (33%)
 Profound hearing impairment1 (9%)
 CVI or other significant visual impairment2 (4%)1 (9%)
 ADD/ADHD
  Confirmed3 (7%)1 (9%)
  Suspected6 (13%)1 (50%)
 ASD2 (4%)
 DCD4 (9%)1 (9%)
 Dyslexia2 (4%)1 (9%)
 Need for special educational support7 (16%)2 (18%)1 (33%)
  • Among children with a history of Sarnat stage II HIE, two (of whom one was born late preterm) were lost to follow-up early due to relocating abroad. One child still residing in Sweden did not participate on either occasion. Two children with a history of Sarnat stage II HIE and favourable outcome at 6–8 years did not participate in the assessments at 10–12 years of age. Outcome was known for all children with a history of Sarnat stage III HIE. Outcomes among children treated outside of the protocol (Sarnat stage I HIE, GA<36 weeks, delayed initiation of active TH) are also presented separately. Two of the children with a history of Sarnat stage I HIE were lost to follow-up early due to relocating abroad. Infants for whom active TH was initiated at >6 hours postpartum had been passively cooled as they were on the borderline between Sarnat stage I and II HIE initially.

  • ADD/ADHD, attention deficit disorder/attention deficit and hyperactivity disorder; ASD, autism spectrum disorder; BIF, borderline intellectual functioning; CP, cerebral palsy; CVI, cerebral/cortical visual impairment; DCD, developmental coordination disorder; GA, gestational age; HIE, hypoxic–ischaemic encephalopathy; TH, therapeutic hypothermia.