TY - JOUR
T1 - Antiseizure medication at discharge in infants with hypoxic-ischaemic encephalopathy
T2 - An observational study
AU - Sewell, Elizabeth K.
AU - Shankaran, Seetha
AU - McDonald, Scott A.
AU - Hamrick, Shannon
AU - Wusthoff, Courtney J.
AU - Adams-Chapman, Ira
AU - Chalak, Lina F.
AU - Davis, Alexis S.
AU - Van Meurs, Krisa
AU - Das, Abhik
AU - Maitre, Nathalie
AU - Laptook, Abbott
AU - Patel, Ravi Mangal
N1 - Funding Information:
The National Institutes of Health, the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), the National Center for Research Resources (NCRR), and the National Center for Advancing Translational Sciences (NCATS) provided grant support for the Neonatal Research Network’s Induced Hypothermia, Late Hypothermia, and Optimizing Cooling trials through the following cooperative agreements and awards: U10 HD27904, U10 HD21364, U10 HD68284, U10 HD27853, UL1 TR77, U10 HD40492, UL1 TR1117, U10 HD27851, UL1 TR454, U10 HD27856, UL1 TR6, U10 HD21373, U10 HD68278, U10 HD36790, U10 HD27880, UL1 TR93, U10 HD53119, M01 RR54, U10 HD34216, M01 RR32, U10 HD68270, U10 HD40461, U10 HD53109, UL1 TR442, U10 HD21397, M01 RR16587, U10 HD53089, UL1 TR41, U10 HD68244, U10 HD68263, UL1 TR42, U10 HD40689, U10 HD53124, U10 HD21385, U10 HD27871, UL1 TR142.
Publisher Copyright:
© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.
PY - 2023
Y1 - 2023
N2 - Objectives: To assess variability in continuation of antiseizure medication (ASM) at discharge and to evaluate if continuation of ASM at discharge is associated with death or disability among infants with hypoxic-ischaemic encephalopathy (HIE) and seizures. Design: Retrospective study of infants enrolled in three National Institute of Child Health and Human Development Neonatal Research Network Trials of therapeutic hypothermia. Setting: 22 US centres. Patients: Infants with HIE who survived to discharge and had clinical or electrographic seizures treated with ASM. Exposures: ASM continued or discontinued at discharge. Outcomes: Death or moderate-to-severe disability at 18-22 months, using trial definitions. Multivariable logistic regression evaluated the association between continuation of ASM at discharge and the primary outcome, adjusting for severity of HIE, hypothermia trial treatment arm, use of electroencephalogram, discharge on gavage feeds, Apgar Score at 5 min, birth year and centre. Results: Of 302 infants included, 61% were continued on ASMs at discharge (range 13%-100% among 22 centres). Electroencephalogram use occurred in 92% of the cohort. Infants with severe HIE comprised 24% and 22% of those discharged with and without ASM, respectively. The risk of death or moderate-to-severe disability was greater for infants continued on ASM at discharge, compared with those infants discharged without ASM (44% vs 28%, adjusted OR 2.14; 95% CI 1.13 to 4.05). Conclusions: In infants with HIE and seizures, continuation of ASM at discharge varies substantially among centres and may be associated with a higher risk of death or disability at 18-22 months of age.
AB - Objectives: To assess variability in continuation of antiseizure medication (ASM) at discharge and to evaluate if continuation of ASM at discharge is associated with death or disability among infants with hypoxic-ischaemic encephalopathy (HIE) and seizures. Design: Retrospective study of infants enrolled in three National Institute of Child Health and Human Development Neonatal Research Network Trials of therapeutic hypothermia. Setting: 22 US centres. Patients: Infants with HIE who survived to discharge and had clinical or electrographic seizures treated with ASM. Exposures: ASM continued or discontinued at discharge. Outcomes: Death or moderate-to-severe disability at 18-22 months, using trial definitions. Multivariable logistic regression evaluated the association between continuation of ASM at discharge and the primary outcome, adjusting for severity of HIE, hypothermia trial treatment arm, use of electroencephalogram, discharge on gavage feeds, Apgar Score at 5 min, birth year and centre. Results: Of 302 infants included, 61% were continued on ASMs at discharge (range 13%-100% among 22 centres). Electroencephalogram use occurred in 92% of the cohort. Infants with severe HIE comprised 24% and 22% of those discharged with and without ASM, respectively. The risk of death or moderate-to-severe disability was greater for infants continued on ASM at discharge, compared with those infants discharged without ASM (44% vs 28%, adjusted OR 2.14; 95% CI 1.13 to 4.05). Conclusions: In infants with HIE and seizures, continuation of ASM at discharge varies substantially among centres and may be associated with a higher risk of death or disability at 18-22 months of age.
KW - Infant Development
KW - Intensive Care Units, Neonatal
KW - Neonatology
KW - Neurology
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UR - http://www.scopus.com/inward/citedby.url?scp=85148675989&partnerID=8YFLogxK
U2 - 10.1136/archdischild-2022-324612
DO - 10.1136/archdischild-2022-324612
M3 - Article
C2 - 36732048
AN - SCOPUS:85148675989
SN - 1359-2998
JO - Archives of Disease in Childhood: Fetal and Neonatal Edition
JF - Archives of Disease in Childhood: Fetal and Neonatal Edition
M1 - fetalneonatal-2022-324612
ER -