Association of EEG Background and Neurodevelopmental Outcome in Neonates With Hypoxic-Ischemic Encephalopathy Receiving Hypothermia

被引:11
作者
Glass, Hannah C. [1 ,2 ,3 ,4 ]
Numis, Adam L. [1 ,2 ,3 ]
Comstock, Bryan A. [5 ]
Gonzalez, Fernando F.
Mietzsch, Ulrike [6 ]
Bonifacio, Sonia Lomeli [7 ]
Massey, Shavonne [8 ,9 ]
Thomas, Cameron [10 ,11 ]
Natarajan, Niranjana [12 ]
Mayock, Dennis E.
Sokol, Gregory M. [13 ]
Van Meurs, Krisa P. [7 ]
Ahmad, Kaashif A. [14 ]
Maitre, Nathalie [15 ,16 ]
Heagerty, Patrick J. [5 ]
Juul, Sandra E. [6 ]
Wu, Yvonne W. [1 ,2 ,3 ]
Wusthoff, Courtney J. [17 ]
机构
[1] UCSF Benioff Childrens Hosp, Dept Neurol, San Francisco, CA 94158 USA
[2] UCSF Benioff Childrens Hosp, Weill Inst Neurosci, San Francisco, CA 94158 USA
[3] UCSF Benioff Childrens Hosp, Dept Pediat, San Francisco, CA 94158 USA
[4] Univ Calif San Francisco, Epidemiol & Biostat, San Francisco, CA 94118 USA
[5] Univ Washington, Dept Biostat, Seattle, WA USA
[6] Univ Washington, Seattle Childrens Hosp, Dept Pediat, Div Neonatol,Sch Med, Seattle, WA USA
[7] Stanford Univ, Dept Pediat, Div Neonatal & Dev Med, Palo Alto, CA USA
[8] Univ Penn, Childrens Hosp Philadelphia, Dept Neurol & Pediat, Philadelphia, PA USA
[9] Univ Penn, Perelman Sch Med, Philadelphia, PA USA
[10] Univ Cincinnati, Dept Pediat, Cincinnati, OH USA
[11] Cincinnati Childrens Hosp Med Ctr, Div Neurol, Cincinnati, OH USA
[12] Univ Washington, Sch Med, Dept Neurol, Seattle, WA USA
[13] Indiana Univ Sch Med, Dept Pediat, Indianapolis, IN USA
[14] Pediatrix Neonatol San Antonio, San Antonio, TX USA
[15] Emory Univ, Dept Pediat, Atlanta, GA USA
[16] Emory Univ, Emory Childrens Pediat Inst, Atlanta, GA USA
[17] Stanford Univ, Dept Neurol, Palo Alto, CA USA
关键词
AMPLITUDE-INTEGRATED ELECTROENCEPHALOGRAPHY; SEIZURE BURDEN; INFANTS; ASPHYXIA;
D O I
10.1212/WNL.0000000000207744
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and ObjectivesPredicting neurodevelopmental outcome for neonates with hypoxic-ischemic encephalopathy (HIE) is important for clinical decision-making, care planning, and parent communication. We examined the relationship between EEG background and neurodevelopmental outcome among children enrolled in a trial of erythropoietin or placebo for neonates with HIE treated with therapeutic hypothermia.MethodsParticipants had EEG recorded throughout hypothermia. EEG background was classified as normal, discontinuous, or severely abnormal (defined as burst suppression, low voltage suppressed, or status epilepticus) at 5 1-hour epochs: onset of recording, 24, 36, 48, and 72 hours after birth. The predominant background pattern during the entire continuous video EEG monitoring recording was calculated using the arithmetic mean of the 5 EEG background ratings (normal = 0; discontinuous = 1; severely abnormal = 2) as follows: "predominantly normal" (mean = 0), "normal/discontinuous" (0 < mean<1), "predominantly discontinuous" (mean = 1), "discontinuous/severely abnormal" (1 < mean<2), or "predominantly severely abnormal" (mean = 2). Primary outcome was death or neurodevelopmental impairment (NDI) defined as cerebral palsy, Gross Motor Function Classification Score >= 1, or cognitive score <90 on Bayley Scales of Infant Toddler Development, third edition at age 2 years. Neurodevelopment was also categorized into a 5-level ordinal measure: no, mild, moderate, severe NDI, or death for secondary analysis. We used generalized linear regression models with robust standard errors to assess the relative risk of death or NDI by EEG background in both unadjusted and adjusted analyses controlling for the effects of treatment group, sex, HIE severity, and study recruitment site.ResultsAmong 142 neonates, the predominant background EEG pattern was predominantly normal in 35 (25%), normal/discontinuous in 68 (48%), predominantly discontinuous in 11 (7.7%), discontinuous/severely abnormal in 16 (11%), and predominantly severely abnormal in 12 (8.5%). Increasing severity of background across monitoring epochs was associated with increasingly worse clinical outcomes. Children with severe EEG background abnormality at any time point (n = 36, 25%) were significantly more likely to die or have severe NDI at 2 years (adjusted relative risk: 7.95, 95% CI 3.49-18.12).DiscussionEEG background is strongly associated with NDI at age 2 years. These results can be used to assist health care providers to plan follow-up care and counsel families for decision-making related to goals of care.
引用
收藏
页码:E2223 / E2233
页数:11
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