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Postanoxic Myoclonic Seizures After Pediatric Cardiac Arrest: Characteristics and Outcomes in a Single-Center Cohort,
Ashley M Bach1,2, Kathleen Walsh1, Dominique D Cooper1,2
1Department of Pediatrics, Division of Neurology, Children's Hospital of Philadelphia, PA.
Insights
Postanoxic myoclonic seizures (PAMS) in children after cardiac arrest (CA) often lead to severe disability or death. Continuous EEG background and limited MRI diffusion restriction may indicate better outcomes in PAMS patients.
Area of Science:
- Pediatric Neurology
- Critical Care Medicine
- Neurophysiology
Background:
- Postanoxic myoclonic seizures (PAMS) are a challenging complication in children following cardiac arrest (CA).
- Understanding the clinical features and outcomes of PAMS is crucial for improving patient management.
Purpose of the Study:
- To describe the clinical characteristics and outcomes of pediatric patients experiencing postanoxic myoclonic seizures (PAMS) after cardiac arrest (CA).
Main Methods:
- Retrospective cohort study at a single children's hospital.
- Identified pediatric patients (<18 years) with PAMS on video continuous electroencephalography (CEEG) within 24 hours of CA.
- Analyzed clinical seizure manifestations, electroencephalography (EEG) patterns, treatments, and neurological outcomes.
Main Results:
- Twenty-six children with PAMS were identified; median age was 6.3 years.
- PAMS commonly presented as limb jerking and rhythmic eye opening, with burst-suppressed/burst-attenuated EEG background in most.
- Seventeen of 26 patients died before hospital discharge; survivors experienced severe disability (PCPC 3-5).
- Brain MRI revealed restricted diffusion in cortical areas supplied by the posterior cerebral artery in all evaluated patients.
Conclusions:
- Pediatric PAMS exhibit diverse EEG characteristics and are associated with high rates of mortality and severe disability.
- A continuous EEG background and limited MRI diffusion restriction may correlate with a less severe outcome, as seen in one survivor with moderate disability.
Objectives:
To describe clinical features and outcomes among children with postanoxic myoclonic seizures (PAMS) after cardiac arrest (CA).
Design:
Retrospective cohort.
Setting:
Single-center, children's hospital in the United States.
Patients:
Patients younger than 18 years old with in- or out-of-hospital CA with PAMS identified on video continuous electroencephalography (CEEG) within 24 hours of CA (2018-2024).
Interventions:
None.
Measurements And Main Results:
Twenty-six children with in-hospital or out-of-hospital CA and PAMS, defined as clinical myoclonus with electrographic correlates, were identified from a CA database. PAMS was verified on video CEEG. Median (interquartile range [IQR]) age was 6.3 years (IQR, 1.1-11.9 yr). Baseline Pediatric Cerebral Performance Category (PCPC) was 1 (normal) for 17 children. PAMS were observed within 1 hour of CEEG initiation for 19 children and within 12 hours for all children. PAMS manifested as limb jerking (18/25) and rhythmic eye opening (13/25). The range in electroencephalography (EEG) background was continuous (1/26), discontinuous (2/26), burst-suppressed/burst-attenuated (20/26), and entirely suppressed (3/26). Bursts were often highly epileptiform (15/20) and identical (10/20). All patients received at least 1 anti-seizure medication, and 16 of 26 received at least 1 anesthetic infusion. Death before hospital discharge occurred in 17 of 26, and causes of death were withdrawal of life-sustaining therapy (10/17), brain death (6/17), and rearrest (1/17). Among nine survivors, PCPC scores ranged from 3 to 5, eight had gastrostomies, and one a tracheostomy. A brain MRI was available for 15 of 26 at a median 4 days (IQR, 3-5 d) after CA. All had restricted diffusion involving the precentral and postcentral gyri and cortex supplied by the posterior cerebral artery. The one child with moderate disability (PCPC = 3) at hospital discharge had continuous EEG background and limited MRI diffusion restriction.
Conclusions:
Children with PAMS have a range of EEG characteristics. Severe disability and death were common following PAMS. The child with moderate disability had a continuous EEG background and limited MRI diffusion restriction.
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