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Cerebral palsy patients discovered dead during sleep: experience from a comprehensive tertiary pediatric center
Ali F Karatas1, Elissa G Miller1, Freeman Miller1
1Nemours/Alfred I. duPont Hospital for Children, Wilmington, DE, USA.
Insights
Children with cerebral palsy (CP) who died suddenly during sleep (DDDS) often had severe motor and respiratory issues. Further research is needed to understand and prevent these sleep-related deaths in CP patients.
Area of Science:
- Pediatrics
- Neurology
- Pulmonology
Background:
- Sudden deaths during sleep (DDDS) in children with cerebral palsy (CP) are a concern, but associated factors are poorly understood.
- Understanding these factors is crucial for improving care and potentially preventing mortality in this vulnerable population.
Purpose of the Study:
- To describe the characteristics and co-morbidities of children with CP who experienced DDDS.
- To identify potential risk factors associated with DDDS in children with CP.
Main Methods:
- Retrospective, case-only study design.
- Analysis of patient data from a single tertiary care center between 1993 and 2011.
- Examination of mortality patterns, patient demographics, and co-morbidities.
Main Results:
- 19 out of 177 children with CP died from DDDS.
- DDDS patients frequently had gastrointestinal feeding tubes, seizure disorders, respiratory disorders, and were non-ambulatory.
- A high prevalence of respiratory issues was observed, including recurrent aspiration pneumonia, asthma pneumonitis, reactive airway disease, respiratory failure, chronic bronchitis, COPD, and nocturnal respiratory insufficiency.
Conclusions:
- Severe motor disability, seizures, intellectual status, and particularly respiratory disorders are potential co-morbidities linked to DDDS in children with CP.
- Further investigation is required to determine effective monitoring and care strategies to prevent DDDS in this population.
Objectives:
It is not uncommon for children with cerebral palsy (CP) to be discovered dead during sleep (DDDS); however, the factors associated with this pattern of mortality remain unknown. The current study aims to describe the mortality associated with children with CP from a single, tertiary care center who were DDDS.
Methods:
A retrospective (case-only) design to examine proportionate mortality and patient characteristics and co-morbidities that may be related to children DDDS between 1993 and 2011.
Results:
There were 177 patients with CP whose deaths were reported to our institution during the study period, of which 19 were DDDS at home. The period proportionate mortality (PPM) was 114.5 per 1000. The average age at time of death was 17 years and 6 months (minimum, 6 years; maximum, 25 years). All but one of the DDDS patients had gastrointestinal feeding tubes, seizure disorders, respiratory disorders, and were non-ambulatory. Very importantly, our DDDS patients manifested clusters of respiratory disorders, namely recurrent aspiration pneumonia (10/19), asthma pneumonitis (4/19), food/vomitius inhalation (6/19), reactive airway disease (16/19), respiratory failure (14/19), chronic bronchitis (7/19), chronic obstructive lung disease (9/19), and nocturnal respiratory insufficiency (16/19).
Conclusions:
Respiratory disorders, severe motor disability, seizures, and intellectual status are possible co-morbidities that may be associated with DDDS. There is a need for further study in order to understand what type of monitoring and care (if any) may help prevent DDDS related to these co-morbidities and sleep disorders/abnormalities.
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