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The investigators hypothesize that critical care trained registered nurses and physicians can perform measurements of cognitive impairment in critically ill pediatric patients in a reliable and valid manner. To test this hypothesis, the investigators will incorporate an instrument (psCAM-ICU) to assess both components of consciousness, arousal and content, in critically ill pediatric patients at least 6 months to children 5 years of age, both on and off mechanical ventilation, and compare these assessments to those of the reference standard.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Critically Ill Children | Children in the Pediatric Critical Care Unit regardless of admitting diagnosis aged at least 6 months of age up to 5 years of age. |
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| Measure | Description | Time Frame |
|---|---|---|
| Validation of psCAM-ICU | The investigators will validate the psCAM-ICU against a reference standard delirium assessment in critically ill infants and young children. Critical care physicians and registered nurses will use the psCAM-ICU to determine presence or absence of delirium once daily in critically ill infants and young children from 6 months to less than 5 years of age. The reference standard, a pediatric delirium expert (child psychiatrist or equivalent), will independently evaluate the same patients for presence or absence of delirium using the Diagnostic and Statistical Manual of Mental Disorders (DSM IV-TR) as the foundation of assessment. | Participants will be followed for the duration of hospital stay, an expected average of 2 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Inter-rater reliability of diagnosing delirium | The investigators will assess inter-rater reliability between physician, practitioner, and nursing assessment using the psCAM-ICU. The psCAM-ICU should consistently diagnose delirium in the critically ill pediatric patient, independent of the type of medical care provider assessing the patient. | Participants will be followed for the duration of hospital stay, an expected average of 2 weeks |
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Inclusion Criteria:
Exclusion Criteria:
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Critically ill pediatric patients at least 6 months to children 5 years of age, both on and off mechanical ventilation
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| Name | Affiliation | Role |
|---|---|---|
| Heidi Smith, MD | Vanderbilt University School of Medicine | Principal Investigator |
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| ID | Term |
|---|---|
| D003693 | Delirium |
| D060825 | Cognitive Dysfunction |
| ID | Term |
|---|---|
| D003221 | Confusion |
| D019954 | Neurobehavioral Manifestations |
| D009461 | Neurologic Manifestations |
| D009422 | Nervous System Diseases |
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| Validation of the Richmond Agitation Sedation Scale (RASS) | The investigators will validate the RASS against the Glasgow Coma Scale in critically ill infants and young children less than 5 years of age. | Participants will be followed for the duration of hospital stay, an expected average of 2 weeks |
| Validation of the Withdrawal Assessment Tool-1 (WAT-1) | The investigators will validate the WAT-1 against a reference standard (child psychiatrist) in critically ill infants and young children less than 5 years of age. | Participants will be followed for the duration of hospital stay, an expected average of 2 weeks |
| Long-term cognitive impairment composite | Clinical data will be obtained from the medical record to determine a composite measure of long-term cognitive impairment. The composite will include specific outcomes, and follow-up phone interviews with be conducted with a parent/legal guardian at 12 months post-hospital discharge of enrolled patients to assess cognitive function using a validated questionnaire that is compared to expected developmental trajectories based on age adjusted norms. | 1 year |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D019965 | Neurocognitive Disorders |
| D001523 | Mental Disorders |
| D003072 | Cognition Disorders |