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Delirium Op de PICU studie (DOP-studie).

The delirium at the PICU study: an evaluation of the usefulness of the pCAM-ICU, PAED and-Comfort and SOS scores for the diagnosis of pediatric delirium at the Pediatric Intensive Care Unit (PICU) of the Maastricht Universitair Medisch Centrum (MUMC+). A quality of care improvement program.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON27483
Enrollment
125
Registered
2009-10-12
Start date
2009-01-11
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric Delirium Pediatric Intensive Care Unit

Interventions

If the first team suspects a pediatric delirium, they will always and immediately alert the reference rater team in order to confirm the diagnosis of delirium and treat the patient according to pediat

Sponsors

MUMC+
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All non-elective patients admitted to the PICU between the age of 1 and 17, ventilated or non-ventilated, will be screened for eligibility regardless of admitting diagnosis which includes both surgical and medical population. This also regards children who have been admitted to the PICU after an elective surgical procedure and who are still at the PICU after 48 hours.

Exclusion criteria

Exclusion criteria: 1. All patients admitted to the PICU on an elective base; 2. Regarding the use of the pCAM- ICU and the neurocognitive items: 3, 5, 6, & 13 of the DRS 88/98: A. Children less than five years of age, because the pCAM-ICU will require some degree of education and baseline level of functioning of the child; B. Children of at least five years of age, but with a level of cognition less than five years of age, for the same reasons as given above; C. Non-Dutch speakers; D. Children with visual or hearing impairments who are unable to be assessed using the pCAM-ICU.

Design outcomes

Primary

MeasureTime frame
The primary study parameters are: Delirium yes or no with a positive result after diagnostic testing.

Secondary

MeasureTime frame
During the use of the diagnostic instruments, a few 'points' will be collected in order to test the cut-off value. The current use of medication will be documented as well as the reason of admission in order to examine the etiology in retrospect of pediatric delirium.

Contacts

Public ContactJ. Schieveld

P. O. Box 5800

jan.schieveld@mumc.nl+31 (0)43 3877499

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)