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Plasma glutamine is associated with multiple organ failure in critically ill children

Plasma glutamine is associated with multiple organ failure in critically ill children

Status
Completed
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12613001298707
Enrollment
150
Registered
2013-11-22
Start date
2007-10-15
Completion date
2008-06-06
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Low plasma glutamine concentration (< 420 micromol/L) is an independent risk factor for mortality in critically ill adult patients. Glutamine metabolism in children is less well characterized. However, the PICU mortality is low and therefore mortality is difficult to use as an endpoint. Here we evaluated if plasma glutamine concentration at admission to the PICU relates to the development of multiple organ failure, using PELOD-score as a surrogate marker of mortality. In this observational study, consecutive critically ill children (n = 149) admitted to the PICU of a tertiary university hospital as well as a reference group of healthy children (n=60) were included. Plasma glutamine concentration and the pediatric logistic organ dysfunction score (PELOD) were determined at admission and at day 5 for patients still in the PICU.

Interventions

In this observational study, consecutive critically ill children (n = 149) admitted to the PICU of a tertiary university hospital as well as a reference group of healthy children (n=60) were included. Plasma glutamine concentration and the pediatric logistic organ dysfunction score (PELOD) were determined at admission and at day 5 for patients still in the PICU.

Sponsors

Stockholms lans landstng. The Country Council of Stockholm (projects 502033 and 511126).
Lead SponsorUniversity

Eligibility

Sex/Gender
All
Age
0 to 18 Years
Healthy volunteers
No

Inclusion criteria

An expected PICU-stay > 24 hours, informed consent and sampling within 48 hours after admittance.

Exclusion criteria

Absence of informed consent at 48 hours after admittance, failure of sampling or age > 18 years.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026