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Acute hyperglycemia is a reliable outcome predictor in children with severe traumatic brain injury

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Abstract

Purpose

Hyperglycemia in the acute phase after trauma could adversely affect outcome in children with severe traumatic brain injury (TBI). The goal of this study was to identify the relationship between acute spontaneous hyperglycemia and outcome in children with severe TBI at hospital discharge and 6 months later.

Methods

A retrospective analysis of blood glucose levels in children with severe TBI at a Pediatric level I Trauma Center, between January 2000 and December 2005. Hyperglycemia was considered for a cut-off value of 11.1 mmol/l (200 mg/dl). Outcome was measured with Glasgow Outcome Scale (GOS) at hospital discharge and at 6 months. A multiple logistic regression analysis, the Student's t test and the χ 2 test were done.

Results

Hyperglycemia was noted within the first 48 h in 34% of the patients. Mortality (70% vs 14%, p < 10-5) was more frequent in hyperglycemic children and bad outcome upon hospital discharge in those who remained hyperglycemic during the first 48 h of hospitalization. GOS after 6 months demonstrated that those normoglycemic children had a better outcome (95%) than those who developed hyperglycemia during the first 48 h (83%, p = 0.01) after trauma.

Conclusion

Hyperglycemia could be considered as a marker of brain injury and when present upon admission, could reflect extensive brain damage with frequently associated mortality and bad outcome. The inability to maintain normal blood glucose levels during the first 48 h could be a predictive factor of bad outcome. Avoiding hyperglycemia in the initial phase could be a major issue in children with severe TBI.

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Acknowledgment

The authors acknowledge Mrs. Adeline Noiriat, secretary of the Department of Pediatric Neurosurgery-Hôpital Necker-Enfants Malades.

CAPES Brazil (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior), Exchange Program for PhD studies, is a source of support.

This study is supported in part by a grant from Direction Régionale de la Recherche Clinique Assistance Publique Hôpitaux de Paris PHRC 2003 No. AOM 03018.

Conflicts of interest

The authors declare that they have no conflicts of interest.

Comments

The deleterious effect of hyperglycemia in the acute stage of critically ill patients, especially on their brain, whatever the age and cause be is not new information. However, few articles dedicated on this topic in children suffering from severe TBI (admitted with GCS < 8)have been previously published. The article from Tude Melo et al. brings a well-constructed retrospective analysis of 286 children admitted in their unit after a TBI with a GCS < 8. The cases have been stratified in four groups according to initial and the follow-up glycemia in the first 48 h, and the outcome was analyzed considering mortality and GOS at 6 months. A sound statistical analysis confirms the deleterious effect of the initial hyperglycemia persisting in the first 2 days after admission as an independent factor of increased mortality and bad functional outcome. Normoglycemic patients had a statistically significant better outcome than those who developed hyperglycemia during the first 48 h. Prevention of iatrogenic increase of glycemia (avoidance of fluid maintenance with solution containing glucose and steroid administration) is recommended by the authors, and although one could be tempted to try to treat hyperglycemia with insulin, there is, up to now, no proof of any benefit of such treatment. On the contrary, randomized multicenter studies in adults admitted in a ICU in a critical state that were assigned intensive versus conventional glucose control showed an increased mortality.

Benedict Rilliet

Geneva, Switzerland

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Correspondence to José Roberto Tude Melo.

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Melo, J.R.T., Di Rocco, F., Blanot, S. et al. Acute hyperglycemia is a reliable outcome predictor in children with severe traumatic brain injury. Acta Neurochir 152, 1559–1565 (2010). https://doi.org/10.1007/s00701-010-0680-z

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  • DOI: https://doi.org/10.1007/s00701-010-0680-z

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