Successful use of the new high-dose mannitol treatment in patients with Glasgow Coma Scale scores of 3 and bilateral abnormal pupillary widening: a randomized trial

Successful use of the new high-dose mannitol treatment in patients with Glasgow Coma Scale scores of 3 and bilateral abnormal pupillary widening: a randomized trial

Autor Cruz, J. Google Scholar
Minoja, G. Google Scholar
Okuchi, K. Google Scholar
Facco, E. Google Scholar
Instituição Comprehens Int Ctr Neuroemergencies
Universidade Federal de São Paulo (UNIFESP)
Univ Insubria
Nara Med Univ
Univ Padua E Meneghetti
Resumo Object. the authors evaluated long-term clinical outcomes in selected acutely comatose patients with severe diffuse brain swelling and recent clinical signs of impending brain death who received a novel high-dose mannitol treatment compared with those who received conventional-dose mannitol in the emergency room.Methods. Forty-four adult patients with traumatic, nonmissile-inflicted, acute, severe diffuse brain swelling were prospectively and randomly evaluated. All patients were selected based on the presence of recent clinical signs of impending brain death on the first emergency room evaluation. These signs included bilateral abnormal pupillary widening and lack of motor responses to painful stimulation (Glasgow Coma Scale score of 3). the study group (23 patients) received ultra-early and fast intravenous high-dose mannitol treatment (similar to1.4 g/kg), whereas the control group (21 patients) received half that dose (similar to0.7 g/kg).Ultra-early improvement of bilateral abnormal pupillary widening was significantly more frequent in the high-dose mannitol group than in the conventional-dose group (p < 0.02). High-dose mannitol treatment in the emergency room was also associated with significantly better 6-month clinical outcomes (p < 0.02); the best rate of favorable outcomes was 43.5%, compared with only 9.5% in the conventional-dose mannitol group. the two groups of patients were well matched with respect to all emergency room and head computerized tomography findings, as well as the timing of initial mannitol treatment (similar to80-90 minutes after the first evaluation at the scene of the injury).Comparative evaluation of bilateral pupillary widening between the scene of the injury and the emergency room showed no significant differences between groups, whereas mannitol dose dependence was statistically significant (p < 0.05), insofar as early pupillary improvement in the emergency room was concerned.Conclusions. Ultra-early high-dose mannitol administration in the emergency room is the first known treatment strategy significantly to reverse recent clinical signs of impending brain death, and also to contribute directly to improved long-term clinical outcomes for these patients who have previously been considered unsalvageable.
Assunto head injury
brain swelling
impending brain death
mannitol
outcome
Idioma Inglês
Data 2004-03-01
Publicado em Journal of Neurosurgery. Charlottesville: Amer Assoc Neurological Surgeons, v. 100, n. 3, p. 376-383, 2004.
ISSN 0022-3085 (Sherpa/Romeo, fator de impacto)
Editor Amer Assoc Neurological Surgeons
Extensão 376-383
Fonte http://dx.doi.org/10.3171/jns.2004.100.3.0376
Direito de acesso Acesso restrito
Tipo Artigo
Web of Science WOS:000220186400006
URI http://repositorio.unifesp.br/handle/11600/27669

Mostrar registro completo




Arquivos deste item

Arquivos Tamanho Formato Visualização

Não existem arquivos associados a este item.

Este item aparece na(s) seguinte(s) coleção(s)

Buscar DSpace


Navegar

Minha conta