Acidosis láctica severa asociada a infusión de propofol. Caso clínico
Author | dc.contributor.author | Romero P., Carlos | |
Author | dc.contributor.author | Morales R., Mónica | es_CL |
Author | dc.contributor.author | Donaire R., Luisa | es_CL |
Author | dc.contributor.author | Llanos V., Osvaldo | es_CL |
Author | dc.contributor.author | Cornejo R., Rodrigo | es_CL |
Author | dc.contributor.author | Gálvez A., Ricardo | es_CL |
Author | dc.contributor.author | Castro Ormazábal, José | es_CL |
Admission date | dc.date.accessioned | 2010-01-15T16:56:39Z | |
Available date | dc.date.available | 2010-01-15T16:56:39Z | |
Publication date | dc.date.issued | 2008-01 | |
Cita de ítem | dc.identifier.citation | REVISTA MEDICA DE CHILE, Volume: 136, Issue: 1, Pages: 88-92, 2008 | en_US |
Identifier | dc.identifier.issn | 0034-9887 | |
Identifier | dc.identifier.uri | https://repositorio.uchile.cl/handle/2250/128226 | |
Abstract | dc.description.abstract | Propofol infusion syndrome (PRIS) is a rare but potentially lethal complications. This disorder is triggered under unknown circumstances by a propofol infusion of more than 5 mg/kg/h for more than 48 h. PRIS is characterized by a multiorgan failure and rhabdomyolysis and is induced by a disturbance in mitochondrial long chain fatty acid oxidation. We report a 43 year-old woman who underwent brain surgery due to a vascular malformation. In the immediate postoperative period, she had an unexplained and severe lactic acidosis. During anaesthesia, she received a propofol infusion of 7 mg/kg/h that continued in the UCI at a rate of 3.5 mg/kg/h, for 8 hours more. The suspicion of PRIS motivated immediate discontinuation of propofol with rapid correction of lactic acidosis and full recovery of the patient | en_US |
Lenguage | dc.language.iso | es | en_US |
Publisher | dc.publisher | SOC MEDICA SANTIAGO | en_US |
Keywords | dc.subject | Acidosis, lactic | en_US |
Título | dc.title | Acidosis láctica severa asociada a infusión de propofol. Caso clínico | en_US |
Document type | dc.type | Artículo de revista |
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