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1.
An. pediatr. (2003, Ed. impr.) ; 73(1): 12-18, jul. 2010. tab, ilus
Article in Spanish | IBECS | ID: ibc-82577

ABSTRACT

Introducción y objetivo: La hipertensión intracraneal (HITC) es la principal causa de mortalidad y secuelas de los pacientes con traumatismo craneoencefálico grave. La craniectomía descompresiva (CD) es una técnica quirúrgica que permite disminuir la presión intracraneal y mejorar la presión de perfusión cerebral (PPC). El objetivo del trabajo es presentar la experiencia con la CD para el tratamiento de la hipertensión intracraneal. Pacientes y métodos: Revisión retrospectiva de los pacientes ingresados entre los años 2005–2008 con lesión cerebral e hipertensión intracraneal incontrolable médicamente a los que se les realizó una CD como terapia. Resultados: Se incluyen 14 pacientes con traumatismo craneoencefálico grave con una mediana de edad de 14,2 años (4–20 años). Las lesiones detectadas más frecuentemente en la TC craneal de los niños con traumatismo fueron las lesiones encefálicas difusas II y III. En todos se practicó una CD por presentar cifras de presión intracraneal elevadas refractarias a la terapéutica instaurada. La evolución fue favorable en todos los pacientes salvo en 2. El 78,8% presenta una buena evolución neurológica (Glasgow Outcome Score 4 y 5) a los 6 meses de la intervención. Conclusión: La CD es una alternativa en el manejo de la hipertensión intracraneal refractaria al tratamiento médico en niños y adolescentes que han sufrido un traumatismo craneoencefálico grave y puede ser usada simultáneamente o como alternativa al coma barbitúrico sobre todo en aquellos pacientes con inestabilidad hemodinámica (AU)


Introduction and objective: Intracranial hypertension (ICH) is the main cause of morbidity and mortality in patients with severe traumatic head injuries. Decompressive craniectomy (DC) is a surgical technique that allows to reduce intracranial pressure (ICP) and to improve cerebral blood flow. Objective: To present our experience on DC for the treatment of ICH. Patients and methods: Retrospective review of patients admitted from January 2005 to December 2008 who had a traumatic brain injury (TBI) and uncontrollable intracranial hypertension despite optimal medical treatment and who needed DC. Results: Fourteen patients with severe TBI were included in this series. Mean age was 14.2 years (4–20 years). The more frequent damages detected in cranial computerized tomography were diffuse brain lesions types II and III. Indication for DC was made if ICP levels were above 25mmHg for more than 30min despite optimal medical treatment. Clinical outcome was favourable in all patients apart from two. Neurological outcome was correct in 78.8% of patients (Glasgow Outcome Score 4 and 5) six months after PICU discharge. Conclusion: DC is an alternative for the management of refractory intracranial hypertension in children and adolescents with severe TBI. It could be used simultaneously with the barbiturate coma or as an alternative, particularly in haemodynamically unstable patients (AU)


Subject(s)
Humans , Male , Female , Child , Intracranial Hypertension/surgery , Craniotomy , Decompression, Surgical/methods , Craniocerebral Trauma/complications , Coma/chemically induced
2.
An Pediatr (Barc) ; 73(1): 12-8, 2010 Jul.
Article in Spanish | MEDLINE | ID: mdl-20466606

ABSTRACT

INTRODUCTION AND OBJECTIVE: Intracranial hypertension (ICH) is the main cause of morbidity and mortality in patients with severe traumatic head injuries. Decompressive craniectomy (DC) is a surgical technique that allows to reduce intracranial pressure (ICP) and to improve cerebral blood flow. OBJECTIVE: To present our experience on DC for the treatment of ICH. PATIENTS AND METHODS: Retrospective review of patients admitted from January 2005 to December 2008 who had a traumatic brain injury (TBI) and uncontrollable intracranial hypertension despite optimal medical treatment and who needed DC. RESULTS: Fourteen patients with severe TBI were included in this series. Mean age was 14.2 years (4-20 years). The more frequent damages detected in cranial computerized tomography were diffuse brain lesions types II and III. Indication for DC was made if ICP levels were above 25 mmHg for more than 30 min despite optimal medical treatment. Clinical outcome was favourable in all patients apart from two. Neurological outcome was correct in 78.8% of patients (Glasgow Outcome Score 4 and 5) six months after PICU discharge. CONCLUSION: DC is an alternative for the management of refractory intracranial hypertension in children and adolescents with severe TBI. It could be used simultaneously with the barbiturate coma or as an alternative, particularly in haemodynamically unstable patients.


Subject(s)
Decompressive Craniectomy , Intracranial Hypertension/surgery , Adolescent , Child , Child, Preschool , Female , Humans , Male , Retrospective Studies , Young Adult
4.
Rev Neurol ; 46(7): 385-91, 2008.
Article in Spanish | MEDLINE | ID: mdl-18389456

ABSTRACT

PATIENTS AND METHODS: A total of 12 patients with moyamoya disease or syndrome with a mean age of 6 years were analyzed in a retrospective fashion. RESULTS: Infarction was the most frequent presentation feature (8 out of 12 patients), 2 had epilepsy and 2 were incidental findings. Seven cases were classified as idiopathic while the other five were related to systemic illnesses. Diagnosis was initially made by magnetic resonance angiography in 9 cases, and conventional angiography in 3 cases. Mean follow-up is 5 years; six patients experienced clinical worsening of symptoms, while 6 cases remained clinically stable. However, all of them showed angiographic progression. Four patients underwent revascularization surgery. Two children died due to complications associated with moyamoya disease, and six have moderate handicaps. CONCLUSION: Due to the fact moyamoya disease is not an indolent disorder and readily progress to cause complications, surgical revascularization should always be considered in the management of these patients.


Subject(s)
Moyamoya Disease/diagnosis , Adolescent , Child , Child, Preschool , Female , Humans , Infant , Longitudinal Studies , Male , Retrospective Studies
5.
Rev. neurol. (Ed. impr.) ; 46(7): 385-391, 1 abr., 2008. ilus, tab
Article in Es | IBECS | ID: ibc-65446

ABSTRACT

Pacientes y métodos. Estudio descriptivo, longitudinal, de 12 niños no asiáticos con síndrome o enfermedad de moyamoya, con el objetivo de analizar su presentación y evolución clinicorradiológica. Resultados. La edad promedio de inicio fue de 6 años; ocho se iniciaron con infarto cerebral, dos con epilepsia y dos fueron hallazgo casual. Siete se consideraron idiopáticos(enfermedad de moyamoya) y cinco asociados a enfermedades sistémicas (síndrome de moyamoya). El diagnóstico inicial se confirmó por angiorresonancia en nueve casos y en tres por arteriografía convencional. El seguimiento promedio fue de 5 años; seis evidenciaron progresividad clínica y seis estabilidad clínica. Todos tuvieron progresividad angiográfica. En cuatroniños se realizaron siete cirugías de revascularización. Dos niños fallecieron, uno por hemorragia cerebral y otro por un infarto cerebral expansivo, mientras que seis pacientes presentaron secuelas leves a moderadas. Conclusión. Es importante identificara los niños afectados por esta patología, ya que se pueden beneficiar de cirugía de revascularización, una de las pocas opciones terapéuticas para evitar la progresión y complicaciones de esta grave enfermedad


A total of 12 patients with moyamoya disease or syndrome with a mean age of 6 years wereanalyzed in a retrospective fashion. Results. Infarction was the most frequent presentation feature (8 out of 12 patients), 2 had epilepsy and 2 were incidental findings. Seven cases were classified as idiopathic while the other five were related to systemicillnesses. Diagnosis was initially made by magnetic resonance angiography in 9 cases, and conventional angiography in 3 cases. Mean follow-up is 5 years; six patients experienced clinical worsening of symptoms, while 6 cases remained clinicallystable. However, all of them showed angiographic progression. Four patients underwent revascularization surgery. Two children died due to complications associated with moyamoya disease, and six have moderate handicaps. Conclusion. Due to the fact moyamoya disease is not an indolent disorder and readily progress to cause complications, surgical revascularizationshould always be considered in the management of these patients


Subject(s)
Humans , Male , Female , Infant , Child, Preschool , Child , Adolescent , Moyamoya Disease/epidemiology , Moyamoya Disease/surgery , Cerebral Revascularization , Brain Ischemia/surgery , Early Diagnosis
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