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1.
Rev Neurol ; 46(1): 7-12, 2008.
Article in Spanish | MEDLINE | ID: mdl-18214820

ABSTRACT

AIM: To analyze the safety profile and clinical outcome of patients with acute cerebral ischemia who received open treatment with tissue plasminogen activator (rt-PA) in a hospital without previous experience. PATIENTS AND METHODS: This prospective and observational study were realized from January 2004 to January 2007. A total of 1,704 consecutive patients with ischemic stroke were attended. 72 of them (4.2%) were treated with rt-PA within 3 hours from the symptoms onset. We analyzed age, vascular risk factors, initial and 24 hours neurological state by the National Institute of Health Stroke Scale (NIHSS), incidence of intracerebral hemorrhage and mortality and independence at 90 days. Patients were treated by neurologist and stroke monitoring was performed in the emergency area. RESULTS: Baseline median NIHSS was 16. At 24 hours, 53% of patients had improved = or > 4 points in the NIHSS and 33% showed = or > 10 points improvement or total recovery. The median time from stroke onset to rt-PA treatment was 160 minutes. Symptomatic intracerebral hemorrhage occurred in two patients (2.7%). Overall mortality at 90 days was 9.7%, but was due to hemorrhagic brain complications only in one case. At three months, 51% of patients were independent according to the modified Rankin scale. CONCLUSIONS: Treatment of acute ischemic stroke within three hours with intravenous rt-PA is safe and is associated with favorable outcome when it is applied by neurologists following approved protocols even in hospitals without previous experience.


Subject(s)
Brain Ischemia/drug therapy , Fibrinolytic Agents/therapeutic use , Stroke/drug therapy , Thrombolytic Therapy , Tissue Plasminogen Activator/therapeutic use , Aged , Brain Ischemia/complications , Female , Humans , Infusions, Intravenous , Male , Prospective Studies , Stroke/etiology
2.
Rev. neurol. (Ed. impr.) ; 46(1): 007-012, 1 ene., 2008. ilus, tab
Article in Es | IBECS | ID: ibc-65382

ABSTRACT

Analizar los resultados obtenidos en administración de trombólisis intravenosa en el ictus isquémicoagudo en el Complejo Universitario Hospitalario de Albacete, un centro sin experiencia previa adquirida en ensayos clínicos en la administración de este tratamiento. Pacientes y métodos. Estudio observacional y prospectivo, realizado entre enero de2004 y enero de 2007. En este período se atendieron 1.704 ictus isquémicos, 343 de los cuales fueron remitidos como código ictus. Se trató a 72 pacientes (4,2%) con activador del plasminógeno tisular recombinante (rt-PA). Analizamos las variablesedad, factores de riesgo vascular, tiempos de latencia intra y extrahospitalaria, evolución clínica temprana, incidencia de hemorragias cerebrales, mortalidad y situación funcional tres meses después del ictus. Resultados. La edad media fue de 69 años, y la puntuación mediana de la escala de ictus del National Institute of Health (NIHSS) inicial, de 16 puntos. A las 24 horas del inicio, el 53% de los pacientes manifestó mejoría igual o superior a 4 puntos en la NIHSS. El 33% mejoró en 10 puntos o más o presentó una recuperación completa. El tiempo medio desde el inicio de los síntomas-administración rt-PA fue de 160 minutos. Dos casos (2,7%) presentaron hemorragia cerebral sintomática. A los tres meses, el 51% presentaba independencia para sus actividades (escala de Rankin modificada igual o inferior a 2) y la mortalidad era del 9,7%. Conclusiones. El establecimiento y aplicación estandarizada de protocolos extra e intrahospitalarios de atención urgente al ictus permite ofrecer tratamiento trombolítico intravenoso en el infarto cerebral de manera segura y eficaz desde el principio, aun en centros que, como éste, carecían de experiencia previa en este tipo de tratamiento


To analyze the safety profile and clinical outcome of patients with acute cerebral ischemia who received opentreatment with tissue plasminogen activator (rt-PA) in a hospital without previous experience. Patients and methods. This prospective and observational study were realized from January 2004 to January 2007. A total of 1,704 consecutive patients with ischemic stroke were attended. 72 of them (4.2%) were treated with rt-PA within 3 hours from the symptoms onset. Weanalyzed age, vascular risk factors, initial and 24 hours neurological state by the National Institute of Health Stroke Scale (NIHSS), incidence of intracerebral hemorrhage and mortality and independence at 90 days. Patients were treated by neurologist and stroke monitoring was performed in the emergency area. Results. Baseline median NIHSS was 16. At 24 hours,53% of patients had improved = or > 4 points in the NIHSS and 33% showed = or > 10 points improvement or total recovery. The median time from stroke onset to rt-PA treatment was 160 minutes. Symptomatic intracerebral hemorrhage occurred in two patients (2.7%). Overall mortality at 90 days was 9.7%, but was due to hemorrhagic brain complications only in one case. Atthree months, 51% of patients were independent according to the modified Rankin scale. Conclusions. Treatment of acute ischemic stroke within three hours with intravenous rt-PA is safe and is associated with favorable outcome when it is applied byneurologists following approved protocols even in hospitals without previous experience


Subject(s)
Humans , Thrombolytic Therapy/methods , Stroke/drug therapy , Prospective Studies , Tissue Plasminogen Activator/pharmacokinetics , Cerebral Hemorrhage/epidemiology , Stroke/epidemiology , Risk Factors
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