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[Idiosyncratic drug-induced agranulocytosis]. / Agranulocytoses médicamenteuses idiosyncrasiques.
Andrès, E; Maloisel, F.
Afiliación
  • Andrès E; Service de Médecine Interne, Clinique Médicale B, Hôpitaux Universitaires de Strasbourg, France. emmanuel.andres@chru-strasbourg.fr
Rev Med Interne ; 27(3): 209-14, 2006 Mar.
Article en Fr | MEDLINE | ID: mdl-16043267
BACKGROUND: Agranulocytosis is a life-threatening disorder that frequently occurs as an adverse reaction to drugs. CURRENT DATA: Idiosyncratic drug-induced agranulocytosis is characterized by a neutrophil count <0.5x10(9)/l, in serious forms <0,1x10(9)/l that currently occurs especially in association with antibiotics, antithyroid drugs ant ticlopidine (>60% of the incriminated drugs). The overall incidence of idiosyncratic agranulocytosis ranges from 2.4 to 15.4 cases per million patients exposed to drugs per year. Although patients experiencing idiosyncratic agranulocytosis may be asymptomatic (50%), the severity of the neutropenia usually leads to severe sepsis: fever of unknown origin, septicemia, septic shock or localized documented infections such as sore throat, various cutaneous infections or pneumonia. Nevertheless, the mortality rate of idiosyncratic agranulocytosis is now around 5% with appropriate management. PERSPECTIVES: In the future, management of drug-induced agranulocytosis may include pre-established procedures using in critically situations, broad-spectrum antibiotic therapy and hematopoietic growth factors (G-CSF).
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Agranulocitosis Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Humans Idioma: Fr Revista: Rev Med Interne Año: 2006 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Francia
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Agranulocitosis Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Humans Idioma: Fr Revista: Rev Med Interne Año: 2006 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Francia