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Ceftizoxime-induced immune hemolytic anemia associated with multi-organ failure / 영남의대학술지
Article en Ko | WPRIM | ID: wpr-84525
Biblioteca responsable: WPRO
ABSTRACT
Drug-induced immune hemolytic anemia (DIIHA) is a rare side effect of drugs. DIIHA may cause a systemic inflammatory response that results in acute multi-organ failure and death. Ceftizoxime belongs to the class of third generation cephalosporins, which are the most common drugs associated with DIIHA. Herein, we present a case of a 66-year-old man who developed fatal DIIHA after receiving a second dose of ceftizoxime. He was admitted to receive photodynamic therapy. He had a history of a single parenteral dose of ceftizoxime 3 months prior to admission. On the day of the procedure — shortly after the infusion of ceftizoxime — the patient's mental status was altered. The blood test results revealed hemolysis. Oliguric acute kidney injury developed, and continuous renal replacement therapy had to be applied. On the suspicion of DIIHA, the patient underwent plasmapheresis. Diagnosis was confirmed by a detection of drug-dependent antibody with immune complex formation. Although his hemolysis improved, his liver failure did not improve. He was eventually discharged to palliative care, and subsequently died.
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Texto completo: 1 Índice: WPRIM Asunto principal: Cuidados Paliativos / Fotoquimioterapia / Ceftizoxima / Cefalosporinas / Plasmaféresis / Fallo Hepático / Terapia de Reemplazo Renal / Diagnóstico / Lesión Renal Aguda / Pruebas Hematológicas Tipo de estudio: Diagnostic_studies Límite: Aged / Humans Idioma: Ko Revista: Yeungnam University Journal of Medicine Año: 2017 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Cuidados Paliativos / Fotoquimioterapia / Ceftizoxima / Cefalosporinas / Plasmaféresis / Fallo Hepático / Terapia de Reemplazo Renal / Diagnóstico / Lesión Renal Aguda / Pruebas Hematológicas Tipo de estudio: Diagnostic_studies Límite: Aged / Humans Idioma: Ko Revista: Yeungnam University Journal of Medicine Año: 2017 Tipo del documento: Article