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头孢曲松致一名患血红蛋白SC病青少年发生溶血性贫血和肝炎。

Ceftriaxone-induced hemolytic anemia and hepatitis in an adolescent with hemoglobin SC disease.

作者信息

Bell Michael J, Stockwell David C, Luban Naomi L C, Shirey R Sue, Shaak Lorraine, Ness Paul M, Wong Edward C C

机构信息

Division of Critical Care Medicine, Children's National Medical Center and The George Washington University School of Medicine, Washington, DC, USA.

出版信息

Pediatr Crit Care Med. 2005 May;6(3):363-6. doi: 10.1097/01.PCC.0000161285.12396.FF.

Abstract

OBJECTIVES

To describe a case of a ceftriaxone-induced hemolytic anemia and hepatitis leading to multiple organ failure and death in an adolescent with hemoglobin SC disease and to review the previous cases of this rare and potentially fatal disorder in children.

DESIGN

Case report and literature review.

SETTING

Intensive care unit.

PATIENT

Adolescent with hemoglobin SC.

INTERVENTIONS

Emergency treatment.

MEASUREMENTS AND MAIN RESULTS

After 4 days of ceftriaxone therapy, the adolescent experienced an acute hemolytic reaction (hemoglobin decreased to 5 g/dL with hemoglobinuria) and severe hepatitis (all enzymes increasing dramatically including aminoaspartate transferase >20,000 IU/L). Renal failure and ultimately multiple organ failure ensued, and the patient died on hospital day 19. Direct antiglobulin tests on red cells obtained from the patient on hospital day 2 showed microscopic agglutination with polyspecific and anticomplement (C3) antiglobulin reagents. Plasma samples showed macroscopic agglutination reactions when incubated in the presence of ceftriaxone, many days after cessation of ceftriaxone, indicating the continued presence of ceftriaxone-dependent antibodies.

CONCLUSIONS

Drug reactions leading to hemolysis are relatively uncommon, and a total of ten cases of ceftriaxone-induced hemolytic anemia have been reported in children. The present case describes an adolescent who ultimately died on hospital day 19 from multiple organ failure, although the presentation of this case seems atypical in several respects. Children with clinical syndromes that place them at risk for hemolysis and children who frequently require broad spectrum antibiotics present unique diagnostic challenges, and the possibility that hemolytic syndromes may be due to ceftriaxone must be considered.

摘要

目的

描述1例头孢曲松引起的溶血性贫血和肝炎导致1名患有血红蛋白SC病的青少年多器官功能衰竭和死亡的病例,并回顾以往儿童中这种罕见且可能致命疾病的病例。

设计

病例报告及文献综述。

地点

重症监护病房。

患者

患有血红蛋白SC病的青少年。

干预措施

紧急治疗。

测量指标及主要结果

头孢曲松治疗4天后,该青少年出现急性溶血反应(血红蛋白降至5g/dL,出现血红蛋白尿)和严重肝炎(所有酶显著升高,包括天冬氨酸转氨酶>20,000IU/L)。继而出现肾衰竭并最终发展为多器官功能衰竭,患者于住院第19天死亡。住院第2天采集的患者红细胞直接抗球蛋白试验显示,与多特异性和抗补体(C3)抗球蛋白试剂发生显微镜下凝集。血浆样本在头孢曲松停用多日后,在有头孢曲松存在的情况下孵育时出现肉眼可见的凝集反应,表明存在持续的头孢曲松依赖性抗体。

结论

导致溶血的药物反应相对少见,儿童中总共报告了10例头孢曲松引起的溶血性贫血病例。本病例描述了1名青少年最终于住院第19天死于多器官功能衰竭,尽管该病例在几个方面的表现似乎不典型。患有临床综合征使其有溶血风险的儿童以及经常需要使用广谱抗生素的儿童面临独特的诊断挑战,必须考虑溶血性综合征可能由头孢曲松引起的可能性。

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