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[卡马西平诱发的再生障碍性贫血:一例报告]

[Carbamazepine-induced aplastic anaemia: a case report].

作者信息

Yáñez-Rubal J C, Estévez-Rodríguez J, Crespo-López M C, Martín-Herranz I

机构信息

Servicio de Farmacia, Complejo Hospitalario Juan Canalejo, A Coruña, España.

出版信息

Rev Neurol. 2002;35(7):647-9.

Abstract

INTRODUCTION

The widespread use of carbamazepine in multiple neurological disorders makes it a drug whose most frequent side effects are well known and controlled. Aplastic anaemia is a very rare side effect, although it is the most serious since it presents a high mortality rate.

CASE REPORT

We report the case of a 51 year old male patient who suffered brain injury that required daily treatment with 600 mg of carbamazepine. In the sixth month of treatment he was found to have a decrease in the number of platelets, which was confirmed a month later. He was admitted to hospital and diagnosed as having a medullar aplasia. Despite therapy with immunosuppressants, he died 12 weeks later.

DISCUSSION

The appearance of aplastic anaemia does not seem to be related to age, the disease treated or to be dose dependent. Most cases are seen 3 4 months after treatment and the risk period is the first year. The choice treatment is a bone marrow transplant in patients under the age of 50; in older patients the recommended treatment is immunosuppressant therapy. The early diagnosis of aplastic anaemia is essential, although the difficulty lies in determining how often haematological controls are to be performed, since some cases have appeared a few days after beginning treatment. The frequency of the controls must be based on the clinical judgement of the doctor with regular check ups to detect haematological problems (infections, high temperature, ecchymosis) and to warn the patient and relatives should any of the symptoms appear.

摘要

引言

卡马西平在多种神经系统疾病中的广泛应用使其成为一种副作用广为人知且易于控制的药物。再生障碍性贫血是一种非常罕见的副作用,尽管它最为严重,因为其死亡率很高。

病例报告

我们报告一例51岁男性患者,该患者脑部受伤,需要每日服用600毫克卡马西平进行治疗。在治疗的第六个月,发现他的血小板数量减少,一个月后得到证实。他入院后被诊断为骨髓发育不全。尽管接受了免疫抑制剂治疗,但他在12周后死亡。

讨论

再生障碍性贫血的出现似乎与年龄、所治疗的疾病或剂量无关。大多数病例在治疗后3至4个月出现,风险期为第一年。对于50岁以下的患者,首选治疗方法是骨髓移植;对于老年患者,推荐的治疗方法是免疫抑制剂治疗。再生障碍性贫血的早期诊断至关重要,尽管难点在于确定血液学检查的频率,因为有些病例在开始治疗几天后就出现了。检查的频率必须基于医生的临床判断,定期进行检查以发现血液学问题(感染、高烧、瘀斑),并在出现任何症状时提醒患者及其亲属。

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