Diagnosis And Management Of Antithyroid Drug Induced Agranulocytosis

Maulina Debbyousha, Hendra Zufry
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Abstract

Agranulocytosis as adversed effect of antithyroid drug (ATD) in patients with Graves disease is a rare complication but it can be serious and life threatening. The mortality rate 2-10% caused by severe infection as complications. Immediate diagnosis and management are essential for proper treatment and good prognosis. A 35-year-old female with Graves disease was complaining of fever and sore throat. She was initially treated with Thiamizole 1x20 mg for 2 weeks. Physical examination revealed leukoplakia and diffuse struma. Laboratory test : FT4 43 pmol/L, TSHs :0,005 uIu/mL, ANC <100/ul. Patient is diagnosed with ATD induced agranulocytosis. Treatment includes meropenem, fluconazole and GCSFs. The clinical and laboratory parameter improved after two weeks of treatment. Agranulocytosis in Graves’ disease patient which had ATD is a rare occurrence, with an incidence 0,2- 0,5% (66,7% had severe infection). The diagnostic criteria for agranulocytosis caused by ATD are hyperthyroid patients who are confirmed with an increase T4 and/or T3, decrease in TSH, ANC of 1500/ul before receiving ATD, ANC < 500/ul after initiation ATD and other causes of agranulocytosis have been excluded. In fact, most patients had ANC <100/ul. There are no symptom difference with agranulocytosis caused by other cause. High fever and sore throat are the most common symptom. Initial management are to identify, immediately stop the drug use, broad spectrum antibiotics and GCSFs. The hyperthyroidism will continue and alternative therapies should still be given. The best prevention is to educate patient and to examine granulocyte count frequently.
抗甲状腺药物致粒细胞缺乏症的诊断与治疗
抗甲状腺药物(ATD)引起的粒细胞缺乏症在Graves病患者中是一种罕见的并发症,但其严重程度可危及生命。严重感染引起的并发症死亡率为2-10%。及时诊断和处理是正确治疗和良好预后的必要条件。一名35岁女性,患有格雷夫斯病,主诉发烧和喉咙痛。患者最初使用噻咪唑1x20 mg治疗2周。体格检查发现白斑和弥漫性瘤。实验室检测:FT4 43 pmol/L, TSHs: 0.005 uIu/mL, ANC <100/ul。患者被诊断为ATD所致粒细胞缺乏症。治疗包括美罗培南、氟康唑和gcsf。治疗两周后临床及实验室指标均有改善。伴有ATD的Graves病患者出现粒细胞缺乏症较为少见,发生率为0.2% ~ 0.5%,其中66.7%为重度感染。ATD所致粒细胞缺乏症的诊断标准为甲状腺功能亢进患者,确诊为T4和/或T3升高,TSH降低,ATD前ANC为1500/ul, ATD开始后ANC < 500/ul,排除其他原因的粒细胞缺乏症。事实上,大多数患者的ANC <100/ul。与其他原因引起的粒细胞缺乏症无症状差异。高烧和喉咙痛是最常见的症状。最初的管理是确定并立即停止药物使用,广谱抗生素和gcsf。甲状腺功能亢进将继续,替代疗法仍应给予。最好的预防措施是教育患者并经常检查粒细胞计数。
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