Chen Jie, Song Xianmin, Yang Peng, Wang Jianmin
Department of Hematology, Changhai Hospital, The Second Military Medical University, Shanghai, China.
Ann Pharmacother. 2009 Mar;43(3):537-41. doi: 10.1345/aph.1L343. Epub 2009 Mar 3.
To report a rare but severe adverse effect of intravenous itraconazole, anaphylactic shock with hypotension and hypoxemia, in a female patient with acute lymphoblastic leukemia (ALL).
A 36-year-old woman with ALL received antifungal therapy for pulmonary fungal infections. On day 17 of itraconazole treatment, she developed hypotension and hypoxemia shock after intravenous administration of itraconazole 200 mg, which was eventually reversed by steroid treatment. On days 18 and 19, the patient developed the same type of shock 2 more times in the course of itraconazole administration. These 2 episodes of shock occurred more quickly after intravenous itraconazole administration (100 mg on day 18, 40 mg on day 19), and were reversed by stopping itraconazole and applying steroid treatment. In the modified antifungal therapy, intravenous administration of itraconazole was replaced by oral administration of voriconazole 200 mg twice daily. Shock did not recur after discontinuation of itraconazole treatment. The Naranjo probability scale showed a probable relationship between itraconazole treatment and shock occurrence.
Itraconazole is a widely used antifungal drugs and is well tolerated. However, long-term itraconazole treatment might lead to serious and even life-threatening adverse effects such as anaphylactic shock, as seen in our patient. T cell reduction caused by immunosuppression and itraconazole accumulation in patients with ALL are considered to be important causal factors for this delayed-type hypersensitivity reaction.
Anaphylactic shock represents a previously undocumented severe adverse effect associated with long-term itraconazole treatment; patients receiving this therapy and should be monitored closely.
报告1例急性淋巴细胞白血病(ALL)女性患者静脉应用伊曲康唑后出现的罕见但严重的不良反应,即伴有低血压和低氧血症的过敏性休克。
1例36岁的ALL女性患者因肺部真菌感染接受抗真菌治疗。在伊曲康唑治疗的第17天,静脉注射200mg伊曲康唑后,她出现了低血压和低氧血症休克,最终通过类固醇治疗得以逆转。在第18天和第19天,患者在伊曲康唑给药过程中又出现了2次相同类型的休克。这2次休克在静脉注射伊曲康唑后发作更快(第18天100mg,第19天40mg),通过停用伊曲康唑并应用类固醇治疗得以逆转。在改良的抗真菌治疗中,静脉注射伊曲康唑被改为口服伏立康唑,每日2次,每次200mg。停用伊曲康唑治疗后休克未再复发。Naranjo概率量表显示伊曲康唑治疗与休克发生之间可能存在关联。
伊曲康唑是一种广泛使用的抗真菌药物,耐受性良好。然而,长期应用伊曲康唑治疗可能会导致严重甚至危及生命的不良反应,如过敏性休克,正如我们的患者所见。ALL患者免疫抑制导致的T细胞减少以及伊曲康唑蓄积被认为是这种迟发型超敏反应的重要因果因素。
过敏性休克是长期伊曲康唑治疗相关的一种此前未记录的严重不良反应;接受该治疗的患者应密切监测。