Hepatotoxicity and cutaneous reactions after antithyroid drug administration

被引:62
作者
Otsuka, Fumiko [1 ,2 ]
Noh, Jaeduk Y. [1 ]
Chino, Toshiko [1 ]
Shimizu, Taeko [1 ]
Mukasa, Koji [1 ]
Ito, Kunihiko [1 ]
Ito, Koichi [1 ]
Taniyama, Matsuo [2 ]
机构
[1] Ito Hosp, Tokyo, Japan
[2] Showa Univ, Fujigaoka Hosp, Div Endocrinol & Metab, Dept Internal Med, Yokohama, Kanagawa 2278501, Japan
关键词
HEPATIC-INJURY; PROPYLTHIOURACIL; HYPERTHYROIDISM; CARBIMAZOLE;
D O I
10.1111/j.1365-2265.2012.04365.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective Use of the antithyroid drugs (ATDs) thiamazole (MMI) and propylthiouracil (PTU) is associated with a high frequency of side effects. When patients experience side effects with one (the 1st) ATD, it is usually discontinued and another is administered (the 2nd ATD). We investigated side effects associated with the 1st and 2nd ATDs. Design and Patients Four hundred forty-nine patients with untreated Graves' disease (GD) were randomly assigned to three groups according to ATD type and/or dosage: 15 similar to mg/day MMI, 30 similar to mg/day MMI and 300 similar to mg/day PTU. The type, frequency and onset of side effects were assessed. We also studied the side effects associated with the 2nd ATD after cessation of the 1st ATD. Measurements Cutaneous reactions, liver dysfunction and other side effects were examined every 2 similar to weeks after starting ATD administration. Results The overall frequency of side effects in patients taking 15 similar to mg/day MMI was low. The frequencies of cutaneous reactions in patients taking 30 similar to mg/day MMI and hepatotoxicity in those taking 300 similar to mg/day PTU were high. Hepatotoxicity developed later than cutaneous reactions with PTU. Hepatotoxicity developed earlier in the 30 similar to mg/day MMI group than in the other two groups. The frequency of side effects did not differ between the 2nd and 1st ATDs. Hepatotoxicity occurred at a higher frequency in patients who were switched from MMI to PTU because of hepatotoxicity of the former. Conclusion Attention to the onset times of side effects and cross-reactivity of ATDs can lead to safer treatment of GD.
引用
收藏
页码:310 / 315
页数:6
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