Chattaway Jeanne M, Klepser Teresa B
Department of Clinical Pharmacy, College of Pharmacy, Ferris State University, Big Rapids, MI, USA.
Ann Pharmacother. 2007 Jun;41(6):1018-22. doi: 10.1345/aph.1H535. Epub 2007 May 15.
To evaluate the evidence supporting the use of propylthiouracil (PTU) versus methimazole for the treatment of Graves' disease during pregnancy.
An English-language literature search was conducted using MEDLINE (1966-March 2007). Identified articles were then reviewed for additional sources. Search terms included hyperthyroidism, Graves' disease, pregnancy, propylthiouracil, and methimazole.
All clinical trials and case reports that were published in English and reported either subjective or objective outcomes were reviewed.
Rationale supporting the use of PTU over methimazole in treatment of Graves' disease during pregnancy is limited. Theories suggesting that PTU has less placental transfer to the fetus than methimazole are not supported by current literature. Studies demonstrating a causal relationship between methimazole use during pregnancy and congenital anomalies and/or fetal hypothyroidism do not exist.
The selection of PTU versus methimazole for the treatment of Graves' disease during pregnancy should not be based solely on the following assumptions: that PTU crosses the placenta less than methimazole, that PTU leads to less fetal hypothyroidism, or that exposure to methimazole during pregnancy leads to decreased intellectual function in children. However, due to a possible association between the use of methimazole during pregnancy and fetal anomalies such as aplasia cutis, esophageal atresia, and choanal atresia, methimazole may be a less desirable first-line treatment for Graves' disease in pregnancy than PTU. Therefore, in the absence of a compelling indication for the use of methimazole, PTU should still be considered as the first-line agent in the treatment of Graves' disease during pregnancy. Methimazole should be considered a viable second choice if the patient is intolerant to PTU, has an allergic reaction to PTU, or fails to become euthyroid while receiving PTU.
评估支持在妊娠期使用丙硫氧嘧啶(PTU)与甲巯咪唑治疗格雷夫斯病的证据。
使用MEDLINE(1966年 - 2007年3月)进行了英文文献检索。然后对所识别的文章进行审查以获取其他来源。检索词包括甲状腺功能亢进、格雷夫斯病、妊娠、丙硫氧嘧啶和甲巯咪唑。
审查了所有以英文发表并报告主观或客观结果的临床试验和病例报告。
支持在妊娠期使用PTU而非甲巯咪唑治疗格雷夫斯病的理论依据有限。目前的文献并不支持PTU比甲巯咪唑更少通过胎盘转运至胎儿的理论。不存在表明妊娠期使用甲巯咪唑与先天性异常和/或胎儿甲状腺功能减退之间存在因果关系的研究。
在妊娠期治疗格雷夫斯病时,选择PTU还是甲巯咪唑不应仅基于以下假设:PTU比甲巯咪唑更少穿过胎盘、PTU导致胎儿甲状腺功能减退的情况更少,或妊娠期接触甲巯咪唑会导致儿童智力功能下降。然而,由于妊娠期使用甲巯咪唑与胎儿异常如皮肤发育不全、食管闭锁和后鼻孔闭锁之间可能存在关联,与PTU相比,甲巯咪唑可能不太适合作为妊娠期格雷夫斯病的一线治疗药物。因此,在没有使用甲巯咪唑的迫切指征时,PTU仍应被视为妊娠期格雷夫斯病治疗的一线药物。如果患者对PTU不耐受、对PTU过敏或在接受PTU治疗时未能实现甲状腺功能正常,则应将甲巯咪唑视为可行的第二选择。