首页> 外文期刊>Journal of Internal Medicine >Comparison of standardized initial doses of two antithyroid drugs in the treatment of Graves' disease.
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Comparison of standardized initial doses of two antithyroid drugs in the treatment of Graves' disease.

机译:两种抗甲状腺药物标准化初始剂量在Graves病治疗中的比较。

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OBJECTIVES. To obtain a simple standard regimen, suitable for general practice, and based upon the addition of antithyroid drug plus thyroxine for attaining euthyroidism in patients with Graves' disease. DESIGN. Prospective, randomized trial of patients with Graves' disease followed for 3 months after the initiation of therapy with an antithyroid drug and combined with the later addition of triiodothyronine to keep the patient euthyroid. The patients were randomized, according to birth date, between methimazole and propylthiouracil. Three dose schemes were tested for each antithyroid drug. SETTING. The study was performed at the thyroid outpatient units of two general hospitals, with the patients having been referred from primary care. SUBJECTS. Ninety-four patients with Graves' disease who were suitable for treatment with antithyroid drugs. INTERVENTIONS. The patients were allocated into six groups. Three groups received methimazole (10 mg every 6th, 8th or 12th h) and three received propylthiouracil (100 mg every 6th, 8th or 12th h). Twenty micrograms of triiodothyronine was added when the patients were euthyroid to avoid hypothyroidism. MAIN OUTCOME MEASURES. The lowest serum free thyroxine level within 3 months of the initiation of the antithyroid treatment. RESULTS. Fourteen per cent of the patients on methimazole 10 mg every 12th h and 29% on propylthiouracil 100 mg every 12th h did not achieve euthyroidism within the 3-month observation period. All but one patient on methimazole 10 mg every 8th h or propylthiouracil 100 mg every 8th h reduced the free serum thyroxine levels to the normal or hypothyroid range within the observation period. All of the patients on methimazole 10 mg every 6th h and 56% on propylthiouracil 100 mg every 6th h reduced the serum T4 values into the hypothyroid range within the period. CONCLUSION. A standard regimen, based upon the addition of methimazole 10 mg every 8th or 6th h or propylthiouracil 100 mg every 8th or 6th h and followed by the addition of thyroxine or triiodothyronine when euthyroid to avoid hypothyroidism, seems to be suitable for attaining euthyroidism within 3 months in patients with Graves' disease. A dose scheme based on methimazole 10 mg every 12th h or propylthiouracil 100 mg every 12th h were found to be unsuitable due to an unacceptably high incidence of failure to attain euthyroidism or hypothyroidism within 3 months.
机译:目标为了获得适用于一般实践的简单标准方案,并以添加抗甲状腺药和甲状腺素为基础,以使格雷夫斯病患者获得甲状腺功能正常。设计。对Graves病患者进行的一项前瞻性随机试验在开始使用抗甲状腺药物治疗后进行了3个月,并与后来加入的三碘甲甲状腺素相结合以保持患者的甲状腺功能正常。根据出生日期,患者被随机分组​​分配在他巴唑和丙硫氧嘧啶之间。对于每种抗甲状腺药物,测试了三种剂量方案。设置。该研究是在两家综合医院的甲状腺门诊部进行的,患者已从初级保健中转诊。主题。 94名适合使用抗甲状腺药物治疗的Graves病患者。干预措施。将患者分为六组。三组接受甲巯咪唑(每6、8、12h服用10 mg),三组接受丙硫氧嘧啶(每6、8、12h服用100 mg)。甲状腺功能正常的患者加二十微克三碘甲状腺素以避免甲状腺功能减退。主要观察指标。抗甲状腺治疗开始后3个月内的最低血清甲状腺素水平最低。结果。每12h服用甲巯咪唑10 mg的患者中有14%,每12h服用丙硫氧嘧啶100 mg的患者中有29%在三个月的观察期内未达到甲状腺功能正常。除一名患者外,所有患者均每8小时服用一次10 mg甲巯咪唑或每8小时服用100 mg丙基硫氧嘧啶,在观察期内将血清游离甲状腺素水平降低至正常或甲状腺功能减退范围。所有患者每6h服用甲巯咪唑10 mg,每6h服用异丙硫氧嘧啶100 mg的患者中有56%在此期间将血清T4值降低到甲状腺功能减退的范围内。结论。一种标准的治疗方案似乎适合于在3分以内达到甲状腺功能亢进的标准方案,该方案是每8或6小时添加甲巯咪唑10 mg或每8或6小时添加100 mg丙基硫尿嘧啶,然后在甲状腺功能正常的情况下添加甲状腺素或三碘甲甲状腺素以避免甲状腺功能减退。格雷夫斯氏病患者需要几个月的时间。由于在3个月内未能达到甲状腺功能亢进或甲状腺功能减退的发生率过高,令人难以接受,因此,以每12小时10毫克甲硫咪唑或每12小时100毫克丙硫氧嘧啶为基础的剂量方案不合适。

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