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首页> 外文期刊>Medizinische Klinik >Bioequivalence of L-thyroxine tablets and a liquid L-thyroxine solution in the treatment of hypothyroid patients
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Bioequivalence of L-thyroxine tablets and a liquid L-thyroxine solution in the treatment of hypothyroid patients

机译:L-甲状腺素片和L-甲状腺素水溶液在甲状腺功能减退患者中的生物等效性

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BACKGROUND AND PURPOSE: The therapeutic equivalence of L-thyroxine (T(4)) tablets and a new liquid T(4) solution was investigated in patients with hypothyroidism. PATIENTS AND METHODS: The study was unblinded, multicentric and prospective: 136 patients (with autoimmune thyroiditis, after thyroid surgery and/or after therapy with radioiodine), who had been treated with T(4) tablets, were switched to a treatment with a liquid T(4) solution (containing 5 microg T(4) per drop) in the same dosage. Thyrotropin (TSH) was measured after 1, 2, 3, and 6 months; the dose of the T4 solution was adapted to obtain a midnormal TSH level. RESULTS: The T(4) dose remained constant during the 6 months. Dose adaptations were necessary in 19-23% of patients at the different timepoints, with dose reductions and increases, respectively, becoming equally frequently necessary. The mean TSH level was 0.79 mU/l at the beginning and 0.81 mU/l after 6 months; similarly, the mean levels of free triiodothyronine (fT(3)) and free thyroxine (fT(4)) were equivalent.The liquid T(4) solution was well tolerated: adverse events were noted in three patients (1.8%); one serious adverse event (thyroid carcinoma) showed no correlation to the treatment. CONCLUSION: T(4) tablets and liquid T(4) solution have been proven to be therapeutically equivalent; the use of liquid T(4) solutions will have advantages in the treatment of hypothyroid infants or elderly patients with disturbed swallowing, patients who need a differentiated titration of the T(4) dose, as well as patients with an allergy against inactive ingredients of L-thyroxine tablets.
机译:背景与目的:研究了甲状腺功能减退症患者的L-甲状腺素(T(4))片剂和新型液体T(4)溶液的治疗等效性。病人和方法:这项研究是非盲的,多中心的和前瞻性的:将接受过T(4)片治疗的136例患者(患有自身免疫性甲状腺炎,在甲状腺手术后和/或接受放射碘治疗后)转为接受T(4)片治疗。相同剂量的液体T(4)溶液(每滴含5微克T(4))。在1、2、3和6个月后测量促甲状腺激素(TSH);调整T4溶液的剂量以获得中等的TSH水平。结果:T(4)剂量在6个月内保持不变。在19-23%的患者在不同时间点必须进行剂量调整,剂量减少和增加分别变得同样频繁。开始时平均TSH水平为0.79 mU / l,六个月后平均为0.81 mU / l;同样,游离三碘甲状腺素(fT(3))和游离甲状腺素(fT(4))的平均水平是相等的。液体T(4)溶液耐受性良好:三名患者(1.8%)出现不良反应;一项严重的不良事件(甲状腺癌)与治疗无相关性。结论:T(4)片剂和液体T(4)溶液已被证明在治疗上是等效的。使用液态T(4)溶液在治疗甲状腺功能低下的婴儿或吞咽不佳的老年患者,需要差异化滴定T(4)剂量的患者以及对非活性成分过敏的患者方面具有优势L-甲状腺素片。

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