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首页> 外文期刊>Endocrine practice: official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists >Comparison of TSH levels with liquid formulation versus tablet formulations of levothyroxine in the treatment of adult hypothyroidism
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Comparison of TSH levels with liquid formulation versus tablet formulations of levothyroxine in the treatment of adult hypothyroidism

机译:比较左甲状腺素液体制剂和片剂制剂中TSH水平治疗成人甲状腺功能减退症

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Objective: A great number of factors can interfere with levothyroxine (LT4) tablet absorption, leading to increased serum thyroid-stimulating hormone (TSH) levels and, accordingly, to increased LT4 requirements. LT4 oral solution (LT4-OS) is a novel formulation with a pharmacokinetics profile different from those of tablets. The aim of this study was to retrospectively evaluate whether serum TSH levels were decreased after switching adult hypothyroid patients from the tablet to LT-OS.Methods: We retrospectively evaluated 53 outpatients on LT4 replacement therapy (consumed within 1 hour before breakfast) who switched from LT4 tablets to LT4-OS without changing the daily dose. We compared preswitch TSH (TSH1) with TSH level 60 to 90 days after the switch (TSH2) and examined the clinical differences between the patients whose TSH did and did not drop after the switch.Results: After the switch, TSH levels decreased from a median value of 3.04 (interquartile range [IQR] 1.75-6.80) to 2.30 (IQR 1.21-3.81) μIU/mL, and the difference was significant (P = .0034). We observed a TSH reduction (TSH2/TSH1 ratio <1) in 36/53 (67.9%) of patients; the median TSH2/TSH1 ratio was 0.71 (IQR 0.37-1.14). In the group of patients whose TSH dropped, we observed an increased frequency of factors interfering with LT4 absorption (P = .014). The median TSH2/TSH1 ratios were 0.50 (IQR 0.31-0.72) and 0.85 (IQR 0.65-1.36) for patients with and without interfering factors, respectively.Conclusion: Our study confirms that LT4-OS could have an increased absorption rate in comparison to LT4 tablets, especially in the presence of other factors interfering with LT4 absorption.
机译:目的:多种因素可能会干扰左甲状腺素(LT4)片剂的吸收,导致血清促甲状腺激素(TSH)水平升高,从而导致对LT4的需求增加。 LT4口服溶液(LT4-OS)是一种新型制剂,其药代动力学特性与片剂不同。这项研究的目的是回顾性评估成年甲状腺功能减退患者从片剂改为LT-OS后血清TSH水平是否降低。方法:我们回顾性评估了53名接受LT4替代疗法(早餐前1小时内服用)的门诊患者。将LT4片剂改为LT4-OS,无需更改每日剂量。我们将转换前TSH(TSH1)与转换后(TSH2)60天至90天的TSH水平进行了比较,并检查了转换后TSH下降且未下降的患者之间的临床差异。结果:转换后,TSH水平从中位数为3.04(四分位间距[IQR] 1.75-6.80)至2.30(IQR 1.21-3.81)μIU/ mL,差异显着(P = .0034)。我们观察到36/53(67.9%)的患者的TSH降低(TSH2 / TSH1比<1); TSH2 / TSH1中位数比为0.71(IQR 0.37-1.14)。在TSH下降的患者组中,我们观察到干扰LT4吸收的因素的频率增加(P = .014)。结论:有干扰因素和无干扰因素的患者中位数TSH2 / TSH1比分别为0.50(IQR 0.31-0.72)和0.85(IQR 0.65-1.36)。结论:我们的研究证实LT4-OS的吸收率较LT4片剂,尤其是在存在其他干扰LT​​4吸收的因素的情况下。

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