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治疗甲状腺功能减退症的左甲状腺素不同制剂:一项实际应用研究。

Different Formulations of Levothyroxine for Treating Hypothyroidism: A Real-Life Study.

作者信息

Trimboli Pierpaolo, Scappaticcio Lorenzo, De Bellis Annamaria, Maiorino Maria Ida, Knappe Luisa, Esposito Katherine, Bellastella Giuseppe, Giovanella Luca

机构信息

Clinic for Nuclear Medicine and Competence Centre for Thyroid Disease, Imaging Institute of Southern Switzerland, Ente Ospedaliero Cantonale, Bellinzona, Switzerland.

Unit of Endocrinology and Metabolic Diseases, University of Campania "L. Vanvitelli", Naples, Italy.

出版信息

Int J Endocrinol. 2020 Jan 20;2020:4524759. doi: 10.1155/2020/4524759. eCollection 2020.

Abstract

OBJECTIVE

Hypothyroid patients are treated by sodium levothyroxine (LT4). Tablet is the mostly used LT4 formulation, and the fasting regimen is required for the absorption of active principle. Also, gastrointestinal diseases and drugs may impair the LT4 bioavailability when tablet is used. Nonsolid LT4 formulations (i.e., liquid solution (LS) and soft gel (SG) capsule) were manufactured to overcome the limitations of LT4 tablet. This study was conceived to evaluate the performance of nonsolid LT4 formulations in a real-life scenario.

METHODS

Two institutions participated in the study that was conducted in two phases (i.e., enrollment and re-evaluation). Adults with autoimmune or postsurgical hypothyroidism and on LT4 from a few months were selected. A nonparametric statistical analysis for paired or unpaired data was performed.

RESULTS

121 consecutive cases were included. At the enrollment phase, a 52% of patients took the therapy at least 30 min before breakfast with no difference between tablet and SG/LS users. TSH was 1.65 mIU/L (0.86-2.70) in patients on LT4 tablet and 1.70 mIU/L (1.10-2.17) in those on SG/LS (=0.66). At the re-evaluation phase, among the patients using correct LT4 assumption, the TSH value was stable in the tablet group (=0.66). At the re-evaluation phase, among the patients using correct LT4 assumption, the TSH value was stable in the tablet group (=0.66). At the re-evaluation phase, among the patients using correct LT4 assumption, the TSH value was stable in the tablet group (=0.66). At the re-evaluation phase, among the patients using correct LT4 assumption, the TSH value was stable in the tablet group (=0.66). At the re-evaluation phase, among the patients using correct LT4 assumption, the TSH value was stable in the tablet group (.

CONCLUSION

The performance of nonsolid LT4 formulations is not influenced by correct or incorrect use of therapy. On the contrary, LT4 tablet does not guarantee euthyroidism when it is ingested without waiting for at least 30 minutes before breakfast. These new data, obtained in a real-life scenario, suggest that LT4 SG/LS should be regarded as first-line therapy for treating adults with newly diagnosed hypothyroidism.

摘要

目的

甲状腺功能减退患者采用左甲状腺素钠(LT4)治疗。片剂是最常用的LT4制剂,且为使活性成分吸收需采用空腹服药方案。此外,使用片剂时,胃肠道疾病和药物可能会损害LT4的生物利用度。为克服LT4片剂的局限性,研发了非固体LT4制剂(即液体溶液(LS)和软胶囊(SG))。本研究旨在评估非固体LT4制剂在实际应用中的效果。

方法

两家机构参与了该分两阶段(即入组和重新评估)进行的研究。选取患有自身免疫性或手术后甲状腺功能减退且已服用LT4数月的成年人。对配对或非配对数据进行非参数统计分析。

结果

共纳入121例连续病例。在入组阶段,52%的患者在早餐前至少30分钟服药,片剂使用者与SG/LS使用者之间无差异。服用LT4片剂的患者促甲状腺激素(TSH)为1.65 mIU/L(0.86 - 2.70),服用SG/LS的患者为1.70 mIU/L(1.10 - 2.17)(P = 0.66)。在重新评估阶段,在正确服用LT4的患者中,片剂组的TSH值稳定(P = 0.66)。在重新评估阶段,在正确服用LT4的患者中,片剂组的TSH值稳定(P = 0.66)。在重新评估阶段,在正确服用LT4的患者中,片剂组的TSH值稳定(P = 0.66)。在重新评估阶段,在正确服用LT4的患者中,片剂组的TSH值稳定(P = 0.66)。在重新评估阶段,在正确服用LT4的患者中,片剂组的TSH值稳定(P = 0.66)。

结论

非固体LT4制剂的效果不受治疗使用正确与否的影响。相反,LT4片剂在早餐前未等待至少30分钟就服用时不能保证甲状腺功能正常。在实际应用中获得的这些新数据表明,LT4 SG/LS应被视为治疗新诊断甲状腺功能减退成人患者的一线治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d3e/7059087/4e62a4f6c44d/IJE2020-4524759.001.jpg

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