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评估短期卢戈氏液对毒性结节性甲状腺疾病的影响:一项干预前后研究。

Assessing the impact of short-term Lugol's solution on toxic nodular thyroid disease: a pre-post-intervention study.

机构信息

Department of Endocrinology, Karolinska University Hospital, Stockholm, Sweden.

Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

出版信息

Front Endocrinol (Lausanne). 2024 Jul 25;15:1420154. doi: 10.3389/fendo.2024.1420154. eCollection 2024.

Abstract

PURPOSE

Preoperative iodine therapy in toxic nodular goiter (TNG) is discouraged as iodine may cause aggravation of hyperthyroidism. We aimed to examine if a short course of iodine treatment is safe to administer in TNG.

METHODS

Patients with TNG (n=20) and subclinical to mild hyperthyroidism (free (f)T4 <30 pmol/L) without complicating illnesses were included in this pre-post-intervention study at Karolinska University Hospital. All participants received Lugol's solution 5%, three oral drops thrice daily for 10 days. Heart rate, TSH, fT4, fT3 concentrations were collected before (day 0) and after treatment (day 10). Thyroid hormone concentrations were also measured at two time points during treatment to discover aggravations of hyperthyroidism. ThyPRO39se, a quality-of-life questionnaire, was filled out day 0 and day 10. Differences in heart rate, thyroid hormone concentrations, and quality-of-life before and after treatment were compared. Adverse reactions were reported.

RESULTS

The median age was 63.5 years. Female to male ratio 19:1. FT4 and fT3 concentrations decreased (both <0.001), and TSH concentration increased (<0.001) after 10 days of treatment. There was no difference in heart rate. No aggravations of thyrotoxicosis were noticed in any of the participants. ThyPRO39se scores improved on three scales, including hyperthyroid symptoms, while the remaining scale scores were unchanged. Mild and transient symptoms related to or possibly related to treatment were observed in six participants.

CONCLUSION

A short course of Lugol's solution improved thyroid hormone concentrations, reduced patient-reported hyperthyroid symptoms and was safe in TNG. Lugol's solution might be an option for preoperative treatment in TNG.

CLINICAL TRIAL REGISTRATION

https://www.clinicaltrials.gov, identifier NCT04856488.

摘要

目的

在毒性结节性甲状腺肿(TNG)中不提倡术前碘治疗,因为碘可能导致甲状腺功能亢进加重。我们旨在研究在 TNG 中给予短期碘治疗是否安全。

方法

这项在卡罗林斯卡大学医院进行的干预前后研究纳入了 20 例 TNG 患者和亚临床至轻度甲状腺功能亢进(游离(f)T4<30 pmol/L)且无合并症的患者。所有参与者均接受卢戈氏液 5%,口服 3 滴,每日 3 次,共 10 天。在治疗前(第 0 天)和治疗后(第 10 天)收集心率、TSH、fT4、fT3 浓度。在治疗期间的两个时间点还测量了甲状腺激素浓度,以发现甲状腺功能亢进的加重。在第 0 天和第 10 天填写 ThyPRO39se,这是一种生活质量问卷。比较治疗前后心率、甲状腺激素浓度和生活质量的差异。报告不良反应。

结果

中位年龄为 63.5 岁。女性与男性的比例为 19:1。FT4 和 fT3 浓度降低(均<0.001),治疗 10 天后 TSH 浓度升高(均<0.001)。心率没有差异。在任何参与者中均未发现甲状腺毒症加重。在三个包括甲状腺功能亢进症状的量表上,ThyPRO39se 评分有所改善,而其余量表的评分则保持不变。在 6 名参与者中观察到与治疗相关或可能与治疗相关的轻度和短暂症状。

结论

短期卢戈氏液治疗可改善甲状腺激素浓度,减轻患者报告的甲状腺功能亢进症状,且在 TNG 中安全。卢戈氏液可能是 TNG 术前治疗的一种选择。

临床试验注册

https://www.clinicaltrials.gov,标识符 NCT04856488。

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