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EMPATHY: A New Tool for Identifying the Most Suitable Thyroxine Formulation in Hypothyroid Patients

机译:同理心:一种用于鉴定甲状腺功能亢进患者中最合适的甲状腺素配方的新工具

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Background: Therapy of hypothyroidism is based on the administration of appropriate doses of levothyroxine (LT4). A failure to achieve the thyrotropin (TSH) target may be due to poor compliance with the LT4 therapy in about 60% of cases or to malabsorption in about 40% of cases. No tools are available for detecting malab-sorption disorders before the choice of the most appropriate therapy. The aim of this study was to validate the Evaluation of Malabsorption in PATients with HYpothyroidism (EMPATHY) questionnaire and to demonstrate its usefulness in indicating the most appropriate therapy. Methods: EMPATHY consists of seven questions that allow the evaluation of several intolerances and allergies. Three hundred (100 males) newly diagnosed hypothyroid patients were enrolled and randomly assigned to complete an EMPATHY questionnaire (150 patients; group 1) or to a control group (150 patients; group 2). The choice of thyroxine formulation and dose for each group was made on the basis of the questionnaire answers or based on the history. Thyroid hormones and TSH were evaluated at enrollment and then every two months for six months; the number of the dose adjustments in the six months for each patient was recorded. Results: Of the 150 patients in each group, 21 (14%) in group 1 and 42 (28%) in group 2 (p = 0.005) needed more than two dose adjustments within six months. After six months of replacement therapy, six (4%) patients in group 1 and 17 (11%) in group 2 (p = 0.03) did not have appropriately controlled hypothyroidism (TSH ≥ 2.5 mIU/L). A significantly higher LT4 final dose was found in group 2 (148 ±33μg/day) than in group 1 (136 ± 28 μg/day; p = 0.003). Conclusions: Validation of EMPATHY provides endocrinologists with a useful tool in clinical practice, permitting a better personalization of LT4 replacement therapy, a more rapid attainment of the target TSH levels, and a decreased need for dose adjustments after initiating therapy.
机译:背景:甲状腺功能减退症的治疗基于给予适当剂量的左甲苯胺(LT4)。未达到甲状腺激素(TSH)靶标可能是由于约60%的病例或在约40%的病例中遵守LT4治疗的易符合性差。在选择最合适的疗法之前,没有任何工具可用于检测染色体吸附障碍。本研究的目的是验证甲状腺功能减退症(移情)问卷患者的吸收性评估,并证明其在表明最合适的治疗方面的有用性。方法:同理心由七个问题组成,允许评估几种不容忍和过敏症。三百(100名男性)新诊断的甲状腺功能亢进患者被纳入并随机分配,以完成同理心调查问卷(150名患者;第1组)或对照组(150名患者;第2组)。根据调查问卷答案或基于历史,制定每组甲状腺素配方和剂量的选择。甲状腺激素和TSH在注册时评估,然后每两个月评估六个月;记录每位患者的六个月内剂量调整的数量。结果:每组150名患者,21例(14%)的21%(14%),第2组(P = 0.005)在六个月内需要超过两剂调整。在六个月的替代疗法后,第1组和17族(11%)六(4%)患者在第2组(P = 0.03)中没有适当控制的甲状腺功能亢进(TSH≥2.5mIU/ L)。在第2组(148±33μg/天)中发现了显着更高的LT4最终剂量(148±33μg/天)(136±28μg/天; p = 0.003)。结论:验证Empathy在临床实践中提供了具有有用工具的内分泌学家,允许更好地描述LT4替代疗法,更快地获得目标TSH水平,并且在启动治疗后对剂量调节的需求减少。

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