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EMPATHY: A New Tool for Identifying the Most Suitable Thyroxine Formulation in Hypothyroid Patients
Giuseppe Bellastella1, Mariangela Caputo1, Maria Ida Maiorino1
11Endocrinology and Metabolic Diseases Unit, Department of Advanced Medical and Surgical Sciences, University of Campania "L. Vanvitelli," Naples, Italy.
The EMPATHY questionnaire helps identify levothyroxine (LT4) malabsorption in hypothyroidism patients. This tool aids in personalizing LT4 therapy, leading to faster TSH target achievement and fewer dose adjustments.
Area of Science:
- Endocrinology
- Clinical Pharmacology
Background:
- Levothyroxine (LT4) therapy is standard for hypothyroidism, but achieving target thyrotropin (TSH) levels can be challenging.
- Poor compliance (60%) and malabsorption (40%) are primary reasons for treatment failure.
- Currently, no tools exist to pre-emptively detect malabsorption before initiating therapy.
Purpose of the Study:
- To validate the Evaluation of Malabsorption in PATients with HYpothyroidism (EMPATHY) questionnaire.
- To assess the questionnaire's utility in guiding appropriate LT4 therapy selection.
Main Methods:
- The EMPATHY questionnaire, assessing intolerances and allergies, was administered to 150 newly diagnosed hypothyroid patients (group 1).
- A control group (150 patients) received standard care based on history.
- Thyroid hormones and TSH were monitored for six months, with dose adjustments recorded.
Main Results:
- Fewer patients in the EMPATHY group (14%) required more than two dose adjustments compared to the control group (28%).
- Hypothyroidism control (TSH < 2.5 mIU/L) was achieved in more patients using EMPATHY (96%) versus the control group (89%).
- The final LT4 dose was significantly lower in the EMPATHY group (136 ± 28 μg/day) than in the control group (148 ± 33 μg/day).
Conclusions:
- The validated EMPATHY questionnaire is a valuable clinical tool for endocrinologists.
- It facilitates personalized LT4 replacement therapy and accelerates TSH level normalization.
- The questionnaire reduces the need for post-initiation therapy dose adjustments.
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