ETA guidelines for the use of levothyroxine sodium preparations in monotherapy to optimize the treatment of hypothyroidism
- PMID: 40622204
- PMCID: PMC12323320
- DOI: 10.1530/ETJ-25-0123
ETA guidelines for the use of levothyroxine sodium preparations in monotherapy to optimize the treatment of hypothyroidism
Abstract
Sodium levothyroxine (LT4) as a monotherapy represents the mainstay of treatment of hypothyroidism, and its use has increased over time. Nevertheless, it faces several potential barriers in its 'real life' utilization, and hence its clinical effectiveness may be marred. This is suggested by the frequent situation of patients failing to reach the therapeutic goals of symptom relief and serum TSH control. Thus, an expert task force was approved by the Guidelines Board of the European Thyroid Association to examine the available data and to formulate recommendations based on the available evidence and the experts' deduction. The task force provides a body of suggestions to optimize the levothyroxine treatment in monotherapy, considering the key point in the individualization of treatment. Furthermore, the nutritional, pharmacological and pathological factors, potentially leading to the increased need for levothyroxine, are discussed, with a specific focus on the use of liquid and softgel formulations of the hormone.
Keywords: hypothyroidism; levothyroxine formulations; levothyroxine malabsorption; levothyroxine therapy; patient adherence.
Conflict of interest statement
MC, LD, JK, and PR declared no conflicts of interest. UFR received speaker honoraria and travel grants from Merck Darmstadt, Germany. SR received speaker fees from Merck KgaA, Abbott Pharmaceuticals, and Berlin-Chemie. CV has been a consultant for Institut Biochimique SA (Switzerland). PT has been a consultant for Institut Biochimique SA (Switzerland).
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