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      Patient-Tailored Levothyroxine Dosage with Pharmacokinetic/Pharmacodynamic Modeling: A Novel Approach After Total Thyroidectomy

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          Abstract

          Background: After seven decades of levothyroxine (LT4) replacement therapy, dosage adjustment still takes several months. We have developed a decision aid tool (DAT) that models LT4 pharmacometrics and enables patient-tailored dosage. The aim of this was to speed up dosage adjustments for patients after total thyroidectomy.

          Methods: The DAT computer program was developed with a group of 46 patients post-thyroidectomy, and it was then applied in a prospective randomized multicenter validation trial in 145 unselected patients admitted for total thyroidectomy for goiter, differentiated thyroid cancer, or thyrotoxicosis. The LT4 dosage was adjusted after only two weeks, with or without application of the DAT, which calculated individual free thyroxine (fT4) targets based on four repeated measurements of fT4 and thyrotropin (TSH) levels. The individual TSH target was either <0.1, 0.1–0.5, or 0.5–2.0 mIU/L, depending on the diagnosis. Initial postoperative LT4 dosage was determined according to clinical routine without using algorithms. A simplified DAT with a population-based fT4 target was used for thyrotoxic patients who often went into surgery after prolonged TSH suppression. Subsequent LT4 adjustments were carried out every six weeks until target TSH was achieved.

          Results: When clinicians were guided by the DAT, 40% of patients with goiter and 59% of patients with cancer satisfied the narrow TSH targets eight weeks after surgery, as compared with only 0% and 19% of the controls, respectively. The TSH was within the normal range in 80% of DAT/goiter patients eight weeks after surgery as compared with 19% of controls. The DAT shortened the average dosage adjustment period by 58 days in the goiter group and 40 days in the cancer group. For thyrotoxic patients, application of the simplified DAT did not improve the dosage adjustment.

          Conclusions: Application of the DAT in combination with early postoperative TSH and fT4 monitoring offers a fast approach to LT4 dosage after total thyroidectomy for patients with goiter or differentiated thyroid cancer. Estimation of individual TSH-fT4 dynamics was crucial for the model to work, as removal of this feature in the applied model for thyrotoxic patients also removed the benefit of the DAT.

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          Most cited references32

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              Risk for fracture in women with low serum levels of thyroid-stimulating hormone.

              Biochemical evidence of hyperthyroidism may be associated with low bone mass, particularly in older postmenopausal women, but no prospective studies of thyroid function and subsequent fracture risk have been done. To examine the association between low levels of thyroid-stimulating hormone (TSH) and fracture in older women. Prospective cohort study with case-cohort sampling. Four clinical centers in the United States. 686 women older than 65 years of age from a cohort of 9704 women recruited from population-based listings between 1986 and 1988. Baseline assessment of calcaneal bone mass, spine radiography, and history of thyroid disease. Spine radiography was repeated after a mean follow-up of 3.7 years; nonspine fractures were centrally adjudicated. Thyroid-stimulating hormone was measured in sera obtained at baseline from 148 women with new hip fractures, 149 women with new vertebral fractures, and a subsample of 398 women randomly selected from the cohort. After adjustment for age, history of previous hyperthyroidism, self-rated health, and use of estrogen and thyroid hormone, women with a low TSH level (0.1 mU/L) had a threefold increased risk for hip fracture (relative hazard, 3.6 [95% CI, 1.0 to 12.9]) and a fourfold increased risk for vertebral fracture (odds ratio, 4.5 [CI, 1.3 to 15.6]) compared with women who had normal TSH levels (0.5 to 5.5 mU/L). After adjustment for TSH level, a history of hyperthyroidism was associated with a twofold increase in hip fracture (relative hazard, 2.2 [CI, 1.0 to 4.4]), but use of thyroid hormone itself was not associated with increased risk for hip fracture (relative hazard, 0.5 [CI, 0.2 to 1.3]). Women older than 65 years of age who have low serum TSH levels, indicating physiologic hyperthyroidism, are at increased risk for new hip and vertebral fractures. Use of thyroid hormone itself does not increase risk for fracture if TSH levels are normal.
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                Author and article information

                Journal
                Thyroid
                Thyroid
                thy
                Thyroid
                Mary Ann Liebert, Inc., publishers ( 140 Huguenot Street, 3rd Floor New Rochelle, NY 10801 USA )
                1050-7256
                1557-9077
                September 2021
                07 September 2021
                07 September 2021
                : 31
                : 9
                : 1297-1304
                Affiliations
                [ 1 ]Department of Breast and Endocrine Surgery, University Hospital of North Norway, Tromsø, Norway.
                [ 2 ]Institute of Clinical Medicine, University in Tromsø—The Arctic University of Norway, Tromsø, Norway.
                [ 3 ]Department of Surgery, Västervik Hospital, Västervik, Sweden.
                [ 4 ]Department of Breast and Endocrine Surgery, Haukeland University Hospital, Bergen, Norway.
                [ 5 ]Department of Sustainable Energy Technology, SINTEF Industry, Trondheim, Norway.
                Author notes
                [*]Address correspondence to: Vegard Heimly Brun, MD, PhD, Department of Breast and Endocrine Surgery, University Hospital of North Norway, Sykehusvegen 38, 9019 Tromsø, Norway. vegardbrun@ 123456gmail.com vegard.h.brun@ 123456uit.no
                Author information
                https://orcid.org/0000-0002-4136-3073
                Article
                10.1089/thy.2021.0125
                10.1089/thy.2021.0125
                8558060
                33980057
                447e0b0c-d1a7-4df9-b4f2-ded58917b71a
                © Vegard Heimly Brun et al., 2021; Published by Mary Ann Liebert, Inc.

                This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License [CC-BY-NC] ( http://creativecommons.org/licenses/by-nc/4.0/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are cited.

                History
                Page count
                Figures: 5, Tables: 3, References: 34, Pages: 8
                Categories
                Original Studies
                Thyroid Dysfunction: Hypothyroidism, Thyrotoxicosis, and Thyroid Function Tests

                decision aid tool,levothyroxine dosage,patient tailored,pharmacokinetic modeling,thyroidectomy

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