Evidence map›Paper›PMID 40781507›Full record

ArticleEndocrine2025

Comparison of tablet versus liquid ethanol-free Levothyroxine in thyroidectomised patients.

Laura Croce, Spyridon Chytiris, Marsida Teliti, Jacopo Bertini, Lidia Pizzuto, Marzia Dal Molin, Matteo Limiroli, Benedetto Calì, Flavia Magri, Mario Rotondi

Abstract readComparative Study
In one paragraph

Article in Endocrine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Laura CroceDepartment of Internal Medicine and Therapeutics, University of Pavia, Pavia, 27100, Italy.
Spyridon ChytirisIstituti Clinici Scientifici Maugeri IRCCS, Unit of Internal Medicine and Endocrinology, Laboratory for Endocrine Disruptors, Pavia, 27100, Italy.
Marsida TelitiDepartment of Internal Medicine and Therapeutics, University of Pavia, Pavia, 27100, Italy.
Jacopo BertiniInternal Medicine, Endocrinology and Metabolic Diseases Unit, IRCCS Ospedale Galeazzi - Sant'Ambrogio, Milan, 20157, Italy.
Lidia PizzutoDepartment of Internal Medicine and Therapeutics, University of Pavia, Pavia, 27100, Italy.
Marzia Dal MolinDepartment of Internal Medicine and Therapeutics, University of Pavia, Pavia, 27100, Italy.
Matteo LimiroliDepartment of Internal Medicine and Therapeutics, University of Pavia, Pavia, 27100, Italy.
Benedetto CalìIstituti Clinici Scientifici Maugeri IRCCS, Department of General and Minimally Invasive Surgery, Pavia, 27100, Italy.
Flavia MagriDepartment of Internal Medicine and Therapeutics, University of Pavia, Pavia, 27100, Italy.
Mario RotondiDepartment of Internal Medicine and Therapeutics, University of Pavia, Pavia, 27100, Italy. mario.rotondi@icsmaugeri.it.ORCID 0000-0001-6464-2334

Funding

Ministero dell'Istruzione e del Merito PE00000003
6 · The paper itself

Abstract

purposeSince the introduction of an ethanol-free liquid levothyroxine formulation, only few studies assessed its therapeutic efficacy. The present study aimed to compare the efficacy of tablet (T-LT4) versus L-EF-LT4 in achieving the patient-specific TSH target in thyroidectomized patients. The primary objective was to assess whether the required LT4 dose differed between formulations in a real-life setting.

methodsThe study was conducted on 275 patients who underwent total thyroidectomy and were treated with either T-LT4 (n = 152) or L-EF-LT4 (n = 123) between 2020 and 2023. Clinical and biochemical data, including LT4 dose, BMI, TSH levels, and potential causes of malabsorption, were collected. The primary endpoint was the pro-kg LT4 dose required to achieve individualized TSH targets. Multivariate regression analysis was used to evaluate predictors of LT4 requirement.

resultsAt final follow-up, 227 patients (82.5%) achieved their TSH target and were under stable doses of LT4 with no significant difference in mean LT4 dose between groups (T-LT4: 1.54 ± 0.35 µg/kg/day; L-EF-LT4: 1.60 ± 0.32 µg/kg/day, p = 0.160). TSH levels were comparable (p = 0.311). Regression analysis showed that age and BMI were inversely correlated with LT4 dose, while a diagnosis of differentiated thyroid cancer was positively correlated with LT4 dose. Formulation type was not a significant predictor.

conclusionIn patients with post-surgical hypothyroidism, L-EF-LT4 demonstrated equivalent therapeutic efficacy to T-LT4 in terms of dose requirement and TSH control. These findings support the use of L-EF-LT4 as a viable alternative to tablet LT4, particularly in clinical scenarios where flexible timing of ingestion may improve patient compliance.

Indexed as

Hormone Replacement TherapyHypothyroidismThyroidectomyThyroxineAdultAgedEthanolFemaleHumansMaleMiddle AgedTabletsThyrotropinTreatment OutcomeEthanolTabletsThyrotropinThyroxineEthanol-free liquid Levothyroxine - levotirsolHypothyroidismLevothyroxineThyroidTotal thyroidectomy

Identifiers

PMID40781507
PMCPMC12572031

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.