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Peer-reviewedCC BY 4.0Journal of Clinical Medicine

Beyond Euthyroid Sick Syndrome: Pre-Admission Levothyroxine Use and Thyroid Hormone–Outcome Associations in Hospitalized Patients

  1. 1Institute of Endocrinology, Bnai Zion Medical Center, 47 Eliyahu Golomb Avenue, Haifa 3339419, Israel
  2. 2The Ruth and Bruce Rappaport Faculty of Medicine, Technion, Israel Institute of Technology, 1 Efron Street, Haifa 3339101, Israel
  3. 3Clinical Laboratories Division, Bnai Zion Medical Center, Haifa 3339419, Israel

Abstract

Background/Objectives: Pre-admission levothyroxine use may influence the interpretation of thyroid tests beyond the conventional framework of non-thyroidal illness syndrome (NTIS). We examined whether thyroid hormone–outcome associations differed by treatment status. Methods: This retrospective study included medical inpatients with thyroid-stimulating hormone (TSH) < 5 mIU/L during 2006–2024. Propensity-score matching used age, sex, and 16 comorbidity indicators. Complete-case negative-binomial and logistic models examined hospitalization length and in-hospital mortality, with treatment-by-hormone interactions. Results: Among 14,332 matched patients, 3717 had complete data (1986 users; 1731 nonusers). Higher free triiodothyronine (FT3) in nonusers was associated with shorter hospitalization (incidence–rate ratio [IRR] 0.76, 95% confidence interval [CI] 0.73–0.80) and lower mortality odds (odds ratio [OR] 0.47, 95% CI 0.35–0.62). Free thyroxine (FT4) associations differed by levothyroxine use for both hospitalization length (interaction IRR 0.95, 95% CI 0.94–0.97) and mortality (interaction OR 0.83, 95% CI 0.77–0.90; both p < 0.001). At mean hormone concentrations, levothyroxine use was associated with shorter hospitalization (IRR 0.87, 95% CI 0.81–0.94) and lower mortality odds (OR 0.53, 95% CI 0.35–0.82). Crude mortality was 4.6% versus 5.0%, respectively; the conditional estimates represent a different comparison. Conclusions: FT4–outcome associations differed by pre-admission levothyroxine use, extending the established low-T3 prognostic framework to treatment-specific hormone patterns. These findings support considering treatment history when interpreting inpatient thyroid tests. Selective testing and residual confounding limit causal interpretation.

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BibTeX
@article{sheikhahmad2026beyond,
  title = {{Beyond Euthyroid Sick Syndrome: Pre-Admission Levothyroxine Use and Thyroid Hormone–Outcome Associations in Hospitalized Patients}},
  author = {Mohammad Sheikh-Ahmad and Ilana Rosenblatt and Hadas Rabani and Clara Henig and Balsam Dakwar and Ekaterina Yovanovich and Emad Khoury and Leonard Saiegh},
  journal = {Journal of Clinical Medicine},
  year = {2026},
  month = oct,
  doi = {10.3390/jcm15218382},
  url = {https://www.mdpi.com/2077-0383/15/21/8382},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Beyond Euthyroid Sick Syndrome: Pre-Admission Levothyroxine Use and Thyroid Hormone–Outcome Associations in Hospitalized Patients
AU  - Mohammad Sheikh-Ahmad
AU  - Ilana Rosenblatt
AU  - Hadas Rabani
AU  - Clara Henig
AU  - Balsam Dakwar
AU  - Ekaterina Yovanovich
AU  - Emad Khoury
AU  - Leonard Saiegh
PY  - 2026
DA  - 2026/10/28
JO  - Journal of Clinical Medicine
DO  - 10.3390/jcm15218382
UR  - https://www.mdpi.com/2077-0383/15/21/8382
AB  - Background/Objectives: Pre-admission levothyroxine use may influence the interpretation of thyroid tests beyond the conventional framework of non-thyroidal illness syndrome (NTIS). We examined whether thyroid hormone–outcome associations differed by treatment status. Methods: This retrospective study included medical inpatients with thyroid-stimulating hormone (TSH) < 5 mIU/L during 2006–2024. Propensity-score matching used age, sex, and 16 comorbidity indicators. Complete-case negative-binomial and logistic models examined hospitalization length and in-hospital mortality, with treatment-by-hormone interactions. Results: Among 14,332 matched patients, 3717 had complete data (1986 users; 1731 nonusers). Higher free triiodothyronine (FT3) in nonusers was associated with shorter hospitalization (incidence–rate ratio [IRR] 0.76, 95% confidence interval [CI] 0.73–0.80) and lower mortality odds (odds ratio [OR] 0.47, 95% CI 0.35–0.62). Free thyroxine (FT4) associations differed by levothyroxine use for both hospitalization length (interaction IRR 0.95, 95% CI 0.94–0.97) and mortality (interaction OR 0.83, 95% CI 0.77–0.90; both p < 0.001). At mean hormone concentrations, levothyroxine use was associated with shorter hospitalization (IRR 0.87, 95% CI 0.81–0.94) and lower mortality odds (OR 0.53, 95% CI 0.35–0.82). Crude mortality was 4.6% versus 5.0%, respectively; the conditional estimates represent a different comparison. Conclusions: FT4–outcome associations differed by pre-admission levothyroxine use, extending the established low-T3 prognostic framework to treatment-specific hormone patterns. These findings support considering treatment history when interpreting inpatient thyroid tests. Selective testing and residual confounding limit causal interpretation.
SN  - 2077-0383
ER  -