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Elecsys ft4iii

Manufactured by Roche

The Elecsys FT4III is a laboratory instrument used for the quantitative determination of free thyroxine (FT4) in human serum and plasma samples. It is designed to provide accurate and reliable results for the assessment of thyroid function.

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3 protocols using elecsys ft4iii

1

Thyroid Autoantibody Profiles After COVID-19 Vaccine

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TRAb (Elecsys Anti-TRAb v2, Roche Diagnostics; reference range, <2.0 IU/L), TgAb (Elecsys Anti-Tg, Roche Diagnostics; reference range, <28.0 IU/mL), and TPOAb (Elecsys Anti-TPO, Roche Diagnostics; reference range, <16.0 IU/mL) were measured on a Roche Cobas e801 analyzer (Roche Diagnostics) according to the manufacturer’s instructions. TSH (Elecsys TSH v2, Roche Diagnostics; reference range, 0.500-5.000 μIU/mL), free T4 (FT4, Elecsys FT4III, Roche Diagnostics; reference range, 0.90-1.7 ng/dL), and free T3 (FT3, Elecsys FT3III, Roche Diagnostics; reference range, 2.30-4.00 pg/mL) were measured on a Roche Cobas e801 analyzer (Roche Diagnostics) according to the manufacturer’s instructions. Increases of TRAb, TSH, FT4, and FT3 from baseline to 4 weeks after the third dose were defined as ΔTRAb, ΔTSH, ΔFT4, and ΔFT3, respectively, which were calculated as:
(value at 4 weeks after the third dose) - (value at baseline).
Increases of TgAb and TPOAb from 32 weeks after the second dose (pre-third dose) to 4 weeks after the third dose (post-third dose) were also defined as ΔTgAb and ΔTPOAb, respectively, and calculated as:
(vales at 4 weeks after the third dose) - (values at 32 weeks after the second dose).
Responders to increase in TRAb were defined as the subjects who exhibited increase in TRAb in a time dependent manner and had TRAb >1.2 IU/L at 4 weeks after the third dose.
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2

Thyroid Hormone Levels in Liver Disease

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All laboratory tests were conducted at the ISO-certified Department of Laboratory Medicine of the Vienna General Hospital. Blood withdrawals were conducted in a standardized manner after HVPG measurement under fasting conditions and after resting in the supine position for at least 30 min. Serum levels of TSH (normal range 0.27–4.2 μIU/ml; Elecsys TSH, Roche Diagnostics, Mannheim, Germany), as well as fT4 (normal range 0.76–1.66 ng/dl; Elecsys fT4 III, Roche Diagnostics, Mannheim, Germany) and fT3 (normal range 2.15–4.12 pg/ml; Elecsys fT3 III, Roche Diagnostics) were analyzed by electrochemoluminescence immunoassay (Roche Diagnostics). Standard laboratory methods were used for the assessment of routine laboratory parameters. Low fT4 and low fT3 were defined as fT4 upper limit of normal (ULN).
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3

Endocrine Disorder Evaluation Protocol

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The decision to examine serum and plasma hormones for evaluation of the possibility of some endocrine disorders was made by each physician. Blood samples were collected in a sitting position at the time when the patients visited our clinic at late morning time. Information on the following biochemical parameters was also obtained: ACTH, cortisol, growth hormone (GH), insulin-like growth factor (IGF)-I, free thyroxin (FT4), and thyrotropin (TSH). The levels of those parameters were determined by using the auto-analyzer system Cobas 8000 (F. Hoffmann-La Roche AG, Basel, Switzerland) at the Central Laboratory of Okayama University Hospital. Plasma ACTH and serum cortisol were measured by an electro-chemiluminescence immunoassay (ECLIA) method using Elecsys ACTH and Elecsys Cortisol II kits (F. Hoffmann-La Roche AG), respectively. Serum GH and IGF-I were measured using Elecsys GH and Elecsys IGF-I kits (F. Hoffmann-La Roche AG), respectively, and IGF-I levels were shown by the standard deviation (SD) values [18] . Serum FT4 and TSH were determined by Elecsys FT4 III and Elecsys TSH kits (F. Hoffmann-La Roche AG), respectively.
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