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Elecsys ft3iii

Manufactured by Roche
Sourced in Germany

The Elecsys FT3III is a laboratory equipment product developed by Roche. It is designed to measure the level of free triiodothyronine (FT3) in blood samples. FT3 is a thyroid hormone that plays a crucial role in the regulation of the body's metabolism.

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3 protocols using elecsys ft3iii

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

Apatinib-Induced Thyroid Dysfunction Evaluation

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All patients received 500 mg apatinib/day (Jiangsu Heng Rui Medicine Co., Ltd.) orally until the disease progressed, except for 3 patients who were administered a dose of 250 mg/day due to hypertension. Dose reductions occurred often due to toxicity, as such the doses of 11 patients were reduced to 250 mg/day.
Levels of triiodothyronine (T3; normal range, 3.1-6.8 pmol/l), tetraiodothyronine (T4; normal range, 12-22 pmol/l) and thyroid stimulating hormone (TSH; 0.27-4.2 µIU/ml) were evaluated monthly. These parameters were evaluated using Elecsys FT3 III, FT4 III and TSH and Cobase E analyzers supplied by Roche Diagnostics GmbH. Lower levels of T3 and T4 were <3.1 and 12 pmol/l, respectively. Higher levels of TSH were >4.2 µIU/ml.
Additionally, patients underwent a thyroid ultrasound every 2 months while receiving apatinib treatment. Their thyroid function and thyroid ultrastructure was evaluated for at least 24 months or until death. All patients divided into the normal thyroid function group (96 cases) and the hypothyroidism group (53 cases) according to their levels of T3, T4 and TSH. Efficacy measures included complete response(CR), partial response (PR), stable disease (SD) and disease control rate (DCR; including complete response, partial response and sTable disease). Statistical differences in DCR between the two groups were analyzed.
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3

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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