A trial of thyroxine in acute renal failure

• Published in: Kidney international Vol. 57; no. 1; pp. 293 - 298
• Main Authors: Acker, Christopher G., Singh, Asim R., Flick, Richard P., Bernardini, Judith, Greenberg, Arthur, Johnson, John P.
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01.01.2000; Nature Publishing; Elsevier Limited
• Subjects: Acute Kidney Injury - drug therapy; Acute Kidney Injury - pathology; APACHE; Biological and medical sciences; critical care medicine; Double-Blind Method; euthyroid sick syndrome; Female; Humans; ischemia; Male; Medical sciences; Middle Aged; nephrotoxicity; Pharmacology. Drug treatments; Prospective Studies; thyroid hormone; Thyroxine - therapeutic use; Urinary system; critical care medicine; nephrotoxicity; thyroid hormone; euthyroid sick syndrome; ischemia; Kidney disease; Human; Chemotherapy; Urinary system disease; Renal function; Treatment; Acute; Renal failure; Thyroxine; Exploration; Thyroid hormone
• ISSN: 0085-2538; 1523-1755
• DOI: 10.1046/j.1523-1755.2000.00827.x

A trial of thyroxine in acute renal failure. Acute renal failure (ARF) remains a serious medical problem with a high mortality rate. Efforts to shorten the course of ARF might reduce this mortality. Since thyroxine has been shown in experimental models to shorten the course of ARF, we designed a trial to determine if a defined course of thyroxine would alter the course or change the mortality of clinical ARF. A prospective, randomized, placebo-controlled, double-blind trial of thyroxine was carried out in patients with ARF. End points were the percentage requiring dialysis, the percentage recovering renal function, time to recovery, and mortality. Fifty-nine patients were randomized to receive either thyroxine or placebo. The groups were well matched in terms of basal and entry creatinines, age, sex, APACHE II scores at entry, and percentage oliguric. Baseline thyroid functions, including T3, T4, rT3, and thyroid stimulating hormone (TSH) levels, were equal between the two groups and typical of patients with euthyroid sick syndrome. Thyroxine resulted in a progressive and sustained suppression of TSH levels in the treated group, but had no effect on any measure of ARF severity. Mortality was higher in the thyroxine group than the control group (43 vs. 13%) and correlated with suppression of TSH. In contrast to the beneficial effects seen in experimental ARF, thyroxine has no effect on the course of clinical ARF and could have a negative effect on outcome through prolonged suppression of TSH. Critically ill euthyroid sick patients should not be replaced with thyroid hormone.