2014
DOI: 10.1111/bcpt.12338
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Is the Measurement of Serum Formate Concentration Useful in the Diagnostics of Acute Methanol Poisoning? A Prospective Study of 38 Patients

Abstract: The aim of this article was to study the role of serum formate (S-formate) in diagnosing methanol poisoning. A prospective study was undertaken of 38 patients from the Czech methanol mass poisoning in 2012 -median age 51 [interquartile range (IQR) 37-62] years with confirmed methanol poisoning. S-formate was measured enzymatically. The receiver operating characteristics (ROC) curve was used to examine the predictive ability of S-formate. Asymptomatic patients had median S-formate of 1.9 (IQR 1.5-2.4) mmol/L. T… Show more

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Cited by 55 publications
(47 citation statements)
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“…Formate was measured enzymatically using formate dehydrogenase and nicotinamide adenine dinucleotide, according to a previously published method [38, 39]. Day-to-day coefficient of variation was 5.6 %, and the upper reference limit was 0.44 mmol dm −3 .…”
Section: Methodsmentioning
confidence: 99%
“…Formate was measured enzymatically using formate dehydrogenase and nicotinamide adenine dinucleotide, according to a previously published method [38, 39]. Day-to-day coefficient of variation was 5.6 %, and the upper reference limit was 0.44 mmol dm −3 .…”
Section: Methodsmentioning
confidence: 99%
“…As a moderate inhibitor of mitochondrial cytochrome c oxidase (Ki $6 mmol/L), formic acid impairs tissue utilization of oxygen resulting in excess lactic acid production and depletion of ATP in cells [15,16]. Nevertheless, there is no difference in the serum formic acid concentrations in patients with lethal outcome and in survivors with sequelae of poisoning [17]. MRI signs of brain damage can be found in survivors of poisoning with low serum formic acid concentration on admission (2-4 mmol/L), while the patients with high serum formic acid concentration on admission of about 15 mmol/L may survive without CNS sequelae [9].…”
Section: Importancementioning
confidence: 99%
“…Formate was measured enzymatically by a Hitachi analyzer (Hitachi 912, Hitachi Science Systems Ltd., Japan) using formate dehydrogenase (Roche, France) and nicotinamide adenine dinucleotide (NAD) (Roche, France), according to a previously published method [28][29][30][31] . Pure sodium formate (Sigma-Aldrich, USA) was used to prepare a standard of 1.1 mmol/L phosphate buffer and two control sera.…”
Section: Laboratory Investigationsmentioning
confidence: 99%