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Serum potassium level as a biomarker for acute caffeine poisoning
AIM: Acute caffeine poisoning presents with hypokalemia, although a relationship between potassium levels and blood concentrations of caffeine has not been established. A correlation between serum potassium level and blood caffeine concentration could establish serum potassium as a simple marker to...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507111/ https://www.ncbi.nlm.nih.gov/pubmed/32995022 http://dx.doi.org/10.1002/ams2.568 |
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author | Tsuji, Tomoatsu Morita, Seiji Saito, Takeshi Nakagawa, Yoshihide Inokuchi, Sadaki |
author_facet | Tsuji, Tomoatsu Morita, Seiji Saito, Takeshi Nakagawa, Yoshihide Inokuchi, Sadaki |
author_sort | Tsuji, Tomoatsu |
collection | PubMed |
description | AIM: Acute caffeine poisoning presents with hypokalemia, although a relationship between potassium levels and blood concentrations of caffeine has not been established. A correlation between serum potassium level and blood caffeine concentration could establish serum potassium as a simple marker to assess caffeine toxicity in patients with acute toxicity. We investigated whether serum potassium, a symptom of acute caffeine poisoning, could be a parameter correlated with blood caffeine levels. METHODS: We enrolled 85 patients treated for acute caffeine poisoning between January 2012 and March 2019 with blood caffeine levels measured after an overdose of a caffeine‐containing over‐the‐counter drug and for whom serum potassium levels were available. We examined the correlation between serum potassium and blood caffeine concentration. A receiver operating characteristic curve was created with serum potassium values to stratify participants into two groups by blood caffeine concentrations: <20 or ≥20 mg/L (toxic dose) and <80 or ≥80 mg/L (lethal dose). The lethal cut‐off value was calculated. RESULTS: The correlation coefficient between serum potassium level and blood caffeine concentration was −0.612 (R (2) = 0.374), indicating a negative correlation. The areas under the curve at blood caffeine concentrations of 20 mg/L (toxic dose) and 80 mg/L (lethal dose) and serum potassium levels were 0.716 and 0.888 (sensitivity, 0.829 and 0.919; specificity, 0.568 and 0.818; cut‐off, 3.3 mEq/L and 2.9 mEq/L), respectively. CONCLUSION: Serum potassium levels are associated with blood caffeine concentrations; K(+) of 3.3 mEq/L and 2.9 mEq/L indicate acute caffeine poisoning in the toxic and lethal dose, respectively. |
format | Online Article Text |
id | pubmed-7507111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75071112020-09-28 Serum potassium level as a biomarker for acute caffeine poisoning Tsuji, Tomoatsu Morita, Seiji Saito, Takeshi Nakagawa, Yoshihide Inokuchi, Sadaki Acute Med Surg Original Articles AIM: Acute caffeine poisoning presents with hypokalemia, although a relationship between potassium levels and blood concentrations of caffeine has not been established. A correlation between serum potassium level and blood caffeine concentration could establish serum potassium as a simple marker to assess caffeine toxicity in patients with acute toxicity. We investigated whether serum potassium, a symptom of acute caffeine poisoning, could be a parameter correlated with blood caffeine levels. METHODS: We enrolled 85 patients treated for acute caffeine poisoning between January 2012 and March 2019 with blood caffeine levels measured after an overdose of a caffeine‐containing over‐the‐counter drug and for whom serum potassium levels were available. We examined the correlation between serum potassium and blood caffeine concentration. A receiver operating characteristic curve was created with serum potassium values to stratify participants into two groups by blood caffeine concentrations: <20 or ≥20 mg/L (toxic dose) and <80 or ≥80 mg/L (lethal dose). The lethal cut‐off value was calculated. RESULTS: The correlation coefficient between serum potassium level and blood caffeine concentration was −0.612 (R (2) = 0.374), indicating a negative correlation. The areas under the curve at blood caffeine concentrations of 20 mg/L (toxic dose) and 80 mg/L (lethal dose) and serum potassium levels were 0.716 and 0.888 (sensitivity, 0.829 and 0.919; specificity, 0.568 and 0.818; cut‐off, 3.3 mEq/L and 2.9 mEq/L), respectively. CONCLUSION: Serum potassium levels are associated with blood caffeine concentrations; K(+) of 3.3 mEq/L and 2.9 mEq/L indicate acute caffeine poisoning in the toxic and lethal dose, respectively. John Wiley and Sons Inc. 2020-09-19 /pmc/articles/PMC7507111/ /pubmed/32995022 http://dx.doi.org/10.1002/ams2.568 Text en © 2020 The Authors. Acute Medicine & Surgery published by John Wiley & Sons Australia, Ltd on behalf of Japanese Association for Acute Medicine This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Tsuji, Tomoatsu Morita, Seiji Saito, Takeshi Nakagawa, Yoshihide Inokuchi, Sadaki Serum potassium level as a biomarker for acute caffeine poisoning |
title | Serum potassium level as a biomarker for acute caffeine poisoning |
title_full | Serum potassium level as a biomarker for acute caffeine poisoning |
title_fullStr | Serum potassium level as a biomarker for acute caffeine poisoning |
title_full_unstemmed | Serum potassium level as a biomarker for acute caffeine poisoning |
title_short | Serum potassium level as a biomarker for acute caffeine poisoning |
title_sort | serum potassium level as a biomarker for acute caffeine poisoning |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507111/ https://www.ncbi.nlm.nih.gov/pubmed/32995022 http://dx.doi.org/10.1002/ams2.568 |
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