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Metronidazole-induced encephalopathy in a patient with Crohn's disease
Metronidazole is a widely used antibiotic for the treatment of anaerobic bacterial infections. Metronidazole-induced encephalopathy (MIEP) is a rare but potentially reversible disease. The mechanism of MIEP remains unclear, and differences in the neurotoxic effects of oral versus intravenous (IV) me...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association for the Study of Intestinal Diseases
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323302/ https://www.ncbi.nlm.nih.gov/pubmed/28239323 http://dx.doi.org/10.5217/ir.2017.15.1.124 |
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author | Kim, Jihye Chun, Jaeyoung Park, Jae Yong Hong, Seung Wook Lee, Joo Young Kang, Jin Woo Hwang, Seongjun Ko, Sang-Bae Im, Jong Pil Kim, Joo Sung |
author_facet | Kim, Jihye Chun, Jaeyoung Park, Jae Yong Hong, Seung Wook Lee, Joo Young Kang, Jin Woo Hwang, Seongjun Ko, Sang-Bae Im, Jong Pil Kim, Joo Sung |
author_sort | Kim, Jihye |
collection | PubMed |
description | Metronidazole is a widely used antibiotic for the treatment of anaerobic bacterial infections. Metronidazole-induced encephalopathy (MIEP) is a rare but potentially reversible disease. The mechanism of MIEP remains unclear, and differences in the neurotoxic effects of oral versus intravenous (IV) metronidazole administration have not yet been determined. We report the case of a Crohn's disease (CD) patient who experienced encephalopathy immediately after a single IV dose of metronidazole following long-term exposure to the oral form of the drug. The 64-year-old man with intractable CD experienced a sudden change in mental status, aphasia, and muscle weakness after IV administration of metronidazole. He had previously taken metronidazole orally for 13 years and received intermittent IV metronidazole treatments for CD exacerbation. Brain magnetic resonance imaging (MRI) showed high-intensity signals in the bilateral medial thalamus and the midbrain and pontine tegmentum on fluid-attenuated inversion recovery images. After discontinuation of metronidazole, the high-intensity brain MRI signals resolved and the patient's mental status dramatically improved; however, the patient exhibited mild cognitive dysfunction 2 months after the onset of encephalopathy. |
format | Online Article Text |
id | pubmed-5323302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Korean Association for the Study of Intestinal Diseases |
record_format | MEDLINE/PubMed |
spelling | pubmed-53233022017-02-24 Metronidazole-induced encephalopathy in a patient with Crohn's disease Kim, Jihye Chun, Jaeyoung Park, Jae Yong Hong, Seung Wook Lee, Joo Young Kang, Jin Woo Hwang, Seongjun Ko, Sang-Bae Im, Jong Pil Kim, Joo Sung Intest Res Case Report Metronidazole is a widely used antibiotic for the treatment of anaerobic bacterial infections. Metronidazole-induced encephalopathy (MIEP) is a rare but potentially reversible disease. The mechanism of MIEP remains unclear, and differences in the neurotoxic effects of oral versus intravenous (IV) metronidazole administration have not yet been determined. We report the case of a Crohn's disease (CD) patient who experienced encephalopathy immediately after a single IV dose of metronidazole following long-term exposure to the oral form of the drug. The 64-year-old man with intractable CD experienced a sudden change in mental status, aphasia, and muscle weakness after IV administration of metronidazole. He had previously taken metronidazole orally for 13 years and received intermittent IV metronidazole treatments for CD exacerbation. Brain magnetic resonance imaging (MRI) showed high-intensity signals in the bilateral medial thalamus and the midbrain and pontine tegmentum on fluid-attenuated inversion recovery images. After discontinuation of metronidazole, the high-intensity brain MRI signals resolved and the patient's mental status dramatically improved; however, the patient exhibited mild cognitive dysfunction 2 months after the onset of encephalopathy. Korean Association for the Study of Intestinal Diseases 2017-01 2017-01-31 /pmc/articles/PMC5323302/ /pubmed/28239323 http://dx.doi.org/10.5217/ir.2017.15.1.124 Text en © Copyright 2017. Korean Association for the Study of Intestinal Diseases. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kim, Jihye Chun, Jaeyoung Park, Jae Yong Hong, Seung Wook Lee, Joo Young Kang, Jin Woo Hwang, Seongjun Ko, Sang-Bae Im, Jong Pil Kim, Joo Sung Metronidazole-induced encephalopathy in a patient with Crohn's disease |
title | Metronidazole-induced encephalopathy in a patient with Crohn's disease |
title_full | Metronidazole-induced encephalopathy in a patient with Crohn's disease |
title_fullStr | Metronidazole-induced encephalopathy in a patient with Crohn's disease |
title_full_unstemmed | Metronidazole-induced encephalopathy in a patient with Crohn's disease |
title_short | Metronidazole-induced encephalopathy in a patient with Crohn's disease |
title_sort | metronidazole-induced encephalopathy in a patient with crohn's disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323302/ https://www.ncbi.nlm.nih.gov/pubmed/28239323 http://dx.doi.org/10.5217/ir.2017.15.1.124 |
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