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Effects of Acute Organophosphorus Poisoning on Function of Peripheral Nerves: A Cohort Study

BACKGROUND: Following acute organophosphorus (OP) poisoning patients complain of numbness without objective sensory abnormalities or other features of OP induced delayed polyneuropathy. The aim of this study was to measure peripheral nerve function after acute exposure to OP. METHODS: A cohort study...

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Autores principales: Jayasinghe, Sudheera S., Pathirana, Kithsiri D., Buckley, Nick A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502513/
https://www.ncbi.nlm.nih.gov/pubmed/23185328
http://dx.doi.org/10.1371/journal.pone.0049405
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author Jayasinghe, Sudheera S.
Pathirana, Kithsiri D.
Buckley, Nick A.
author_facet Jayasinghe, Sudheera S.
Pathirana, Kithsiri D.
Buckley, Nick A.
author_sort Jayasinghe, Sudheera S.
collection PubMed
description BACKGROUND: Following acute organophosphorus (OP) poisoning patients complain of numbness without objective sensory abnormalities or other features of OP induced delayed polyneuropathy. The aim of this study was to measure peripheral nerve function after acute exposure to OP. METHODS: A cohort study was conducted with age, gender and occupation matched controls. Motor nerve conduction velocity (MNCV), amplitude and area of compound muscle action potential (CMAP), sensory nerve conduction velocity (SNCV), F- waves and electromyography (EMG) on the deltoid and the first dorsal interosseous muscles on the dominant side were performed, following acute OP poisoning. All neurophysiological assessments except EMG were performed on the controls. Assessments were performed on the day of discharge from the hospital (the first assessment) and six weeks (the second assessment) after the exposure. The controls were assessed only once. RESULTS: There were 70 patients (50 males) and 70 controls. Fifty-three patients attended for the second assessment. In the first assessment MNCV of all the motor nerves examined, CMAP amplitude and SNCV of ulnar nerve, median and ulnar F-wave occurrence in the patients were significantly reduced compared to the controls. In the second assessment significant reduction was found in SNCV of both sensory nerves examined, MNCV of ulnar nerve, CMAP amplitude of common peroneal nerve, F-wave occurrence of median and ulnar nerves. No abnormalities were detected in the patients when compared to the standard cut-off values of nerve conduction studies except F-wave occurrence. EMG studies did not show any abnormality. CONCLUSION: There was no strong evidence of irreversible peripheral nerve damage following acute OP poisoning, however further studies are required.
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spelling pubmed-35025132012-11-26 Effects of Acute Organophosphorus Poisoning on Function of Peripheral Nerves: A Cohort Study Jayasinghe, Sudheera S. Pathirana, Kithsiri D. Buckley, Nick A. PLoS One Research Article BACKGROUND: Following acute organophosphorus (OP) poisoning patients complain of numbness without objective sensory abnormalities or other features of OP induced delayed polyneuropathy. The aim of this study was to measure peripheral nerve function after acute exposure to OP. METHODS: A cohort study was conducted with age, gender and occupation matched controls. Motor nerve conduction velocity (MNCV), amplitude and area of compound muscle action potential (CMAP), sensory nerve conduction velocity (SNCV), F- waves and electromyography (EMG) on the deltoid and the first dorsal interosseous muscles on the dominant side were performed, following acute OP poisoning. All neurophysiological assessments except EMG were performed on the controls. Assessments were performed on the day of discharge from the hospital (the first assessment) and six weeks (the second assessment) after the exposure. The controls were assessed only once. RESULTS: There were 70 patients (50 males) and 70 controls. Fifty-three patients attended for the second assessment. In the first assessment MNCV of all the motor nerves examined, CMAP amplitude and SNCV of ulnar nerve, median and ulnar F-wave occurrence in the patients were significantly reduced compared to the controls. In the second assessment significant reduction was found in SNCV of both sensory nerves examined, MNCV of ulnar nerve, CMAP amplitude of common peroneal nerve, F-wave occurrence of median and ulnar nerves. No abnormalities were detected in the patients when compared to the standard cut-off values of nerve conduction studies except F-wave occurrence. EMG studies did not show any abnormality. CONCLUSION: There was no strong evidence of irreversible peripheral nerve damage following acute OP poisoning, however further studies are required. Public Library of Science 2012-11-20 /pmc/articles/PMC3502513/ /pubmed/23185328 http://dx.doi.org/10.1371/journal.pone.0049405 Text en © 2012 Jayasinghe et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Jayasinghe, Sudheera S.
Pathirana, Kithsiri D.
Buckley, Nick A.
Effects of Acute Organophosphorus Poisoning on Function of Peripheral Nerves: A Cohort Study
title Effects of Acute Organophosphorus Poisoning on Function of Peripheral Nerves: A Cohort Study
title_full Effects of Acute Organophosphorus Poisoning on Function of Peripheral Nerves: A Cohort Study
title_fullStr Effects of Acute Organophosphorus Poisoning on Function of Peripheral Nerves: A Cohort Study
title_full_unstemmed Effects of Acute Organophosphorus Poisoning on Function of Peripheral Nerves: A Cohort Study
title_short Effects of Acute Organophosphorus Poisoning on Function of Peripheral Nerves: A Cohort Study
title_sort effects of acute organophosphorus poisoning on function of peripheral nerves: a cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502513/
https://www.ncbi.nlm.nih.gov/pubmed/23185328
http://dx.doi.org/10.1371/journal.pone.0049405
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