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Calgary score and modified calgary score in the differential diagnosis between syncope and genetic generalized epilepsy in children

The purpose of the study is to explore the use of Calgary scoring (CS) and Modified Calgary scoring (MCS) in the differentiation of genetic generalized epilepsy and syncope in children. The study involved 117 patients aged < 18 years who presented to our hospital’s pediatric neurology outpatient...

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Autores principales: Köle, Mehmet Tolga, Sağer, Safiye Günes, Batu, Utku, Çetiner Çine, Nilüfer, Çağ, Yakup, Akin, Yasemin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390527/
https://www.ncbi.nlm.nih.gov/pubmed/37524730
http://dx.doi.org/10.1038/s41598-023-39338-5
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author Köle, Mehmet Tolga
Sağer, Safiye Günes
Batu, Utku
Çetiner Çine, Nilüfer
Çağ, Yakup
Akin, Yasemin
author_facet Köle, Mehmet Tolga
Sağer, Safiye Günes
Batu, Utku
Çetiner Çine, Nilüfer
Çağ, Yakup
Akin, Yasemin
author_sort Köle, Mehmet Tolga
collection PubMed
description The purpose of the study is to explore the use of Calgary scoring (CS) and Modified Calgary scoring (MCS) in the differentiation of genetic generalized epilepsy and syncope in children. The study involved 117 patients aged < 18 years who presented to our hospital’s pediatric neurology outpatient clinic with TLOC between June 2020 and June 2022. In addition to CS and MCS scoring, all patients were subjected to statistical analysis based on their age, sex, number of episodes and distribution during the day, duration of syncope, and family history. Seventy-one patients with syncope and 46 with epilepsy were included in the study. At a CS value >  − 1, sensitivity was 86.9% and specificity 63.4%, while at an MCS value >  − 1, sensitivity was 76.1% and specificity 71.8%. CS had less specificity and sensitivity in predicting epilepsy when focal epilepsies were excluded. Abnormal behavior noted by bystanders, including witnessed unresponsive, unusual posturing, or limb jerking? (Q5) emerged as the most important question for the detection of epilepsy. Compared with other syncope findings, loss of consciousness during prolonged sitting or standing (Q9) emerged as the most important for the detection of syncope.
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spelling pubmed-103905272023-08-02 Calgary score and modified calgary score in the differential diagnosis between syncope and genetic generalized epilepsy in children Köle, Mehmet Tolga Sağer, Safiye Günes Batu, Utku Çetiner Çine, Nilüfer Çağ, Yakup Akin, Yasemin Sci Rep Article The purpose of the study is to explore the use of Calgary scoring (CS) and Modified Calgary scoring (MCS) in the differentiation of genetic generalized epilepsy and syncope in children. The study involved 117 patients aged < 18 years who presented to our hospital’s pediatric neurology outpatient clinic with TLOC between June 2020 and June 2022. In addition to CS and MCS scoring, all patients were subjected to statistical analysis based on their age, sex, number of episodes and distribution during the day, duration of syncope, and family history. Seventy-one patients with syncope and 46 with epilepsy were included in the study. At a CS value >  − 1, sensitivity was 86.9% and specificity 63.4%, while at an MCS value >  − 1, sensitivity was 76.1% and specificity 71.8%. CS had less specificity and sensitivity in predicting epilepsy when focal epilepsies were excluded. Abnormal behavior noted by bystanders, including witnessed unresponsive, unusual posturing, or limb jerking? (Q5) emerged as the most important question for the detection of epilepsy. Compared with other syncope findings, loss of consciousness during prolonged sitting or standing (Q9) emerged as the most important for the detection of syncope. Nature Publishing Group UK 2023-07-31 /pmc/articles/PMC10390527/ /pubmed/37524730 http://dx.doi.org/10.1038/s41598-023-39338-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Köle, Mehmet Tolga
Sağer, Safiye Günes
Batu, Utku
Çetiner Çine, Nilüfer
Çağ, Yakup
Akin, Yasemin
Calgary score and modified calgary score in the differential diagnosis between syncope and genetic generalized epilepsy in children
title Calgary score and modified calgary score in the differential diagnosis between syncope and genetic generalized epilepsy in children
title_full Calgary score and modified calgary score in the differential diagnosis between syncope and genetic generalized epilepsy in children
title_fullStr Calgary score and modified calgary score in the differential diagnosis between syncope and genetic generalized epilepsy in children
title_full_unstemmed Calgary score and modified calgary score in the differential diagnosis between syncope and genetic generalized epilepsy in children
title_short Calgary score and modified calgary score in the differential diagnosis between syncope and genetic generalized epilepsy in children
title_sort calgary score and modified calgary score in the differential diagnosis between syncope and genetic generalized epilepsy in children
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390527/
https://www.ncbi.nlm.nih.gov/pubmed/37524730
http://dx.doi.org/10.1038/s41598-023-39338-5
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