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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Published in: | Scientific reports Vol. 13; no. 1; p. 12376 |
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Abstract | 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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AbstractList | 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. 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. 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. Abstract 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. |
ArticleNumber | 12376 |
Author | Köle, Mehmet Tolga Batu, Utku Çağ, Yakup Çetiner Çine, Nilüfer Sağer, Safiye Günes Akin, Yasemin |
Author_xml | – sequence: 1 givenname: Mehmet Tolga orcidid: 0000-0002-6055-7746 surname: Köle fullname: Köle, Mehmet Tolga email: mehmet_tolga@hotmail.com organization: Department of Pediatrics, University of Health Science, Kartal Dr. Lutfi Kirdar City Hospital – sequence: 2 givenname: Safiye Günes orcidid: 0000-0002-9876-2454 surname: Sağer fullname: Sağer, Safiye Günes organization: Department of Pediatric Neurology, University of Health Science, Kartal Dr. Lutfi Kirdar City Hospital – sequence: 3 givenname: Utku orcidid: 0000-0002-4434-1670 surname: Batu fullname: Batu, Utku organization: Department of Pediatrics, Van Education and Research Hospital – sequence: 4 givenname: Nilüfer orcidid: 0000-0001-6827-5527 surname: Çetiner Çine fullname: Çetiner Çine, Nilüfer organization: Department of Pediatric Cardiology, Koşuyolu Highly Specialized Training and Research Hospital – sequence: 5 givenname: Yakup orcidid: 0000-0002-3855-7280 surname: Çağ fullname: Çağ, Yakup organization: Department of Pediatrics, University of Health Science, Kartal Dr. Lutfi Kirdar City Hospital – sequence: 6 givenname: Yasemin orcidid: 0000-0002-7618-7778 surname: Akin fullname: Akin, Yasemin organization: Department of Pediatrics, University of Health Science, Kartal Dr. Lutfi Kirdar City Hospital |
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Cites_doi | 10.1016/j.pcad.2012.10.011 10.1016/j.yebeh.2012.02.006 10.1038/nrneurol.2009.99 10.1093/eurheartj/ehy037 10.1016/j.eplepsyres.2011.03.009 10.1016/j.hrthm.2015.03.029 10.1007/s00246-006-1140-7 10.1159/000503831 10.1016/S0735-1097(02)01940-X 10.3389/fped.2021.638394 10.1016/j.cjca.2019.12.023 10.1212/WNL.0000000000003509 10.1136/adc.2004.064477 10.1093/eurheartj/ehp298 10.1186/s12883-017-0822-5 10.1111/epi.13709 10.1007/s10072-016-2740-5 10.1111/j.1540-8159.2009.02685.x 10.1016/j.brainres.2016.03.021 10.14581/jer.11007 |
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References | Rodrigues Tda, Sternick, Moreira Mda (CR9) 2010; 33 Sabri, Mahmodian, Sadri (CR20) 2006; 27 Sandhu (CR11) 2020; 36 van Dijk, Thijs, Benditt, Wieling (CR12) 2009; 5 Hu, Liu, Chen, Wang (CR4) 2021; 9 Brignole (CR15) 2018; 39 Scheffer (CR13) 2017; 58 Wirrell, Grossardt, Wong-Kisiel, Nickels (CR6) 2011; 95 Jeong, Moon, Oh, Kim (CR17) 2011; 1 Sheldon (CR14) 2015; 12 Yilmaz, Gökben, Levent, Serdaroğlu, Özyürek (CR16) 2012; 24 Sheldon (CR10) 2002; 40 Moya (CR3) 2009; 30 Fiest (CR5) 2017; 88 Beghi (CR7) 2020; 54 Zou (CR8) 2017; 38 Sheldon (CR1) 2013; 55 Ungar (CR2) 2017; 17 Uldall, Alving, Hansen, Kibaek, Buchholt (CR19) 2006; 91 Romeo (CR18) 2017; 1654 R Sheldon (39338_CR1) 2013; 55 KM Fiest (39338_CR5) 2017; 88 HS Jeong (39338_CR17) 2011; 1 IE Scheffer (39338_CR13) 2017; 58 A Ungar (39338_CR2) 2017; 17 RD Romeo (39338_CR18) 2017; 1654 S Yilmaz (39338_CR16) 2012; 24 R Zou (39338_CR8) 2017; 38 R Rodrigues Tda (39338_CR9) 2010; 33 M Brignole (39338_CR15) 2018; 39 RK Sandhu (39338_CR11) 2020; 36 JG van Dijk (39338_CR12) 2009; 5 R Sheldon (39338_CR10) 2002; 40 E Beghi (39338_CR7) 2020; 54 MR Sabri (39338_CR20) 2006; 27 P Uldall (39338_CR19) 2006; 91 EC Wirrell (39338_CR6) 2011; 95 RS Sheldon (39338_CR14) 2015; 12 A Moya (39338_CR3) 2009; 30 E Hu (39338_CR4) 2021; 9 |
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Electrophysiol. doi: 10.1111/j.1540-8159.2009.02685.x contributor: fullname: R Rodrigues Tda – volume: 58 start-page: 512 issue: 4 year: 2017 ident: 39338_CR13 publication-title: Epilepsia doi: 10.1111/epi.13709 contributor: fullname: IE Scheffer – volume: 36 start-page: 1167 issue: 8 year: 2020 ident: 39338_CR11 publication-title: Can. J. Cardiol. doi: 10.1016/j.cjca.2019.12.023 contributor: fullname: RK Sandhu – volume: 91 start-page: 219 issue: 3 year: 2006 ident: 39338_CR19 publication-title: Arch. Dis. Child doi: 10.1136/adc.2004.064477 contributor: fullname: P Uldall |
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Snippet | 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... Abstract The purpose of the study is to explore the use of Calgary scoring (CS) and Modified Calgary scoring (MCS) in the differentiation of genetic... |
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SubjectTerms | 631/378/1689/178 692/700/1720/3187 Differential diagnosis Epilepsy Fainting Genetics Humanities and Social Sciences multidisciplinary Patients Pediatrics Science Science (multidisciplinary) Statistical analysis Syncope |
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Title | Calgary score and modified calgary score in the differential diagnosis between syncope and genetic generalized epilepsy in children |
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