Child neurology open最新文献_第8页

Cross-Sectional Study of Headache in Flemish Children and Adolescents. 佛兰德儿童和青少年头痛的横断面研究。

Child neurology open Pub Date : 2022-01-01 DOI: 10.1177/2329048X221140783

Sarah Mingels, Marita Granitzer

{"title":"Cross-Sectional Study of Headache in Flemish Children and Adolescents.","authors":"Sarah Mingels, Marita Granitzer","doi":"10.1177/2329048X221140783","DOIUrl":"https://doi.org/10.1177/2329048X221140783","url":null,"abstract":"Background: Although headache is common in pediatrics, data for the Flemish population are missing. We explored headache-prevalence, and its association with communication-technology (CT) and physical activity (PA) in Flemish children and adolescents. Methods: A cross-sectional exploratory school-based questionnaire study was designed. Flemish boys and girls (5-18 years) completed a symptom-questionnaire. Primary outcomes: sociodemographic background, headache-prevalence, headache-characteristics, CT-use and PA characteristics (self-report). Secondary outcomes: associations between headache-characteristics, age, gender, and CT-use and PA-characteristics. Results: Four hundred twenty-four questionnaires were analysed: 5-7-years: n = 58; 8-11-years: n = 84; 12-15-years: n = 137; 16-18-years: n = 145. Fifty-five percent suffered from headache. Prevalence increased with age. More 16-18-year girls versus boys had headache. CT-use was the main headache-provocateur. Headache prevalence was significantly higher in a frequently physical active population. Conclusion: Our results suggest presence of headache in Flemish children and adolescents. PA-level associates with headache prevalence. However, children and adolescents with headache did not report more CT-use compared to controls.","PeriodicalId":72572,"journal":{"name":"Child neurology open","volume":"9 ","pages":"2329048X221140783"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/94/38/10.1177_2329048X221140783.PMC9720830.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10372037","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Startle Seizures and Diffuse Leukoencephalopathy After Resolution of Herpes Simplex Virus 1 Encephalitis in a Child 儿童单纯疱疹病毒1型脑炎消退后首发发作和弥漫性白质脑病

Child neurology open Pub Date : 2022-01-01 DOI: 10.1177/2329048X221083761

A. C. Ng, J. Kassiri, H. Goez, F. Morneau-Jacob, J. Mailo

引用次数: 0

Post-Concussive Orthostatic Tachycardia is Distinct from Postural Orthostatic Tachycardia Syndrome (POTS) in Children and Adolescents 儿童和青少年震荡后直立性心动过速与体位性直立性心动过速综合征（POTS）不同

Child neurology open Pub Date : 2022-01-01 DOI: 10.1177/2329048X221082753

R. Pearson, C. Sheridan, Kaylee Kang, A. Brown, Michael Baham, R. Asarnow, C. Giza, M. Choe

引用次数: 2

Neurologic Complications of Extracorporeal Cardiopulmonary Resuscitation in Neonates and Infants 新生儿和婴儿体外心肺复苏的神经系统并发症

Child neurology open Pub Date : 2022-01-01 DOI: 10.1177/2329048X221114970

M. Schmaedick, Devin Midura, Claire Gerall, D. Garey, W. Middlesworth, J. Bain

{"title":"Neurologic Complications of Extracorporeal Cardiopulmonary Resuscitation in Neonates and Infants","authors":"M. Schmaedick, Devin Midura, Claire Gerall, D. Garey, W. Middlesworth, J. Bain","doi":"10.1177/2329048X221114970","DOIUrl":"https://doi.org/10.1177/2329048X221114970","url":null,"abstract":"Objective: Extracorporeal membrane oxygenation (ECMO) is a lifesaving measure for patients in cardiac or respiratory failure. Extracorporeal cardiopulmonary resuscitation (ECPR) is emergent ECMO cannulation during cardiac arrest. All ECMO patients are at high risk for neurologic complications, but the degree of risk of ECPR relative to ECMO without CPR in progress (non-ECPR ECMO) is not well documented in infants. The goal of the present study is to compare neurologic complication rates between infants who underwent ECPR and those who underwent non-ECPR ECMO. Methods: We performed a retrospective chart review on all patients admitted between 2009 and 2020 to the neonatal intensive care unit (NICU) in our quaternary children's hospital. We separated patients by ECPR vs. non-ECPR ECMO cannulation. We compared rates of death and used neuroimaging and video electroencephalogram (vEEG) to determine incidence of stroke, intracranial hemorrhage, and seizure. Chi-square and Fisher's exact tests were used to compare these categorical variables among groups.Results: A total of 181 infants were cannulated onto ECMO. Of these, 40 received ECPR, 56 received non-ECPR ECMO for a cardiac indication, and 85 received non-ECPR ECMO for a respiratory indication. After excluding patients currently admitted (n=1, ECPR), 180 patients were subjected to analysis. ECPR patients were less likely to survive to hospital discharge than patients who underwent non-ECPR ECMO for respiratory indications, and less likely to survive without any neurologic complication compared with infants who underwent non-ECPR ECMO for cardiac or respiratory indications. Interpretation: Significantly fewer ECPR patients survived without experiencing a neurologic complication, compared with non-ECPR ECMO patients.","PeriodicalId":72572,"journal":{"name":"Child neurology open","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46908409","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

A Case of Infant-Type Hemispheric Glioma with NTRK1 Fusion. 婴儿型半球胶质瘤合并NTRK1融合1例。

Child neurology open Pub Date : 2022-01-01 DOI: 10.1177/2329048X221146982

Mekka R Garcia, Lena Bell, Claire Miller, Devorah Segal

引用次数: 0

Genetic Generalized Epilepsy and Intrafamilial Phenotypic Variability with Distal 7q11.23 Deletion 遗传性全身性癫痫和家族内表型变异与远端7q11.23缺失

Child neurology open Pub Date : 2022-01-01 DOI: 10.1177/2329048X221093173

Veronica Birca, K. Myers

引用次数: 0

Stroke Caused by Arterial Thoracic Outlet Syndrome in an Adolescent 青少年胸动脉出口综合征引起的脑卒中

Child neurology open Pub Date : 2022-01-01 DOI: 10.1177/2329048X221105743

Lindsay Schleifer, S. Vogel, A. Arun, Y. Lum, Courtney E. Lawrence, F. Hui, Lisa R. Sun

引用次数: 1

Refractory MOG-Associated Demyelinating Disease in a Pediatric Patient 顽固性mog相关性脱髓鞘疾病的儿科患者

Child neurology open Pub Date : 2022-01-01 DOI: 10.1177/2329048X221079093

Eve Kroenke, Alex Ankar, Nikita Malani Shukla

引用次数: 1

Faciobrachial Dystonic Seizures as a Sign of Relapse in a Child with LGI-1 Encephalitis 一例LGI-1型脑炎患儿的面臂强直性癫痫作为复发标志

Child neurology open Pub Date : 2022-01-01 DOI: 10.1177/2329048X221105960

WajdA Alotaibi, S. Bashir, A. Mir

{"title":"Faciobrachial Dystonic Seizures as a Sign of Relapse in a Child with LGI-1 Encephalitis","authors":"WajdA Alotaibi, S. Bashir, A. Mir","doi":"10.1177/2329048X221105960","DOIUrl":"https://doi.org/10.1177/2329048X221105960","url":null,"abstract":"We report an interesting case of a young girl with LGI1-antibody encephalitis who presented at 7 years old with very frequent seizures and severe neurocognitive decline. She responded very well to high dose corticosteroids and intravenous immunoglobulin (IVIG) initially but relapsed after 7 months. The relapse included frequent faciobrachial dystonic seizures (FBDS) that were successfully treated with rituximab. This case report highlights a few important points about LGI1-antibody encephalitis in children to help clinicians recognize this condition early and start prompt treatment with immunosuppressants. Data is lacking about LGI1-antibody encephalitis in children as it is mostly reported in adults. Our patient presented with frequent drug-resistant seizures including FBDS, along with amnesia, confusion, medial temporal lobe involvement, and hyponatremia similar to the presentation in adults. In contrast, none of the patients in the recent systematic review had FBDS or hyponatremia, making our case unique and suggesting variability in clinical presentation in children similar to adults. To our knowledge, FBDS have never been reported in children and our patient was initially misdiagnosed as having Childhood Epilepsy with Centrotemporal spikes. Since receiving rituximab, our patient is seizure-free for 1 year and 9 months and was successfully weaned of topiramate. She is going to school and has normal attention, concentration, memory, and mood. We propose early consideration of rituximab to accelerate recovery and prevent relapse.","PeriodicalId":72572,"journal":{"name":"Child neurology open","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49427675","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 1

A Favorable Treatment Outcome in RANBP2 and Influenza Associated Acute Necrotizing Encephalitis. RANBP2和流感相关急性坏死性脑炎的良好治疗结果

Child neurology open Pub Date : 2022-01-01 DOI: 10.1177/2329048X221143689

Fernando Galan, Douglas R Nordli, Milad Yazdani, Jessica Klein

引用次数: 1