Abdullah Aloboudi, A. Al Hammad, Jaffar AlFaraj, Ali Al Hussain
{"title":"Correlation between skeletal manifestations of sickle cell disease (SCD) and transcranial doppler imaging velocities","authors":"Abdullah Aloboudi, A. Al Hammad, Jaffar AlFaraj, Ali Al Hussain","doi":"10.4103/njbcs.njbcs_57_22","DOIUrl":null,"url":null,"abstract":"Context: Sickle cell disease (SCD), a genetic disorder, is a debilitating illness. Among the different complications of SCD, cerebrovascular complication results in stroke in pediatric population. The cause of stroke in those patients is attributed to vasculopathy, stenosis, or vaso-occlusion of distal internal carotid arteries. Another body system that is commonly affected is the musculoskeletal system. Both skeletal manifestations and vasculopathy in Circle of Willis in SCD are known consequences of the same underlying pathology. Aim: This study was conducted to assess the correlation between osseous findings and vasculopathy of Circle of Willis. Settings and Design: It was a chart review study conducted during December 2021 to January 2022. Children suffering from SCD were the study population. Materials and Methods: The sampling was done by using convenience purposive sampling technique. The data were collected as observations using picture archiving and communication system and then entered Excel spreadsheet. Statistical Analysis Used: The data were analyzed using SPSS, Version 28. The descriptive statistics including frequencies and percentages for the skeletal manifestations and transcranial Doppler imaging (TCDI) readings were calculated. To assess the association between skeletal manifestations and TCDI, a Chi-square test of independence was performed. Results: The findings showed that abnormal TCDI readings exhibited higher frequency on abnormal skeletal manifestations as compared to normal TCDI readings. Conclusion: The study showed that an osseous manifestation of disease was associated with vasculopathy of Circle of Willis vasculature. Therefore, osseous manifestations of SCD can be associated with the chance of stroke among the children since it is associated with the vasculopathy of Circle of Willis.","PeriodicalId":19224,"journal":{"name":"Nigerian Journal of Basic and Clinical Sciences","volume":"9 1","pages":"66 - 69"},"PeriodicalIF":0.2000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nigerian Journal of Basic and Clinical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/njbcs.njbcs_57_22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Context: Sickle cell disease (SCD), a genetic disorder, is a debilitating illness. Among the different complications of SCD, cerebrovascular complication results in stroke in pediatric population. The cause of stroke in those patients is attributed to vasculopathy, stenosis, or vaso-occlusion of distal internal carotid arteries. Another body system that is commonly affected is the musculoskeletal system. Both skeletal manifestations and vasculopathy in Circle of Willis in SCD are known consequences of the same underlying pathology. Aim: This study was conducted to assess the correlation between osseous findings and vasculopathy of Circle of Willis. Settings and Design: It was a chart review study conducted during December 2021 to January 2022. Children suffering from SCD were the study population. Materials and Methods: The sampling was done by using convenience purposive sampling technique. The data were collected as observations using picture archiving and communication system and then entered Excel spreadsheet. Statistical Analysis Used: The data were analyzed using SPSS, Version 28. The descriptive statistics including frequencies and percentages for the skeletal manifestations and transcranial Doppler imaging (TCDI) readings were calculated. To assess the association between skeletal manifestations and TCDI, a Chi-square test of independence was performed. Results: The findings showed that abnormal TCDI readings exhibited higher frequency on abnormal skeletal manifestations as compared to normal TCDI readings. Conclusion: The study showed that an osseous manifestation of disease was associated with vasculopathy of Circle of Willis vasculature. Therefore, osseous manifestations of SCD can be associated with the chance of stroke among the children since it is associated with the vasculopathy of Circle of Willis.
背景:镰状细胞病(SCD)是一种遗传性疾病,是一种使人衰弱的疾病。在SCD的各种并发症中,脑血管并发症是导致儿童卒中的主要原因。这些患者中风的原因可归因于血管病变、狭窄或颈动脉远端血管闭塞。另一个常受影响的身体系统是肌肉骨骼系统。SCD中威利斯圈的骨骼表现和血管病变都是相同基础病理的结果。目的:本研究旨在评估威利斯环骨性表现与血管病变的相关性。设置和设计:这是2021年12月至2022年1月期间进行的一项图表审查研究。患有SCD的儿童是研究人群。材料与方法:采用方便目的抽样技术。使用图片存档和通讯系统收集数据作为观察,然后输入Excel电子表格。使用统计分析:数据分析使用SPSS, Version 28。计算描述性统计数据,包括骨骼表现的频率和百分比以及经颅多普勒成像(TCDI)读数。为了评估骨骼表现与TCDI之间的关系,进行了卡方独立性检验。结果:与正常TCDI读数相比,TCDI读数异常对骨骼异常表现的频率更高。结论:该疾病的骨性表现与威利斯循环血管病变有关。因此,SCD的骨骼表现可能与儿童中风的机会有关,因为它与威利斯环血管病变有关。