Komirisetti Anjaneyulu, N. Madhavi, D. Manikyamba, V. V. Lakshmi
{"title":"研究镰状细胞性贫血患儿的临床特征并使用 2d 超声心动图评估其心功能","authors":"Komirisetti Anjaneyulu, N. Madhavi, D. Manikyamba, V. V. Lakshmi","doi":"10.36106/ijar/2303450","DOIUrl":null,"url":null,"abstract":"Introduction: Sickle-cell anemia (SCA), a severe form of sickle-cell disease, is a global hemoglobinopathy with a\nsignicant on affected individuals. The disease is characterized by a single point mutation in the β-globin gene, leading\nto the synthesis of unstable sickle haemoglobin (HbS). This results in HbS polymerization, oxidative stress, inammation, and endothelial\nactivation. Despite advancements in treatment strategies, mortality remains high in this population. Cardiac complications, although\nrecognized, are not well-explored. This study aims to investigate the clinical prole of children with SCA and assess cardiac function using 2D\nechocardiography.\nAims & Objectives:\n1.To assess clinical prole of children with sickle cell anemia\n2.Evaluation of cardiac function in them using 2D Echocardiography.\nMaterials and Methods:\nThis prospective observational study was conducted at a Government General Hospital, enrolling children aged 5 to 12 years with SCA.Detailed\ndemographic information, family history, and clinical data were collected. All enrolled children underwent investigations, including complete\nblood count (CBC) and 2D Echocardiography was performed by a cardiologist. Data was analysed with appropriate statistical methods. Results:\nThe study included 100 children with SCA, with a mean age of 8.7 years. Clinical presentations revealed a prevalence of vascular occlusion\n(73%), splenomegaly (14%), infections (7%), and hepatomegaly (6%). Electrocardiographic parameters indicated sinus bradycardia (24%), left\natrial enlargement (19%) and diastolic dysfunction (84%). Mean values of echocardiographic parameters were also reported. Hydroxyurea\ntherapy showed statically signicant improvement in haemoglobin levels, number of blood transfusions, hospital admissions and other clinical\nparameters. This study provides valuable insights into the clinical prole especially cardiac abnor Conclusions: malities among children with\nSCA.All SCA childrens should be routinely screened for cardiac abnormalities and counselled appropriately. The clinical benits of\nhydroxyurea therapy highlights the importance of early initiation of this drug in all childrens with SCA.","PeriodicalId":13502,"journal":{"name":"Indian journal of applied research","volume":"72 34","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"STUDY OF CLINICAL PROFILE OF CHILDREN WITH SICKLE CELL ANEMIA AND EVALUATION OF CARDIAC FUNCTION IN THEM USING 2D ECHOCARDIOGRAPHY\",\"authors\":\"Komirisetti Anjaneyulu, N. Madhavi, D. Manikyamba, V. V. Lakshmi\",\"doi\":\"10.36106/ijar/2303450\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: Sickle-cell anemia (SCA), a severe form of sickle-cell disease, is a global hemoglobinopathy with a\\nsignicant on affected individuals. The disease is characterized by a single point mutation in the β-globin gene, leading\\nto the synthesis of unstable sickle haemoglobin (HbS). This results in HbS polymerization, oxidative stress, inammation, and endothelial\\nactivation. Despite advancements in treatment strategies, mortality remains high in this population. Cardiac complications, although\\nrecognized, are not well-explored. This study aims to investigate the clinical prole of children with SCA and assess cardiac function using 2D\\nechocardiography.\\nAims & Objectives:\\n1.To assess clinical prole of children with sickle cell anemia\\n2.Evaluation of cardiac function in them using 2D Echocardiography.\\nMaterials and Methods:\\nThis prospective observational study was conducted at a Government General Hospital, enrolling children aged 5 to 12 years with SCA.Detailed\\ndemographic information, family history, and clinical data were collected. All enrolled children underwent investigations, including complete\\nblood count (CBC) and 2D Echocardiography was performed by a cardiologist. Data was analysed with appropriate statistical methods. Results:\\nThe study included 100 children with SCA, with a mean age of 8.7 years. Clinical presentations revealed a prevalence of vascular occlusion\\n(73%), splenomegaly (14%), infections (7%), and hepatomegaly (6%). Electrocardiographic parameters indicated sinus bradycardia (24%), left\\natrial enlargement (19%) and diastolic dysfunction (84%). Mean values of echocardiographic parameters were also reported. Hydroxyurea\\ntherapy showed statically signicant improvement in haemoglobin levels, number of blood transfusions, hospital admissions and other clinical\\nparameters. This study provides valuable insights into the clinical prole especially cardiac abnor Conclusions: malities among children with\\nSCA.All SCA childrens should be routinely screened for cardiac abnormalities and counselled appropriately. 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引用次数: 0
摘要
导言:镰状细胞性贫血(SCA)是镰状细胞病的一种严重形式,是一种全球性的血红蛋白病,对患者的cant。该病的特征是β-球蛋白基因发生单点突变,导致合成不稳定的镰状血红蛋白(HbS)。这导致 HbS 聚合、氧化应激、ammation 和内皮细胞活化。尽管治疗策略有所进步,但这一人群的死亡率仍然很高。心脏并发症虽然已被认识到,但尚未得到很好的研究。本研究旨在调查镰状细胞性贫血患儿的临床原le,并使用二维超声心动图评估心脏功能。Aims & Objectives:1.To assess clinical prole of children with sickle cell anemia2.Evaluation of cardiac function in them using 2D Echocardiography.材料与方法:本前瞻性观察研究在一家政府综合医院进行,共招募了5至12岁的镰状细胞性贫血患儿。收集了详细的人口学信息、家族史和临床数据。所有入组儿童均接受了包括全血细胞计数(CBC)在内的检查,并由心脏病专家进行了二维超声心动图检查。数据采用适当的统计方法进行分析。结果:该研究包括100名患有SCA的儿童,平均年龄为8.7岁。临床表现为血管闭塞(73%)、脾肿大(14%)、感染(7%)和肝肿大(6%)。心电图参数显示窦性心动过缓(24%)、左房扩大(19%)和舒张功能障碍(84%)。此外,还报告了超声心动图参数的平均值。羟基尿疗法在血红蛋白水平、输血次数、入院次数和其他临床参数方面都有显著的改善。这项研究为了解SCA患儿的临床,尤其是心脏异常提供了宝贵的见解。所有SCA患儿都应接受常规的心脏异常筛查,并给予适当的指导。羟基脲治疗的临床良,凸显了对所有SCA患儿尽早使用该药物的重要性。
STUDY OF CLINICAL PROFILE OF CHILDREN WITH SICKLE CELL ANEMIA AND EVALUATION OF CARDIAC FUNCTION IN THEM USING 2D ECHOCARDIOGRAPHY
Introduction: Sickle-cell anemia (SCA), a severe form of sickle-cell disease, is a global hemoglobinopathy with a
signicant on affected individuals. The disease is characterized by a single point mutation in the β-globin gene, leading
to the synthesis of unstable sickle haemoglobin (HbS). This results in HbS polymerization, oxidative stress, inammation, and endothelial
activation. Despite advancements in treatment strategies, mortality remains high in this population. Cardiac complications, although
recognized, are not well-explored. This study aims to investigate the clinical prole of children with SCA and assess cardiac function using 2D
echocardiography.
Aims & Objectives:
1.To assess clinical prole of children with sickle cell anemia
2.Evaluation of cardiac function in them using 2D Echocardiography.
Materials and Methods:
This prospective observational study was conducted at a Government General Hospital, enrolling children aged 5 to 12 years with SCA.Detailed
demographic information, family history, and clinical data were collected. All enrolled children underwent investigations, including complete
blood count (CBC) and 2D Echocardiography was performed by a cardiologist. Data was analysed with appropriate statistical methods. Results:
The study included 100 children with SCA, with a mean age of 8.7 years. Clinical presentations revealed a prevalence of vascular occlusion
(73%), splenomegaly (14%), infections (7%), and hepatomegaly (6%). Electrocardiographic parameters indicated sinus bradycardia (24%), left
atrial enlargement (19%) and diastolic dysfunction (84%). Mean values of echocardiographic parameters were also reported. Hydroxyurea
therapy showed statically signicant improvement in haemoglobin levels, number of blood transfusions, hospital admissions and other clinical
parameters. This study provides valuable insights into the clinical prole especially cardiac abnor Conclusions: malities among children with
SCA.All SCA childrens should be routinely screened for cardiac abnormalities and counselled appropriately. The clinical benits of
hydroxyurea therapy highlights the importance of early initiation of this drug in all childrens with SCA.