...
首页> 外文期刊>Journal of Natural Sciences Research >Growth Parameters Changes (Weight and Height ) in DCM with Acute and Chronic LV Dysfunction
【24h】

Growth Parameters Changes (Weight and Height ) in DCM with Acute and Chronic LV Dysfunction

机译:DCM中急性和慢性LV功能不全的生长参数变化(体重和身高)

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Background: The growth failure is one of the most significant problem in children with dilated cardiomyopathy, one third of those with DCM have growth failure . Echocardiography regarded as the corner stone in the diagnosis of dilated cardiomyopathy. Material and methods: This study included 48 child with dilated cardiomyopathy with LV dysfunction, that diagnosed clinically by history, clinical examination, electrocardiography and echocardiography, including 2D-echocardiography, M-mode and Doppler study. Those patient were subdivided to 15 child present with acute heart failure (Acute DCM) (8 female and 7 male), and 33 child who are known cases of dilated cardiomyopathy reported in the cardiology out clinic with chronic LV dysfunction (18 female and 15 male) ,both groups followed for one year with regular clinical, laboratory and echocardiographic evaluation during treatment coarse for LV dysfunction. another 48 control healthy child with same age groups involved in the study (25 female and 23male), the age of both patient and control groups ranging from 1month- 12 years. Results: All patient had LV dysfunction at the time of attendance . In this study, most patient that had DCM with acute LV dysfunction had normal weight and height at the time of attendance, but after one year , those with LV dysfunction in spite of treatment had defective weight and height, but those with chronic LV dysfunction, that develop normal cardiac function after one year of treatment will improve their weight and height after one year treatment and follow up. Conclusions: Most children with chronic dilated cardiomyopathy have delayed growth regarding weight and height with decrease hemoglobin level .The improvement in the cardiac function of some patients usually followed by increment in their body weight and height over the periods of follow up.
机译:背景:生长障碍是扩张型心肌病患儿最严重的问题之一,DCM患儿中有三分之一患有生长障碍。超声心动图被认为是扩张型心肌病诊断的基石。资料和方法:这项研究包括48例患有LV功能障碍的扩张型心肌病患儿,该患儿通过病史,临床检查,心电图和超声心动图进行临床诊断,包括2D超声心动图,M型和多普勒研究。这些患者被细分为15例患有急性心力衰竭的儿童(急性DCM)(8例女性和7例男性),以及33例慢性左室功能不全的心脏病学门诊报告的已知扩张性心肌病的儿童(18例女性和15例男性) ),两组均在治疗过程中定期进行了为期一年的定期临床,实验室和超声心动图评估,以评估左室功能不全。另有48名健康对照儿童,年龄相同,分别为25位女性和23位男性,患者和对照组的年龄均为1个月至12岁。结果:所有患者在就诊时均患有左室功能不全。在这项研究中,大多数患有LV急性功能障碍的DCM患者出诊时体重和身高均正常,但一年后,尽管经过治疗但患有LV功能障碍的患者体重和身高均存在缺陷,而患有慢性LV功能障碍的患者,治疗一年后恢复正常心功能的患者,治疗一年后将改善体重和身高,并进行随访。结论:大多数慢性扩张型心肌病患儿体重和身高发育迟缓,血红蛋白水平降低。某些患者的心功能改善通常在随访期内体重和身高增加。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号