首页> 外国专利> METHOD FOR DIAGNOSIS OF MACROPHAGE ACTIVATION SYNDROME IN PATIENTS WITH ACTIVE SYSTEM JUVENILE IDIOPATHIC ARTHRITIS

METHOD FOR DIAGNOSIS OF MACROPHAGE ACTIVATION SYNDROME IN PATIENTS WITH ACTIVE SYSTEM JUVENILE IDIOPATHIC ARTHRITIS

机译:活动系统少年特发性关节炎患者巨噬细胞活化综合征的诊断方法

摘要

FIELD: medicine.;SUBSTANCE: method relates to paediatric rheumatology, immunology and haematology and can be used for early diagnosis of severe life-threatening complication of systemic juvenile idiopathic arthritis (SJIA) - macrophage activation syndrome (MAS). Method comprises analysis of biochemical parameters of blood and urine. In presence of at least three values of following parameters: reduced number of platelets ≤211×109/l, reduced number of leukocytes ≤9.9×109/l, increased AST59.7 E/l, increased LDG882 E/l, reduced albumin ≤29 g/l, increased ferritin 400 mcg/l, reduced fibrinogen ≤1.8 g/l and the presence of proteinuria 1.0 g/24 hours, macrophage activation syndrome is diagnosed.;EFFECT: using presented diagnostic technique enables early and highly accurate diagnosis of developing early macrophage activation syndrome with 100% sensitivity and specificity.;1 cl, 3 ex
机译:领域:方法与小儿风湿病学,免疫学和血液学有关,可用于早期诊断严重的威胁生命的系统性幼年特发性关节炎(SJIA)-巨噬细胞活化综合征(MAS)并发症。方法包括分析血液和尿液的生化参数。存在至少三个以下参数值时:血小板数量减少≤211×109 / l,白细胞减少数量≤9.9×109 / l,AST> 59.7 E / l增加,LDG> 882 E / l增加,减少白蛋白≤29g / l,铁蛋白> 400 mcg / l,纤维蛋白原减少≤1.8g / l,蛋白尿<1.0 g / 24小时,诊断为巨噬细胞活化综合征。高度准确地诊断发展中的早期巨噬细胞活化综合征,灵敏度和特异性为100%。; 1 cl,3 ex

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

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