期刊文献+

大剂量地塞米松联合血小板生成素治疗免疫性血小板减少症临床观察 被引量:7

Clinical effect of large dose of dexamethasone combined with thrombopoietin in the treatment of immune thrombocytopenia
下载PDF
导出
摘要 目的评价大剂量地塞米松联合血小板生成素(TPO)治疗免疫性血小板减少症(ITP)的疗效及其对患者细胞免疫功能的影响。方法选取2015年6月至2018年1月就诊于广东医科大学附属医院的92例ITP患者,根据随机数表法分为对照组和联合组各46例。所有患者均接受大剂量地塞米松治疗,联合组在此基础上加用TPO治疗,30 d后比较两组患者的临床疗效、用药安全性,并观察治疗前后两组患者的血小板计数(PLT)和T、B淋巴细胞水平。结果联合组患者的治疗总有效率为91.30%,明显高于对照组的71.74%,差异有统计学意义(P<0.05);治疗7 d、14 d后,两组患者的PLT水平均呈上升趋势,联合组分别为(49.26±21.15)×109/L、(110.32±46.58)×109/L,均高于对照组的(40.61±20.47)×109/L、(92.15±40.27)×109/L,差异均有统计学意义(P<0.05);治疗30 d后,联合组患者的CD4+、CD4+/CD8+分别为(40.26±6.18)%、(1.34±0.64),均高于对照组的(34.11±5.76)%、(1.04±0.52),CD8+、CD19+/CD20+分别为(30.08±7.36)%、(15.17±4.49),均低于对照组的(36.82±9.36)%、(19.25±5.11),差异均有统计学意义(P<0.05);用药和随访期间联合组患者的不良反应发生率为4.35%,略低于对照组的13.04%,但差异无统计学意义(P>0.05)。结论大剂量地塞米松联合TPO治疗ITP有利于提高患者的PLT水平,调节免疫功能,其疗效确切且用药安全性较高。 Objective To evaluate the efficacy of large dose of dexamethasone combined with thrombopoietin(TPO) in the treatment of immune thrombocytopenia(ITP) and its influence on cellular immunity of patients.Methods A total of 92 ITP patients in the Affiliated Hospital of Guangdong Medical University from June 2015 to January 2018 were selected, and they were divided into control group and combined group by random number table, with46 patients in each group. All the patients were treated with large dose of dexamethasone, and on this basis, the combined group was additionally treated with TPO. The clinical efficacy and medication safety of patients in the two groups were compared after 30 days. The changes of blood platelet(PLT), T, B lymphocyte before and after treatment were observed. Results The total effective rate of the combined group(91.30%) was significantly higher than that in the control group(71.74%), P<0.05. After treatment for 7 d and 14 d, the PLT levels of two groups showed an increasing trend,but the levels in the combined group were significantly higher than those in the control group:(49.26 ± 21.15) × 109/L vs(40.61±20.47)×109/L for 7 d, P<0.05;(110.32±46.58)×109/L vs(92.15±40.27)×109/L for 14 d, P<0.05. After treatment for 30 d, the CD4+, CD4+/CD8+in combined group were(40.26±6.18)%,(1.34±0.64), which were significantly higher than(34.11±5.76)%,(1.04±0.52) in the control group, and the CD8+and CD19+/CD20+in the combined group were(30.08±7.36)%,(15.17±4.49), significantly lower than(36.82±9.36)%,(19.25±5.11) in the control group, all with statistically significant differences(P<0.05). The incidence of adverse reactions in the combined group during medication and follow-up(4.35%) was slightly lower than that in control group(13.04%), but there was no statistically significant difference(P>0.05). Conclusion Large dose of dexamethasone combined with TPO in treatment of ITP can increase the levels of PLT and regulate immune function, which has definite efficacy and higher medication safety.
作者 吴国才 李庆华 马境志 WU Guo-cai;LI Qing-hua;MA Jing-zhi(Department of Hematology,Zhanjiang Central People's Hospital,Zhanjiang 524000,Guangdong,CHINA;Department of Hematology,the Affiliated Hospital of Guangdong Medical University,Zhanfiang 524000,Guangdong,CHINA)
出处 《海南医学》 CAS 2019年第2期183-185,共3页 Hainan Medical Journal
基金 2018年广东省湛江市非资助科技攻关项目(编号:2018B01018)
关键词 免疫性血小板减少症 大剂量地塞米松 血小板生成素 临床疗效 细胞免疫 Immune thrombocytopenia Large dose of dexamethasone Thrombopoietin Clinical efficacy Cellular immunity
  • 相关文献

参考文献10

二级参考文献73

  • 1陈诚,王佳,李义德,郑晓敏,张晓春.免疫性血小板减少症患儿外周血CD4+CD25+调节T细胞和Th17细胞的变化[J].宁夏医科大学学报,2013,35(8):864-867. 被引量:8
  • 2杨默,夏文杰,李桂霞,庞雅轩,戚其威,李志光,吴香玲,吴浩强,冯国培,霍泰辉.中枢神经系统表达TPO受体的初步研究[J].中国实验血液学杂志,2004,12(4):494-497. 被引量:24
  • 3夏文杰,项鹏,杨默,冯国培,罗广平,张丽蓉,付涌水,汪传喜,李树浓.血小板生成素thrombopoietin对神经保护作用的体外研究[J].热带医学杂志,2007,7(7):622-625. 被引量:7
  • 4l张之南,郝玉书,赵永强.血液病学[M].2版.北京:人民卫生出版社,2012:459-461.
  • 5LONGA E Z, WEINSTEIN P R, CARLSON S, et al. Rev- ersible middle cerebralartery occlusion without crainiectomy in rat [ J ] .Stroke, 1989,20( 1 ) : 84-91.
  • 6GEDDIS A E, LINDEN H M, KAUSHANSKY K.Thrombo- poietin: a pan-hematopoietic cytokine [ J ]. Cytokine Growth Factor Rev,2002,13( 1 ) :61-73.
  • 7ZHOU J, LI J, ROSENBAUM D M, et al. Thrombopoietin protects the brain and improves sensorimotor functions: reduction of stroke-induced MMP-9 upregulaion and blood- brain barrier injury [ J ] .J Cereb Blood Flow Metab, 2011, 31(3) :924-933.
  • 8SUZUKI S, TANAKA K, NOGAWA S, et al. Phosphory- lation of signal transducer and activator of transcription-3 ( State 3 ) after focal cerebral ischemia in rats [ J ]. Exp Neuro1,2001,170( 1 ) :63-71.
  • 9WEN T C, PENG H, HATA R, et al. Induction of phos- phorylated of Stat 3 following focal cerebral ischemia in mice [J].Neurosci Lett,2001,303(3) :153-156.
  • 10BROWN S, ZEIDLER M P, HOMBRIA J E. JAK-STAT signaling in Drosophila controls cell motility during germ cell migration [ J ]. Dev Dyn, 2006,235 (4) : 958-966.

共引文献249

同被引文献70

引证文献7

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部