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find Keyword "血小板减少" 31 results
  • 婴儿特发性血小板减少性紫癜的临床分析

    目的 分析婴儿期特发性血小板减少性紫癜(ITP)的诱因、临床特点、实验室资料、治疗反应和转归,为临床治疗和预后评估提供依据。 方法 2007年1月-2008年6月共收治32例ITP住院婴儿,男20例,女12例,中位年龄5个月,对其临床特征、治疗、转归进行回顾性分析。 结果 32例中14例有前驱感染,5例发病前2周~3个月内有过疫苗预防接种史。病程<3 d者25例,3~7 d者5例,>7 d者2例。主要表现为不同程度的皮肤、黏膜出血(包括消化道出血)。治疗以地塞米松单独或联合静脉用人血丙种球蛋白冲击,并以适量泼尼松短期维持。出血停止并且血小板计数恢复正常<3 d者16例,3~7 d者14例,>7 d者2例。经地塞米松冲击治疗的21例中,3例停药后又复发,再次给予联合冲击治疗,均在1周内恢复。中位随访时间12个月,无1例转为慢性或难治性病例。 结论 婴儿ITP是一组预后良好的疾病,地塞米松单独或联合静脉用人血丙种球蛋白冲击是有效治疗。免疫接种引起的ITP预后亦佳。

    Release date:2016-09-08 09:16 Export PDF Favorites Scan
  • 脾脏原发性血管肉瘤合并骨髓纤维化并文献复习

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  • 维持性血液透析患者感染新型冠状病毒后并发免疫性血小板减少一例

    Release date:2024-08-21 02:11 Export PDF Favorites Scan
  • Expression and clinical significance of immune cell subsets in elderly patients with primary immune thrombocytopenia

    Objective To investigate the expression and clinical significance of T lymphocyte subsets, natural killer (NK) cells and CD19+ B cells in the elderly with primary immune thrombocytopenia (ITP) before and after treatment. Methods The elderly ITP patients diagnosed and treated in the Songjiang Hospital Affiliated to Shanghai Jiaotong University School of Medicine (preparatory stage) between January 2014 and June 2019 were retrospectively selected as the observation group. The healthy elderly in the same period were selected as the control group. According to the treatment, the observation group was divided into effective group and ineffective group. The expression levels of T lymphocyte subsets (CD3+, CD4+, CD8+ and CD4+/CD8+), NK cells and CD19+ B cells were observed and analyzed. Results A total of 75 subjects were included, including 35 in the observation group and 40 in the control group. The total effective rate was 85.71% (30/35). Before treatment, the expression levels of T lymphocyte subsets (CD3+, CD4+ and CD4+/CD8+) in the observation group were lower than those in the control group (P<0.05). There was no significant difference in other indexes between the two groups (P>0.05). After treatment, except for CD8+, the expression levels of T lymphocyte subsets (CD3+, CD4+ and CD4+/CD8+) in the observation group were higher than those before treatment (P<0.05). The expression levels of NK cells and CD19+ B cells were lower than those before treatment (P<0.05). The expression levels of T lymphocyte subsets (CD3+, CD4+ and CD4+/CD8+) in the effective group were higher than those before treatment (P<0.05), while the expression level of CD19+ B cells was lower than that before treatment (P<0.05). There was no significant difference in other indexes before and after treatment (P>0.05). There was no significant difference in the expression levels of T lymphocyte subsets (CD3+, CD4+, CD8+ and CD4+/CD8+), NK cells and CD19+ B cells in the ineffective group before and after treatment (P>0.05). Conclusions T lymphocyte subsets are abnormal in elderly ITP patients. The immune abnormality of T lymphocyte may be one of the reasons for elderly patients with ITP. With the improvement of therapeutic effect, immune cell subsets have also been improved.

    Release date:2022-06-27 09:55 Export PDF Favorites Scan
  • Effectiveness and Safety of Middle and Low-dose Gamma Globulin for Severe Idiopathic Thrombocytopenic Purpura: A Systematic Review

    ObjectiveTo systematically review the clinical effectiveness and safety of middle and low-dose gamma globulin for severe idiopathic thrombocytopenic purpurar (ITP). MethodsDatabases such as The Cochrane Library (Issue 2, 2013), PubMed, EMbase, CBM, CNKI and WanFang Data were searched to collect randomized controlled trials (RCTs) involving the effectiveness and safety of middle and low-dose gamma globulin for severe ITP from the date of their establishment to July 2013. Two reviewers independently screened studies according to the inclusion and exclusion criteria, extracted data and evaluated the methodological quality of included studies. Then meta-analysis was performed using RevMan 5.2 software. ResultsEleven RCTs involving 548 patients were included. The trial group (n=272) were treated with middle and low dose of gamma globulin, while the control group (n=276) were treated with high dose of gamma globulin. The results of meta-analyses showed that there were no significant differences between the two groups in the total effective rate (RR=0.95, 95%CI 0.87 to 1.04, P=0.30), overall response rate (RR=0.97, 95%CI 0.85 to 1.10, P=0.60) and excellence rate (RR=0.94, 95%CI 0.78 to 1.14, P=0.54). The outcomes of time effect such as the time of platelet starting to rise and haemostasis time between the two groups was similar without significant differences. However, the control group was superior to the trial group in the peak time of platelet. The results of meta-analysis for platelet count of different periods showed that no significant differences were found in platelet count of 3, 7, and 14 days after starting the treatment, so do the peak of platelet count. No severe side effects were reported by both groups. ConclusionMiddle and low-dose gamma globulin could achieve the similar effect with the high-dose gamma globulin in the treatment of ITP. However, more high-quality, large-scale, RCTs are required to validate these results.

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  • Clinical Efficacy of Combined Immunosuppressant Therapy on Chronic Refractory Immune Thrombocytopenia Purpura and Its Effects on the Level of Platelete-associated antibody

    ObjectiveTo observe the clinical efficacy of combined immunosuppressant therapy for patients with chronic refractory immune thrombocytopenia purpura (ITP) and its effects on platelete-associated antibody (PAIG) level. MethodsBetween February 2009 and February 2013, 22 patients with refractory ITP were randomly divided into immunosuppressive drugs combination treatment group and single drug treatment group. The combination treatment group was treated with methylprednisolone and intravenous immunoglobulin (IVIG), and after the fast increasing of platelet count, combined chemotherapy consisting of two or three kinds of immunosuppressive agents was adopted. The single treatment group was also treated with methylprednisolone and IVIG, but took only one immunosuppressive agent after the fast increasing of platelet count. The treatment maintained for 3 to 6 months. The duration of follow-up was 6-36 months. We used flow cytometry to detect PAIG of the patients. ResultsThe total effective rate of combination treatment group was 81.8%, significantly higher than that of the single treatment group (36.4%) (P<0.05). PAIG decreased obviously in both the two groups, and the PAIG level of the combination treatment group was much lower than that of the single treatment group (P<0.05). ConclusionImmunosuppresant combination chemotherapy is a powerful approach for patients with refractory ITP, and it can decrease patient's PAIG level simultaneously.

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  • 乙二胺四乙酸依赖的假性血小板减少症一例

    Release date:2016-09-07 02:34 Export PDF Favorites Scan
  • 狼疮肾炎伴血栓性血小板减少性紫癜一例

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  • 慢性/复发性原发免疫性血小板减少症合并抗 O 升高二例

    Release date:2017-10-27 11:09 Export PDF Favorites Scan
  • Laparoscopic Splenectomy for Idiopathic Thrombocytopenic Purpura in 20 Cases

    目的 探讨腹腔镜下脾切除术(LS)治疗特发性血小板减少性紫癜(ITP)的临床效果。方法 我院2003年1月至2008年8月期间行LS治疗ITP患者20例,将术前与术后1、2、7、14、30、90及180 d的血小板计数进行比较。结果 20例ITP患者均顺利完成LS,平均手术时间为156 min,术中出血平均50 ml,平均住院时间为9 d。完全停用药物14例; 4例患者术后需继续服用激素治疗,但激素用量较前明显减少; 无效2例。总有效率为90%。术后1、2、7、14、30、90及180 d的血小板数量分别为(251.6±91.4)×109/L、(312.6±90.1)×109/L、(343.2±103.7)×109/L、(300.0±98.2)×109/L、(175.6±42.6)×109/L、(151.8±42.1)×109/L及(207.0±53.4)×109/L,分别与术前〔(38.3±19.4)×109/L〕比较,经t检验,差异均有统计学意义(P<0.001)。结论 LS治疗ITP是可行和安全的,手术效果满意。

    Release date:2016-09-08 10:56 Export PDF Favorites Scan
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