期刊文献+

低分子肝素预防高危深静脉置管的恶性肿瘤患者发生静脉血栓栓塞的效果研究 被引量:22

Effect of LMWH in VTE Prevention in High Risk Malignant Tumor Patients
下载PDF
导出
摘要 目的探讨低分子肝素在预防高危的深静脉置管的恶性肿瘤患者发生静脉血栓栓塞(VTE)中的效果。方法选择Caprini模型VTE风险度评分≥5分的31例深静脉置管的恶性肿瘤患者为研究对象,在深静脉置管后进行预防性低分子肝素治疗,分析治疗后血栓发生的情况和各项观察指标(年龄、性别、病种等)与血栓发生的关系。结果 (1)预防性低分子肝素治疗后的血栓发生率为9.7%(3/31);(2)31例患者的各项观察指标不同水平的血栓发生率比较,差异均无统计学意义(P>0.05);(3)3例发生血栓的患者均来源于17例(54.8%)有2项或2项以上高危因素(VTE风险度评分、D-二聚体异常、激素治疗)的患者,余14例(45.2%)有0~1项高危因素,但无一例发生血栓,两组血栓发生率比较,差异无统计学意义(P=0.23);(4)低分子肝素预防用药后D-二聚体及血小板计数异常的患者由5例下降至1例。结论低分子肝素预防用药可以在一定程度上减少深静脉置管后高危患者发生VTE,但需进一步开展前瞻性随机对照研究。 Objective To explore the effect of low molecular weight heparin(LMWH)in preventing high risk malignant tumor patients from venous thromboembolism(VTE).Methods Thirty-one malignant tumor patients evaluated as very high risk grade(≥5)of VTE by Caprini model were chosen as research objects.Prophylactic LMWH was conducted after deep venous catheter.The thrombosis incidence and observed indicators(age,gender,diseases,etc.)after treatment and their relationship were analyzed.Results After prophylactic LMWH,thrombosis incidence was 9.7%(3/31).No significant difference was noted in thrombosis incidence between 31 patients with different levels of observed indicators(P0.05).The 3 patients with thrombosis were among 17 patients(54.8%)having 2 or more risk factors,thrombosis did not occur in the other 14(45.2%)having 0~1 risk factor,the difference was not significant(P=0.23).The number of patients with abnormal D-dimer and platelet count dropped from 5 to 1 after prevent LMWH.Conclusion LMWH can reduce VTE incidence of high risk patients after deep venous cartheter,but some further,prospective,randomized and comparative studies should be conducted.
出处 《中国全科医学》 CAS CSCD 北大核心 2012年第33期3836-3838,共3页 Chinese General Practice
关键词 肝素 低分子量 预防 肿瘤 静脉血栓形成 Heparin low-molecular-weight Prevention Neoplasms Venous thrombosis
  • 相关文献

参考文献9

  • 1Blom JW, Doggen C J, Osanto S, et al. Malignancies, prothrombotic mutations, and the risk of venous thrombosis [J]. JAMA, 2005, 293 (6) : 715 -722.
  • 2Heit JA, Silverstein MD, Mohr DN, et al. Risk factors for deep vein thrombosis and pulmonary embolism: a population - based case - control study [J]. Arch Intern Med, 2000, 160 (6) : 809 -815.
  • 3Cunningham MS, White B, Hollywood D, et al. Primary thremboprophylaxis for cancer patients with central venous cathetersa reappraisal of the evidence [J]. Br J Cancer, 2006, 94 (2) : 189,194.
  • 4Geerts WH, Bergqvist D, Pineo GF, et al. Prevention of venous thromboembolism: American college of chest physicians evidence - based clinical practice guidelines (8th edition) [J]. Chest, 2008, 133 (6): 381-453.
  • 5Lyman GH, Khorana AA, Falanga A, et al. American society of clinical oncology guideline: recommendations for venous thromboembolism prophylaxis and treatment in patients with cancer [ J ]. J Clin Oncol, 2007, 25 (34) : 5490 - 5505.
  • 6Khorana AA, Francis CW, Culakova E. Thromboembolism is a leading cause of death in cancer patients receiving outpatient chemotherapy [J]. J Thromb Haemost, 2007, 5 (3) : 632 - 634.
  • 7Nalluri SR, Chu D, Keresztes R, et al. Risk of venous thromboembolism with the angiogenesis inhibitor bevacizumab in cancer patients: a meta-analysis [J]. JAMA, 2008, 300 (19): 2277-2285.
  • 8Khorana AA, Francis CW, Culakova E, et al. Thromboembolism in hospitalized neutronpenic cancer patients [ J ]. J Clin Oncol, 2006, 24 (3) : 484 - 490.
  • 9王金万,孙燕,刘永煜,于起涛,张沂平,李凯,朱允中,周清华,侯梅,管忠震,李维廉,庄武,王东林,梁后杰,秦凤展,卢辉山,刘晓晴,孙红,张燕军,王杰军,罗素霞,杨瑞合,涂远荣,王秀问,宋恕平,周静敏,游丽芬,王竞,姚晨.重组人血管内皮抑素联合NP方案治疗晚期NSCLC随机、双盲、对照、多中心Ⅲ期临床研究[J].中国肺癌杂志,2005,8(4):283-290. 被引量:625

二级参考文献31

  • 1杨林,王金万,汤仲明,刘秀文,黄镜,李树婷,董英,张和平,薛岚,储大同,孙燕.重组人血管内皮抑制素Ⅰ期临床研究[J].中国新药杂志,2004,13(6):548-553. 被引量:154
  • 2周清华,孙燕.加强我国肺癌分子靶向治疗基础和临床研究[J].中国肺癌杂志,2004,7(4):267-269. 被引量:51
  • 3杨林,王金万,崔成旭,黄镜,张和平,李树亭,孙燕.重组人血管内皮抑制素YH-16联合用药治疗晚期非小细胞肺癌的多中心Ⅱ期临床试验[J].中国新药杂志,2005,14(2):204-207. 被引量:116
  • 4Folkman J. Role of angiogenesis in tumor growth and metastasis.Semin Oncol,2002,29(6 Suppl 16) : 15-18.
  • 5Huang X, Wong MK, Zhao Q, et al. Soluble recombinant endostatinpurified from Escherichia coli: antiangiogenic activity and antitumor effect. Cancer Res,2001,61(2): 478-481. Erratum in:Cancer Res, 2001,61 ( 15 ) : 5956. Cancer Res, 2001,61 (10) :4297.
  • 6Li B, Wu XY, Zhou H, et al. Acid-induced unfolding mechanism of recombinant human endostatin. Biochemistry, 2004, 43 (9) :2550-2557.
  • 7Eder JP Jr, Supko JG, Clark JW, et al. Phase Ⅰ clinical trial of recombinant human endostatin administered as a short intravenous infusion repeated daily. J Clin Oncol, 2002,20(18) : 3772-3784.
  • 8Kulke M, Bergsland E, Ryan DP, et al. A phase Ⅱ , open-label,safety, pharmacokinetic, and efficacy study of recombinant human endostatin in patients with advanced neuroendocrine tumors. Proc ASCO,2003,22: 958a.
  • 9Scagliotti GV, De Marinis F, Rinaldi M, et al. Phase Ⅲ randomized trial comparing three platinum-based doublets in advanced nonsmall cell lung cancer. J Clin Oncol,2002,20(21) : 4285-4291.
  • 10Gebbia V, Galetta D, Caruso M, et al. Gemcitabine and cisplatin versus vinorelbine and cisplatin versus ifosfamide+gemcitabine fol lowed by vinorelbine and cisplatin versus vinorelbine and cisplatin followed by ifosfamide and gemcitabine in stage Ⅲ B-Ⅳ non small cell lung carcinoma: a prospective randomized phase Ⅲ trial of the Gruppo Oncologico Italia Meridionale. Lung Cancer,2003,39(2) :179-189.

共引文献624

同被引文献237

引证文献22

二级引证文献163

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