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首页> 外文期刊>Journal of Thoracic Disease >Effect of Huisheng oral solution on coagulation function in perioperative period in patients with primary lung cancer
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Effect of Huisheng oral solution on coagulation function in perioperative period in patients with primary lung cancer

机译:惠生口服液对原发性肺癌患者围手术期凝血功能的影响

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Background: The incidence of venous thromboembolism (VTE) is about 4–10% in lung cancer patients. Huisheng oral solution (HSOS) has been previously demonstrated to inhibit carageenan induced acute thrombosis in rats, reduce the incidence of thrombosis in the lungs and mesentery of tumor-bearing mice and inhibit tumor cell metastasis. The purpose of this study was to assess the anticoagulant effect of HSOS in lung cancer patients in the perioperative period. Methods: This study was a multicenter, randomized, single-blind, blank-controlled clinical trial. A total of patients at five hospitals in Hebei Province, China were included. The patients were randomly divided into study group or control group according to random number table. The primary outcome was the blood test indices in both groups. The study group was given oral HSOS (20 mL, bid) from admission until 24 h before surgery. If no active bleeding was observed, the patients were given oral HSOS (20 mL, tid) from 24 h to 24 d postoperatively. The patients in the study group did not receive any other anticoagulation therapy during the study period and the control group only underwent surgery. The study protocol was approved by the local ethics committee of principal investigator hospital. Blood samples were taken at admission (before therapy), 24 h, 72 h, 10 d (before discharge) and 24 d (first visit after discharge) after surgery. Routine blood tests [red blood cell (RBC) count, white blood cell (WBC) count, hemoglobin (HGB), and platelet (PLT) count] and coagulation function test [prothrombin time (PT), activated partial thromboplastin time (APTT), thrombin time (TT), fibrinogen (FIB), and plasma D-dimer] were performed. The changes in outcome measures over time were analyzed by repeated measures analysis of variance to compare the differences between groups and between different time points and assess the impact of tumor stage and mode of surgery on them. All tests were two-tailed, and P values Results: The results differed between different tumor stage groups. In stage III–IV group, there was no significant difference in various indices between the study group and control group. In stage I–II group, there was significant difference in hemoglobin (P=0.004), platelet count (P=0.007), fibrinogen (P=0.046), and plasma D-dimer (24 d: P=0.032) between two groups. Fibrinogen reach the peak 72 h after surgery, and other indices reach the peak 7–10 d postoperatively and declined one month after surgery, and the decline tendency was different between two groups. In addition, no adverse drug reaction was observed in both the study group and control group. Conclusions: HSOS (20 mL, tid) is of good safety profile and does not increase the risk of bleeding. With its unique characteristic of convenience for being taken, HSOS (20 mL, tid) could be a proper treatment for lung cancer patients in the perioperative period.
机译:背景:肺癌患者的静脉血栓栓塞(VTE)发生率约为4-10%。先前已证明惠生口服液(HSOS)抑制角叉菜胶诱发的大鼠急性血栓形成,降低肺部血栓形成和荷瘤小鼠肠系膜的发生率以及抑制肿瘤细胞转移。这项研究的目的是评估围手术期HSOS对肺癌患者的抗凝作用。方法:本研究是一项多中心,随机,单盲,空白对照的临床试验。包括中国河北省五家医院的患者。根据随机数字表将患者随机分为研究组或对照组。主要结果是两组的血液检查指标。从入院到手术前24小时,给研究组口服HSOS(20 mL,bid)。如果未观察到活动性出血,则在术后24 h至24 d给予患者口服HSOS(20 mL,tid)。在研究期间,研究组的患者未接受任何其他抗凝治疗,对照组仅接受了手术。研究方案已得到主要研究者医院当地伦理委员会的批准。入院时(治疗前),手术后24 h,72 h,10 d(出院前)和24 d(出院后首次就诊)采集血样。常规血液检查[红细胞(RBC)计数,白细胞(WBC)计数,血红蛋白(HGB)和血小板(PLT)计数]和凝血功能检查[凝血酶原时间(PT),活化的部分凝血活酶时间(APTT) ,凝血酶时间(TT),纤维蛋白原(FIB)和血浆D-二聚体]。通过重复测量方差分析来分析结局指标随时间的变化,以比较各组之间以及不同时间点之间的差异,并评估肿瘤分期和手术方式对其的影响。所有测试都是两尾的,P值结果:不同肿瘤阶段组的结果不同。在III–IV期组中,研究组和对照组之间的各项指标没有显着差异。在I–II期组中,两组之间的血红蛋白(P = 0.004),血小板计数(P = 0.007),纤维蛋白原(P = 0.046)和血浆D-二聚体(24 d:P = 0.032)存在显着差异。 。纤维蛋白原在术后72 h达到高峰,其他指标在术后7-10 d达到高峰,术后1个月下降,两组的下降趋势不同。此外,在研究组和对照组中均未观察到药物不良反应。结论:HSOS(20 mL,tid)具有良好的安全性,不会增加出血的风险。 HSOS(20 mL,tid)具有服用方便的独特特征,可以作为围手术期肺癌患者的适当治疗方法。

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