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. 2017 Jul;9(7):1891-1902.
doi: 10.21037/jtd.2017.06.64.

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

Xiaoguang Yang et al. J Thorac Dis. 2017 Jul.

Abstract

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 <0.05 were considered statistically significant.

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.

Keywords: Huisheng oral solution (HSOS); coagulation function; primary lung cancer.

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Conflict of interest statement

Conflicts of Interest: The authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Flowchart illustrating the process of patient enrollment.
Figure 2
Figure 2
Changes in HGB over time in stages I–II patients. HGB, hemoglobin.
Figure 3
Figure 3
Changes in PLT over time in stages I–II patients. PLT, platelet.
Figure 4
Figure 4
Changes in FIB over time in stages I–II patients. FIB, fibrinogen.
Figure 5
Figure 5
Changes in D-dimer over time in stages I–II patients.

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References

    1. Farge D, Durant C, Villiers S, et al. Lessons from French National Guidelines on the treatment of venous thrombosis and central venous catheter thrombosis in cancer patients. Thromb Res 2010;125:S108-116. 10.1016/S0049-3848(10)70027-X - DOI - PubMed
    1. The Ministry of Health of the People’s Republic of China. Third national retrospect spot-check of death-causation. Beijing: Peking Union Medical College Press, 2008.
    1. Tagalakis V, Levi D, Agulnik JS, et al. High risk of deep vein thrombosis in patients with non-small cell lung cancer: a cohort study of 493 patients. J Thorac Oncol 2007;2:729-34. 10.1097/JTO.0b013e31811ea275 - DOI - PubMed
    1. Heit JA, Silverstein MD, Mohr DN, et al. Risk factors for deep vein thrombosis and pulmonary embolism: a population-based case-control study. Arch Intern Med 2000;160:809-15. 10.1001/archinte.160.6.809 - DOI - PubMed
    1. Cavo M, Zamagni E, Cellini C, et al. Deep-vein thrombosis in patients with multiple myeloma receiving first-line thalidomide-dexamethasone therapy. Blood 2002;100:2272-3. 10.1182/blood-2002-06-1674 - DOI - PubMed

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