利伐沙班用于肺栓塞患者维持期抗凝治疗的临床研究OA北大核心CSTPCD
Clinical trial of rivaroxaban in the treatment of anticoagulation in patients with pulmonary embolism during maintenance period
目的 比较不同剂量利伐沙班在肺血栓栓塞症(PTE)患者维持期抗凝治疗中的应用效果,并评估其获益-风险.方法 将PTE患者按队列法分为常规剂量组和低剂量组.常规剂量组给予利伐沙班每次15 mg,每天2次,3周后改为每次20 mg,每天1次;低剂量组给予利伐沙班每次10 mg,每天2次,3周后改为每次15 mg,每天1次,抗凝治疗时间均≥3个月.记录2组患者的临床疗效,比较治疗前及治疗3个月的血清指标[D-二聚体(D-D)、N末端脑钠肽前体(NT-proBNP)、肌钙蛋白Ⅰ(cTnⅠ)]、肝肾功能[谷丙转氨酶(GPT)、谷草转氨酶(GOT)、血尿素氮(BUN)、肌酸酐(Cr)],治疗后随访3个月,记录2组PTE复发、死亡等终点事件及出血事件发生情况.结果 常规剂量组入组42例,低剂量组入组44例.治疗3个月后,低剂量组和常规剂量组的总有效率均为100.00%,在统计学上差异无统计学意义(P>0.05).治疗3个月后,低剂量组和常规剂量组的血清D-D分别为(0.31±0.08)和(0.29±0.07)mg·L-1,NT-proBNP分别为(125.49±24.16)和(121.39±22.08)ng·L-1,cTn Ⅰ 分别为(0.02±0.00)和(0.02±0.00)µg·L-1,在统计学上差异均无统计学意义(均P>0.05).2组患者治疗前后GPT、GOT、BUN、Cr比较,在统计学上差异均无统计学意义(均P>0.05).低剂量组与常规剂量组随访期间出血事件总发生率分别为6.82%和23.81%,在统计学上差异有统计学意义(P<0.05).结论 相较于常规剂量的利伐沙班,低剂量利伐沙班具有相似的抗凝效果,但能降低PTE患者出血事件发生风险.
Objective To compare the application effect of different doses of rivaroxaban on anticoagulation therapy in patients with pulmonary thromboembolism(PTE)during maintenance period,and to evaluate its benefit-risk.Methods The patients with PTE were divided into conventional-dose group and low-dose group according to the cohort method.Conventional-dose group were given of rivaroxaban 15 mg,twice a day and changed to 20 mg once a day after 3 weeks;low-dose group were given rivaroxaban 10 mg twice a day and changed to 15 mg once a day after 3 weeks,and the anticoagulation treatment time in both groups was ≥ 3 months.The clinical efficacy in the two groups was recorded.Serum indicators[D-dimer(D-D),N-terminal pro-brain natriuretic peptide(NT-proBNP),cardiac troponin Ⅰ(cTn Ⅰ)]and liver-kidney function[glutamic-pyruvic transaminase(GPT),glutamic-oxaloacetic transaminase(GOT),blood urea nitrogen(BUN),creatinine(Cr)]were compared before treatment and after 3 months of treatment.The patients were followed up for 3 months after treatment,and the endpoint events such as PTE recurrence and death and the bleeding events were recorded in the two groups.Results There were 42 cases in conventional-dose group,44 cases in low-dose group.After 3 months of treatment,the total effective rates in low-dose group and conventional-dose group were both 100.00%,with no significant difference(P>0.05).After 3 months of treatment,serum D-D levels in low-dose group and conventional-dose group were(0.31±0.08)and(0.29±0.07)mg·L-1,NT-proBNP levels were(125.49±24.16)and(121.39±22.08)ng·L-1,cTn Ⅰ levels were(0.02±0.00)and(0.02±0.00)μg·L-1,all with significant differences(all P>0.05).There were no significant changes in GPT,GOT,BUN and Cr in the two groups before and after treatment(all P>0.05),and there were no statistically significant differences between the two groups(all P>0.05).The total incidences of bleeding events during follow-up was 6.82%in low-dose group and was 23.81%in conventional-dose group(P<0.05).Conclusion Compared with conventional-dose rivaroxaban,low-dose rivaroxaban has similar anticoagulant effect,but the latter one can better reduce the risk of bleeding events in patients with PTE.
钱会;刘魁;蒋亚林;赵侠
亳州市人民医院呼吸与危重症医学科,安徽亳州 236800
药学
利伐沙班片肺血栓栓塞症抗凝剂量复发出血
rivaroxabanpulmonary thromboembolismanticoagulationdoserecurrencebleeding
《中国临床药理学杂志》 2024 (007)
959-962 / 4
亳州市卫生健康委科研基金资助项目(bzwj2022b001)
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