Albabtain Monirah A, Alhebaishi Yahya, Al-Yafi Ola, Kheirallah Hatim, Othman Adel, Alghosoon Haneen, Arafat Amr A, Alfagih Ahmed
Pharmacy Department, Prince Sultan Cardiac Center, Riyadh, Saudi Arabia.
Adult Cardiology Department, Prince Sultan Cardiac Center, Riyadh, Saudi Arabia.
Egypt Heart J. 2021 May 1;73(1):41. doi: 10.1186/s43044-021-00164-7.
Rivaroxaban has been recently introduced for the management of non-valvular intra-cardiac thrombosis with variable results. We aimed to compare the results of the off-label use of rivaroxaban versus warfarin in the management of patients with left ventricle (LV) thrombus. This research is a retrospective study conducted on 63 patients who had LV thrombus from January to December 2016. We compared patients treated with warfarin (n=35) to patients who had rivaroxaban (n=28), and study outcomes were time to thrombus resolution, bleeding, stroke, and mortality.
The median duration of treatment was 9.5 (25th-75th percentiles: 6-32.5) months for rivaroxaban and 14 (3-41) months for warfarin. Thrombus resolution occurred in 24 patients in the warfarin group (68.6%) and 20 patients in the rivaroxaban group (71.4%). The median time to resolution in the warfarin group was 9 (4-20) months and 3 (2-11.5) months in the rivaroxaban group. Thrombus resolution was significantly faster in patients on rivaroxaban (p= 0.019). Predictors of thrombus resolution were thrombus surface area (HR: 1.21; CI 95% (1.0-1.46); p= .048) and the use of rivaroxaban (HR: 1.92; CI 95% (1.01-3.65); p= 0.048). There was no difference in stroke, bleeding, and mortality between both groups.
Rivaroxaban was as effective and safe as warfarin in managing patients with left ventricle thrombus. Larger randomized clinical trials are recommended to confirm our findings.
利伐沙班最近被用于非瓣膜性心内血栓的治疗,但其效果不一。我们旨在比较利伐沙班与华法林在左心室(LV)血栓患者治疗中的非适应证使用效果。本研究是一项回顾性研究,对2016年1月至12月期间63例患有LV血栓的患者进行。我们将接受华法林治疗的患者(n = 35)与接受利伐沙班治疗的患者(n = 28)进行比较,研究结果包括血栓溶解时间、出血、中风和死亡率。
利伐沙班治疗的中位持续时间为9.5(第25 - 75百分位数:6 - 32.5)个月,华法林为14(3 - 41)个月。华法林组24例患者(68.6%)血栓溶解,利伐沙班组20例患者(71.4%)血栓溶解。华法林组血栓溶解的中位时间为9(4 - 20)个月,利伐沙班组为3(2 - 11.5)个月。接受利伐沙班治疗的患者血栓溶解明显更快(p = 0.019)。血栓溶解的预测因素是血栓表面积(HR:1.21;95%CI(1.0 - 1.46);p = 0.048)和利伐沙班的使用(HR:1.92;95%CI(1.01 - 3.65);p = 0.048)。两组之间的中风、出血和死亡率没有差异。
在治疗左心室血栓患者方面,利伐沙班与华法林同样有效且安全。建议进行更大规模的随机临床试验以证实我们的发现。