Incidence of residual perfusion defects by lung scintigraphy in patients treated with rivaroxaban compared with warfarin for acute pulmonary embolism

被引:4
|
作者
Lim, Ming Sheng [1 ]
Nandurkar, Dee [2 ]
Jong, Ian [2 ]
Cummins, Anita [1 ]
Tran, Huyen [3 ,4 ,5 ]
Chunilal, Sanjeev [1 ,5 ]
机构
[1] Monash Med Centre, Haematol Dept, Monash Hlth, Clayton Rd, Clayton, Vic 3168, Australia
[2] Diagnost Imaging, Monash Hlth, Melbourne, Vic, Australia
[3] Monash Univ, Australian Centre Blood Dis, Alfred Med Res, Educ Precinct, Melbourne, Vic, Australia
[4] Alfred Hosp, Clin Haematol Dept, Melbourne, Vic, Australia
[5] Monash Univ, Fac Med Nursing, Hlth Sci, Melbourne, Vic, Australia
关键词
Anticoagulants; Pulmonary embolism; Rivaroxaban; Ventilation-perfusion scan; Warfarin; UNPROVOKED VENOUS THROMBOEMBOLISM; TERM-FOLLOW-UP; COMPUTED-TOMOGRAPHY; RECANALIZATION RATE; 1ST EPISODE; HYPERTENSION; RECURRENCE; RESOLUTION; DIAGNOSIS; RISK;
D O I
10.1007/s11239-019-01944-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Residual perfusion defects (RPD) as detected by lung scintigraphy occur in over 50% of patients with acute pulmonary embolism (PE) treated with vitamin K antagonists but there is lack of data in patients treated with direct oral anticoagulants. The aim of this retrospective study was to estimate the incidence of RPD detected by ventilation perfusion (VQ) scan at 3-6 months in patients with first acute symptomatic PE treated with rivaroxaban compared to warfarin. Consecutive eligible patients treated with rivaroxaban as part of a previous study were identified. The Monash Health Radiology database was used to identify a historical cohort of age matched (+/- 5 years) patients treated with warfarin. Follow-up VQ scans were classified as normal (no perfusion defect) or abnormal (matched or unmatched perfusion defects) by two independent nuclear medicine physicians blinded to treatment. Any disagreement was resolved by consensus. One hundred and ninety patients with PE (95 in each cohort) were included (mean age 56.8 years; 41.1% males; 54.2% unprovoked). In the overall cohort, 31.1% had RPD with a significantly lower incidence of RPD in rivaroxaban treated patients 23.2% (95% CI 15.8-32.6), compared to warfarin 38.9% (95% CI 29.8-49.0). Treatment with rivaroxaban was associated with a significantly lower incidence of RPD detected by VQ scan at 3-6 months compared to warfarin. This supports recent in-vitro data suggesting an indirect enhancement of fibrinolysis by direct oral Xa inhibitors but requires confirmation in larger studies.
引用
收藏
页码:220 / 227
页数:8
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