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WATCHMAN device-related thrombus successfully treated with apixaban A case report
被引:4
|作者:
Wong, Chun-Ka
[1
]
Chan, Pak-Hei
[1
]
Lam, Cheung-Chi
[1
]
Kwok, On-Hing
[2
]
Lam, Yat-Yin
[3
]
Siu, Chung-Wah
[1
]
机构:
[1] Univ Hong Kong, Dept Med, Cardiol Div, Happy Valley, Hong Kong, Peoples R China
[2] Hong Kong Sanat & Hosp, Cardiol Ctr, Happy Valley, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Prince Wales Hosp, Fac Med, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China
来源:
关键词:
apixaban;
atrial fibrillation;
device related thrombus;
left atrial appendage occlusion;
stroke;
LEFT ATRIAL APPENDAGE;
FIBRILLATION;
CLOSURE;
D O I:
10.1097/MD.0000000000008693
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Rationale: Among atrial fibrillation patients with high risk of bleeding, left atrial appendage occlusion has emerged as an alternative to long-term oral anticoagulation therapy for stroke prevention. Device-related thrombus remains a major concern because it may result in recurrent embolic events. To date, there is no consensus on the optimal method of treating device-related-thrombus. Patient concerns: A 78-year-old man with atrial fibrillation had an episode of intracranial hemorrhage while taking warfarin. He subsequently underwent percutaneous placement of a 30-mm Watchman device to the left atrial appendage. He was prescribed dual anti-platelet therapy with aspirin and clopidogrel. Diagnosis: Reassessment echocardiography 3 months later found device-related thrombus. Interventions: The antithrombotic regimen was switched from dual antiplatelet therapy to apixaban. Outcomes: Reassessment echocardiography 3 months later revealed complete resolution of the device-related thrombus. Apixaban was stopped. He had dual antiplatelet therapy for 6 more months followed by life-long aspirin. There was no bleeding complication since implantation of Watchman device. Lessons: We demonstrated successful treatment of device-related thrombus with a short course of apixaban with complete resolution of thrombus. Further randomized controlled trials are required to determine the choice and duration of drug therapy for device-related thrombus.
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