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Warfarin-induced intracerebral hemorrhage associated with microbleeds
Gha-Hyun Lee1, Sun U Kwon, Dong-Wha Kang
1Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Background:
Microbleeds (MBs), proposed as a biomarker for microangiopathy, have been suggested as a predictor of spontaneous or thrombolysis-related intracerebral hemorrhage (ICH) in acute ischemic stroke. However, the relationship between MBs and warfarin-induced ICH is not clear.
Case Report:
We describe two patients who developed warfarin-induced ICH at the site of MBs documented in previous MRI.
Conclusions:
The presence of MBs might increase the risk of ICH after warfarin use in ischemic stroke patients. A large cohort study is required to confirm the relationship of MBs with warfarin-induced ICH.
Insights
Microbleeds (MBs) may increase the risk of warfarin-induced intracerebral hemorrhage (ICH) in acute ischemic stroke patients. Further research is needed to confirm this association.
Area of Science:
- Neurology
- Radiology
Background:
- Cerebral microbleeds (MBs) are potential biomarkers for microangiopathy.
- MBs may predict spontaneous or thrombolysis-related intracerebral hemorrhage (ICH) in acute ischemic stroke.
- The link between MBs and warfarin-induced ICH remains unclear.
Purpose of the Study:
- To investigate the relationship between pre-existing microbleeds and the occurrence of warfarin-induced ICH.
- To present case studies of patients experiencing ICH at MB sites after warfarin administration.
Main Methods:
- Case report methodology.
- Review of previous MRI scans to identify documented microbleeds.
- Analysis of patient cases involving warfarin-induced ICH.
Main Results:
- Two cases of warfarin-induced ICH were identified.
- ICH occurred at the specific sites of previously documented MBs.
Conclusions:
- The presence of MBs may elevate the risk of ICH in ischemic stroke patients using warfarin.
- Larger cohort studies are necessary to validate the association between MBs and warfarin-induced ICH.
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