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Published on: July 21, 2013
Does anticoagulation promote mural hematoma growth or delayed occlusion in spontaneous cervical artery dissections?
A Machet1, A C Fonseca, C Oppenheim
1Department of Neuroradiology, Université Paris-Descartes, Sorbonne Paris Cité, INSERM UMR 894, Centre Hospitalier Sainte-Anne, Paris, France.
Insights
Cervical artery dissection (CAD) treatment with anticoagulation (AC) or antiplatelet (AP) drugs showed similar, limited mural hematoma growth in about one-third of patients. Neither AC nor AP agents caused lumen narrowing or recurrent dissection.
Area of Science:
- Neurology
- Vascular Medicine
- Radiology
Background:
- Spontaneous cervical artery dissection (CAD) requires medical treatment to prevent ischemic stroke.
- Anticoagulant (AC) or antiplatelet (AP) drugs are used, but evidence from randomized trials is limited.
- Concerns exist that AC may enlarge the dissecting hematoma, potentially narrowing the artery lumen.
Purpose of the Study:
- To compare the evolution of mural hematoma in CAD patients treated with AP agents versus AC during the first week.
- To assess the impact of AC and AP treatments on arterial lumen patency and hematoma size using dedicated cervical MRI.
Main Methods:
- A comparative study using cervical MRI (T1-weighted fat-suppressed axial sequences) at admission and during the first week of treatment.
- Two readers measured mural hematoma volume, length, and lumen patency.
- Assessment for recurrent CAD, ischemic brain lesions, and hemorrhagic transformation was performed.
Main Results:
- 44 patients (31 AC, 13 AP) with 49 CAD events were analyzed.
- No recurrent CAD, lumen reduction, recurrent DWI lesions, or hemorrhagic transformation were observed in either group.
- Mean mural hematoma volume and length decreased in both groups, but approximately one-third of patients in each group showed some growth.
Conclusions:
- Limited mural hematoma growth occurred in about one-third of CAD patients irrespective of AC or AP treatment during the first week.
- Neither AC nor AP agents were found to promote lumen reduction or recurrent dissection in this study.
- Cervical MRI is crucial for monitoring mural hematoma evolution in CAD management.
Background:
In case of spontaneous cervical artery dissection (CAD), a medical treatment with anticoagulant or antiplatelet (AP) drugs would avoid the occurrence of an ischemic stroke. Although immediate anticoagulation (AC) is advocated, evidence from randomized trials is lacking. Since CAD is characterized by a mural accumulation of blood, the dissecting hematoma may enlarge under AC, with subsequent lumen narrowing. Although direct evidence of mural hematoma enlargement is lacking in the literature, such a complication may not only be theoretical. Magnetic resonance imaging (MRI) of the mural hematoma on transverse sections through the neck is the current diagnostic gold standard. Our aim was to compare the evolution of the mural hematoma in CAD during the first week after treatment initiation (AP agent: groupAP, AC: groupAC), using dedicated cervical MRI of the arterial wall.
Methods:
The study was -approved by the Ethics Committee of Ile de France III. Informed consent was waived. The manuscript was prepared in accordance with the STROBE statement. Fast spin-echo T1-weighted fat-suppressed axial sequences were performed at admission (MRI1) and during the first week after initiation of the treatment (MRI2). Two readers measured volumes, craniocaudal length of the mural hematoma and lumen patency, and searched for early recurrent CAD. They also searched for extension or recurrence of ischemic brain lesions and for hemorrhagic transformation on diffusion-weighted imaging (DWI) and gradient echo T2 (T2*) sequences, respectively.
Results:
The population included 44 patients (31 in groupAC, 13 in groupAP) with 49 CAD (35 carotid, 14 vertebral). Recurrent CAD and reduction of the lumen did not occur in either group. We did not observe recurrent DWI lesions or occurrence of hemorrhagic transformation. Interobserver agreement [intraclass correlation coefficient (95% CI)] was excellent for volume measurement [0.98 (0.97-0.99) and 0.99 (0.98-1.0) for volume1 and volume2, respectively]. While mean volumes and length of the mural hematoma decreased after treatment in both groups (volume: groupAC -13 ± 22%, groupAP -12 ± 24%, p = 0.33; length: groupAC -10 ± 27%, groupAP -10 ± 20%, p = 0.18), approximately one third of patients in each group had some growth of the mural hematoma as well as an increase in length.
Conclusion:
Limited growth of the mural hematoma was seen with both treatments in approximately one third of patients during the first week after treatment initiation. However, neither AC nor AP agents promote reduction of the lumen or recurrent dissection.
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