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Published on: September 4, 2017
Bleeding risk evaluation in cerebral cavernous malformation, the role of medications, and hemorrhagic factors: a
Alba Scerrati1,2, Giorgio Mantovani1,2, Francesco Travaglini1,2
1Departments of1Translational Medicine and.
Insights
Cerebral cavernous malformations (CCMs) bleeding risk is primarily predicted by lesion volume. Antithrombotic agents and propranolol may offer protection, while the HAS-BLED score did not correlate with increased bleeding risk in this study.
Area of Science:
- Neurology
- Vascular Biology
- Medical Diagnostics
Background:
- Cerebral cavernous malformations (CCMs) are vascular lesions with a significant annual rupture risk, leading to morbidity and mortality.
- Increasing diagnostic incidence necessitates improved patient risk stratification for rupture.
- The influence of patient coagulative status on CCM bleeding risk remains unclear, despite suggestions that certain medications may reduce bleeding.
Purpose of the Study:
- To evaluate the impact of radiological, clinical, and pharmacological factors on the bleeding risk of CCMs.
- To assess the predictive capability of the HAS-BLED score for CCM bleeding events.
Main Methods:
- A multicenter retrospective observational study was conducted.
- Data on imaging, clinical status, and therapy were collected from 257 patients with bleeding and nonbleeding CCMs.
- Univariate and multivariate logistic regression analyses identified predictors of bleeding.
Main Results:
- Lesion volume ≥ 300 mm³ was the sole significant predictor of bleeding (adjusted OR 3.11).
- Patients with bleeding CCMs were younger and less likely to have hypertension or use antiplatelet drugs and beta-blockers.
- A volume threshold of ≥ 300 mm³ demonstrated high specificity (78.2%) but limited sensitivity (36.7%) for predicting bleeding.
Conclusions:
- CCM lesion volume is the primary factor influencing bleeding risk.
- Antithrombotic agents and propranolol may confer a protective effect against CCM bleeding.
- The HAS-BLED score was not associated with an increased risk of bleeding in this cohort.
Objective:
Cerebral cavernous malformations (CCMs) are vascular lesions with an overall risk of rupture from 2% to 6% per year, which is associated with significant morbidity and mortality. The diagnostic incidence is increasing, so it is of paramount importance to stratify patients based on their risk of rupture. Data in the literature seem to suggest that specific medications, particularly antithrombotic and cardiovascular agents, are associated with a reduced risk of bleeding. However, the effect of the patient coagulative status on the cumulative bleeding risk remains unclear. The aim of this study was to assess the impact of different radiological, clinical, and pharmacological factors on the bleeding risk of CCMs and to assess the predictive power of an already validated scale for general bleeding risk, the HAS-BLED (hypertension, abnormal renal/liver function, stroke, bleeding history or predisposition, labile international normalized ratio, elderly, drugs/alcohol concomitantly).
Method:
This was a multicenter retrospective observational study. The authors collected imaging, clinical status, and therapy data on patients with bleeding and nonbleeding CCMs. Univariate analysis and subsequent multivariate logistic regression were performed between the considered variables and bleeding or nonbleeding status to identify potential independent predictors of bleeding.
Results:
The authors collected data on 257 patients (46.7% male, 25.3% with bleeding CCMs). Compared with patients with nonbleeding lesions, those with bleeding CCMs were younger, less frequently had hypertension, and less frequently required antiplatelet drugs and beta-blockers (all p < 0.05). Bleeding lesions, however, had significantly higher median volumes (1050 mm3 vs 523 mm3 , p < 0.001). On multivariate analyses, after adjusting for age, history of hypertension and diabetes, and use of antiplatelet drugs or beta-blockers, lesion volume ≥ 300 mm3 was the only significant predictor of bleeding (adjusted OR 3.11, 95% CI 1.09-8.86). When the diagnostic accuracy of different volume thresholds was explored, volume ≥ 300 mm3 showed a limited sensitivity (36.7%, 95% CI 24.6%-50.0%), but a high specificity 78.2% (95% CI 71.3%-84.2%), with an area under the curve of 0.57 (95% CI 0.51-0.64).
Conclusions:
This study supports previous findings that the CCM volume is the only factor influencing the bleeding risk. Antithrombotic agents and propranolol seem to have a protective role against the bleeding events. A high HAS-BLED score was not associated with an increased bleeding risk. Further studies are needed to confirm these results.
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