Back to Search Start Over

Role of aspirin and statin therapy in patients with cerebral cavernous malformations

Authors :
Mohamed M. Salem
Santiago Gomez-Paz
Kimberly P. Kicielinski
Justin M. Moore
Ajith J. Thomas
Luis C. Ascanio
Alejandro Enriquez-Marulanda
Georgios A Maragkos
Christopher S. Ogilvy
Michelle Lee
Source :
Journal of Clinical Neuroscience. 78:246-251
Publication Year :
2020
Publisher :
Elsevier BV, 2020.

Abstract

Stagnant blood flow and organizing thrombus are intralesional components of patients with cerebral cavernous malformations (CCM). Stasis and inflammation are mechanisms of growth, lesional instability and acute hemorrhages with or w/o symptoms. We evaluate the association of pre-diagnostic aspirin and/or statin use with acute hemorrhages at diagnosis. Patients with a CCM diagnosis were identified and categorized according to their medications on admission into four groups (no therapy, statin, aspirin, combined). The primary outcome was an acute hemorrhage (with or w/o symptoms) at diagnosis reported in a standardized manner from the T2 weighted magnetic resonance image. A multivariate generalized linear mixed models (GLMM) was utilized to conduct per-lesion analysis. We identified 446 patients with 635 lesions. An acute hemorrhage at diagnosis was observed in 31% of the patients. There were 328 patients without statin or aspirin therapy, 34% of whom presented with acute hemorrhage. Of patients on aspirin therapy at diagnosis, 25% presented with hemorrhage. Of patients on statin therapy, 26% had a hemorrhage at diagnosis. Combined therapy in 44 patients demonstrated a lower proportion of patients with acute hemorrhages (7 patients, 16% incidence). A GLMM showed that patients in the combined therapy group to have significantly lower odds of having an acute hemorrhage at diagnosis compared to the reference group of no therapy (OR 0.24; 95% CI 0.09–0.59; P = 0.002). Patients with a CCM receiving therapy with both aspirin and statins were less likely to present at diagnosis with acute hemorrhage.

Details

ISSN :
09675868
Volume :
78
Database :
OpenAIRE
Journal :
Journal of Clinical Neuroscience
Accession number :
edsair.doi.dedup.....6b2cd985aa53a24190a3640b7ac1cc85
Full Text :
https://doi.org/10.1016/j.jocn.2020.04.012