TY - JOUR
T1 - Long-term antithrombotic therapy and risk of intracranial haemorrhage from cerebral cavernous malformations
T2 - a population-based cohort study, systematic review, and meta-analysis
AU - Zuurbier, Susanna M.
AU - Hickman, Charlotte R.
AU - Tolias, Christos S.
AU - Rinkel, Leon A.
AU - Leyrer, Rebecca
AU - Flemming, Kelly D.
AU - Bervini, David
AU - Lanzino, Giuseppe
AU - Wityk, Robert J.
AU - Schneble, Hans Martin
AU - Sure, Ulrich
AU - Al-Shahi Salman, Rustam
N1 - Funding Information:
This study was supported by the Medical Research Council (clinical training fellowship G84/5176, clinician scientist fellowship G108/613, and senior clinical fellowship G1002605), the Chief Scientist Office of the Scottish Government (project grants K/MRS/50/C2704 and CZB/4/35), and the Stroke Association (project grant TSA04/01). SMZ was supported by the Remmert Adriaan Laan Foundation and Cavernoma Alliance UK (Caver-no-more 2030 essay prize). We thank Rosemary Anderson, Aidan Hutchison, and all the patients and collaborators in the Scottish Audit of Intracranial Vascular Malformations.
Funding Information:
This study was supported by the Medical Research Council (clinical training fellowship G84/5176 , clinician scientist fellowship G108/613, and senior clinical fellowship G1002605), the Chief Scientist Office of the Scottish Government (project grants K/MRS/50/C2704 and CZB/4/35 ), and the Stroke Association (project grant TSA04/01). SMZ was supported by the Remmert Adriaan Laan Foundation and Cavernoma Alliance UK (Caver-no-more 2030 essay prize). We thank Rosemary Anderson, Aidan Hutchison, and all the patients and collaborators in the Scottish Audit of Intracranial Vascular Malformations.
Funding Information:
SMZ reports a grant from Remmert Adriaan Laan Foundation, during the conduct of the study. RA-SS reports grants from Medical Research Council, the Chief Scientist Office of the Scottish Government, and The Stroke Association during the conduct of the study; and consultancy fees from BiovelocITA, paid to the University of Edinburgh, outside the submitted work. All other authors declare no competing interests.
Publisher Copyright:
© 2019 The Authors. Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
PY - 2019/10
Y1 - 2019/10
N2 - Background: Antithrombotic (anticoagulant or antiplatelet) therapy is withheld from some patients with cerebral cavernous malformations, because of uncertainty around the safety of these drugs in such patients. We aimed to establish whether antithrombotic therapy is associated with an increased risk of intracranial haemorrhage in adults with cerebral cavernous malformations. Methods: In this population-based, cohort study, we used data from the Scottish Audit of Intracranial Vascular Malformations, which prospectively identified individuals aged 16 years and older living in Scotland who were first diagnosed with a cerebral cavernous malformation during 1999–2003 or 2006–10. We compared the association between use of antithrombotic therapy after first presentation and the occurrence of intracranial haemorrhage or persistent or progressive focal neurological deficit due to the cerebral cavernous malformations during up to 15 years of prospective follow-up with multivariable Cox proportional hazards regression assessed in all individuals identified in the database. We also did a systematic review and meta-analysis, in which we searched Ovid MEDLINE and Embase from database inception to Feb 1, 2019, to identify comparative studies to calculate the intracranial haemorrhage incidence rate ratio according to antithrombotic therapy use. We then generated a pooled estimate using the inverse variance method and a random effects model. Findings: We assessed 300 of 306 individuals with a cerebral cavernous malformation who were eligible for study. 61 used antithrombotic therapy (ten [16%] of 61 used anticoagulation) for a mean duration of 7·4 years (SD 5·4) during follow-up. Antithrombotic therapy use was associated with a lower risk of subsequent intracranial haemorrhage or focal neurological deficit (one [2%] of 61 vs 29 [12%] of 239, adjusted hazard ratio [HR] 0·12, 95% CI 0·02–0·88; p=0·037). In a meta-analysis of six cohort studies including 1342 patients, antithrombotic therapy use was associated with a lower risk of intracranial haemorrhage (eight [3%] of 253 vs 152 [14%] of 1089; incidence rate ratio 0·25, 95% CI 0·13–0·51; p<0·0001; I2=0%). Interpretation: Antithrombotic therapy use is associated with a lower risk of intracranial haemorrhage or focal neurological deficit from cerebral cavernous malformations than avoidance of antithrombotic therapy. These findings provide reassurance about safety for clinical practice and require further investigation in a randomised controlled trial. Funding: UK Medical Research Council, Chief Scientist Office of the Scottish Government, The Stroke Association, Cavernoma Alliance UK, and the Remmert Adriaan Laan Foundation.
AB - Background: Antithrombotic (anticoagulant or antiplatelet) therapy is withheld from some patients with cerebral cavernous malformations, because of uncertainty around the safety of these drugs in such patients. We aimed to establish whether antithrombotic therapy is associated with an increased risk of intracranial haemorrhage in adults with cerebral cavernous malformations. Methods: In this population-based, cohort study, we used data from the Scottish Audit of Intracranial Vascular Malformations, which prospectively identified individuals aged 16 years and older living in Scotland who were first diagnosed with a cerebral cavernous malformation during 1999–2003 or 2006–10. We compared the association between use of antithrombotic therapy after first presentation and the occurrence of intracranial haemorrhage or persistent or progressive focal neurological deficit due to the cerebral cavernous malformations during up to 15 years of prospective follow-up with multivariable Cox proportional hazards regression assessed in all individuals identified in the database. We also did a systematic review and meta-analysis, in which we searched Ovid MEDLINE and Embase from database inception to Feb 1, 2019, to identify comparative studies to calculate the intracranial haemorrhage incidence rate ratio according to antithrombotic therapy use. We then generated a pooled estimate using the inverse variance method and a random effects model. Findings: We assessed 300 of 306 individuals with a cerebral cavernous malformation who were eligible for study. 61 used antithrombotic therapy (ten [16%] of 61 used anticoagulation) for a mean duration of 7·4 years (SD 5·4) during follow-up. Antithrombotic therapy use was associated with a lower risk of subsequent intracranial haemorrhage or focal neurological deficit (one [2%] of 61 vs 29 [12%] of 239, adjusted hazard ratio [HR] 0·12, 95% CI 0·02–0·88; p=0·037). In a meta-analysis of six cohort studies including 1342 patients, antithrombotic therapy use was associated with a lower risk of intracranial haemorrhage (eight [3%] of 253 vs 152 [14%] of 1089; incidence rate ratio 0·25, 95% CI 0·13–0·51; p<0·0001; I2=0%). Interpretation: Antithrombotic therapy use is associated with a lower risk of intracranial haemorrhage or focal neurological deficit from cerebral cavernous malformations than avoidance of antithrombotic therapy. These findings provide reassurance about safety for clinical practice and require further investigation in a randomised controlled trial. Funding: UK Medical Research Council, Chief Scientist Office of the Scottish Government, The Stroke Association, Cavernoma Alliance UK, and the Remmert Adriaan Laan Foundation.
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U2 - 10.1016/S1474-4422(19)30231-5
DO - 10.1016/S1474-4422(19)30231-5
M3 - Article
C2 - 31401075
AN - SCOPUS:85071968173
SN - 1474-4422
VL - 18
SP - 935
EP - 941
JO - The Lancet Neurology
JF - The Lancet Neurology
IS - 10
ER -