TY - JOUR
T1 - Time in therapeutic range of anticoagulation among patients with atrial fibrillation and cerebral amyloid angiopathy
AU - Ward, Robert C.
AU - Graff-Radford, Jonathan
AU - Ponamgi, Shiva
AU - English, Stephen
AU - Meskill, Alayna
AU - Challa, Apurva B.
AU - Hodge, David O.
AU - Slusser, Joshua P.
AU - Rabinstein, Alejandro A.
AU - Asirvatham, Samuel J.
AU - Holmes, David
AU - DeSimone, Christopher V.
N1 - Funding Information:
This study was made possible using the resources of the Rochester Epidemiology Project, which is supported by the National Institute on Aging of the National Institutes of Health under award number R01AG034676. Additional support was given through K76 AG 57015. Dr. DeSimone is supported by the Earl A. Wood Career Development Award.
Publisher Copyright:
© Copyright © 2021 Baylor University Medical Center.
PY - 2022
Y1 - 2022
N2 - Atrial fibrillation (AF) and cerebral amyloid angiopathy (CAA) present risks of ischemic stroke and intracerebral hemorrhage (ICH). Vitamin K antagonist use is associated with fluctuations in international normalized ratio (INR), which predispose to a higher bleeding risk. Patients with a diagnosis of AF and ICH while on a vitamin K antagonist were identified using the Rochester Epidemiology Project. Sixty patients were identified (mean age 81.3 years; 24 men). Thirty-three (55%) exhibited characteristics consistent with possible (n = 25) or probable (n = 8) CAA. Mean time in therapeutic range in the 30 days preceding ICH was 55.4%, with no difference between CAA and non-CAA patients. Mean time spent above therapeutic range (INR > 3.0) was 17.7%, with no difference between CAA and non-CAA patients. Following ICH, 21 (35%) died within 30 days, with total mortality at 76.7% after 176.4 person-years of follow-up (mean 2.9 years). Time in therapeutic range in the 30 days prior to ICH had no significant impact on 7-day mortality, nor risk of recurrent ICH or ischemic stroke. Patients with warfarin-related ICH were often outside of the therapeutic range within the month preceding hemorrhage but more frequently were subtherapeutic. Even with careful avoidance of supratherapeutic INR, vitamin K antagonist use in CAA patients is unlikely to have a major effect in preventing ICH and must be used with caution.
AB - Atrial fibrillation (AF) and cerebral amyloid angiopathy (CAA) present risks of ischemic stroke and intracerebral hemorrhage (ICH). Vitamin K antagonist use is associated with fluctuations in international normalized ratio (INR), which predispose to a higher bleeding risk. Patients with a diagnosis of AF and ICH while on a vitamin K antagonist were identified using the Rochester Epidemiology Project. Sixty patients were identified (mean age 81.3 years; 24 men). Thirty-three (55%) exhibited characteristics consistent with possible (n = 25) or probable (n = 8) CAA. Mean time in therapeutic range in the 30 days preceding ICH was 55.4%, with no difference between CAA and non-CAA patients. Mean time spent above therapeutic range (INR > 3.0) was 17.7%, with no difference between CAA and non-CAA patients. Following ICH, 21 (35%) died within 30 days, with total mortality at 76.7% after 176.4 person-years of follow-up (mean 2.9 years). Time in therapeutic range in the 30 days prior to ICH had no significant impact on 7-day mortality, nor risk of recurrent ICH or ischemic stroke. Patients with warfarin-related ICH were often outside of the therapeutic range within the month preceding hemorrhage but more frequently were subtherapeutic. Even with careful avoidance of supratherapeutic INR, vitamin K antagonist use in CAA patients is unlikely to have a major effect in preventing ICH and must be used with caution.
KW - Anticoagulation
KW - atrial fibrillation
KW - cerebral amyloid angiopathy
KW - intracranial hemorrhage
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U2 - 10.1080/08998280.2021.2013393
DO - 10.1080/08998280.2021.2013393
M3 - Article
AN - SCOPUS:85121877817
SN - 0899-8280
VL - 35
SP - 162
EP - 167
JO - Baylor University Medical Center Proceedings
JF - Baylor University Medical Center Proceedings
IS - 2
ER -