TY - JOUR
T1 - Safety Outcomes of Antiplatelet Therapy During Endovascular Treatment of Tandem Lesions in Acute Ischemic Stroke Patients
AU - Farooqui, Mudassir
AU - Divani, Afshin A.
AU - Galecio-Castillo, Milagros
AU - Hassan, Ameer E.
AU - Jumaa, Mouhammad A.
AU - Ribo, Marc
AU - Abraham, Michael
AU - Petersen, Nils
AU - Fifi, Johanna
AU - Guerrero, Waldo R.
AU - Malik, Amer M.
AU - Siegler, James E.
AU - Nguyen, Thanh N.
AU - Sheth, Sunil A.
AU - Yoo, Albert J.
AU - Linares, Guillermo
AU - Janjua, Nazli
AU - Quispe-Orozco, Darko
AU - Ikram, Asad
AU - Tekle, Wondewossen G.
AU - Zaidi, Syed F.
AU - Zevallos, Cynthia B.
AU - Rizzo, Federica
AU - Barkley, Tiffany
AU - De Leacy, Reade
AU - Khalife, Jane
AU - Abdalkader, Mohamad
AU - Salazar-Marioni, Sergio
AU - Soomro, Jazba
AU - Gordon, Weston
AU - Rodriguez-Calienes, Aaron
AU - Vivanco-Suarez, Juan
AU - Turabova, Charoskhon
AU - Mokin, Maxim
AU - Yavagal, Dileep R.
AU - Ortega-Gutierrez, Santiago
N1 - Publisher Copyright:
© 2023, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2023
Y1 - 2023
N2 - Risk of hemorrhage remains with antiplatelet medications required with carotid stenting during endovascular therapy (EVT) for tandem lesion (TLs). We evaluated the safety of antiplatelet regimens in EVT of TLs. This multicenter study included anterior circulation TL patients from 2015 to 2020, stratified by periprocedural EVT antiplatelet strategy: (1) no antiplatelets, (2) single oral, (3) dual oral, and (4) intravenous IV (in combination with single or dual oral). Primary outcome was symptomatic intracranial hemorrhage (sICH). Secondary outcomes were any hemorrhage, favorable functional status (mRS 0–2) at 90 days, successful reperfusion (mTICI score ≥ 2b), in-stent thrombosis, and mortality at 90 days. Of the total 691 patients, 595 were included in the final analysis. One hundred and nineteen (20%) received no antiplatelets, 134 (22.5%) received single oral, 152 (25.5%) dual oral, and 196 (31.9%) IV combination. No significant association was found for sICH (ref: no antiplatelet: 5.7%; single:4.2%; aOR 0.64, CI 0.20–2.06, p = 0.45, dual:1.9%; aOR 0.35, CI 0.09–1.43, p = 0.15, IV combination: 6.1%; aOR 1.05, CI 0.39–2.85, p = 0.92). No association was found for parenchymal or petechial hemorrhage. Odds of successful reperfusion were significantly higher with dual oral (aOR 5.85, CI 2.12–16.14, p = 0.001) and IV combination (aOR 2.35, CI 1.07–5.18, p = 0.035) compared with no antiplatelets. Odds of excellent reperfusion (mTICI 2c/3) were significantly higher for cangrelor (aOR 4.41; CI 1.2–16.28; p = 0.026). No differences were noted for mRS 0–2 at 90 days, in-stent thrombosis, and mortality rates. Administration of dual oral and IV (in combination with single or dual oral) antiplatelets during EVT was associated with significantly increased odds of successful reperfusion without an increased rate of symptomatic hemorrhage or mortality in patients with anterior circulation TLs.
AB - Risk of hemorrhage remains with antiplatelet medications required with carotid stenting during endovascular therapy (EVT) for tandem lesion (TLs). We evaluated the safety of antiplatelet regimens in EVT of TLs. This multicenter study included anterior circulation TL patients from 2015 to 2020, stratified by periprocedural EVT antiplatelet strategy: (1) no antiplatelets, (2) single oral, (3) dual oral, and (4) intravenous IV (in combination with single or dual oral). Primary outcome was symptomatic intracranial hemorrhage (sICH). Secondary outcomes were any hemorrhage, favorable functional status (mRS 0–2) at 90 days, successful reperfusion (mTICI score ≥ 2b), in-stent thrombosis, and mortality at 90 days. Of the total 691 patients, 595 were included in the final analysis. One hundred and nineteen (20%) received no antiplatelets, 134 (22.5%) received single oral, 152 (25.5%) dual oral, and 196 (31.9%) IV combination. No significant association was found for sICH (ref: no antiplatelet: 5.7%; single:4.2%; aOR 0.64, CI 0.20–2.06, p = 0.45, dual:1.9%; aOR 0.35, CI 0.09–1.43, p = 0.15, IV combination: 6.1%; aOR 1.05, CI 0.39–2.85, p = 0.92). No association was found for parenchymal or petechial hemorrhage. Odds of successful reperfusion were significantly higher with dual oral (aOR 5.85, CI 2.12–16.14, p = 0.001) and IV combination (aOR 2.35, CI 1.07–5.18, p = 0.035) compared with no antiplatelets. Odds of excellent reperfusion (mTICI 2c/3) were significantly higher for cangrelor (aOR 4.41; CI 1.2–16.28; p = 0.026). No differences were noted for mRS 0–2 at 90 days, in-stent thrombosis, and mortality rates. Administration of dual oral and IV (in combination with single or dual oral) antiplatelets during EVT was associated with significantly increased odds of successful reperfusion without an increased rate of symptomatic hemorrhage or mortality in patients with anterior circulation TLs.
KW - Antiplatelet therapy
KW - Ischemic stroke
KW - Tandem lesions
KW - Thrombectomy
UR - http://www.scopus.com/inward/record.url?scp=85177832366&partnerID=8YFLogxK
U2 - 10.1007/s12975-023-01214-9
DO - 10.1007/s12975-023-01214-9
M3 - Artículo
AN - SCOPUS:85177832366
SN - 1868-4483
JO - Translational Stroke Research
JF - Translational Stroke Research
ER -