Efficacy of Monitoring for Multiple Antiplatelet Therapy during Intracranial Stent Placement: A Preliminary Study
Objective: During cerebral aneurysm embolization using intracranial stents, platelet aggregation increases owing to increased wall shear stress and a loss of vascular endothelial function at the stent implantation site. Preoperative multiple antiplatelet therapy was introduced to prevent severe thro...
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Published in | Journal of Neuroendovascular Therapy Vol. 15; no. 8; pp. 533 - 539 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Japan
The Japanese Society for Neuroendovascular Therapy
01.01.2021
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Subjects | |
Online Access | Get full text |
ISSN | 1882-4072 2186-2494 2186-2494 |
DOI | 10.5797/jnet.oa.2020-0137 |
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Abstract | Objective: During cerebral aneurysm embolization using intracranial stents, platelet aggregation increases owing to increased wall shear stress and a loss of vascular endothelial function at the stent implantation site. Preoperative multiple antiplatelet therapy was introduced to prevent severe thromboembolic complications due to increased platelet aggregation. However, specific guidelines for the administration and pharmacological evaluation of this therapy do not exist currently. We examined the benefits of perioperative platelet aggregation monitoring in a cohort of patients.Methods: We had 377 patients with unruptured intracranial aneurysms who underwent stent-assisted embolization at our hospital between December 2012 and November 2019. We ultimately included 181 patients in our final analysis. These patients were continuously administered aspirin (100 mg/day) and clopidogrel (75 mg/day) for more than 5 days before the procedure to the post-procedural period. Of these patients, 30 patients who underwent light transmission aggregometry (LTA) before procedure, post-procedure (3 days after procedure), and at first post-discharge clinic visit were included as the subjects. The following characteristics were studied: age; sex; presence/absence of hypertension, dyslipidemia, and/or diabetes mellitus; location of aneurysm; type/number of stent; technique for stent placement; duration of preoperative multiple antiplatelet therapy; perioperative platelet aggregation test results; and postoperative ischemic or hemorrhagic complications.Results: Among these 30 patients, the median duration of antiplatelet therapy prior to the preoperative platelet aggregation measurements was 7 (interquartile range [IQR]: 6–8) days, and post-discharge measurement of LTA was performed at a median period of 27 (IQR: 22–35.5) days after procedure. The preoperative, postoperative, and first post-discharge clinic visit LTA values for adenosine diphosphate (ADP)-induced platelet aggregation were 50% (IQR: 44–54%), 42.5% (IQR: 36–48%), and 36% (IQR: 32–40%), respectively. These results represented gradual decrease in LTA values and a significant difference between the preoperative and post-discharge values. The LTA values for collagen aggregation showed a significant difference evident between the preoperative and post-discharge values; preoperative 38% (IQR: 27–60%), postoperative 42% (IQR: 30–58%), post-discharge 28% (IQR: 20–42%), respectively. We had one thromboembolic complication and one hemorrhagic complication. The results indicated that appropriate platelet aggregation monitoring during multiple antiplatelet therapy prevents thromboembolic complications such as stent thrombosis. However, we also found that many patients demonstrated increased postoperative platelet aggregation inhibitory effects due to the postoperative continuation of the same multiple antiplatelet therapy that was used preoperatively.Conclusion: This study demonstrates that postoperative, continuous, oral antiplatelet therapy induces increased platelet aggregation inhibition effects, which may lead to hemorrhagic complications. Therefore, continued platelet aggregation monitoring after surgery may be important to allow for any necessary alterations to the therapeutic dose and regimen. |
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AbstractList | During cerebral aneurysm embolization using intracranial stents, platelet aggregation increases owing to increased wall shear stress and a loss of vascular endothelial function at the stent implantation site. Preoperative multiple antiplatelet therapy was introduced to prevent severe thromboembolic complications due to increased platelet aggregation. However, specific guidelines for the administration and pharmacological evaluation of this therapy do not exist currently. We examined the benefits of perioperative platelet aggregation monitoring in a cohort of patients.
We had 377 patients with unruptured intracranial aneurysms who underwent stent-assisted embolization at our hospital between December 2012 and November 2019. We ultimately included 181 patients in our final analysis. These patients were continuously administered aspirin (100 mg/day) and clopidogrel (75 mg/day) for more than 5 days before the procedure to the post-procedural period. Of these patients, 30 patients who underwent light transmission aggregometry (LTA) before procedure, post-procedure (3 days after procedure), and at first post-discharge clinic visit were included as the subjects. The following characteristics were studied: age; sex; presence/absence of hypertension, dyslipidemia, and/or diabetes mellitus; location of aneurysm; type/number of stent; technique for stent placement; duration of preoperative multiple antiplatelet therapy; perioperative platelet aggregation test results; and postoperative ischemic or hemorrhagic complications.
Among these 30 patients, the median duration of antiplatelet therapy prior to the preoperative platelet aggregation measurements was 7 (interquartile range [IQR]: 6-8) days, and post-discharge measurement of LTA was performed at a median period of 27 (IQR: 22-35.5) days after procedure. The preoperative, postoperative, and first post-discharge clinic visit LTA values for adenosine diphosphate (ADP)-induced platelet aggregation were 50% (IQR: 44-54%), 42.5% (IQR: 36-48%), and 36% (IQR: 32-40%), respectively. These results represented gradual decrease in LTA values and a significant difference between the preoperative and post-discharge values. The LTA values for collagen aggregation showed a significant difference evident between the preoperative and post-discharge values; preoperative 38% (IQR: 27-60%), postoperative 42% (IQR: 30-58%), post-discharge 28% (IQR: 20-42%), respectively. We had one thromboembolic complication and one hemorrhagic complication. The results indicated that appropriate platelet aggregation monitoring during multiple antiplatelet therapy prevents thromboembolic complications such as stent thrombosis. However, we also found that many patients demonstrated increased postoperative platelet aggregation inhibitory effects due to the postoperative continuation of the same multiple antiplatelet therapy that was used preoperatively.
This study demonstrates that postoperative, continuous, oral antiplatelet therapy induces increased platelet aggregation inhibition effects, which may lead to hemorrhagic complications. Therefore, continued platelet aggregation monitoring after surgery may be important to allow for any necessary alterations to the therapeutic dose and regimen. Objective: During cerebral aneurysm embolization using intracranial stents, platelet aggregation increases owing to increased wall shear stress and a loss of vascular endothelial function at the stent implantation site. Preoperative multiple antiplatelet therapy was introduced to prevent severe thromboembolic complications due to increased platelet aggregation. However, specific guidelines for the administration and pharmacological evaluation of this therapy do not exist currently. We examined the benefits of perioperative platelet aggregation monitoring in a cohort of patients.Methods: We had 377 patients with unruptured intracranial aneurysms who underwent stent-assisted embolization at our hospital between December 2012 and November 2019. We ultimately included 181 patients in our final analysis. These patients were continuously administered aspirin (100 mg/day) and clopidogrel (75 mg/day) for more than 5 days before the procedure to the post-procedural period. Of these patients, 30 patients who underwent light transmission aggregometry (LTA) before procedure, post-procedure (3 days after procedure), and at first post-discharge clinic visit were included as the subjects. The following characteristics were studied: age; sex; presence/absence of hypertension, dyslipidemia, and/or diabetes mellitus; location of aneurysm; type/number of stent; technique for stent placement; duration of preoperative multiple antiplatelet therapy; perioperative platelet aggregation test results; and postoperative ischemic or hemorrhagic complications.Results: Among these 30 patients, the median duration of antiplatelet therapy prior to the preoperative platelet aggregation measurements was 7 (interquartile range [IQR]: 6–8) days, and post-discharge measurement of LTA was performed at a median period of 27 (IQR: 22–35.5) days after procedure. The preoperative, postoperative, and first post-discharge clinic visit LTA values for adenosine diphosphate (ADP)-induced platelet aggregation were 50% (IQR: 44–54%), 42.5% (IQR: 36–48%), and 36% (IQR: 32–40%), respectively. These results represented gradual decrease in LTA values and a significant difference between the preoperative and post-discharge values. The LTA values for collagen aggregation showed a significant difference evident between the preoperative and post-discharge values; preoperative 38% (IQR: 27–60%), postoperative 42% (IQR: 30–58%), post-discharge 28% (IQR: 20–42%), respectively. We had one thromboembolic complication and one hemorrhagic complication. The results indicated that appropriate platelet aggregation monitoring during multiple antiplatelet therapy prevents thromboembolic complications such as stent thrombosis. However, we also found that many patients demonstrated increased postoperative platelet aggregation inhibitory effects due to the postoperative continuation of the same multiple antiplatelet therapy that was used preoperatively.Conclusion: This study demonstrates that postoperative, continuous, oral antiplatelet therapy induces increased platelet aggregation inhibition effects, which may lead to hemorrhagic complications. Therefore, continued platelet aggregation monitoring after surgery may be important to allow for any necessary alterations to the therapeutic dose and regimen. [Objective] : During cerebral aneurysm embolization using intracranial stents, platelet aggregation increases owing to increased wall shear stress and a loss of vascular endothelial function at the stent implantation site. Preoperative multiple antiplatelet therapy was introduced to prevent severe thromboembolic complications due to increased platelet aggregation. However, specific guidelines for the administration and pharmacological evaluation of this therapy do not exist currently. We examined the benefits of perioperative platelet aggregation monitoring in a cohort of patients. [Methods] : We had 377 patients with unruptured intracranial aneurysms who underwent stent-assisted embolization at our hospital between December 2012 and November 2019. We ultimately included 181 patients in our final analysis. These patients were continuously administered aspirin (100 mg/day) and clopidogrel (75 mg/day) for more than 5 days before the procedure to the post-procedural period. Of these patients, 30 patients who underwent light transmission aggregometry (LTA) before procedure, post-procedure (3 days after procedure), and at first post-discharge clinic visit were included as the subjects. The following characteristics were studied : age ; sex ; presence/absence of hypertension, dyslipidemia, and/or diabetes mellitus ; location of aneurysm ; type/number of stent ; technique for stent placement ; duration of preoperative multiple antiplatelet therapy ; perioperative platelet aggregation test results ; and postoperative ischemic or hemorrhagic complications. [Results] : Among these 30 patients, the median duration of antiplatelet therapy prior to the preoperative platelet aggregation measurements was 7 (interquartile range [IQR] : 6-8) days, and post-discharge measurement of LTA was performed at a median period of 27 (IQR : 22-35.5) days after procedure. The preoperative, postoperative, and first post-discharge clinic visit LTA values for adenosine diphosphate (ADP)-induced platelet aggregation were 50% (IQR : 44-54%), 42.5% (IQR : 36-48%), and 36% (IQR : 32-40%), respectively. These results represented gradual decrease in LTA values and a significant difference between the preoperative and post-discharge values. The LTA values for collagen aggregation showed a significant difference evident between the preoperative and post-discharge values ; preoperative 38% (IQR : 27-60%), postoperative 42% (IQR : 30-58%), post-discharge 28% (IQR : 20-42%), respectively. We had one thromboembolic complication and one hemorrhagic complication. The results indicated that appropriate platelet aggregation monitoring during multiple antiplatelet therapy prevents thromboembolic complications such as stent thrombosis. However, we also found that many patients demonstrated increased postoperative platelet aggregation inhibitory effects due to the postoperative continuation of the same multiple antiplatelet therapy that was used preoperatively. [Conclusion] : This study demonstrates that postoperative, continuous, oral antiplatelet therapy induces increased platelet aggregation inhibition effects, which may lead to hemorrhagic complications. Therefore, continued platelet aggregation monitoring after surgery may be important to allow for any necessary alterations to the therapeutic dose and regimen. |
ArticleNumber | oa.2020-0137 |
Author | Oishi, Hidenori Yamamoto, Munetaka Arai, Hajime Suga, Yasuo |
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Cites_doi | 10.3174/ajnr.A3658 10.1016/j.jacc.2010.04.047 10.1016/S0140-6736(13)61170-8 10.1136/neurintsurg-2013-010976 10.3171/2012.8.JNS12185 10.1001/jama.2011.290 10.1160/TH06-01-0046 10.1111/j.1552-6569.2008.00322.x 10.1111/j.1538-7836.2009.03709.x 10.3174/ajnr.A3418 10.1161/STROKEAHA.109.558114 10.1161/STROKEAHA.108.531400 10.1136/neurintsurg-2013-011023 10.1136/neurintsurg-2013-010808 10.5797/jnet.oa.2017-0004 10.1111/j.1538-7836.2011.04570.x 10.1160/TH08-09-0577 10.1227/NEU.0b013e3181efe3ef 10.1160/TH07-07-0478 10.1161/CIRCULATIONAHA.111.029165 10.3174/ajnr.A0641 10.1136/neurintsurg-2012-010582 10.3174/ajnr.A2963 10.1136/neurintsurg-2013-010809 |
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Keywords | platelet aggregation test stent antiplatelet therapy intracranial aneurysm monitoring |
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References | 1) Yamada NK, Cross DT, Pilgram TK, et al: Effect of antiplatelet therapy on thromboembolic complications of elective coil embolization of cerebral aneurysms. AJNR Am J Neuroradiol 2007; 28: 1778–1782. 23) Delgado Almandoz JE, Kadkhodayan Y, Crandall BM, et al: Variability in initial response to standard clopidogrel therapy, delayed conversion to clopidogrel hyper-response, and associated thromboembolic and hemorrhagic complications in patients undergoing endovascular treatment of unruptured cerebral aneurysms. J Neurointerv Surg 2014; 6: 767–773. 24) Endo H, Kataoka T, Ogino T, et al: Delayed clopidogrel hyper-response after neuroendovascular therapy associated with hemorrhagic complications. JNET J Neurovasc Ther 2017; 11: 570–574. 18) Pandya DJ, Fitzsimmons BF, Wolfe TJ, et al: Measurement of antiplatelet inhibition during neurointerventional procedures: the effect of antithrombotic duration and loading dose. J Neuroimaging 2010; 20: 64–69. 15) Sibbing D, Braun S, Jawansky S, et al: Assessment of ADP-induced platelet aggregation with light transmission aggregometry and multiple electrode platelet aggregometry before and after clopidogrel treatment. Thromb Haemost 2008; 99: 121–126. 4) Piotin M, Blanc R, Spelle L, et al: Stent-assisted coiling of intracranial aneurysms: clinical and angiographic results in 216 consecutive aneurysms. Stroke 2010; 41: 110–115. 21) Li Y, Tang HL, Hu YF, et al. The gain-of-function variant allele CYP2C19* 17: a double-edged sword between thrombosis and bleeding in clopidogrel-treated patients. Thromb Haemost 2012; 10: 199–206. 20) Sibbing D, Schulz S, Braun S, et al: Antiplatelet effects of clopidogrel and bleeding in patients undergoing coronary stent placement. Thromb Haemost 2010; 8: 250–256. 2) Kang HS, Han MH, Kwon BJ, et al: Is clopidogrel premedication useful to reduce thromboembolic events during coil embolization for unruptured intracranial aneurysms? Neurosurgery 2010; 67: 1371–1376; discussion 1376. 3) Riedel CH, Tietke M, Alfke K, et al: Subacute stent thrombosis in intracranial stenting. Stroke 2009; 40: 1310–1314. 12) Chandra RV: Point of care platelet function testing in routine neurointerventional care is unjustified. J Neurointerv Surg 2013; 5: 280–282. 17) Price MJ, Berger PB, Teirstein PS, et al: Standard- vs high-dose clopidogrel based on platelet function testing after percutaneous coronary intervention: the GRAVITAS randomized trial. JAMA 2011; 305: 1097–1105. 13) Hussein HM, Emiru T, Georgiadis AL, et al: Assessment of platelet inhibition by point-of-care testing in neuroendovascular procedures. AJNR Am J Neuroradiol 2013; 34: 700–706. 16) Gremmel T, Steiner S, Seidinger D, et al: Comparison of methods to evaluate clopidogrel-mediated platelet inhibition after percutaneous intervention with stent implantation. Thromb Haemost 2009; 101: 333–339. 7) Delgado Almandoz JE, Crandall BM, Scholz JM, et al: Pre-procedure P2Y12 reaction units value predicts perioperative thromboembolic and hemorrhagic complications in patients with cerebral aneurysms treated with pipeline embolization device. J Neurointerv Surg 2013; 5: iii3–iii10. 6) Oran I, Cinar C, Bozkaya H, et al: Tailoring platelet inhibition according to multiple electrode aggregometry decreases the rate of thrombotic complications after intracranial flow-diverting stent implantation. J Neurointerv Surg 2015; 7: 357–362. 8) Rossen JD, Chalouhi N, Wassef SN, et al: Incidence of cerebral ischemic events after discontinuation of clopidogrel in patients with intracranial aneurysms treated with stent-assisted techniques. J Neurosurg 2012; 117: 929–933. 11) Leslie-Mazwi TM: Antiplatelet testing in neurointervention: we cannot ignore the signs. J Neurointerv Surg 2013; 5: 277–279. 9) Bonello L, Tantry US, Marcucci R, et al: Consensus and future directions on the definition of high on-treatment platelet reactivity to adenosine diphosphate. J Am Coll Cardiol 2010; 56: 919–933. 10) Stone GW, Witzenbichler B, Weisz G, et al: Platelet reactivity and clinical outcomes after coronary artery implantation of drug-eluting stents (ADAPT-DES): a prospective multicentre registry study. Lancet 2013; 382: 614–623. 14) von Beckerath N, Pogatsa-Murray G, Wieczorek A, et al: Correlation of a new point-of-care test with conventional optical aggregometry for the assessment of clopidogrel responsiveness. Thromb Haemost 2006; 95: 910–911. 22) Goh C, Churilov L, Mitchell P, et al: Clopidogrel hyper-response and bleeding risk in neurointerventional procedures. AJNR Am J Neuroradiol 2013; 34: 721–726. 5) Nishido H, Piotin M, Bartolini B, et al: Analysis of complications and recurrences of aneurysm coiling with special emphasis on the stent-assisted technique. AJNR Am J Neuroradiol 2014; 35: 339–344. 19) Price MJ, Angiolillo DJ, Teirstein PS, et al: Platelet reactivity and cardiovascular outcomes after percutaneous coronary intervention: a time-dependent analysis of the gauging responsiveness with a VerifyNow P2Y12 assay: impact on thrombosis and safety (GRAVITAS) trial. Circulation 2011; 124: 1132–1137. 11 22 12 23 13 24 14 15 16 17 18 19 1 2 3 4 5 6 7 8 9 20 10 21 |
References_xml | – reference: 1) Yamada NK, Cross DT, Pilgram TK, et al: Effect of antiplatelet therapy on thromboembolic complications of elective coil embolization of cerebral aneurysms. AJNR Am J Neuroradiol 2007; 28: 1778–1782. – reference: 6) Oran I, Cinar C, Bozkaya H, et al: Tailoring platelet inhibition according to multiple electrode aggregometry decreases the rate of thrombotic complications after intracranial flow-diverting stent implantation. J Neurointerv Surg 2015; 7: 357–362. – reference: 15) Sibbing D, Braun S, Jawansky S, et al: Assessment of ADP-induced platelet aggregation with light transmission aggregometry and multiple electrode platelet aggregometry before and after clopidogrel treatment. Thromb Haemost 2008; 99: 121–126. – reference: 20) Sibbing D, Schulz S, Braun S, et al: Antiplatelet effects of clopidogrel and bleeding in patients undergoing coronary stent placement. Thromb Haemost 2010; 8: 250–256. – reference: 16) Gremmel T, Steiner S, Seidinger D, et al: Comparison of methods to evaluate clopidogrel-mediated platelet inhibition after percutaneous intervention with stent implantation. Thromb Haemost 2009; 101: 333–339. – reference: 24) Endo H, Kataoka T, Ogino T, et al: Delayed clopidogrel hyper-response after neuroendovascular therapy associated with hemorrhagic complications. JNET J Neurovasc Ther 2017; 11: 570–574. – reference: 23) Delgado Almandoz JE, Kadkhodayan Y, Crandall BM, et al: Variability in initial response to standard clopidogrel therapy, delayed conversion to clopidogrel hyper-response, and associated thromboembolic and hemorrhagic complications in patients undergoing endovascular treatment of unruptured cerebral aneurysms. J Neurointerv Surg 2014; 6: 767–773. – reference: 2) Kang HS, Han MH, Kwon BJ, et al: Is clopidogrel premedication useful to reduce thromboembolic events during coil embolization for unruptured intracranial aneurysms? Neurosurgery 2010; 67: 1371–1376; discussion 1376. – reference: 10) Stone GW, Witzenbichler B, Weisz G, et al: Platelet reactivity and clinical outcomes after coronary artery implantation of drug-eluting stents (ADAPT-DES): a prospective multicentre registry study. Lancet 2013; 382: 614–623. – reference: 5) Nishido H, Piotin M, Bartolini B, et al: Analysis of complications and recurrences of aneurysm coiling with special emphasis on the stent-assisted technique. AJNR Am J Neuroradiol 2014; 35: 339–344. – reference: 13) Hussein HM, Emiru T, Georgiadis AL, et al: Assessment of platelet inhibition by point-of-care testing in neuroendovascular procedures. AJNR Am J Neuroradiol 2013; 34: 700–706. – reference: 3) Riedel CH, Tietke M, Alfke K, et al: Subacute stent thrombosis in intracranial stenting. Stroke 2009; 40: 1310–1314. – reference: 4) Piotin M, Blanc R, Spelle L, et al: Stent-assisted coiling of intracranial aneurysms: clinical and angiographic results in 216 consecutive aneurysms. Stroke 2010; 41: 110–115. – reference: 18) Pandya DJ, Fitzsimmons BF, Wolfe TJ, et al: Measurement of antiplatelet inhibition during neurointerventional procedures: the effect of antithrombotic duration and loading dose. J Neuroimaging 2010; 20: 64–69. – reference: 21) Li Y, Tang HL, Hu YF, et al. The gain-of-function variant allele CYP2C19* 17: a double-edged sword between thrombosis and bleeding in clopidogrel-treated patients. Thromb Haemost 2012; 10: 199–206. – reference: 7) Delgado Almandoz JE, Crandall BM, Scholz JM, et al: Pre-procedure P2Y12 reaction units value predicts perioperative thromboembolic and hemorrhagic complications in patients with cerebral aneurysms treated with pipeline embolization device. J Neurointerv Surg 2013; 5: iii3–iii10. – reference: 9) Bonello L, Tantry US, Marcucci R, et al: Consensus and future directions on the definition of high on-treatment platelet reactivity to adenosine diphosphate. J Am Coll Cardiol 2010; 56: 919–933. – reference: 8) Rossen JD, Chalouhi N, Wassef SN, et al: Incidence of cerebral ischemic events after discontinuation of clopidogrel in patients with intracranial aneurysms treated with stent-assisted techniques. J Neurosurg 2012; 117: 929–933. – reference: 14) von Beckerath N, Pogatsa-Murray G, Wieczorek A, et al: Correlation of a new point-of-care test with conventional optical aggregometry for the assessment of clopidogrel responsiveness. Thromb Haemost 2006; 95: 910–911. – reference: 17) Price MJ, Berger PB, Teirstein PS, et al: Standard- vs high-dose clopidogrel based on platelet function testing after percutaneous coronary intervention: the GRAVITAS randomized trial. JAMA 2011; 305: 1097–1105. – reference: 19) Price MJ, Angiolillo DJ, Teirstein PS, et al: Platelet reactivity and cardiovascular outcomes after percutaneous coronary intervention: a time-dependent analysis of the gauging responsiveness with a VerifyNow P2Y12 assay: impact on thrombosis and safety (GRAVITAS) trial. Circulation 2011; 124: 1132–1137. – reference: 22) Goh C, Churilov L, Mitchell P, et al: Clopidogrel hyper-response and bleeding risk in neurointerventional procedures. AJNR Am J Neuroradiol 2013; 34: 721–726. – reference: 12) Chandra RV: Point of care platelet function testing in routine neurointerventional care is unjustified. J Neurointerv Surg 2013; 5: 280–282. – reference: 11) Leslie-Mazwi TM: Antiplatelet testing in neurointervention: we cannot ignore the signs. 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Snippet | Objective: During cerebral aneurysm embolization using intracranial stents, platelet aggregation increases owing to increased wall shear stress and a loss of... [Objective] : During cerebral aneurysm embolization using intracranial stents, platelet aggregation increases owing to increased wall shear stress and a loss... During cerebral aneurysm embolization using intracranial stents, platelet aggregation increases owing to increased wall shear stress and a loss of vascular... |
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SubjectTerms | antiplatelet therapy intracranial aneurysm monitoring Original platelet aggregation test stent |
Title | Efficacy of Monitoring for Multiple Antiplatelet Therapy during Intracranial Stent Placement: A Preliminary Study |
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