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...

Full description

Saved in:
Bibliographic Details
Published inJournal of Neuroendovascular Therapy Vol. 15; no. 8; pp. 533 - 539
Main Authors Yamamoto, Munetaka, Arai, Hajime, Oishi, Hidenori, Suga, Yasuo
Format Journal Article
LanguageEnglish
Published Japan The Japanese Society for Neuroendovascular Therapy 01.01.2021
Subjects
Online AccessGet full text
ISSN1882-4072
2186-2494
2186-2494
DOI10.5797/jnet.oa.2020-0137

Cover

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.
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
Author_xml – sequence: 1
  fullname: Yamamoto, Munetaka
  organization: Department of Neurosurgery, Juntendo University School of Medicine, Tokyo, Japan
– sequence: 1
  fullname: Arai, Hajime
  organization: Department of Neurosurgery, Juntendo University School of Medicine, Tokyo, Japan
– sequence: 1
  fullname: Oishi, Hidenori
  organization: Department of Neuroendovascular Therapy, Juntendo University School of Medicine, Tokyo, Japan
– sequence: 1
  fullname: Suga, Yasuo
  organization: Department of Neurosurgery, Juntendo University School of Medicine, Tokyo, Japan
BackLink https://www.ncbi.nlm.nih.gov/pubmed/37502768$$D View this record in MEDLINE/PubMed
BookMark eNqNUdtuEzEQtVARLaUfwAvyD2zwZb12eEFRVUqlVlSiPFsT72ziyLGDd7cof4-3KaG8YckztuacM-Pjt-QkpoiEvOdspvRcf9xEHGYJZoIJVjEu9StyJrhpKlHP6xNyxo0RVc20OCUXfb9hZTWMG16_IadSKyZ0Y87Iz6uu8w7cnqaO3qXoh5R9XNEuZXo3hsHvAtJFnDIMGHCgD2vMsNvTdnwC3sQhg8sQPQT6fcA40PsADrfl9Iku6H3G4Lc-Qt6X8tju35HXHYQeL57zOfnx5erh8mt1--365nJxWzlVS11pZKJuDWJroAPHoTNi2QKfS2ZaxQCk4kq1DtQclk3DmHaya2oQWPNyE_KciIPuGHew_wUh2F322zKH5cxOFtrJQpvAThbaycJC-nwg7cblFluH0-v-EhN4-28l-rVdpcciKTVTpikKH14qHKl_LC8AfgC4nPo-Y_dfY10fOEWx_FZIMfiIdpPGHIuH1nVqIq0nCreMccVMSWUrKacwl0az-qn7s9KmH2CFx96QB-8CHnpzZc0UXs5wRLg1ZItR_gbuNsky
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
ContentType Journal Article
Copyright 2021 The Japanese Society for Neuroendovascular Therapy
2021 The Japanese Society for Neuroendovascular Therapy.
2021 The Japanese Society for Neuroendovascular Therapy 2021
Copyright_xml – notice: 2021 The Japanese Society for Neuroendovascular Therapy
– notice: 2021 The Japanese Society for Neuroendovascular Therapy.
– notice: 2021 The Japanese Society for Neuroendovascular Therapy 2021
CorporateAuthor Department of Neuroendovascular Therapy
Juntendo University School of Medicine
Department of Neurosurgery
CorporateAuthor_xml – name: Juntendo University School of Medicine
– name: Department of Neurosurgery
– name: Department of Neuroendovascular Therapy
DBID AAYXX
CITATION
NPM
5PM
ADTOC
UNPAY
DOI 10.5797/jnet.oa.2020-0137
DatabaseName CrossRef
PubMed
PubMed Central (Full Participant titles)
Unpaywall for CDI: Periodical Content
Unpaywall
DatabaseTitle CrossRef
PubMed
DatabaseTitleList PubMed


Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: UNPAY
  name: Unpaywall
  url: https://proxy.k.utb.cz/login?url=https://unpaywall.org/
  sourceTypes: Open Access Repository
DeliveryMethod fulltext_linktorsrc
DocumentTitleAlternate Suga Y, et al
EISSN 2186-2494
EndPage 539
ExternalDocumentID 10.5797/jnet.oa.2020-0137
PMC10370586
37502768
10_5797_jnet_oa_2020_0137
cf5jneth_2021_001508_008_0533_05393870468
article_jnet_15_8_15_oa_2020_0137_article_char_en
Genre Journal Article
GroupedDBID ABDBF
ABJNI
ALMA_UNASSIGNED_HOLDINGS
GROUPED_DOAJ
JMI
JSF
JSH
KQ8
MOJWN
OK1
RJT
RPM
RZJ
AAYXX
CITATION
NPM
5PM
ADTOC
UNPAY
ID FETCH-LOGICAL-c5437-7e024d8eed8afac1af82bda19308d50aa35155dca59ab66007c3f64a2e4160023
IEDL.DBID UNPAY
ISSN 1882-4072
2186-2494
IngestDate Wed Oct 01 16:16:49 EDT 2025
Thu Aug 21 18:36:57 EDT 2025
Thu Jan 02 22:51:00 EST 2025
Tue Jul 01 01:32:34 EDT 2025
Thu Jul 10 16:15:14 EDT 2025
Wed Sep 03 06:31:06 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 8
Keywords platelet aggregation test
stent
antiplatelet therapy
intracranial aneurysm
monitoring
Language English
License https://creativecommons.org/licenses/by-nc-nd/4.0
2021 The Japanese Society for Neuroendovascular Therapy.
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives International License
cc-by-nc
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c5437-7e024d8eed8afac1af82bda19308d50aa35155dca59ab66007c3f64a2e4160023
Notes Email: yssuga@juntendo.ac.jp
OpenAccessLink https://proxy.k.utb.cz/login?url=https://www.jstage.jst.go.jp/article/jnet/15/8/15_oa.2020-0137/_pdf
PMID 37502768
PageCount 7
ParticipantIDs unpaywall_primary_10_5797_jnet_oa_2020_0137
pubmedcentral_primary_oai_pubmedcentral_nih_gov_10370586
pubmed_primary_37502768
crossref_primary_10_5797_jnet_oa_2020_0137
medicalonline_journals_cf5jneth_2021_001508_008_0533_05393870468
jstage_primary_article_jnet_15_8_15_oa_2020_0137_article_char_en
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 20210101
PublicationDateYYYYMMDD 2021-01-01
PublicationDate_xml – month: 1
  year: 2021
  text: 20210101
  day: 1
PublicationDecade 2020
PublicationPlace Japan
PublicationPlace_xml – name: Japan
PublicationTitle Journal of Neuroendovascular Therapy
PublicationTitleAlternate JNET
PublicationYear 2021
Publisher The Japanese Society for Neuroendovascular Therapy
Publisher_xml – name: The Japanese Society for Neuroendovascular Therapy
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. J Neurointerv Surg 2013; 5: 277–279.
– ident: 5
  doi: 10.3174/ajnr.A3658
– ident: 9
  doi: 10.1016/j.jacc.2010.04.047
– ident: 10
  doi: 10.1016/S0140-6736(13)61170-8
– ident: 23
  doi: 10.1136/neurintsurg-2013-010976
– ident: 8
  doi: 10.3171/2012.8.JNS12185
– ident: 17
  doi: 10.1001/jama.2011.290
– ident: 14
  doi: 10.1160/TH06-01-0046
– ident: 18
  doi: 10.1111/j.1552-6569.2008.00322.x
– ident: 20
  doi: 10.1111/j.1538-7836.2009.03709.x
– ident: 22
  doi: 10.3174/ajnr.A3418
– ident: 4
  doi: 10.1161/STROKEAHA.109.558114
– ident: 3
  doi: 10.1161/STROKEAHA.108.531400
– ident: 6
  doi: 10.1136/neurintsurg-2013-011023
– ident: 12
  doi: 10.1136/neurintsurg-2013-010808
– ident: 24
  doi: 10.5797/jnet.oa.2017-0004
– ident: 21
  doi: 10.1111/j.1538-7836.2011.04570.x
– ident: 16
  doi: 10.1160/TH08-09-0577
– ident: 2
  doi: 10.1227/NEU.0b013e3181efe3ef
– ident: 15
  doi: 10.1160/TH07-07-0478
– ident: 19
  doi: 10.1161/CIRCULATIONAHA.111.029165
– ident: 1
  doi: 10.3174/ajnr.A0641
– ident: 7
  doi: 10.1136/neurintsurg-2012-010582
– ident: 13
  doi: 10.3174/ajnr.A2963
– ident: 11
  doi: 10.1136/neurintsurg-2013-010809
SSID ssj0000601814
ssib040212986
ssib051641539
ssib058493112
ssib002919271
Score 2.1337688
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...
SourceID unpaywall
pubmedcentral
pubmed
crossref
medicalonline
jstage
SourceType Open Access Repository
Index Database
Publisher
StartPage 533
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
URI https://www.jstage.jst.go.jp/article/jnet/15/8/15_oa.2020-0137/_article/-char/en
http://mol.medicalonline.jp/library/journal/download?GoodsID=cf5jneth/2021/001508/008&name=0533-0539e
https://www.ncbi.nlm.nih.gov/pubmed/37502768
https://pubmed.ncbi.nlm.nih.gov/PMC10370586
https://www.jstage.jst.go.jp/article/jnet/15/8/15_oa.2020-0137/_pdf
UnpaywallVersion publishedVersion
Volume 15
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
ispartofPNX Journal of Neuroendovascular Therapy, 2021, Vol.15(8), pp.533-539
journalDatabaseRights – providerCode: PRVAFT
  databaseName: Open Access Digital Library
  customDbUrl:
  eissn: 2186-2494
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0000601814
  issn: 1882-4072
  databaseCode: KQ8
  dateStart: 20070101
  isFulltext: true
  titleUrlDefault: http://grweb.coalliance.org/oadl/oadl.html
  providerName: Colorado Alliance of Research Libraries
– providerCode: PRVAON
  databaseName: DOAJ Directory of Open Access Journals
  customDbUrl:
  eissn: 2186-2494
  dateEnd: 20211231
  omitProxy: true
  ssIdentifier: ssj0000601814
  issn: 1882-4072
  databaseCode: DOA
  dateStart: 20160101
  isFulltext: true
  titleUrlDefault: https://www.doaj.org/
  providerName: Directory of Open Access Journals
– providerCode: PRVHPJ
  databaseName: ROAD: Directory of Open Access Scholarly Resources
  customDbUrl:
  eissn: 2186-2494
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssib051641539
  issn: 1882-4072
  databaseCode: M~E
  dateStart: 20070101
  isFulltext: true
  titleUrlDefault: https://road.issn.org
  providerName: ISSN International Centre
– providerCode: PRVAQN
  databaseName: PubMed Central
  customDbUrl:
  eissn: 2186-2494
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0000601814
  issn: 1882-4072
  databaseCode: RPM
  dateStart: 20200101
  isFulltext: true
  titleUrlDefault: https://www.ncbi.nlm.nih.gov/pmc/
  providerName: National Library of Medicine
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lj9MwEB4tXSRAiIdYlvKofOAESto0cexyolp1tSC1qsRWWk6WYzu7lG5aSitUDvx2ZuI0tHtBiIt9iG3F48d8Mx5_BnhtZYZaJEoDLq0IiEIryGJceKbnJNobsTOW7g4PR-nZJPl4wS8O4GR7F4bCKqeIiy4dZeHlPJwu2pUQ21Oy1iPelpioObEGdSmqKhZttbD5LThM6ZSpAYeT0bj_mUwtwo9EAUZPzEUyDdDYSPzZJhc9UTYY7ja0p51u-x-5B_ev_aGJJ6_Y0VU34yjvrIuF3vzQs9mOkjp9CHbbPR-b8jVcr7LQ_LzB_Pif_X8EDyoQy_q-wmM4cMUT-DYgNgptNmyeM79VkM-QISpmwypskfULyhHf4nRh557RgPmrkuwDdc-g7sQlwT4hll-xMTn5yX_5jvXZeOlm5Rtkyw2j8MfNEUxOB-cnZ0H1oENgeBKLQDhEBFaiWpY61ybSuexmViOG7EjLO1rH9OCMNZr3dEZjKUycp4nuOoSNhC6eQqOYF-4ZsMih3WZsbnMpE9yktJGI1bSIjeVci6wJb7YDqRaet0OhvUOjrkiMKD5F4lMkvia89zKvi1YS90VR2FKVEv9TpS5Bl-Nwh8Em9iaJqraC78rknFq5orqRKikdpSrf_kSkTUkvxj0zSWUTjv10qv8iRjjXFfRF7k20ugBxg-9_Kb5clRzhdP2zw2XahLf1nPy7IJ7_U-kXcJf65B1SL6GxWq7dK4Roq6xVujYwHf4aYDoaD1ulH61VLc3fxn8_WQ
linkProvider Unpaywall
linkToUnpaywall http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3db9MwED-NDgnQxIcY0PEhP_AEStrUcezyRDVtGkibKrFK48lybGejlLSUVlP313MXp6HdC0K8JA-xrfh8vvudff4Z4K1TOXqRJIuEcjIiCq0o5zjxbN8rjDe4t47ODp-eZSej9POFuNiBw_VZGEqrHCMuuvT0ii-n8XjWqYXYGVO0noiOwoeeEmtQj7KquOzomSvuwG5Gu0wt2B2dDQdfKdQi_EgUYHTFXKKyCIONNOxtCtmXVYPxZkNb3ulu-JEHsPcjbJoE8ooNX3U7j_LespyZ1bWZTDac1PEjcOvuhdyU7_Fykcf25hbz43_2_zE8rEEsG4QKT2DHl0_h5xGxURi7YtOCBVNBa4YMUTE7rdMW2aCkN-JbVBd2HhgNWDgqyT5R9yz6TpwS7Ati-QUb0iI_rV9-YAM2nPtJdQfZfMUo_XG1D6Pjo_PDk6i-0CGyIuUykh4RgVPolpUpjE1MoXq5M4ghu8qJrjGcLpxx1oi-yWkspeVFlpqeR9hI6OIZtMpp6V8ASzzGbdYVrlAqRSNlrEKsZiS3Tggj8za8Ww-kngXeDo3xDo26JjGi-DSJT5P42vAxyLwpWks8FEVhK11J_E-VpgQdjkMLg01sKYmuTcEvbQtBrVxR3URXlI5KV3d_ItKmR5-jzUwz1YbnQZ2av-AI53qSvqgtRWsKEDf49pfy21XFEU7HP7tCZW143-jk3wVx8E-lX8J96lNYkHoFrcV86V8jRFvkb-op-BsSITsX
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Efficacy+of+Monitoring+for+Multiple+Antiplatelet+Therapy+during+Intracranial+Stent+Placement%3A+A+Preliminary+Study&rft.jtitle=Journal+of+neuroendovascular+therapy&rft.au=Suga%2C+Yasuo&rft.au=Oishi%2C+Hidenori&rft.au=Yamamoto%2C+Munetaka&rft.au=Arai%2C+Hajime&rft.date=2021-01-01&rft.pub=The+Japanese+Society+for+Neuroendovascular+Therapy&rft.issn=1882-4072&rft.eissn=2186-2494&rft.volume=15&rft.issue=8&rft.spage=533&rft.epage=539&rft_id=info:doi/10.5797%2Fjnet.oa.2020-0137&rft.externalDocID=PMC10370586
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1882-4072&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1882-4072&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1882-4072&client=summon