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      KCI등재 SCIE SCOPUS

      Low Exposure to Direct Oral Anticoagulants Is Associated with Ischemic Stroke and Its Severity

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      https://www.riss.kr/link?id=A108004568

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      다국어 초록 (Multilingual Abstract)

      Background and purpose In acute stroke patients, plasma concentrations of direct oral anticoagulants (DOAC) at hospital admission only poorly mirror DOAC exposure or the coagulation status at the time of the event. Here, we evaluated whether DOAC expo...

      Background and purpose In acute stroke patients, plasma concentrations of direct oral anticoagulants (DOAC) at hospital admission only poorly mirror DOAC exposure or the coagulation status at the time of the event. Here, we evaluated whether DOAC exposure and DOAC plasma concentration at the time of transient ischemic attacks (TIA) and ischemic strokes correlate with their likelihood of occurrence.




      Methods Prospectively, consecutive DOAC patients with acute ischemic stroke or TIA were included. Admission DOAC plasma concentrations were measured by ultraperformance liquid chromatography–tandem mass spectrometry. Individual DOAC exposure (area under the curve) and DOAC concentrations at event onset were derived from population pharmacokinetic analyses.




      Results DOAC exposure was successfully modeled in 211 patients (ischemic stroke 74.4%, TIA 25.6%). Compared to published values, 63.0% had relatively lower DOAC exposure and they more often received lower DOAC doses than recommended (odds ratio [OR], 2.125; 95% confidence interval [CI], 1.039 to 4.560; P=0.044). These patients more likely suffered ischemic strokes than TIA (OR, 2.411;95% CI, 1.254 to 4.638; P=0.008) and their strokes were more severe (slope, 3.161; 95% CI, 0.741 to 5.58; P=0.011). Low relative DOAC concentrations at event onset were likewise associated with ischemic strokes (OR, 4.123; 95% CI, 1.834 to 9.268; P=0.001), but not to stroke severity (P=0.272). DOAC exposure had a higher explanatory value for stroke severity than concentrations at event.




      Conclusions Low DOAC exposure is strongly associated to ischemic stroke and its severity. By monitoring DOAC plasma concentrations, patients prone to ischemic stroke might be identified.

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      참고문헌 (Reference)

      1 Reilly PA, "The effect of dabigatran plasma concentrations and patient characteristics on the frequency of ischemic stroke and major bleeding in atrial fibrillation patients: the RE-LY Trial (Randomized Evaluation of Long-Term Anticoagulation Therapy)" 63 : 321-328, 2014

      2 Foerster KI, "Simultaneous quantification of direct oral anticoagulants currently used in anticoagulation therapy" 148 : 238-244, 2018

      3 Kubitza D, "Safety, pharmacodynamics, and pharmacokinetics of BAY 59-7939–an oral, direct Factor Xa inhibitor: after multiple dosing in healthy male subjects" 61 : 873-880, 2005

      4 Seiffge DJ, "Rivaroxaban plasma levels in acute ischemic stroke and intracerebral hemorrhage" 83 : 451-459, 2018

      5 Gallagher AM, "Risks of stroke and mortality associated with suboptimal anticoagulation in atrial fibrillation patients" 106 : 968-977, 2011

      6 Woo HG, "Recurrent ischemic stroke in atrial fibrillation with non-vitamin K antagonist oral anticoagulation" 64 : 127-133, 2019

      7 Leil TA, "Quantification of apixaban’s therapeutic utility in prevention of venous thromboembolism : selection of phase III trial dose" 88 : 375-382, 2010

      8 Byon W, "Population pharmacokinetics, pharmacodynamics, and exploratory exposure-response analyses of apixaban in subjects treated for venous thromboembolism" 6 : 340-349, 2017

      9 Krekels EH, "Population pharmacokinetics of edoxaban in patients with non-valvular atrial fibrillation in the ENGAGE AF-TIMI 48 study, a phase III clinical trial" 55 : 1079-1090, 2016

      10 Cirincione B, "Population pharmacokinetics of apixaban in subjects with nonvalvular atrial fibrillation" 7 : 728-738, 2018

      1 Reilly PA, "The effect of dabigatran plasma concentrations and patient characteristics on the frequency of ischemic stroke and major bleeding in atrial fibrillation patients: the RE-LY Trial (Randomized Evaluation of Long-Term Anticoagulation Therapy)" 63 : 321-328, 2014

      2 Foerster KI, "Simultaneous quantification of direct oral anticoagulants currently used in anticoagulation therapy" 148 : 238-244, 2018

      3 Kubitza D, "Safety, pharmacodynamics, and pharmacokinetics of BAY 59-7939–an oral, direct Factor Xa inhibitor: after multiple dosing in healthy male subjects" 61 : 873-880, 2005

      4 Seiffge DJ, "Rivaroxaban plasma levels in acute ischemic stroke and intracerebral hemorrhage" 83 : 451-459, 2018

      5 Gallagher AM, "Risks of stroke and mortality associated with suboptimal anticoagulation in atrial fibrillation patients" 106 : 968-977, 2011

      6 Woo HG, "Recurrent ischemic stroke in atrial fibrillation with non-vitamin K antagonist oral anticoagulation" 64 : 127-133, 2019

      7 Leil TA, "Quantification of apixaban’s therapeutic utility in prevention of venous thromboembolism : selection of phase III trial dose" 88 : 375-382, 2010

      8 Byon W, "Population pharmacokinetics, pharmacodynamics, and exploratory exposure-response analyses of apixaban in subjects treated for venous thromboembolism" 6 : 340-349, 2017

      9 Krekels EH, "Population pharmacokinetics of edoxaban in patients with non-valvular atrial fibrillation in the ENGAGE AF-TIMI 48 study, a phase III clinical trial" 55 : 1079-1090, 2016

      10 Cirincione B, "Population pharmacokinetics of apixaban in subjects with nonvalvular atrial fibrillation" 7 : 728-738, 2018

      11 Girgis IG, "Population pharmacokinetics and pharmacodynamics of rivaroxaban in patients with non-valvular atrial fibrillation : results from ROCKET AF" 54 : 917-927, 2014

      12 Liesenfeld KH, "Population pharmacokinetic analysis of the oral thrombin inhibitor dabigatran etexilate in patients with non-valvular atrial fibrillation from the RE-LY trial" 9 : 2168-2175, 2011

      13 Wang X, "Pharmacokinetics, pharmacodynamics, and safety of apixaban in subjects with end-stage renal disease on hemodialysis" 56 : 628-636, 2016

      14 Sakaguchi T, "Monitoring of anti-Xa activity and factors related to bleeding events: a study in Japanese patients with nonvalvular atrial fibrillation receiving rivaroxaban" 70 : 244-249, 2017

      15 Purrucker JC, "Management of acute stroke in patients on oral anticoagulants" 30 : 1-7, 2017

      16 Vuong QH, "Likelihood ratio tests for model selection and non-nested hypotheses" 57 : 307-333, 1989

      17 Stoll S, "Ischemic stroke and dose adjustment of oral Factor Xa inhibitors in patients with atrial fibrillation" 267 : 2007-2012, 2020

      18 Gosselin RC, "International Council for Standardization in Haematology (ICSH) recommendations for laboratory measurement of direct oral anticoagulants" 118 : 437-450, 2018

      19 Nakamura A, "Intensity of anticoagulation and clinical outcomes in acute cardioembolic stroke : the Fukuoka Stroke Registry" 44 : 3239-3242, 2013

      20 Steinberg BA, "Frequency and outcomes of reduced dose non-vitamin K antagonist anticoagulants: results from ORBIT-AF II (The Outcomes Registry for Better Informed Treatment of Atrial Fibrillation II)" 7 : e007633-, 2018

      21 Seiffge DJ, "Feasibility of rapid measurement of rivaroxaban plasma levels in patients with acute stroke" 43 : 112-116, 2017

      22 Hylek EM, "Effect of intensity of oral anticoagulation on stroke severity and mortality in atrial fibrillation" 349 : 1019-1026, 2003

      23 Yin OQ, "Edoxaban population pharmacokinetics and exposure-response analysis in patients with non-valvular atrial fibrillation" 70 : 1339-1351, 2014

      24 Volbers B, "Dabigatran plasma levels in acute cerebrovascular events" 25 : 877-882, 2016

      25 Purrucker JC, "Coagulation testing in acute ischemic stroke patients taking non-vitamin k antagonist oral anticoagulants" 48 : 152-158, 2017

      26 Stangier J, "Clinical pharmacokinetics and pharmacodynamics of the oral direct thrombin inhibitor dabigatran etexilate" 47 : 285-295, 2008

      27 Herink MC, "Clinical management of pharmacokinetic drug interactions with direct oral anticoagulants (DOACs)" 79 : 1625-1634, 2019

      28 Macha K, "Cerebral ischemia in patients on direct oral anticoagulants" 50 : 873-879, 2019

      29 Connolly SJ, "Benefit of oral anticoagulant over antiplatelet therapy in atrial fibrillation depends on the quality of international normalized ratio control achieved by centers and countries as measured by time in therapeutic range" 118 : 2029-2037, 2008

      30 RuffCT, "Association between edoxaban dose, concentration, anti-factor Xa activity, and outcomes: an analysis of data from the randomised, double-blind ENGAGE AF-TIMI 48trial" 385 : 2288-2295, 2015

      31 "Assessment report Xarelto VHF"

      32 Ay H, "Admission international normalized ratio and acute infarct volume in ischemic stroke" 64 : 499-506, 2008

      33 Borne RT, "Adherence and outcomes to direct oral anticoagulants among patients with atrial fibrillation : findings from the veterans health administration" 17 : 236-, 2017

      34 Yeo IK, "A new family of power transformations to improve normality or symmetry" 87 : 954-959, 2000

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      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2014-11-01 평가 SCIE 등재 (기타) KCI등재
      2013-01-01 평가 등재후보학술지 유지 (기타) KCI등재후보
      2011-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 3.63 0.55 3.13
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      2.37 1.91 1.175 0.1
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