2019
DOI: 10.1016/j.jacc.2019.08.1031
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Anticoagulation in Concomitant Chronic Kidney Disease and Atrial Fibrillation

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Cited by 118 publications
(117 citation statements)
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References 63 publications
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“…Although efficacy and safety outcome data is limited, to reduce the risk of stroke and systemic embolism for patients with non-valvular AF (except with moderate-to-severe mitral stenosis or a mechanical heart valve) with an elevated CHA2DS2-VASc score (Congestive heart failure, Hypertension, Age ( > 65 = 1 point, > 75 = 2 points), Diabetes, previous Stroke/transient ischemic attack (2 points) vascular disease) and moderate-to-severe CKD, both the United States (US) Food and Drug Administration (FDA) and European Medicines Agency have approved reduced doses of both edoxaban and rivaroxaban in CKD patients with a creatinine clearance (CrCl) of 15 to 50 ml/min [16]. For apixaban, in patients with at least two of the following characteristics: age ≥ 80 years, body weight ≤ 60 kg, or serum creatinine ≥ 1.5 mg/dL, the recommended dose is 2.5 mg orally twice daily.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Although efficacy and safety outcome data is limited, to reduce the risk of stroke and systemic embolism for patients with non-valvular AF (except with moderate-to-severe mitral stenosis or a mechanical heart valve) with an elevated CHA2DS2-VASc score (Congestive heart failure, Hypertension, Age ( > 65 = 1 point, > 75 = 2 points), Diabetes, previous Stroke/transient ischemic attack (2 points) vascular disease) and moderate-to-severe CKD, both the United States (US) Food and Drug Administration (FDA) and European Medicines Agency have approved reduced doses of both edoxaban and rivaroxaban in CKD patients with a creatinine clearance (CrCl) of 15 to 50 ml/min [16]. For apixaban, in patients with at least two of the following characteristics: age ≥ 80 years, body weight ≤ 60 kg, or serum creatinine ≥ 1.5 mg/dL, the recommended dose is 2.5 mg orally twice daily.…”
Section: Discussionmentioning
confidence: 99%
“…For apixaban, in patients with at least two of the following characteristics: age ≥ 80 years, body weight ≤ 60 kg, or serum creatinine ≥ 1.5 mg/dL, the recommended dose is 2.5 mg orally twice daily. The FDA has also approved the use of a specific low-dose dabigatran (75 mg twice daily) based solely on pharmacokinetic data for these patients [16]. For patients with AF who have a CHA2DS2-VASc score of 2 or greater in men or 3 or greater in women and who have end-stage CKD (CrCl < 15 mL/min) or are on dialysis, it might also be reasonable to prescribe dose-adjusted apixaban for oral anticoagulation [17].…”
Section: Discussionmentioning
confidence: 99%
“…As a result of fixed dosing, no need for routine laboratory monitoring, few drug interactions, at least equal efficacy to vitamin K antagonists and lower risks of bleeding, DOACs (dabigatran, apixaban, rivaroxaban and edoxaban) have become the oral anticoagulants of choice in several conditions, including AF, in the general population and patients with mild to moderate CME: Renal medicine CKD. 3,4,7,21 However, all DOACs have an element of renal excretion. Although patients with advanced CKD/ESKD have been generally excluded from the large DOAC clinical trials, 3 on the basis of pharmacological modelling, rivaroxaban, apixaban and edoxaban have been approved for use in Europe for patients with severe CKD ( Table 2 ).…”
Section: Direct Oral Anticoagulantsmentioning
confidence: 99%
“…Наличие ХБП является независимым фактором риска развития нарушений мозгового кровообращения: существует линейная взаимосвязь между значениями расчетной скорости клубочковой фильтрации (рСКФ) и риском инсульта -с каждым снижением показателя почечной функции на 10 мл/мин/1,73 м 2 вероятность возникновения указанного осложнения увеличивается на 7% [18]; похожие ассоциации описаны для альбуминурии [15]. Также на фоне снижения функции почек отмечается соразмерное увеличение риска крупных кровотечений при назначении антикоагулянтов пациентам с ФП: в регистре ORBIT-AF их частота составила 2,7% у пациентов без ХБП и смерти от всех причин [3].…”
Section: нарушение функции почек как предиктор неблагоприятных исходоunclassified
“…в виде интерстициального фиброза и апоптоза кардио миоцитов в предсердиях путем активации ренинангиотензин-альдостероновой системы [12], а также с процессами воспаления [13] и оксидативного стресса [3]. Также в качестве потенциальных механизмов возникновения ФП обсуждаются нарушения минерального обмена и электролитного баланса, увеличение активности симпатической нервной системы и субклиническая гиперволемия [14,15]. Реализация всех этих механизмов происходит на фоне воздействия общих для возникновения ФП и ХБП клинических состояний (рис.…”
unclassified