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      Practical issues in clinical scenarios involving CKD patients requiring antithrombotic therapy in light of the 2017 ESC guideline recommendations

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          Abstract

          Background

          The choice of the most appropriate antithrombotic regimen that balances ischemic and bleeding risks was addressed by the August 2017 European Society of Cardiologists (ESC)/European Association for Cardio-Thoracic Surgery Focused Update recommendations, which propose new evaluation scores and protocols for patients requiring a coronary stent or patients with an acute coronary syndrome, atrial fibrillation, or a high bleeding risk and indication for oral anticoagulation therapy.

          Discussion

          Numerous questions remain regarding antithrombotic regimens and risk management algorithms for both ischemic and hemorrhagic events in patients with chronic kidney disease (CKD) in various clinical scenarios. Limitations of current studies include a general ack of advanced CKD patients in major randomized controlled trials, of evidence on algorithm implementation, and of robust assessment tools for hemorrhagic risk. Herein, we aim to analyze the ESC Update recommendations and the newly implemented risk scores (DAPT, PRECISE-DAPT, PARIS) from the point of view of CKD, providing suggestions on drug choice (which combination has the best evidence), dosage, and duration (the same or different as for non-CKD population) of antithrombotics, as well as to identify current shortcomings and to envision directions of future research.

          Conclusion

          We provide an evidence-based perspective on the new proposed bleeding management protocol, with focus on the CKD population. Despite previous important steps on antithrombotic therapy of renal patients, there remain many unsolved questions for which our suggestions could fundament new randomized controlled trials and specific protocols.

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          Most cited references46

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          Derivation and validation of the predicting bleeding complications in patients undergoing stent implantation and subsequent dual antiplatelet therapy (PRECISE-DAPT) score: a pooled analysis of individual-patient datasets from clinical trials

          Dual antiplatelet therapy (DAPT) with aspirin plus a P2Y12 inhibitor prevents ischaemic events after coronary stenting, but increases bleeding. Guidelines support weighting bleeding risk before the selection of treatment duration, but no standardised tool exists for this purpose.
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            Development and Validation of a Prediction Rule for Benefit and Harm of Dual Antiplatelet Therapy Beyond 1 Year After Percutaneous Coronary Intervention.

            Dual antiplatelet therapy after percutaneous coronary intervention (PCI) reduces ischemia but increases bleeding.
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              Thrombolysis in Myocardial Infarction (TIMI) Trial, Phase I: A comparison between intravenous tissue plasminogen activator and intravenous streptokinase. Clinical findings through hospital discharge.

              Intravenous administration of 80 mg of recombinant tissue plasminogen activator (rt-PA, 40, 20, and 20 mg in successive hours) and streptokinase (SK, 1.5 million units over 1 hr) was compared in a double-blind, randomized trial in 290 patients with evolving acute myocardial infarction. These patients entered the trial within 7 hr of the onset of symptoms and underwent baseline coronary arteriography before thrombolytic therapy was instituted. Ninety minutes after the start of thrombolytic therapy, occluded infarct-related arteries had opened in 62% of 113 patients in the rt-PA and 31% of 119 patients in the SK group (p less than .001). Twice as many occluded infarct-related arteries opened after rt-PA compared with SK at the time of each of seven angiograms obtained during the first 90 min after commencing thrombolytic therapy. Regardless of the time from onset of symptoms to treatment, more arteries were opened after rt-PA than SK. The reduction in circulating fibrinogen and plasminogen and the increase in circulating fibrin split products at 3 and 24 hr were significantly less in patients treated with rt-PA than in those treated with SK (p less than .001). The occurrence of bleeding events, administration of blood transfusions, and reocclusion of the infarct-related artery was comparable in the two groups. Thus, in patients with acute myocardial infarction, rt-PA elicited reperfusion in twice as many occluded infarct-related arteries as compared with SK at each of seven serial observations during the first 90 min after onset of treatment.
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                Author and article information

                Contributors
                alburlacu@yahoo.com
                Journal
                BMC Med
                BMC Med
                BMC Medicine
                BioMed Central (London )
                1741-7015
                19 September 2018
                19 September 2018
                2018
                : 16
                : 158
                Affiliations
                [1 ]Nephrology Clinic, Dialysis and Renal Transplant Center – ‘C.I. Parhon’ University Hospital, Iasi, Romania
                [2 ]‘Grigore T. Popa’ University of Medicine, Iasi, Romania
                [3 ]ISNI 0000 0001 2174 1754, GRID grid.7563.7, Department of Medicine and Surgery, , University of Milan-Bicocca, ; Monza, Italy
                [4 ]ISNI 0000 0004 1756 8604, GRID grid.415025.7, Nephrology Unit, , San Gerardo Hospital, ; Monza, Italy
                [5 ]ISNI 0000 0004 1765 1301, GRID grid.410527.5, Inserm, Centre d’Investigations Cliniques-Plurithématique 14-33, Inserm U1116, CHRU Nancy, ; Nancy, France
                [6 ]ISNI 0000 0001 2194 6418, GRID grid.29172.3f, Université de Lorraine, Association Lorraine de Traitement de l’Insuffisance Rénale (ALTIR) and F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), ; Nancy, France
                [7 ]ISNI 0000 0001 0237 2025, GRID grid.412346.6, The University of Manchester, Manchester Academic Health Science Centre, Salford Royal NHS Foundation Trust, ; Stott Lane, Salford, UK
                [8 ]GRID grid.419651.e, IIS-Fundacion Jimenez Diaz UAM, FRIAT and REDINREN, ; Madrid, Spain
                [9 ]ISNI 0000 0001 2165 3025, GRID grid.8267.b, Department of Hypertension, Chair of Nephrology and Hypertension, , Medical University of Lodz, ; Lodz, Poland
                [10 ]Department of Interventional Cardiology, Cardiovascular Diseases Institute, ‘Grigore T. Popa’ University of Medicine, Iasi, Romania
                Author information
                http://orcid.org/0000-0002-3424-1588
                Article
                1145
                10.1186/s12916-018-1145-0
                6145111
                30227855
                930c1de8-8896-46bd-8212-5aa2ad6a8599
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 11 April 2018
                : 3 August 2018
                Categories
                Opinion
                Custom metadata
                © The Author(s) 2018

                Medicine
                anticoagulation,antithrombotics,bleeding,cardiovascular disease,chronic kidney disease,ischemic heart disease,risk score

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