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      Prevention of Contrast-Induced Nephropathy After Emergency Percutaneous Coronary Intervention With a Single Bolus Administration of High-Concentrate Sodium Bicarbonate ― Rationale and Design of a Single-Arm Study Compared With Historical Controls ―

      methods-article
      , MD 1 , , MD, PhD 1 , , , MD, PhD 1 , , MD, PhD 2 , , MD, PhD 1 , , MD, PhD 1 , , MD, PhD 3 , , MD, PhD 4 , , MD, PhD 5 , , MD, PhD 6 , , MD, PhD 7 , , MD, PhD 8 , , MD, PhD 9 , , MD, PhD 10 , , MD, PhD 11 , , 12 , , 12 , , MD, PhD 12 , , MD, PhD 1 , 3
      Circulation Reports
      The Japanese Circulation Society
      Acute myocardial infarction, Contrast-induced nephropathy, Emergency percutaneous coronary intervention, Sodium bicarbonate

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          Abstract

          Background: Contrast-induced nephropathy (CIN) is clinically important because of its poor prognosis. The incidence of CIN is higher in emergency than elective percutaneous coronary intervention (PCI) because there is no established method to prevent CIN. The aim of this study is to evaluate whether bolus administration of a concentrated solution of sodium bicarbonate can prevent CIN in patients undergoing emergency PCI.

          Methods and Results: This multicenter prospective single-arm trial with historical controls will include patients who are aged ≥20 years and will undergo cardiac catheterization for suspected acute myocardial infarction (AMI). Patients will receive an intravenous bolus administration of concentrated sodium bicarbonate solution (7% or 8.4%, 20 mEq) and will be observed for 72±12 h. Data for the control group, comprising all patients who underwent PCI for AMI between January 1, 2020 and December 31, 2020 across participating hospitals, will be extracted. The primary endpoint is the incidence of CIN, defined as an increase in serum creatinine of >0.5 mg/dL or >25% from baseline within 48±12 h. We will evaluate the endpoints in the prospective group and compare them with those in the historical control group.

          Conclusions: This study will evaluate whether a single bolus administration of concentrated sodium bicarbonate can prevent CIN after emergency PCI.

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          Most cited references14

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          Reactive oxygen species generated at mitochondrial complex III stabilize hypoxia-inducible factor-1alpha during hypoxia: a mechanism of O2 sensing.

          During hypoxia, hypoxia-inducible factor-1alpha (HIF-1alpha) is required for induction of a variety of genes including erythropoietin and vascular endothelial growth factor. Hypoxia increases mitochondrial reactive oxygen species (ROS) generation at Complex III, which causes accumulation of HIF-1alpha protein responsible for initiating expression of a luciferase reporter construct under the control of a hypoxic response element. This response is lost in cells depleted of mitochondrial DNA (rho(0) cells). Overexpression of catalase abolishes hypoxic response element-luciferase expression during hypoxia. Exogenous H(2)O(2) stabilizes HIF-1alpha protein during normoxia and activates luciferase expression in wild-type and rho(0) cells. Isolated mitochondria increase ROS generation during hypoxia, as does the bacterium Paracoccus denitrificans. These findings reveal that mitochondria-derived ROS are both required and sufficient to initiate HIF-1alpha stabilization during hypoxia.
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            JCS 2018 Guideline on Diagnosis and Treatment of Acute Coronary Syndrome.

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              Renal parenchymal hypoxia, hypoxia adaptation, and the pathogenesis of radiocontrast nephropathy.

              Renal parenchymal Po(2) declines after the administration of iodinated radiocontrast agents, reaching critically low levels of approximately 10 mmHg in medullary structures. In this review, the causes of renal parenchymal hypoxia and its potential role in the pathogenesis of contrast nephropathy are appraised. Commonly associated predisposing factors are associated with a propensity to enhance renal hypoxia. Indeed, animal models of radiocontrast nephropathy require the induction of such predisposing factors, mimicking clinical scenarios that lead to contrast nephropathy in high-risk individuals. In these models, in association with medullary hypoxic damage, a transient local cellular hypoxia response is noted, initiated at least in part by hypoxia-inducible factors. Some predisposing conditions that are distinguished by chronically aggravated medullary hypoxia, such as tubulointerstitial disease and diabetes, are characterized by a priori upregulation of hypoxia-inducible factors, which seems to confer tolerance against radiocontrast-related hypoxic tubular damage. Renal dysfunction under such circumstances likely reflects to some extent altered intrarenal hemodynamics, rather than acute tubular injury. Real-time, noninvasive novel methods may help to differentiate between evolving tubular damage and altered hemodynamics and in the design of appropriate preventive interventions.
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                Author and article information

                Journal
                Circ Rep
                Circ Rep
                Circulation Reports
                The Japanese Circulation Society
                2434-0790
                9 March 2023
                10 April 2023
                : 5
                : 4
                : 152-156
                Affiliations
                [1) ] Department of Cardiovascular Medicine, Nara Medical University Kashihara Japan
                [2) ] Department of Nephrology, Nara Medical University Kashihara Japan
                [3) ] Department of Cardiology, Nara Prefecture Seiwa Medical Center Nara Japan
                [4) ] Department of Cardiology, Nara Prefecture General Medical Center Nara Japan
                [5) ] Department of Cardiovascular Medicine, Nara City Hospital Nara Japan
                [6) ] Department of Cardiology, Osaka Saiseikai Suita Hospital Suita Japan
                [7) ] Department of Internal Medicine, Yamato Kashihara Hospital Kashihara Japan
                [8) ] Department of Cardiology, Faculty of Medicine, University of Tsukuba Tsukuba Japan
                [9) ] Department of Cardiology, Tokyo Metropolitan Bokutoh Hospital Tokyo Japan
                [10) ] Department of Cardiovascular Medicine, Shinshu University School of Medicine Matsumoto Japan
                [11) ] Division of Cardiology, Nihon University Itabashi Hospital Tokyo Japan
                [12) ] Clinical and Translational Science, Nara Medical University Hospital Kashihara Japan
                Author notes
                Mailing address

                Makoto Watanabe, MD, PhD

                [*] Department of Cardiovascular Medicine, Nara Medical University 840 Shijo-cho, Kashihara 634-8521 Japan wmakoto07@ 123456kcn.jp
                Article
                10.1253/circrep.CR-22-0105
                10072897
                b3e419d7-58c4-43f7-a40d-095ac9ac2322
                Copyright © 2023, THE JAPANESE CIRCULATION SOCIETY

                This article is licensed under a Creative Commons [Attribution-NonCommercial-NoDerivatives 4.0 International] license.

                History
                : 20 November 2022
                : 8 February 2023
                : 13 February 2023
                Categories
                Protocol Paper

                acute myocardial infarction,contrast-induced nephropathy,emergency percutaneous coronary intervention,sodium bicarbonate

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