FASN Brochure

Total Page:16

File Type:pdf, Size:1020Kb

FASN Brochure Fellow of American Society of Nephrology Fellowship in the American Society of Nephrology (FASN) recognizes the dedicated member’s proven professional contributions and their diverse set of skills and comprehensive knowledge of all aspects of nephrology. The FASN designation lets colleagues and patients know that you are part of an outstanding group of nephrology professionals. Fellowship is open to practitioners from all specialties and investigators conducting research in areas relevant to nephrology who meet the rigorous standards outlined below. Apply for Fellowship To apply for fellowship, applicants must meet four of the seven pathway requirements: 1. ASN Activity Serve ASN in one of these areas within the previous two years: + ASN Council + ASN Committee or another panel + Editor-in-Chief, Deputy Editor, or Editorial Board member for any ASN publication as well as Education Director for any of the Society’s activities + Reviewer for ASN abstract submissions 2. Board Certification in Nephrology Document certification by one of the American Board of Medical Specialty’s certification boards in nephrology, pediatric nephrology, or pathology (with a specialization in renal pathology). International candidates may submit an equivalent credential. 3. Continuing Medical Education (CME) Credits Complete a total of at least 70 hours during the past two years of AMA PRA Category 1 CME credits. 4. Grant Support/Funding Receive peer-reviewed, extramural support within the past five years from a federal entity (such as the National Institutes of Health, the Agency for Healthcare Research and Quality, or the Department of Veterans Affairs), the American Society of Nephrology, or another organization. 5. Publications Publish at least five articles in peer-reviewed journals during the past five years or present poster or oral abstract(s) during two of the last five ASN Kidney Weeks. 6. Public Service Unpaid, volunteer service to the nephrology or primary-care medicine community or as a peer reviewer. (Submit one letter from a supervisor.) 7. Teaching Teach at least 30 hours in a local, state, or national instruction in nephrology during the past two years (Submit one letter from a supervisor.) REV. 2.2019 AMERICAN SOCIETY OF NEPHROLOGY FASN Application Please complete all the information on this form. FASN candidates are required to be an ASN member. Membership status must remain current to avoid an interruption in FASN status. If an interruption occurs, the candidate must reapply. Applicant Name (List as it should appear on the certificate) Credential(s) ☐ MD ☐ PhD ☐ DO ☐ MBChB ☐ MBBS ☐ Other (Check all that apply) Contact Information Street Apt/Suite# City State/Province Zip/Postal Code Country Office Phone Email Business Name (if applicable) Pathway Requirements Document achievement in four of the seven following areas: ☐ ASN Activity ☐ Grant Support/Funding Applicants must submit their CV with the application. ☐ Board Certification in ☐ Publications Nephrology ☐ Public Service CME Credits ☐ ☐ Teaching Payment Information (All funds in USD dollars) ☐ Visa ☐ MasterCard ☐ American Express FASN application fee - $150.00 Card Holder Name Send application, CV and payment to: ASN Member Services Card # 1401 H Street, NW Suite 900 Expiration Date Security Code Washington, DC 20005 Fax: 202-478-0477 Email: [email protected] ☐ Check Enclosed (Payable to American Society of Nephrology) For questions, email [email protected].
Recommended publications
  • Study Guide Medical Terminology by Thea Liza Batan About the Author
    Study Guide Medical Terminology By Thea Liza Batan About the Author Thea Liza Batan earned a Master of Science in Nursing Administration in 2007 from Xavier University in Cincinnati, Ohio. She has worked as a staff nurse, nurse instructor, and level department head. She currently works as a simulation coordinator and a free- lance writer specializing in nursing and healthcare. All terms mentioned in this text that are known to be trademarks or service marks have been appropriately capitalized. Use of a term in this text shouldn’t be regarded as affecting the validity of any trademark or service mark. Copyright © 2017 by Penn Foster, Inc. All rights reserved. No part of the material protected by this copyright may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, or by any information storage and retrieval system, without permission in writing from the copyright owner. Requests for permission to make copies of any part of the work should be mailed to Copyright Permissions, Penn Foster, 925 Oak Street, Scranton, Pennsylvania 18515. Printed in the United States of America CONTENTS INSTRUCTIONS 1 READING ASSIGNMENTS 3 LESSON 1: THE FUNDAMENTALS OF MEDICAL TERMINOLOGY 5 LESSON 2: DIAGNOSIS, INTERVENTION, AND HUMAN BODY TERMS 28 LESSON 3: MUSCULOSKELETAL, CIRCULATORY, AND RESPIRATORY SYSTEM TERMS 44 LESSON 4: DIGESTIVE, URINARY, AND REPRODUCTIVE SYSTEM TERMS 69 LESSON 5: INTEGUMENTARY, NERVOUS, AND ENDOCRINE S YSTEM TERMS 96 SELF-CHECK ANSWERS 134 © PENN FOSTER, INC. 2017 MEDICAL TERMINOLOGY PAGE III Contents INSTRUCTIONS INTRODUCTION Welcome to your course on medical terminology. You’re taking this course because you’re most likely interested in pursuing a health and science career, which entails ­proficiency­in­communicating­with­healthcare­professionals­such­as­physicians,­nurses,­ or dentists.
    [Show full text]
  • Management of Anemia in Non-Dialysis Chronic Kidney Disease: Current Recommendations, Real-World Practice, and Patient Perspectives
    Kidney360 Publish Ahead of Print, published on July 1, 2020 as doi:10.34067/KID.0001442020 Management of Anemia in Non-Dialysis Chronic Kidney Disease: Current recommendations, real-world practice, and patient perspectives Murilo Guedes1,2, Bruce M. Robinson1,3, Gregorio Obrador4, Allison Tong5,6, Ronald L. Pisoni1, Roberto Pecoits-Filho1,2 1Arbor Research Collaborative for Health, Ann Arbor, MI, USA 2School of Medicine, Pontifícia Universidade Católica do Paraná, Curitiba, Brazil 3University of Michigan, Department of Internal Medicine, Ann Arbor, MI, USA 4Universidad Panamericana - Campus México, DF, MX, Mexico 5 Sydney School of Public Health, University of Sydney, Sydney, Australia 6 Centre for Kidney Research, The Children’s Hospital at Westmead, Sydney, Australia Corresponding Author Roberto Pecoits-Filho Arbor Research Collaborative for Health 3700 Earhart Road Ann Arbor, MI 48105 [email protected] 1 Copyright 2020 by American Society of Nephrology. Abstract In non-dialysis chronic kidney disease (ND-CKD), anemia is a multi-factorial and complex condition in which several dysfunctions dynamically contribute to a reduction in circulating hemoglobin (Hb) levels in red blood cells. Anemia is common in CKD, and represents an important and modifiable risk factor for poor clinical outcomes. Importantly, symptoms related to anemia, including reduced physical functioning and fatigue, have been identified as high priorities by patients with CKD. The current management of anemia in ND-CKD, i.e., parameters to initiate treatment, Hb and iron indexes targets, choice of therapies, and impact of treatment on clinical and patient-reported outcomes, remains controversial. In this review article, we explore the epidemiology of anemia in NDD-CKD, and revise current recommendations and controversies in its management.
    [Show full text]
  • Supplemental Guide: Nephrology
    Supplemental Guide for Nephrology Supplemental Guide: Nephrology March 2020 1 Supplemental Guide for Nephrology TABLE OF CONTENTS INTRODUCTION ............................................................................................................................. 3 PATIENT CARE .............................................................................................................................. 4 Acute Kidney Injury ...................................................................................................................... 4 Chronic Dialysis Therapy ............................................................................................................. 6 Chronic Kidney Disease ............................................................................................................... 8 Transplant .................................................................................................................................. 10 Fluid and Electrolytes ................................................................................................................. 12 Hypertension .............................................................................................................................. 13 Competence in Procedures ........................................................................................................ 15 MEDICAL KNOWLEDGE .............................................................................................................. 17 Physiology and Pathophysiology ..............................................................................................
    [Show full text]
  • 2012 CKD Guideline
    OFFICIAL JOURNAL OF THE INTERNATIONAL SOCIETY OF NEPHROLOGY KDIGO 2012 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease VOLUME 3 | ISSUE 1 | JANUARY 2013 http://www.kidney-international.org KDIGO 2012 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease KDIGO gratefully acknowledges the following consortium of sponsors that make our initiatives possible: Abbott, Amgen, Bayer Schering Pharma, Belo Foundation, Bristol-Myers Squibb, Chugai Pharmaceutical, Coca-Cola Company, Dole Food Company, Fresenius Medical Care, Genzyme, Hoffmann-LaRoche, JC Penney, Kyowa Hakko Kirin, NATCO—The Organization for Transplant Professionals, NKF-Board of Directors, Novartis, Pharmacosmos, PUMC Pharmaceutical, Robert and Jane Cizik Foundation, Shire, Takeda Pharmaceutical, Transwestern Commercial Services, Vifor Pharma, and Wyeth. Sponsorship Statement: KDIGO is supported by a consortium of sponsors and no funding is accepted for the development of specific guidelines. http://www.kidney-international.org contents & 2013 KDIGO VOL 3 | ISSUE 1 | JANUARY (1) 2013 KDIGO 2012 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease v Tables and Figures vii KDIGO Board Members viii Reference Keys x CKD Nomenclature xi Conversion Factors & HbA1c Conversion xii Abbreviations and Acronyms 1 Notice 2 Foreword 3 Work Group Membership 4 Abstract 5 Summary of Recommendation Statements 15 Introduction: The case for updating and context 19 Chapter 1: Definition, and classification
    [Show full text]
  • Chapter 10: Radiation Nephropathy
    Chapter 10: Radiation Nephropathy † Amaka Edeani, MBBS,* and Eric P. Cohen, MD *Kidney Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland; and †Nephrology Division, Department of Medicine, University of Maryland School of Medicine, and Baltimore Veterans Affairs Medical Center, Baltimore, Maryland INTRODUCTION Classical radiation nephropathy occurred after external beam radiation for treatment of solid The occurrence of renal dysfunction as a consequence cancers such as seminomas (6); the incidence has of ionizing radiation has been known for more than declined with the advent of more effective chemo- 100 years (1,2). Initial reports termed this condition therapy. In recent years, radiation nephropathy has “radiation nephritis,” but that is a misnomer, because occurred due to TBI used as part of chemo-irradiation it is not an inflammatory condition. Renal radiation conditioning just before hematopoietic stem cell injury may be avoided by the exclusion of an ade- transplantation (HSCT) and also from targeted ra- quate volume of kidney exposure during radiation dionuclide therapy used for instance in the treatment therapy, but the kidneys’ central location can make of neuroendocrine malignancies. TBI may be myelo- this difficult to impossible when tumors of the abdo- ablative or nonmyeloablative, with myeloablative men or retroperitoneum are treated, or during total regimens using radiation doses of 10–12 Gy to de- body irradiation (TBI) (3). stroy or suppress the recipient’s bone marrow. These doses are given in a single fraction or in nine fractions over 3 days (4). In addition, TBI for bone marrow BACKGROUND/CLINICAL SIGNIFICANCE transplantation (BMT) is preceded or accompanied by cytotoxic chemotherapy, which potentiates the Radiation nephropathy is renal injury and loss of effects of ionizing radiation (7).
    [Show full text]
  • Glomerulonephritis
    Adolesc Med 16 (2005) 67–85 Glomerulonephritis Keith K. Lau, MDa,b, Robert J. Wyatt, MD, MSa,b,* aDivision of Pediatric Nephrology, Department of Pediatrics, University of Tennessee Health Sciences Center, Room 301, WPT, 50 North Dunlap, Memphis, TN 38103, USA bChildren’s Foundation Research Center at the Le Bonheur Children’s Medical Center, Room 301, WPT, 50 North Dunlap, Memphis, TN 38103, USA Early diagnosis of glomerulonephritis (GN) in the adolescent is important in initiating appropriate treatment and controlling chronic glomerular injury that may eventually lead to end-stage renal disease (ESRD). The spectrum of GN in adolescents is more similar to that seen in young and middle-aged adults than to that observed in prepubertal children. In this article, the authors discuss the clinical features associated with GN and the diagnostic evaluation required to determine the specific type of GN. With the exception of hereditary nephritis (Alport’s disease), virtually all types of GN are immunologically mediated with glomerular deposition of immunoglobulins and complement proteins. The inflammatory events leading to GN may be triggered by a number of factors. Most commonly, immune complexes deposit in the glomeruli or are formed in situ with the antigen as a structural component of the glomerulus. The immune complexes then initiate the production of proinflammatory mediators, such as complement proteins and cytokines. Subsequently, the processes of sclerosis within the glomeruli and fibrosis in the tubulointerstitial cells lead to chronic or even irreversible renal injury [1]. Less commonly, these processes occur without involvement of immune complexes—so-called ‘‘pauci-immune GN.’’ * Corresponding author.
    [Show full text]
  • IDF Guide for Nurses Imimmmunnoogglolboubliun Ltinhe Trahpeyr Faopr Y Fopr Rpirmimaarryy I Mimmumnoudneoficdieenfciyc Ideisnecasy Es Diseases IDF GUIDE for NURSES
    IDF Guide for Nurses ImImmmunnoogglolboubliun lTinhe Trahpeyr faopr y foPr rPirmimaarryy I mImmumnoudneoficdieenfciyc iDeisnecasy es Diseases IDF GUIDE FOR NURSES IMMUNOGLOBULIN THERAPY FOR PRIMARY IMMUNODEFICIENCY DISEASES THIRD EDITION COPYRIGHTS 2004, 2007, 2012 IMMUNE DEFICIENCY FOUNDATION Copyright 2012 by the Immune Deficiency Foundation, USA. PRINT: 12/2013 Readers may redistribute this publication to other individuals for non-commercial use, provided that the text, html codes, and this notice remain intact and unaltered in any way. The IDF Guide for Nurses may not be resold, reprinted or redistributed for compensation of any kind without prior written permission from the Immune Deficiency Foundation. If you have any questions about permission, please contact: Immune Deficiency Foundation, 40 West Chesapeake Avenue, Suite 308, Towson, MD 21204, USA, or by telephone: 800.296.4433. This publication has been made possible through a generous grant from IDF Guide for Nurses Immunoglobulin Therapy for Primary Immunodeficiency Diseases Third Edition Immune Deficiency Foundation 40 West Chesapeake Avenue, Suite 308 Towson, MD 21204 800.296.4433 www.primaryimmune.org Editor: M. Elizabeth M. Younger CRNP, PhD Johns Hopkins, Baltimore, Maryland Vice Chair, Immune Deficiency Foundation Nurse Advisory Committee Associate Editors: Rebecca H. Buckley, MD Duke University School of Medicine, Durham, NC Chair, Immune Deficiency Foundation Medical Advisory Committee Christine M. Belser Immune Deficiency Foundation, Towson, Maryland Kara Moran Immune Deficiency
    [Show full text]
  • Renal Papillary Necrosis Following Mesenteric Artery Stenting
    Open Access Case Report DOI: 10.7759/cureus.10824 Renal Papillary Necrosis Following Mesenteric Artery Stenting Zachary A. Glusman 1, 2 , Kenneth J. Sample 1, 2 , Kevin S. Landau 1, 2 , Ronald B. Vigo 2 1. Internal Medicine, St. George's University School of Medicine, St. George's, GRD 2. Nephrology, Delray Medical Center, Delray Beach, USA Corresponding author: Zachary A. Glusman, [email protected] Abstract A 62-year-old man presented with left flank pain and hematuria four days after undergoing mesenteric artery balloon angioplasty and stent placement. Imaging revealed left renal infarction with associated papillary necrosis and a thrombus in the left collecting system causing acute renal obstruction. Complete obstruction was confirmed using MAG3 Renal Scan with Lasix. A nephrostomy tube was inserted under CT guidance by interventional radiology with complete resolution of obstruction and hematuria. Categories: Cardiac/Thoracic/Vascular Surgery, Internal Medicine, Nephrology Keywords: renal papillary necrosis, renal infarction, renal thrombus, kidney, papillary necrosis, renal obstruction Introduction Renal papillary necrosis (RPN) is a rare presentation of coagulative necrosis of the papilla and medullary pyramids. It is most often associated with analgesic nephropathy, sickle cell nephropathy, and diabetes mellitus complicated by urinary tract infection. However, it may also present in the setting of pyelonephritis, obstructive uropathy, hepatopathology, tuberculosis, renal transplant rejection, and some vasculitides or coagulopathies [1,2]. This potentially devastating process can lead to secondary infection of necrotic areas and may involve sloughing of the affected cells that can cause obstructive nephropathy and even complete renal failure [1]. Case Presentation A 62-year-old Caucasian man presented with complaints of palpitations and leg pain with toe discoloration.
    [Show full text]
  • Report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference
    Nomenclature for Kidney Function and Disease: Report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference Andrew S. Levey 1, Kai-Uwe Eckardt 2, Nijsje M. Dorman 3, Stacy L. Christiansen 4, Ewout J. Hoorn 5, Julie R. Ingelfinger 6, Lesley A. Inker 1, Adeera Levin 7, Rajnish Mehrotra 8, Paul M. Palevsky 9, Mark A. Perazella 10 , Allison Tong 11 , Susan J. Allison 12 , Detlef Bockenhauer 13 , Josephine P. Briggs 14 , Jonathan S. Bromberg 15 , Andrew Davenport 16 , Harold I. Feldman 17 , Denis Fouque 18 , Ron T. Gansevoort 19 , John S. Gill 20 , Eddie L. Greene 21 , Brenda R. Hemmelgarn 22 , Matthias Kretzler 23 , Mark Lambie 24 , Pascale H. Lane 25 , Joseph Laycock 26 , Shari Leventhal 27 , Michael Mittelman 28 , Patricia Morrissey 29 , Marlies Ostermann 30 , Lesley Rees 31 , Pierre Ronco 32 , Franz Schaefer 33 , Jennifer St. Clair Russell 34 , Caroline Vinck 35 , Stephen B. Walsh 36 , Daniel E. Weiner 1, Michael Cheung 37; Michel Jadoul 38, Wolfgang C. Winkelmayer 39 1 Division of Nephrology, Tufts Medical Center, Boston, MA, USA 2 Department of Nephrology and Medical Intensive Care, Charité Universitätsmedizin Berlin, Berlin, Germany 3 Managing Editor , AJKD 4 Managing Editor , JAMA 5 Department of Internal Medicine, Division of Nephrology and Transplantation, Erasmus Medical Center, University Medical Center Rotterdam, The Netherlands 6 Harvard Medical School, Boston, Mass; Department of Pediatrics, Massachusetts General Hospital, Boston, MA, USA 7 Division of Nephrology, University of British Columbia, Vancouver,
    [Show full text]
  • Use of Ultrasound in Kidney Disease and Nephrology Procedures
    CJASN ePress. Published on January 23, 2014 as doi: 10.2215/CJN.03170313 Renal Relevant Radiology: Use of Ultrasound in Kidney Disease and Nephrology Procedures W. Charles O’Neill Abstract Ultrasound is commonly used in nephrology for diagnostic studies of the kidneys and lower urinary tract and to guide percutaneous procedures, such as insertion of hemodialysis catheters and kidney biopsy. Nephrologists must, therefore, have a thorough understanding of renal anatomy and the sonographic appearance of normal Renal Division, Department of kidneys and lower urinary tract, and they must be able to recognize common abnormalities. Proper interpretation Medicine, Emory requires correlation with the clinical scenario. With the advent of affordable, portable scanners, sonography has University School of become a procedure that can be performed by nephrologists, and both training and certification in renal Medicine, Atlanta, ultrasonography are available. Georgia Clin J Am Soc Nephrol 9: ccc–ccc, 2014. doi: 10.2215/CJN.03170313 Correspondence: Dr.W.Charles O’Neill, Emory Introduction decisions (Figure 1). Given its poor precision (5), this University School of Sonography is an essential tool in nephrology for not measurement should be performed several times. Medicine, Renal only the diagnosis and management of kidney dis- Since the poor precision stems mostly from under- Division WMB 338, 1639 Pierce Drive, ease, but also for the guidance of invasive procedures. measurement, the maximum length is the value that Atlanta, GA 30322. For this reason, it is essential for nephrologists to should be reported. Measurement of other dimen- Email: woneill@ have a thorough understanding of sonography and its sionsisevenmoreimpreciseandisofnoutility. emory.edu uses in nephrology.
    [Show full text]
  • College-Regulations Nephrology.Pdf
    CMSA The Colleges of Medicine of South Africa NPC Nonprofit Company (Reg. No. 1955/000003/08) Nonprofit Organisation (Reg No 009 - 8 7 4 N P O ) 27 Rhodes Ave, PARKTOWN WEST 2193 Private Bag X23, BRAAMFONTEIN 2017 Tel: +27 11 726 -7 0 3 7 /8 /9 Fax: +27 11 726 -4 0 3 6 General: a dmin@cmsa -jhb.co.za Academic Registrar: a lv@cmsa -jhb.co.za JOHANNESBURG Website: www.collegemedsa.ac.za ACADEMIC OFFICE September 2014 THE COLLEGE OF PHYSICIANS OF SOUTH AFRICA R E G U L A T I O N S FOR ADMISSION TO THE EXAMINATION FOR THE POST-SPECIALISATION SUB-SPECIALTY CERTIFICATE IN NEPHROLOGY Cert Nephrology(SA) Phys 1.0 ELIGIBILITY TO TAKE THE EXAMINATION In order to be eligible to enter for this examination, the candidate:- 1.1 must comply with the requirements for registration as a medical practitioner, as prescribed by the Medical, Dental and Supplementary Health Services Act. 1.2 must be registered as a specialist Physician 2.0 ADMISSION TO THE EXAMINATION (to be read in conjunction with the Instructions) The following are the requirements for admission to the examination: 2.1 registration as a specialist Physician 2.2 certification of having completed at least eighteen months as a subspecialty trainee in accredited specialist department(s) / division(s) / unit(s) of nephrology, registered and approved by the Health Professions Council of South Africa. 2.3 submission of the prescribed logbook, filled in up to date, and certified by the head(s) of the department(s)/division(s)/unit(s) in which the candidate trained.
    [Show full text]
  • Proteinuria and Nephrotic Syndrome
    Proteinuria and Nephrotic Syndrome Rebecca Hjorten, MD Division of Nephrology Speaker Disclosures • Relevant Financial Relationships: No disclosure. • Relevant Nonfinancial Relationships: No disclosure. • I have no actual or potential conflict of interest in relation to this program/presentation. Division of NephrologyDivision of Nephrology Urine Dip Concern for Positive for Urine Positive for Glomerulonephritis Protein Protein AND Blood (GN) …PIGN, MPGN, IgA, HSP Lupus, ANCA vasculitis, Urine Positive for Anti-GBM Asymptomatic Protein AND NORMAL Concerning Ex. Nephrotic Syndrome False Positive Symptoms Non-Significant Levels Persistent of Urine Protein Asymptomatic Consider Proteinuria Further Orthostatic Proteinuria Evaluation and Referral to Transient Proteinuria Pediatric Nephrology Division of Nephrology Urine Dip Concern for Positive for Urine Positive for Glomerulonephritis Protein Protein AND Blood (GN) …PIGN, MPGN, IgA, HSP Lupus, ANCA vasculitis, Urine Positive for Anti-GBM Asymptomatic Protein AND NORMAL Concerning Ex. Nephrotic Syndrome False Positive Symptoms Non-Significant Levels Persistent of Urine Protein Asymptomatic Consider Proteinuria Further Orthostatic Proteinuria Evaluation and Referral to Transient Proteinuria Pediatric Nephrology Division of Nephrology Objectives • Asymptomatic Proteinuria without Hematuria • Identification of transient and orthostatic proteinuria • Initial workup and referral or persistent proteinuria • Nephrotic syndrome • Early recognition of nephrotic syndrome • Initiation of management •
    [Show full text]