Hemolytic Uremic Syndrome And Thrombotic Thrombocytopenic Purpura
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Hemolytic Uremic Syndrome And Thrombotic Thrombocytopenic Purpura
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Author : Bernard S. Kaplan
language : en
Publisher: CRC Press
Release Date : 1992-07-14
Hemolytic Uremic Syndrome And Thrombotic Thrombocytopenic Purpura written by Bernard S. Kaplan and has been published by CRC Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 1992-07-14 with Medical categories.
This reference presents detailed discussions of the history, pathology, pathophysiology, and approaches to treatment of the complicated, constantly evolving syndromes known as thrombotic thromocytopenic purpura (TTP), from many different points of view. Hemolytic Uremic syndrome and Thrombotic Thrombocytopenic Purpura offers: extensive analyses of the relationship between HUS and TTP; epidemiological studies of HUS from the UK, Canada, Asia, South Africa and Argentina; investigations of non-renal complications of HUS; perspectives on atypical HUS and post-transplantation HUS; delineations of the association between verotoxin and HUS, HUS and pregnancy, and HUS and cancer and cancer tharapy; information on HUS/TTP in HIV-infected patients; explications of the pathology and pathogenesis of HUS; and approaches to treatment of HUS, prognosis, and long-term follow-up.;In addition, it covers the history and pathogenesis of TTP, von Willebrand factor abnormalities in TTP and HUS, platelet agglutinating proteins in TTP, and the treatment of TTP.;With over 2000 literature citations and figures, this book is for nephrologists, hematologists, oncologists, paediatricians, pathologists, gastroenterologists, internists, endocrinologists, infectious disease specialists, neurologists, gynaecologists, microbiologists, surgeons, geneticsts, epidemiologists, radiologists, and medical school students in these disciplines.
Studies Of The Pathogenesis Of Hemolytic Uremic Syndrome And Thrombotic Thrombocytopenic Purpura
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Author : Diana O. Karpman
language : en
Publisher:
Release Date : 1997
Studies Of The Pathogenesis Of Hemolytic Uremic Syndrome And Thrombotic Thrombocytopenic Purpura written by Diana O. Karpman and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1997 with Endotoxins categories.
Thrombotic Thrombocytopenic Purpura And The Hemolytic Uremic Syndrome
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Author : Hau C. Kwaan
language : en
Publisher:
Release Date : 1997
Thrombotic Thrombocytopenic Purpura And The Hemolytic Uremic Syndrome written by Hau C. Kwaan and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1997 with categories.
Thrombotic Thrombocytopenic Purpura Ttp And Hemolytic Uremic Syndrome Hus
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Author : J. T. Thomas
language : en
Publisher: CreateSpace
Release Date : 2015-04-18
Thrombotic Thrombocytopenic Purpura Ttp And Hemolytic Uremic Syndrome Hus written by J. T. Thomas and has been published by CreateSpace this book supported file pdf, txt, epub, kindle and other format this book has been release on 2015-04-18 with categories.
This book is written to help the reader further understand the Thrombotic Thrombocytopenic Purpura (TTP) and Hemolytic Uremic Syndrome (HUS). This book is written in a simple and easy to read format designed for medical students, residents and physicians who are preparing for boards. This book simplifies a complicated medical issue so you will remember the important details.
Fast Facts Thrombotic Thrombocytopenic Purpura
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Author : Marie A. Scully
language : en
Publisher: Karger Medical and Scientific Publishers
Release Date : 2020-02-26
Fast Facts Thrombotic Thrombocytopenic Purpura written by Marie A. Scully and has been published by Karger Medical and Scientific Publishers this book supported file pdf, txt, epub, kindle and other format this book has been release on 2020-02-26 with Medical categories.
Thrombotic thrombocytopenic purpura (TTP) is a rare disorder of the blood coagulation system. In most cases, a lack of the ADAMTS13 enzyme leads to an accumulation of ultra-large von Willebrand factor molecules in the plasma which, in turn, initiate the formation of microscopic thromboses in small blood vessels. TTP is a medical emergency. Timely diagnosis and urgent and effective management are vital – mortality in those untreated is in the region of 90%. The understanding of TTP pathogenesis has increased markedly in recent decades. It is now known that TTP is acquired (immunemediated) or congenital, and that the most common type – the acquired form – predominantly affects women in their 40s. It is also clear that the prompt delivery of plasma exchange saves lives. 'Fast Facts: Thrombotic Thrombocytopenic Purpura' sets out, in a clear and accessible format, the steps to suspecting, diagnosing and treating this potentially devastating disease. These steps are complemented by clear descriptions of the disease mechanism and epidemiology. Differential diagnosis, which is of the utmost importance for this disease, is explored in detail. Contents: • Disease overview • Clinical presentation • Differential diagnosis • Laboratory findings and diagnosis • Management
Hemolytic Uremic Syndrome New Insights For The Healthcare Professional 2012 Edition
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Author :
language : en
Publisher: ScholarlyEditions
Release Date : 2012-12-10
Hemolytic Uremic Syndrome New Insights For The Healthcare Professional 2012 Edition written by and has been published by ScholarlyEditions this book supported file pdf, txt, epub, kindle and other format this book has been release on 2012-12-10 with Medical categories.
Hemolytic-Uremic Syndrome: New Insights for the Healthcare Professional / 2012 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about Hemolytic-Uremic Syndrome in a compact format. The editors have built Hemolytic-Uremic Syndrome: New Insights for the Healthcare Professional / 2012 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Hemolytic-Uremic Syndrome in this eBook to be deeper than what you can access anywhere else, as well as consistently reliable, authoritative, informed, and relevant. The content of Hemolytic-Uremic Syndrome: New Insights for the Healthcare Professional / 2012 Edition has been produced by the world’s leading scientists, engineers, analysts, research institutions, and companies. All of the content is from peer-reviewed sources, and all of it is written, assembled, and edited by the editors at ScholarlyEditions™ and available exclusively from us. You now have a source you can cite with authority, confidence, and credibility. More information is available at http://www.ScholarlyEditions.com/.
Thrombotic Thrombocytopenic Purpura Hemolytic Uremic Syndrome In Relapsing Remitting Multiple Sclerosis Patients On High Dose Interferon
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Author :
language : en
Publisher:
Release Date : 2014
Thrombotic Thrombocytopenic Purpura Hemolytic Uremic Syndrome In Relapsing Remitting Multiple Sclerosis Patients On High Dose Interferon written by and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2014 with categories.
Three women aged 34–47 years old, on high dose interferon beta-1a for relapsing–remitting multiple sclerosis, were hospitalized between 2009–2012 for thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Patients sought medical attention for neurological symptoms including cephalalgia, blurred vision, confusion, focal deficits and seizures. All patients presented thrombocytopenia, hemolytic anemia and arterial hypertension. Despite plasma exchanges, corticosteroids and anti-CD20 treatments, all patients progressed towards severe renal insufficiency and one patient died of hemorrhagic shock. In this report we identify a rare but morbid complication of interferon beta-1a treatment associated with female gender, Caucasian background and low body mass index.
Hemolytic Uremic Syndrome New Insights For The Healthcare Professional 2011 Edition
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Author :
language : en
Publisher: ScholarlyEditions
Release Date : 2012-01-09
Hemolytic Uremic Syndrome New Insights For The Healthcare Professional 2011 Edition written by and has been published by ScholarlyEditions this book supported file pdf, txt, epub, kindle and other format this book has been release on 2012-01-09 with Medical categories.
Hemolytic-Uremic Syndrome: New Insights for the Healthcare Professional: 2011 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about Hemolytic-Uremic Syndrome in a compact format. The editors have built Hemolytic-Uremic Syndrome: New Insights for the Healthcare Professional: 2011 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Hemolytic-Uremic Syndrome in this eBook to be deeper than what you can access anywhere else, as well as consistently reliable, authoritative, informed, and relevant. The content of Hemolytic-Uremic Syndrome: New Insights for the Healthcare Professional: 2011 Edition has been produced by the world’s leading scientists, engineers, analysts, research institutions, and companies. All of the content is from peer-reviewed sources, and all of it is written, assembled, and edited by the editors at ScholarlyEditions™ and available exclusively from us. You now have a source you can cite with authority, confidence, and credibility. More information is available at http://www.ScholarlyEditions.com/.
Thrombotic Microangiopathies Advances In Research And Treatment 2011 Edition
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Author :
language : en
Publisher: ScholarlyEditions
Release Date : 2012-01-09
Thrombotic Microangiopathies Advances In Research And Treatment 2011 Edition written by and has been published by ScholarlyEditions this book supported file pdf, txt, epub, kindle and other format this book has been release on 2012-01-09 with Medical categories.
Thrombotic Microangiopathies: Advances in Research and Treatment: 2011 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about Thrombotic Microangiopathies in a compact format. The editors have built Thrombotic Microangiopathies: Advances in Research and Treatment: 2011 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Thrombotic Microangiopathies in this eBook to be deeper than what you can access anywhere else, as well as consistently reliable, authoritative, informed, and relevant. The content of Thrombotic Microangiopathies: Advances in Research and Treatment: 2011 Edition has been produced by the world’s leading scientists, engineers, analysts, research institutions, and companies. All of the content is from peer-reviewed sources, and all of it is written, assembled, and edited by the editors at ScholarlyEditions™ and available exclusively from us. You now have a source you can cite with authority, confidence, and credibility. More information is available at http://www.ScholarlyEditions.com/.
Fast Facts For Patients Thrombotic Thrombocytopenic Purpura
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Author : Marie Scully
language : en
Publisher: Karger Medical and Scientific Publishers
Release Date : 2022-03-24
Fast Facts For Patients Thrombotic Thrombocytopenic Purpura written by Marie Scully and has been published by Karger Medical and Scientific Publishers this book supported file pdf, txt, epub, kindle and other format this book has been release on 2022-03-24 with Medical categories.
Thrombotic thrombocytopenic purpura (TTP) is a rare disorder of the blood coagulation system. In most cases, a lack of the ADAMTS13 enzyme leads to an accumulation of ultra-large von Willebrand factor molecules in the plasma which, in turn, initiate the formation of microscopic thromboses in small blood vessels. TTP is a medical emergency. Timely diagnosis and urgent and effective management are vital – mortality in those untreated is in the region of 90%. The understanding of TTP pathogenesis has increased markedly in recent decades. It is now known that TTP is acquired (immunemediated) or congenital, and that the most common type – the acquired form – predominantly affects women in their 40s. It is also clear that the prompt delivery of plasma exchange saves lives. 'Fast Facts: Thrombotic Thrombocytopenic Purpura' sets out, in a clear and accessible format, the steps to suspecting, diagnosing and treating this potentially devastating disease. These steps are complemented by clear descriptions of the disease mechanism and epidemiology. Differential diagnosis, which is of the utmost importance for this disease, is explored in detail. Table of Contents: · Disease overview · Clinical presentation · Differential diagnosis · Laboratory findings and diagnosis · Management