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Saturday, May 2, 2020 | History

2 edition of Acquired disorders of haemostasis found in the catalog.

Acquired disorders of haemostasis

Acquired disorders of haemostasis

pathophysiology, clinical practice and basic research

by

  • 354 Want to read
  • 19 Currently reading

Published by Baillière Tindall in London .
Written in English


Edition Notes

StatementJ.J. Michiels, guest editor.
SeriesBaillière"s clinical haematology : international practice and research -- 11/2, Baillière"s clinical haematology -- 11/2.
ContributionsMichiels, J. J.
The Physical Object
Paginationp.287-523 ;
Number of Pages523
ID Numbers
Open LibraryOL22472720M
ISBN 100702024597

  Haemostasis: Biochemistry, Physiology, and Pathology, edited by D. Ogston and B. Bennett, is a repository for much of this new information. The book, composed of 26 chapters authored by 24 contributors, focuses predominantly on the biochemistry of the hemostatic constituents (the first pages), and in the last ten chapters deals with Author: David Green. Platelets, Fourth Edition, integrates the entire field of platelet biology, pathophysiology, and clinical medicine with contributions from world experts from 18 award-winning reference provides clear presentations by basic scientists on the cellular, molecular, and genetic mechanisms of platelets and the role of platelets in thrombosis, hemorrhage, inflammation.   Hodgkin's lymphoma. Non-Hodgkin's lymphoma. Myeloma. MYELOPROLIFERATIVE DISORDERS. Polycythaemia. Essential thrombocythaemia and myelofibrosis. HAEMOSTASIS AND THROMBOSIS. Thrombocytopenia. Disorders of platelet function and vascular purpuras. Haemophilia. Von Willebrand's disease and other inherited coagulation disorders. Acquired disorders of Pages:   Many advances have been made in the field of thrombosis and haemostasis since the publication of the second edition of this book. This thoroughly revised third edition of Practical Hemostasis and Thrombosis encompasses the major progress in the understanding of the genetics and molecular biology, new drugs and treatment regimens available, and updated content on direct oral .


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Acquired disorders of haemostasis Download PDF EPUB FB2

Acquired disorders of coagulation may be the consequence of many underlying conditions, and although they may share abnormality of a coagulation test, e.g. a prolonged prothrombin time, their clinical effects are diverse and often sis—most acquired disorders of coagulation can be identified by screening haemostasis tests, including (1) prothrombin time (PT); (2) activated.

Get this from a library. Acquired disorders of haemostasis: pathophysiology, clinical practice and basic research. [J J Michiels;]. 4 5 On behalf of the International Society on Thrombosis and Haemostasis (ISTH), it is a pleasure to welcome you to the Second Advanced Training Course of the ISTH in Cascais, Portugal.

The course is designed to provide the latest training in biological and clinical. This book: Provides essential practical management for all those working in the field of hemostasis and thrombosis; Includes new chapters on direct oral anticoagulants and, acquired inhibitors of coagulation; Covers in a clear and succinct format, the diagnosis, treatment and prevention of thrombotic and haemostatic disorders3/5(1).

This book will offer a comprehensive guide to disorders of thrombosis and haemostasis in pregnancy. It will highlight the latest developments and controversial issues.

The multidisciplinary approach will provide authoritative clinical advice on state-of-the-art management. The disorders to be covered are highly pertinent to successful pregnancy outcome, and many may be associated with. Recombinant factor VIII or IX are the products of choice for previously untreated patients with haemophilia A and B respectively.

A wide variety of acquired disorders may lead to bleeding. DIC is a complex disorder that results from excessive activation of the haemostatic system that can have haemorrhagic or thrombotic : Vickie McDonald, Samuel J.

Machin. Hemostasis and Thrombosis: Practical Guidelines in Clinical Managementcovers all aspects of the practical management of commonly encountered thrombotic and bleeding disorders, with emphasis on clinical diagnosis, treatment, and day-to-day management. Assessing haemostasis - The coagulation system - Laboratory tests - Platelets - Bleeding - Bleeding: laboratory investigations - Bleeding: therapeutic products - von Willebrand disease - Haemophilia A and B - Rare congenital coagulation disorders - Congenital thrombocytopenias - Congenital platelet function defects - Congenital vascular disorders - Haemorrhagic disease of the newborn Author: Drew Provan.

BMA Medical Book Awards Highly Commended in Internal Medicine category. A unique clinical focus makes Consultative Hemostasis and Thrombosis, 3rd Edition your go-to guide for quick, practical answers on managing the full range of bleeding and clotting disorders.

Emphasizing real-world problems and solutions, Dr. Craig S. Kitchens, Dr. Barbara A. Konkle, and Dr. Craig M. Kessler provide. Acquired hemostatic disorders comprise thrombocytopenia and platelet dysfunction, coagulation factor deficiencies, excessive anticoagulation, and hemorrhagic complications due to antiplatelet.

This chapter sets out diagnostic and management strategies for acquired hemostatic disorders, with a particular emphasis on features that can prove useful in a perioperative context.

Antiplatelet and anticoagulant drug complications are presented in Chap. by: 1. Normal haemostasis is a balance between procoagulant and anticoagulant factors.

Abnormalities can occur as a result of both inherited or acquired abnormalities. This book is an updated comprehensive guide to disorders of thrombosis and haemostasis in pregnancy ; The book provides authoritative, practical clinical advice on the management of women with both common and rare disorders of thrombosis and haemostasis, in the context of available scientific evidence.

Hereditary disorders of platelet function consist of von Willebrand disease, the most common hereditary hemorrhagic disease, and hereditary intrinsic platelet disorders, which are much less common. Acquired disorders of platelet dysfunction are commonly due to diseases (eg.

The second edition includes a new chapter on acquired disorders of haemostasis. Online Resource Centre The Online Resource Centre to accompany Haematology features: For registered adopters of the book: DT Figures from the book, available to download For students: DT Answers to case study and self-check questions/5(37).

With authoritative coverage of rare and common hemostatic disorders, Consultative Hemostasis and Thrombosis, 4th Edition, keeps you both up to date with all that's new in this fast-moving field as well as reviewing background and development and citing pertinent classical literature.

Broad differential diagnoses are provided, underscoring the editors' position that correct treatment begins Pages: Dysregulation of hemostasis can also lead to venous thromboembolic disease, with hereditary causes including protein C, protein S and antithrombin deficiency and gain-of-function disorders such as factor V Leiden and prothrombin GA mutation, and acquired disorders such as the antiphospholipid antibody syndrome and thrombotic microangiopathies.

What is haemostasis. Haemostasis is the human body's response to blood vessel injury and bleeding. It involves a coordinated effort between platelets and numerous blood clotting proteins (or factors), resulting in the formation of a blood clot and subsequent stopping of the bleed.

BLEEDING DISORDERS Slideshare uses cookies to improve functionality and performance, and to provide you with relevant advertising. If you continue browsing the site, you agree to the use of cookies on this website. Hemostasis and Thrombosis, Sixth Edition Since publication of the First Edition inHemostasis and Thrombosis has established itself as the pre-eminent book in the field of coagulation disorders.

No other book is as inclusive in scope, with coverage of the field from the standpoint of both basic scientists and clinicians. This comprehensive resource details the essentials of bleeding and Price: $ Ratnoff OD () Hemostatic defects in liver and biliary tract disease and disorders of vitamin K metabolism.

In: Ratnoff OD, Forbes CD (eds) Disorders of hemostasis. Grune and Stratton, New York, pp – Google ScholarCited by:   2-Thrombasthenia (glanzman’s disease). 3- Bernard – soulier syndrome. 4- Von Willebrand disease. • Acquired disorders: 1- Aspirin therapy. 2- Hyperglobulinemia.

3- Myeloproliferative disorders. INHERITED COAGULATION DISORDERS VON WILLEBRAND DISEASE • The most common inherited disorder due to deficiency or dysfunction of vWF.

Hemostasis or haemostasis is a process to prevent and stop bleeding, meaning to keep blood within a damaged blood vessel (the opposite of hemostasis is hemorrhage).It is the first stage of wound involves coagulation, blood changing from a liquid to a blood vessels are central to moderating blood's tendency to form endothelial cells of intact vessels prevent.

Perioperative dental management strategies of value in patients with different congenital and acquired disorders of hemostasis are carefully explained, and the role of surgical techniques and local and topical agents in helping to minimize and control bleeding is described.

Hemostasis is the physiological process by which bleeding ceases. Hemostasis involves three basic steps: vascular spasm, the formation of a platelet plug, and coagulation, in which clotting factors promote the formation of a fibrin clot. Fibrinolysis is the process in which a clot is degraded in a healing vessel.

The second edition includes a new chapter on acquired disorders of haemostasis. Online Resource Centre The Online Resource Centre to accompany Haematology features: For registered adopters of the book: DT Figures from the book, available to download For students: DT Answers to case study and self-check s: 1.

Primary Haemostasis. Primary haemostasis is the initial response of the body to vascular injury, and involves interaction between platelets, adhesive proteins located in the subendothelial matrix (including collagen and von Willebrand factor), and circulating fibrinogen.

1 The end result of primary haemostasis is the formation of a stable platelet plug around which a fibrin network can then be. Coagulation Disorders: Definition Coagulation disorders deal with disruption of the body's ability to control blood clotting.

The most commonly known coagulation disorder is hemophilia, a condition in which patients bleed for long periods of time before clotting. There are other coagulation disorders with a variety of causes.

Description. The book is augmented by an Online Resource Centre, which includes an interactive digital microscope, video interviews with practicing biomedical scientists, and 'in the lab' footage showing biomedical science in practice Acquired disorders of haemostasis Haemostasis and anticoagulation Part 5: Case Studies Case studies in haematology.

COVID Resources. Reliable information about the coronavirus (COVID) is available from the World Health Organization (current situation, international travel).Numerous and frequently-updated resource results are available from this ’s WebJunction has pulled together information and resources to assist library staff as they consider how to handle coronavirus.

Vascular disorders Scurvy, easy bruising, Henoch-Schonlein purpura. Platelet disorders Quantitative - Thrombocytopenia Qualitative - Platelet function disorders – Glanzmans 3. Coagulation disorders Congenital - Haemophilia (A, B), Von-Willebrands Acquired - Vitamin-K deficiency, Liver disease 4.

Following the familiar, easy-to-use at a Glance format, Haematology at a Glance, Fourth Edition is a broad and accessible introduction to the study of blood. Fully revised and updated to reflect advances in the field and in clinical practice, this new edition covers essential knowledge, from basic hematological physiology to blood disorders and their diagnosis and treatment.

Primary Hemostasis. Platelets are small anuclear cell fragments that bud off from megakaryocytes, specialized large polyploid blood cells that originate in the bone marrow (Schulze et al., ).Platelets are present at to million per milliliter of blood and circulate for about ten days (Zucker-Franklin, ).In a healthy blood vessel, and under normal blood flow, platelets do not Cited by: Buy Acquired Disorders of Haematostasis: Pathophysiology, Clinical Practice and Basic Research (Bailliere's Clinical Infectious Diseases S.) by Michiels, J.

(ISBN: ) from Amazon's Book Store. Everyday low prices and free delivery on eligible : Paperback. The Textbook of Human Disease in Dentistry is structured around the systems of the body and includes chapters on immunological disease, cardiovascular diseases, respiratory medicine, gastroenterology, dermatology, musculoskeletal disorders and neurological and special senses.

A key aspect of the book is the relevance of particular diseases and Author: Mark Greenwood. Bleeding is often a presenting manifestation of systemic disease and requires a multidisciplinary team approach. Iatrogenic causes of abnormal haemostasis are of particular importance to the emergency physician.

This CME article aims to provide an approach to the diagnosis and management of acquired bleeding disorders encountered in general Author: N Alli, J Vaughan, S Louw, S Moodly, M Patel.

Part 6 Haemostasis. 39 Normal haemostasis I: vessel wall and platelets 40 Normal haemostasis II: coagulation factors and fi brinolysis 41 Disorders of haemostasis I: vessel wall and platelets 42 Disorders of haemostasis II: inherited disorders of coagulation 43 Disorders of haemostasis III: acquired disorders of coagulation Brand: Atul B.

Mehta. We have shared a review and a free pdf download link (Google Drive) of Haematology at a Glance 4th Edition. Following the familiar, easy-to-use at a Glance format, Haematology at a Glance, Fourth Edition is a broad and accessible introduction to the study of blood.

Fully revised and updated to reflect advances in the field and in clinical [ ]. Haematology. Second Edition. Gary Moore, Gavin Knight, and Andrew Blann Fundamentals of Biomedical Science. A blend of science theory and biomedical science practice make this series ideal for those seeking both the knowledge and skills to become proficient Biomedical Scientists.

The disorders covered are highly pertinent to successful pregnancy outcome, and many may be associated with significant maternal and/or fetal morbidity, and even mortality.

This book is relevant for individuals in all disciplines involved in the care of women with disorders of thrombosis and hemostasis in pregnancy.

Contents: 1. The format is designed to provide quick reference information on diagnosis - both clinical and laboratory - and management of common haematologic disorders. In addition, the basic physiologic and biochemical mechanisms of haemostasis are presented as a basis to further discussion of pathophysiology which follow later in the text.Haemostasis: Normal Physiology, Disorders of Haemostasis and Thrombosis With Elizabeth Jones, Russell David Keenan This chapter aims to provide the physiological and practical knowledge to manage three main scenarios to come across disorders of haemostasis .acquired; elderly most likely acquired B.

General consideration Does patient have a history of venous thrombosis. Does patient have a family history of venous thrombosis. Are the thrombotic events recurrent. Was the thrombosis idiopathic. Is there a history of cancer. Has the patient been treated for a clot before.

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