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Titlebook: Sickle Cell Disease in Clinical Practice; Jo Howard,Paul Telfer Book 2015 Springer-Verlag London 2015 Hematology.Sickle Cell

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发表于 2025-3-21 16:47:23 | 显示全部楼层 |阅读模式
书目名称Sickle Cell Disease in Clinical Practice
编辑Jo Howard,Paul Telfer
视频video
概述A concise practical guide on how to manage sickle cell disease.A clear guide to outpatient management of sickle cell patients, including management plans for the chronic complications of sickle cell d
丛书名称In Clinical Practice
图书封面Titlebook: Sickle Cell Disease in Clinical Practice;  Jo Howard,Paul Telfer Book 2015 Springer-Verlag London 2015 Hematology.Sickle Cell
描述Sickle Cell Disease is the most common genetic disease world wide and in the UK. It has marked geographical variation in its distribution in the UK, with a concentration in London and other major conurbations (Birmingham and Manchester). In these areas, specialist centres have become established offering expert, up to date care for both inpatients and out patients with Sickle Cell Disease. Although patient numbers are increasing outside these areas, the expertise of health professionals can be patchy. This book aims to provide a user friendly, accessible resource for areas with smaller numbers of patients, to allow them to provide equitable care with the larger well established centres. Sickle Cell Disease can be associated with acute life threatening complications, when clear, easily available advice is needed, and with chronic long term complications which may need liaison with other health professionals. Clear treatment protocols for all the common complications of sickle cell disease, are outlined here, with summaries of key evidence and references.
出版日期Book 2015
关键词Hematology; Sickle Cell
版次1
doihttps://doi.org/10.1007/978-1-4471-2473-3
isbn_softcover978-1-4471-2472-6
isbn_ebook978-1-4471-2473-3Series ISSN 2199-6652 Series E-ISSN 2199-6660
issn_series 2199-6652
copyrightSpringer-Verlag London 2015
The information of publication is updating

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The Spleend and this results in splenic damage and dysfunction early in life. Here, we cover the presentation and clinical management of acute splenic sequestration and chronic splenomegaly. Prophylaxis for hyposplenia and asplenia are covered in the following chapter.
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2199-6652 agement plans for the chronic complications of sickle cell dSickle Cell Disease is the most common genetic disease world wide and in the UK. It has marked geographical variation in its distribution in the UK, with a concentration in London and other major conurbations (Birmingham and Manchester). In
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Book 2015ith a concentration in London and other major conurbations (Birmingham and Manchester). In these areas, specialist centres have become established offering expert, up to date care for both inpatients and out patients with Sickle Cell Disease. Although patient numbers are increasing outside these are
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Respiratory and Cardiac ComplicationsACS is a common acute respiratory complication which is often misdiagnosed or delayed in diagnosis. ACS can rapidly progress to respiratory failure. There is a high risk of mortality if not diagnosed and treated appropriately. We describe the pathology, clinical features, diagnosis and management. P
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Renal and Urological Complications mechanism in the medulla are all involved in the disease process. HbSS patients are generally the most severely affected, but significant pathology is also frequently observed in adults with HbSC, and even in carriers of SCD. A distal renal tubule concentrating defect is usually the first manifesta
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