New PDF release: Essential Guide to Blood Coagulation

By Jovan P. Antovic, Margareta Blombäck

ISBN-10: 1405196270

ISBN-13: 9781405196277

A functional advisor to laboratory analysis and therapy of hemostatic disorders.

This concise publication covers all you want to understand to control thrombotic and bleeding issues, distilling the main clinically up to date details, and together with the most recent therapy suggestions for key stipulations and diseases. Essential advisor to Blood Coagulation covers either the good and the intense phases of hereditary and purchased bleeding and thrombotic disorders.

Faced with a bleeding sufferer, it can be tough to figure out even if blood loss is because of an area issue or an underlying hemostatic illness. there are a selection of laboratory assessments which are played to spot the reason for bleeding in a sufferer. This ebook highlights the assessments that may be utilized in the laboratory to help diagnosis.

Originally released in Swedish, Essential consultant to Blood Coagulation, has been revised to incorporate the most recent remedy concepts to be had for sufferers and should aid clinicians to extend their wisdom of hemostatic disorders.

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Additional resources for Essential Guide to Blood Coagulation

Sample text

Se). An increased fibrin D-dimer level is, however, more difficult to evaluate and cannot be used to predict the presence of a thrombosis. Some methods for measuring D-dimer have a relatively high detection limit and do not identify the minor elevations that sometimes occur in a thrombotic disease. Contact your laboratory concerning the detection limit (and the clinical prediction capacity). It is desirable to have a detection level of about 100 µg/L, which is above the upper reference limit in healthy individuals.

In patients with this mutation, the risk of developing DVT/LE is increased about seven times, while for those who are homozygous for this mutation the risk is increased more than 50-fold. This means that many heterozygous individuals will be asymptomatic for the rest of their lives. See also APC resistance. Laboratory investigations | 27 Mutation 20210G > A in the prothrombin gene This mutation (polymorphism) is present in about 2% of the normal population and is a weak but independent risk factor for DVT/LE.

Therefore, high levels are also present in many intensive care patients but often decrease quickly after adequate treatment. High levels inhibit fibrinolytic activity and can possibly contribute to poor “revascularization” of the microcirculation and organ damage. High levels correlate to a poorer prognosis. The level is elevated about five times in pregnancy. PAI-1 levels are often elevated in preeclampsia. In severe pre-eclampsia, the increased resistance in the placental circulation is correlated with a further increase in PAI-1.

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Essential Guide to Blood Coagulation by Jovan P. Antovic, Margareta Blombäck


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