Clotting Cascade PowerPoint Templates

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Clotting cascade plays a very important role in healing the injury of the blood vessel and other injury site of the body. To explain the Coagulation factors and the Clotting cascade pathway to your audience in a very creative way you can use Clotting cascade PowerPoint templates. Know more: http://www.medicalppttemplates.com/medical-ppt-templates.aspx/Clotting-Cascade-473

Thrombosis & Haemostasis: Research is an open access, peer reviewed, scholarly journal dedicated to publish articles covering all areas of Thrombosis & Haemostasis. The journal aims to promote research communications and provide a forum for doctors, researchers, physicians and healthcare professionals to find most recent advances in all areas of Thrombosis & Haemostasis. Thrombosis & Haemostasis: Research accepts original research articles, reviews, mini reviews, case reports and rapid communication covering all aspects of Thrombosis & Haemostasis. Thrombosis & Haemostasis: Research strongly supports the scientific up gradation and fortification in related scientific research community by enhancing access to peer reviewed scientific literary works. Austin Publishing Group also brings universally peer reviewed journals under one roof thereby promoting knowledge sharing, mutual promotion of multidisciplinary science.

Download online hematology powerpoint template

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Antiphospholipid syndrome

Saurabh Gupta

Antiphospholipid syndrome (APS) is an autoimmune disorder characterized by arterial or venous blood clots and/or pregnancy morbidity. It results from antibodies that target phospholipids or proteins that bind phospholipids. APS can occur alone (primary) or with other autoimmune diseases like lupus (secondary). The antibodies are associated with an increased risk of blood clots, heart attacks, strokes, preeclampsia, and fetal loss. Diagnosis requires both clinical criteria of vascular events or pregnancy complications and laboratory detection of antiphospholipid antibodies. Treatment focuses on blood thinners to prevent new clots.

Blood intro,vol& poiesis by Dr.M.Anthony David MD

antdavsku

The document discusses blood physiology and erythropoiesis. It provides details on the composition of blood including plasma, red blood cells, white blood cells and platelets. It also describes the production of blood cells known as hematopoiesis starting from pluripotent stem cells and progenitor cells that give rise to the various cell lineages through a series of differentiation steps in the bone marrow. Specifically, it outlines the process of erythropoiesis or red blood cell production from the proerythroblast stage through the basophilic, polychromatophilic and orthochromic stages in both the fetal liver and postnatal bone marrow.

Hemorragia subaracnoidea tanya final

Hospital Regional Atlantida

La hemorragia subaracnoidea no traumática es una emergencia neurológica causada principalmente por la ruptura de un aneurisma cerebral. Representa el 2-5% de todos los derrames cerebrales y afecta a miles de personas cada año en los EE. UU. El diagnóstico se realiza mediante TAC cerebral o punción lumbar, y el tratamiento incluye la fijación del aneurisma roto mediante clipaje quirúrgico o coiling endovascular. Las complicaciones comunes son el vasoespasmo, hidrocefalia y nuevas

Thromboembolism in pregnancy

hanaa adnan

1) This document discusses hemostasis, coagulation during pregnancy, thromboembolism in pregnancy including superficial thrombophlebitis, deep vein thrombosis, pulmonary embolism, and thrombophilias. 2) Pregnancy causes a hypercoagulable state due to increased fibrinogen, factors V, VII, VIII, IX, X and XII. This helps control bleeding after delivery but also increases risk of thrombosis. 3) Thromboembolism is a leading cause of maternal death. Risk factors include prior VTE, thrombophilia, older age, obesity, cesarean delivery, and medical comorbidities. Superficial thrombophlebitis causes pain while

La isoinmunización materno-fetal ocurre cuando una madre desarrolla anticuerpos contra los antígenos de glóbulos rojos del feto, lo que puede causar anemia y otras complicaciones graves en el feto o recién nacido. Los dos tipos principales son la incompatibilidad ABO, causada por diferencias en los tipos de sangre A, B, AB u O; y la incompatibilidad Rh, que ocurre cuando una madre Rh- tiene un feto Rh+. La detección temprana y el tratamiento, como transfusiones fetales o interrupción del embaraz

4 hemostasis&thrombosis

Prasad CSBR

Hemostasis and thrombosis involve the regulation of blood clotting. Normal hemostasis maintains blood fluidity but allows clotting at sites of injury. Thrombosis is pathological clotting in uninjured or minimally injured vessels. It involves platelet adhesion and activation, coagulation cascade activation, and fibrin clot formation. Counter-regulatory mechanisms normally limit clotting to the injury site. Abnormalities in blood components, vessel walls, or flow can cause hypercoagulability and thrombosis.

Introduction to Phlebotomy

payneje

The document discusses phlebotomy, which is defined as the collection of blood specimens for laboratory analysis and diagnosis. It describes the duties of a phlebotomist, which include correctly identifying patients, collecting the proper amount of blood in labeled containers, and transporting samples to the lab in a timely manner while interacting professionally with patients. The document also lists desirable personal characteristics for phlebotomists such as dependability, compassion, and strong communication and listening skills when interacting with patients.

Coagulation assays part 1

derosaMSKCC

This document provides an overview of routine coagulation assays including PT, aPTT, fibrinogen, D-dimer, and mixing studies. It discusses the clinical utility and interpretation of these assays for monitoring coagulation and detecting coagulation disorders or abnormalities. Key points include that PT measures the extrinsic pathway and factors VII, X, and prothrombin, while aPTT is more sensitive to deficiencies in the intrinsic pathway and contact factors. D-dimer has high negative predictive value for ruling out VTE but low positive predictive value due to non-specific elevations. Mixing studies can help distinguish between factor deficiencies and inhibitors like lupus anticoagulant.

Pathogenesis & Lab diagnosis of Hemolytic Anemia

Ramachandran Thiruvengadam

This document discusses the pathogenesis and laboratory diagnosis of sickle cell anemia and thalassemia. It describes how abnormal red blood cells are destroyed in the spleen, releasing hemoglobin. The heme portion of hemoglobin is broken down into bilirubin and stored iron, while the globin portion is recycled to amino acids. This leads to anemia. Specific tests are used to diagnose these conditions based on abnormal hemoglobin levels, types or variants seen on electrophoresis or peripheral smears. Genetic testing can also identify mutations that cause these hemolytic anemias.

Hereditary spherocytosis

Asif Zeb

Sql Antipatterns Strike Back

Karwin Software Solutions LLC

Coagulation cascade

templatesforpowerpoint.com

Coagulation cascade PowerPoint templates designed by skilled, experienced and professional graphic designers that are intended to solve the big issue of time consumption. These are fully editable slides and organized in a way to simplify the most complex topics and present it in an attractive manner. You can easily incorporate charts, diagrams and animations along with the content to these layouts in order to explore new technologies and trends of businesses in a unique way. All editable slides are digitally created to pinpoint and clarify the message, and summarize information regarding topic.

Collection and handling of blood

Umm Alqura University, Makkah, SA.

This document provides guidelines for proper blood collection and handling. It discusses selecting the appropriate collection tubes based on required tests and filling order. Venous blood is most commonly collected from the antecubital fossa, but other sites like the hand, leg or neck may be used if needed. Capillary or arterial blood can also be taken for certain tests. Labels must include full patient details and specimens should be promptly delivered to the lab. Following sterile technique and avoiding complications like stasis is important to obtain quality samples.

Thalassemia Case presentation

aazma

The document summarizes a case of a 16 month old female patient named Naseeba who presented with pallor and difficulty breathing for the past month and 5 days respectively. She was diagnosed with thalassemia major based on her history of severe anemia requiring regular blood transfusions since 8 months of age. Her examination revealed signs of severe anemia, failure to thrive, and secondary malnutrition. The discussion section provided an overview of thalassemia including pathogenesis, classification, management with regular blood transfusions and chelation therapy, as well as complications. It emphasized the importance of lifelong management, counseling, and screening to improve quality of life for patients with thalassemia major.

Coagulation

shabeel pn

The document discusses the process of coagulation and fibrinolysis. It describes the three major systems involved - the vessel wall, platelets, and the coagulation cascade. The coagulation cascade involves multiple coagulation factors and pathways. Fibrinolysis is the breakdown of clots by plasmin. The document also discusses inhibitors and regulators of coagulation, including the roles of vitamin K, thrombomodulin, and tissue factor pathway inhibitor.

Paediatric hematology

Ahmed Yousef

The document discusses the scope of pediatric hematology, including red blood cell disorders like anemias and thalassemias, platelet and coagulation disorders, and pediatric oncology. It provides objectives for an introductory lecture on understanding the hematopoietic system, normal pediatric investigation values, and evaluating anemias. Key aspects of the hematopoietic system development and composition are outlined.

Seminar thalassemia

siti hamidah

1. Thalassemia is caused by a defective production of the globin portion of hemoglobin, resulting in an imbalance between alpha and beta globin chains. 2. There are two main types - alpha thalassemia affects alpha chain production while beta thalassemia affects beta chain production. 3. Beta thalassemia major is the most severe form, characterized by severe anemia starting in early childhood requiring lifelong regular blood transfusions and iron chelation therapy to prevent iron overload.

Incompatibilidad rh final

Hospital Regional Atlantida

Este documento describe la incompatibilidad Rh materna, una condición en la que los glóbulos rojos del feto tienen el antígeno Rh positivo mientras que la madre es Rh negativa, lo que puede provocar una respuesta inmune de la madre. Explica que la incompatibilidad Rh puede causar enfermedad hemolítica perinatal en embarazos posteriores y describe los mecanismos fisiopatológicos, el diagnóstico, la vigilancia y el tratamiento de esta afección potencialmente grave.

Thalassaemia

Azilah Sulaiman

This document discusses non-transfusion dependent thalassemia (NTDT), including HbE/β thalassemia. It classifies HbE/β thalassemia into severe, moderate, and mild based on hemoglobin levels and clinical symptoms. It also discusses transfusion therapy for NTDT, indicating when regular transfusions should start based on hemoglobin drop, organ enlargement, and other factors. The document further discusses chelation therapy for managing iron overload in NTDT, covering various chelating agents like deferoxamine, deferiprone, and deferasirox.

Coagulation Disorders and Anesthesia-Basic pathophysiology

Unnikrishnan Prathapadas

Thalassemia

Livson Thomas

This document discusses thalassemia, an inherited blood disorder characterized by reduced or absent hemoglobin. There are two main types: alpha thalassemia affects hemoglobin production; beta thalassemia has four forms ranging from mild (trait) to severe (major). Symptoms include anemia, fatigue, bone changes. Treatment involves blood transfusions, iron chelation therapy, and potentially splenectomy or bone marrow transplant.

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