There are two main causes of a low platelet count

Similar documents
Haemostasis & Coagulation disorders Objectives:

Chapter 3 Diseases of the Blood and Bloodforming Organs and Certain Disorders Involving the Immune Mechanism D50-D89

The importance of thrombocytopenia and its causes

Dr. MUBARAK ABDELRAHMAN MD PEDIATRICS AND CHILD HEALTH Assistant Professor FACULTY OF MEDICINE -JAZAN

Clinical & Laboratory Assessment

Immune Thrombocytopenia (ITP)

Bleeding Disorders. Dr. Mazen Fawzi Done by Saja M. Al-Neaumy Noor A Mohammad Noor A Joseph Joseph

Easy Bleeding General Presentation

Dr. Rai Muhammad Asghar Associate Professor Head of Pediatric Department Rawalpindi Medical College

Bone Marrow Transplantation

Coagulation Disorders. Dr. Muhammad Shamim Assistant Professor, BMU

HEME 10 Bleeding Disorders

Medical Surgical Review Handout- Hematology/Oncology 2016

Haemorrhagic Disorders. Dr. Bashar Department of Pathology Mosul Medical College

Leukemia. There are different types of leukemia and several treatment options for each type.

Thrombocytopenia: a practial approach

Most Common Hemostasis Consults: Thrombocytopenia

Immune Thrombocytopenic Purpura (ITP)

PATHOLOGY & PATHOPHYSIOLOGY

Hematology. The Study of blood

r). SUPPLEMENTARY/SECOND OPPORTUNITY EXAMINATION PAPER nnmlbih UNIVERSITY Sophia Blaauw INSTRUCTIONS FACULTY OF HEALTH AND APPLIED SCIENCES

Platelet Disorders. By : Saja Al-Oran

Average adult = 8-10 pints of blood. Functions:

Unit 6: Circulatory System. 6.1 Blood

Moath Darweesh. Omar Sami. Saleem Khreisha. 1 P a g e

Contents SECTION 1: PHYSIOLOGY OF BLOOD

Year 2002 Paper two: Questions supplied by Jo 1

12 Dynamic Interactions between Hematopoietic Stem and Progenitor Cells and the Bone Marrow: Current Biology of Stem Cell Homing and Mobilization

Chapter 46. Care of the Patient with a Blood or Lymphatic Disorder

Getting started with PROMACTA (eltrombopag)

Hematologic changes in systemic diseases. Chittima Sirijerachai

Bleeding disorders. Hemostatic failure: Inappropriate and excessive bleeding either spontaneous or in response to injury.

Anaemia / SCD/ Bleeding disorders in Children

Wiskott-Aldrich Syndrome

WISKOTT-ALDRICH SYNDROME. An X-linked Primary Immunodeficiency

Hemostatic System - general information

Bleeding Disorders: (Hemorrhagic Diatheses) Tests used to evaluate different aspects of hemostasis are the following:

Sysmex Educational Enhancement and Development No

The Complete Blood Count

Hematologic Disorders. Assistant professor of anesthesia

BLEEDING DISORDERS. JC Opperman 2012

Have a healthy discussion. Use this guide to start a. conversation. with your. healthcare provider

Disorders of Blood Cells & Blood Coagulation

Preferred Clinical Services for Leading Age Florida August 26-27, 2015

What should I discuss with my health care provider before taking eltrombopag?

Bleeding and Thrombotic Disorders. Kristine Krafts, M.D.

Thrombocytopenia. Dr Lynda Vandertuin May 6, 2014

The Child with a Hematologic Alteration

Scrub In. Lymphocytes are a type of what?

The LaboratoryMatters

For the Patient: Rituximab injection Other names: RITUXAN

For platelet control as individual as you

City State Zip Code. Ethnic Background: Caucasian African-American Asian Hispanic Native American. Previous. Hobbies/Leisure activities:,,,

M B Garvey. University of Toronto

Guidelines for Shared Care Centres and Community Staff

Elements for a Public Summary

Care of the Patient with a Blood or Lymphatic Disorder. ph Volume pints. Red blood cells (RBC) White blood cells (WBC)

Do Now pg What part of the blood causes a blood clot? 2. Could you survive without this? Why?

The primary medical content categories of the blueprint are shown below, with the percentage assigned to each for a typical exam:

Blood Transfusion Guidelines in Clinical Practice

BLEEDING DISORDERS Simple complement:

Anemia (3).ms4.25.Oct.15 Hemolytic Anemia. Abdallah Abbadi

INHERITED COAGULOPATHY

PCCN Review Hematology

What are the four parts of blood and what are their main functions?

For the Patient: Cyclosporine injection Other names: SANDIMMUNE I.V.

V.N. KARAZIN KHARKOV NATIONAL UNIVERSITY

READ THIS FOR SAFE AND EFFECTIVE USE OF YOUR MEDICINE PATIENT MEDICATION INFORMATION. LEMTRADA (alemtuzumab)

QUESTIONS OF HEMATOLOGY AND THEIR ANSWERS

Assessing thrombocytopenia in the intensive care unit: The past, present, and future

Pathology note 8 BLEEDING DISORDER

CH 11 Blood OUTLINE: Functions of Blood Composition of Blood Blood Cell Disorders Blood Types Blood Clotting Functions of Blood Transportation

Approach To A Bleeding Patient

37 2 Blood and the Lymphatic System

John Davidson Consultant in Intensive Care Medicine Freeman Hospital, Newcastle upon Tyne

EDUCATIONAL COMMENTARY PLATELET DISORDERS

Bio& 242 Unit 3 / Lecture 1

Bleeding Disorders HOPE Maram Al-anbar

Definition Chronic autoimmune disease The body s immune system starts attacking itself Can affect most organs and tissues in the body Brain, lungs, he

Platelet disorders. Information for families. Great Ormond Street Hospital for Children NHS Foundation Trust

Acute Immune Thrombocytopenic Purpura (ITP) in Childhood

LAMA SHATAT TTP, ITP, DIC

Pharmacy Prior Authorization

NON- HODGKIN LYMPHOMA

BLEEDING (PLATELET) DISORDER. IAP UG Teaching slides

UNIT VI. Chapter 37: Platelets Hemostasis and Blood Coagulation Presented by Dr. Diksha Yadav. Copyright 2011 by Saunders, an imprint of Elsevier Inc.

Thrombotic Thrombocytopenic Purpura and the Role of ADAMTS-13

DIC. Disseminated intravascular coagulation, is a life threatening pathological process in which clotting factors are abnormally activated.

Blood. BIOLOGY OF HUMANS Concepts, Applications, and Issues. Judith Goodenough Betty McGuire

POSTGRADUATE INSTITUTE OF MEDICINE UNIVERSITY OF COLOMBO POSTGRADUATE DIPLOMA IN CLINICAL HAEMATOLOGY EXAMINATION - JUNE 2014 PAPER I - ESSAY

It s a bird, It s a plane, No It s a. Presented by Julie Kirkegaard & Miche Swofford

General approach to the investigation of haemostasis. Jan Gert Nel Dept. of Haematology University of Pretoria 2013

Dairion Gatot, Soegiarto Ganie, Savita Handayani. Divisi Hematologi & Onkologi Medik Departemen Ilmu Penyakit Dalam FK-USU/RS H.Adam Malik Medan 2009

Blood transfusion. Dr. J. Potgieter Dept. of Haematology NHLS - TAD

MEDICATION GUIDE Prasugrel (pra-su-grel) tablets Read this Medication Guide before you start taking prasugrel and each time you get a refill.

Anaemia is a shortage of red blood cells and haemoglobin. If you have anaemia, doctors say that you are anaemic.

ACQUIRED COAGULATION ABNORMALITIES

Large granular lymphocytic leukaemia (LGLL)

BLOOD TRANSFUSION. Dr Lumka Ntabeni

Chapter 11. Lecture and Animation Outline

Transcription:

Thrombocytopenia Thrombocytopenia is a condition in which a person's blood has an unusually low level of platelets Platelets, also called thrombocytes, are found in a person's blood along with red blood cells and white blood cells They stop bleeding by helping the blood to clot and plugging damaged blood vessels Thrombocytopenia happens when the body does not make enough platelets, is losing platelets, or destroys platelets, and sometimes associated with abnormal bleeding Thrombocytopenia is common in people with cancer, especially in those receiving chemotherapy A healthy person usually has a platelet count of 150,000 to 400,000. You have thrombocytopenia if your number falls under 150,000 Platelet function abnormalities (thrombocytopathy) include a range of inherited and acquired defects of platelet function. Thrombocytopathy may cause a thrombotic or a bleeding tendency or may be part of a wider disorder such as myelodysplasia

Signs and symptoms People with thrombocytopenia may experience some of these symptoms: Unexpected bruising Small purple or red spots under the skin, called petechiae Bleeding from the nose or gums Heavier than usual menstrual periods in women Black or bloody bowel movements or red- or pink-colored urine Bloody vomit Severe headaches Dizziness Pain in the joints or muscles Increased weakness Often, symptoms do not occur until the level of platelets is very low. Many patients do not know they have thrombocytopenia until it is diagnosed during a blood test

Causes Platelets and red and white blood cells are made in bone marrow, the soft, spongy tissue found inside larger bones Some types of chemotherapy and other medications damage the bone marrow, lowering its production of platelets. However, thrombocytopenia caused by chemotherapy is usually temporary In addition, a person's body can make specialized proteins called antibodies that cause a person s immune system to attack platelets Normally, antibodies help destroy substances that appear harmful to the body, such as bacteria and viruses, but sometimes this process works incorrectly and antibodies are produced that destroy healthy parts of a person s body Radiation therapy alone usually does not cause thrombocytopenia, unless a significant amount of radiation is directed at the pelvis, the patient is receiving chemotherapy at the same time, or the cancer spreads to the bone Thrombocytopenia may also occur when cancer cells, such as leukemia or lymphoma cells, crowd normal bone marrow cells. Although rare, thrombocytopenia can occur when other cancers, such as prostate or breast cancer, spread to the bone marrow Cancer of the spleen is another uncommon cause of thrombocytopenia. Excess platelets are stored in the spleen, and cancer of the spleen can cause the spleen to enlarge, trapping too many platelets

There are two main causes of a low platelet count Not enough platelets being made in the bone marrow Conditions that can cause too few platelets to be made include aplastic anaemia, cancers in the bone marrow, such as leukaemia, cirrhosis (scarring of the liver), folate or vitamin B12 deficiency and myelodysplastic syndrome (where the bone marrow does not make enough blood cells or makes defective cells The use of certain drugs may also lead to a low production of platelets in the bone marrow the most common example here is chemotherapy treatment and Druginduced - eg, heparin, ibuprofen, quinine, Cytosine arabinoside, and vancomycin Viral infections, including chickenpox, parvovirus, hepatitis C, Epstein-Barr, mononucleosis, or HIV Severe bacterial infection in your blood Inherited platelet function disorders: von Willebrand's disease (vwd), It is usually associated with a low plasma factor VIII level Immune - idiopathic thrombocytopenia purpura (ITP), systemic lupus erythematosus, rheumatoid arthritis, sarcoidosis, antiphospholipid syndrome and can be treated by one of these: a) Eltrombopag, b)! Rituximab c) Cyclosporin, d) Cyclophosphamide. It is more common in women than men, and It may be treated by gammaglobulin infusions Increased breakdown of platelets in the bloodstream or in the spleen/liver Increased breakdown of platelets either in the bloodstream or in the spleen/liver can be caused by disseminated intravascular coagulation (DIC), drug-induced thrombocytopenia (immune or non-immune types), hypersplenism (swollen spleen), immune thrombocytopenic purpura (ITP) and thrombotic thrombocytopenic purpura

What tests are needed? Low platelet count can be picked up on a routine blood test. Blood tests include a full blood count (FBC) and blood clotting studies, such as the partial thromboplastin time (PTT) and prothrombin time (PT). Other tests that may help diagnose this condition include bone marrow aspiration or biopsy

How is thrombocytopenia treated? The treatment and long-term outcomes of thrombocytopenia depends on the cause of the condition In some cases, a transfusion of platelets may be required to stop or prevent bleeding The main complication of thrombocytopenia is severe bleeding and this may occur in the brain or gastrointestinal tract Polycythaemia vera is associated with a rise in platelet counts: is a neoplasm in which the bone marrow makes too many red blood cells. It may also result in the overproduction of white blood cells and platelets