Instructor s Manual Chapter 26 Hematological Alterations. 1. A man and woman both test positive for the sickle cell trait. The couple asks the

Size: px
Start display at page:

Download "Instructor s Manual Chapter 26 Hematological Alterations. 1. A man and woman both test positive for the sickle cell trait. The couple asks the"

Transcription

1 1 Instructor s Manual Chapter 26 Hematological Alterations Answers to Study Questions 1. A man and woman both test positive for the sickle cell trait. The couple asks the nurse how many of their children with have sickle cell disease. The nurse understands that when both parents carry the sickle cell trait gene: a. out of four children, only one will have the sickle cell disease. b. only male children will be affected. c. all of their children will carry the sickle cell trait. d. each pregnancy will have a 25% chance of having the disease. Answer: d. Sickle cell anemia is an autosomal recessive disorder, which means that when both parents carry the recessive gene, each pregnancy has a 25% chance of not having the disease or carrying the disease. There is a 50% chance that each pregnancy will carry the gene and a 25% chance that each pregnancy will have the disease. It is important to remember that each pregnancy is an individual event; that is, the outcome of a previous pregnancy in no way affects the outcome of the current pregnancy. 2. A 6-year-old child has been admitted to the emergency department with the diagnosis of vaso-occlusive crisis. What should the nurse anticipate as a priority medical intervention? a. IV pain medications and IV fluids

2 2 b. CBC and IV fluids c. IV antibiotics and oxygen d. transfuse platelets Answer: a. Vaso-occlusive crisis is a painful event occurring when a group of sickled red blood cells obstruct a vessel. Often this crisis can be managed at home but if the child is seeking care at an emergency room then the nurse can assume this particular crisis is very painful. IV fluids are necessary to rehydrate the child and reverse the sickling. 3. The nurse identifies which group as being most at risk for developing iron-deficiency anemia? a. school-aged children enrolled in an after-school program b. breast-fed infants under the age of 6 months c. children ages 6 months to 2 years of age d. 3- to 5-year-old children in daycare five days a week Answer: c. School-aged children regardless of their afterschool activities are at least risk of developing iron-deficiency anemia. Infants under the age of 6 month have adequate stores of iron from birth and preschool children in daycare receive supplemental dietary iron. Children ages 6 months to 2 years are most at risk due to depleting maternal stores and picky eating. 4. An important nursing intervention for the prevention of infection in a child with sickle disease includes which of the following?

3 3 a. encouraging compliance of regular exchange transfusions b. administering hepatitis b and pneumococcal vaccines c. explaining the importance of frequent urination d. preparing the child for IV replacement therapy Answer: b. Adherence to recommended immunizations including hepatitis b and pneumococcal vaccines is the only choice that prevents disease. 5. A mother of a 3-month-old infant newly diagnosed with sickle cell anemia asks the nurse why her baby does not have any symptoms. The nurse understands that most newborns are asymptomatic because: a. newborns have sufficient maternal stores of iron. b. newborns have a higher percentage of HbF. c. newborns blood is relatively high in water content. d. newborns have immature liver function. Answer: b. Newborns have a higher percentage of fetal hemoglobin (HbF) which does not sickle. Gradually HbF will be replaced with hemoglobin that does sickle (HbS). 6. The nurse is caring for a 5-year-old hemophiliac complaining of knee pain. The nurse understands that hemarthrosis predisposes the child to long-term joint dysfunction. What is an important nursing intervention? a. starting active range of motion exercises b. administering aspirin for pain relief

4 4 c. appling heat to the affected joint d. immobilizing and elevating the extremity Answer: d. Active range of motion exercises should not be started until 48 hours after ice or cold is applied to the area. Aspirin is not used for pain therapy due to the anticoagulation properties of the drug. Immobilization and elevation prevents further damage. 7. A child is admitted with immune thrombocytopenic purpura (ITP). What will the nurse anticipate the history to include? a. petechial rash following a viral infection b. frequent urinary tract infections c. recent transfusion of platelets d. recent aspirin use Answer: a. Immune thrombocytopenic purpura (ITP) is often preceded by viral infection. 8. The nurse is caring for a child with septicemia in the intensive care unit and notices blood oozing from around the arterial line. The nurse would suspect which of the following? a. hand-foot syndrome b. aplastic anemia c. hemosiderosis d. disseminated intravascular coagulation

5 5 Answer: d. DIC is a coagulation disorder in which the stimulus for coagulation overwhelms the control mechanisms that normally confine coagulation to the area of bleeding. This sequence of events can lead to hemorrhage, which in this case is seen as blood oozing from the arterial line. 9. The nurse is performing a well-baby checkup on a 12-month-old infant. What finding would be of most concern? a. cannot walk yet b. has increased bruising c. eating less variety of foods d. straining during bowel movements Answer: b. Increased bruising may be a sign of anemia, which is abnormal for a 12 month old. 10. Which of the following foods are a good dietary sources of iron? Check all that apply. a. meat b. red potatoes c. whole grains d. green beans e. canned peaches f. raisins g. seafood Answer: a, c, f & g. Red potatoes, canned peaches, and green beans are not good sources of dietary iron.

The Child with a Hematologic Alteration

The Child with a Hematologic Alteration 47 The Child with a Hematologic Alteration HELPFUL HINT Review the anatomy and physiology of the hematologic system in an anatomy and physiology textbook. MATCHING KEY TERMS Match the term with the correct

More information

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

Dr. MUBARAK ABDELRAHMAN MD PEDIATRICS AND CHILD HEALTH Assistant Professor FACULTY OF MEDICINE -JAZAN Dr. MUBARAK ABDELRAHMAN MD PEDIATRICS AND CHILD HEALTH Assistant Professor FACULTY OF MEDICINE -JAZAN The student should be able:» To identify the mechanism of homeostasis and the role of vessels, platelets

More information

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

DIC. Disseminated intravascular coagulation, is a life threatening pathological process in which clotting factors are abnormally activated. Miss. kamlah 1 DIC Disseminated intravascular coagulation, is a life threatening pathological process in which clotting factors are abnormally activated. Resulting in wide spread of clot formation in the

More information

QUESTIONS OF HEMATOLOGY AND THEIR ANSWERS

QUESTIONS OF HEMATOLOGY AND THEIR ANSWERS QUESTIONS OF HEMATOLOGY AND THEIR ANSWERS WHAT IS TRUE AND WHAT IS FALSE? Questions 1 Iron deficiency anemia a) Is usually associated with a raised MCV. b) The MCH is usually low. c) Is most commonly due

More information

NEW HEMATOLOGY PARAMETERS

NEW HEMATOLOGY PARAMETERS NEW HEMATOLOGY PARAMETERS CASE STUDIES and IMPLEMENTATION WHAT WE WILL COVER new parameters Ret-He, IPF (and some not so new parameters) - anemias - hemoglobinopathies - problem platelets - uncommon things

More information

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

Chapter 3 Diseases of the Blood and Bloodforming Organs and Certain Disorders Involving the Immune Mechanism D50-D89 Chapter 3 Diseases of the Blood and Bloodforming Organs and Certain Disorders Involving the Immune Mechanism D50-D89 Presented by Jennifer Kurkulonis 1 FOUR MAJOR TYPES OF BLOOD CELLS White blood cells

More information

SICKLE CELL BROCHURE

SICKLE CELL BROCHURE SICKLE CELL BROCHURE SICKLE CELL DIESEASE According to CDC, Sickle cell disease (SCD) is a group of inherited red blood cell disorders. Healthy red blood cells are round and SCD C -shaped farm tool called

More information

Anaemia Patient information

Anaemia Patient information Anaemia Patient information What is anaemia? Anaemia is the result of either not having enough red cells to take oxygen around the body, or having faulty red cells that are unable to carry enough oxygen.

More information

Putting some hematology into Pediatric Hematology/Oncology: a review of Hemophilia and Sickle Cell Disease in the Pediatric Patient

Putting some hematology into Pediatric Hematology/Oncology: a review of Hemophilia and Sickle Cell Disease in the Pediatric Patient Putting some hematology into Pediatric Hematology/Oncology: a review of Hemophilia and Sickle Cell Disease in the Pediatric Patient Kristina Haley, DO March 10, 2012 Jovita Reyes Memorial Pediatric Hematology/Oncology

More information

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

It s a bird, It s a plane, No It s a. Presented by Julie Kirkegaard & Miche Swofford It s a bird, It s a plane, No It s a Presented by Julie Kirkegaard & Miche Swofford 55 year old woman admitted 11/23/2015 for colon cancer that metastasized to her liver History of 3 pregnancies Surgery

More information

1. Adequate diet and iron intake to prevent iron deficiency 2. Signs and symptoms of malignant disease

1. Adequate diet and iron intake to prevent iron deficiency 2. Signs and symptoms of malignant disease Hematology/Oncology Description: The pediatric hematology-oncology division sees a wide spectrum of pediatric disease including but not limited to leukemia, hemophilia, solid tumors, ITP, and other blood

More information

Anemia s. Troy Lund MSMS PhD MD

Anemia s. Troy Lund MSMS PhD MD Anemia s Troy Lund MSMS PhD MD lundx072@umn.edu Hemoglobinopathy/Anemia IOM take home points. 1. How do we identify the condtion? Smear, CBC Solubility Test (SCD) 2. How does it present clincally? 3. How

More information

Hematology/Oncology/BMT

Hematology/Oncology/BMT The University of Arizona Pediatric Residency Program Primary Goals for Rotation Hematology/Oncology/BMT 1. GOAL: Understand the role of the pediatrician in preventing hematologic or oncologic conditions,

More information

Hydroxyurea. for Sickle Cell Disease. A Guide for Starting Treatment. Hydroxyurea is a medicine proven to prevent pain from sickle cell disease.

Hydroxyurea. for Sickle Cell Disease. A Guide for Starting Treatment. Hydroxyurea is a medicine proven to prevent pain from sickle cell disease. Hydroxyurea for Sickle Cell Disease A Guide for Starting Treatment Hydroxyurea is a medicine proven to prevent pain from sickle cell disease. This handbook was created to help answer common questions about

More information

Anaemia in Pregnancy

Anaemia in Pregnancy Anaemia in Pregnancy Definition :anaemia is a pathological condition in which the oxygen-carrying capacity of red blood cells is insufficient to meet the body needs. The WHO : haemoglobin concentration

More information

Tenth Visit posttest

Tenth Visit posttest Test Code 10C Patient s name: Tenth Visit posttest Patient s birth date: Your name and relationship to patient: Today s date: 1. Which one of the medications listed below should every child with a sickle

More information

There are two main causes of a low platelet count

There are two main causes of a low platelet count 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

More information

AOHS Global Health. Unit 3, Lesson 9. Causes and Effects of Malnutrition

AOHS Global Health. Unit 3, Lesson 9. Causes and Effects of Malnutrition AOHS Global Health Unit 3, Lesson 9 Causes and Effects of Malnutrition Copyright 2012 2016 NAF. All rights reserved. Nutritional status has a major impact on health status Health of pregnant women and

More information

Most Common Hemostasis Consults: Thrombocytopenia

Most Common Hemostasis Consults: Thrombocytopenia Most Common Hemostasis Consults: Thrombocytopenia Cindy Neunert, MS MSCS Assistant Professor, Pediatrics CUMC Columbia University TSHNA Meeting, April 15, 2016 Financial Disclosures No relevant financial

More information

Managing Emergencies

Managing Emergencies Managing Emergencies Richard Ward, MSc, MRCP, FRCPath Director, Red Blood Cell Disorders Program, UHN Assistant Professor, Hematology, University of Toronto Chair, Canadian Hemoglobinopathy Association

More information

Schematic Of Heparin Induced Thrombocytopenia Platelet Count

Schematic Of Heparin Induced Thrombocytopenia Platelet Count Schematic Of Heparin Induced Thrombocytopenia Platelet Count Normal IgG and IgG2 differentially inhibit HIT antibody-dependent platelet activation that platelet counts were lower in FcγRIIA 131RR patients

More information

What You Need to Know About Blood Transfusion. Elianna Saidenberg May 2014

What You Need to Know About Blood Transfusion. Elianna Saidenberg May 2014 What You Need to Know About Blood Transfusion Elianna Saidenberg May 2014 Objectives Why your doctor might order transfusion therapy Where does the blood come from The beginning of your transfusion Consent

More information

Immune Thrombocytopenia (ITP)

Immune Thrombocytopenia (ITP) Immune Thrombocytopenia (ITP) ITP - What is it? ITP is a blood disorder affecting platelets in the blood. Platelets are small cells in your blood that help your blood to clot. In ITP the body s immune

More information

Education Visit #1 *** All Sickle Cell Patients*** from A Parent s Handbook for Sickle Cell Disease Booklet.

Education Visit #1 *** All Sickle Cell Patients*** from A Parent s Handbook for Sickle Cell Disease Booklet. Education Visit #1 *** All Sickle Cell Patients*** Step 1: Administer Pretest A. Step 2: Education Watch DVD: Education Visit #1 For All Patients Handout So You Have Sickle Cell Disorder Handout Infection

More information

Hydroxyurea and Transfusion Therapy for the Treatment of Sickle Cell Disease

Hydroxyurea and Transfusion Therapy for the Treatment of Sickle Cell Disease Hydroxyurea and Transfusion Therapy for the Treatment of Sickle Cell Disease A Pocket Guide for the Clinician Susan E. Creary, MD, MSc 1 John J. Strouse, MD, PhD 2 1 The Ohio State University School of

More information

نظام تأديب الطلبة في جامعة آل البيت ( 27 /لسنة 2000( ينص على أن :

نظام تأديب الطلبة في جامعة آل البيت ( 27 /لسنة 2000( ينص على أن : Al-Albayte University Faculty of Nursing Child Health Nursing (2008/2009) Student Name: Instructor: ID#: section: Questions One 1 2 3 A B C D Questions 21 22 23 24 A B C D 4 25 5 6 7 8 9 10 11 12 13 14

More information

Wiskott-Aldrich Syndrome

Wiskott-Aldrich Syndrome chapter 7 Wiskott-Aldrich Syndrome Wiskott-Aldrich syndrome is a primary immunodeficiency disease involving both T- and B-lymphocytes. In addition, the blood cells that help control bleeding, called platelets

More information

Medical Surgical Review Handout- Hematology/Oncology 2016

Medical Surgical Review Handout- Hematology/Oncology 2016 Medical Surgical Review Handout- Hematology/Oncology 2016 Overview Blood circulates in the cardiovascular system o Carries oxygen to the cells o Carries waste away from the cells Functions of blood o Transportation:

More information

Wellness Preventive Health Guide

Wellness Preventive Health Guide Wellness Preventive Health Guide Protect Your Health with Good Preventive Care Plan Now for Better Health One of the best ways to maintain good health and lower the risk of future health concerns for you

More information

Other labs 4/24/2012. N 24: Pediatric Hematological Alterations & Cancer Intro. Cabrillo College ADN Program C. Madsen RN, MSN 1.

Other labs 4/24/2012. N 24: Pediatric Hematological Alterations & Cancer Intro. Cabrillo College ADN Program C. Madsen RN, MSN 1. Evaluation of CBC Evaluate type of WBCs Reticulocyte count RBC size, shape, color MCV: size RBC color (hypo or normo chromic) Mean corpuscular hemoglobin concentration (MCHC) Mean corpuscular hemoglobin

More information

Blood is serious business

Blood is serious business Transfusion at RCH BLOOD TRANSFUSION Anthea Greenway Dept of Clinical Haematology >10000 fresh blood products per year Supports craniofacial and cardiac surgery Support bone marrow, liver transplant and

More information

Hematologic Disorders. Assistant professor of anesthesia

Hematologic Disorders. Assistant professor of anesthesia Preoperative Evaluation Hematologic Disorders Dr M.Razavi Assistant professor of anesthesia Anemia Evaluation needs to consider the extent and type of surgery, the anticipated blood loss, and the patient's

More information

Chapter 06 Lecture Outline. See separate PowerPoint slides for all figures and tables preinserted into PowerPoint without notes.

Chapter 06 Lecture Outline. See separate PowerPoint slides for all figures and tables preinserted into PowerPoint without notes. Chapter 06 Lecture Outline See separate PowerPoint slides for all figures and tables preinserted into PowerPoint without notes. Copyright 2016 McGraw-Hill Education. 2012 Pearson Permission Education,

More information

The Power of Peripheral Blood Smears: Apparent Diagnostic Clues (Part 1) (Wednesday, October 19, 2011)

The Power of Peripheral Blood Smears: Apparent Diagnostic Clues (Part 1) (Wednesday, October 19, 2011) The Power of Peripheral Blood Smears: Apparent Diagnostic Clues (Part 1) (Wednesday, October 19, 2011) By Gene Gulati, Ph.D., SH(ASCP) Conflict of Interest None Plan for the Course Review blood smears,

More information

Disseminated Intravascular Coagulation (DIC) Seminar. Ron Kopilov 4 th year Medical Student, Tel Aviv University Internal Medicine A 8.3.

Disseminated Intravascular Coagulation (DIC) Seminar. Ron Kopilov 4 th year Medical Student, Tel Aviv University Internal Medicine A 8.3. Disseminated Intravascular Coagulation (DIC) Seminar Ron Kopilov 4 th year Medical Student, Tel Aviv University Internal Medicine A 8.3.2012 1 Our plan: Understand the pathophysiology Identify risk factors

More information

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

Do Now pg What part of the blood causes a blood clot? 2. Could you survive without this? Why? Do Now pg 95 1. What part of the blood causes a blood clot? 2. Could you survive without this? Why? What is Hemostasis? The stopping of bleeding, which is vitally important when blood vessels are damaged.

More information

C. treatment with Desferal (deferoxamine mesylate USP, iron-chelating agent)

C. treatment with Desferal (deferoxamine mesylate USP, iron-chelating agent) HEMOLYTIC ANEMIAS Single choice tests 1. Select the clinical manifestation that is not characteristic for the hemolytic crisis: A. decrease of the red blood cell count B. reticulocytosis C. jaundice D.

More information

Principles of Anatomy and Physiology

Principles of Anatomy and Physiology Principles of Anatomy and Physiology 14 th Edition CHAPTER 19 The Cardiovascular System: The Blood Functions and Properties of Blood Blood is a liquid connective tissue consisting of cells surrounded by

More information

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

Dr. Rai Muhammad Asghar Associate Professor Head of Pediatric Department Rawalpindi Medical College Dr. Rai Muhammad Asghar Associate Professor Head of Pediatric Department Rawalpindi Medical College AN APPROACH TO BLEEDING DISORDERS NORMAL HEMOSTASIS After injury, 3 processes halt bleeding Vasoconstriction

More information

WHAT IT MEANS or WHY YOU DO IT

WHAT IT MEANS or WHY YOU DO IT WHAT IT MEANS or WHY YOU DO IT Dr. Patrick Sauer Billings Clinic Pediatrics Objective Increase understanding of prenatal tests Increase understanding of routine newborn procedures Increase knowledge to

More information

CURRENT RESEARCH STUDIES

CURRENT RESEARCH STUDIES CURRENT RESEARCH STUDIES SCAGO SICKLE CELL RESEARCH DAY MAY 12, 2018 REBECCA LEROUX RN, BSCN, CCRP RED BLOOD CELL DISORDERS PROGRAM, UNIVERSITY HEALTH NETWORK MANUELA MERELLES-PULCINI RN, BSCN, MSN, CCRP

More information

Symptoms and Signs in Hematology (2)/ 2013

Symptoms and Signs in Hematology (2)/ 2013 Symptoms and Signs in Hematology (2)/ 2013 Abdallah Abbadi.MD.FRCP Professor of Medicine,Hematology & Oncology University of Jordan & JUH Email: abdalla.awidi@gmail.com Case one: A 24 yr old female complains

More information

78 The Power of Peripheral Blood Smears-Apparent Diagnostic Clues (Part 1) Gene Gulati PhD, SH(ASCP)

78 The Power of Peripheral Blood Smears-Apparent Diagnostic Clues (Part 1) Gene Gulati PhD, SH(ASCP) 78 The Power of Peripheral Blood Smears-Apparent Diagnostic Clues (Part 1) Gene Gulati PhD, SH(ASCP) 2011 Annual Meeting Las Vegas, NV AMERICAN SOCIETY FOR CLINICAL PATHOLOGY 33 W. Monroe, Ste. 1600 Chicago,

More information

Approach to Hemolysis

Approach to Hemolysis Objectives: Approach to Hemolysis To know the function of platelets and the relationship between the platelet count in peripheral blood and the extent of abnormal bleeding. To know about the diseases associated

More information

Index. Note: Page numbers of article titles are in boldface type.

Index. Note: Page numbers of article titles are in boldface type. Note: Page numbers of article titles are in boldface type. A Abdominal tumors, in children, 530 531 Alkalinization, in tumor lysis syndrome, 516 Allopurinol, in tumor lysis syndrome, 515 Anaphylaxis, drug

More information

HEME 10 Bleeding Disorders

HEME 10 Bleeding Disorders HEME 10 Bleeding Disorders When injury occurs, three mechanisms occur Blood vessels Primary hemostasis Secondary hemostasis Diseases of the blood vessels Platelet disorders Thrombocytopenia Functional

More information

Coagulation Disorders. Dr. Muhammad Shamim Assistant Professor, BMU

Coagulation Disorders. Dr. Muhammad Shamim Assistant Professor, BMU Coagulation Disorders Dr. Muhammad Shamim Assistant Professor, BMU 1 Introduction Local Vs. General Hematoma & Joint bleed Coagulation Skin/Mucosal Petechiae & Purpura PLT wound / surgical bleeding Immediate

More information

Sickle cell disease. Fareed Omar 10 March 2018

Sickle cell disease. Fareed Omar 10 March 2018 Sickle cell disease Fareed Omar 10 March 2018 Physiology Haemoglobin structure HbA2: 2α and 2δ chains (2-3%) HbF: 2α and 2γ chains (

More information

Miss. kamlah ahmed 1

Miss. kamlah ahmed 1 Miss. kamlah ahmed 1 Anatomy & Physiology Blood has two compartments: 1- a fluid portion called plasma. 2- a cellular portion known as the formed elements of the blood. Which are RBC (erythrocytes), WBC

More information

A Guide for Understanding Genetics and Health

A Guide for Understanding Genetics and Health 2 Does it Run in the Family? A Guide for Understanding Genetics and Health National Council of La Raza Contents Why is genetics important to my family and me? 1 What makes me unique? 2 Tell me more about

More information

Anti-Tumor Necrosis Factor (Anti-TNF)

Anti-Tumor Necrosis Factor (Anti-TNF) Anti-Tumor Necrosis Factor (Anti-TNF) 110465 Anti-TNF.indd 1 9/20/16 9:01 AM s About your medicine Anti-tumor necrosis factor (anti-tnf) is a type of medicine called biologic agent that targets substance

More information

Immunohaematology: a branch of immunology that deals with the immunologic properties of blood.

Immunohaematology: a branch of immunology that deals with the immunologic properties of blood. 1 Immunohaematology: a branch of immunology that deals with the immunologic properties of blood. The red blood cells have on their surface hundreds of antigens and according to the antigen on their surface

More information

Hydroxyurea Treatment for Sickle Cell Disease

Hydroxyurea Treatment for Sickle Cell Disease Hydroxyurea Treatment for Sickle Cell Disease Before Hydroxyurea After Hydroxyurea Hydroxyurea Treatment for Sickle Cell Disease This document is not intended to take the place of the care and attention

More information

Idiopathic Thrombocytopenic Purpura

Idiopathic Thrombocytopenic Purpura Idiopathic Thrombocytopenic Purpura Title of Guideline Contact Name and Job Title (author) Directorate & Speciality Guideline for the management of idiopathic thrombocytopenic purpura Dr S Stokley, Consultant

More information

Index. Note: Page numbers of article titles are in boldface type.

Index. Note: Page numbers of article titles are in boldface type. Index Note: Page numbers of article titles are in boldface type. A Activated partial thromboplastin time abnormality, perioperative approach to, 104 105 Acute kidney injury, perioperative, 89 99 early

More information

Things to never miss in the office. Brett Houston MD FRCPC (PYG-5, hematology) Leonard Minuk MD FRCPC

Things to never miss in the office. Brett Houston MD FRCPC (PYG-5, hematology) Leonard Minuk MD FRCPC Things to never miss in the office Brett Houston MD FRCPC (PYG-5, hematology) Leonard Minuk MD FRCPC Presenter Disclosure Faculty / Speaker s name: Brett Houston / Leonard Minuk Relationships with commercial

More information

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

Moath Darweesh. Omar Sami. Saleem Khreisha. 1 P a g e 7 Moath Darweesh Omar Sami Saleem Khreisha 1 P a g e -First of all, I want to give a quick revision to simplify the whole hemostasis mechanism, it will be much easier here with me. Enjoy (you can skip

More information

got anemia? IT COULD BE THALASSEMIA TRAIT

got anemia? IT COULD BE THALASSEMIA TRAIT got anemia? IT COULD BE THALASSEMIA TRAIT 1 in 20 people worldwide carry some type of thalassemia trait You are especially at risk of carrying the thalassemia trait if you have ancestry from: Southeast

More information

Platelet Disorders. By : Saja Al-Oran

Platelet Disorders. By : Saja Al-Oran Platelet Disorders By : Saja Al-Oran Introduction The platelet arise from the fragmentation of the cytoplasm of megakaryocyte in the bone marrow. circulate in the blood as disc-shaped anucleate particles

More information

Screening for haemoglobinopathies in pregnancy

Screening for haemoglobinopathies in pregnancy Policy Statement All Southern Health patients will receive clinical care that reflects best practice and is based on the best available evidence. Index of chapters within background 1. Prevalence of haemoglobinopathies

More information

Treating sickle cell disease: Is hydroxyurea right for you?

Treating sickle cell disease: Is hydroxyurea right for you? Treating sickle cell disease: Is hydroxyurea right for you? What is sickle cell disease? Sickle cell disease changes the shape and texture of hemoglobin, which is a protein in red blood cells. People with

More information

Hydroxyurea Treatment for Sickle Cell Disease

Hydroxyurea Treatment for Sickle Cell Disease Hydroxyurea Treatment for Sickle Cell Disease Hydroxyurea Treatment for Sickle Cell Disease 1 This document is not intended to take the place of the care and attention of your personal physician. Our aim

More information

Preventive care guidelines Blue Cross and Blue Shield of Minnesota

Preventive care guidelines Blue Cross and Blue Shield of Minnesota Service Recommendation Adult men Adult Children Pregnant abdominal aortic aneurysm One-time screening by ultrasound in men aged 65 to 75 who have ever smoked Screening and counseling to reduce alcohol

More information

Extra Notes 3. Warm. In the core (center) of the body, where the temperature is 37 C.

Extra Notes 3. Warm. In the core (center) of the body, where the temperature is 37 C. Extra Notes 3 *The numbers of the slides are according to the last year slides. Slide 33 Autoimmune hemolytic anemia : Abnormal circulating antibodies that target normal antigen on the RBC and cause lysis.

More information

MI Newborn Screening Program: An Overview of Follow-up & Case Management for Sickle Cell Conditions

MI Newborn Screening Program: An Overview of Follow-up & Case Management for Sickle Cell Conditions Michigan Department of Community Health MI Newborn Screening Program: An Overview of Follow-up & Case Management for Sickle Cell Conditions Dominic Smith, MSA - Linda Carter, BSW - Ben Frazier, BSW - Ruth

More information

Do you have Iron Deficient Anemia?

Do you have Iron Deficient Anemia? Do you have Iron Deficient Anemia? Do you ever just have this overwhelming feeling all day, every day, that you have no energy?! Ever just sat there thinking, I eat well and healthily, I exercise, I take

More information

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

Bleeding Disorders. Dr. Mazen Fawzi Done by Saja M. Al-Neaumy Noor A Mohammad Noor A Joseph Joseph Bleeding Disorders Dr. Mazen Fawzi Done by Saja M. Al-Neaumy Noor A Mohammad Noor A Joseph Joseph Normal hemostasis The normal hemostatic response involves interactions among: The blood vessel wall (endothelium)

More information

Blood Transfusion Guidelines in Clinical Practice

Blood Transfusion Guidelines in Clinical Practice Blood Transfusion Guidelines in Clinical Practice Salwa Hindawi Director of Blood Transfusion Services Associate Professor in Haematology and Transfusion Medicine King Abdalaziz University, Jeddah Saudi

More information

Case Studies: Congenital Platelet Disorders

Case Studies: Congenital Platelet Disorders Case Studies: Congenital Platelet Disorders Presented to Atlanta Wednesday, November 2, 2016 Disclosures for Michele P. Lambert, MD, MTR In compliance with COI policy, ISTH requires the following disclosures

More information

Contemporary perspectives and initial management of pediatric ITP. William Beau Mitchell, MD Weill Cornell Medical College New York, NY USA

Contemporary perspectives and initial management of pediatric ITP. William Beau Mitchell, MD Weill Cornell Medical College New York, NY USA Contemporary perspectives and initial management of pediatric ITP William Beau Mitchell, MD Weill Cornell Medical College New York, NY USA Case Presentation 5 year old female Bruises on trunk, extremities

More information

Non-malignant hematologic disorders associated arthropathies: hemoglobinopathy-associated musculoskeletal manifestations, hemophilia

Non-malignant hematologic disorders associated arthropathies: hemoglobinopathy-associated musculoskeletal manifestations, hemophilia Non-malignant hematologic disorders associated arthropathies: hemoglobinopathy-associated musculoskeletal manifestations, hemophilia HAEMOGLOBINOPATHIES = inherited disorders of globin divided into: Thalassaemia

More information

How to Write a Life Care Plan for a Child with Hemoglobinopathy

How to Write a Life Care Plan for a Child with Hemoglobinopathy How to Write a Life Care Plan for a Child with Hemoglobinopathy Tamar Fleischer, BSN, MSN, CNLCP & Mona Yudkoff, RN, MPH, CRRN, CNLCP BalaCare Solutions March 2018 St. Peterburg, Florida What is Hemoglobinopathy?

More information

Third Visit Posttest

Third Visit Posttest Test code 03C Patient s name: Third Visit Posttest Patient s birth date: Your name and relationship to patient: Today s date: Please mark only one answer for each of the following questions: 1. Which one

More information

Bone Marrow Transplant Exercise Manual While You Are in the Hospital

Bone Marrow Transplant Exercise Manual While You Are in the Hospital Bone Marrow Transplant Exercise Manual While You Are in the Hospital Why Do I Need to Exercise While I Am In The Hospital? You will feel tired and weak because of your cancer treatments. Exercise helps

More information

For platelet control as individual as you

For platelet control as individual as you For platelet control as individual as you Explore the possibilities of Immune Thrombocytopenic Purpura (ITP) treatment. Important Risk Information WARNING: INTRAVASCULAR HEMOLYSIS (IVH) Intravascular hemolysis

More information

RBCs Disorders 1. Dr. Nabila Hamdi MD, PhD

RBCs Disorders 1. Dr. Nabila Hamdi MD, PhD RBCs Disorders 1 Dr. Nabila Hamdi MD, PhD ILOs Discuss the classification of anemia into hypochromic-microcytic, normochromicnormocytic and macrocytic. Categorize laboratory test procedures used in the

More information

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

What should I discuss with my health care provider before taking eltrombopag? 1 of 6 6/10/2016 3:57 PM Generic Name: eltrombopag (el TROM boe pag) Brand Name: Promacta What is eltrombopag? Eltrombopag is a man-made form of a protein that increases production of platelets (blood-clotting

More information

Every day matters. To help you stay out of the hospital, you can: Live healthy with sickle cell disease

Every day matters. To help you stay out of the hospital, you can: Live healthy with sickle cell disease Living with sickle cell disease (SCD) can be difficult. There can be severe pain and discomfort. AmeriHealth Caritas Louisiana wants to help you manage this life-threatening disease. To help you stay out

More information

THE KENYA POLYTECHNIC UNIVERSITY COLLEGE

THE KENYA POLYTECHNIC UNIVERSITY COLLEGE THE KENYA POLYTECHNIC UNIVERSITY COLLEGE SCHOOL OF HEALTH SCIENCES AND TECHNOLOGY DEPARTMENT OF BIOMEDICAL LABORATORY SCIENCES AND TECHNOLOGY DIPLOMA IN MEDICAL LABORATORY SCIENCES FINAL YEAR EXAMINATION

More information

Dialogue between Clinician and Pathologist on CBC report

Dialogue between Clinician and Pathologist on CBC report Dialogue between Clinician and Pathologist on CBC report Dr. Seema Bhatwadekar Haematologist, Oncohaematologist & Transplant Physician Vadodara. CBC PBS Most important test to make probable diagnosis Crucial

More information

Newborn Screening: Blood Spot Disorders

Newborn Screening: Blood Spot Disorders Newborn Screening: Blood Spot Disorders Arizona s Newborn Screening Program Program Overview Panel of Disorders Disorder Descriptions Program Components Hospitals ADHS Lab ADHS Follow-up ADHS Billing Medical

More information

Fever in the Newborn Period

Fever in the Newborn Period Fever in the Newborn Period 1. Definitions 1 2. Overview 1 3. History and Physical Examination 2 4. Fever in Infants Less than 3 Months Old 2 a. Table 1: Rochester criteria for low risk infants 3 5. Fever

More information

A Guide for Understanding Genetics and Health

A Guide for Understanding Genetics and Health 2 D o e s i t Ru n i n t h e Fa m i ly? A Guide for Understanding Genetics and Health Institute for Cultural Partnerships Contents Why is genetics important to my family and me? 1 What makes me unique?

More information

Aneurin Bevan University Health Board Sickle Cell Anaemia and Haemoglobinopathy Screening and Management in Pregnancy Guidelines

Aneurin Bevan University Health Board Sickle Cell Anaemia and Haemoglobinopathy Screening and Management in Pregnancy Guidelines Sickle Cell Anaemia and Haemoglobinopathy Screening and Management in Pregnancy Guidelines N.B. Staff should be discouraged from printing this document. This is to avoid the risk of out of date printed

More information

CHILD HEALTH. There is a list of references at the end where you can find more information. FACT SHEETS

CHILD HEALTH. There is a list of references at the end where you can find more information. FACT SHEETS SOME 18,000 CHILDREN STILL DIE EVERY DAY FROM DISEASES THAT ARE MOSTLY PREVENTABLE. This fact sheet outlines some of the basic information related to the health and wellbeing of children under five years

More information

Information for health professionals

Information for health professionals Introduction of a new screening test for newborn babies in Wales Newborn bloodspot screening for Medium chain acyl-coa dehydrogenase deficiency (MCADD) Newborn bloodspot screening for MCADD is being introduced

More information

QUICK REFERENCE Clinical Practice Guideline on the Evaluation and Management of Immune Thrombocytopenia (ITP)

QUICK REFERENCE Clinical Practice Guideline on the Evaluation and Management of Immune Thrombocytopenia (ITP) QUICK REFERENCE 2011 Clinical Practice Guideline on the Evaluation and Management of Immune Thrombocytopenia (ITP) Presented by the American Society of Hematology, adapted from: The American Society of

More information

CASE STUDIES PERIPHERAL BLOOD AND BODY FLUIDS

CASE STUDIES PERIPHERAL BLOOD AND BODY FLUIDS CASE STUDIES PERIPHERAL BLOOD AND BODY FLUIDS WHERE TO START anemias hemoglobinopathies new and old parameters uncommon things fluids.benign and malignant.yuk! really annoying stuff and maybe some entertainment

More information

Fatty Acid Oxidation Disorders

Fatty Acid Oxidation Disorders Genetic Fact Sheets for Parents Fatty Acid Oxidation Disorders Screening, Technology, and Research in Genetics is a multi-state project to improve information about the financial, ethical, legal, and social

More information

GUIDELINES FOR THE TRANSFUSION OF BLOOD COMPONENTS

GUIDELINES FOR THE TRANSFUSION OF BLOOD COMPONENTS CHILDREN S HOSPITALS AND CLINICS OF MINNESOTA Introduction: GUIDELINES FOR THE TRANSFUSION OF BLOOD COMPONENTS These guidelines have been developed in conjunction with the hospital Transfusion Committee.

More information

Diagnostic Approach to Patients with Anemia

Diagnostic Approach to Patients with Anemia J KMA Special Issue Diagnostic Approach to Patients with Anemia Seonyang Park, MD Department of Internal Medicine, Seoul National University College of Medicine E mail : seonpark@snu.ac.kr J Korean Med

More information

Abnormal blood counts in children Dr Tina Biss Consultant Paediatric Haematologist Newcastle upon Tyne Hospitals NHS Foundation Trust

Abnormal blood counts in children Dr Tina Biss Consultant Paediatric Haematologist Newcastle upon Tyne Hospitals NHS Foundation Trust Abnormal blood counts in children Dr Tina Biss Consultant Paediatric Haematologist Newcastle upon Tyne Hospitals NHS Foundation Trust Regional Paediatric Specialty Trainees teaching 4 th July 2017 Scope

More information

Symptoms and Signs in Hematology/ 2013

Symptoms and Signs in Hematology/ 2013 Symptoms and Signs in Hematology/ 2013 Abdallah Abbadi.MD.FRCP Professor of Hematology & Oncology University of Jordan & JUH Email: abdalla.awidi@gmail.com Diseases of Blood & Blood forming organs A- Benign

More information

Information for fathers invited for a screening test for sickle cell disease and thalassaemia major

Information for fathers invited for a screening test for sickle cell disease and thalassaemia major Information for fathers invited for a screening test for sickle cell disease and thalassaemia major Who is this leaflet for? This leaflet is for fathers invited to have a screening test for haemoglobin

More information

Description of the evidence collection method. (1). Each recommendation was discussed by the committee and a consensus

Description of the evidence collection method. (1). Each recommendation was discussed by the committee and a consensus Special Article Guidelines on the treatment of primary immune thrombocytopenia in children and adolescents: Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular Sandra Regina Loggetto 1

More information

The importance of thrombocytopenia and its causes

The importance of thrombocytopenia and its causes SYSMEX EDUCATIONAL ENHANCEMENT AND DEVELOPMENT NO 4 2017 SEED HAEMATOLOGY The importance of thrombocytopenia and its causes Key words: Thrombocytopenia, thrombocytopenic, low levels of platelets What is

More information

201 Low Hematocrit/Low Hemoglobin

201 Low Hematocrit/Low Hemoglobin 201 Low Hematocrit/Low Hemoglobin Definition/Cut off Value Hemoglobin or hematocrit concentration below the 95 percent confidence interval (i.e., below the.025 percentile) for healthy, well nourished individuals

More information

2. Does the patient have a diagnosis of chronic idiopathic thrombocytopenic purpura (ITP)?

2. Does the patient have a diagnosis of chronic idiopathic thrombocytopenic purpura (ITP)? Pharmacy Prior Authorization MERC CARE (MEDICAID) Promacta (Medicaid) This fax machine is located in a secure location as required by HIPAA regulations. Complete/review information, sign and date. Fax

More information

DONE BY : RaSHA RAKAN & Bushra Saleem

DONE BY : RaSHA RAKAN & Bushra Saleem DONE BY : RaSHA RAKAN & Bushra Saleem Hemolytic anemias (2 of 2) Sickle Cell Anemia The most common familial hemolytic anemia in the world Sickle cell anemia is the prototypical (and most prevalent) hemoglobinopathy

More information