The Complete Blood Cell Count (CBC) Part 1
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
The Hematological Complications of Alcoholism
The Hematological Complications of Alcoholism HAROLD S. BALLARD, M.D. Alcohol has numerous adverse effects on the various types of blood cells and their functions. For example, heavy alcohol consumption can cause generalized suppression of blood cell production and the production of structurally abnormal blood cell precursors that cannot mature into functional cells. Alcoholics frequently have defective red blood cells that are destroyed prematurely, possibly resulting in anemia. Alcohol also interferes with the production and function of white blood cells, especially those that defend the body against invading bacteria. Consequently, alcoholics frequently suffer from bacterial infections. Finally, alcohol adversely affects the platelets and other components of the blood-clotting system. Heavy alcohol consumption thus may increase the drinker’s risk of suffering a stroke. KEY WORDS: adverse drug effect; AODE (alcohol and other drug effects); blood function; cell growth and differentiation; erythrocytes; leukocytes; platelets; plasma proteins; bone marrow; anemia; blood coagulation; thrombocytopenia; fibrinolysis; macrophage; monocyte; stroke; bacterial disease; literature review eople who abuse alcohol1 are at both direct and indirect. The direct in the number and function of WBC’s risk for numerous alcohol-related consequences of excessive alcohol increases the drinker’s risk of serious Pmedical complications, includ- consumption include toxic effects on infection, and impaired platelet produc- ing those affecting the blood (i.e., the the bone marrow; the blood cell pre- tion and function interfere with blood cursors; and the mature red blood blood cells as well as proteins present clotting, leading to symptoms ranging in the blood plasma) and the bone cells (RBC’s), white blood cells from a simple nosebleed to bleeding in marrow, where the blood cells are (WBC’s), and platelets. -
Thrombotic Microangiopathy Score As a New Predictor for Neurologic Outcome in Patients Undergoing Targeted Temperature Management After Out-Of-Hospital Cardiac Arrest
Thrombotic Microangiopathy Score as a New Predictor for Neurologic Outcome in Patients Undergoing Targeted Temperature Management After Out-of-hospital Cardiac Arrest Taeyoung Kong Yonsei University College of Medicine Hye Sun Lee Yonsei University College of Medicine Soyoung Jeon Yonsei University College of Medicine Jong Wook Lee Konyang University Hospital Hyun Soo Chung Yonsei University College of Medicine Sung Phil Chung Yonsei University College of Medicine Je Sung You ( [email protected] ) Yonsei University College of MedicineGangnam Severance Hospital https://orcid.org/0000-0002-2074- 6745 Original research Keywords: Out-of-hospital cardiac arrest, Targeted temperature management, Thrombotic microangiopathy score, Mortality, Predictor, Schistocytes Posted Date: July 8th, 2020 DOI: https://doi.org/10.21203/rs.3.rs-40096/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/21 Abstract Background: Given the morphological characteristics of schistocytes, thrombotic microangiopathy (TMA) score can be benecial as it can be quickly and serially measured without additional effort or costs. This study aimed to investigate whether the serial TMA scores until 48 h post admission are associated with clinical outcomes in patients undergoing targeted temperature management (TTM) after out-of-hospital cardiac arrest (OHCA). Methods:We retrospectively evaluated a cohort of 185 patients using a prospective registry. We analyzed the TMA score at admission and after 12, 24, and -
Hematology Unit Lab 1 Review Material
Hematology Unit Lab 1 Review Material Objectives Laboratory instructors: 1. Facilitate lab discussion and answer questions Students: 1. Review the introductory material below 2. Study and review the assigned cases and questions in small groups before the Lab. This includes the pathological material using Virtual Microscopy 3. Be prepared to present your cases, questions and answers to the rest of your Lab class during the Lab Erythropoiesis: The process of red blood cell (RBC) production • Characterized by: − Increasing hemoglobin synthesis Erythroid maturation stages (Below): − Decreasing cell size - Average of 4 cell divisions during maturation − Decreasing cytoplasmic basophilia [One pronormoblast gives rise to 16 red cells] (increasing pink color) - pronormoblast → reticulocyte = 7 days − Progressive chromatin condensation of the - reticulocytes → mature RBC =1-2 days nuclei − Extrusion of nucleus (orthochromatic stage) − Extruded nuclei are subsequently phagocytized − Loss of mitotic capability after the early stage of polychromatophilic normoblast • Picture below: Erythroid progenitors (normoblasts) cluster around macrophages (arrows) in the bone marrow and spleen • Macrophages store iron • Iron is transferred from macrophages to erythroid precursor cells • Iron is used by normoblasts for hemoglobin synthesis aka nucleated rbc aka reticulocyte 1 Mature Red Blood Cell 7-8 microns; round / ovoid biconcave disc with orange-red cytoplasm, no RNA, no nucleus; survives ~120 days in circulation Classification of Anemia by Morphology 1. -
The Use of Mean Corpuscular Volume (MCV) to Classify the Anemia As
The Frequency of Iron Deficiency Anemia and Thalassemia Trait among Children: Experience at Prince Rashed Bin Al- Hassan Military Hospital Zuhair Nusair MD*, Abdelrazzaq Al-Wraikat MD**, Nazih Abu Al-Shiekh MD**, Sameer Kofahi MD^, Mohammad Zoubi MD^ ABSTRACT Objectives: To determine the frequency of iron deficiency anemia and thalassemia trait among children attending the Pediatric Department at Prince Rashed Bin Al-Hassan Military Hospital in the North of Jordan. Methods: This hospital based study was conducted in the year 2008 on 1,012 children aged 6 months to 14 years who attended the Pediatric Department at Prince Rashed Bin Al-Hassan Military Hospital in North of Jordan using fully automated blood count of the mean corpuscular volume, serum ferritin level and high performance liquid chromography, or genotyping. None of the subjects included in the study had been on any hematinic in the previous six months, had infection in the past one month or had a chronic disease. The diagnosis of iron deficiency anemia was defined as mean corpuscular volume ≤ mean – 1 standard deviation corrected for age, with a ferritin level < 7 ng/ml of the serum (normal reference range 7 – 140 ng/ml). The diagnosis of thalassemia trait, for subjects with normal or high serum ferritin and those whose mean corpuscular volume was non-compliant to iron therapy, was obtained by high performance liquid chromography or polymerase chain reaction, which was performed at Princess Eman Research and Laboratory Science Center. Results: The frequency of iron deficiency anemia and thalassemia trait was 13.3% and 5.8% respectively. They were equally frequent among males and females. -
Morphological Study of Human Blood for Different Diseases
Research Article ISSN: 2574 -1241 DOI: 10.26717/BJSTR.2020.30.004893 Morphological Study of Human Blood for Different Diseases Muzafar Shah1*, Haseena1, Kainat1, Noor Shaba1, Sania1, Sadia1, Akhtar Rasool2, Fazal Akbar2 and Muhammad Israr3 1Centre for Animal Sciences & Fisheries, University of Swat, Pakistan 2Centre for Biotechnology and Microbiology, University of Swat, Pakistan 3Department of Forensic Sciences, University of Swat, Pakistan *Corresponding author: Muzafar Shah, Centre for Animal Sciences & Fisheries, University of Swat, Pakistan ARTICLE INFO ABSTRACT Received: August 25, 2020 The aim of our study was the screening of blood cells on the basis of morphology for different diseased with Morphogenetic characters I e. ear lobe attachment, clinodactyly Published: September 07, 2020 and tongue rolling. For this purpose, 318 blood samples were collected randomly. Samples were examined under the compound microscopic by using 100x with standard Citation: Muzafar Shah, Haseena, method. The results show 63 samples were found normal while in 255 samples, different Kainat, Noor Shaba, Sania, Sadia, et al. types of morphological changes were observed which was 68.5%, in which Bite cell 36%, Morphological Study of Human Blood for Elliptocyte 34%, Tear drop cell 30%, Schistocyte 26%, Hypochromic cell 22.5%, Irregular Different Diseases. Biomed J Sci & Tech Res contracted cell 16%, Echinocytes 15.5%, Roleaux 8%, Boat shape 6.5%, Sickle cell 5%, Keratocyte 4% and Acanthocytes 1.5%. During the screening of slides, bite cell, elliptocyte, tear drop cell, schistocytes, hypochromic cell, irregular contracted cells were found 30(1)-2020.Keywords: BJSTR.Human MS.ID.004893. blood; Diseases; frequently while echinocytes, boat shape cell, acanthocytes, sickle cells and keratocytes Morphological; Acanthocytes; Keratocyte were found rarely. -
Complete Blood Count in Primary Care
Complete Blood Count in Primary Care bpac nz better medicine Editorial Team bpacnz Tony Fraser 10 George Street Professor Murray Tilyard PO Box 6032, Dunedin Clinical Advisory Group phone 03 477 5418 Dr Dave Colquhoun Michele Cray free fax 0800 bpac nz Dr Rosemary Ikram www.bpac.org.nz Dr Peter Jensen Dr Cam Kyle Dr Chris Leathart Dr Lynn McBain Associate Professor Jim Reid Dr David Reith Professor Murray Tilyard Programme Development Team Noni Allison Rachael Clarke Rebecca Didham Terry Ehau Peter Ellison Dr Malcolm Kendall-Smith Dr Anne Marie Tangney Dr Trevor Walker Dr Sharyn Willis Dave Woods Report Development Team Justine Broadley Todd Gillies Lana Johnson Web Gordon Smith Design Michael Crawford Management and Administration Kaye Baldwin Tony Fraser Kyla Letman Professor Murray Tilyard Distribution Zane Lindon Lyn Thomlinson Colleen Witchall All information is intended for use by competent health care professionals and should be utilised in conjunction with © May 2008 pertinent clinical data. Contents Key points/purpose 2 Introduction 2 Background ▪ Haematopoiesis - Cell development 3 ▪ Limitations of reference ranges for the CBC 4 ▪ Borderline abnormal results must be interpreted in clinical context 4 ▪ History and clinical examination 4 White Cells ▪ Neutrophils 5 ▪ Lymphocytes 9 ▪ Monocytes 11 ▪ Basophils 12 ▪ Eosinophils 12 ▪ Platelets 13 Haemoglobin and red cell indices ▪ Low haemoglobin 15 ▪ Microcytic anaemia 15 ▪ Normocytic anaemia 16 ▪ Macrocytic anaemia 17 ▪ High haemoglobin 17 ▪ Other red cell indices 18 Summary Table 19 Glossary 20 This resource is a consensus document, developed with haematology and general practice input. We would like to thank: Dr Liam Fernyhough, Haematologist, Canterbury Health Laboratories Dr Chris Leathart, GP, Christchurch Dr Edward Theakston, Haematologist, Diagnostic Medlab Ltd We would like to acknowledge their advice, expertise and valuable feedback on this document. -
Laboratory Diagnosis Review
Laboratory Diagnosis Review Hematology Definition: The study of the three cellular elements of blood: Red Blood Cells (RBCs), White Blood Cells (WBCs), and Platelets Hemoglobin (Hgb or Hb): The oxygen carrying compound in RBCs Reference Range: Men 14-18 g/dL, Women 12-16 g/dL, Boy and girl levels are equal till age 11 Smoking increases, Pregnancy decreases, Capillary levels in newborns are higher than venous levels, Race, Position, and Time of day have minor effects, High WBCs may falsely raise Hgb. Below normal Hgb = anemia Red Blood Cell Count Reference Range: Men 4l5-6 million / cubic ml, Women4.0-5.5 million / ml3. Hematocrit (Hct): The ratio of RBCs to plasma Reference Range, Men 40%-54%, Women 37%-47%, Depends mostly on the number of RBCs but is slightly effected by the average RBC size, Not measured directly, but is calculated from the RBC count and the mean corpuscular volume (MCV). Increased by smoking, Decrease = anemia Useful Relationships: Hb X 3 = Hct RBCs (millions) X 3 = Hgb RBCs (millions) X 9 = Hct Wintrobe Indices: These indices are only significant if the RBCs, Hgb, and/or Hct. is abnormal MCV: Mean Corpuscular Volume MCH: Mean Corpuscular Hemoglobin MCHC: Mean Corpuscular Hemoglobin Concentration RDW: Red blood cell Distribution Width MCV: Reference Ranges: Men 80-95 fl (femtoliters), Women 81-99 fl (femto = 1 quadrillionth) Increased MCV = Macrocytosis, Decreased = Microcytosis MCV is increased by smoking, by B12 and/or folic acid deficiency, chronic liver disease, chronic alcoholism, Cardiorespiratory problems… Some macrocytic patients will not have macrocytosis MCV is decreased by iron deficiency, thalassemia, and anemia of chronic disease MCH: Reference Range 27-31 pg MCH is increased by Macrocytic anemias. -
Mean Corpuscular Hemoglobin (MCH) As a Predictor of Iron Deficiency in Infants
Pediatr. Res. 16: 168-170 (1982) Diagnosis of Iron Deficiency: Mean Corpuscular Hemoglobin (MCH) as a Predictor of Iron Deficiency in Infants G. J. KNIGHT, H. DE V. HEESE,"'' W. S. DEMPSTER, AND G. KIRSTEN Department of Paediatrics and Child Health, Institute of Child Health, University of Cape Town and Red Cross War Memorial Children's Hospital, Rondebosch 7700, Cape Town, Republic of South Africa Summary an infant population. Their interpretation during childhood is further compounded by factors such as age and periods of rapid Hematologic variables were measured in 240 apparently healthy growth. To overcome some of these difficulties, various combi- infants ranging from 1-12 months of age attending a well baby nations of tests have been suggested to assist in the diagnosis of clinic. There were 20 infants for each month of age. Hematologic mild iron deficiency (3, 7, 10, 12, 13, 14). In our hands they have parameters were measured in each infant by Coulter Counter not proved satisfactory and their cost prohibitive in a developing Model S. Serum iron, total iron binding capacity, free erythrocyte country. protoporphyrin (FEP) and serum ferritin levels were measured in A statistical exercise was embarked upon to establish the most most infants. Their weights together with their serum iron, total useful single hematologic parameter for the assessment of the iron iron binding capacity, and serum ferritin were judged to be inde- status of an infant. It formed part of a study to determine the pendent variables of iron status, whereas the hematologic variables prevalence of iron deficiency anemia during infancy in a com- were considered to be response variables indicative of iron status. -
Complete Blood Count
Print Entire Test Page 1 of 6 Close Window email this page print this page Complete Blood Count Also known as: CBC, Hemogram, CBC with differential Related tests: Blood smear, Hemoglobin, Hematocrit, Red blood cell (RBC) count, White blood cell (WBC) count, White blood cell differential count, Platelet count At A Glance Why get tested? To determine general health status and to screen for a variety of disorders, such as anemia and infection When to get tested? As part of a routine medical exam or as determined by your doctor Sample required? A blood sample drawn from a vein in the arm or a fingerstick or heelstick (newborns) The Test Sample What is being tested? The Complete Blood Count (CBC) test is an automated count of the cells in the blood. It provides information about the white blood cell (WBC), red blood cell (RBC), and platelet populations present. This information includes the number, type, size, shape, and some of the physical characteristics of the cells. In only a minute or two, the hematology instrument (the machine that is used to run the test) can measure thousands of RBCs, WBCs, and platelets and compare them against established normal ranges. Any abnormalities found are noted, and the clinical laboratory scientist (CLS) running the instrument then uses his or her expertise and experience to accept the automated findings and/or to target the sample for further analysis. In most cases, the automated CBC is very accurate and the test is complete at this point. If, however, there are significant abnormalities in one or more of the cell populations, a blood smear test may be performed. -
Drinking Water Health Advisory for the Cyanobacterial Toxin Cylindrospermopsin
United States Office of Water EPA- 820R15101 Environmental Mail Code 4304T June 2015 Protection Agency Drinking Water Health Advisory for the Cyanobacterial Toxin Cylindrospermopsin Drinking Water Health Advisory for the Cyanobacterial Toxin Cylindrospermopsin Prepared by: U.S. Environmental Protection Agency Office of Water (4304T) Health and Ecological Criteria Division Washington, DC 20460 EPA Document Number: 820R15101 Date: June 15, 2015 ACKNOWLEDGMENTS This document was prepared by U.S. EPA Scientists Lesley V. D’Anglada, Dr.P.H. (lead) and Jamie Strong, Ph.D. Health and Ecological Criteria Division, Office of Science and Technology, Office of Water. EPA gratefully acknowledges the valuable contributions from Health Canada’s Water and Air Quality Bureau, in developing the Analytical Methods and Treatment Technologies information included in this document. This Health Advisory was provided for review and comments were received from staff in the following U.S. EPA Program Offices: U.S. EPA Office of Ground Water and Drinking Water U.S. EPA Office of Science and Technology U.S. EPA Office of Research and Development U.S. EPA Office of Children’s Health Protection U.S. EPA Office of General Counsel This Health Advisory was provided for review and comments were received from the following other federal and health agencies: Health Canada U.S. Department of Health and Human Services, Centers for Disease Control and Prevention Drinking Water Health Advisory for Cylindrospermopsin - June 2015 i TABLE OF CONTENTS ACKNOWLEDGMENTS.....................................................................................................................I -
Blood and Immunity
Chapter Ten BLOOD AND IMMUNITY Chapter Contents 10 Pretest Clinical Aspects of Immunity Blood Chapter Review Immunity Case Studies Word Parts Pertaining to Blood and Immunity Crossword Puzzle Clinical Aspects of Blood Objectives After study of this chapter you should be able to: 1. Describe the composition of the blood plasma. 7. Identify and use roots pertaining to blood 2. Describe and give the functions of the three types of chemistry. blood cells. 8. List and describe the major disorders of the blood. 3. Label pictures of the blood cells. 9. List and describe the major disorders of the 4. Explain the basis of blood types. immune system. 5. Define immunity and list the possible sources of 10. Describe the major tests used to study blood. immunity. 11. Interpret abbreviations used in blood studies. 6. Identify and use roots and suffixes pertaining to the 12. Analyse several case studies involving the blood. blood and immunity. Pretest 1. The scientific name for red blood cells 5. Substances produced by immune cells that is . counteract microorganisms and other foreign 2. The scientific name for white blood cells materials are called . is . 6. A deficiency of hemoglobin results in the disorder 3. Platelets, or thrombocytes, are involved in called . 7. A neoplasm involving overgrowth of white blood 4. The white blood cells active in adaptive immunity cells is called . are the . 225 226 ♦ PART THREE / Body Systems Other 1% Proteins 8% Plasma 55% Water 91% Whole blood Leukocytes and platelets Formed 0.9% elements 45% Erythrocytes 10 99.1% Figure 10-1 Composition of whole blood. -
10 11 Cyto Slides 81-85
NEW YORK STATE CYTOHEMATOLOGY PROFICIENCY TESTING PROGRAM Glass Slide Critique ~ November 2010 Slide 081 Diagnosis: MDS to AML 9 WBC 51.0 x 10 /L 12 Available data: RBC 3.39 x 10 /L 72 year-old female Hemoglobin 9.6 g/dL Hematocrit 29.1 % MCV 86.0 fL Platelet count 16 x 109 /L The significant finding in this case of Acute Myelogenous Leukemia (AML) was the presence of many blast forms. The participant median for blasts, all types was 88. The blast cells in this case (Image 081) are large, irregular in shape and contain large prominent nucleoli. It is difficult to identify a blast cell as a myeloblast without the presence of an Auer rod in the cytoplasm. Auer rods were reported by three participants. Two systems are used to classify AML into subtypes, the French- American-British (FAB) and the World Health Organization (WHO). Most are familiar with the FAB classification. The WHO classification system takes into consideration prognostic factors in classifying AML. These factors include cytogenetic test results, patient’s age, white blood cell count, pre-existing blood disorders and a history of treatment with chemotherapy and/or radiation therapy for a prior cancer. The platelet count in this case was 16,000. Reduced number of platelets was correctly reported by 346 (94%) of participants. Approximately eight percent of participants commented that the red blood cells in this case were difficult to evaluate due to the presence of a bluish hue around the red blood cells. Comments received included, “On slide 081 the morphology was difficult to evaluate since there was a large amount of protein surrounding RBC’s”, “Slide 081 unable to distinguish red cell morphology due to protein” and “Unable to adequately assess morphology on slide 081 due to poor stain”.