Hematology is the study of blood and blood components. The document discusses the components of blood including red blood cells, white blood cells, platelets, and plasma. It describes their functions such as oxygen transport, immune response, and blood clotting. Various blood disorders are also summarized like anemia, which can result from blood loss, decreased production, or increased destruction. The stages of blood cell production and normal ranges for blood counts are also outlined.
A basic and worth information for diagnostic is urine microscopy. ideally it should be by the physician at his clinic to add and correlate diagnosis promptly. this will make physician confident in dealing with patients. it also help in follow up the consequences in some important glomerulopathies.
Hematopoiesis: Origin and development of blood cellsVarun Singh
The process of hematopoiesis, its microenvironment and regulators. the process of erythropoiesis, myelopoiesis and megakaryopoiesis and their regulators with illustrated figures.
A basic and worth information for diagnostic is urine microscopy. ideally it should be by the physician at his clinic to add and correlate diagnosis promptly. this will make physician confident in dealing with patients. it also help in follow up the consequences in some important glomerulopathies.
Hematopoiesis: Origin and development of blood cellsVarun Singh
The process of hematopoiesis, its microenvironment and regulators. the process of erythropoiesis, myelopoiesis and megakaryopoiesis and their regulators with illustrated figures.
Physicians working in the field of hematology are called hematologists. Initially, hematologists complete a four-year medical degree and this is followed by three or four years in an internship or residency program. Thereafter, they spend two or three more years learning how to diagnose and treat blood disorders.
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An illustrative presentation on Microscopic examination of Urine for Medical, Dental, Pharmacology and Biotechnology students to facilitate easy- learning and self-study..
Physicians working in the field of hematology are called hematologists. Initially, hematologists complete a four-year medical degree and this is followed by three or four years in an internship or residency program. Thereafter, they spend two or three more years learning how to diagnose and treat blood disorders.
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An illustrative presentation on Microscopic examination of Urine for Medical, Dental, Pharmacology and Biotechnology students to facilitate easy- learning and self-study..
This Presentation for technologist, to learned the basic Hematology cell morphology of RBC, WBC & Platelet count. It will be very useful for technical personnel.
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
2. Hematology
2
Hematology is the study of blood and blood components
Blood is biological fluid that has the supernatant fluid plasma and
cellular components (RBCs, WBCs and platelets).
Blood is 6-8% of total body weight and equals approximately 5-6
liters.
The fluid portion of anticoagulated blood is called plasma.
The fluid portion of coagulated blood is called serum.
Tassew Tefera
3. Hematology…
3
Serum vs Plasma
Both are fluid portions of blood
Serum:
Is from clotted blood, has no clotting factors (used up in the
clotting process)
Serum = Plasma - clotting factor (fibrinogen)
Plasma:
Is from anticoagulated blood, has clotting factors, makes up
about 45-55% of blood’s volume.
Plasma contains water (95%) and many solutes, including
proteins, mineral ions, organic molecules, hormones,
enzymes, products of digestion, and waste products for
excretion.
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4. Functions of blood
4
Blood has important transport, distribution, regulatory,
and protective functions in the body.
Blood assists in regulating the temperature of the body
by absorbing and distributing heat throughout the
body.
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5. Function of plasma
5
Plasma maintain the pH of the blood between pH 7.35–7.45 and the
pH in body tissues within the physiological limits required for normal
cellular activity.
Proteins (particularly albumin) and salts (particularly sodium chloride)
regulate plasma osmotic pressure, preventing excessive loss of fluid
from the blood into tissues spaces.
When a blood vessel is damaged, platelets and blood coagulation
factors interact to control blood loss.
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6. Functions of RBCs
6
Carry Oxygen from the lungs to the tissues.
This function is performed by hemoglobin which is present in large
amounts in mature red cells.
Nutrients absorbed from the digestive tract and are transported to the
cells of the body for use or storage.
Waste products are transported from the tissues to site of excretion,
e.g. Co2 is carried to the lungs, and the waste products of protein
metabolism (urea, creatinine, uric acid) are transported to the kidneys
Hormones are carried from endocrine glands to the organs where they
are needed.
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8. Function of platelets
8
Cause clotting of blood
When a blood vessel is damaged, platelets and blood
coagulation factors interact to control blood loss.
Platelets adhere to the damaged tissue and to one another
and activated coagulation factors lead to the formation of
fibrin and a thrombus clot which reinforce the platelet plug.
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9. Function of WBCs
9
Leukocytes are involved in the body’s defenses
producing antibodies in response to infection
protecting the body from damage by viruses, bacteria,
parasites, toxins and tumor cells.
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10. Blood cell production
10
The process by which blood cells are formed is called hematopoiesis or
haemopoiesis.
Blood is produced in bone marrow
Hematopoiesis during fetal life and infancy
The liver and spleen become the main sites of blood cell
production during the second trimester of pregnancy and fetal bone
marrow in the third trimester.
At birth, hematopoiesis is confined to the bone marrow.
Hematopoiesis during adult life
By about 25 years of age, the main sites of hematopoiesis is bone
marrow.
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11. Blood cell production…
11
Production of RBCs is called erythropoiesis
Production WBCs is called leucopoiesis
Production of platelets is called thrombopoiesis
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12. Erythrocyte(RBCs)
12
It is mainly composed of hemoglobin surrounded by a flexible
protein membrane and outer lipid bilayer.
Have life-span of about 120 days, degenerated red cells are
removed from the circulation by reticuloendothelial cells, mainly
in the spleen.
Normal Values:
Males: 4.5 to 6.0 million/mm3 blood
Females: 4.0 to 5.5 million/mm3 blood
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13. Erythrocyte(RBCs)
13
Visual description of RBC morphology useful for diagnostic
information.
1. Normocytic—cells are of normal size.
2. Macrocytic—abnormally large cell.
3. Microcytic—abnormally small cell.
4. Normochromic—cells are of normal color.
5. Polychromatic—variation in color of the cells..
6. Hypochromatic—decrease in staining density of the cells, usually
due to a lack of hemoglobin.
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14. 14
The main disorders of red cells are:
Anemia
Hemoglobinopathies (thalassemia, abnormal hemoglobin)
Disorders due to red cell enzyme defects, e.g. G6PD
deficiency
Disorders due to red cell membrane defects, e.g. hereditary
spherocytosis
Polycythemia
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15. 15
Anemia
It occurs when the concentration of hemoglobin falls
below what is normal for a person’s age, gender, and
environment,
Results in reduced oxygen carrying capacity of the blood.
Sign and Symptoms of anemia
Fatigue, weakness, breathless on exertion, have
palpitations , headaches and dizziness, pallor of the skin,
mucous membranes and conjunctiva.
Pregnant women with untreated anemia are at increased
risk of dying during or following childbirth.
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16. Mechanisms of anemia
16
BLOOD LOSS
Acute bleeding, e.g. accident, surgical, ectopic pregnancy.
Chronic blood loss, e.g. hookworm infection, schistosomiasis,
gastrointestinal bleeding, menorrhagia
DECREASED RED CELL PRODUCTION
Lack of essential nutrients,
Depressed bone marrow activity
Due to drugs
INCREASED RED CELL DESTRUCTION (HAEMOLYSIS)
hemolytic anemias:
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17. 17
Microcytic hypochromic anemia
Iron deficiency (commonest cause)
Thalassemia syndromes (see later text)
Hemolytic anemia
Aplastic anemia
Megaloblastic anemia
Normocytic normochromic anemia
Types of anemia
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18. 18
RBCs are microcytic (microcytic anemia).
Ferrous (Fe2+) iron is better absorbed than ferric (Fe3+) iron.
Total body iron store about 4g.
Iron deficiency is common at reproductive age since menstrual
losses account for ~20mg Fe/month and in pregnancy an
additional 500–1000mg Fe may be lost (transferred from mother
to fetus).
Causes of iron deficiency Esophagitis, pregnancy, elderly,
hemorrhoids, hookworm infection.
Iron Deficiency Anemia
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19. 19
Laboratory diagnosis
Reduced Hgb and HCT
Reduced MCV (<76FLz) and MCHC
Increased Red cell distribution width (RDW) in iron deficiency.
Treatment of iron deficiency
FeSO4 oral dose of 150–200mg/dl per day for 3-6 months.
Liquid iron occasionally necessary, e.g. children or adults with
swallowing difficulties.
Iron Deficiency Anemia
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20. Megaloblastic anemia
20
Macrocytic anemia (MCV usually >110fL).
RBC become megaloblasts (large in size).
Hyper segmented neutrophils.
Leucopenia and thrombocytopenia common.
Iron stores usually increased.
Caused by vit B12 and Folate deficiency .
Treatment-hydroxocobalamin 1mg IM and folic acid PO
should be given immediately.
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21. Hemolytic anemia
21
Is any situation in which there is a reduction in RBC life-span due
to increased RBC destruction.
Failure of compensatory marrow response results in anemia.
Lab diagnosis
Complete blood count (CBC).
Peripheral blood film:- polychromasia, spherocytosis,
fragmentation (schistocytes), echinocytes.
Increased reticulocytes.
Increased serum bilirubin (unconjugated).
Treatment
folic acid and iron supplements.
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22. 22
A gross reduction or absence of hemopoietic
precursors in all 3 cell lineages peripheral blood.
Cause pancytopenia
It a total reduction in;
Leukocyte
Platelets
Reticulocytes
Aplastic anemia
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23. 23
Is an increase in total red cell mass.
It is suspected by finding a raised hematocrit (Hct)
(packed cell volume, PCV).
Polycythemia Vera (PV) is a neoplastic clonal disorder of
the BM stem cell causing excessive proliferation of the
erythroid carrying a risk of thrombotic complications.
Hct >0.48 in adult female and >0.54 in adult male is PV.
Polycythemia Vera (PV)
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24. WHITE BLOOD CELLS
24
In an adult there are about 4.0-10.0 x 109 WBCs
(leukocytes) per litter of blood.
The white blood cells consist of the granulocytes
(neutrophils; eosinophils; and basophils) and the
agranulocytes (lymphocytes and monocytes).
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27. Neutrophils
27
They are highly mobile phagocytes and important in defending
the body from infection.
Mature neutrophils have a lobulated nucleus.
They function as phagocytes and are important in infectious
conditions and in inflammation.
Increased neutrophil (neutrophilia) are caused by
inflammation, bacterial infection, acute stress, and myeloid
leukemia.
Decreased neutrophil (neutropenia) are caused by viral
infections, toxin exposure (including foodborne toxins),
autoimmune destruction of neutrophils, and typhoid.
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28. Eosinophil
28
They inactivate histamine and inhibit edema formation.
Bi-lobed cell
Increased eosinophil (eosinophilia) are caused by
parasitic infections, tissue injury, allergic reaction, mast cell
tumors, and pregnancy.
Decreased eosinophil (eosinopenia) is almost always
caused by the action of glucocorticoids, Stress response;
due to trauma, shock, burns, surgery.
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29. Basophil
29
They are closely related to mast cells and initiate the
inflammatory response by releasing histamine.
Increased basophil (basophilia): occur in hypersensitivity
reaction, myeloproliferative disorders (myeloid leukemia).
Basophils bind IgE on their surface and are involved in
anaphylactic, hypersensitivity, and inflammatory reactions.
Decreased basophil: occur in miscellaneous disorders;
hyperthyroidism, ovulation, pregnancy, stress.
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30. Monocytes
30
Monocytes are large cells with a kidney bean-shaped
nucleus.
Their main function is phagocytosis.
An increased monocyte count (monocytosis) may occur
in chronic inflammation, lymphoid leukemia, subacute
bacterial endocarditis, tuberculosis, hepatitis, malaria,
systemic lupus erythromatus, rheumatoid arthritis.
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31. Lymphocytes
31
They are the smallest of the white cells, with a round, evenly
staining nucleus and sparse cytoplasm.
Their primary function is immunologic, including both antibody
production and cell-mediated immune responses.
An increased lymphocyte count (lymphocytosis) may occur in
leukemia, viral infection and mycobacterium tuberculosis.
Decreased lymphocyte counts (lymphopenia) are usually due to
an effect of corticosteroids, stress, and in parvoviruses infections.
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32. Disorders of white blood cells
32
The disorders of white cells could be two types:
Leukocytosis (increased WBCs)
Leukopenia (decreased WBCs)
Absolute increases in leukocyte numbers in response to bacterial,
viral, or parasitic infections, tissue injury, and inflammation.
Absolute decreases in leukocyte can be caused by some infections
(especially HIV), hypersplenism, immune destruction of cells,
treatment with cytotoxic drugs, bone marrow dysfunction,
megaloblastic anemia, collagen disorders, and malignant conditions.
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34. Acute myeloblastic leukemia (AML)
34
Malignant tumor of hemopoietic precursor cells of myeloid
lineage, almost certainly arising in the bone marrow.
Commonest leukemia in adults.
Caused by cytotoxic chemotherapy (particularly alkylating agents),
ionizing radiation, chromosomal abnormalities and smoking.
Diagnosis
Examination of the peripheral blood film and bone marrow ≥20%
blasts.
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35. Acute lymphoblastic leukemia (ALL)
35
Malignant tumor of hemopoietic precursor cells of the
lymphoid lineage due to marrow failure in most cases.
Commonest malignancy in childhood.
Rare leukemia in adults.
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36. Chronic myeloid leukemia (CML)
36
Malignant tumor of an early hemopoietic progenitor
cell.
Rare in children and median age of onset is 50 years.
Irradiation is the only known epidemiological factor.
Diagnosis and investigations
Blood film show increased WBC (>25 x 109/L, often
100–300 x 109/L): predominantly neutrophils and
myelocytes; basophilia; eosinophilia.
Anemia common; platelets typically normal or
increased.
ESR increased in absence of secondary infection.
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37. Chronic lymphocytic leukemia (CLL)
37
Progressive accumulation of mature-appearing,
functionally incompetent, long-lived B lymphocytes in
peripheral blood.
Commonest leukemia in adults.
Predominantly disease of elderly and median age of 65
years.
Diagnosis
CBC shows: lymphocytosis >5.0 x 109/L; usually >20 x
109/L, occasionally >400 x109/L
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38. Platelets
38
Formed from multinucleate megakaryocytes in the bone marrow.
They maintain the integrity of the endothelium and act as part of
the clotting process to repair damaged endothelium, where they
ensure mechanical strength of the clot.
Increased platelet counts (thrombocytosis) occur following
injury, after splenectomy, and in megakaryocytic leukemia.
Decreased platelet counts (thrombocytopenia) are caused by
autoimmune reactions, thrombotic/thrombocytopenic purpura,
bone marrow suppression and aplasia, bone marrow neoplasia.
Signs are petechiation and hemorrhage.
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39. Discussion
39
1. Describe the etiologies and types of anemia
2. What are the functions of cells and their reference range?
3. What are the disorder of red blood cells?
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40. 40
Blood must be collected with care and adequate safety
precautions to ensure test results are reliable,
contamination of the sample is avoided and infection
from blood transmissible pathogens is prevented.
Types of blood sample
Capillary blood
Venous blood
Arterial blood
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41. Capillary blood
41
Collected when the volume of blood required is small, e.g. to
measure hemoglobin, perform a WBC count, and to make
thick and thin blood films.
Collected when the patient is an infant or young child.
Thick blood films for malaria parasites are best made from
capillary.
Capillary blood can be collected from:
The ‘ring’ finger of a child or adult.
The heel of an infant up to one year old.
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42. Technique for collecting capillary blood
42
Make sure the puncture area is warm to allow the blood to flow freely.
On cold days soak the hand or foot of an infant in warm water prior
to collecting a sample.
1. Cleanse the puncture area with 70% ethanol and allow the area to
dry.
2. Using a sterile lancet make a rapid puncture, sufficiently deep to
allow the free flow of blood.
3. Wipe away the first drop of blood with a dry piece of cotton wool
and use the next few drops for the test. Do not squeeze too hard
because this will result in an unreliable test result.
4. When sufficient blood has been collected, press a piece of dry
cotton wool over the puncture area until bleeding stops.
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43. Venous blood
43
Venous blood is used when more than 100 μl of whole blood is
required or when serum or plasma blood sample is needed.
Venous blood is preferable to capillary blood particularly when the
patient is an adult and several tests are required.
Technique for collecting venous blood
1. Select a vein.
2. Apply tourniquet the upper arm of the patient to enable the
veins to be seen. Do not apply the tourniquet too tightly.
3. Using the index finger, feel for a suitable vein, selecting a
sufficiently large straight vein that does not roll.
4. Cleanse the puncture site with 70% ethanol and allow to dry.
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44. Venous blood…
44
5. Make the venepuncture with needle directed upwards in the line of the
vein(with angle of 45 degree) and steadily withdraw required volume
of sample.
6. When sufficient blood has been collected, release the tourniquet and
remove the needle and immediately press on the puncture site with a
piece of dry cotton wool.
7. Remove the needle from the syringe and carefully fill the container(s)
with the required volume of blood. Discard the needle safely.
8. Mix immediately the blood in an EDTA or citrate anti-coagulated
container.
9. Check that bleeding from the venepuncture site has stopped.
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45. Blood film
45
Two types
a) Thin blood film:
Examination of thin blood films is important in the
investigation and management of anemia, infections, and
other conditions which produce changes in the appearance
of blood cells and differential white cell count.
b) Thick blood film
For examining blood parasites; e.g. malaria parasites,
trypanosomes, and microfilariae.
Concentrate parasites.
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46. Staining of blood films
46
Blood films are usually stained by;
Leishman stain usually used for staining leishmania
parasites.
Wright’s stain used for morphology blood cells and
rarely for malaria parasites.
Giemsa stain preferable for staining malaria parasites.
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47. Hematological tests are mainly used:
47
To investigate anemia,
To investigate infections and pyrexia (fever) of unknown origin
To investigate clinically important hemoglobinopathies.
To monitor patients receiving antiretroviral therapy (ART).
To investigate a bleeding disorder
To diagnose and monitor a coagulation disorder.
To diagnose and treat major blood cell disorders (leukemia or
myelomatosis).
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48. Hematological tests performed in
district laboratories
48
Measurement of hemoglobin.
Measurement of packed cell volume (hematocrit).
Red cell indices (MCV,MCH.MCHC RDW).
Total White blood cell (WBC) count.
Platelet count.
Differential WBC count.
Erythrocyte sedimentation rate(ESR).
Reticulocyte count.
Blood film examination.
Tests to screen for a bleeding and coagulation disorder
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49. Measurement of hemoglobin
49
Hemoglobin (Hgb)
Hgb is the pigment part of the erythrocyte.
It accounts three fourth of the red cell membrane.
Hgb is made up of iron-containing molecules called heme which
are attached to polypeptide chains called globin.
It has the ability to combine reversibly with oxygen and carbon
dioxide.
Oxygen is taken up in the lungs and pumped to the tissues.
After it has been used, the oxygen is replaced by unwanted carbon
dioxide which is carried back to the lungs by the red cells.
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50. Measurement of hemoglobin
50
Value of test:
Hemoglobin is measured to detect anemia and its severity and to
monitor an anemic patient’s response to treatment.
Monitoring the Hgb (or PCV) is also required when patients with
HIV disease are being treated with drugs such as AZT.
The test is also performed to check the hemoglobin level of a blood
donor prior to donating blood.
Specimen: Capillary blood or EDTA anticoagulated venous blood
can be used.
Measured by
Sahli hilage /acid haematin method,
Haemiglobincyanide (Methemoglobin method),
Hemoglobino meter method (HemoCue system).
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52. Interpretation of hemoglobin results
52
Clinician/health worker at point-of-care should identify
anemia and judge its severity in the following clinical
categories:
Hgb 12 g/dl Not anemia
Hgb 10–11 g/dl Mild anemia
Hgb 8–9 g/dl Moderate anemia
Hgb 6–7 g/dl Marked anemia
Hgb 4–5 g/dl Severe anemia
Hgb 4 g/dl Critical
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53. Packed Cell Volume (PCV)
53
PCV also referred to as hematocrit
PCV is that proportion of whole blood occupied by red cells,
expressed as a ratio (%).
Anticoagulated blood in a glass capillary is centrifuged in a
microhematocrit centrifuge at 1000–5000 rpm for 3–5 minutes
to obtain constant packing of the red cells.
The PCV value is read from the scale of a microhematocrit
reader or calculated by dividing the height of the red cell
column by the height of the total column of blood.
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54. Packed Cell Volume (PCV)…
54
Increased PCV(HCT)Polycythemia Vera.
Abnormally low PCV in anemia may be caused by loss of blood
(hemorrhage), break-down of erythrocytes in circulation
(hemolysis), or lack of production of erythrocytes by the bone
marrow (hypoplasia or aplasia).
Aplastic anemia is always chronic in onset because anemia
occurs gradually as existing cells reach the end of their lifespan.
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55. Reference value of HCT
55
PCV values vary according to age, gender, and altitude.
Normal reference value
Children at birth . . . . . . . . . . . . . . . . . . . .0.44–0.54
Children 2–5 y . . . . . . . . . . . . . . . . . . . . . 0.34–0.40
Children 6–12 y . . . . . . . . . . . . . . . . . . . . 0.35–0.45
Adult men. . . . . . . . . . . . . . . . . . . . . . . . . 0.40–0.54
Adult women . . . . . . . . . . . . . . . . . . . . . . 0.36–0.48
Specimen: EDTA anticoagulated blood or capillary blood
collected into a heparinized capillary .
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56. RED CELL INDICES
56
Red cell indices most frequently used in the investigation of anemia are:
Mean cell hemoglobin concentration (MCHC)
Mean cell volume (MCV)
Mean cell hemoglobin (MCH)
MCHC
The MCHC gives the concentration of hemoglobin in g/l in 1 littre of packed red
cells.
MCHC= Hgb g/dl x100
PCV (%)
A normal reference range for MCHC in health is 31.5–36.0 g/dl.
Low MCHC values are found in iron deficiency anemia.
An increased MCHC can occur in marked spherocytosis.
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57. Mean Red Cell Volume (MCV)
57
It provides provides information on red cell size.
Classify RBCs as microcytic and macrocytic.
Measured in femtolitres (fl) and is determined from the
PCV and electronically obtained RBC count.
A normal reference range is 80–100 fl.
Low MCV values: are found in microcytic anemias particularly
iron deficiency, anemia of chronic disease and thalassemia.
Raised MCV values: are found in macrocytic anemias, marked
B12 or folate deficiency, acquired sideroblastic anemia,
hypothyroidism, chronic respiratory failure, aplastic anemia
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58. Mean cell hemoglobin (MCH)
58
The MCH gives the amount of hemoglobin in picograms
(pg) in an average red cell.
It is calculated from the hemoglobin and electronically
obtained RBC count:
MCH (pg) = Hgb x10
RBCs
A normal reference range for MCH in health is 27–32 pg.
Low MCH values: are found in microcytic hypochromic
anemias.
Raised MCH values: are found in macrocytic
normochromic anemias.
MCH is also raised in newborns.
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59. Factors that affect measurements of
erythrocyte parameters:
59
1. Old samples cause RBC to swell, thus increasing PCV and
MCV and decreasing MCHC.
2. Lipemia causes a falsely high Hgb reading, and hence a
falsely high MCHC.
3. Hemolysis causes PCV to decrease while Hgb remains
unchanged, again leading to a falsely high MCHC.
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60. WHITE BLOOD CELL COUNT
60
A white blood cell (WBC) count is used to investigate
HIV/AIDS, infections and unexplained fever, and to monitor
treatments which can cause leukopenia or leukocytosis.
Principle of test
Whole blood is diluted 1 in 20 in an acid reagent which
hemolyzes the red cells (non nucleated red cells), leaving the
white cells to be counted.
White cells are counted microscopically using an Improved
Neubauer ruled counting chamber (hemocytometer) and the
number of WBCs per littre of blood calculated.
Blood sample: EDTA anticoagulated blood or capillary blood.
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61. WHITE BLOOD CELL COUNT
61
Methods
A) Thoma pipette(o.5 blood to 11 parts of diluting fluid)
B) Tube method(20 microlittre blood to 380 microlittre
fluid)
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62. Interpretation of WBC counts
62
Reference ranges vary with gender and age.
WBC reference range
These are guideline figures which should be checked
locally.
Children at 1 y . . . . . . . . . . . . . . . . 6.0– 18.0 109/l
Children 4–7 y . . . . . . . . . . . . . . . . 5.0– 15.0 109/l
Adults . . . . . . . . . . . . . . . . . . . . . . . 4.0– 10.0 109/l
Adults women . . . . . . . . . . . . . . . . .4.0– 8.0 109/l
Pregnant women . . . . . . . . . . . . . . Up to 15 109/l
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63. Leukocytosis
63
The main causes of a raised WBC count are:
Acute infections; pneumonia, meningitis, abscess,
acute rheumatic fever, septic abortion.
Inflammation and tissue necrosis.
Metabolic disorders; diabetic coma and acidosis.
Poisoning; chemicals, drugs, snake venoms.
Acute hemorrhage
Leukemia
Stress, menstruation, strenuous exercise.
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64. Leukopenia
64
The main causes of a reduced WBC count are:
Viral, bacterial, parasitic infections e.g. HIV/AIDS,
viral hepatitis, measles, rubella, influenza, rickettsial
infections, relapsing fever, typhoid, paratyphoid,
brucellosis etc.
Drugs (e.g. cytotoxic)
Aplastic anaemia
Folate and vitamin B12 deficiencies
Anaphylactic shock
Ionizing radiation
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65. PLATELET COUNT
65
A platelet count may be requested to investigate abnormal
skin and mucosal bleeding which can occur when the platelet
count is very low (usually below 20 x 109/l).
Principle of test
Blood is diluted 1 in 20 in a filtered solution of ammonium
oxalate reagent which lyzes the red cells.
Platelets are counted microscopically using an Improved
Neubauer ruled counting chamber.
Blood sample: Use EDTA anticoagulated venous blood.
Capillary blood should not be used because platelets clumpas
the blood is being collected.
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66. Interpretation of platelets counts
66
Normal reference value 150–400 x 109 platelets/littre of
blood.
Thrombocytopenia (reduction in platelet number)is due
to:
Reduced production of platelets (Aplastic anemia).
Infections, e.g. typhoid, brucellosis
Deficiency of folate or vitamin B12
Drugs (e.g. cytotoxic, quinine, aspirin),
Leukemia, carcinoma
Hereditary thrombocytopenia (rare condition).
Disseminated intravascular coagulation (DIC)
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67. Thrombocytosis
67
Causes of an increase in platelet numbers include:
Chronic myeloproliferative diseases, e.g. essential
thrombocythemia, polycythemia Vera, chronic myeloid leukemia,
myelofibrosis.
Chronic inflammatory disease, e.g. tuberculosis
Haemorrhage
Splenectomy.
Iron deficiency anemia, associated with active bleeding.
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68. Erythrocyte sedimentation (ESR)
68
ESR is a non-specific test.
It is raised in a wide range of infectious, inflammatory,
degenerative, and malignant conditions associated with
changes in plasma proteins, particularly increases in
fibrinogen, immunoglobulins, and C-reactive protein.
The ESR is also affected anemia, pregnancy,
haemoglobinopathies, hemoconcentration and treatment
with anti-inflammatory drugs.
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69. Principle of test of ESR
69
When citrated blood in a vertically positioned Westergren
pipette is left undisturbed, red cells aggregate, stack together
to form rouleaux, and sediment through the plasma.
The ESR is the rate at which this sedimentation occurs in 1
hour as indicated by the length of the column of clear
plasma above the red cells, measured in mm/hr.
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70. Interpretation of ESR test results
70
Reference range
Men . . . . . . . . . . . . . . . . . . . . . Up to 10 mm/hour*
Women . . . . . . . . . . . . . . . . . . . Up to 15 mm/hour*
Elderly . . . . . . . . . . . . . . . . . . . . Up to 20 mm/hour*
Causes of a significantly raised ESR
Anemia,
Acute and chronic inflammatory conditions,
Infections including: HIV disease, Tuberculosis, Pelvic
inflammatory disease , Ruptured ectopic pregnancy , Systemic
lupus erythematosus.
Drugs, including oral contraceptives
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71. Reduced ESR
71
Sedimentation is falsely low in polycythemia, dehydration,
dengue hemorrhagic fever, and other conditions associated
with hemoconcentration.
Abnormally shaped red cells as in sickle cell disease also
lower sedimentation rate.
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73. Assignment
73
1. The importance of clinical laboratory in prevention and
control of Disease
2. List and discuss types of laboratory testes
3. What is leukemia and how it is caused
4. Write detail about laboratory and medical laboratory
5. Describe the etiologies and types of anemia
6. Discuss about chemistry tests
7. Discuss about microbiological laboratory examination
8. discuss briefly about sensitivity , specificity , positive
predictive value and Negative predictive value
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