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Hematology: Principles and Procedures

✍ Scribed by Barbara A. Brown


Publisher
Lea & Febiger
Year
1993
Tongue
English
Leaves
496
Edition
6
Category
Library

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✦ Synopsis


Tufts New England Medical Center Hospital, Boston, Massachusetts. New edition of a Brandon/Hill Allied Health List first -purchase selection. Textbook for medical technology students. Halftone illustrations and color plates. Previous edition 1988. DNLM: Hematologic Diseases - diagnosis laboratory manuals.

✦ Table of Contents


  1. • Basic Laboratory Techniques
    COMPOSITION OF BLOOD 1
    UNIVERSAL PRECAUTIONS 1
    COLLECTION OF BLOOD 2
    Microsample Technique 3
    Venipuncture 7
    Isolation Techniques 11
    ANTICOAGULANTS 12
    THE MICROSCOPE 13
    Operating Procedures 15
    Phase Microscopy 17
    Electron Microscopy 18
    PHOTOMETER/SPECTROPHOTOMETER 18
    Optical Density vs. % Transmittance 20
    Determination of the Wavelength 20
    Preparation of a Curve 20
    CENTRIFUGATION 21
    STATISTICAL TOOLS USED TO EVALUATE LABORATORY TESTING 22
    Quality Control of Test Results 22
    Evaluation of Test Procedures 28
    Determination of Normal Range (Reference Interval) 32
  2. • Hematopoiesis
    ORIGIN AND INTERRELATIONSHIP OF BLOOD CELLS 36
    CELL STRUCTURE 37
    NORMAL CELL MATURATION 39
    Cytoplasmic Maturation 39
    Nuclear Maturation 39
    Cell Size 39
    Identification of Cells 39
    RED BLOOD CELLS 40
    Erythropoiesis 41
    Hemoglobin Structure and Synthesis , 42
    Function of Hemoglobin 44
    Erythrocyte Membrane 46
    Metabolism of the Red Blood Cell 46
    Breakdown of the Red Blood Cell 47
    Megaloblastic Erythropoiesis 49
    Red Blood Cell Morphology 51
    WHITE BLOOD CELLS AND PLATELETS 57
    Granulocytes 57
    Monocytes 66
    Lymphocytes 70
    Megakaryocytes 77
    White Blood Cell and Platelet Morphology 81
  3. • Routine Hematology Procedures
    COMPLETE BLOOD COUNT 83
    HEMOGLOBIN 83
    Cyanmethemoglobin Method 83
    Preparation of a Standard Hemoglobin Curve 84
    Abnormal Hemoglobin Pigments 84
    HEMATOCRIT 85
    Microhematocrit Method 86
    BLOOD CELL COUNTS 87
    Units of Reporting 87
    THE UNOPETTE SYSTEM 88
    WHITE BLOOD CELL COUNT 89
    Manual White Blood Cell Count 90
    RED BLOOD CELL COUNT 95
    PREPARATION AND STAINING PROCEDURES FOR THE BLOOD SMEAR 97
    Cover Glass Smears 97
    Wedge Blood Smears 98
    Automated Spun Smear 99
    Buffy Coat Smear 99
    Thick Blood Film 99
    Staining Procedure for Blood Smears 100
    DIFFERENTIAL CELL COUNT 102
    Procedure for Examination of the Stained Blood Smear 102
    RED BLOOD CELL INDICES 105
    Mean Corpuscular Volume (MCV) 106
    Mean Corpuscular Hemoglobin (MCH) 106
    Mean Corpuscular Hemoglobin Concentration (MCHC) 106
    Examples of Red Blood Cell Indices with Corresponding Red Blood Cell 107
    Morphology
    ERYTHROCYTE SEDIMENTATION RATE 107
    Westergren Method 108
    Wintrobe and Landsberg Method 109
    RETICULOCYTE COUNT HI
    PLATELET COUNT 116
    EOSINOPHIL COUNT lig
    SICKLE CELL TESTS 121
    Sodium Metabisulfite Method 121
    Solubility Test 122
    Hemocard Hb A and S Procedure 124
  4. • Special Hematology Procedures
    SPECIAL STAINING TECHNIQUES
    EXAMINATION OF THE BONE MARROW 127
    Preparation of the Bone Marrow for Study 127
    Examination of Marrow Slides 129
    IRON STAIN (PRUSSIAN BLUE REACTION) 130
    LEUKOCYTE ALKALINE PHOSPHATASE STAIN 132
    PEROXIDASE STAIN 133
    PERIODIC ACID-SCHIFF (PAS) REACTION 135
    SUDAN BLACK B STAIN 136
    ACID PHOSPHATASE STAIN (WITH TARTRATE RESISTANCE) 137
    NONSPECIFIC ESTERASE STAIN (WITH FLUORIDE INHIBITION) 139
    CHLOROACETATE ESTERASE STAIN 140
    NITROBLUE TETRAZOLIUM (NBT) NEUTROPHIL REDUCTION TEST 141
    HEINZ BODY PREPARATION 143
    Stain for Heinz Bodies 144
    Heinz Body Preparation with Acetylphenylhydrazine 144
    BLOOD SMEAR PREPARATION AND EXAMINATION FOR PARASITES 145
    Blood Smear Preparation and Stain 146
    Examination of the Smear for Parasites 148
    HEMOGLOBIN TESTS
    RED CELL ZINC PROTOPORPHYRIN 149
    DETECTION/IDENTIFICATION OF HEMOGLOBINOPATHIES 152
    HEMOGLOBIN ELECTROPHORESIS BY CELLULOSE ACETATE 153
    CITRATE AGAR GEL ELECTROPHORESIS 157
    HEMOGLOBIN A2 160
    QUANTITATION OF HEMOGLOBIN F 163
    Betke Method of Alkali Denaturation 163
    Singer Method of Alkali Denaturation 164
    Radial Immunodiffusion Procedure for Hemoglobin F 166
    ACID ELUTION TEST 168
    HEMOGLOBIN H PREPARATION 170
    HEAT PRECIPITATION TEST 171
    ISOPROPANOL PRECIPITATION TEST 172
    TESTS FOR HEMOLYTIC ANEMIA, RED BLOOD CELL ENZYME DEFICIENCIES
    OSMOTIC FRAGILITY TEST 174
    OSMOTIC FRAGILITY TEST WITH INCUBATION 177
    AUTOHEMOLYSIS TEST 179
    ASCORBATE-CYANIDE SCREENING TEST 180
    Jacob and Jandl Method 181
    GLUCOSE-6-PHOSPHATE DEHYDROGENASE TEST 182
    PYRUVATE KINASE TEST 184
    GLUTATHIONE REDUCTASE TEST 186
    QUANTITATION OF METHEMOGLOBIN 187
    SERUM HAPTOGLOBIN TEST 188
    TESTS FOR PAROXYSMAL NOCTURNAL HEMOGLOBINURIA
    SUGAR WATER SCREENING TEST 192
    SUCROSE HEMOLYSIS TEST 193
    ACID SERUM TEST 195
    Ham Method 195
    MISCELLANEOUS TESTS
    LUPUS ERYTHEMATOSUS (L.E.) PREPARATION 197
    L.E. Cell Technique Using Heparinized Blood 198
    L.E. Cell Technique Using Clotted Blood 199
    SERUM VISCOSITY TEST 199
    REAGENTS 201
  5. • CoagoSafion
    HEMOSTASIS AND FIBRINOLYSIS 203
    Outline of Section 203
    Introduction 203
    Coagulation Mechanism 203
    The Coagulation Factors 206
    Fibrinolysis 208
    Limiting Mechanisms of Hemostasis 209
    Primary Hemostasis 210
    COAGULATION SCREENING PROCEDURES 212
    COAGULATION TESTING REQUIREMENTS 212
    SCREENING TESTS
    COAGULATION TIME OF WHOLE BLOOD 215
    Lee and White Method 215
    PROTHROMBIN TIME 216
    ACTIVATED PARTIAL THROMBOPLASTIN TIME 218
    PLASMA RECALCIFICATION TIME 220
    STYPVEN TIME 220
    REPTILASE TIME ' 221
    THROMBIN TIME 222
    PREKALUKREIN (FLETCHER FACTOR) SCREENING TEST 223
    FACTOR XIII SCREENING TEST 224
    FACTOR IDENTIFICATION (PT AND APTT SUBSTITUTION TEST) 225
    ASSAYS
    QUANTITATIVE FIBRINOGEN 226
    FACTOR V (II, VII, X) ASSAY 229
    FACTOR VIII (VIII:C, IX, XI, XII) ASSAY 232
    VONWILLEBRAND FACTOR ANTIGEN 234
    RISTOCETIN COFACTOR ASSAY 237
    HEPARIN (ANTI-XA) ASSAY 239
    TESTS FOR DIC/FIBRINOLYSIS
    FIBRINOGEN DEGRADATION PRODUCTS 240
    Thrombo-Wellcotest Procedure 241
    D-DIMER TEST FOR FIBRIN DEGRADATION PRODUCTS 242
    F.S. TEST FOR SOLUBLE FIBRIN MONOMER COMPLEXES 244
    ETHANOL GELATION TEST 246
    PROTAMINE SULFATE 247
    CLOT LYSIS 249
    EUGLOBULIN CLOT LYSIS TIME 249
    TESTS FOR INHIBITORS/ANTICOAGULANTS
    CIRCULATING ANTICOAGULANTS (INHIBITORS) 251
    PLATELET NEUTRALIZATION PROCEDURE 253
    DILUTE RUSSELL VIPER VENOM TEST 254
    INHIBITOR ASSAY 256
    Factor VIII Inhibitor Assay (Bethesda Method) 256
    TESTS FOR THROMBOTIC DISORDERS
    ANTITHROMBIN III 258
    PLASMINOGEN ASSAY 260
    PROTEIN C 261
    Protein C Chromagenic Method 261
    Protein C Clotting Assay 263
    PROTEIN S 264
    ELISA Method 264
    Free Protein S 266
    Protein S Clotting Assay 266
    PLATELET PROCEDURES
    BLEEDING TIME 267
    TOURNIQUET TEST (CAPILLARY FRAGILITY TEST) 270
    CLOT RETRACTION 271
    PLATELET AGGREGATION 271
    PLATELET ADHESIVENESS TEST 274
    Salzman Method 275
    HEPARIN ASSOCIATED THROMBOCYTOPENIA TEST (HATT TEST) 276
    REAGENTS 278
  6. • Diseases
    RED BLOOD CELL DISORDERS 279
    Introduction to the Anemias 279
    Morphologic Classification of Anemias 281
    Classification of Anemias According to Cause 281
    Disorders Related to Iron and Heme Metabolism 282
    Aplastic Anemia 286
    Pure Red Blood Cell Aplasia 287
    Congenital Dyserythropoietic Anemias 288
    Megaloblastic Anemias 288
    ANEMIAS RELATED TO OTHER (PRIMARY) DISORDERS 291
    Hemolytic Anemias 293
    WHITE BLOOD CELL DISORDERS 309
    Neutrophil Disorders 309
    The Leukemias 310
    The Myeloproliferative Disorders 317
    The Myelodysplastic Syndromes (MDS) 320
    Infectious Mononucleosis 321
    Malignant Lymphomas 322
    Plasma Cell Disorders 325
    Storage Diseases 328
    Histiocytosis X 328
    PLATELET DISORDERS 329
    Quantitative Disorders 329
    Qualitative Platelet Disorders 332
    VASCULAR DISORDERS 334
    COAGULATION DISORDERS 335
    Coagulation Factor Deficiencies 335
    Circulating Anticoagulants and Inhibitors 340
    Liver Disease 341
    Disseminated Intravascular Coagulation 342
    Fibrinolysis 343
    Hypercoagulable States 343
  7. • Automation
    CELL COUNTERS 345
    Sysmex™ E-5000 345
    Sysmex™ NE-8000 34g
    Sysmex™ Total Hematology System (HS) 355
    Coulter Counter Analyzers 355
    Technicon H™ Systems 3gg
    Cell-Dyn 3000/3000 SL 375
    BLOOD SMEAR PREPARATION AND STAINING 379
    Miniprep® Automatic Blood Smearing Instrument 379
    Hemaspinner Automatic Blood Cell Spinner 381
    Hemastainer Automatic Slide Stainer 381
    Hema-Tek 1000 Slide Stainer 383
    Hema-Tek 2000 Slide Stainer 384
    RETICULOCYTE TESTING 386
    Sysmex R-1000 386
    ERYTHROCYTE SEDIMENTATION TESTING 390
    Automated ESR System 3g0
    COULTER Zetafuge™ 3gi
    COAGULATION TESTING 393
    Fibrosystem® (Fibrometer®) 393
    Coag-A-Mate XC 396
    Coag-A-Mate XM 398
    Coag-A-Mate 2001 401
    Coag-A-Mate Dual Channel Analyzer 401
    Coag-A-Mate X2 404
    MDA-180 406
    MLA Electra® 750 408
    MLA Electra® 800 408
    MLA Electra® 900/900C 411
    MLA Electra® 1000C 413
    KoaguLab 40-A Automated Coagulation System 414
    KoaguLab 16-S Coagulation System 416
    Ortho KoaguLab 60 S 417
    ACL 3000 419
    PLATELET AGGREGOMETRY AND CHROMOGENIC TESTING 422
    Bio/Data Platelet Aggregation Profiler Model PAP-4 422
    Bio/Data Platelet Aggregation Profiler PAP-4C 424
    Bibliography 427
    Index 435

📜 SIMILAR VOLUMES


General Principles and Procedures
✍ Christopher Miller, Efraim Racker (auth.), R. D. O’Brien (eds.) 📂 Library 📅 1979 🏛 Springer US 🌐 English

<p>The following remarks are intended to serve as an introduction to this particular volume as well as to the whole series of volumes of which this is the first. The intent of the series is to provide an authentic and relatively complete statement about the status of our understanding of the recepto