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Dacie and Lewis Practical Haematology E-Book

Dacie and Lewis Practical Haematology E-Book

S. Mitchell Lewis | Barbara J. Bain | Imelda Bates

(2006)

Additional Information

Book Details

Abstract

Often referred to as "the bible of hematology," this highly successful, practical manual is the place to turn to for every aspect of laboratory hematology. The book covers all of the techniques used in the investigation of patients with blood disorders, including the latest technologies as well as the tried-and-true manual methods of measurement. It comprehensively discusses which test to use for each situation, the principles of each test, possible causes of error, and the interpretation and clinical significance of the findings. Each chapter conforms to a template, providing quick, easy access to key information. Extensive updates throughout bring you expert guidance on advancing technologies as well as contemporary laboratory organization and management, while retaining the strengths that have made this book an essential reference on laboratory hematology for over 50 years!

  • Contains crucial instructions for performing and interpreting lab tests in any sized laboratory.
  • Provides complete coverage of all levels of diagnostic testing from the basic to the most advanced.
  • Uses helpful decision trees to make the critical information you need easy to locate and understand.
  • Features state-of-the-art information on the hottest areas of the field, including Diagnostic Radionuclides in Hematology and Molecular and Cytogenetic Techniques.
  • Demonstrates important lab findings with over 300 illustrations and color photographs.

Table of Contents

Section Title Page Action Price
Front Cover Cover
Dacie and Lewis Practical Haematology iii
Copyright iv
Contents v
Preface vii
Contributors ix
Chapter 1: Collection and handling of blood xiii
Biohazard precautions xiii
Standardized procedure xiii
Venous blood 2
Phlebotomy Tray 2
Disposable Plastic Syringes and Disposable Needles 2
Specimen Containers 2
Phlebotomy Procedure 3
Post-phlebotomy Procedure 3
Waste Disposal 3
Capillary blood 4
Collection of Capillary Blood 4
Blood Film Preparation 4
Differences between capillary and venous blood 5
Sample homogeneity 5
Serum 5
Defibrinating Whole Blood 5
Cold Agglutinins 6
Anticoagulants 6
Ethylenediaminetetra-acetic Acid (EDTA) 6
Trisodium Citrate 7
Heparin 7
Effects of storage on the blood count 7
Effects of storage on blood cell morphology 7
References 9
Chapter 2: Reference ranges and normal values 11
Reference ranges 11
Statistical procedures 12
Confidence Limits 12
Normal reference values 13
Physiological variations in the blood count 15
Red Cell Components 15
Pregnancy 15
The Elderly 18
Exercise 18
Posture 18
Diurnal and Seasonal Variation 18
Altitude 18
Smoking 19
Leucocyte Count 19
Platelet Count 20
Other Blood Constituents 20
Effects of Smoking 20
References 20
Chapter 3: Basic haematological techniques 23
Haemoglobinometry 24
Measurement of haemoglobin concentration using a spectrometer (spectrophotometer) or photoelectric colorimeter 24
Haemiglobincyanide (cyanmethaemoglobin) method 25
Diluent 25
Haemiglobincyanide Reference Standard 25
Method 26
Calculation of Haemoglobin Concentration 26
Preparation of Standard Graph and Standard Table 26
Oxyhaemoglobin method 27
Method 27
Standard 27
Direct spectrometry 27
Direct reading portable haemoglobinometers 28
Colour Comparators 28
Portable Haemoglobinometers 28
Non-invasive Screening Tests 28
Range of Haemoglobin Concentration in Health 28
Packed cell volume or haematocrit 28
Microhaematocrit Method 29
Accuracy of Microhaematocrit 29
Anticoagulant 29
Blood Sample 29
Capillary Tubes 29
Centrifuge 29
Reading 29
Plasma Trapping 29
International Council for Standardization in Haematology Reference Method 30
Surrogate Reference Method 30
Equipment 30
Method 30
Range of Packed Cell Volume in Health 30
Manual cell counts and red cell indices 30
Range of MCHC in Health 30
Manual differential leucocyte count 30
Method 31
Basophil and eosinophil counts 32
Range of Eosinophil Count in Health 32
Range of Basophil Count in Health 32
Reporting the Differential Leucocyte Count 32
Correcting the Count for Nucleated Red Blood Cells 32
Reference Differential White Cell Count 32
Range of Differential White Cells in Health 33
Platelet count 33
Range of Platelet Count in Health 33
Reticulocyte count 33
Reticulocyte Stains and Count 33
Staining Solution 33
Method 33
Counting Reticulocytes 35
Calculation 35
Differentiating between Reticulocytes and Other Red Cell Inclusions 35
Fluorescence Methods for Performing a Reticulocyte Count 36
Manual Reference Method 36
Range of Reticulocyte Count in Health 36
Automated blood count techniques 36
Haemoglobin concentration 37
Red blood cell count 37
Counting systems 37
Impedance Counting 37
Light Scattering 38
Reliability of electronic counters 38
Setting Discrimination Thresholds 39
Packed cell volume and mean cell volume 39
Red cell indices 41
Mean Cell Volume 41
Mean Cell Haemoglobin and Mean Cell Haemoglobin Concentration 41
Variations in red cell volumes: red cell distribution width 41
Percentage hypochromic red cells and variation in red cell haemoglobinization: haemoglobin distribution width 42
Total white blood cell count 42
Automated differential count 43
The automated immature granulocyte count 44
The automated nucleated red blood cell count 44
Automated digital imaging analysis of blood cells 44
New White Cell Parameters 45
Automated instrument graphics 45
Platelet count 47
Platelet Count in Health 47
Mean Platelet Volume 47
Reticulated Platelets and Immature Platelet Fraction 48
Reticulocyte count 48
Immature Reticulocyte Fraction 48
Reticulocyte Counts in Health 49
Measurement of Reticulocyte Haemoglobin 49
Point-of-care instruments 49
Calibration of automated blood cell counters 49
Flagging of automated blood counts 50
Microscopy 51
Microscope Components 51
Setting Up the Microscope Illumination 52
Examination of Slides 52
Routine Maintenance of the Microscope 52
References 53
Chapter 4: Preparation and staining methods for blood and bone marrow films 57
Preparation of blood films on slides 57
Manual Method 57
Automated Methods 58
Labelling Blood Films 58
Fixing Blood Films 58
Bone Marrow Films 59
Staining blood and bone marrow films 59
Preparation of Solutions of Romanowsky Dyes 59
May-Grünwald Stain 59
Jenner's Stain 59
Giemsa's Stain 59
Azure B-Eosin Y Stock Solution 60
Chapter 5: Blood cell morphology in health and disease 69
Examination of blood films 70
Red cell morphology 70
Abnormal erythropoiesis 71
Anisocytosis (αiotaσzeta, unequal) and Poikilocytosis (πiotaκiotaλzeta, varied) 71
Macrocytes 73
Microcytes 73
Basophilic Stippling 74
Inadequate haemoglobin formation 74
Hypochromia (Hypochromasia) (πρ, under) 74
Anisochromasia (αiotaσzeta, unequal) and Dimorphic Red Cell Population 76
Damage to red cells after formation 76
Hyperchromasia (Hyperchromia) (περ, over) 76
Spherocytosis (σφαiotaρα, a sphere) 76
Irregularly Contracted Red Cells 77
Elliptocytosis and Ovalocytosis 79
Spiculated cells and red cell fragmentation 80
Schistocytosis (Fragmentation) (σχiotaστzeta, cleft) 80
Keratocytes (κεραzeta, horn) 81
Acanthocytosis (ακαnuθα, spine) 81
Echinocytosis (εχiotanuzeta, sea-urchin or hedgehog) 82
Miscellaneous erythrocyte abnormalities 82
Leptocytosis (λεπτzeta, thin) 82
Target Cells 83
Stomatocytosis (στμα, mouth) 83
Sickle Cells 84
Haemoglobin C Crystals and SC Poikilocytes 85
Erythrocyte Inclusions 85
Howell-Jolly Bodies 85
Pappenheimer Bodies 85
Rouleaux and Autoagglutination 86
Changes associated with a compensatory increase in erythropoiesis 86
Polychromasia (πλθzeta, many) 86
Erythroblastaemia 87
Effects of splenectomy and hyposplenism 88
Scanning electron microscopy 88
Morphology of leucocytes 88
Polymorphonuclear neutrophils 89
Granules 90
Vacuoles 92
Bacteria 92
Döhle Bodies 92
Nuclei 93
Hypersegmentation 93
Pelger-Huët Cells 93
Pyknotic Neutrophils (Apoptosis) 94
Eosinophils 94
Basophils 94
Monocytes 95
Lymphocytes 95
Platelet morphology 97
References 99
Chapter 6: Supplementary techniques including blood parasite diagnosis 101
Tests for the acute-phase response 101
Erythrocyte Sedimentation Rate 102
Conventional Westergren Method 102
Method 102
Range in health 102
Modified methods 103
Length of tube 103
Plastic glass tubes 103
Disposable glass tubes 103
Capillary method 103
Time 103
Sloping tube 103
Anticoagulant 103
Evaluation of a new routine method 103
Quality Control 104
Semiquantitative Slide Method 104
Mechanism of Erythrocyte Sedimentation 104
Plasma Viscosity 105
Reference Values 105
Whole Blood Viscosity 105
Heterophile antibodies in serum: diagnosis of infectious mononucleosis 105
Screening Tests for Infectious Mononucleosis 106
Clinical Value 106
Demonstration of Lupus Erythematosus Cells 106
Erythropoietin 107
Reference Range 107
Significance 107
Autonomous in vitro Erythropoiesis 107
Thrombopoietin 107
Haematological tests in sports medicine 108
Reticulocytes 108
Haemoglobin and Hct 108
Whole Blood Viscosity and ESR 108
Erythropoietin 108
Principles of parasite detection 108
Examination of blood films for parasites 109
General Principles 109
Staining Thin Films 109
Microscopic diagnosis of malaria 109
Fluorescence Microscopy 110
Quantitative Buffy Coat Method 110
Rapid diagnostic tests for malaria 110
Leishmaniasis 116
Diagnosis of Leishmaniasis in the Haematology Laboratory 116
Trypanosomiasis 116
African Trypanosomiasis 116
American Trypanosomiasis 116
Diagnosis of Trypanosomiasis in the Haematology Laboratory 116
Wet Preparations 117
Thick Blood Films or Chancre Aspirates 117
Concentration Techniques 117
Quantitative buffy coat method 117
Capillary tube method 117
Filariasis and loiasis 118
Diagnosis of Filariasis in the Haematology Laboratory 118
Wet Preparation 118
Concentration Techniques 118
Filtration method 118
Quantitative buffy coat and microhaematocrit methods 118
Lysed capillary blood 118
Babesiosis 118
Ehrlichiosis 118
References 119
Chapter 7: Bone marrow biopsy 123
Aspiration of the bone marrow 124
Consent and Safety 124
Performing a Bone Marrow Aspiration 124
Puncture of the Ilium 125
Puncture of the Sternum 125
Comparison of Different Sites for Marrow Puncture 125
Aspiration of the bone marrow in children 125
Marrow puncture needles 126
Processing of aspirated bone marrow 126
Preparing Films from Bone Marrow Aspirates 126
Concentration of Bone Marrow by Centrifugation 128
Preparation of Films of Post-mortem Bone Marrow 128
Examination of aspirated bone marrow 128
Principles of Marrow Aspirate Examination 128
Quantitative Cell Counts on Aspirated Bone Marrow 129
Differential Cell Counts on Aspirated Bone Marrow 129
Sources of Error and Physiological Variations 129
Cellular Ratios 130
Reporting bone marrow aspirate films 130
Systematic Scheme for Examining Bone Marrow Aspirate Films 130
Low Power (x10) 130
Higher Power (x40, x100 Oil-Immersion) 130
Reporting Results 131
Preparation of sections of aspirated bone marrow fragments 131
Percutaneous trephine biopsy of the bone marrow 131
Principles Behind Marrow Trephine Biopsy Examination 133
Imprints from Bone Marrow Trephine Biopsy Specimens 133
Processing of Bone Marrow Trephine Biopsy Specimens 133
Staining of Sections of Bone Marrow Trephine Biopsy Specimens 135
References 137
Chapter 8: Molecular and cytogenetic analysis 139
Introduction to the analysis of DNA 139
Extraction of DNA 140
DNA Extraction Kits 140
Polymerase chain reaction 140
Principle 140
Reagents 141
Method 142
Modifications and Developments 143
Problems and Interpretation 143
Analysis of polymerase chain reaction products 143
Presence or Absence of a Polymerase Chain Reaction Product 143
Amplification Refractory Mutation System 143
Principle 143
Interpretation 143
Gap-PCR 144
Size of the PCR Product 144
Chapter 9: Iron deficiency anaemia and iron overload 175
Iron metabolism 176
Dietary Iron Absorption 176
Dietary and Luminal Factors 177
Iron Absorption at the Molecular Level 177
Regulation of Iron Absorption 177
Cellular Iron Uptake and Release 177
Iron Storage 178
Regulation of Iron Metabolism 178
Plasma Iron Transport 178
Iron status 179
Disorders of iron metabolism 179
Methods for assessing iron status 179
Serum Ferritin Assay 179
Immunoassay for Ferritin 180
Preparation and Storage of Ferritin 180
Antibodies to Human Ferritin 180
Reagents and Materials 180
Conjugation of Antiferritin IgG Preparation to Horseradish Peroxidase36 180
Buffer A 182
Buffer B 182
Buffer C 182
Buffer D 183
Substrate Solution 183
Sulphuric Acid 183
Preparation and Storage of a Standard Ferritin Solution 183
Coating of Plates 183
Preparation of Test Sera 183
Assay Procedure 183
Calculation of Results 183
Selecting an Assay Method 183
Interpretation 184
Estimation of serum iron concentration 185
Reagents and Materials 185
Preparation of Glassware 185
Protein Precipitant 185
Chromogen Solution (Ferrozine) 185
Iron-free Water 185
Iron Standard 80μmol/l 185
Method 185
Calculation 185
Alternative procedure: serum iron without protein precipitation 186
Reagents and Materials 186
Iron Standards 80 μmol/l and 40 μmol/l 186
Phosphate-Ascorbate Buffer (Stock) 186
Chromogen Solution 186
Microtitre Trays 186
Control Serum 186
Method 186
Calculations 186
Automated Methods for Serum Iron 187
Serum iron concentrations in health and disease 187
Iron-binding capacity, serum transferrin and transferrin saturation 187
Estimation of Total Iron-Binding Capacity 187
Principle 187
Reagents 187
Method 187
Determination of unsaturated iron-binding capacity 188
Reagents and Materials 188
Saturating Solution 188
Tris Buffer (Stock) 188
Tris-Ascorbate-Iron Buffer 188
Chromogen Solution 188
Microtitre Trays 188
Control Serum 188
Method 188
Calculations 188
Fully Automated Methods 189
Serum transferrin 189
Normal Ranges of Transferrin and Total Iron-Binding Capacity 189
Transferrin saturation 189
Transferrin Index 189
Serum transferrin receptor 190
Assays for the Serum Transferrin Receptor 190
Reference Ranges 191
Samples 191
Transferrin Receptor Concentrations in Diagnosis 191
Erythropoiesis 191
Iron Deficiency 191
Iron Overload 191
Erythrocyte protoporphyrin 192
Analysers 192
Diagnostic Applications 193
Units 193
Hepcidin 193
Methodological and biological variability of assays 193
Predictive value of blood tests for iron deficiency 194
Iron Deficiency Anaemia in Adults 194
Detection of Iron Deficiency in Acute or Chronic Disease 194
Functional Iron Deficiency 195
Iron Deficiency in Infancy and Childhood 196
Pregnancy 196
Conclusion 196
References 196
Chapter 10: Investigation of megaloblastic anaemia 201
Cobalamin absorption and metabolism 202
Folate absorption and metabolism 202
Rationale for Investigation of Cobalamin or Folate Status 204
Haematological features of megaloblastic anaemia 204
Differential Diagnosis of Macrocytic Anaemia 205
Testing strategy for suspected cobalamin or folate deficiency 205
Limitations of Cobalamin Assays 210
Sensitivity and Specificity of Cobalamin and Holotranscobalamin Assays 210
Utility of receiver operator characteristic curves 210
Utility of holotranscobalamin, methylmalonic acid and homocysteine assays 211
Clinical and Diagnostic Pitfalls of Folate Assays 213
Standards, Accuracy and Precision of Cobalamin and Folate Assays 213
Genetic Factors 214
Pre-analytical Sample Preparation 214
Analytical Factors 215
Limitations and Interference 215
Post-analytical Factors 216
Methods for cobalamin and folate analysis 216
General Principles of Competitive protein binding assays 216
Serum B12 assays 216
Release from Endogenous Binders and Conversion of Analyte to Appropriate Form 216
Binding of B12 to Kit Binder 216
Separation of Bound and Unbound B12 216
Signal Generation 217
Electrochemiluminescence Immunoassay 217
Enzyme-linked Fluorescence Generation 217
Holotranscobalamin assays 217
Principle 217
Holotranscobalamin `Active B12´ Immunoassay 217
HoloTC Radioimmunoassay 217
Quantitation of Transcobalamin Saturation 218
Serum folate methods 218
Release from Endogenous Binders 218
Binding of Folate to Folate-Binding Protein 218
Separation of Bound and Unbound Folate 218
Signal Generation 218
Red cell folate methods 218
Haemolysate Preparation 219
Calculation of Red Blood Cell Folate from Haemolysate Folate Result 219
Serum B12 and Folate and Red Cell Folate Assay Calibration 219
Whole Blood Folate Standards 220
Primary Instrument Calibration 220
Internal Adjustment Calibration 220
Internal Quality Control 220
Methylmalonic acid measurement 220
Chapter 11: Laboratory methods used in the investigation of the haemolytic anaemias 229
Investigation of haemolytic anaemia 230
Is There Evidence of Increased Haemolysis? 230
What is the Type of Haemolytic Mechanism? 231
What is the Precise Diagnosis? 231
Plasma haemoglobin 231
Sample Collection 231
Peroxidase Method3 232
Reagents 232
Benzidine compound 232
Hydrogen peroxide 232
Acetic acid 232
Standard 232
Method 232
Spectrophotometric Method 232
Normal Range 232
Significance of increased plasma haemoglobin 232
Serum haptoglobin 233
Electrophoresis Method 233
Principle 233
Reagents 233
Buffer (pH 7.0, ionic strength 0.05) 233
Haemolysates 233
Stain 233
Clearing solution 233
Acetic acid rinse 233
Method 233
Interpretation 233
Radial Immunodiffusion (RID) Method 234
Principle 234
Reagents 234
Single diffusion plates 234
Reference sera 234
Test serum 234
Method 234
Normal Ranges 234
Significance 235
Serum haemopexin 235
Examination of plasma (or serum) for methaemalbumin 235
Schumm´s Test 236
Chapter 12: Investigation of the hereditary haemolytic anaemias 245
Investigation of membrane defects 246
Osmotic fragility as measured by lysis in hypotonic saline 246
Principle 246
Reagents 246
Method 246
Notes 246
Osmotic Fragility after Incubating the Blood at 37C for 24 Hours 247
Method 247
Factors Affecting Osmotic Fragility Tests 248
Recording the Results of Osmotic Fragility Tests 248
Alternative methods of recording osmotic fragility 249
Interpretation of Results 249
Flow cytometric (dye-binding) test 250
Principle 250
Reagents 250
EMA 250
Bovine serum albumin (30%) solution (BSA) 251
PBS 251
Chapter 13: Acquired haemolytic anaemias 273
Assessing the likelihood of acquired haemolytic anaemia 273
Assessment of the blood film and count in suspected acquired haemolytic anaemia 273
Immune haemolytic anaemias 274
Types of Autoantibody 275
Warm Autoantibodies 276
Cold Autoantibodies 277
Combined Warm and Cold Autoantibodies 277
Methods of Investigation 277
Collection of Samples of Blood and Serum 277
Storage of Samples 278
Scheme for Serological Investigation of Haemolytic Anaemia Suspected to be of Immunological Origin 278
Detection of Incomplete Antibodies by Means of the Direct Antiglobulin (Coombs) Test 279
Principle 279
Precautions 280
Method 280
DAT Using Column Agglutination Technology 280
Significance of Positive Direct Antiglobulin Test 280
Positive DATs in Normal Subjects 281
Positive DATs in Hospital Patients 281
False-Negative Antiglobulin Test Results 281
DAT-Negative Autoimmune Haemolytic Anaemia 281
Preparing and Testing a Concentrated Eluate 282
Manual Direct Polybrene Test 282
Reagents 282
Method 282
Positive control 282
Negative control 282
Determination of the Blood Group of a Patient with AIHA 283
ABO Grouping 283
RhD Grouping 283
Demonstration of Free Antibodies in Serum 283
Identification by Adsorption Techniques of Coexisting Alloantibodies in the Presence of Warm Autoantibodies 283
Use of ZZAP Reagent in Autoadsorption Techniques 283
Reagents 283
Method 283
Notes 283
Alloadsorption Using Papainized R1R1, R2R2 and rr Cells 284
Method for Testing Alloadsorbed Sera 284
Example of alloantibody detection using the alloadsorption technique in a recently transfused patient with AIHA 284
Explanation of the results of testing alloadsorbed sera, A, B and C 284
Additional notes on adsorption techniques 284
Elution of Antibodies from Red Cells 284
Notes 286
Heat Elution 286
Freeze and Thaw Elution (Lui) 286
Screening Eluates 286
Determination of the Specificity of Warm Autoantibodies in Eluates and Sera 286
Titration of Warm Antibodies in Eluates or Sera 286
Determination of the Specificity of Cold Autoantibodies 286
Titration of Cold Antibodies 286
Normal range 287
Cold Agglutinin Titration Patterns 287
Determination of the Thermal Range of Cold Agglutinins 287
Detection and Titration of the Donath-Landsteiner Antibody 287
Direct Donath-Landsteiner Test 287
Indirect Donath-Landsteiner Test 287
Two-Stage Indirect Donath-Landsteiner Test 288
Titration of a Donath-Landsteiner Antibody 288
Detection of a Donath-Landsteiner Antibody by the Indirect Antiglobulin Test 288
Method 288
Thermal range of Donath-Landsteiner antibody 288
Specificity of the Donath-Landsteiner antibody 288
Treatment of Serum with 2-Mercaptoethanol or Dithiothreitol 289
Method 289
2-Mercaptoethanol 289
Dithiothreitol 289
Drug-Induced Haemolytic Anaemias of Immunological Origin 289
Drug-Induced Autoimmune Haemolytic Anaemias 289
Detection of Antipenicillin Antibodies 290
Reagents 290
Penicillin-Coated Normal Red Cells 290
Control normal red cells 290
Method 290
Note 290
Detection of Antibodies against Drugs Other than Penicillin 290
Interpretation 291
Oxidant-induced haemolytic anaemia 291
Microangiopathic and mechanical haemolytic anaemias 291
Paroxysmal nocturnal haemoglobinuria 291
Acidified-Serum Lysis Test (Ham test) 293
Principle 293
Chapter 14: Investigation of abnormal haemoglobins and thalassaemia 301
The haemoglobin molecule 302
Structural variants of haemoglobin 302
Haemoglobins with Reduced Solubility 303
Hb S 303
Sickle Cell Disease 303
Other Forms of Sickle Cell Disease 303
Hb C 303
Other Sickling Haemoglobins 303
Unstable Haemoglobins 304
Haemoglobins with Altered Oxygen Affinity 304
Hb M 304
Thalassaemia syndromes 304
β Thalassaemia Syndromes 305
α Thalassaemia Syndromes 306
Thalassaemic Structural Variants 306
Increased Hb F in Adult Life 307
Inherited Abnormalities That Increase Hb F Concentration 307
Investigation of patients with a suspected haemoglobinopathy 307
Laboratory detection of haemoglobin variants 308
Blood Count and Film 308
Collection of Blood and Preparation of Haemolysates 309
Preparation of Haemolysate for Qualitative Haemoglobin Electrophoresis 309
Preparation of Haemolysate for the Quantification of Haemoglobins and Stability Tests 309
Control Samples 310
Quality Assurance 310
Cellulose Acetate Electrophoresis at Alkaline pH 310
Principle 310
Equipment 310
Reagents 311
Method 311
Interpretation and Comments 311
Citrate Agar Electrophoresis at pH 6.0 312
Equipment 312
Reagents 313
Buffer 313
Method 313
Interpretation and Comments 313
Agarose Gel Electrophoresis 313
Reagents and Method 313
Interpretation 314
Automated High-Performance Liquid Chromatography 314
Principle 314
Chapter 15: Erythrocyte and leucocyte cytochemistry 333
Erythrocyte cytochemistry 333
Siderocytes and Sideroblasts 333
Method of Staining Siderotic Granules 334
Significance of siderocytes 335
Haemoglobin Derivatives 336
Heinz Bodies in Red Cells 336
Demonstration of Heinz Bodies 336
Unstained preparations 336
Stained preparations 337
Demonstration of Haemoglobin H Inclusions 337
Method 337
Carboxyhaemoglobin and Methaemoglobin 338
Fetal Haemoglobin 338
Reagents 338
Method 338
Haemoglobin S and Other Haemoglobin Variants 339
Leucocyte cytochemistry 339
Myeloperoxidase 339
Method with 3,3-Diaminobenzidine 340
Reagents 340
Method 340
Technical considerations 340
Results and interpretation 340
Pathological variations 341
Sudan Black B 341
Chapter 16: Immunophenotyping 353
Introduction 353
Methods for the study of immunological markers 354
Preparation of the Specimens and Cell Separation 354
Ficoll-Gradient Method of Separation 354
Red Blood Cell Lysing Methods 354
Multicolour Flow Cytometry Methods 354
Detection of membrane antigens 354
Rationale for choosing antibody panels 356
Detection of Surface Immunoglobulin 356
Method 1: Wash-Stain-Lyse-Wash 356
Method 2: Lyse-Stain-Wash 357
Detection of Intracellular Antigens 357
Chapter 17: Diagnostic radioisotopes in haematology 373
Sources of radioisotopes 374
Radiation protection 374
Apparatus for Measuring Radioactivity in Vitro 375
Apparatus for Measuring Radioactivity in Vivo 376
Surface Counting 376
Imaging 376
Measurement of Radioactivity with a Scintillation Counter 376
Standardization of Working Conditions 376
Counting Technique 377
Measurement of radioactivity 377
Correction for Physical Decay 377
Double Radioisotope Measurements 377
Differential decay 377
Physical separation 377
Blood volume 377
Measurement of Blood Volume 377
Principle 377
Red Cell Volume 378
Radioactive Chromium Method 378
Technetium Method 378
Chapter 18: Investigation of haemostasis 393
Components of normal haemostasis 394
The Blood Vessel 394
General Structure of the Blood Vessel 394
Endothelial Cell Function 394
Vasoconstriction 395
Platelets 395
Platelet Function in the Haemostatic Process 395
Platelet Aggregation 396
Blood Coagulation 396
The Contact Activation System 397
Tissue Factor 397
The Vitamin K-Dependent Factors 398
Cofactors 398
Fibrinogen 399
Factor XIII 399
Inhibitors of Coagulation 399
The Fibrinolytic System 399
General approach to investigation of haemostasis 400
Clinical Approach 400
Principles of Laboratory Analysis 400
Immunological 400
Assays using chromogenic peptide substrates (amidolytic assays) 401
Coagulation assays 401
Other Assays 401
Notes on equipment 401
Waterbaths 401
Refrigerators and Freezers 402
Centrifuges 402
Reagents and Buffers 402
Plastic and Glass Tubes 402
Pipettes 402
Stopwatches and Stopclocks 402
Automated Coagulation Analysers 402
Evaluating and choosing an automated analyser 402
Mandatory requirements 402
Desirable additional requirements 402
Safety 403
Pre-analytical variables including sample collection 403
Collection of Venous Blood 403
Blood Sample Anticoagulation 403
Time of Sample Collection 404
Transportation to the Laboratory 404
Centrifugation: Preparation of Platelet-Poor Plasma 404
Storage of Plasma and Sample Thawing 404
Some Common `Technical´ Errors 404
Calibration and Quality Control 405
Reference Standard (Calibrator) 405
Calibration of Standard Pools and Suggested Calibration Procedure 405
Control Plasma 405
Variability of Coagulation Assays 405
Performance of Coagulation Tests 405
Handling of Samples and Reagents 405
Eliminating a Time Trend 406
Assay Monitoring and Endpoint Detection 406
Manual Methods 406
Electromechanical 406
Impedance, steel ball 406
Photo-Optical Analysis 406
Scattered light detection for clotting assays (660nm) 406
Transmitted light detection for chromogenic assays (405nm, 575nm, 800nm) 406
Transmitted light detection for immunoassays (405nm, 575nm, 800nm) 406
Nephelometry 406
Photo-optical endpoint determination and analyses 406
Percentage Detection Method 406
Rate Method 407
VLin Integral Method 407
Analysis Time Over 407
Turbidity Level Over 408
Clot Signatures: Normal and Abnormal APTT Clot Waveforms 408
Molecular Mechanism of the Biphasic Waveform: LC-CRP 408
Commonly Used Reagents 409
CaCl2 409
Barbitone buffer 409
Barbitone buffered saline, pH 7.4 409
Glyoxaline buffer 409
Owren's veronal buffer 409
Factor-Deficient Plasmas 409
The `clotting screen´ 409
Prothrombin Time 409
Principle 409
Reagents 409
Patient and control plasma samples 409
Thromboplastin 409
CaCl2 410
Method 410
Expression of Results 410
Normal Values 410
Interpretation 410
Activated Partial Thromboplastin Time 410
Principle 410
Reagents 410
Chapter 19: Investigation of a thrombotic tendency 447
Introduction to thrombophilia 447
Tests for the presence of a lupus anticoagulant 448
Sample Preparation 448
Dilute Russell's Viper Venom Time 449
Principle 449
Reagents 449
Reagent Preparation 449
Method 449
Interpretation 449
Platelet Neutralization Test 450
Principle 450
Reagents for preparation of platelet neutralization reagent 450
Method 450
Interpretation 450
Interpretation of Tests for Lupus Anticoagulant 450
Kaolin Clotting Time 451
Chapter 20: Laboratory control of anticoagulant, thrombolytic and antiplatelet therapy 467
Oral anticoagulant treatment using vitamin K antagonists 467
Selection of Patients 468
Methods Used for the Laboratory Control of Oral Anticoagulant Treatment 468
Standardization of Oral Anticoagulant Treatment 468
Calibration of Thromboplastins 468
Principle 468
Reagents 468
Method 468
Calibration 469
Calculation of International Sensitivity Index 469
Local Calibration of Thromboplastins 470
Geometric Mean Normal Prothrombin Time 470
Calibration Audits 470
Determination of the International Normalized Ratio 470
Capillary Reagent 470
Therapeutic Range and Choice of Thromboplastin 470
Management of Overanticoagulation 470
Point-of-Care Testing 471
Heparin treatment 472
Selection of Patients 472
Laboratory Control of Heparin Treatment 472
Activated Partial Thromboplastin Time for Heparin Monitoring 473
Principle 473
Reagents and Method 473
Therapeutic Range 473
Near-Patient Heparin Monitoring 474
Chapter 21: Blood cell antigens and antibodies 483
Erythrocytes 483
Red Cell Antigens 483
ABO System 485
ABO Antigens and Encoding Genes 486
Secretors and Non-Secretors 487
ABO Antigens and Disease 488
ABO Antibodies 488
Anti-A and anti-B 488
Anti-A1 and anti-H 488
Lewis System 488
Lewis Antigens and Encoding Genes 488
Lewis Antibodies 489
The P System and Globoside Collection 489
Antigens 489
Antibodies 489
Rh System 489
Rh Antigens and Encoding Genes 489
Antibodies 490
Kell and Kx Systems 491
Antigens and Encoding Genes 491
Kell Antibodies 491
Duffy System 491
Duffy antigens and encoding genes 491
Duffy antibodies 491
Kidd (JK) System 491
Kidd antigens and encoding genes 491
Kidd antibodies 491
MNSs System 491
MNSs antigens and encoding genes 491
MNSs antibodies 492
Other Blood Group Systems 492
Lutheran system 492
Yt (Cartwright) system 492
Colton system 492
Dombrock system 492
Clinical Significance of Red Cell Alloantibodies 492
Mechanisms of Immune Destruction of Red Cells 494
Antigen-Antibody Reactions 495
Quality Assurance within the Laboratory 495
General Points of Serological Technique 496
Serum versus Plasma 496
Collection and Storage of Blood Samples 497
Storage of Sera or Plasma 497
Red Cell Suspensions 497
Normal ionic strength saline 497
Low ionic strength saline 497
Reagent Red Cells 497
Use of Enzyme-Treated Cells 498
Agglutination of Red Cells by Antibody: A Basic Method 498
Tube Tests 498
Tubes 498
Temperature and Time of Exposure of Red Cells to Antibody 498
Slide Tests 498
Reading Results of Tube Tests 498
Microscopic reading 498
Macroscopic reading 498
Demonstration of Lysis 499
Controls 500
Antiglobulin Test 500
Antiglobulin Reagents 500
Polyspecific (broad-spectrum) reagents 500
Monospecific reagents 500
Quality Control of Antiglobulin Reagents 500
Recommended Antiglobulin Test Procedure 501
Alternative Technology for Antibody Detection by the Antiglobulin Test 502
Assessment of Individual Worker Performance 502
Titration of Antibodies 503
Preparation of serial dilutions of patient's or other sera 503
Addition of red cell suspensions to dilutions of serum 503
Test for ABH Substance Secretion 504
Method 504
Red Cell Genotyping 504
Platelet and Neutrophils 504
Platelet and Neutrophil Alloantigen Systems 504
Clinical Significance of Platelet and Neutrophil Antibodies 504
Alloantibodies 504
Isoantibodies 506
Autoantibodies 506
Drug-Induced Antibodies 507
Demonstration of Platelet and Neutrophil Antibodies 507
Alloantibodies 507
Autoantibodies 508
Drug-Induced Antibodies 508
Methods of Demonstrating Antibodies 508
The Immunofluorescent Antiglobulin Methods 509
Patient's and Screening Panel Cells 509
Patient's Serum 509
Control Sera 509
Eluate from Patient's Sensitized Cells 509
Heat Eluate 509
Platelet Preparation 509
Granulocyte Preparation 509
Platelet and Granulocyte Immunofluorescence Tests 510
Indirect Test 510
Scoring Results 511
Use of Flow Cytometry 511
Chloroquine Treatment of Platelets and Granulocytes 511
Interpretation of Results with Chloroquine-Treated Cells 512
MAIPA Assay 512
Other Methods 513
Molecular Genotyping of Platelet Alloantigens 513
References 514
Chapter 34: Laboratory aspects of blood transfusion 519
Technology and automation in blood transfusion laboratories 520
Pre-transfusion compatibility systems 522
Documentation of the Transfusion Process 523
Identification and Storage of Blood Samples 523
ABO and D grouping 524
ABO Grouping 524
Reagents for ABO Grouping 524
D Grouping 524
Reagents for D Grouping 524
Methods 524
Tube and slide tests 525
EDTA for diluents 525
Slide method 525
Liquid-phase microplate methods 525
Column agglutination techniques 525
Solid-phase techniques 526
Controls 526
Causes of Discrepancies in ABO/D Grouping 526
False-Positive Reactions 526
Rouleaux 526
Cold autoagglutination and cold reacting alloantibodies 526
T-activation/polyagglutination 526
Acquired B 527
Potentiators 527
In vitro bacterial contamination 527
False-Negative Reactions 527
Failure to add reagents 527
Loss of potency 527
Failure to identify lysis 527
Mixed-field appearance 527
D variant phenotypes 527
Antibody screening 528
Red Cell Reagents 528
Methods 528
Indirect Antiglobulin Techniques 529
Column Agglutination 529
Solid-Phase Systems 529
Liquid-Phase Techniques - Tubes and Microplates 529
Controls 529
Antibody identification 530
Principles 530
Phenotyping 530
Additional Panels/Techniques 531
Reagents 531
Antibody Cards 531
Selection and transfusion of red cells 531
Crossmatching 532
Choice of Test 532
Indirect Antiglobulin Crossmatch 532
Immediate Spin Crossmatch 533
False-negative results (in immediate spin crossmatch) 533
False-positive results (in immediate spin crossmatch) 533
Electronic Issue 533
Emergency blood issue 534
Rapid ABO and D Typing 534
Confirmation 534
Selection of Units 534
Compatibility Testing 534
Antibody Screening 534
Massive Transfusion 534
Selection of Platelets and Plasma 535
Potential Errors 535
Antenatal serology and haemolytic disease of the newborn 535
Haemolytic Disease of the Fetus and Newborn 535
Antenatal Serology 535
ABO and D Grouping and Antibody Screening 535
Follow-Up Antibody Screening 535
Prediction of Fetal Blood Group 536
Partner Testing 536
Testing Fetal DNA in the Maternal Circulation 536
Fetal Blood Sampling 536
Antenatal Assessment of the Severity of Haemolytic Disease of the Fetus and Newborn 536
Antibody Titrations during Pregnancy 536
Antibody Quantitation 536
Assessment of Fetal Anaemia 536
Tests on Maternal and Cord Blood at Delivery 537
Prevention of Haemolytic Disease of the Fetus and Newborn as a Result of Anti-D 538
Anti-D Prophylaxis 538
Measurement of Fetomaternal Haemorrhage 539
Recommended Action at Delivery (or Potentially Sensitizing Event) 539
ABO Haemolytic Disease of the Newborn 540
Serological Investigation 540
Compatibility testing in special transfusion situations 540
Neonates and Infants within First 4 Months of Life 540
Investigations on the Maternal Sample 540
Investigations on the Infant Sample 540
Selection of Blood and Other Components 540
Intrauterine (Fetal) Transfusion 541
Patients Receiving Transfusions at Close Intervals 541
Chronic Transfusion Programmes 541
Allogeneic Haemopoietic Stem Cell Transplantation 542
Investigation of a transfusion reaction 542
Acute Transfusion Reactions 543
Acute Intravascular Haemolysis 543
Documentation check 544
Serological investigations 544
Tests for haemolysis 544
Microbiological tests 544
Delayed Haemolytic Transfusion Reaction 544
Haematological Investigation 544
Serological Investigation 544
References 545
Chapter 23: Approach to the diagnosis and classification of blood diseases 549
Common presentations of haematological diseases 549
Initial screening tests 549
Interpretation of Screening Tests 550
Quantitative Abnormalities of Blood Cells 550
Increased Numbers of Cells 550
Increases affecting more than one cell line 550
Erythrocytosis 550
Leucocytosis 550
Neutrophilia 550
Lymphocytosis 550
Monocytosis 550
Eosinophilia 551
Basophilia 551
Thrombocytosis 551
Reduced Numbers of Cells 551
Reductions in more than one cell line 551
Anaemia 551
Microcytic Anaemia 551
Macrocytic Anaemia 553
Normocytic Anaemia 554
Leucopenia 554
Neutropenia 554
Reduced numbers of lymphocytes, monocytes, eosinophils and basophils 554
Thrombocytopenia 554
Pancytopenia 554
Qualitative Abnormalities of Blood Cells 554
Abnormalities of All Cell Lines 554
Abnormalities of Individual Cell Lines 555
Red cells 555
White cells 555
Platelets 555
Specific tests for common haematological disorders 555
Red Cell Disorders 555
Microcytic Hypochromic Anaemias 555
Macrocytic Anaemias 556
Aplastic Anaemia11 556
Haemolytic Anaemias 556
White Cell Disorders 556
Acute Leukaemia 556
Neutropenia 556
Chronic Myelogenous Leukaemia 556
Chronic Lymphoproliferative Disorders/Lymphadenopathy 556
Myelomatosis (Plasma Cell Myeloma) 557
Other Disorders 557
Myeloproliferative Neoplasms 557
Myelodysplastic syndromes 557
Pancytopenia with Splenomegaly 557
Classification of haematological neoplasms 557
Classification of Acute Myeloid Leukaemia 558
Classification of the Myelodysplastic Syndromes 558
Classification of Acute Lymphoblastic Leukaemia 559
Classification of Myeloproliferative Neoplasms and Related Conditions 559
References 562
Chapter 24: Laboratory organization and management 563
Management structure and function 564
Staff Appraisal 564
Continuing Professional Development 565
Strategic and Business Planning 565
Workload Assessment and Costing of Tests 565
Financial Control 566
Calculation of Test Costs 566
Test reliability 567
Test selection 567
Likelihood Ratio 568
Receiver-Operator Characteristic Analysis 568
Test Utility 568
Instrumentation 569
Equipment Evaluation 569
Principles of Evaluation 569
Precision 569
Linearity 569
Carryover 570
Accuracy and Comparability 570
Maintenance logs 570
Data processing 570
Laboratory Computers 571
Pre-analytical and post-analytical stages of testing 572
Test Requesting 572
Specimen Collection and Delivery 572
Pre-Analytical Phase 572
Post-Analytical Phase 572
Test Turnaround Time 574
Point-of-Care Testing 574
Point-of-Care Testing Beyond the Laboratory 575
Patient Self-Testing 575
Laboratory Services for General Practitioners 575
Pre-Analytical Service 575
Post-Analytical Service 575
Standard Operating Procedures 575
Laboratory audit and accreditation 576
Audit 576
Accreditation 577
International standards of practice 578
Benchmarking 579
Laboratory Safety 579
Principles of Safety Policy 579
Design of Laboratory 580
Electrical and Radiation Safety 580
Fire Hazard 581
Chemical Safety 581
Eyewash Facilities 581
Biohazardous Specimens 581
Universal Precautions 581
Disinfectants 582
Sodium hypochlorite (chlorine) 582
Alcohols 582
Applications of Disinfectants 583
Automated equipment 583
Centrifuges 583
Syringes and needles 583
Gloves 583
Laundry 583
Waste Disposal 583
Specimen Shipping 584
References 585
Chapter 25: Quality assurance 587
Standardization 587
Control materials and reference standards 588
Reference Standards 589
Assigning Values to Reference Materials 590
Quality assurance procedures 590
Internal Quality Control 592
Control Charts 592
Duplicate Tests on Patients' Specimens 593
Correlation Check 593
External Quality Assessment 594
Standardization of EQA Schemes 595
Assessment of Participant Performance 596
Quantitative Tests 596
Deviation index 596
Consecutive monitoring 597
Out of consensus method 597
Target values and bias 597
Youden (xy) plot 597
Methodology check 598
Clinical significance 598
Semi-Quantitative Tests 598
Interpretive Tests 598
Internal audit for total quality management 598
Internal Audit of Examination Processes 599
Continuous Quality Improvement 599
Control of Non-Compliance 599
Preparation of extended-life material for use in quality assessment 599
Preparation of Preserved Whole Blood 599
Method4,15 599
Preparation of Haemolysate 599
Method 599
Preparation of Stabilized Whole Blood Control Material 600
Chapter 26: Haematology in under-resourced laboratories 603
Introduction: types of laboratories 603
Organization of clinical laboratory services 604
Level A: Sub-District Facilities Including Health Centres 604
Level B: District Hospitals 604
Level C: Central and Teaching Hospitals 605
Availability of tests at each level 605
Level A 605
Level B 605
Level C 605
Microscopes 606
Care of the Microscope 606
`Essential´ haematology tests 606
Cost per Test 606
Diagnostic Reliability 606
Clinical Usefulness 607
Maintaining quality and reliability of tests 607
Quality Control of a Test Method (Technical Quality) 607
Internal Quality Control 607
External Quality Assessment 607
Basic haematology tests 607
Haemoglobinometry 607
Direct Reading Haemoglobinometers 608
HemoCue Blood Hemoglobin System**Available from HemoCue AB, Angelholm, Sweden; www.hemocue.com (Accessed 25 January 2010). 608
Haemoglobin Colour ScaleAvailable from Teaching Aids at Low Cost; www.talcuk.org/accessories/haemoglobin-colour-scale.htm (Acce 608
Packed Cell Volume 609
Manual Cell Counts Using Counting Chambers 609
Counting Chambers 609
Total White Blood Cell Count 610
Diluent 610
Appendix 619
Preparation of commonly used reagents 619
Water 619
Anticoagulants and Preservative Solutions 619
Acid-Citrate-Dextrose (ACD) Solution - NIH-A 619
Acid-Citrate-Dextrose (Alsever's) Solution 619
Citrate-Phosphate-Dextrose (CPD) Solution, pH 6.9 620
Citrate-Phosphate-Dextrose (CPD) Solution, pH 5.6-5.8 620
Citrate-Phosphate-Dextrose-Adenine (CPD-A) Solution, pH 5.6-5.8 620
Low Ionic Strength Solution (LISS)1 620
EDTA 620
Neutral EDTA, pH 7.0, 110mmol/l 620
Neutral Buffered EDTA, pH 7.0 620
Saline (Normal Ionic Strength) 621
Trisodium Citrate (Na3C6H5O7.2H2O), 109mmol/l 621
Heparin 621
Buffers 621
Barbitone Buffer, pH 7.4 621
Barbitone Buffered Saline, pH 7.4 621
Barbitone Buffered Saline, pH 9.5 621
Barbitone-Bovine Serum Albumin Buffer, pH 9.8 621
Citrate-Saline Buffer 621
Glycine Buffer, pH 3.0 621
HEPES Buffer, pH 6.6 621
HEPES-Saline Buffer, pH 7.6 622
Imidazole Buffered Saline, pH 7.4 622
Phosphate Buffer, Iso-Osmotic 622
Phosphate Buffered Saline 622
Phosphate Buffer, Sörensen's 622
Tris-HCl Buffer (200mmol/l) 623
Tris-HCl Bovine Serum Albumin (BSA) Buffer, pH 7.6, 20mmol/l 623
Buffered Formal Acetone 623
Preparation of glassware 623
Siliconized Glassware 623
Cleaning Slides 623
New Slides 623
Dirty Slides 623
Cleaning Glassware 623
Iron-free Glassware 623
Sizes of tubes 623
Speed of centrifuging 624
Statistical procedures 624
Calculations 625
Variance (s2) 625
Standard deviation (SD) 625
Coefficient of variation (CV) as percentage 625
Standard error mean (SEM) 625
Standard deviation of paired results 625
Standard deviation of median 625
Confidence interval 625
Analysis of Differences by t-Test 625
Index 633