Clinical Biochemistry

Höfundur Michael Murphy; Rajeev Srivastava; Kevin Deans

Útgefandi Elsevier Limited (UK)

Snið ePub

Print ISBN 9780702072987

Útgáfa 6

Útgáfuár 2019

4.990 kr.

Description

Efnisyfirlit

  • Cover image
  • Title Page
  • Table of Contents
  • Copyright
  • Preface
  • Acknowledgements
  • Part 1 Introducing clinical biochemistry
  • 1 The clinical biochemistry laboratory
  • The use of biochemical tests
  • Core biochemistry
  • Specialised tests
  • Urgent samples
  • Automation and computerisation
  • Test repertoire
  • Laboratory personnel
  • 2 The use of the laboratory
  • Specimen collection
  • Sampling errors
  • Analysing the specimen
  • Timing
  • Unnecessary testing
  • 3 Interpretation of results
  • How biochemical results are expressed
  • 4 Interpretation of results
  • Diagnostic test outcomes
  • The impact of prevalence on test utility
  • Final thoughts
  • 5 Interpretation of results
  • Sources of variation
  • Pre-analytical variation
  • Analytical variation
  • Biological variation
  • Other biological variation
  • 6 Analytical aspects
  • Precision and accuracy
  • Analytical sensitivity and specificity
  • Quality assurance
  • Part 2 Core biochemistry
  • 7 Fluid and electrolytes
  • Body fluid compartments
  • Evaluation of hydration
  • Osmolality
  • Oncotic pressure
  • 8 Water and sodium balance
  • Water
  • AVP and the regulation of osmolality
  • Sodium
  • Regulation of volume
  • 9 Hyponatraemia
  • Mechanisms of hyponatraemia
  • Water retention
  • Sodium loss
  • Pseudohyponatraemia
  • 10 Hyponatraemia
  • Clinical assessment
  • Severity
  • Mechanism
  • Treatment
  • 11 Hypernatraemia
  • Water loss
  • Sodium gain
  • Clinical features
  • Treatment
  • Other osmolality disorders
  • 12 Hyperkalaemia
  • Serum potassium and potassium balance
  • Hyperkalaemia
  • Treatment
  • Pseudohyperkalaemia
  • 13 Hypokalaemia
  • Diagnosis
  • Redistribution into cells
  • Treatment
  • 14 Intravenous fluid therapy
  • Does this patient need IV fluids?
  • Which IV fluids should be given?
  • How much fluid should be given?
  • How quickly should the fluids be given?
  • How should the fluid therapy be monitored?
  • 15 Investigation of renal function (1)
  • Functions of the kidney
  • Glomerular function
  • 16 Investigation of renal function (2)
  • Renal tubular function
  • Investigation of tubular function
  • Specific tubular defects
  • 17 Urinalysis
  • Procedure
  • 18 Proteinuria
  • Ways of measuring proteinuria
  • 19 Acute kidney injury
  • Aetiology
  • Detection of AKI
  • Identifying the cause of AKI
  • Recovery
  • 20 Chronic kidney disease
  • Consequences of CKD
  • Clinical features
  • Detection
  • Classification
  • Management
  • 21 Acid–base
  • Hydrogen ion concentration [H+]
  • H+ production
  • Buffering
  • Renal handling of H+ and HCO3−
  • Assessing status
  • Acid–base disorders
  • 22 Metabolic acid–base disorders
  • Metabolic acidosis
  • Metabolic alkalosis
  • 23 Respiratory and mixed acid–base disorders
  • Respiratory acidosis
  • Respiratory alkalosis
  • Mixed acid–base disorders
  • 24 Acid–base disorders
  • Specimens for blood gas analysis
  • Clinical cases
  • Management of acid–base disorders
  • 25 Proteins and enzymes
  • Enzymes
  • Plasma proteins
  • 26 Immunoglobulins
  • Structure
  • Electrophoresis of serum proteins
  • Increased immunoglobulins
  • Deficiencies or absence of immunoglobulins
  • 27 Myocardial infarction
  • Pathology
  • Cardiac biomarkers
  • Diagnosis
  • Definitions
  • 28 Liver function tests
  • Introduction
  • Liver function tests
  • 29 Jaundice
  • Biochemical tests
  • Differential diagnosis
  • 30 Liver disease
  • Acute liver disease
  • Investigation
  • Outcome
  • Chronic liver disease
  • Aetiology
  • Clinical features
  • Unusual causes of cirrhosis
  • Other liver problems
  • 31 Glucose metabolism and diabetes mellitus
  • Insulin
  • Diabetes mellitus
  • 32 Diagnosis and monitoring of diabetes mellitus
  • Diagnosis of diabetes mellitus
  • Monitoring of diabetes
  • 33 Diabetic ketoacidosis
  • How diabetic ketoacidosis develops
  • Treatment
  • Laboratory investigations
  • Hyperosmolar hyperglycaemic state (HHS)
  • Diagnosis
  • Treatment
  • 34 Hypoglycaemia
  • Clinical effects
  • Assessment
  • Specific causes of hypoglycaemia
  • Diabetic patients
  • Neonatal hypoglycaemia
  • 35 Calcium regulation and hypocalcaemia
  • Calcium homeostasis
  • Serum calcium
  • Hypocalcaemia
  • Treatment
  • 36 Hypercalcaemia
  • Clinical features
  • Diagnosis
  • Treatment
  • Familial benign hypercalcaemia
  • 37 Phosphate and magnesium
  • Phosphate
  • Inorganic phosphate
  • Hyperphosphataemia
  • Hypophosphataemia
  • Magnesium
  • Magnesium homeostasis
  • Serum magnesium
  • Magnesium deficiency
  • 38 Metabolic bone disease
  • Bone metabolism
  • Common bone disorders
  • Other bone diseases
  • Biochemistry testing in calcium disorders or bone disease
  • 39 Osteoporosis and fragility fractures
  • Risk factors
  • Diagnosis
  • Principles of treatment
  • Part 3 Endocrinology
  • 40 Endocrine control
  • Biochemical regulators
  • Hormone structure
  • Assessment of endocrine control
  • Types of endocrine control
  • Pitfalls in interpretation
  • Dynamic function tests
  • 41 Dynamic function tests
  • Insulin stress test
  • TRH test
  • GnRH test
  • Oral glucose tolerance test with GH measurement
  • Synacthen tests
  • Dexamethasone suppression tests
  • Dynamic function tests – protocol variation
  • 42 Pituitary function
  • The pituitary gland
  • Pituitary tumours
  • Hypopituitarism
  • 43 Growth disorders and acromegaly
  • Normal growth
  • Growth hormone insufficiency
  • Excessive growth
  • Acromegaly
  • 44 Thyroid pathophysiology
  • Goitre
  • Thyroid hormone action
  • Thyroid function tests
  • 45 Hypothyroidism
  • Clinical features
  • Causes
  • Diagnosis
  • Treatment
  • Screening for neonatal hypothyroidism
  • Non-thyroidal illness
  • 46 Hyperthyroidism
  • Clinical features
  • Causes
  • Diagnosis
  • Treatment
  • 47 Adrenocortical pathophysiology
  • Cortisol
  • Adrenal androgens
  • Assessing the function of the HPA axis
  • Aldosterone
  • Congenital adrenal hyperplasia
  • Relationship of adrenal cortex and medulla
  • 48 Hypofunction of the adrenal cortex
  • Adrenal insufficiency
  • Clinical features
  • 49 Hyperfunction of the adrenal cortex
  • Cortisol excess
  • Confirming the diagnosis
  • Androgen excess
  • Aldosterone excess
  • 50 Gonadal function
  • Sex steroid hormones
  • Hypothalamic–pituitary–gonadal axis
  • Male gonadal function
  • Female gonadal function
  • 51 Subfertility
  • Endocrine investigations in the subfertile woman
  • Endocrine investigations in the subfertile man
  • Part 4 Specialised investigations
  • 52 Nutritional assessment
  • History
  • Examination
  • Biochemistry
  • Preoperative nutritional assessment
  • 53 Nutritional support
  • What do patients need?
  • How should they receive nutrition?
  • Monitoring patients
  • 54 Parenteral nutrition
  • Indications for parenteral nutrition
  • Route of administration
  • Components of TPN
  • Complications
  • Monitoring patients on TPN
  • 55 The metabolic response to injury
  • The phases of the metabolic response to injury
  • The acute phase protein response
  • Clinical uses
  • Starvation and the metabolic response to injury
  • 56 Gastrointestinal disorders
  • Physiology of digestion and absorption
  • Malabsorption
  • Gastrointestinal disorders
  • Inflammatory bowel disease
  • Malignant disease
  • 57 Iron
  • Iron physiology
  • Laboratory investigation of iron disorders
  • Iron deficiency
  • Iron overload
  • 58 Zinc and copper
  • Zinc
  • Zinc physiology
  • Copper
  • 59 Therapeutic drug monitoring
  • Sampling for TDM
  • Interpretation of drug levels
  • Drug interactions
  • Pharmacokinetics
  • 60 Toxicology
  • Confirming poisoning
  • Measurement of drug levels
  • Treatment
  • Common causes of poisoning
  • Chronic poisoning
  • 61 Metal poisoning
  • Metals associated with poisoning
  • Treatment
  • Common sources
  • 62 Alcohol
  • Metabolism of ethanol
  • Acute alcohol poisoning
  • Chronic alcohol abuse
  • 63 Ascites
  • Peritonitis
  • Malignant ascites
  • 64 Pleural fluid
  • Transudate or exudate?
  • Is it empyema?
  • Is it malignant?
  • Is it chyle?
  • Is it tuberculosis?
  • 65 Cerebrospinal fluid
  • 66 Identification of body fluids
  • Cerebrospinal fluid
  • Lymph and chyle
  • Urine
  • Other
  • 67 Lipoprotein metabolism
  • Nomenclature
  • Metabolism
  • Apolipoproteins
  • The LDL receptor
  • 68 Clinical disorders of lipid metabolism
  • Classification
  • Atherogenic profiles
  • 69 Hypertension
  • Causes of hypertension
  • Treatment of hypertension
  • 70 Cancer and its consequences
  • Local effects of tumours
  • Cancer cachexia
  • Paraneoplastic syndromes and ectopic hormone production
  • Consequences of cancer treatment
  • 71 Tumour markers
  • The use of tumour markers
  • A practical application of tumour markers
  • Tumour markers with established clinical value
  • The future
  • 72 Multiple endocrine neoplasia
  • MEN 1
  • MEN 2
  • Screening and treatment
  • The APUD concept
  • 73 Hyperuricaemia
  • Urate formation and excretion
  • Lesch–Nyhan syndrome
  • Gout
  • Renal disease and hyperuricaemia
  • Urate in pregnancy
  • 74 Myopathy
  • Muscle weakness
  • Rhabdomyolysis
  • Duchenne muscular dystrophy
  • 75 Fetal monitoring and prenatal diagnosis
  • HCG
  • Fetoplacental function
  • Prenatal diagnosis
  • 76 Pregnancy
  • Maternal physiology
  • Weight gain
  • Pregnancy-associated pathology
  • 77 Antenatal screening
  • Overview of screening programmes
  • Screening for Down syndrome
  • First-trimester screening
  • Nuchal translucency
  • Biochemical tests
  • Risk calculation
  • Diagnostic tests
  • Second-trimester screening
  • Diagnostic tests
  • Other factors affecting interpretation of biochemical markers
  • 78 Screening the newborn for disease
  • Neonatal screening programmes
  • Follow-up of screening tests
  • 79 Paediatric biochemistry
  • Immaturity
  • Prematurity
  • Practical considerations
  • 80 Inborn errors of metabolism
  • Patterns of inheritance
  • Mechanisms of disease
  • Clinical diagnosis
  • Laboratory diagnosis
  • 81 Selected inherited disorders
  • Part 5 Case history comments
  • 82 Case history comments
  • Case history 1
  • Case history 2
  • Case history 3
  • Case history 4
  • Case history 5
  • Case history 6
  • Case history 7
  • Case history 8
  • Case history 9
  • Case history 10
  • Case history 11
  • Case history 12
  • Case history 13
  • Case history 14
  • Case history 15
  • Case history 16
  • Case history 17
  • Case history 18
  • Case history 19
  • Case history 20
  • Case history 21
  • Case history 22
  • Case history 23
  • Case history 24
  • Case history 25
  • Case history 26
  • Case history 27
  • Case history 28
  • Case history 29
  • Case history 30
  • Case history 31
  • Case history 32
  • Case history 33
  • Case history 34
  • Case history 35
  • Case history 36
  • Case history 37
  • Case history 38
  • Case history 39
  • Case history 40
  • Case history 41
  • Case history 42
  • Case history 43
  • Case history 44
  • Case history 45
  • Case history 46
  • Case history 47
  • Case history 48
  • Case history 49
  • Case history 50
  • Case history 51
  • Case history 52
  • Case history 53
  • Case history 54
  • Case history 55
  • Case history 56
  • Case history 57
  • Case history 58
  • Case history 59
  • Case history 60
  • Index
  • IBC

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