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Essentials of Kumar and Clark's Clinical Medicine E-Book

Essentials of Kumar and Clark's Clinical Medicine E-Book

Nicola Zammitt | Alastair O'Brien

(2017)

Additional Information

Book Details

Abstract

‘Baby Kumar & Clark’, best-selling portable revision reference, is now in its sixth edition.

Features

  • Normal values
  • Medical emergencies
  • Useful websites
  • Abbreviations
  • Dictionary of terms

 

  • New author team: Nicola Zammitt and Alastair O’Brien
  • Now comes with a free e-book on StudentConsult
  • Fully updated and revised in line with the new edition of Kumar & Clark’s Clinical Medicine

Table of Contents

Section Title Page Action Price
Front Cover Cover
Inside Front Cover ES2
Essentials of Kumar & Clark’s Clinical Medicine iii
Copyright iv
Contents v
Preface vii
Contributors ix
Medical emergencies xi
Abbreviations xv
Significant websites xxix
General websites xxix
Medical dictionaries xxix
Guidelines and evidence-based medicine xxix
Medical calculators xxx
Healthcare journals and magazines xxx
Medical societies and organizations xxx
Others xxx
Chapter-specific websites xxx
1. Ethics and communication xxx
2. Infectious diseases xxxi
3. Gastroenterology and nutrition xxxi
Chapter 1: Ethics and communication 1
Legally valid consent 1
Capacity 2
Information disclosure 2
Obtaining consent 3
Special circumstances 3
Adults who lack capacity to consent 3
Advance decisions 3
Children 4
Teaching 4
Human immunodeficiency virus testing 4
End-of-life decisions including assisted dying 4
Cardiopulmonary resuscitation 5
Confidentiality 5
Communication 5
The medical interview 6
1. Building a relationship 6
2. Opening the discussion 6
3. Gathering information 6
4. Understanding the patient 6
5. Sharing information 7
6. Reaching agreement on management 7
7. Providing closing 7
Breaking bad news 7
Communication in difficult circumstances 8
When things go wrong 8
Complaints 9
Culture and communication 9
Patients with impaired faculties for communication 9
Medical record keeping 9
Team communication 10
Chapter 2: Infectious diseases 11
Common investigations in infectious disease 11
Pyrexia of unknown origin 12
Investigations 13
Management 14
Septicaemia 14
Aetiology 15
Clinical features 15
Investigations 15
Management 15
Common viral infections 16
Measlesnd 16
Clinical features 16
Complications 16
Chapter 3: Gastroenterology and nutrition 67
Gastroenterology 67
Symptoms of gastrointestinal disease 67
Dyspepsia and indigestion 67
Dysphagia 67
Vomiting 67
Flatulence 68
Diarrhoea and constipation 68
Steatorrhoea 68
Abdominal pain 69
Investigation of gastrointestinal disease 69
Endoscopy 70
Oesophagogastroduodenoscopy (OGD, `gastroscopy) 70
Sigmoidoscopy 70
Colonoscopy 70
Endoscopic retrograde cannulation of biliary and pancreatic duct (ERCP) 71
Endoscopic ultrasound (EUS) 71
Endoanal and endorectal ultrasonography 71
Balloon enteroscopy, 71
Capsule endoscopy 71
Imaging 71
Plain X-rays 71
Ultrasound 71
Transabdominal ultrasound 71
Computed tomography (CT) scan 71
Magnetic resonance imaging (MRI) 72
Positron emission tomography (PET) 73
Contrast studies 73
Oesophageal physiology testing 73
The mouth 73
Mouth ulcers 73
Non-infective 73
Infective 74
Oral white patches 74
The tongue 74
Periodontal disorders 74
Salivary gland disorders 75
The oesophagus 75
Symptoms of oesophageal disorders 75
Gastro-oesophageal reflux disease (GORD) 76
Pathophysiology 76
Clinical features 76
Investigations 76
OGD 76
24-Hour intraluminal pH monitoring or impedance 76
Management 76
Complications 78
Peptic stricture 78
Barrett's oesophagus 78
Achalasia 79
Clinical features 79
Investigations 79
Management 79
Complications 79
Systemic sclerosis 80
Other oesophageal dysmotility disorders 80
Hiatus hernia 80
Benign oesophageal strictures 80
Oesophageal perforation 80
Iatrogenic perforation 80
Traumatic or spontaneous oesophageal rupture 81
Malignant oesophageal tumours 81
Pathology 81
Epidemiology and aetiological factors 81
Squamous carcinoma 81
Adenocarcinoma 81
Clinical features 81
Investigations 81
Management 82
Prognosis 82
Benign oesophageal tumours 82
The stomach and duodenum 82
Helicobacter pylori infection 82
Chapter 4: Liver, biliary tract and pancreatic disease 139
Liver biochemistry and liver function tests 139
Approach to interpretation of abnormal liver biochemistry 141
Other investigations in liver and biliary disease 141
Hepatic stiffness (transient elastography) 141
Endoscopic ultrasound (EUS) 143
Computed tomography (CT) examination 143
Magnetic resonance imaging (MRI) 143
Magnetic resonance cholangiopancreatography (MRCP) 143
Upper gastrointestinal (GI) endoscopy 143
ERCP 143
Percutaneous transhepatic cholangiography (PTC) 143
Liver biopsy 143
Markers of liver fibrosis 144
Symptoms and signs of liver disease 145
Jaundice 145
Haemolytic jaundice 145
Congenital hyperbilirubinaemia 147
Cholestatic jaundice 147
Investigations 148
Hepatitis 149
Acute hepatitis 149
Chronic hepatitis 150
Viral hepatitis 150
Hepatitis A 150
Epidemiology 150
Clinical features 151
Investigations 151
Differential diagnosis 153
Management 153
Prophylaxis 153
Hepatitis B 153
Epidemiology 153
Viral structure 153
Acute HBV infection 154
Chronic HBV infection 155
Treatment of chronic infection: whom to treat 156
Antiviral agents 157
Hepatitis B and HIV co-infection 157
Prophylaxis 157
Hepatitis D (delta or δ agent) 158
Hepatitis C 158
Hepatitis C virus 159
Chronic hepatitis C infection 159
Hepatitis End 160
Acute hepatic failure 160
Alcohol use 161
Screening for problem drinking 162
Consequences of alcohol use and dependence 162
Physical complications 162
Alcohol withdrawal 163
Autoimmune hepatitis 164
Aetiology 164
Clinical features 164
Investigations 164
Treatment 165
Prognosis 165
Non-alcoholic fatty liver disease 165
Cirrhosis 165
Chapter 5: Haematological disease 197
Anaemia 197
Clinical features 198
Classification of anaemia (Table 5.2) 198
Microcytic anaemia 199
Iron deficiency 199
Causes of iron deficiency 200
Clinical features 201
Investigations 201
Differential diagnosis 201
Management 201
Sideroblastic anaemia 202
Anaemia of chronic disease 202
Macrocytic anaemia 202
Megaloblastic anaemia 202
Vitamin B12 deficiency 203
Pernicious anaemia 203
Epidemiology 204
Clinical features 204
Investigation of B12 deficiency 204
Differential diagnosis 204
Chapter 6: Malignant disease 253
Diagnosis of malignancy 253
Investigations 254
Cancer treatment 255
Chemotherapy 255
Radiotherapy 255
Endocrine therapy 256
Biological therapy 256
Myeloablative therapy and haemopoietic stem cell transplantation 257
Oncological emergencies 257
Neutropenic sepsis 257
Superior vena cava syndrome 257
Acute tumour lysis syndrome 257
The leukaemias 258
General classification 258
Aetiology 258
Acute leukaemia 259
Epidemiology 259
Clinical features 259
Investigations 259
Management 260
Supportive care 260
Treatment 260
Acute myeloid leukaemia 260
Low risk of treatment failure (based on the cytogenetic pattern) 261
Intermediate risk 261
High risk of treatment failure 261
Acute promyelocytic leukaemia 261
Prognosis 261
Acute lymphoblastic leukaemia 261
Chronic myeloid leukaemia 262
Chapter 7: Rheumatology 273
The normal joint 273
Musculoskeletal symptoms 273
Common investigations in musculoskeketal disease 275
Blood tests 275
Simple blood tests 275
Autoantibodies 275
Imaging 275
Plain X-rays 275
Bone scintigraphy (isotope bone scan) 276
Ultrasound 276
Magnetic resonance imaging (MRI) 277
DXA 277
Arthroscopy 277
Synovial fluid analysis 277
Investigation of suspected muscle disease 277
Common regional musculoskeletal problems 277
Pain in the neck and shoulder 277
Elbow pain 278
Hip problems 278
The knee 278
Back pain 278
Lumbar back pain 278
Investigations 279
Management 280
Intervertebral disc disease 280
Acute disc disease 280
Clinical features 280
Investigations 281
Management 281
Chronic disc disease 281
Mechanical problems 282
Spondylolisthesis 282
Spinal stenosis 282
Neck pain 282
Osteoarthritis 282
Epidemiology 283
Pathology and pathogenesis 283
Clinical features 283
Differential diagnosis 284
Investigations 285
Management 285
Inflammatory arthritis 286
Rheumatoid arthritis 286
Epidemiology 286
Aetiology and pathogenesis 286
Pathology 286
Clinical features 287
Non-articular manifestations 288
Investigations 289
Differential diagnosis 289
Management 290
NSAIDs and coxibs 290
Corticosteroids 290
Disease-modifying antirheumatic drugs 290
Biological DMARDs 291
Prognosis 292
The seronegative spondyloarthritis 292
Axial spondylarthritis 292
Clinical features 293
Investigations 294
Management 295
Psoriatic arthritis 295
Clinical features 295
Investigations 295
Treatment 295
Reactive arthritis 296
Clinical features 296
Investigations 296
Management 296
Enteropathic arthritis 297
Crystal arthritis 297
Gout and hyperuricaemia 297
Epidemiology 297
Pathogenesis 297
Clinical features 297
Investigations 298
Management 299
Pseudogout (pyrophosphate arthropathy) 299
Investigations 300
Chapter 8: Water, electrolytes and acid-base balance 327
Water and electrolyte requirements 327
Body fluid compartments 327
Osmotic pressure 327
Distribution of extracellular fluid 328
Intravenous fluids in clinical practice 330
Regulation of body fluid homeostasis 331
Regulation of extracellular volume 332
Abnormalities of extracellular volume 332
Increased extracellular volume 332
Clinical features 332
Chapter 9: Renal disease 355
Presenting features of renal disease 355
Dysuria 357
Polyuria and nocturia 357
Oliguria 357
Haematuria 358
Pain 358
Investigation of renal disease 358
Blood tests 358
Glomerular filtration rate 358
Calculation of creatinine clearance using the Cockroft–Gault equation: 359
Men 359
Women 359
Urine dipstick testing 359
Proteinuria 359
Haematuria 360
Glycosuria 361
Urine microscopy 361
White cells 362
Red cells 362
Casts 362
Bacteria 363
Imaging techniques 363
Plain X-ray 363
Ultrasonography 363
CT 363
Magnetic resonance imaging (MRI) 363
Excretion urography 363
Renal arteriography (angiography) 363
Anterograde pyelography 364
Retrograde pyelography 364
Renal scintigraphy 364
Transcutaneous renal biopsy 364
Glomerular diseases 364
Normal glomerular structure 364
Pathogenesis and terms in glomerular disease 365
Classification and presentation of glomerulopathies 366
Nephrotic syndrome 367
Aetiology 367
Nephrotic syndrome with 'bland' urine sediments 367
Nephrotic syndrome with 'active' urine sediments (mixed nephrotic/nephritic) 368
Clinical features 368
Differential diagnoses 369
Investigations 369
Management 369
General oedema 369
Specific treatment 369
Complications 370
Acute glomerulonephritis (acute nephritic syndrome) 371
Clinical features 371
Investigations 372
Management 372
Rapidly progressive glomerulonephritis 372
Urinary tract infection 372
Pathogenesis 372
Risk factors for UTI 373
Clinical features 373
Natural history 374
Uncomplicated versus complicated infection 374
Acute pyelonephritis 374
Reflux nephropathy 374
Recurrent UTI 374
Investigations 374
Diagnosis 374
Management 375
Treatment of single isolated attack 375
Recurrent infection 376
UTI in pregnancy 376
Abacteriuric frequency or dysuria ('urethral syndrome') 376
Bacterial prostatitis 376
Tuberculosis of the urinary tract 377
Tubulointerstitial nephritis 377
Acute tubulointerstitial nephritis 377
Chronic tubulointerstitial nephritis 377
Hypertension and the kidney 378
Essential hypertension 378
Renal hypertension 378
Bilateral renal disease 378
Renovascular disease 378
Options for renal artery imaging 380
Management 380
Renal calculi and nephrocalcinosis 380
Aetiology 380
Calcium stones 380
Hypercalciuria 380
Hyperoxaluria 381
Uric acid stones 381
Infection-induced stones 381
Cystine stones 381
Clinical features 381
Differential diagnosis 382
Investigations 382
Management 382
Initial treatment 382
Prevention of recurrence 383
Nephrocalcinosis 384
Urinary tract obstruction 384
Aetiology 384
Clinical features 384
Investigations 385
Management 386
Acute kidney injury 386
Epidemiology 387
Approaching AKI 388
1. Prerenal AKI 388
2. Postrenal AKI 389
3. Renal parenchymal AKI 389
Clinical and biochemical features 390
Investigation of the uraemic emergency 390
Investigations 391
Management 391
Prognosis 392
Chronic kidney disease 393
Aetiology 393
Clinical features and investigations 394
Anaemia 394
Bone disease 394
Neurological complications 395
Cardiovascular disease 396
Other complications 396
Differentiating AKI from CKD 397
Management 397
Renoprotection 397
Reduce cardiovascular risk 397
Correction of complications 397
Hyperkalaemia 397
Calcium and phosphate 397
Anaemia 398
Acidosis 398
Infections 398
Referral to a nephrologist 398
Renal replacement therapy 399
Dialysis 399
Haemodialysis 399
Peritoneal dialysis 399
Haemofiltration 400
Complications of all long-term dialysis 400
Transplantation 401
Cystic renal disease 401
Solitary and multiple renal cysts 401
Autosomal-dominant polycystic kidney disease 401
Clinical features 402
Diagnosis 402
Management 402
Medullary sponge kidney 402
Tumours of the kidney and genitourinary tract 403
Renal cell carcinoma 403
Clinical features 403
Investigations 403
Management 403
Localized disease 403
Metastatic or locally advanced disease 403
Prognosis 404
Urothelial tumours 404
Clinical features 404
Investigations 404
Management 404
Diseases of the prostate gland 404
Benign enlargement of the prostate gland 405
Clinical features 405
Investigations 405
Management 405
Prostatic carcinoma 405
Chapter 10: Cardiovascular disease 409
Common presenting symptoms of heart disease 409
Chest pain 409
Dyspnoea 409
Palpitations 409
Syncope 409
Other symptoms 411
Investigations in cardiac disease 411
The chest X-ray 411
The electrocardiogram 411
ECG waveform and definitions (Fig. 10.5) 412
Heart rate 412
Exercise electrocardiography 418
24-hour ambulatory taped electrocardiography 418
Tilt testing 418
Echocardiography 419
Cardiac nuclear imaging 419
Cardiac computed tomography 421
Cardiovascular magnetic resonance 421
Cardiac catheterization 421
Cardiac arrhythmias 421
General principles of management of arrhythmias 422
Sinus rhythms 422
Sinus arrhythmia 422
Bradycardia 422
Sinus bradycardia 422
Heart block 423
Atrioventricular block 423
First-degree AV block 423
Second-degree AV block 423
Third-degree AV block 423
Bundle branch block 425
Supraventricular tachycardias 425
Sinus tachycardia 425
Atrioventricular junctional tachycardias 425
Atrioventricular nodal re-entry tachycardia 425
Atrioventricular reciprocating tachycardia 428
Symptoms 428
Acute management 428
Long-term management 429
Atrial tachyarrhythmias 429
Atrial fibrillation 430
Management 430
Assessment for anticoagulation 431
Atrial flutter 432
Ventricular tachyarrhythmias 432
Ventricular ectopic premature beats (extrasystoles) 432
Sustained ventricular tachycardia 432
Non-sustained ventricular tachycardia 433
Ventricular fibrillation 433
Long QT syndrome 433
Cardiac arrest 436
Prognosis 436
Heart failure 436
Aetiology 436
Pathophysiology 436
Activation of the sympathetic nervous system 437
Renin–angiotensin system 437
Natriuretic peptides 437
Ventricular dilatation 438
Ventricular remodelling 438
Clinical features 439
Symptoms 439
Signs 439
Investigations 440
Treatment of chronic heart failure 441
Drug treatment 441
Vasodilator therapy 441
β-Blockers 442
Diuretics 443
Digoxin 443
Inotropes 443
Non-pharmacological treatment 443
Revascularization 443
Cardiac resynchronization therapy 443
Implantable cardioverter–defibrillator 443
Cardiac transplantation 443
Prognosis 444
Acute heart failure 444
Clinical features 444
Management 444
Ischaemic heart disease 445
Irreversible risk factors for coronary artery disease 446
Age 446
Gender 446
Family history 446
Potentially changeable risk factors 446
Hyperlipidaemia 446
Cigarette smoking 446
Hypertension 446
Metabolic factors 446
Diets 446
Other risk factors 446
Estimation of cardiovascular risk 447
Angina 447
Clinical features 447
Diagnosis 447
Investigations 448
Management 448
Secondary prevention 448
Symptomatic treatment 448
Percutaneous coronary intervention (PCI) 449
Coronary artery bypass grafting 450
Acute coronary syndromes 450
Clinical features 450
Treatment of NSTEMI and unstable angina 451
Risk stratification 451
ST segment elevation myocardial infarction (STEMI) 453
Clinical features 453
Investigations 453
The ECG 454
Cardiac markers 455
Other investigations 455
Management 455
Limitation of infarct size 455
Immediate primary angioplasty 455
Fibrinolytic agents 455
Subsequent management 457
Complications (Table 10.9) 457
Disturbances of rate, rhythm and conduction (p. 421) 457
Heart failure 458
Embolism 458
Pericarditis 458
Post-ACS drug therapy and assessment 459
Rheumatic fever 459
Epidemiology 459
Clinical features 459
Investigations 460
Blood count 460
Treatment 460
Chronic rheumatic heart disease 460
Valvular heart disease 460
Prosthetic heart valves 460
Mitral stenosis 461
Aetiology 461
Pathophysiology 461
Symptoms 461
Signs 461
Investigations 462
Chest X-ray 462
ECG 462
Echocardiography 462
Management 462
General 462
Specific 462
Mitral regurgitation 462
Aetiology 462
Pathophysiology 463
Symptoms 463
Signs 463
Investigations 463
Chapter 11: Respiratory disease 505
Basic structure of the respiratory system 505
Function of the respiratory system 505
Symptoms of respiratory disease 506
Cough 506
Sputum 506
Haemoptysis 507
Breathlessness 507
Wheezing 507
Chest pain (p. 409) 508
Investigation of respiratory disease 508
Sputum 508
Respiratory function tests 508
Peak expiratory flow rate 508
The spirometer 509
Arterial blood gas sampling 509
Walking distance 509
Imaging 509
Chest X-ray 509
Computed tomography (CT scan) 509
Magnetic resonance imaging (MRI) 511
Positron emission tomography (PET) 511
Scintigraphic imaging 511
Pleural aspiration and biopsy 511
Bronchoscopy 512
Mediastinoscopy 512
Video-assisted thoracoscopic (VATS) lung biopsy 512
Smoking 512
Diseases of the upper respiratory tract 513
The common cold (acute coryza) 513
Sinusitis (see p. 707) 513
Rhinitis 513
Seasonal rhinitis 513
Perennial rhinitis 513
Diagnosis 513
Management 513
Acute pharyngitis 513
Acute laryngotracheobronchitis (croup) 514
Influenza 514
Clinical features 514
Diagnosis 514
Management 514
Complications 515
Prophylaxis 515
Inhalation of foreign bodies 515
Diseases of the lower respiratory tract 515
Acute bronchitis 515
Chronic obstructive pulmonary disease (COPD) 516
Epidemiology and aetiology 516
Pathophysiology 516
Pathogenesis 516
Clinical features 517
Complications 518
Investigations 518
Management 519
Cessation of smoking 520
Bronchodilators 520
Phosphodiesterase type 4 inhibitors 520
Corticosteroids 520
Prevention of infection 520
Oxygen 520
Additional treatments 520
Acute exacerbation of COPD 520
Long term prognosis 521
Obstructive sleep apnoea (OSA) 522
Aetiology 522
Clinical features 522
Diagnosis 522
Management 522
Bronchiectasis 523
Aetiology 523
Clinical features 523
Investigations 523
Management 523
Complications 524
Cystic fibrosis 524
Clinical features 525
Investigations 525
Management 525
Prognosis 526
Asthma 526
Epidemiology 526
Classification 526
Aetiology 527
Pathogenesis 527
Inflammation 527
Remodelling 527
Precipitating factors 528
Clinical features 528
Investigations 528
Management 529
Avoidance of precipitating factors 530
Drug treatment 530
Acute severe asthma 532
Clinical features 532
Pneumonia 532
Clinical features 534
Investigations 535
Differential diagnosis 536
Management 537
Complications 537
Specific forms of pneumonia 537
Mycoplasma pneumoniae 537
Haemophilus influenzae 537
Chlamydia 537
Staphylococcus aureus 539
Legionella pneumophila 539
Pseudomonas aeruginosa 539
Pneumocystis jiroveci 539
Aspiration pneumonia 539
Complications of pneumonia: lung abscess and empyema 539
Clinical features 540
Investigations 540
Management 540
Tuberculosis 540
Epidemiology 540
Pathology 541
Clinical features 541
Investigations 543
Management 543
Prevention and chemoprophylaxis 545
Diffuse diseases of the lung parenchyma 545
Granulomatous lung disease 546
Sarcoidosis 546
Epidemiology 546
Immunopathology 546
Clinical features 547
Investigations 548
Differential diagnosis 548
Management 548
Prognosis 549
Granulomatous lung disease with vasculitis 549
Idiopathic interstitial pneumonias 549
Idiopathic pulmonary fibrosis (IPF) 549
Clinical features 549
Investigations 550
Differential diagnosis 550
Treatment 550
Prognosis 550
Hypersensensitivity pneumonitis 550
Clinical features 551
Investigations 551
Management 552
Other types of diffuse lung disease 552
Occupational lung disease 552
Coal worker's pneumoconiosis 552
Asbestosis 553
Carcinoma of the lung 554
Epidemiology 554
Aetiology 554
Pathology 554
Clinical features 554
Local effects of tumour within a bronchus 554
Spread within the chest 554
Metastatic disease 554
Non-metastatic manifestations 555
Investigations 555
Confirm the diagnosis 555
Determine the histology 556
Assess spread of the tumour 556
Determine patient suitability for major operation 557
Treatment 557
Non-small cell lung cancer 557
Small cell lung cancer 557
Symptomatic treatments 557
Differential diagnosis 557
Metastatic tumours in the lung 557
Diseases of the chest wall and pleura 558
Rib fractures 558
Kyphosis and scoliosis of the spine 558
Pleurisy 558
Pleural effusion 558
Aetiology 558
Investigations 560
Diagnostic pleural fluid aspiration 560
Contrast-enhanced thoracic CT scan 560
Pleural biopsy 561
Chapter 12: Intensive care medicine 571
ICUs 571
High-dependency units 571
Patient selection - withholding and withdrawing treatment 571
Critical care outreach and early warning systems 572
Acute disturbances of haemodynamic function (shock) 572
Pathophysiology 572
The sympathoadrenal response to shock 572
Neuroendocrine response 574
Release of mediators 574
Microcirculatory changes 575
Activation of the coagulation system 575
Progressive organ failure 575
Clinical features 576
Hypovolaemic shock 577
Cardiogenic shock 577
Mechanical shock 577
Anaphylactic shock 577
Sepsis 577
Management 577
Expansion of the circulating volume (preload) 577
Myocardial contractility and inotropic agents 579
Additional treatment 579
Specific treatment of the cause 581
Monitoring 581
Clinical 581
Invasive 581
Respiratory failure 582
Monitoring 582
Clinical 582
Pulse oximetry 582
Forced vital capacity (FVC) 583
Arterial blood gas analysis 583
Capnography 584
Management 584
Respiratory support 584
Acute respiratory distress syndrome (ARDS) 586
Definition and causes 586
Pathophysiology 586
Clinical features 587
Management 587
Prognosis 587
Chapter 13: Clinical pharmacology and toxicology 589
Drug prescribing 589
Concordance with medication 589
Adverse drug reactions 589
Writing a prescription 590
Best practice for drug prescribing 590
Specific drugs 591
Drug poisoning 591
The general approach to the poisoned patient 592
History 592
Investigations 592
Management 592
Emergency resuscitation (ABCDE, p. 742) 592
Prevention of further drug absorption 594
Increasing drug elimination 594
Antagonizing the effects of specific poisons 595
Psychiatric assessment 595
Specific drug problems 595
Aspirin 595
Clinical features 595
Investigations 595
Chapter 14: Endocrine disease 607
Common presenting symptoms in endocrine disease 607
The hypothalamus and pituitary 609
Control and feedback 609
Pituitary space-occupying lesions and tumours 611
Underproduction 611
Overproduction 611
Local effects 612
Investigation 612
Hypopituitarism 613
Aetiology 613
Clinical features 613
Investigation 614
Management 615
Pituitary hypersecretion syndromes 615
Hyperprolactinaemia 615
Aetiology 616
Clinical features 616
Investigations 616
Management 616
Acromegaly and gigantism 617
Clinical features 617
Investigations 617
Management 618
Transsphenoidal surgical resection 618
Medical therapy 618
External radiotherapy 619
Cushing's disease 619
Hypersecretion of other hormones 619
The thyroid axis 619
Assessment of thyroid function tests 620
Hypothyroidism 620
Aetiology 620
Autoimmune thyroiditis 621
Post-partum thyroiditis 621
Iatrogenic 621
Drug induced 621
Iodine deficiency 621
Congenital hypothyroidism 621
Clinical features 621
Investigations 621
Management 621
Borderline or subclinical hypothyroidism (compensated euthyroidism) 622
Myxoedema coma 623
Myxoedema madness 623
Hyperthyroidism 624
Graves' disease 624
Toxic multinodular goitre 624
Solitary toxic nodule/adenoma 624
de Quervain's thyroiditis 624
Post-partum thyroiditis 624
Clinical features 624
Investigations 624
Management 626
Antithyroid drugs 626
Radioactive iodine 626
Surgery 626
Thyroid crisis or `thyroid storm 626
Graves' orbitopathy (ophthalmopathy) 627
Aetiology 627
Clinical features 627
Investigations 627
Management 627
Goitre (thyroid enlargement) 628
Clinical features 628
Investigations 628
Management 629
Thyroid malignancy 630
Male reproduction and sex 630
Male hypogonadism 631
Klinefelters syndrome 631
Congenital deficiency of gonadotrophin-releasing hormone 632
Investigations 632
Management 632
Loss of libido and erectile dysfunction 632
Gynaecomastia 633
Female reproduction and sex 634
The menopause 634
Female hypogonadism and amenorrhoea 635
Aetiology 635
Investigations 636
Management 636
Hirsutism and polycystic ovary syndrome 636
Clinical features 637
Criteria for diagnosis 637
Investigations and differential diagnosis 637
Management 637
Local therapy for hirsutism 637
Systemic therapy for hirsutism 637
Treatment of menstrual disturbance 638
Treatment for infertility 638
The glucocorticoid axis 638
Synthetic steroids 638
Addison's disease: primary hypoadrenalism 638
Aetiology 638
Clinical features 639
Investigations 639
Management 640
Uses and problems of therapeutic steroid therapy 641
Secondary hypoadrenalism 641
Cushings syndrome 642
Clinical features 643
Investigations 643
Confirm raised cortisol 643
Establishing the cause of Cushing's syndrome 644
Management 645
Incidental adrenal tumours 645
Endocrinology of blood pressure control 645
The renin–angiotensin system 646
Aldosterone 646
Primary hyperaldosteronism 646
Clinical features 646
Chapter 15: Diabetes mellitus and other disorders of metabolism 667
Diabetes mellitus 667
Glucose metabolism 667
Classification of diabetes 667
Aetiology and pathogenesis 668
Type 1 diabetes mellitus 668
Type 2 diabetes mellitus 668
Clinical features 669
Investigations 669
Impaired glucose tolerance 670
Management 670
Principles of treatment 671
Diet 671
Tablet treatments for type 2 diabetes 672
Insulin treatment 674
Complications of insulin therapy 675
Hypoglycaemia 675
Whole pancreas and pancreatic islet transplantation 676
Measuring the metabolic control of diabetes 676
Home testing 676
Hospital (clinic) testing 676
Diabetic metabolic emergencies 677
Diabetic ketoacidosis 677
Pathogenesis 677
Clinical features 677
Investigations 678
Management 678
Hyperosmolar hyperglycaemic state 680
Clinical features 680
Management 680
Prognosis 681
Lactic acidosis 681
Complications of diabetes 681
Vascular 681
Macrovascular complications 681
Microvascular complications 681
Diabetic eye disease 682
Retinopathy 682
The diabetic kidney 682
Diabetic nephropathies 683
Ischaemic lesions 684
Infective lesions 684
Diabetic neuropathy 684
Symmetrical mainly sensory neuropathy 685
Acute painful neuropathy 685
Mononeuritis and mononeuritis multiplex (multiple mononeuropathy) 685
Diabetic amyotrophy 686
Autonomic neuropathy 686
The diabetic foot 686
Infections 686
The skin 687
Special situations 687
Surgery 687
Major surgery (i.e. having a general anaesthetic) 687
Minor surgery (e.g. endoscopy) 688
Insulin-treated patients 688
Tablet-controlled diabetes 688
Pregnancy and diabetes 688
Acutely ill hospital inpatients 688
Unstable diabetes 689
Hypoglycaemia in the non-diabetic 689
Insulinomas 689
Clinical features 689
Investigations 689
Treatment 691
Disorders of lipid metabolism 691
Measurement of plasma lipids 692
The primary hyperlipidaemias 693
Disorders of VLDL and chylomicrons - hypertriglyceridaemia alone 693
Disorders of LDL - hypercholesterolaemia alone 693
Combined hyperlipidaemia (hypercholesterolaemia and hyperlipidaemia) 693
Management of hyperlipidaemia 694
Guidelines to therapy 694
Lipid-lowering diet 694
Lipid-lowering drugs (Table15.12) 694
Whom to treat 695
Primary prevention for people at risk of cardiovascular disease 695
Secondary prevention 695
Aims of treatment 695
The porphyrias 696
Acute intermittent porphyria 697
Clinical features 697
Investigations 697
Management 697
Other porphyrias 697
Amyloidosis 698
Therapeutics 698
Oral antidiabetic drugs 698
Metformin 698
Mechanism of action 698
Chapter 16: The special senses 703
The ear 703
Hearing loss 703
Vertigo 703
Benign paroxysmal positional vertigo 704
Vestibular neuronitis 704
Ménières disease 705
Central causes 705
Ear infections 705
The nose and nasal cavity 706
Epistaxis (nose bleeds) 706
Sinusitis 707
The throat 707
Hoarseness (dysphonia) 707
Stridor 707
Sore throat 708
The eye 708
The red eye 708
Visual loss 709
Chapter 17: Neurology 717
Common neurological symptoms 717
Headache 717
Difficulty walking 717
Spasticity and hemiparesis 717
Parkinson's disease: shuffling gait 718
Cerebellar ataxia: broad-based gait 718
Sensory ataxia: stamping gait 718
Lower limb weakness: high-stepping and waddling gaits 719
Gait apraxia 719
Dizziness, faints and 'funny turns' 719
Dizziness and syncope 719
Investigation 721
Weakness 721
The corticospinal (or pyramidal) tracts 721
The upper motor neurone 721
The lower motor neurone 723
Numbness 724
The sensory system 724
Peripheral nerve lesions 724
Spinal root lesions 724
Spinal cord lesions 724
Pontine lesions 724
Thalamic lesions 727
Cortical lesions 727
Tremor 727
Coordination of movement 727
The cerebellum 727
The cranial nerves 728
The olfactory nerve (first cranial nerve) 728
The optic nerve (second cranial nerve) and the visual system 728
Visual field defects 729
Optic nerve lesions 729
Defects of the optic chiasm 731
Defects of the optic tract and radiation 731
Defects of the occipital cortex 732
Optic disc oedema (papilloedema) and optic atrophy 732
Papilloedema 732
Optic atrophy 732
The pupils 732
Cranial nerves III-XII 733
The ocular movements and the third, fourth and sixth cranial nerves 733
The trigeminal nerve (fifth cranial nerve) 735
Trigeminal neuralgia 736
Clinical features 736
Management 736
Differential diagnosis 736
The facial nerve (seventh cranial nerve) 736
Lower motor neurone lesions 737
Bell's palsy 737
Clinical features 737
Investigations 737
Management 737
Prognosis 737
Ramsay Hunt syndrome 737
Upper motor neurone lesions 738
The vestibulocochlear nerve (eighth cranial nerve) 738
Vertigo 738
Nystagmus 738
Pendular nystagmus 738
Jerk nystagmus 738
Glossopharyngeal, vagus, accessory and hypoglossal nerves (ninth to twelfth cranial nerves) 739
Common investigations in neurological disease 739
Blood tests 739
Imaging 739
Skull and spinal X-rays 739
Computed tomography 739
Magnetic resonance imaging 739
Positron emission tomography 740
Doppler studies 740
Electroencephalography 740
Lumbar puncture and cerebrospinal fluid examination 740
Electromyography 740
Investigation of suspected muscle disease 740
Unconsciousness and coma 741
Aetiology 742
Assessment 742
Immediate assessment 742
Further assessment 742
Investigations 744
Blood and urine tests 744
Radiology 744
CSF examination 744
Management 744
Prognosis 745
Brain death 745
Stroke and cerebrovascular disease 745
Definitions 745
Stroke 745
Stroke in evolution 746
A minor stroke 746
Transient ischaemic attack 746
Pathophysiology 746
Completed stroke 746
Transient ischaemic attacks 746
Risk factors 746
Transient ischaemic attacks 747
Investigations 747
Blood 747
Brain imaging 747
Carotid artery imaging 748
Other investigations 748
Treatment 748
Antithrombotic treatment 748
Other secondary prevention 748
Carotid endarterectomy 748
Cerebral infarction 749
Clinical features 749
Cerebral hemisphere infarcts 749
Brainstem infarction 749
Multi-infarct dementia 749
Management 750
Prognosis 752
Primary intracranial haemorrhage 753
Intracerebral haemorrhage 753
Subarachnoid haemorrhage 753
Incidence 753
Aetiology 753
Clinical features 754
Investigation 754
Management 755
Prognosis 755
Subdural haematoma 755
Extradural haemorrhage 756
Epilepsy and loss of consciousness 756
Epilepsy 756
Classification 756
Aetiology and precipitants 757
Evaluation and investigation 758
Management 758
Emergency measures 758
Status epilepticus 758
Antiepileptic drugs 759
Drug withdrawal 760
Neurosurgical treatment 761
Advice to patients 761
Movement disorders 761
Akinetic-rigid syndromes 762
Idiopathic Parkinsons disease 762
Aetiology 762
Clinical features 762
Investigations 763
Management 763
Levodopa 763
Dopamine agonists 763
Monoamine oxidase B inhibitors 763
Additional treatment 764
Other akinetic-rigid syndromes 764
Drug-induced parkinsonism 764
'Parkinsonism plus' 764
Dyskinesias 764
Benign essential tremor 764
Chorea 765
Huntington's disease 765
Hemiballismus 765
Myoclonus 765
Tics 766
Dystonias 766
Multiple sclerosis 766
Epidemiology 766
Aetiology 766
Pathology 767
Clinical features 767
Optic neuropathy 767
Brainstem demyelination 767
Spinal cord lesions 767
Differential diagnosis 768
Investigations 768
Management 768
Nervous system infection and inflammation 769
Meningitis 769
Clinical features 769
Acute bacterial meningitis 769
Viral meningitis 769
Chronic meningitis 769
Differential diagnosis 769
Management 770
Notification 770
Meningococcal prophylaxis 770
Encephalitis 771
Acute viral encephalitis 772
Clinical features 772
Investigations 772
Treatment 773
Brain and spinal abscesses 773
Cerebral abscess 773
Clinical features 773
Investigations 773
Management 773
Spinal epidural abscess 773
Neurosyphilis 773
Management 774
Transmissible spongiform encephalopathy (Creutzfeldt-Jakob disease) 774
HIV and neurology 775
CNS and peripheral nerve disease in HIV 775
HIV seroconversion 775
Chronic meningitis 775
AIDS-dementia complex 775
Encephalitis and brain abscess 775
CNS lymphoma 775
Progressive multifocal leucoencephalopathy 775
Spinal vacuolar myelopathy 775
Peripheral nerve disease 775
Brain tumours 775
Clinical features 775
Neurological deficit 776
Raised intracranial pressure 776
Epilepsy 776
Differential diagnosis 777
Investigations 777
Management 777
Hydrocephalus 777
Aetiology 778
Clinical features 778
Management 778
Headache, migraine and facial pain 778
Tension headache 779
Migraine 779
Pathogenesis 779
Clinical features 779
Differential diagnosis 780
Management 780
General measures 780
Treatment of the acute attack 780
Prophylaxis 780
Facial pain 781
Trigeminal autonomic cephalgias 781
Cluster headaches (migrainous neuralgia) 781
Giant cell arteritis (cranial or temporal arteritis) 781
Clinical features 781
Investigations 782
Management 782
Spinal cord disease 782
Spinal cord compression 782
Clinical features 782
Aetiology 784
Investigations 784
Management 784
Differential diagnosis 784
Cauda equina lesion 785
Syringomyelia and syringobulbia 785
Aetiology 785
Clinical features 785
Investigation 785
Treatment 785
Friedreich's ataxia 786
Management of the paraplegic patient 787
Degenerative neuronal diseases 787
Motor neurone disease 787
Clinical features 787
Investigations 788
Differential diagnosis 788
Management 788
Spinal muscular atrophies 788
Dementia 788
Alzheimer's disease 788
Clinical features 789
Investigations 789
Management 790
Prognosis 790
Vascular (multi-infarct) dementia 791
Dementia with Lewy bodies 791
Diseases of the peripheral nerves 791
Mononeuropathies 791
Carpal tunnel syndrome 791
Aetiology 791
Clinical features 792
Management 792
Mononeuritis multiplex 792
Polyneuropathy 792
Guillain-Barré syndrome 793
Pathogenesis 793
Clinical features 793
Investigations 794
Differential diagnosis 794
Management 794
Vitamin deficiency neuropathies 795
Thiamin (vitamin B1) 795
Pyridoxine (vitamin B6) 795
Vitamin B12 795
Hereditary sensorimotor neuropathy 795
Muscle diseases 795
Acquired muscle disease 796
Myasthenia gravis 796
Aetiology 797
Clinical features 797
Investigations 797
Differential diagnosis 797
Management 798
Anticholinesterases 798
Immunosuppressant drugs 798
Plasmapheresis and intravenous immunoglobulin 798
Thymectomy 798
Muscular dystrophies 798
Myotonias 798
Dystrophia myotonica 799
Myotonia congenita 799
Delirium 799
Delirium (toxic confusional state) 799
Management 799
Therapeutics 800
Hypnotics 800
Mechanism of action 800
Chapter 18: Dermatology 807
Introduction 807
Skin and soft tissue infections 807
Cellulitis and erysipelas 807
Clinical features 808
Diagnosis 808
Treatment 808
Necrotizing fasciitis 809
Gas gangrene 809
Fungal infections 809
Candida albicans 810
Common skin conditions 810
Acne vulgaris 810
Clinical features 810
Management 811
First-line therapy 811
Second-line therapy 811
Third-line therapy 811
Psoriasis 811
Aetiology 811
Clinical features 812
Associated features 812
Management 813
Topical treatment 813
Phototherapy 813
Systemic therapy 813
Urticaria/angio-oedema 813
Aetiology 813
Management 814
Eczema 814
Atopic eczema 814
Aetiology 814
Clinical features 814
Management 815
Exogenous eczema (contact dermatitis) 815
Clinical features 815
Normal values 823
Dictionary of terms 827
Index 837