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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_2683_Библиотеки_им_академика_М_И_Перельмана.pdf
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- •Series Editors’ foreword
- •Prefaces
- •Acknowledgements
- •Series Editors’ acknowledgements
- •History of the presenting complaint (HPC)
- •Past medical history (PMH)
- •Medications and allergies (DHX)
- •Family history (FHX)
- •Social history (SHX)
- •Systems review (SR)
- •General symptoms
- •Fatigue
- •Appetite
- •Weight change
- •Sweats
- •Pruritus (itching)
- •Sleep pattern
- •Cardiovascular symptoms
- •Chest pain
- •Shortness of breath (dyspnoea) and exercise tolerance
- •Loss of consciousness (syncope)
- •Palpitations
- •Ankle and calf swelling
- •Calf, thigh or buttock pain on exertion (claudication)
- •Respiratory symptoms
- •Dyspnoea
- •Cough
- •Sputum
- •Chest pain
- •Wheeze
- •Hoarse voice
- •Gastrointestinal disease
- •Abdominal pain
- •Dysphagia
- •Nausea and vomiting
- •Indigestion
- •Change in bowel habit or stools
- •Jaundice and itch
- •Abdominal swelling
- •Genitourinary symptoms
- •Dysuria
- •Change in urine appearance
- •Frequency and nocturia
- •Hesitancy
- •Contents
- •Loin pain
- •Incontinence
- •Menstruation
- •Discharge
- •Neurological symptoms
- •Headache
- •Dizziness and vertigo
- •Loss of consciousness
- •Visual disturbance
- •Altered hearing
- •General principles
- •Altered smell
- •Speech disturbance
- •Limb weakness, paraesthesiae and sensory loss
- •Metabolic and endocrine symptoms
- •Musculoskeletal symptoms
- •Pain
- •Weakness
- •Overview
- •The history
- •Presenting complaint (PC)
- •Visual survey
- •Position
- •Hands
- •Radial pulse
- •Blood pressure
- •Brachial and carotid artery
- •Jugular Venous Pressure
- •Face
- •Praecordium
- •Apex beat
- •Palpation
- •Auscultation
- •Summary
- •The respiratory system
- •Visual survey
- •Stiffness
- •Joint swelling
- •Disability
- •Skin symptoms
- •Rash
- •Pruritus
- •Precipitants
- •Haematological symptoms
- •Fatigue
- •Excessive bleeding or bruising
- •Recurrent infections
- •Glandular swelling
- •Conclusion of history taking
- •2 Clinical examination
- •ABCDE approach
- •Massive Blood Loss Protocol
- •General principles
- •Visual survey
- •Patient position, general behaviour and around the bed
- •Pallor
- •Cyanosis
- •Jaundice
- •Fluid status
- •Pigmentation
- •The face and body habitus
- •The hands
- •Hands
- •Nails
- •Tendons
- •Joints
- •Neuromuscular
- •Miscellaneous
- •The cardiovascular system
- •Position
- •Hands
- •Pulse
- •Blood pressure
- •Jugular venous pressure
- •Face and mouth
- •Trachea
- •Thorax
- •Inspection
- •Expansion
- •Tactile fremitus and vocal fremitus
- •Percussion
- •Auscultation
- •Summary
- •The abdomen
- •Visual survey
- •Position
- •Hands
- •Arms
- •Face and mouth
- •Neck
- •Trunk and back
- •Abdomen
- •Inspection
- •Palpation
- •Percussion
- •Auscultation
- •Concluding your examination
- •The nervous system
- •Visual survey
- •Cranial nerves
- •Cranial nerve I (olfactory nerve)
- •Cranial nerve II (optic nerve)
- •Cranial nerves III, IV and VI and eye movements
- •Cranial nerve III (oculomotor nerve)
- •Cranial nerve IV (trochlear nerve)
- •Cranial nerve VI (abducens nerve)
- •Cranial nerve V (trigeminal nerve)
- •Cranial nerve VII (facial nerve)
- •Cranial nerve VIII (vestibulocochlear nerve)
- •Cranial nerve IX (glossopharyngeal nerve)
- •Cranial nerve X (vagus nerve)
- •Cranial nerve XI (accessory nerve)
- •Cranial nerve XII (hypoglossal nerve)
- •Upper limb
- •Visual survey
- •Tone
- •Power
- •Coordination
- •Reflexes
- •Sensation
- •Lower limb
- •Visual survey
- •Tone
- •Power
- •Coordination
- •Reflexes
- •Sensation
- •Gait
- •Musculoskeletal examination
- •Visual survey
- •Look
- •Feel
- •Move
- •Assessment of disability
- •Hands
- •Skin and lymphadenopathy
- •Breast examination
- •Neck examination
- •3 Writing in the medical notes
- •General principles
- •Sample clerking
- •4 Chest pain
- •Introduction
- •History and examination findings
- •History
- •Type of chest pain
- •Onset and progression
- •Site and radiation
- •Nature of pain
- •Associated symptoms
- •Examination
- •Investigations
- •5 Shortness of breath
- •Introduction
- •History and examination findings
- •History
- •Onset
- •Severity
- •Precipitating and aggravating factors
- •Associated features
- •Other factors
- •Examination
- •Inspection
- •Palpation
- •Percussion
- •Auscultation
- •Investigations
- •Acute presentation
- •Chronic presentation
- •6 Cough and haemoptysis
- •Introduction
- •History and examination findings
- •History
- •Examination
- •Investigations
- •Bedside
- •Blood tests
- •Imaging
- •Further investigations
- •7 Palpitations
- •Introduction
- •History and examination findings
- •History
- •Causes and contributing factors
- •Examination
- •Investigations
- •8 Pyrexia of unknown origin
- •Introduction
- •History and examination findings
- •Investigations
- •Bedside investigations
- •Blood tests
- •Microbiology tests
- •Further investigations
- •Differential diagnosis
- •9 Abdominal pain
- •Introduction
- •History and examination findings
- •History
- •Examination
- •Ascertaining the underlying causes of abdomnal pain
- •Investigations
- •Bedside investigations
- •Blood tests
- •Imaging
- •Further investigations
- •10 Heartburn and indigestion
- •Introduction
- •History and examination findings
- •Investigations
- •Common investigations
- •Specialized investigations
- •11 Gastrointestinal bleed
- •Introduction
- •History and examination findings
- •History
- •Examination
- •Investigations
- •Bedside investigations
- •Blood tests
- •Further investigations
- •12 Change in bowel habit
- •Introduction
- •History and examination findings
- •History
- •Examination
- •Investigations
- •Bedside investigations
- •Blood tests
- •Imaging
- •Noninvasive
- •Invasive
- •Further investigations
- •13 Weight loss
- •Introduction
- •History and examination findings
- •History
- •Examination
- •Investigations
- •Blood tests
- •Imaging
- •14 Jaundice
- •Introduction
- •History and examination
- •History
- •Examination
- •Investigations
- •Haemolysis screen
- •Hepatocellular screen
- •Introduction
- •Micturition disturbances
- •History and examination findings
- •Examination
- •General appearance
- •Cardiovascular system
- •Abdominal examination
- •Neurological examination
- •Investigations
- •Urine tests
- •Blood tests
- •Imaging
- •Further investigations
- •Haematuria
- •History and examination findings
- •Initial tests
- •Imaging
- •Other investigations
- •Proteinuria
- •16 Headache and facial pain
- •Introduction
- •History and examination findings
- •History
- •Solitary acute episode
- •Progressive headache
- •Recurrent episodic headache and facial pain
- •Chronic headache and facial pain
- •Examination
- •Investigations
- •Blood tests
- •Imaging
- •Introduction
- •History and examination findings
- •Investigations
- •Imaging
- •Further investigations
- •Differential diagnosis
- •Thyroid disease
- •Hypothyroidism
- •Aetiology
- •Clinical features
- •Investigations
- •Blood tests
- •Other
- •Imaging
- •Hyperthyroidism
- •Aetiology
- •Primary hyperthyroidism
- •Clinical features
- •Investigations
- •Subacute (de Quervain) thyroiditis
- •Thyroid malignancy
- •Papillary thyroid carcinoma
- •Follicular thyroid carcinoma
- •Anaplastic carcinoma
- •Medullary thyroid carcinoma
- •Primary thyroid lymphoma
- •Further reading
- •18 Loss of consciousness
- •Introduction
- •History and examination findings
- •History
- •Before the event
- •The event itself
- •After the event
- •Risk factors
- •Examination
- •Comatose patient
- •Patient with blackouts
- •Investigations
- •19 Confusion and delirium
- •Introduction
- •History and examination findings
- •History
- •Pattern of confusion
- •Underlying causes
- •Examination
- •Investigations
- •Bedside investigations
- •Blood tests
- •Further tests
- •20 Stroke and TIA
- •Introduction
- •Causes and pathophysiology
- •History and examination findings
- •History
- •Examination
- •Investigations
- •Bedside investigations
- •Blood tests
- •Imaging
- •Further investigations
- •Management
- •Acute treatment
- •Prevention
- •21 Lumps
- •Introduction
- •History and examination findings
- •Investigations
- •Differential diagnosis
- •Localized lymphadenopathy
- •Generalized lymphadenopathy
- •Splenomegaly
- •22 Focal neurological deficits
- •Introduction
- •History and examination findings
- •History
- •Pattern of deficit
- •Onset
- •Precipitants
- •Progression
- •Evidence of cause
- •Examination
- •The anatomical site of the lesion
- •The underlying cause
- •The resultant disability
- •Investigations
- •Bedside investigations
- •Blood tests
- •Cerebrospinal fluid analysis
- •Imaging
- •Further investigations
- •23 Dizziness and vertigo
- •Introduction
- •History and examination findings
- •History
- •Onset and pattern of vertigo
- •Aural symptoms
- •Neurological symptoms
- •Examination
- •Investigations
- •24 Back pain and joint pain
- •Introduction
- •History and examination findings
- •History
- •Ask about associated features:
- •Other important points to consider include:
- •Examination
- •Investigations
- •Bedside investigations
- •Blood tests
- •Imaging
- •Differential diagnosis
- •Joint disease
- •Back pain
- •25 Skin lesions and rash
- •Introduction
- •History and examination
- •History
- •Examination
- •Investigations
- •Differential diagnosis
- •Pigmented lesions
- •Scaly lesions
- •Vesicular lesions
- •Weepy or pustular lesions
- •Figurate erythema
- •Bullous lesions
- •Papular and nodular lesions
- •Photodermatoses
- •Maculopapular lesions
- •Ulcerated lesions
- •Petechial and purpuric lesions
- •Miscellaneous lesions
- •Introduction
- •History and examination findings
- •Investigations
- •Differential diagnosis
- •Platelet abnormality
- •Thrombocytopenia
- •Platelet dysfunction
- •Coagulation abnormality
- •Vitamin K deficiency
- •Factor deficiency
- •Acquired factor inhibitors
- •Vessel wall abnormalities
- •Hereditary
- •Acquired
- •27 Cardiovascular system
- •Coronary heart disease
- •General overview
- •Risk factors
- •Nonmodifiable risk factors
- •Family history
- •Ethnicity
- •Modifiable risk factors
- •Smoking
- •Poor nutrition
- •Hyperlipidaemia
- •Hypertension
- •Diabetes mellitus
- •Obesity
- •Pathophysiology
- •Clinical features
- •Investigations
- •Electrocardiogram
- •Exercise tolerance test
- •Echocardiography
- •CT coronary angiography
- •Nuclear imaging
- •Coronary angiography
- •Treatment
- •Lifestyle changes
- •Drug agents
- •Antiplatelet drugs
- •Nitrates
- •β-Blockers
- •Calcium channel blockers
- •Potassium channel activators
- •Angiotensin-converting enzyme inhibitors
- •Lipid-lowering drugs
- •Revascularization
- •Acute coronary syndrome
- •ST elevation myocardial infarction
- •General overview
- •Clinical features
- •Investigations
- •Management
- •Acute management
- •Non-ST elevation myocardial infarction and unstable angina
- •General overview
- •Clinical features
- •Investigations
- •Risk scoring
- •Management
- •Acute management
- •Subsequent inpatient management of patients with acute coronary syndrome
- •Complications of myocardial infarction
- •Cardiac failure and cardiogenic shock
- •Cardiac rupture
- •Mitral regurgitation
- •Arrhythmias and conduction disturbances
- •Supraventricular arrhythmias
- •Arrhythmias
- •General overview
- •Investigations
- •Sinus tachycardia
- •Atrial fibrillation
- •Aetiology and pathophysiology
- •Complications
- •Management
- •Atrial flutter
- •Paroxysmal supraventricular tachycardia
- •Atrioventricular reentry tachycardia
- •Atrioventricular nodal reentry tachycardia
- •Management
- •Ventricular tachycardia
- •Torsades de pointes
- •Ventricular fibrillation
- •Bradycardias
- •Sinus bradycardia
- •Sick sinus syndrome
- •Heart block
- •Antiarrhythmic drugs
- •Supraventricular arrhythmias only
- •Supraventricular and ventricular arrhythmias
- •Ventricular arrhythmias
- •Heart failure
- •General overview
- •Aetiology
- •Clinical features
- •Left-sided heart failure
- •Right-sided heart failure
- •Congestive cardiac failure
- •Investigations
- •Blood tests
- •Imaging
- •Other
- •Management of acute heart failure
- •Management of chronic heart failure
- •Drug treatment
- •Angiotensin-converting enzyme inhibitors
- •β-Blockers
- •Diuretics
- •Aldosterone antagonists
- •Hydralazine in combination with a nitrate
- •Digoxin
- •Ivabradine
- •Nondrug therapy
- •Implantable cardioverter defibrillator and cardiac resynchronization therapy
- •Left ventricular assist devices
- •Transplantation
- •Hypertension
- •General overview
- •Clinical features
- •Investigations
- •Management
- •Drug treatment
- •Angiotensin-converting enzyme inhibitors
- •Angiotensin II receptor blockers
- •Calcium channel blockers
- •Thiazide diuretics
- •β-Blockers
- •α-Adrenergic receptor blockers
- •Central acting agents
- •Vasodilators
- •Management of hypertension in pregnancy
- •Malignant (accelerated) hypertension
- •Valvular heart disease
- •General overview
- •Mitral stenosis
- •Clinical features
- •Management
- •Mitral regurgitation
- •Clinical features
- •Management
- •Mitral valve prolapse
- •Aortic stenosis
- •Clinical features
- •Management
- •Aortic regurgitation
- •Clinical features
- •Management
- •Tricuspid regurgitation
- •Pulmonary valve lesions
- •Miscellaneous conditions
- •Pericarditis and pericardial effusion
- •Clinical features
- •Management
- •Constrictive pericarditis
- •Cardiomyopathy
- •Hypertrophic obstructive cardiomyopathy
- •Dilated cardiomyopathy
- •Restrictive/infiltrative cardiomyopathy
- •Arrhythmogenic right ventricular dysplasia
- •Infective endocarditis
- •Clinical features
- •Management
- •Rheumatic fever
- •Major Jones criteria
- •Carditis (40%–50%)
- •Polyarthritis (80%)
- •Sydenham chorea (10%)
- •Erythema marginatum (5%)
- •Subcutaneous nodules (rare)
- •Management
- •Atrial myxomata
- •Congenital heart disease in adults
- •Acyanotic conditions
- •Atrial septal defect
- •Ventricular septal defect
- •Patent ductus arteriosus
- •Aortic coarctation
- •Aortic and pulmonary stenosis
- •Cyanotic conditions
- •Tetralogy of Fallot
- •Further reading
- •28 Respiratory system
- •Respiratory failure
- •General overview
- •Type I respiratory failure
- •Causes
- •Management
- •Type II respiratory failure
- •Causes
- •Management
- •Asthma
- •General overview
- •Aetiology
- •Pathophysiology
- •Clinical features
- •Investigations
- •Management
- •Emergency management
- •Long-term management
- •Chronic obstructive pulmonary disease
- •General overview
- •Aetiology
- •Cigarette smoking
- •α1-Antitrypsin deficiency
- •Occupation
- •Pathophysiology
- •Clinical features
- •Investigations
- •Management
- •Short-term management
- •Long-term management
- •Bronchiectasis
- •General overview
- •Clinical features
- •Investigations
- •Management
- •Pneumonia
- •General overview
- •Aetiology
- •Community-acquired pneumonia
- •Atypical pneumonia
- •Hospital-acquired pneumonia (nosocomial)
- •Aspiration pneumonia
- •Opportunistic pneumonia
- •Clinical features
- •Typical
- •Atypical
- •Investigations
- •Bedside
- •Imaging
- •Other tests
- •CURB65 score
- •Management
- •Pulmonary embolism
- •Clinical features
- •Investigations
- •Management
- •Lung cancer
- •General overview
- •Aetiology
- •Pathology
- •Clinical features
- •Paraneoplastic syndrome
- •Investigations
- •Tumour, Node, Metastasis (TNM) staging
- •Management
- •Tuberculosis
- •General overview
- •Pathogenesis
- •Pulmonary tuberculosis
- •Extrapulmonary tuberculosis
- •Clinical features
- •Systemic
- •Pulmonary
- •Extrapulmonary
- •Investigations
- •Management
- •Pneumothorax
- •General overview
- •Clinical features
- •Management
- •Pleural effusion
- •General overview
- •Clinical features
- •Investigations
- •Management
- •Interstitial lung disease
- •General overview
- •Aetiology
- •Known cause:
- •Unknown cause:
- •Clinical features
- •Investigations
- •Management
- •Idiopathic pulmonary fibrosis
- •Sarcoidosis
- •Occupational lung disease
- •Aspergillus and the lung
- •Hypoventilation syndromes and sleep-related respiratory disorders
- •General overview
- •Obstructive sleep apnoea syndrome
- •Obesity hypoventilation syndrome
- •Congenital hypoventilation syndrome
- •Acute respiratory distress syndrome
- •General overview
- •Management
- •Cystic fibrosis
- •General overview
- •Clinical features
- •Management
- •Further Reading
- •Upper gastrointestinal tract
- •Oesophageal disorders
- •Gastro-oesophageal reflux disease
- •Clinical features
- •Investigations
- •Management
- •Complications
- •Hiatus hernia
- •Sliding hiatus hernia
- •Rolling (or paraoesophageal) hiatus hernia
- •Barrett oesophagus
- •Eosinophilic oesophagitis
- •Oesophageal motility disorders
- •Achalasia
- •Oesophageal cancer
- •Clinical features
- •Investigations
- •Management
- •Gastroduodenal disorders
- •Gastroduodenitis and peptic ulcer disease
- •Clinical features
- •Investigations
- •Management
- •Upper gastrointestinal tract haemorrhage
- •Management
- •Gastric cancer
- •Clinical features
- •Management
- •Gastrointestinal stromal tumour
- •Small bowel disorders
- •Malabsorption
- •Coeliac disease
- •Bacterial overgrowth
- •Tropical sprue
- •Whipple disease
- •Neuroendocrine tumours of the bowel
- •Carcinoid tumours
- •Gastrinoma
- •Insulinomas
- •VIPomas
- •Glucagonomas
- •Lower gastrointestinal tract
- •Colorectal disorders
- •Colorectal neoplasia
- •Benign disease
- •Colorectal cancer
- •Screening
- •Diverticular disease
- •Clinical features
- •Investigations
- •Management
- •Clostridium difficile and pseudomembranous colitis
- •Lower gastrointestinal tract bleeding
- •Ischaemic colitis
- •Microscopic colitis
- •Irritable bowel syndrome
- •Clinical features
- •Investigations
- •Management
- •Nonulcer dyspepsia
- •Inflammatory bowel disease
- •General overview
- •Ulcerative colitis
- •Crohn disease
- •Hepatobiliary system
- •Gallbladder disorders
- •Gallstones and biliary colic
- •Clinical features
- •Investigations
- •Management
- •Acute cholecystitis
- •Clinical features
- •Investigations
- •Management
- •Recurrent cholecystitis
- •Biliary tract cancer
- •Cholangiocarcinoma
- •Gallbladder cancer
- •Cancer of the ampulla of Vater
- •Pancreatic disorders
- •Acute pancreatitis
- •Clinical features
- •Investigations
- •Management
- •Chronic pancreatitis
- •Investigations
- •Management
- •Pancreatic cancer
- •Clinical features
- •Investigations
- •Management
- •Liver disorders
- •Chronic liver disease
- •Established chronic liver disease
- •Hepatitis
- •Acute hepatitis
- •Acute viral hepatitis
- •Hepatitis A
- •Epidemiology
- •Hepatitis B
- •Hepatitis C
- •Investigations
- •Management
- •Autoimmune hepatitis
- •Alcoholic liver disease
- •Pathology
- •Clinical features
- •Investigations
- •Prognosis
- •Nonalcoholic steatohepatitis
- •Haemochromatosis
- •Investigations
- •Management
- •Primary biliary cholangitis
- •Primary sclerosing cholangitis
- •Wilson disease (hepatocellular degeneration)
- •Clinical features
- •Investigations
- •Management
- •Hepatic tumours
- •Benign tumours
- •Malignant tumours
- •Miscellaneous conditions
- •α1-Antitrypsin deficiency
- •Liver abscess
- •Budd–Chiari syndrome
- •Further reading
- •Haematuria and proteinuria
- •Proteinuria
- •Benign proteinuria
- •Pathological proteinuria
- •Overflow proteinuria
- •Clinical Features
- •Investigations
- •Urine
- •Blood tests
- •Imaging
- •Histological diagnosis
- •Acute kidney injury
- •Aetiology
- •Clinical features
- •Investigations
- •Urine
- •Blood tests
- •Other tests
- •Management
- •Hyperkalaemia
- •Acidosis
- •Pulmonary oedema
- •Renal replacement therapies
- •Supportive management
- •Summary
- •Chronic kidney disease
- •Aetiology
- •Clinical features
- •Investigations
- •Management
- •Prevention of decline in renal function
- •Prevention of complications
- •Cardiovascular
- •Renal osteodystrophy
- •Acidosis
- •Anaemia
- •Hyperkalaemia
- •End-stage renal failure
- •Glomerular disease
- •Clinical features
- •Nephritic syndrome
- •Nephrotic syndrome
- •History
- •Investigations
- •Urine
- •Blood tests
- •Imaging
- •Renal biopsy
- •Management
- •Important primary and secondary glomerular diseases
- •Rapidly progressive glomerulonephritis
- •Antiglomerular basement membrane disease
- •IgA nephropathy
- •Lupus nephritis
- •Minimal change nephropathy
- •Focal segmental glomerulosclerosis
- •Membranous glomerulonephritis
- •Membranoproliferative glomerulonephritis
- •Poststreptococcal glomerulonephritis
- •Urinary tract infections
- •Lower urinary tract infections
- •Upper urinary tract infections
- •Clinical features
- •Investigations
- •Management
- •Renal calculi
- •General overview
- •Clinical features
- •Management
- •Urinary tract malignancies
- •Renal cell carcinoma
- •Transitional cell carcinoma
- •Prostatic carcinoma
- •Testicular cancer
- •Miscellaneous conditions
- •Adult polycystic kidney disease
- •Hepatorenal syndrome
- •Thrombotic microangiopathies
- •Sexually transmitted diseases
- •Chlamydia
- •Gonorrhoea
- •Syphilis
- •Further reading
- •Sodium and water balance
- •Hyponatraemia
- •Investigations
- •Hypernatraemia
- •Focal onset seizures
- •Normal awareness
- •Impaired awareness
- •Focal evolving to bilateral convulsive seizures
- •Generalized onset seizures
- •Tonic–clonic (grand mal) seizures
- •Absence attacks (petit mal)
- •Myoclonic seizure
- •Atonic or akinetic epilepsy
- •Aetiology
- •Hypokalaemia
- •Investigations
- •Management
- •Hyperkalaemia
- •Investigations
- •Management
- •Calcium balance
- •Hypocalcaemia
- •Hypercalcaemia
- •Investigations
- •32 Nervous system
- •Cerebrovascular disease
- •Stroke and TIA
- •Intracerebral haemorrhage
- •Subarachnoid haemorrhage
- •Clinical features
- •Investigations
- •Management
- •Subdural haematoma
- •Extradural haematoma
- •Headache
- •Migraine
- •General overview
- •Clinical features
- •Management
- •Cluster headache
- •Tension-type headache
- •Idiopathic intracranial hypertension
- •Trigeminal neuralgia
- •Persistent idiopathic facial pain (atypical facial pain)
- •Dementia
- •Epilepsy
- •General overview
- •Classification
- •Investigations
- •Bedside
- •Imaging
- •Electroencephalogram
- •Management
- •Drug treatment
- •First-line drugs
- •Second-line drugs
- •Withdrawing drugs
- •Other treatment
- •Status epilepticus
- •Pregnancy and epilepsy
- •Driving and work and epilepsy
- •Sudden unexpected death in epilepsy
- •Intracranial tumours
- •General overview
- •Clinical features
- •Raised intracranial pressure
- •Investigations
- •Management
- •Movement disorders
- •Parkinsonism
- •Clinical features
- •Tremor
- •Rigidity
- •Bradykinesia
- •Other features
- •Management
- •Drug therapy
- •Other therapy
- •Tremor
- •Essential tremor
- •Cerebellar tremor
- •Huntington Disease
- •Sydenham chorea
- •Other movement disorders
- •Multiple sclerosis
- •General overview
- •Pathogenesis
- •Clinical features
- •Optic neuritis
- •Diplopia
- •Sensory symptoms
- •Motor weakness
- •Cerebellar signs
- •Other manifestations
- •Investigations
- •Management
- •Central nervous system infection
- •Meningitis
- •General overview
- •Causative organisms
- •Clinical features
- •Meningism
- •Sepsis
- •Raised intracranial pressure
- •Investigations
- •Management
- •Encephalitis
- •Central nervous system abscess
- •Spinal cord infection
- •Spinal cord disorders
- •Spinal cord compression
- •Subacute combined degeneration of the cord
- •Syringomyelia and syringobulbia
- •Peripheral nervous system disorders
- •Peripheral neuropathy
- •Guillain–Barré syndrome
- •Clinical features
- •Investigations
- •Management
- •Entrapment/compression neuropathies
- •Neuromuscular disorders
- •Muscle disorders
- •Myotonic dystrophy (myotonia dystrophica)
- •Muscular dystrophy
- •Duchenne and Becker muscular dystrophy (pseudohypertrophic)
- •Facioscapulohumeral dystrophy (Landouzy–Dejerine syndrome)
- •Limb girdle dystrophy
- •Neuromuscular junction disorders
- •Myasthenia gravis
- •Clinical features
- •Investigations
- •Management
- •Lambert–Eaton myasthenic syndrome
- •Miscellaneous disorders
- •Motor neurone disease
- •Management
- •Horner syndrome
- •Bulbar and pseudobulbar palsy
- •Bell palsy
- •Further reading
- •Diabetes mellitus
- •Aetiology and Pathophysiology
- •Clinical features
- •Macrovascular disease
- •Microvascular disease
- •Diabetic retinopathy
- •Diabetic nephropathy
- •Diabetic neuropathy
- •Diabetic feet
- •Skin
- •Infections
- •Management
- •Diet and lifestyle
- •Oral hypoglycaemic agents
- •Biguanides
- •Sulphonylureas
- •Meglitinides; rapid-acting insulin secretagogues
- •Thiazolidinediones
- •Dipeptidyl peptidase 4 inhibitors
- •Glucagon-like peptide 1 agonists
- •Acarbose
- •Insulin
- •Diabetes and surgery
- •Diabetic emergencies
- •Hypoglycaemia
- •Diabetic ketoacidosis
- •Hyperosmolar hyperglycaemic state
- •Obesity and metabolic syndrome
- •Lipid disorders
- •Aetiology and pathophysiology
- •Primary hyperlipidaemia
- •Secondary hyperlipidaemia
- •Investigations
- •Management
- •Primary prevention
- •Secondary prevention
- •Drugs
- •Thyroid disease
- •Hypothyroidism
- •Management
- •Hyperthyroidism
- •Management
- •Antithyroid drugs
- •Radioiodine
- •Subtotal thyroidectomy
- •Thyroid emergencies
- •Thyrotoxic crisis (‘thyroid storm’)
- •Myxoedema coma
- •Parathyroid disease
- •Hypoparathyroidism
- •Aetiology
- •Clinical features
- •Investigations
- •Management
- •Hyperparathyroidism
- •Aetiology
- •Clinical features
- •Investigations
- •Management
- •Pituitary disorders
- •Hypopituitarism
- •Aetiology
- •Clinical features
- •Investigations
- •Management
- •Pituitary tumours
- •Clinical features
- •Investigations
- •Management
- •Acromegaly
- •Aetiology
- •Clinical features
- •Investigations
- •Management
- •Surgery
- •Radiotherapy
- •Medical therapies
- •Prognosis
- •Prolactin disorders
- •Aetiology
- •Clinical features
- •Investigations
- •Management
- •Diabetes insipidus
- •Cranial diabetes insipidus
- •Nephrogenic diabetes insipidus
- •Management
- •Adrenal disorders
- •Cushing syndrome
- •Clinical features
- •Investigations
- •Management
- •Cushing disease
- •Adrenocortical tumours
- •Ectopic adrenocorticotrophic hormone syndrome
- •Addison disease
- •Aetiology
- •Clinical features
- •Investigations
- •Management
- •Conn syndrome (primary hyperaldosteronism)
- •Clinical features
- •Investigations
- •Management
- •Phaeochromocytoma
- •Clinical features
- •Investigations
- •Management
- •Hypothalamus–pituitary–adrenal axis
- •Dynamic tests for cortisol excess
- •Tests for cortisol deficiency
- •Pituitary function tests
- •Miscellaneous endocrine conditions
- •Multiple endocrine neoplasia
- •Autoimmune polyendocrine syndrome
- •Congenital adrenal hyperplasia
- •Metabolic bone disease
- •Osteoporosis
- •Aetiology
- •Primary osteoporosis
- •Secondary osteoporosis
- •Clinical features
- •Investigations
- •Management
- •General principles
- •Drugs
- •Paget disease
- •Clinical features
- •Investigations
- •Management
- •Bisphosphonates
- •Calcitonin
- •Surgery
- •Osteomalacia
- •Aetiology
- •Clinical features
- •Investigations
- •Biochemistry
- •Imaging
- •Management
- •Renal osteodystrophy
- •Management
- •Further reading
- •34 Musculoskeletal system
- •Osteoarthritis
- •Pathology
- •Clinical features
- •Management
- •Rheumatoid arthritis
- •Pathology
- •Clinical features
- •Management
- •Spondyloarthropathies
- •Ankylosing spondylitis
- •Pathology
- •Clinical features
- •Management
- •Reactive arthritis
- •Pathology
- •Clinical features
- •Management
- •Psoriatic arthritis
- •Enteropathic arthropathies
- •Crystal arthropathy
- •Gout
- •Pathology
- •Clinical features
- •Management
- •Pseudogout
- •Connective tissue disorders
- •Systemic lupus erythematosus
- •Pathology
- •Clinical features
- •Treatment
- •Systemic sclerosis
- •Pathology
- •Clinical features
- •Management
- •Polymyositis and dermatomyositis
- •Pathology
- •Clinical features
- •Management
- •Sjögren syndrome
- •Vasculitis
- •General overview
- •Eosinophilic granulomatosis with polyangiitis
- •Granulomatosis with polyangiitis
- •Henoch–Schönlein purpura
- •Kawasaki disease
- •Microscopic polyangiitis
- •Polyarteritis nodosa
- •Behçet disease
- •Polymyalgia rheumatica and giant cell arteritis
- •Polymyalgia rheumatica
- •Giant cell arteritis
- •Antiphospholipid syndrome
- •35 Skin disease
- •Skin manifestations of systemic disease
- •Diabetes mellitus
- •Inflammatory bowel disease
- •Coeliac disease
- •Hyperthyroidism
- •Malignant disease
- •Sarcoidosis
- •Rheumatic fever
- •Neurofibromatosis
- •Lyme disease (borreliosis)
- •Hyperlipidaemia
- •Skin disease
- •Psoriasis
- •Clinical features
- •Management
- •Eczema/dermatitis
- •Clinical features
- •Management
- •Acne vulgaris
- •Actinic keratosis
- •Seborrhoeic keratosis
- •Herpes simplex
- •Herpes (varicella) zoster
- •Lichen planus
- •Erythema multiforme
- •Stevens–Johnson syndrome and toxic epidermal necrolysis
- •Pemphigus vulgaris and bullous pemphigoid
- •Erythema nodosum
- •Vitiligo
- •Pyoderma gangrenosum
- •Neoplastic disease
- •Basal cell carcinoma
- •Squamous cell carcinoma
- •Malignant melanoma
- •Infections
- •Impetigo
- •Cellulitis
- •Necrotizing fasciitis
- •36 Haematological disorders
- •Anaemia
- •Diagnosis
- •Management
- •Iron replacement
- •Vitamin B12 and folate replacement
- •Blood transfusion
- •Splenectomy
- •Erythropoietin
- •Causes of anaemia
- •Anaemia of chronic disease
- •Clinical features
- •Management
- •Haemolytic anaemia
- •Clinical features
- •Management
- •Sickle cell anaemia
- •Clinical features
- •Management
- •Thalassaemia
- •Clinical features
- •Management
- •Aplastic anaemia
- •Clinical features
- •Management
- •Leukaemia
- •Acute lymphoblastic leukaemia
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Acute myeloid leukaemia
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Chronic lymphocytic leukaemia
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Chronic myeloid leukaemia
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Multiple myeloma
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Lymphoma
- •Hodgkin disease
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Non-Hodgkin lymphoma
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Myelodysplastic syndromes
- •Classification
- •Clinical features
- •Management
- •Myeloproliferative disease
- •Polycythaemia vera
- •Essential thrombocythaemia
- •Primary myelofibrosis
- •Bleeding disorders
- •Haemophilia A
- •Haemophilia B (Christmas disease)
- •Von Willebrand disease
- •Immune thrombocytopenia
- •Disseminated intravascular coagulation
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Thrombotic disorders and thromboembolism
- •Aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Thrombotic thrombocytopenic purpura
- •Haemolytic uraemic syndrome
- •37 Infectious diseases
- •General overview
- •HIV and AIDS
- •Epidemiology and aetiology
- •Pathology
- •Clinical features
- •Primary HIV infection
- •Clinical stage 1
- •Clinical stage 2
- •Clinical stages 3 and 4
- •Treatment and prognosis
- •Prevention
- •Malaria
- •Epidemiology and aetiology
- •Pathology
- •Clinical features
- •Treatment and prognosis
- •Prevention
- •Diarrhoeal disease
- •Drug-resistant bacteria
- •Other resistant bacteria
- •38 Drug overdose and abuse
- •General overview
- •Common presentation, investigations and management
- •History
- •Examination
- •How ill is the patient?
- •Is there any evidence to suggest an underlying cause?
- •Have any complications occurred?
- •Investigations
- •Management
- •Supportive care
- •Preventing absorption
- •Increase elimination of drug
- •Specific antidotes
- •Psychiatric and social assessment
- •Paracetamol overdose
- •Illegal drugs
- •Alcohol misuse and withdrawal
- •Alcohol withdrawal
- •Wernicke encephalopathy/Korsakoff psychosis
- •Long-term treatment
- •Further reading
- •Self-Assessment
- •SBA answers
- •EMQ answers
- •Index

Contents
Series Editors’ foreword ........................v
Prefaces ................................... vi
Acknowledgements. . . . . . . . . . . . . . . . . . . . . . . . . . . vii
Series Editors’ acknowledgements ............... ix
1. History taking and communication ..............1
General principles ......................................................... 1
The history ....................................................................1
Conclusion of history taking .........................................8
2. Clinical examination .........................11
ABCDE approach ........................................................11
General principles ....................................................... 12
Visual survey ............................................................... 12
The face and body habitus .........................................13
The hands ...................................................................13
The cardiovascular system .........................................15
The respiratory system................................................17
The abdomen .............................................................. 20
The nervous system .................................................... 23
Musculoskeletal examination ...................................... 33
Hands .......................................................................... 33
Skin and lymphadenopathy ........................................33
Breast examination .....................................................34
Neck examination .......................................................34
3. Writing in the medical notes ..................37
General principles ....................................................... 37
Sample clerking ..........................................................38
Section 1 Clinical Presentations ...... 41
4. Chest pain .................................43
Introduction .................................................................43
History and examination findings................................44
5. Shortness of breath .........................47
Introduction .................................................................47
History and examination findings................................47
Investigations .............................................................. 50
6. Cough and haemoptysis ......................53
Introduction .................................................................53
History and examination findings................................53
Investigations .............................................................. 54
7. Palpitations ................................57
Introduction .................................................................57
History and examination findings................................57
Investigations .............................................................. 58
8. Pyrexia of unknown origin ....................61
Introduction .................................................................61
History and examination findings................................61
Investigations .............................................................. 61
Differential diagnosis ...................................................62
9. Abdominal pain .............................65
Introduction .................................................................65
History and examination findings................................66
Investigations .............................................................. 68
10. Heartburn and indigestion ....................71
Introduction .................................................................71
History and examination findings................................71
Investigations .............................................................. 72
11. Gastrointestinal bleed ........................75
Introduction .................................................................75
History and examination findings................................75
Investigations .............................................................. 76
12. Change in bowel habit .......................81
Introduction .................................................................81
History and examination findings................................81
Investigations .............................................................. 82
13. Weight loss ................................85
Introduction .................................................................85
History and examination findings................................86
Investigations .............................................................. 86
14. Jaundice ...................................89
Introduction .................................................................89
History and examination .............................................89
Investigations .............................................................. 91
15. Urinary symptoms and haematuria .............93
Introduction .................................................................93
16. Headache and facial pain ....................101
Introduction ...............................................................101
17. Goitre, thyroid disease and thyroid
malignancy. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .107
Introduction ...............................................................107
Further reading .........................................................110
18. Loss of consciousness ......................111
Introduction ...............................................................111
History and examination findings..............................111
19. Confusion and delirium .....................117
Introduction ...............................................................117
History and examination findings..............................117
20. Stroke and TIA .............................121
Introduction ...............................................................121
Causes and pathophysiology ...................................122
History and examination findings..............................122
xi

Contents
21. Lumps. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .129
Introduction ...............................................................129
History and examination findings..............................129
Investigations ............................................................ 130
Differential diagnosis .................................................130
22. Focal neurological deficits ...................133
Introduction ...............................................................133
History and examination findings..............................135
23. Dizziness and vertigo .......................141
Introduction ...............................................................141
History and examination findings..............................142
24. Back pain and joint pain .....................145
Introduction ...............................................................145
History and examination findings..............................145
Investigations ............................................................ 147
Differential diagnosis .................................................148
25. Skin lesions and rash .......................151
Introduction ...............................................................151
History and examination ...........................................151
Investigations ............................................................ 152
Differential diagnosis .................................................153
26. Excessive bruising and bleeding ..............159
Introduction ...............................................................159
History and examination findings..............................159
Investigations ............................................................ 160
Differential diagnosis .................................................162
Section 2 Diagnoses ............... 165
27. Cardiovascular system ......................167
Coronary heart disease .............................................167
Acute coronary syndrome .........................................171
Arrhythmias ............................................................... 175
Heart failure ...............................................................180
Hypertension ............................................................. 183
Valvular heart disease ...............................................187
Miscellaneous conditions..........................................192
Further reading ..........................................................199
28. Respiratory system .........................201
Respiratory failure .....................................................201
Asthma ...................................................................... 203
Chronic obstructive pulmonary disease ...................206
Bronchiectasis ..........................................................209
Pneumonia ................................................................ 209
Pulmonary embolism ................................................212
Lung cancer ..............................................................213
Tuberculosis ..............................................................216
Pneumothorax ........................................................... 219
Pleural effusion..........................................................221
Interstitial lung disease .............................................222
Hypoventilation syndromes and sleep-related
respiratory disorders ..............................................224
Acute respiratory distress syndrome ........................224
Cystic fibrosis............................................................225
Further reading ..........................................................227
29. Gastrointestinal and hepatobiliary systems .....229
Upper gastrointestinal tract ......................................229
Lower gastrointestinal tract ......................................234
Hepatobiliary system ................................................241
Further reading ..........................................................252
30. Renal, genitourinary and sexual health
medicine. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .253
Haematuria and proteinuria ......................................253
Acute kidney injury .................................................... 256
Chronic kidney disease .............................................259
Glomerular disease ................................................... 262
Urinary tract infections .............................................. 267
Renal calculi .............................................................. 268
Urinary tract malignancies ........................................269
Miscellaneous conditions..........................................270
Sexually transmitted diseases ..................................272
Further reading ..........................................................273
31. Fluid balance and electrolyte disturbances .....275
Sodium and water balance ....................................... 275
Hyponatraemia .......................................................... 275
Hypernatraemia.........................................................277
Hypokalaemia ...........................................................278
Hyperkalaemia ..........................................................278
Calcium balance .......................................................279
32. Nervous system ............................283
Cerebrovascular disease...........................................283
Dementia ................................................................... 286
Epilepsy ..................................................................... 286
Intracranial tumours .................................................. 289
Movement disorders .................................................291
Multiple sclerosis ......................................................294
Central nervous system infection..............................296
Spinal cord disorders ................................................298
Peripheral nervous system disorders ........................299
Neuromuscular disorders ..........................................300
Miscellaneous disorders ...........................................301
Further reading ..........................................................303
33. Metabolic and endocrine disorders ...........305
Diabetes mellitus ....................................................... 305
Obesity and metabolic syndrome .............................313
Lipid disorders ..........................................................314
Thyroid disease .........................................................315
Pituitary disorders .....................................................319
Adrenal disorders ......................................................323
Miscellaneous endocrine conditions.........................328
Metabolic bone disease ............................................ 329
Further reading ..........................................................334
34. Musculoskeletal system .....................335
Osteoarthritis.............................................................335
Rheumatoid arthritis .................................................. 336
Spondyloarthropathies ..............................................338
Crystal arthropathy ...................................................340
Connective tissue disorders......................................341
Vasculitis ...................................................................344
xii

Contents
Polymyalgia rheumatica and giant cell arteritis ........345
Antiphospholipid syndrome ......................................346
35. Skin disease. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .347
Skin manifestations of systemic disease .................. 347
Skin disease .............................................................. 348
Neoplastic disease .................................................... 353
Infections...................................................................355
36. Haematological disorders ...................357
Anaemia ....................................................................357
Leukaemia ................................................................. 362
Multiple myeloma ...................................................... 365
Lymphoma ................................................................366
Myelodysplastic syndromes .....................................369
Myeloproliferative disease ........................................369
Bleeding disorders ....................................................370
Disseminated intravascular coagulation ................... 371
Thrombotic disorders and thromboembolism ..........372
37. Infectious diseases .........................375
General overview ......................................................375
HIV and AIDS ............................................................375
Malaria ......................................................................379
Diarrhoeal disease ....................................................381
Drug-resistant bacteria .............................................382
38. Drug overdose and abuse ...................385
General overview ......................................................385
Common presentation, investigations and
management ..........................................................385
Paracetamol overdose ..............................................388
Illegal drugs ............................................................... 388
Alcohol misuse and withdrawal ................................388
Further reading ..........................................................291
Self-Assessment ..............................393
Single best answer (SBA) questions ..............395
Extended-matching questions (EMQs) ............409
SBA answers .................................421
EMQ answers .................................431
Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 441
xiii

History taking and
communication
GENERAL PRINCIPLES
Overview
Medical students are often told that ‘90% of the diagnosis
is in the history’. Although there is a large amount of truth
in this statement, this is only the case if your history- taking
skills are focused, accurate and relevant. This, in turn, is
largely dependent on your bedside manner and your ability
to build up a good rapport with your patient.
There is no easy recipe for developing a good bedside
manner, but courtesy, patience and letting patients express
their ideas, concerns and expectations are essential ingredients. Whenever you meet a patient, introduce yourself politely and do not forget relatives or friends who may also be
present. Try to put the patient at ease, as visiting the doctor
is very stressful for most people, particularly if they think
that they have a serious illness. If you cannot speak the same
language, try to get an interpreter. Language Line solutions,
a telephone-based translation service, is a useful resource;
avoid using members of the family as interpreters. If a patient has hearing difficulties, sit closer or write things down.
The aims of history taking are:
• to establish rapport with the patient;
• to obtain an accurate, sequential account of the
patient's symptoms through open questions and make a
differential diagnosis;
• to ask specific questions to focus on the most likely
diagnoses;
• to determine risk factors for these possible diagnoses;
• to put this problem or problems into the context of the
patient's life.
This chapter provides a framework for taking a comprehensive history. However, the important thing is that you develop an approach with which you are comfortable and then
practise it. In this way, you will not miss things, and you will
be able to concentrate more on what the patient is telling you
rather than what comes next. With experience, you will recognize patterns and explore different avenues in the history.
Make sure not to miss nonverbal clues, as facial expression and body posture can sometimes tell you more than the
words themselves. If you are looking up, patients will also
feel that you are genuinely listening to what they are saying.
It is important to strike a good balance between recording
the history accurately and maintaining eye contact.
As a general principle, start the consultation by asking
very open-ended questions, such as ‘How are you?’ or ‘What
problems have made you come to the clinic today?’ This
gives patients the opportunity to say what they want. Then
ask more specific questions to clarify important aspects.
1
Try to take the history and then write it down afterwards; this enables you to listen and appear to be listening
without distraction, plus you can organize your thoughts
before committing them to paper. However, when you are
learning, it may be easier to make notes as you go along; you
can also have prompts on your paper to enable you to fill in
all sub-sections of this history detailed below. As you gain
experience, you will find it easier to memorize the patient's
history and write it down later.
THE HISTORY
At the start of every history you should always:
• Document the date, time and place of the consultation.
This should be done on both sides and each subsequent
sheet of paper (remember that the clinical record is a
legal document).
• Document your name, grade and role.
• Record the age, sex and occupation of the patient.
• Document who referred the patient and if the patient
was seen as an emergency.
CLINICAL NOTES
With the move to electronic notes, some of these
steps will be done for you. It is important that you
use only your own computer log-in details, and if
you move away from your computer you lock the
screen so no patient information is on display.
A comprehensive medical history is detailed below. The separate headings help ensure a good flow and that information
is not missed. Depending on the situation, the importance of
each part of the history will differ; for instance, family history
is crucial with genetic conditions, and a detailed social history is particularly relevant in the elderly. The history needs
to be adapted to the situation; it is obviously unsafe and inappropriate to take a detailed history from an acutely unwell patient in the resuscitation unit of the emergency department.
Presenting complaint (PC)
This is a sentence or short list explaining the reason the
patient has seen you today. Resist the temptation to write
the entire history in this section, particularly when there are
multiple symptoms; however, mentioning an obvious background condition can be helpful (e.g. ‘One week increasing
1

History taking and communication
shortness of breath and productive cough. Background: 10year history of COPD’).
History of the presenting complaint (HPC)
This is where the presenting complaint is explored in detail. It is impossible to describe a system that will work for
all complaints in every situation. You will need to develop
your own techniques, likes and dislikes. Inadequate relevant
detail in this section is the commonest problem in medical
student histories:
• Aim to obtain a coherent, sequential chronological
description of the events leading to the consultation.
• Ask the questions relevant to the symptoms (e.g. for
pain, ‘Where is it?’, ‘What is its character?’)
• Keep the differential diagnoses for a symptom in your
mind and seek evidence to confirm or refute them.
• Use the review of symptoms questions for the system
you suspect to fill in extra detail (e.g. if the complaint
is a cough, ask about dyspnoea, pain, sputum, etc. and
record it in the presenting complaint section).
• Ask about the relevant risk factors (e.g. if
pulmonary embolus is suspected, ask about
immobility, travel, etc.).
• Recapitulate the history to the patient, as this helps
cement the story in your mind and reassures the
patient that you are listening.
• If the history is long, or vague, using the opening
question ‘So when did you last feel well?’ gives a
platform to begin from.
• Seek collateral history from witnesses, friends or family
where necessary (e.g. after a seizure). It is always worth
asking patients first whether they mind you speaking to
family or friends.
• With chronic complaints, it is vital to ask about how
the symptoms are affecting the patient's life.
• Document relevant negative findings (e.g. headache,
but no photophobia or neck stiffness).
Finally, ask if the patient has any thoughts or worries as to
what the diagnosis might be; this can be very enlightening
and will help you build a good working relationship as you
will be addressing the patient’s concerns. What the doctor
is interested in and what the patient is interested in can be
diametrically different.
HINTS AND TIPS
If the patient presents with pain, the SOCRATES
principle is a useful framework for remembering
to ask all the relevant questions: site, onset,
character, radiation, associated features, timing,
exacerbating/relieving factors, severity.
Past medical history (PMH)
Ask the patient if he or she has had any previous operations
or medical problems. It is prudent to probe a little about each
illness and how the diagnosis was made. Previous histories
are sometimes incorrect and can be carried forward from
one hospital visit to the next. Record the history in chronological order and, where possible, record the year, hospital
and consultant involved for each episode. Many patients may
forget past illnesses, particularly if they are anxious, and it is
worth developing a routine to ask them specifically about
diabetes, hypertension, angina or heart disease, rheumatic
fever, tuberculosis, epilepsy, asthma/emphysema/bronchitis,
jaundice, stroke or transient ischaemic attacks.
HINTS AND TIPS
MJTHREADS is a useful mnemonic for
remembering to ask about specific medical
conditions: myocardial infarction, jaundice,
tuberculosis, hypertension, rheumatic fever,
epilepsy, asthma, diabetes, stroke.
Medications and allergies (DHX)
Record which medications the patient is currently taking,
how often and at what dose. If the prescribed medications
are not being taken, ask why. Ask if there have been any
recent changes in medication. Always ask what drugs the
patient has taken in the past. For example, a patient with
pulmonary fibrosis caused by amiodarone may well have
stopped taking it years before! Ask about any nonprescription medications or herbal remedies that the patient may be
taking. Ask about illicit drug use, and whether the patient
smokes or injects the substance.
Does the patient have any allergies to any medications
or anything else at all, no matter how trivial? If yes, what
was the exact nature of the reaction? Was it anaphylaxis or
did the patient experience a rash? It is worth asking about
penicillin directly as many patients state they have a penicillin allergy, but on being questioned more closely they may
describe a nonspecific symptom, and a β-lactam antibiotic
can be given safely if the need is there.
If the patient says he or she has no allergies, it is traditional to write ‘No known drug allergies’ (NKDA).
Family history (FHX)
Do any diseases run in the patient's family—in particular,
ischaemic heart disease, cancer, diabetes and autoimmune
disorders? Record illnesses in close relatives, including age
of death where relevant. Generally speaking, family members affected before the age of 60years are deemed to be relevant. Drawing a family tree can be helpful in some patients.
2

The history
Units of alcohol
of wine
lager or cider
e
of s
pirit
1 unit
11
Social history (SHX)
The importance of this part of the history is to establish how
the illness affects the patient's life and whether the patient
is coping at home. It can provide important information on
the patient’s baseline functional status, and this is key when
one is considering whether it will be safe for the patient to
return home. Ask:
• Who is at home? Do you have a partner? Is your
partner fit and well?
• What is the home like? Is it a flat or are there stairs?
Can you manage these? Do you leave the house, and
how often? If the patient is in a home, clarify if this is a
warden-controlled flat, a residential home or a nursing
home as these offer different levels of support.
• Do you need help with daily tasks, such as washing,
dressing, feeding, cleaning or shopping? Do you have
carers or a nearby relative who helps? How often do
they come, and what do they help with?
• Do you have dependent children? Who is looking after
them now?
• Do you have any other responsibilities, such as caring
for an infirm parent or pets?
• What is your occupation? Details of the patient's
past and present occupation can be important (e.g.
industrial lung disease).
• Are you still able to work despite the current problem?
Some diagnoses can be particularly important in
relation to work, such as heavy goods vehicle drivers and
epilepsy.
• Do you, or did you, smoke? Smoking is a significant
cause of many diseases. Record smoking in pack-years.
• How much alcohol do you drink (past and present)?
Record the number of units per week (Fig.1.1).
• Have you recently been abroad, and if so, where? Was
this urban or rural? Were you vaccinated?
• Do you have pets (particularly budgerigars, pigeons
and parrots)?
Sexual history is not appropriate in every history but may be
important (e.g. for hepatitis or human immunodeficiency
virus infection).
Systems review (SR)
Patients occasionally focus on one minor symptom while
omitting to tell you of another more significant symptom.
In fact, this can be a deliberate act, asking the doctor to
deal with a simple problem (e.g. sore throat) while deciding
whether to ask for help with the real worry such as impotence or rectal bleeding. Performing a quick systems review
will prevent you from missing other important diseases.
Some of these you will have covered in the history of
the presenting complaint, and you do not need to ask about
them again.
General symptoms
Fatigue
This is a nonspecific symptom that can accompany many
organic as well as psychiatric diseases. Look particularly for
evidence of anaemia or hypothyroidism.
Appetite
Anorexia is a feature of many diseases, again organic and
psychiatric; increased appetite despite weight loss is seen
in hyperthyroidism. Distinguish between reduced appetite,
nausea and dysphagia.
Weight change
Weight loss can be deliberate (dieting) or due to chronic
disease. The causes are discussed in detail in Chapter13.
Weight gain is seen in pregnancy, hypothyroidism,
Cushing syndrome, polycystic ovary syndrome and ‘comfort eating’ due to anxiety or depression.
Sweats
Drenching sweats occurring at night are seen in lymphoma,
chronic leukaemia and tuberculosis. These are commonly
referred to as B symptoms (including also weight loss and
fever).
== =
2
/3 small glass
Fig.1.1 Units of alcohol. These refer to a standard pub
measure of wine (12% alcohol by volume), a small pub
measure of spirits (40% alcohol by volume) and standard
strength beer (3%–4% alcohol by volume). An easy way
to work out the units for a drink is to remember that the
alcohol percentage is equivalent to the number of units in
1 L of the drink (e.g. 1 L of 40% whisky contains 40 units,
and a 330-mL bottle of 6% lager contains 2 units).
1
pint of beer,
/
2
1 small measur
Pruritus (itching)
Pruritus can be due to local skin disease or systemic disease,
as shown in Table1.1.
Sleep pattern
If there is difficulty in sleeping, ask if the problem is in going
to sleep or in waking early. Difficulty in getting off to sleep
is often due to worry or anxiety, whereas early morning
wakening is a feature of depression. Sleep apnoea is common, and can be debilitating as excessive sleepiness limits
daytime function. The commonest medical condition affecting sleep is obstructive sleep apnoea (see Chapter28).
Ask about snoring, whether sleep is refreshing, morning
headaches and restless leg movements. The patient's partner is often the best source of information.
3

History taking and communication
Table1.1 Causes of pruritus
Cause Examples
Skin disease Scabies, eczema, lichen planus,
urticaria, dry skin (elderly,
hypothyroidism)
Systemic disease Hepatic (biliary obstruction,
pregnancy)
Malignancy (particularly lymphoma)
Haematological (polycythaemia,
iron deficiency)
Chronic renal failure
Drugs (sensitivity, opiates)
Endocrine (diabetes mellitus,
hyperthyroidism/hypothyroidism,
carcinoid syndrome)
Parasitic (trichinosis)
Neurological (multiple sclerosis)
Psychogenic
Cardiovascular symptoms
Chest pain
Establish the site, radiation, character, exacerbating and
relieving factors and severity; this is discussed in detail in
Chapter4.
Shortness of breath (dyspnoea) and exercise tolerance
Exertional dyspnoea can be due to poor left ventricular
function, pulmonary oedema, arrhythmia or valvular disease (see Chapter27).
Orthopnoea is breathlessness on lying flat, usually from
increased pulmonary venous congestion. This symptom can
be present in diaphragmatic weakness and even in chronic
obstructive pulmonary disease, as diaphragmatic input to
ventilation is less efficient when the patient is lying flat.
Paroxysmal nocturnal dyspnoea is waking during the
night because of severe breathlessness (pulmonary oedema).
Sudden onset of breathlessness, irrespective of body position or exercise, is often due to arrhythmia, pneumothorax or pulmonary embolism (see Chapter5).
Taking a relevant exercise tolerance history is important.
Ask the patient whether they can walk up a set of stairs (in one
go, without being out of breath once upstairs) and how far they
can walk on the flat. Remember that joint problems rather than
cardiorespiratory reserve may be the limiting factor.
Loss of consciousness (syncope)
Syncope is the transient loss of consciousness and motor
tone, which may be due to arrhythmia, valvular heart disease, postural hypotension or vertebrobasilar insufficiency
(see Chapter18).
Palpitations
Palpitations mean different things to different people, and
they should be explored carefully as they may be insignificant or they may be life threatening. Most commonly they
refer to awareness of one's heart beating (see Chapter7).
Ankle and calf swelling
This can be due to right ventricular failure, low plasma oncotic pressure (e.g. decreased albumin levels) or drugs (e.g.
calcium channel blockers), or it can be gravitational.
Calf swelling can be due to:
• deep vein thrombosis: consider underlying risk
factors such as – recent travel, immobility or surgery,
pregnancy, combined oral contraceptive pill use, family
history, malignancy;
• ruptured Baker cyst: more common in the elderly and
can be secondary to osteoarthritis of the knee;
• muscle trauma;
• cellulitis.
Calf, thigh or buttock pain on exertion (claudication)
Intermittent claudication due to peripheral vascular disease
causes calf, thigh or buttock pain on exercise. The amount
of exercise required to cause pain tends to be consistent although it often deteriorates slowly. Pain is relieved within a
predictable period of rest.
Spinal claudication due to spinal stenosis also causes
calf, thigh or buttock pain on exertion, possibly by causing
occlusion of the spinal arteries. However, the claudication
distance tends to be variable.
Respiratory symptoms
Dyspnoea
Clarify the degree of dyspnoea and its consequences for everyday tasks; try to separate respiratory dyspnoea from cardiac causes, although there is much overlap (see Chapter5).
Cough
The causes of cough are multiple. Associated features will help
in developing a sensible differential diagnosis (see Chapter6).
Sputum
How much sputum is produced? Ask about its colour, texture and time course:
• yellow/green: usually infection, acute asthma (due to
eosinophils);
• frothy: pulmonary oedema;
• rusty: lobar pneumonia (pneumococcal);
• blood: pulmonary embolism, lung cancer, pneumonia
(see Chapter6);
• taste: foul in bronchiectasis and abscess;
• smell: foul in bronchiectasis.
Chest pain
This needs a careful assessment of character, position, timing, precipitating factors, etc. Chest pain is usually pleuritic
in respiratory disease (see Chapter4), and is potentially due
to pneumonia, pneumothorax or pulmonary embolus.
Wheeze
Patients with airway obstruction sometimes notice an audible expiratory wheeze.
4

The history
11
Hoarse voice
This may be caused, for example, by recurrent laryngeal
nerve palsy in bronchial carcinoma.
Gastrointestinal disease
Abdominal pain
Establish the site, radiation, character, exacerbating and
relieving factors and severity. This is discussed in detail in
Chapter9.
Dysphagia
Dysphagia means difficulty in swallowing. Ask about:
• The onset and progression of symptoms.
• Where things get stuck. This may give a clue as to the
site of the lesion.
• If there is difficulty with solids, fluids or both.
Neuromuscular disorders tend to present with
dysphagia for fluids at onset, whereas mechanical
obstruction results in dysphagia for solids at onset.
The causes of dysphagia are outlined in Table1.2.
Nausea and vomiting
What does the vomitus look like?
• Yellow-green: upper gastrointestinal (GI) tract contents
plus bile.
Table1.2 Causes of dysphagia
Disorder Examples
Oropharyngeal
lesions
Intrinsic oesophageal
and gastric lesions
Extrinsic
oesophageal
compression
Neuromuscular
disorders
Psychological Globus hystericus
Pharyngitis, quinsy, lymphoma
Peptic stricture
Carcinoma of oesophagus or
gastric fundus
Foreign body
Oesophageal web (Paterson–
Brown–Kelly syndrome or
Plummer–Vinson syndrome)
Infection (Candida albicans)
Pharyngeal pouch
Schatzki ring (lower oesophageal
narrowing)
Leiomyoma of oesophageal muscle
Goitre with retrosternal extension
Intrathoracic tumours (lymphoma,
bronchial carcinoma)
Enlarged left atrium
Achalasia
Scleroderma
Diffuse oesophageal spasm
Diabetes mellitus
Myasthenia gravis
Myotonia dystrophica
Bulbar or pseudobulbar palsy, e.g.
motor neurone disease or stroke
Diphtheria
• Brown (feculent): lower small bowel contents.
• Bright-red blood: active upper GI tract bleeding (see
Chapter11).
• ‘Coffee grounds’: ‘old’ upper GI tract bleeding.
How ‘violent’ was the vomiting? Projectile vomiting indicates pyloric stenosis, most commonly seen in infants, but
may arise because of duodenal ulceration in adults.
Indigestion
Heartburn or dyspepsia is due to reflux of the gastric contents into the oesophagus. Be aware that heartburn can
easily be confused with cardiac chest pain. Always explore
these symptoms carefully.
Change in bowel habit or stools
Has there been a change? Ask about diarrhoea and constipation, or the presence of one alternating with the other (see
Chapter12).
Is there any rectal bleeding? Is the bleeding with or
without mucus? The causes of rectal bleeding are summarized in Box1.1. Anal and rectal lesions result in fresh
blood on the outside of the stool, on the paper on wiping or
in the pan. Higher lesions result in blood intermixed with
the stool. Melaena implies upper GI tract bleeding and the
passage of altered blood originating proximal to the hepatic flexure.
Inquire about tenesmus. Tenesmus is the painful desire
to defecate when there is no stool in the rectum. This is due
to a lesion in the lumen or wall of the rectum mimicking
faeces.
Jaundice and itch
Jaundice can be insidious or acute, and the patient may
therefore not have noticed it. Ask the patient’s family or
friends whether they have noticed a change in skin colour.
Itching is caused by build-up of bile salts in the skin and is
a feature of obstructive jaundice (see Chapter14). It can be
asked about directly and may even be evident on clinical
examination through scratch marks. Jaundice may indicate
liver function impairment and bruising, and should therefore be asked about directly as clotting factor biosynthesis
may be impaired.
BOX1.1 CAUSES OF RECTAL BLEEDING
Haemorrhoids
Anal fissure
Carcinoma (anus, rectum or colon)
Polyps
Diverticulitis (including Meckel diverticulum) but not
diverticulosis
Colitis (infective, ulcerative, Crohn disease,
ischaemic)
Angiodysplasia
5

History taking and communication
Abdominal swelling
Ask whether the patient has noticed a change in the size
of the abdomen. Remember the seven F's: foetus, flatus, fat,
fluid, flipping great mass, faeces and full bladder.
Genitourinary symptoms
Dysuria
This is discomfort during or after micturition due to urinary tract infection or recent urethral instrumentation
(catheter or cystoscope).
Change in urine appearance
What does the urine look like?
• Cloudy: infection, precipitated urates or phosphates.
• Frothy: proteinuria.
• Orange: very concentrated urine, bilirubin, rifampicin.
• Red/smoky: haematuria, haemoglobinuria, myoglobinuria,
rifampicin, blackwater fever due to haemolysis in
Plasmodium falciparum malaria, eating beetroot.
• Dark on standing: porphyria.
• Green: drugs containing methylene blue (commercial
analgesics).
See Chapter15 for the causes of haematuria and proteinuria.
Frequency and nocturia
Increased frequency of micturition can be due to:
• bladder irritation: infection, stones, tumour;
• outflow obstruction: prostatic hypertrophy, urethral
stricture;
• neurological causes: multiple sclerosis, cauda equina
syndrome.
In polyuria there is an increased volume of urine as well as
increased frequency of micturition.
Nocturia can be due to any of the causes of polyuria (see
Chapter15) and increased frequency.
Hesitancy
Hesitancy followed by a poor stream with terminal dribbling is a feature of prostatic enlargement. These symptoms
are often associated with benign prostatic hypertrophy, but
could indicate carcinoma of the prostate.
Loin pain
This can be associated with a renal calculus or a pyelonephritis (see Chapter15).
Incontinence
This can be either urge incontinence (e.g. detrusor instability) or stress incontinence (e.g. weak pelvic musculature following childbirth). It can be functional, as people
with mobility problems may not be able to get to the toilet
quickly enough.
Menstruation
Determine the pattern of the normal cycle. Then ask about
flow (heavy or light), intermenstrual bleeding, postcoital
bleeding and dysmenorrhoea.
Discharge
Vaginal or penile discharge can indicate infection.
Neurological symptoms
Headache
This is a difficult symptom for the doctor, with the diagnosis ranging from the trivial to the fatal. Ask about red flag
symptoms (see Chapter16).
Dizziness and vertigo
Ask about any perceived movement of the room. Establish
when it is occurring, in bed (classically benign positional
vertigo) or with a change in posture; that is, going from sitting to standing (i.e. orthostatic hypotension). Is there any
associated tinnitus or recent coryzal symptoms, suggesting
a vestibular cause? Be aware that the patient may refer to
unsteadiness as a sensation of feeling dizzy; consider peripheral neuropathy and visual/hearing impairment (see
Chapter23)
Loss of consciousness
Establish the situation, when it occurred (at rest, on
sitting to standing or on exertion), any warning symptoms, any seizure activity and the postictal period. See
Chapter18.
Visual disturbance
Vision can be affected by lesions of the optic pathway and
lesions of the nerves controlling eye movements (third,
fourth and sixth).
Altered hearing
Ask about deafness, tinnitus and vertigo (see Chapter23).
Altered smell
Anosmia can result from head injury, nasal polyps, following viral upper respiratory tract infections or frontal lobe
tumours and can be a feature of Parkinson disease.
Speech disturbance
There are three types of disordered speech:
• dysarthria: difficulty in articulating speech but
language content is completely normal;
• dysphonia: difficulty in voice production;
• dysphasia: difficulty in understanding or expressing
language, caused by lesions affecting the dominant
cerebral hemisphere (usually the left).
Table1.3 shows the characteristic speech abnormalities that
result from lesions at specific anatomical sites.
Limb weakness, paraesthesiae and sensory loss
This may result from a stroke leading to negative symptoms
of weakness or sensory loss. Positive features of paraesthesiae or pins and needles are referred to as positive symptoms,
seen in migrainous conditions or with seizures. These are
covered in detail in Chapter32.
6

The history
Table1.3 Causes and features of abnormalities of speech arising from lesions at specific anatomical sites
Site of lesion Causes Features of speech
Dysarthria
Mouth Ulcers, macroglossia Slurred
Lower cranial nerve
lesions (9th to 12th)
Upper cranial nerve
lesions (9th to 12th)
Cerebellum Multiple sclerosis, stroke, tumour, hereditary
Extrapyramidal Parkinsonism Difficulty initiating speech
Toxic Acute alcohol intoxication Slurred
Dysphonia
Neuromuscular junction Myasthenia gravis Weak, nasal speech
Vocal cord disease Tumour, viral laryngitis, tuberculosis, syphilis Weak volume, husky quality
Vocal cord paralysis Recurrent laryngeal nerve palsy (mediastinal
Dysphasia
Broca area (inferior
frontal gyrus)
Wernicke area (superior
temporal gyrus)
Frontotemporoparietal
lesion
Posterior part of
superior temporal/
inferior parietal lobe
Bulbar palsy (stroke, poliomyelitis, motor
neurone disease, syringobulbia, malignancy)
Pseudobulbar palsy (stroke, motor neurone
disease, multiple sclerosis)
ataxias, alcohol, hypothyroidism
carcinoma, intrathoracic surgery or trauma,
aortic aneurysm)
Infarction, bleeding, space-occupying lesion Expressive dysphasia
Infarction, bleeding, space-occupying lesion Receptive dysphasia
Infarction (left middle cerebral artery),
bleeding, space-occupying lesion and raised
intracranial pressure, dementia
Nasal quality, slurred
Associated features such as dysphagia
Spastic speech, like ‘Donald Duck’
Associated features such as dysphagia and
emotional lability
Scanning (staccato) speech
Flow is broken
Syllables explosive
Monotonous and slightly slurred
Deteriorates on repetition
Weak volume, husky quality
Comprehension intact
Difficulty in finding appropriate words and so
speech nonfluent
Fluent speech but words are disorganized or
unintelligible
Comprehension impaired
Global dysphasia
Marked receptive and expressive dysphasia
Nominal aphasia
Unable to name specific objects
Other aspects of speech preserved
11
Metabolic and endocrine symptoms
Symptoms associated with metabolic and endocrine
problems are varied and multiple—these symptoms are
described in detail in Chapter33. The two commonest endocrine conditions to consider and ask about are disorders
of the thyroid (Table1.4) and diabetes (Table1.5).
Musculoskeletal symptoms
Pain
Pain can arise in the muscles, joints (see Chapter 24) or
bones (see Table1.6).
Weakness
This can be either secondary to a neurological condition
or from nutritional deficiency, medications (e.g. long-term
Table1.4 Differences in the history between
hyperthyroidism and hypothyroidism
Symptom Hyperthyroidism Hypothyroidism
Temperature
intolerance
Weight Decreased Increased
Appetite Increased Decreased
Bowel habit Diarrhoea Constipation
Psychiatric Anxiety, irritability Poor memory,
Menstruation Oligomenorrhoea Menorrhagia
Other
symptoms
Heat Cold
depression
Palpitations, sweating,
eye changes, pretibial
myxoedema, acropachy
Dry skin, brittle
hair, arthralgia,
myalgia
7
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