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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

Abdominal pain
INVESTIGATIONS
Investigations will depend on a focused differential diagnosis. The diagnostic pathway is outlined in Fig.9.2.
Bedside investigations
• Blood glucose: hypoglycaemia in advanced liver
failure or Addison disease; hyperglycaemia will be
present in ketoacidosis and may complicate acute
pancreatitis.
• Urine dipstick test: positive for nitrites and leucocytes
indicates urinary tract infection; ketone positive
may indicate dehydration, anorexia or diabetic
ketoacidosis.
• Pregnancy test: any female of childbearing age presenting
with abdominal pain must have a pregnancy test.
Blood tests
• Full blood count: leucocytosis is seen in infection and
occasionally inflammation and malignancy. Anaemia
may be due to acute blood loss or chronic disease such
as malignancy.
• Serum amylase: hallmark of acute pancreatitis but
its level may also be raised in perforated peptic ulcer,
diabetic ketoacidosis, cholecystitis, ectopic pregnancy,
abdominal trauma and myocardial infarction. Note that
in chronic pancreatitis, serum amylase level may not be
raised.
• Urea and electrolytes: dehydration, acute kidney injury,
deranged electrolytes (e.g. low potassium level in
diarrhoea), high urea level in an upper gastrointestinal
tract bleed.
• Serum calcium: hypercalcaemia may cause renal stones
and pancreatitis; it may also indicate malignancy;
hypocalcaemia may be a consequence of pancreatitis.
• Liver function tests: abnormal findings in liver disease,
biliary disease and shock.
• Arterial blood gas: high lactate level in dehydration or
ischaemic bowel.
Imaging
• Abdominal X-ray: obstruction (dilated loops of bowel);
pancreatitis (sentinel loop due to ileus in overlying
loop of small bowel); volvulus (sigmoid and caecal);
infarction (‘thumb printing’ representing mucosal
oedema); renal stone (90% are radio-opaque).
• Erect chest X-ray: check for free gas under the
diaphragm – a sign of perforated viscus.
• Abdominal ultrasound scan: dilatation of biliary tree
and ureters; intraabdominal mass; ascites; abscess;
hydronephrosis.
• CT: useful in diagnosis of abdominal aortic aneurysm,
perforation of a viscus, abdominal malignancy.
Abdominal pain
History
Examination
MSU
Simple haematology
and biochemistry
Sudden onset,
severe pain
Urgent admission
Haemoglobin
2+
U&Es, Ca
Consider laparoscopy/
Fig.9.2 Diagnosis in the patient with abdominal pain. AXR, Abdominal X-ray; CT, computed tomography; CXR, chest
X-ray; Gluc, glucose; LFTs, liver function tests; MSU, midstream urine; U&Es, urea and electrolytes; US, ultrasound.
, Gluc, LFTs,
amylase
AXR: free gas?
US scan: aneurysm?
laparotomy
Perforation or
rupture of bowel
Aneurysm
Spleen
Pancreatits
Colicky pain
CXR erect
and supine
US scan
Bowel obstruction
Strangulated hernia
Gallstones
Renal stones
Irritable bowel
syndrome
Gradual onset,
sustained pain
Consider:
US scan
CT scan
Colonoscopy
Endoscopy
Small bowel enema
Abscess
Malignancy
Inflammatory
bowel disease
Atypical pain with
normal investigations
Consider:
Anxiety
Munchausen
syndrome
Unusual causes
68

Investigations
99
Further investigations
• Urine sample: microscopy, culture and sensitivity of
midstream urine.
• ECG to rule out myocardial infarction.
• Stool sample: microscopy, culture and sensitivity. Toxin
testing for Clostridium difficile.
• Endoscopic tests: upper gastrointestinal tract
endoscopy, flexible sigmoidoscopy and colonoscopy.
• Diagnostic laparoscopy: occasionally the
aforementioned investigations do not yield a
diagnosis and the abdominal pain persists. Diagnostic
laparoscopic surgery can be helpful in making a
diagnosis, but is more commonly useful in ruling out a
specific disease.
Chapter Summary
• Careful history taking and examination will point towards the diagnosis and guide
management.
• Cardiorespiratory conditions such as myocardial infarction or chest infection can present
as abdominal pain and mimic abdominal diseases.
• Acute abdomen can signify a medical emergency such as septic shock or ruptured
abdominal aortic aneurysm, and requires urgent assessment and management.
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Heartburn and indigestion
10
INTRODUCTION
‘Heartburn’ and ‘indigestion’, also known as ‘dyspepsia’, describe a group of symptoms that relate to the upper gastrointestinal tract. These include upper abdominal discomfort,
retrosternal pain, anorexia, nausea, vomiting, bloating, fullness, heartburn and early satiety.
The approach to this common presenting complaint
involves directing investigations towards those most likely
to benefit (e.g. those at risk of cancer, where a firm endoscopic/histological diagnosis must be made) as opposed to
those in whom empirical therapy is safe and a firm diagnosis would not significantly alter the management (e.g.
a young, otherwise well, patient with dyspepsia and no
Helicobacter pylori infection).
CLINICAL NOTES
CAUSES OF DYSPEPSIA (SEE CHAPTER29)
Duodenal ulcer
Gastric ulcer
Oesophageal/gastric cancer
Oesophagitis/GORD
Gastritis/duodenitis
Nonulcer dyspepsia
Hiatus hernia
Oesophageal motility disorders
Biliary disease
GORD, Gastro-oesophageal reflux disease.
a
Condition associated with Helicobacter pylori infection. It is
unclear whether this infection is causative in all the conditions.
b
Responds favourably to eradication of Helicobacter pylori.
a,b
a,b
a
a,b
a,b
HISTORY AND EXAMINATION FINDINGS
Ask about the following, although correlation between
symptoms and the underlying cause is poor:
• Dyspepsia: usually retrosternal discomfort, often worse
with leaning forward or lying flat. May be associated
with waterbrash, excessive sour or tasteless saliva in
the back of the mouth, either in response to acid in
the lower oesophagus or due to reflux of fluid into the
upper pharynx.
• Chest pain: burning retrosternal pain, not related to
exertion (unlike angina), which may radiate between
the shoulder blades. This can relate to acid-provoked
oesophageal spasm, which, like angina, is relieved by
nitrates.
• Nocturnal cough/asthma: occasionally due to acid
reflux.
• Epigastric pain: feature of peptic ulcer disease.
Classically, a gastric ulcer is aggravated by food, and a
duodenal ulcer is aggravated by fasting, but these are
unreliable symptoms.
Aggravating factors for reflux include:
• Increased intraabdominal pressure: stooping/bending/
obesity/pregnancy.
• Spicy or fatty foods.
• Alcohol ingestion: also causes gastritis.
• Cigarettes, caffeine, theophylline, calcium channel
blockers, β-blockers, anticholinergic drugs: reduce
lower oesophageal sphincter tone.
• Nonsteroidal antiinflammatory drugs, which interfere
with prostaglandin cytoprotection of the gastric mucosa.
• Hiatus hernia.
Identifying patients who require endoscopy is key. This
depends on the presence of the ‘red flag’ features listed in
clinical notes: symptoms in patients with dyspepsia which
indicate that diagnostic endoscopy should be performed,
which must be looked for specifically. These features all
suggest an elevated risk of cancer.
CLINICAL NOTES
SYMPTOMS IN PATIENTS WITH DYSPEPSIA
WHICH INDICATE THAT DIAGNOSTIC
ENDOSCOPY SHOULD BE PERFORMED
Unintentional weight loss >3 kg
Evidence of gastrointestinal bleeding
Previous gastric surgery
Epigastric mass
Previous gastric ulcer
Unexplained iron-deficiency anaemia
Dysphagia/odynophagia
Upper abdominal pain
Persistent vomiting/nausea
Suspicious barium meal findings
Age ≥55years with recent-onset dyspepsia lasting
more than 4weeks
Raised platelet count
71

Heartburn and indigestion
INVESTIGATIONS
An approach to the dyspeptic patient is outlined in Fig.10.1.
The management of specific conditions is further explained
in Chapter29.
The investigations used are explained below. Specialized investigations are used predominantly in cases such as persistent
symptoms not responding to the approach in Fig.10.1 or atypical symptoms (e.g. laryngeal discomfort or atypical chest pain
that may result from acid reflux or oesophageal dysmotility).
It is important to remember that most patients with dyspepsia
can be managed safely without extensive investigations.
Dyspepsia >4 weeks
<55 years
No alarm symptoms/signs
HP breath test/serology
* Empirical therapy while
awaiting result
Negative
Alarm symptoms/signs
(see Fig. 9.2)
Positive
HINTS AND TIPS
Although dyspepsia or heartburn is
usually a gastrointestinal complaint, some older
patients with ‘dyspepsia’ actually have angina
pectoris. Make sure you take an adequate history
to ensure that the problem is gastrointestinal in
origin.
>55 years
Endoscopy ± HP testing
* Diagnosis confirmed
appropriate treatment
* Diagnosis uncertain
Modify lifestyle
Remove aggravating factors
(e.g., NSAID)
Consider empirical
anti-secretory treatment
Consider further
investigation
* Modify lifestyle
Remove aggravating factors
Consider empirical anti-secretory
treatment
Consider further investigation
** HP eradication regime
Asymptomatic
No action
* Re-evaluate
Modify lifestyle
Remove aggravating factors
Consider empirical antisecretory treatment
Consider further investigation
Symptomatic
HP breath test
Negative Positive
Repeat eradication
Fig.10.1 Algorithm for the investigation and management of patients with dyspepsia. See Chapter29. Seek local
microbiological advice. Further information on the management of dyspepsia can be obtained from https://www.nice.org.
uk/guidance/cg184. HP, Helicobacter pylori; NSAID, nonsteroidal antiinflammatory drug.
72

Investigations
1010
Common investigations
• Full blood count: iron-deficiency anaemia and/or
thrombocytosis may suggest gastrointestinal blood loss
and needs further investigation.
• Electrocardiography: if you are considering the
diagnosis of angina in cases of atypical chest pain.
• Helicobacter pylori testing: several tests are available.
Carbon-13 urea breath test (which depends on H.
pylori in the gastric lumen using urease to break down
urea to ammonia and CO2) is the most accurate, and
can confirm eradication following treatment. It is
unreliable in patients taking proton pump inhibitors or
bismuth or who have taken antibiotics within the past
4weeks. Stool antigen tests can be used. Urease tests
can be used on endoscopic specimens, and histology/
culture can confirm these findings.
• Endoscopy (oesophagogastroduodenoscopy): a
relatively safe investigation. It allows visualization of
the upper gastrointestinal tract to the second part
of the duodenum. It allows biopsy and therapeutic
manoeuvres (see Chapter29).
• Barium meal: an alternative for patients in whom
endoscopy is not possible (e.g. elderly frail patients in
whom sedation is dangerous). It is useful in diagnosing
strictures and dysmotility, but does not allow
intervention at the time of the procedure.
Specialized investigations
• Oesophageal motility studies: manometry demonstrates
motility disorders (e.g. achalasia, systemic sclerosis,
diffuse oesophageal spasm).
• Twenty-four-hour intraluminal pH monitoring:
confirms acid reflux in difficult cases.
• Abdominal ultrasound scan: if a mass or biliary disease
is suspected (see Chapter29).
Chapter Summary
• Symptom management is an approach appropriate for most patients presenting with
dyspepsia.
• Identifying patients at increased risk of a sinister cause for symptoms is key.
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Gastrointestinal bleed
11
INTRODUCTION
Haematemesis is the vomiting of blood; it can be fresh
bright red blood or altered (‘coffee grounds’). Melaena
is black, tarry, offensive smelling stool; it is usually due
to bleeding in the gastrointestinal (GI) tract above the
hepatic flexure. Both are typical signs of an upper GI
tract bleed. GI bleeding is an emergency, and treatment
is usually initiated before a diagnosis can be made (see
Chapter29).
Table11.1 gives the differential diagnosis of haemateme-
sis and melaena. It is important to note that melaena which
occurs in the absence of haematemesis may be caused by
disease in the small bowel or ascending colon.
HISTORY AND EXAMINATION FINDINGS
History
It is important to clarify whether the blood has been vomited or coughed up. Food mixed with the blood or an acid
pH suggests haematemesis. Haematemesis may also be due
to blood swallowed from the nasopharynx or mouth.
You must ask about:
• Nonspecific symptoms of hypovolaemia: faintness,
weakness, dizziness, sweating, palpitations, dyspnoea,
pallor, collapse. These symptoms may precede the
actual haematemesis/melaena.
• Symptoms of the blood loss being chronic (see later):
consider gastric carcinoma if the patient gives a history
of anorexia and weight loss.
• Heartburn: oesophagitis.
• Weight loss and anorexia: carcinoma.
• Dysphagia or odynophagia (pain on swallowing):
oesophageal carcinoma or oesophagitis.
• Retching, especially after an alcohol binge: Mallory–
Weiss tear.
• Sudden severe abdominal pain: possible bowel
perforation.
• Intermittent epigastric pain relieved with antacids:
peptic ulceration.
• Current drugs: antiplatelet agents, nonsteroidal
antiinflammatory drugs, steroids or excessive alcohol
consumption are suggestive of gastric erosions; iron
therapy causes black stools but this is not melaena;
anticoagulation will exacerbate bleeding.
Table11.1 The differential diagnosis of haematemesis
and melaena
Cause Notes
Peptic ulcer
disease
Erosive gastritis Causes 20% of upper GI tract
Mallory–Weiss tear Causes 10% of upper GI tract
Oesophagitis Due to GORD
Ruptured
oesophageal
varices
Vascular
abnormalities
Gastric neoplasm Causes 5% of upper GI tract bleeds
Rare causes Oesophageal ulcers or tumours,
GI, Gastrointestinal; GOJ, gastro-oesophageal junction; GORD,
gastro-oesophageal reflux disease.
• Chronic excessive alcohol intake and other causes
of liver disease (see Chapter14): oesophageal
varices.
• A history of GI bleeds and their cause.
• Family history: inherited bleeding disorders.
HINTS AND TIPS
NOVEL ANTICOAGULANT DRUGS AND
BLEEDING
If a patient presents with bleeding and gives a
history of taking any of the novel oral anticoagulants
(e.g. rivaroxaban, apixaban, dabigatran), consider
how you are going to manage this as the effects
of these drugs are difficult to reverse in an
emergency. Idarucizumab is a reversal agent
specific for dabigatran. Currently, there are no
Causes 50% of major upper GI tract
bleeds. Mortality 10%
bleeds, rarely severe
bleeds. Laceration in GOJ mucosa,
often following retching (e.g. after
alcohol binge)
Causes 10%–20% of upper GI tract
bleeds. High mortality. Due to portal
hypertension
Vascular ectasias or
angiodysplasias
aortoenteric fistula after abdominal
aortic surgery, pancreatic tumour,
biliary bleeding, blood dyscrasias
75

Gastrointestinal bleed
— Peutz–Jeghers
Eyes
Rectum
— Rectal
examination
Abdomen
— Rigid
(perforation)
bowel disease)
chycardia
approved reversal agents for the other novel oral
anticoagulants, and management of bleeding
includes use of antifibrinolytics or plasma factors
(prothrombin complex concentrates, fresh frozen
plasma and cryoprecipitate) and attempts to reduce
the drug’s absorption (consider activated charcoal
for apixaban, rivaroxaban and dabigatran) or
increase its removal from the circulation (consider
haemodialysis/haemofiltration for dabigatran). Seek
the advice of a coagulation specialist early.
Examination
The approach to examining the patient with haematemesis
and melaena is given in Fig.11.1. Step back from the patient
for a few seconds. Does the patient look well, or pale and
clammy? If the patient is clearly unwell, follow the ABCDE
approach. Volume replacement in actively bleeding patients
should be started quickly, and the source of bleeding should
be identified and the ‘blood tap’ turned off. Once it is rec-
— Anaemia/
jaundice
— Xanthelasmata
(primary biliary cirrhosis)
Lymph nodes
— Virchow node
and other
lymphadenopathy
Stomach
— Epigastric mass/
tenderness
Mouth
syndrome
Blood
pressure
ognized that the patient needs transfusion, resuscitation
with O-negative blood should be commenced until groupspecific crossed-matched blood is available. Consider the
need for further blood products, platelets, clotting factors
and cryoprecipitate and whether a major transfusion protocol needs to be initiated.
Examination and findings include:
• Pulse and blood pressure: tachycardia is a reflex
response to hypovolaemia (due to bleeding) and usually
precedes a blood pressure fall. A young and healthy
patient may lose more than 500 mL of blood before a
rise in heart rate or fall in blood pressure occurs. If the
patient is hypotensive, intravenous fluid resuscitation
should be initiated.
• Skin: bruises, purpura (bleeding disorders) and
telangiectasia suggest Osler–Weber–Rendu disease
(hereditary haemorrhagic telangiectasia—autosomal
dominant); neurofibromata; pale and cold peripheries
(suggesting the patient is in hypovolaemic shock)
• Jaundice: may indicate liver disease, portal
hypertension and a potential clotting abnormality.
• Clubbing: inflammatory bowel disease, cirrhosis.
• Anaemia: mucous membranes. If the patient is
clinically anaemic, this may indicate chronic blood loss.
• Lymphadenopathy: especially Virchow node (left
supraclavicular lymph node) associated with gastric
carcinoma (Troisier sign).
• Mouth: pharyngeal lesions; pigmented macules (Peutz–
Jeghers syndrome).
• Cachexia.
• A rigid abdomen, suggesting bowel perforation.
• Epigastric tenderness, suggesting peptic ulcer disease,
oesophagitis or gastric carcinoma.
• Epigastric mass: gastric carcinoma.
• Signs of chronic liver disease and portal hypertension,
which are associated with a variceal bleed (see
Chapter14).
Skin
— Bruising/purpura
(bleeding disorders)
— Slate-grey pigmentation
(haemachromatosis)
— Osler–Weber–Rendu
disease
— Neurofibromata
Fig.11.1 Examining the patient with haematemesis and
melaena.
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Pulse
— Ta
Hands
— Clubbing
(inflammatory
INVESTIGATIONS
HINTS AND TIPS
A large upper GI tract bleed may cause the
passage of fresh blood via the rectum rather than
melaena; in this setting the patient is likely to be
haemodynamically unstable.
An algorithm for investigating the patient with a GI
bleed is given in Fig.11.2. Investigations will aid in diagnosis and contribute to estimating mortality and morbidity
(see Further investigations and Tables 11.2 and 11.3)

Haematemesis/melaena
Investigations
1111
Non-GI bleeding
Further investigation,
e.g. haemoptysis
— Oesophagus
(e.g. Mallory–Weiss
tear, oesophagitis,
ulcer, tumour)
— Duodenum (e.g. ulcer)
— Stomach (e.g. ulcer,
erosions, tumour)
GI bleeding: local GI cause GI bleeding: systemic cause
FBC: chronic versus acute
U&Es: urea raised
ECG
CXR: perforation of bowel
Clotting: bleeding diatheses
LFTs: hepatic failure
Upper GI tract: endoscopy ± barium studies
No cause found
(~10%)
History suggests
Mallory–Weiss tear
Specialist investigations,
e.g. for bleeding diatheses
+
Observe
–
Melaena alone
(especially older patient)
–
Consider:
— Angiography
— Isotope scan
— Enteroscopy
— Laparotomy
— SB follow-through or enema
— Videocapsule endoscopy
Diagnosis
+
Investigate lower
GI tract
Observe: repeat
‘top-up’ transfusions
Fig.11.2 Algorithm for the investigation of the patient with haematemesis and melaena. ECG, Electrocardiogram; CXR,
chest X-ray; FBC, full blood count; GI, gastrointestinal; LFTs, liver function tests; SB, small bowel; U&Es, urea and
electrolytes.
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