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Medicine at a Glance

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Medicine at a Glance

The market‐leading at a Glance series is popular among healthcare students and newly qualified practitioners for its concise and simple approach and excellent illustrations.

Each bite‐sized chapter is covered in a double‐page spread with clear, easy‐to‐follow diagrams, supported by succinct explanatory text.

Covering a wide range of topics, books in the at a Glance series are ideal as introductory texts for teaching, learning and revision, and are useful throughout university and beyond.

Everything you need to know about Medicine… at a Glance!

Discover a fully updated and comprehensive revision guide for the core medical curriculum

In the newly revised Fifth Edition of Medicine at a Glance, expert general physicians and cardiologists, Dr Patrick Davey and Dr Alex Pitcher, deliver a fully updated and comprehensive overview of the core medical curriculum. All topics are presented in an intuitive, double-page spread style with four-colour illustrations included to aid in learning and retention. The book is an essential tool for medical students revising for exams and an excellent reference for those on clinical attachments.

The Fifth Edition includes expanded coverage of COVID, neurology, fluid management, and medical emergencies. As the perfect practical companion for medical students for on-the-go study and review, Medicine at a Glance offers access to a companion website and a bundled “Core Cases” book.

Every bite-sized chapter is supported by clear, easy-to-follow diagrams and succinct explanatory text. The book also offers:

  • A thorough introduction to the practice of medicine generally and how to be a medical student, including discussions of patient confidentiality and consent, patient relationships, complaint history, medical history, and the principles of examination
  • Comprehensive explorations of clinical presentations at a glance, including cardiovascular disease, respiratory disease, renal medicine, and more
  • Practical discussions of diseases and treatments at a glance, including endocrinology, infectious disease, haematology, and more
  • In-depth examinations of miscellaneous medical issues, including fluid replacement therapy, psychiatric disorders, and substance misuse

Perfect for medical students, Foundation Programme Doctors, and Physician Associates, Medicine at a Glance is also an indispensable resource for anyone training in the allied health professions seeking a fully updated and comprehensive clinical medicine revision guide.

Table of Contents:

  1. How to use your revision guide
  2. About the companion website
  3. Part 1: Introduction
  4. 1 How to be a medical student
  5. Good doctors
  6. Hippocratic oath and the modern perspective
  7. Healthcare systems
  8. How to learn
  9. How to behave on the wards
  10. 2 Patient confidentiality
  11. The duty to maintain confidentiality
  12. Consent to disclose confidential information
  13. Breaches of confidentiality
  14. Confidentiality, privacy and data protection
  15. 3 Consent
  16. Mental capacity and consent
  17. Consent and children
  18. 4 Relationship with the patient
  19. Sequence of the consultation
  20. Privacy
  21. Language
  22. Relatives, friends and chaperones
  23. Hand washing and hospital‐acquired infection
  24. 5 History of presenting complaint
  25. Let the patient talk
  26. More specific questioning
  27. Premorbid functional status
  28. Patients’ understanding of their illness
  29. Focus on the main problems
  30. Summarize your findings
  31. 6 Past medical history, drugs and allergies
  32. Past medical history
  33. Drug history
  34. Allergies
  35. Smoking
  36. Alcohol
  37. 7 Family and social history
  38. Family history
  39. Social history
  40. Travel history
  41. 8 Functional enquiry
  42. 9 Basic clinical skills
  43. Clinical assessment of the patient
  44. Taking the history
  45. Examination of the patient
  46. Formulating a differential diagnosis
  47. Co‐ordinating diagnosis with safe care of the patient
  48. Presenting the case
  49. 10 Principles of examination
  50. Inspect
  51. Palpate
  52. Percuss
  53. Auscultate
  54. Record findings
  55. 11 Is the patient ill?
  56. Assessment of ill patients
  57. General findings
  58. Consciousness
  59. 12 The critically ill patient
  60. Recognition of the critically ill patient
  61. Examination of the critically ill patient
  62. Examination of critically ill patients’ charts
  63. Admission to intensive care
  64. Treatment of the critically sick patient
  65. Part 2: Clinical presentations at a glance
  66. 13 Chest pain
  67. Diagnostic assessment of acute chest pain
  68. Typical myocardial ischaemic pain (cardiac pain)
  69. Aortic dissection
  70. Pleuritic pain
  71. Musculoskeletal chest pain
  72. Gastro‐oesophageal pain
  73. Gall bladder disease
  74. 14 Oedema
  75. Presentation
  76. Diagnosis
  77. Investigations
  78. Treatment
  79. 15 Palpitations
  80. 16 The painful leg
  81. 17 Heart murmurs
  82. Aetiology of valvar lesions
  83. Investigations
  84. Treatment
  85. Valve intervention
  86. 18 Shock
  87. Useful investigations in diagnosis and management
  88. General principles of management
  89. Specific treatments
  90. 19 Breathlessness, cough and haemoptysis
  91. Breathlessness
  92. Cough
  93. Haemoptysis
  94. 20 Wheeze (stridor)
  95. Investigations
  96. 21 Pleural effusion
  97. Definition
  98. Introduction
  99. Clinical approach
  100. Investigations
  101. Management
  102. 22 Pneumothorax
  103. Definition
  104. Epidemiology
  105. Aetiology
  106. Pathophysiology
  107. Clinical features
  108. Investigations
  109. Management
  110. Prognosis
  111. 23 Unintentional weight loss
  112. Overall approach
  113. Epidemiology
  114. Differential diagnosis
  115. Consequences of weight loss
  116. Clinical features
  117. History
  118. Examination
  119. Investigations
  120. Management
  121. 24 Constipation and change in bowel habit
  122. Chronic constipation
  123. Change in bowel habit in older patients
  124. 25 Diarrhoea: acute and chronic
  125. Acute diarrhoea
  126. Chronic diarrhoea
  127. 26 Vomiting and intestinal obstruction
  128. Intestinal obstruction
  129. Chronic vomiting
  130. 27 Haematemesis and melaena
  131. Introduction
  132. Differential diagnosis
  133. Clinical clues to the diagnosis
  134. Examination
  135. Investigations
  136. Management
  137. Surgery
  138. 28 Rectal bleeding
  139. Acute lower GI haemorrhage
  140. Chronic rectal bleeding
  141. 29 Dysphagia
  142. Introduction
  143. Differential diagnosis
  144. Clinical features
  145. History
  146. Examination
  147. Investigations
  148. Management
  149. Neuromuscular dysphagia
  150. 30 Abdominal pain and dyspepsia
  151. Abdominal pain
  152. Dyspepsia
  153. 31 Jaundice
  154. Introduction
  155. Aetiology
  156. Differential diagnosis
  157. Clinical features and history
  158. Examination
  159. Investigations
  160. Management
  161. 32 Abdominal mass
  162. Differential diagnosis
  163. Investigations
  164. 33 Ascites
  165. Clinical features and investigations
  166. Management
  167. 34 Polyuria and oliguria
  168. Polyuria
  169. Oliguria in the hospital setting
  170. Urinary retention
  171. 35 Dysuria, frequency and urgency
  172. Acute pyelonephritis
  173. Acute cystitis
  174. Urethritis
  175. Investigations
  176. 36 Haematuria
  177. History and examination
  178. Investigations
  179. 37 Sweating, flushing and thyroid swellings
  180. Sweating
  181. Flushing
  182. Thyroid swellings
  183. 38 Obesity
  184. Definition
  185. Epidemiology
  186. Aetiopathogenesis of ‘simple obesity’
  187. Assessment of the obese patient
  188. Complications
  189. Management
  190. 39 Hirsutism and infertility
  191. Hirsutism
  192. Infertility
  193. 40 Erectile dysfunction and gynaecomastia
  194. Erectile dysfunction
  195. Gynaecomastia
  196. 41 Principles of infection
  197. The scope of infectious disease
  198. Principles of managing infection
  199. Host and microbial factors leading to infection
  200. Disease production
  201. Potential clinical consequences of infection
  202. Prevention of infection
  203. Treatment of infection
  204. 42 Investigation of suspected infection
  205. Full blood count
  206. CRP and ESR
  207. Liver function tests
  208. Microscopy
  209. Culture
  210. Serology
  211. Histology
  212. Molecular methods
  213. Imaging
  214. 43 An approach to the patient with fever of short duration
  215. Fever
  216. Assessment of the patient with fever
  217. Examination
  218. Investigations
  219. Non‐infective causes of fever in acutely unwell patients
  220. Infective causes
  221. Specific conditions that should not be missed
  222. 44 Healthcare‐associated infections
  223. Nosocomial fever
  224. Antimicrobial resistance (AMR)
  225. Fever in the neutropenic patient
  226. 45 Fever of unknown origin
  227. Classic fever of unknown origin
  228. Approach to diagnosis
  229. Investigations (see Chapter 42 for details)
  230. 46 Fever and rash
  231. Diffuse erythema
  232. Vesiculo‐bullous rashes
  233. Petechial–purpuric rashes
  234. Maculopapular rashes
  235. Nodular lesions
  236. Other rashes/lesions of importance
  237. 47 Fever in HIV‐infected patients
  238. History
  239. Examination
  240. Diagnosis
  241. Management
  242. 48 Fever in the returned traveller
  243. Incidence
  244. Most common imported infections
  245. Diagnosis
  246. Management
  247. 49 Vaginal discharge and urethritis in men
  248. Vaginal discharge
  249. Urethritis in men
  250. 50 Anaemia
  251. Clinical features
  252. Classification
  253. Functional classification
  254. Investigations
  255. Treatment
  256. 51 Clinical approach to lymphadenopathy and splenomegaly
  257. Lymphadenopathy
  258. Splenomegaly
  259. 52 The patient with abnormal bleeding or bruising
  260. Examination
  261. Investigations
  262. Treatment
  263. 53 Leukopenia
  264. Neutropenia
  265. Lymphopenia
  266. 54 Oncological emergencies
  267. Superior vena caval obstruction
  268. Malignant spinal cord compression
  269. Tumour lysis syndrome
  270. 55 Introduction to neurological diagnosis 1: Neuroepidemiology
  271. 56 Introduction to neurological diagnosis 2
  272. Six steps to neurological diagnosis
  273. Lesion localization
  274. 57 Introduction to neurological diagnosis 3
  275. Eye movements
  276. Spinal cord
  277. Nerve roots
  278. Lesion localization in peripheral nerve and muscle
  279. 58 Common neurological symptoms
  280. Difficulty walking
  281. Differential diagnosis of ataxia
  282. Dizziness
  283. 59 Weakness
  284. Weakness of all four limbs
  285. Weakness of one limb
  286. Weakness of one side of the body
  287. Weakness of both lower limbs (paraparesis)
  288. Weakness of both upper limbs
  289. 60 Disturbance of vision: a neurological perspective
  290. Visual loss
  291. Typical clinical presentations of ‘neurological’ causes of visual loss
  292. Double vision
  293. Pupils
  294. 61 Sudden painless loss of vision
  295. More urgent
  296. Less urgent
  297. 62 Tremor and other involuntary movements
  298. Common causes of tremor
  299. Other abnormal movements
  300. 63 Headache and facial pain
  301. Classification of primary headache
  302. Other causes of headache
  303. 64 Episodic alterations in awareness and consciousness
  304. Cardiovascular causes of loss of consciousness
  305. Neurological causes of loss of consciousness
  306. Prognosis in syncope
  307. Other causes of altered consciousness
  308. 65 The red eye
  309. No pain/just uncomfortable, with normal vision
  310. Painful, vision might be affected
  311. Painful, vision affected
  312. 66 Introduction to rheumatological disease
  313. Key points in clinical assessment
  314. History
  315. Examination
  316. Investigation
  317. Core principles in rheumatology
  318. 67 Low back pain and other regional pain syndromes
  319. Low back pain
  320. Regional pain syndromes
  321. 68 Introduction to dermatology
  322. History
  323. Morphology
  324. Special investigations
  325. Dermatological treatment
  326. 69 Pruritus and rashes
  327. Pruritus
  328. Rashes
  329. 70 Hair and nail disorders
  330. Hirsutes and hypertrichosis
  331. Alopecia
  332. Nail disorders
  333. 71 Leg ulcers
  334. Clinical features
  335. Examination
  336. Investigations
  337. Treatment
  338. 72 Photodermatoses
  339. 73 Pelvic pain
  340. Clinical approach
  341. Acute pelvic pain
  342. Chronic pelvic pain
  343. 74 Urinary incontinence
  344. Diagnosis
  345. Types of urinary incontinence
  346. 75 Attempted suicide by drug poisoning
  347. History
  348. Drug information
  349. Examination
  350. Immediate treatment
  351. Some specific commonly ingested poisons
  352. 76 Anaphylaxis
  353. Mechanism
  354. Clinical features
  355. Source of allergen
  356. Differential diagnosis
  357. Management
  358. Prognosis
  359. 77 Allergic reactions
  360. Inhalant allergy
  361. Food allergy
  362. Angioedema
  363. Urticaria
  364. Investigation of allergic disease
  365. 78 Cardiac and respiratory arrest
  366. Causes of cardiac and respiratory arrest
  367. Cardiopulmonary resuscitation
  368. 79 Delirium
  369. Recognition of delirium
  370. Diagnosing the cause of delirium
  371. Prevention and management of delirium
  372. 80 Coma
  373. Assessment of the level of consciousness
  374. Priorities in the management of the comatose patient
  375. Clinical assessment of the comatose patient
  376. Further management
  377. Prognosis
  378. Part 3: Diseases and treatments at a glance
  379. 81 Hypertension
  380. Definition
  381. Incidence
  382. Pathophysiology
  383. Clinical features
  384. Effects of hypertension
  385. Severity
  386. Investigations
  387. Treatment
  388. Hypertension urgencies and emergencies
  389. 82 Hyperlipidaemia
  390. Definition and incidence
  391. Lipid metabolism and lipoproteins
  392. Secondary hyperlipidaemias
  393. Genetic hyperlipidaemias
  394. Lipids in atherosclerosis
  395. Lipid lowering and risk factor modification
  396. Multiple risk factor modification
  397. 83 Acute coronary syndromes
  398. General approach
  399. Diagnosis of myocardial ischaemia
  400. Differential diagnosis of myocardial ischaemia
  401. Physical examination
  402. Investigations
  403. Acute coronary syndromes including acute STEMI
  404. 84 ST segment elevation myocardial infarction
  405. Demographics
  406. Clinical features
  407. Investigations
  408. Management
  409. Complications
  410. Prognosis and rehabilitation
  411. Risk stratification
  412. 85 Chronic coronary syndromes
  413. Diagnosis
  414. Diagnostic testing in chronic chest pain syndromes
  415. Risk stratification
  416. Treatment
  417. 86 Acute aortic dissection
  418. Risk factors
  419. Pathology
  420. Clinical features
  421. Investigations
  422. Management
  423. Prognosis
  424. 87 Heart failure
  425. Symptoms and signs
  426. Pathophysiology
  427. Classification
  428. Demographics and prognosis
  429. Aetiology
  430. Investigations
  431. Treatment
  432. Complications
  433. 88 Aortic valve disease
  434. Aortic stenosis
  435. Aortic regurgitation
  436. 89 Mitral valve disease
  437. Mitral stenosis
  438. Mitral prolapse
  439. Mitral regurgitation
  440. 90 Cardiomyopathies
  441. Dilated cardiomyopathy
  442. Hypertrophic cardiomyopathy
  443. Arrhythmogenic cardiomyopathy
  444. Restrictive cardiomyopathy
  445. 91 Pericardial disease
  446. Acute pericarditis
  447. Pericardial effusion
  448. Constrictive pericarditis
  449. 92 Pulmonary embolism
  450. Definition
  451. Risk factors
  452. Clinical features
  453. Investigations
  454. Treatment (Table

92. 1)

Chronic thromboembolic disease Thrombophilia 93 Cardiac infections Infective endocarditis Myocarditis Pericarditis Rheumatic fever 94 Tachyarrhythmias Clinical features Key facts for understanding arrhythmias Supraventricular arrhythmias Atrial flutter Ventricular tachycardias Ventricular fibrillation 95 Bradyarrhythmias Definition and clinical features Aetiology Sinoatrial node disease Atrioventricular block Investigations Treatment 96 Congenital heart disease Definition and incidence Classification Ventricular septal defect Atrial septal defect Patent ductus arteriosus Eisenmenger syndrome Coarctation of the aorta Complex congenital heart disease Adult congenital heart disease 97 Lung function tests Spirometric tests of airway function Lung volumes Tests of gas exchange Other investigations 98 Overnight oximetry and sleep apnoea Obstructive sleep apnoea 99 Respiratory failure What is the A–a gradient? Causes of hypoxaemia Causes of hypercapnia Symptoms and signs of respiratory failure Treatment of respiratory failure 100 Arterial blood gas analysis Blood gas values Acid–base homeostasis A practical approach to blood gas interpretation 101 Chest X‐ray anatomy Chest anatomy seen on posteroanterior view Important anatomical landmarks and structures on a normal chest X‐ray 102 Basic chest X‐ray interpretation 103 Chest X‐ray cases 1 Cardiomegaly Pulmonary oedema Pleural effusion Prosthetic heart valves Pleural plaques 104 Chest X‐ray cases 2 Pneumothorax Haemothorax Lobar collapse Tubes, lines and prostheses 105 Non‐invasive ventilation Indications Continuous positive airways pressure Negative and positive pressure ventilation 106 Mechanical ventilation Indications Ventilator set‐up Mode of ventilation Physiological responses to mechanical ventilation Complications Rescue therapies 107 Lower respiratory tract infection: pneumonia Community‐acquired pneumonia Hospital‐acquired pneumonia Lung abscess Pneumonia in the immunocompromised 108 Upper respiratory tract infection 109 Asthma Definition Epidemiology Aetiology Pathology Clinical features Investigations Management Prognosis 110 Chronic obstructive pulmonary disease Definition Epidemiology Aetiology Pathology Clinical features Investigations Management Prognosis 111 Bronchiectasis Definition and epidemiology Aetiology Pathophysiology Clinical features Complications Investigations Management Prognosis 112 Cystic fibrosis Definition Epidemiology Aetiology Pathophysiology Clinical features Investigations Management Prognosis 113 Sarcoidosis and other granulomatous lung diseases Sarcoidosis Beryllium disease Histiocytosis X (Langerhans cell histiocytosis) 114 Hypersensitivity pneumonitis (extrinsic allergic alveolitis) Definition Epidemiology Aetiology Pathophysiology Clinical features Investigations Management Prognosis 115 Pulmonary fibrosis Definition Aetiology Epidemiology Pathology Clinical features Investigations Management Prognosis 116 Pulmonary eosinophilia and vasculitis Pulmonary eosinophilia Vasculitis without eosinophilia Granulomatosis with polyangiitis (GPA) Other immunologically mediated disease of the lung 117 Fungi and the lung Common fungal lung infections Other fungal lung infections 118 Industrial lung disease Dust inhalation diseases Asbestosis Other asbestos‐related diseases: mesothelioma Pleural plaques, pleural thickening and pleural effusion Coal worker’s pneumoconiosis Silicosis 119 Lung disease caused by drugs Clinical features Radiological features Investigations 120 BOOP and ARDS Bronchiolitis obliterans organizing pneumonia Acute respiratory distress syndrome 121 Primary tumours of the lung Epidemiology Aetiology Clinical features Investigations Management Prognosis 122 Gastrointestinal infections Acute gastroenteritis Chronic infections 123 Reflux Incidence Pathophysiology Clinical features Investigations Management and prognosis Barrett’s oesophagus 124 Peptic ulcer disease Duodenal ulcer Gastric ulcer 125 Iron deficiency Clinical features History Examination Investigations Management 126 Abnormal liver chemistry Overall approach Examination Investigations Management 127 Diverticular disease Incidence Pathophysiology Clinical features Investigations Management and prognosis 128 Inflammatory bowel disease Ulcerative colitis Crohn’s disease 129 Gallstone disease Pathophysiology Clinical features Investigations Management and prognosis 130 Malabsorption Clinical features and examination Investigations Management Diseases causing malabsorption 131 Pancreatitis and pancreatic cancer Acute pancreatitis Chronic pancreatitis Pancreatic cancer 132 Inflammatory liver disease: viral and immune Viral hepatitis Autoimmune hepatitis Primary biliary cirrhosis Clinical features Investigations Management and prognosis Primary sclerosing cholangitis Clinical features Investigations Management and prognosis 133 Metabolic liver disease (including alcohol) Alcoholic liver disease Haemochromatosis Wilson disease 134 Acute and chronic liver disease Acute hepatitis Acute liver failure Chronic liver disease 135 Functional gastrointestinal disorders Incidence and pathophysiology Clinical features Management and prognosis 136 Upper gastrointestinal cancer Oesophageal carcinoma Gastric carcinoma 137 Colorectal cancer Incidence Pathophysiology Clinical features Investigations Management and prognosis Screening 138 Nutrition Identification of malnutrition in hospital patients Nutritional support Refeeding syndrome 139 Renal physiology and function tests Glomerular function Renal concentrating ability Amino acid conserving function Renal acid–base control Electrolyte control Hormonal function 140 Hypokalaemia and hyperkalaemia Hypokalaemia Hyperkalaemia 141 Hyponatraemia and hypernatraemia Hyponatraemia Syndrome of inappropriate ADH secretion Hypernatraemia 142 Disorders of acid–base balance Metabolic acidosis Metabolic alkalosis Respiratory acidosis Respiratory alkalosis Mixed acid–base disorders 143 Urinary calculi Aetiology Presentation Investigations Management Prevention 144 Nephrotic and nephritic syndromes Proteinuria and the nephrotic syndrome The nephrotic syndrome The nephritic syndrome 145 Glomerulonephritis Acute glomerulonephritis Chronic glomerulonephritis 146 Renal involvement in systemic disease Diabetes mellitus Myeloma Amyloidosis Haemolytic uraemic syndrome Renovascular disease Renal vasculitis Granulomatosis with polyangiitis (GPA) Microscopic polyangiitis Goodpasture syndrome Polyarteritis nodosa Systemic lupus erythematosus Henoch–Schönlein purpura Scleroderma Cryoglobulinaemia 147 Hereditary renal disorders Autosomal dominant polycystic kidney disease Simple cysts Other inherited disorders affecting the kidney 148 Tubulointerstitial disease Acute interstitial nephritis Cholesterol emboli Chronic interstitial nephritis and chronic pyelonephritis Isolated/specific tubular defects Reflux nephropathy Other congenital malformations of the urinary tract 149 Acute renal failure Pre‐renal causes Renal causes Postrenal causes Diagnostic approach Management 150 Chronic renal failure and the dialysis patient Management (see Table

150. 1)

151 The renal transplant recipient 152 Drugs and renal failure Effect of renal impairment on excretion Effect of renal impairment on drug action Effect of drug on the kidneys 153 Benign prostatic hypertrophy Examination Investigations Management 154 Urinary tract infection Investigations Management 155 Diabetes and its complications Definition Diagnosis Classification and pathophysiology Management Complications of diabetes 156 Diabetic emergencies Diabetic ketoacidosis Hyperosmolar hyperglycaemic state Lactic acidosis 157 Hyperprolactinaemia and acromegaly Hyperprolactinaemia Acromegaly 158 Hypothyroidism Epidemiology Causes Clinical features Investigations Management Myxoedema coma Congenital hypothyroidism 159 Hyperthyroidism Definition and epidemiology Causes Clinical features Investigations Management 160 Calcium metabolism Acute hypercalcaemia Hypocalcaemia 161 Adrenal disease Adrenal failure Hyperaldosteronism Phaeochromocytoma Cushing’s syndrome 162 Miscellaneous endocrine disorders Diseases of the pituitary gland Pituitary tumours Arginine Vasopressin Deficiency (AVP‐D) or Arginine Vasopressin Resistance (AVP‐R) Syndrome of inappropriate ADH secretion Multiple endocrine neoplasia 163 Hypogonadism Male hypogonadism Female hypogonadism Menstrual failure (amenorrhoea) 164 Bacteraemia and septic shock Definitions Epidemiology Clinical manifestations of sepsis Management Prognosis 165 Herpes virus infections in adults Epstein–Barr virus Diagnosis and treatment Herpes simplex virus Varicella‐zoster virus Cytomegalovirus 166 HIV infection and advanced HIV disease Epidemiology Pathogenesis Clinical patterns Diagnosis of HIV infection Treatment of HIV infection Common opportunistic infections 167 Common fungal infections Candida species Aspergillus species Cryptococcal disease 168 Specific bacterial infections Listeriosis Brucellosis Tetanus Lyme disease Syphilis 169 Malaria Epidemiology Pathogenesis Clinical features Diagnosis Differential diagnosis Treatment and management 170 Tuberculosis Epidemiology Pathogenesis Primary infection Pulmonary TB Extrapulmonary disease Diagnosis Treatment 171 Tropical infectious diseases Enteric fever Dengue Schistosomiasis Rickettsial/other tick‐borne infections Leptospirosis Viral haemorrhagic fevers 172 Diseases predisposing to infection Diseases predisposing to infections with common bacterial pathogens Structural factors predisposing to infection Miscellaneous conditions Diseases predisposing to infection with unusual pathogens 173 Immunological deficiency syndromes Antibody deficiency syndromes T‐cell deficiencies Severe combined immunodeficiency Neutrophil disorders Complement deficiency 174 Haematinic deficiency anaemias Iron deficiency Vitamin B12 deficiency Pernicious anaemia Folate deficiency 175 Haemolytic anaemia General laboratory abnormalities in haemolysis Hereditary haemolytic anaemias Acquired haemolytic anaemias Microangiopathic haemolytic anaemia Cardiac haemolysis Thrombotic thrombocytopenic purpura (TTP) Haemolytic uraemic syndrome 176 Thalassaemia and sickle cell disease Thalassaemia Sickle cell disease Other haemoglobin variants 177 Bone marrow failure Acquired aplastic anaemia Paroxysmal nocturnal haemoglobinuria Congenital aplastic anaemia 178 Acute leukaemia Epidemiology Symptoms and signs Investigations Management Prognosis 179 Lymphoma General principles Suspecting and investigating malignant lymphoid diseases Classical Hodgkin lymphoma Nodular lymphocyte‐predominant HL 180 Non‐Hodgkin lymphoma Aetiology Clinical classification Low‐grade NHL High‐grade NHL 181 Myeloproliferative neoplasms Chronic myeloid leukaemia Myelofibrosis Polycythaemia vera (PV) Essential thrombocythaemia (ET) 182 Myeloma Pathophysiology Clinical features and investigations Treatment and prognosis Monoclonal gammopathy of undetermined significance 183 Myelodysplasia Clinical features Diagnosis Treatment and prognosis 184 The blood in systemic disease Anaemia of chronic disease Anaemia of acute disease Leukoerythroblastic anaemia Polycythaemia Leukocytosis Thrombocytosis 185 Platelet disorders Physiology of haemostasis Platelet disorders 186 Disorders of coagulation In vitro tests of clotting In vivo coagulation Inherited disorders of coagulation Acquired disorders of coagulation 187 Anticoagulation and antiplatelet drugs Antiplatelet agents Anticoagulants 188 Thrombophilia Inherited thrombophilia Acquired thrombophilia 189 Aetiology of cancer Environmental causes of carcinogenesis Inherited factors contributing to the development of cancer Genetic mechanisms underlying carcinogenesis Factors underlying the growth and spread of tumours 190 Diagnostic strategies and basic principles of cancer management Important diagnostic strategies Principles of surgical oncology Basic principles of radiotherapy Systemic anticancer therapy Basic principles of chemotherapy Other therapies 191 Cancer screening and early detection Principles of screening Breast cancer Colorectal cancer Cervical cancer The future for screening Education and awareness 192 Breast cancer Epidemiology and aetiology Molecular genetics Pathology Histological grading and pathology Investigations Staging Treatment of early‐stage breast cancer Follow‐up Locally advanced breast cancer Metastatic/advanced breast cancer 193 Prostate cancer Aetiology Pathology Clinical presentation Staging (see Table

193. 1)

Clinical approach Investigations Genetics Treatment of localized prostate cancer Metastatic prostate cancer 194 Cancer with an unknown primary Initial work‐up Neoplasms of unknown primary site Neuroendocrine carcinoma General approach to management 195 Paraneoplastic cancer syndromes and hormone‐producing cancers Pathogenesis Anaemia Cachexia Syndrome of inappropriate ADH secretion Hypercalcaemia Cushing syndrome Hypoglycaemia Neurological paraneoplastic syndromes Dermatological paraneoplastic syndromes Rare syndromes 196 Palliative care Pain The terminal phase of illness and end‐of‐life care 197 Head computed tomography cases Intracranial haemorrhage Cerebral infarction Intracranial tumours 198 Head magnetic resonance imaging cases Intracranial haemorrhage Cerebral infarction and diffusion‐weighted MRI Intracranial tumours 199 Stroke Key features Time course of strokes Anatomy of strokes Risk factors for stroke 200 Management of stroke Acute management Long‐term management (see Table

200. 1)

201 Other vascular disorders of the brain Subarachnoid haemorrhage Subdural haemorrhage Venous sinus thrombosis 202 Dementias Alzheimer disease Frontotemporal dementia Vascular dementia Dementia with Lewy bodies Prion diseases Cognitive impairment in younger patients 203 Epilepsy Causes of seizures Epidemiology Simplified classification Diagnosis Specific syndromes Treatment 204 Multiple sclerosis Clinical spectrum Clinical features Diagnosis Differential diagnosis Prognosis Treatment Neuromyelitis optica 205 Infections of the central nervous system Meningitis Encephalitis Cerebral abscess Prion diseases Parasitic diseases Neurological consequences of HIV disease 206 Tumours and the nervous system Neoplasia and the CNS Specific tumours Malignant meningitis Paraneoplastic disorders Neurocutaneous syndromes 207 Spinal cord disease Acute spinal cord compression Progressive spastic paraparesis Transverse myelitis Anterior spinal artery thrombosis Disc prolapse Syringomyelia Spinal shock 208 Neuromuscular disease The motor unit Motor neuron disease Poliomyelitis Myasthenia gravis Inflammatory myopathies Muscular dystrophies Myotonic dystrophy Metabolic myopathies 209 Peripheral neuropathy Clinical approach Neuropathy classification Polyneuropathies Common mononeuropathies Rarer mononeuropathies Mononeuritis multiplex 210 Movement disorders Parkinsonism Neurodegenerative akinetic–rigid syndromes mimicking Parkinson disease Dystonia Huntington disease Drug‐induced movement disorders Movement disorders in young people 211 Osteoarthritis Epidemiology Aetiology and pathogenesis Classification Clinical features Physical findings Subsets of osteoarthritis Investigations Management 212 Gout and pseudogout (calcium pyrophosphate dihydrate arthropathy) Gout Pseudogout (CPPD arthropathy) 213 Arthritis associated with infectious agents Definitions Epidemiology of joint infection Septic arthritis Arthritis as a feature of systemic infection 214 Vasculitis Definition Key points Epidemiology and pathogenesis History and examination Investigations (See also Table

66. 1)

Prognosis and treatment Kawasaki arteritis 215 Metabolic bone disease Osteoporosis Osteomalacia/rickets Parathyroid and renal bone disease 216 Other bone disease Paget disease Osteonecrosis (avascular necrosis) Osteomyelitis 217 Rheumatoid arthritis Epidemiology Aetiology and pathogenesis Clinical features at onset/early Clinical features: established/chronic RA Investigations Management Pharmacological therapy (Table

217. 2)

Prognosis and outcome 218 Inflammatory spondyloarthropathies Epidemiology Clinical features Ankylosing spondylitis (r‐AxSpA) Psoriatic arthritis (pPsA ± axSpA) Management of psoriatic arthritis and ankylosing spondylitis Reactive arthritis Enteropathic arthritis 219 Systemic lupus erythematosus Aetiology and epidemiology Clinical features and classification criteria Immunology and other investigations in SLE Management and therapy Prognosis 220 Myositis syndromes, polymyalgia rheumatica and systemic sclerosis Myositis Polymyalgia rheumatica Systemic sclerosis 221 Eczema and urticaria Atopic dermatitis Other types of endogenous eczema Contact dermatitis Urticaria Urticarial vasculitis Hereditary angioedema 222 Psoriasis Aetiology, pathogenesis and clinical features Investigations, management and prognosis Management and prognosis Reactive arthritis 223 Blistering diseases Congenital blistering diseases Toxic epidermal necrolysis: Lyell syndrome Bullous pemphigoid Pemphigus vulgaris Dermatitis herpetiformis 224 Skin infections and infestations Staphylococci Streptococci Herpes skin infections Warts Mollusca Fungal infections Parasitosis Mycobacteria and the skin 225 Acne, rosacea and hidradenitis Acne vulgaris Rosacea Hidradenitis suppurativa 226 The skin and systemic disease Raynaud phenomenon Human immunodeficiency virus Drug eruptions Vasculitis Skin markers of internal malignancy Systemic sclerosis 227 Disorders of skin pigmentation Hyperpigmentation Hypopigmentation Vitiligo 228 Skin tumours Premalignant disease Malignant disease Lymphoma 229 Orogenital disease Oral disorders Vulval disorders Penile disorders Genital ulceration Orogenital syndromes 230 Endometriosis and adenomyosis Endometriosis Adenomyosis 231 Polycystic ovary syndrome Diagnosis Clinical consequences Management 232 Hypertensive disorders of pregnancy Effects of pregnancy on maternal cardiovascular system Classification Gestational hypertension Pre‐eclampsia 233 Cardiovascular disease in pregnancy Maternal heart disease in pregnancy Thromboembolic disease in pregnancy 234 Other medical and surgical conditions in pregnancy Neurological diseases in pregnancy Neurological emergencies in pregnancy Psychiatric disorders in pregnancy Pulmonary disease in pregnancy Renal disease in pregnancy Autoimmune diseases in pregnancy Surgical conditions in pregnancy 235 Fluid replacement therapy Assessment of hypovolaemia Management of severely hypovolaemic patients Which fluid should be chosen? 236 Illness in elderly people Premorbid condition Polypharmacy Differential diagnosis Clinical presentations and diseases Specific issues Diagnostic issues Consequence and treatment of illness Rehabilitation 237 Chronic tiredness and other medically unexplained symptoms Chronic fatigue Medically unexplained symptoms Somatic symptom disorder (SSD, formerly known as somatization disorder) Chronic fatigue syndrome 238 Psychiatric disorders Common psychological illnesses seen in medical practice Schizophrenia Affective (mood) disorders Substance misuse 239 Substance misuse Aetiology and management Specific substances 240 Alcohol misuse Safe limits Classification Epidemiology Detection and screening Aetiology Complications Management Prognosis 241 Drug toxicity (adverse drug reactions) Predictable side‐effects Increased tissue action of the drug Toxicity arising from predictable drug–drug interactions Toxicity arising from other predictable mechanisms Immune reactions Unpredictable and other mechanisms giving rise to toxicity Diagnosis Management 242 COVID‐19 Epidemiology Pathogenesis Clinical features Diagnosis Treatment and management Preventing infection Index End User License Agreement

Details
  • ISBN: 9781119430490
  • Authors: Patrick Davey, Alex Pitcher
  • Language: en
  • Publication Year: 2024
  • Pages: 608
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