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Handbook of Liver Disease E-Book

Handbook of Liver Disease E-Book

Lawrence S. Friedman | Emmet B. Keeffe

(2011)

Additional Information

Book Details

Abstract

The Handbook of Liver Disease, 3rd Edition, by Drs. Lawrence S. Friedman and Emmet B. Keeffe, gives you quick reference to the most recent diagnostic and treatment options for patients with liver disorders. International authorities share the latest clinical findings and procedures to help you expertly manage illnesses like hepatitis B and C and hepatocellular carcinoma, as well as apply new practices like genetic testing, noninvasive imaging techniques, and so much more. Quickly access updated information on all aspects of liver disease including new drugs, therapy trials, and post-transplant conditions with this full-color, templated edition–in print and online at www.expertconsult.com.

  • Expedite diagnostic and therapeutic decision making with a highly templated outline format that uses full-color illustrations, tables, algorithms and figures, key point boxes, and alert symbols to present information at a glance.
  • Apply some of the latest treatments for liver disease including the role of pretreatment IL28B testing for patients with hepatitis B and C;  radiofrequency ablation and sorafenib in cases of hepatocellular carcinoma;  the use of the drug rifaximin to treat hepatic encephalopathy;  and much more.

Make optimal use of genetic testing to assess your patients’ risk of metabolic liver disease and to personalize treatment regimens for chronic hepatitis C.

  • Offer your liver transplantation patients the best prognosis and follow-up with the latest information on outcomes and the management of complications.

Use blood test panels and noninvasive imaging techniques to evaluate the degree of liver fibrosis.

  • Make informed treatment decisions with the latest clinical trial results for portal hypertension, autoimmune liver diseases, acute liver failure, and hepatic infections.

  • Search the complete text online, download all the images, and test your knowledge with 200 board-style review questions at www.expertconsult.com.

Table of Contents

Section Title Page Action Price
Front Cover Cover
Handbook of Liver Disease iii
Copyright iv
Contributors v
Foreword xi
Dedication xiv
Preface To The Third Edition xv
Acknowledgments xvi
Special Tribute xvi
Contents xvii
Chapter 1 - Assessment of liver function and diagnostic studies 1
Key Points 1
Routine Liver Biochemical Tests 1
Assessment of Hepatic Metabolic Capacity 9
Other Tests of Liver Function 11
Liver Biopsy 12
Hepatic Imaging 14
Chapter 2 - Acute liver failure 20
Key Points 20
Definitions 20
Epidemiology 21
Causes 22
Pathophysiology 22
Clinical Features 23
Complications 28
Treatment 29
Chapter 3 - Acute viral hepatitis 34
Key Points 34
Importance 34
Agents 35
Epidemiology and Risk Factors 37
Pathophysiology 40
Clinical Features 40
Laboratory Features 41
Histology 42
Diagnosis 43
Natural History and Outcome 47
Treatment 48
Prevention 49
Chapter 4 - Chronic viral hepatitis 53
Key points 53
Overview 53
Chronic Hepatitis B 53
Chronic Hepatitis C 61
Hepatitis D Virus (HDV) 67
Chronic Hepatitis E 69
Chapter 5 - Autoimmune hepatitis 70
Key Points 70
Definition 70
Diagnosis 71
Pathogenesis 72
Subclassifications 76
Epidemialogy 79
Prognosis 79
Clinical Features 81
Treatment 83
Chapter 6 - Alcoholic liver disease 95
Key Points 95
Epidemiology 95
Risk Factors for Alcoholic Liver Disease 96
Clinical Features 97
Diagnosis 99
Histology and Spectrum of Disease 99
Indices of Liver Dysfunction for Alcoholic Hepatitis 101
Treatment 101
Chapter 7 - Fatty liver and nonalcoholic steatohepatitis 106
Key Points 106
Overview 106
Pathogenesis 107
Clinical Features 108
Risk Factors 108
Diagnosis 110
Prognosis (Fig. 7.1) 113
Treatment 113
Chapter 8 - Drug-induced and toxic liver disease 115
Key Points 115
Overview 115
Clinical Presentation 116
Characterization of Drug-Induced Liver Injury 116
Pathophysiology 118
Biotransformation 118
Diagnosis of Drug-induced Liver Injury 120
Hepatotoxicity of Specific Medications 120
Chapter 9 - Cirrhosis and portal hypertension: an overview 136
Key Points 136
Cirrhosis 136
Portal Hypertension 144
Chapter 10 - Portal hypertension and gastrointestinal bleeding 150
Key Points 150
Portal Hypertension: Overview 150
Prevention of Initial Variceal Hemorrhage 152
Treatment of Acute Variceal Hemorrhage 153
Prevention of Recurrent Variceal Hemorrhage 156
Management of Nonesophageal Variceal Sources of Bleeding Related to Portal Hypertension 157
Chapter 11 - Ascites and spontaneous bacterial peritonitis 159
Key Points 159
Overview of Ascites 159
Evaluation of the Patient with Ascites 160
Ascitic Fluid Analysis 162
Treatment of Ascites in Patients with Cirrhosis 163
Spontaneous Bacterial Peritonitis and other Ascitic Fluid Infections 166
Prophylaxis of Ascitic Fluid Infection 170
Chapter 12 - Hepatorenal syndrome 173
Key Points 173
Overview 173
Definition 173
Pathogenesis 173
Pathogenesis 176
Diagnosis 177
Other Causes of Acute Kidney Injury in Cirrhosis 177
Clinical Features 178
Treatment 178
Prevention 180
Chapter 13 - Hepatic encephalopathy 183
Key Points 183
Definition and Classification 183
Pathophysiology 183
Clinical Features 184
Diagnosis 185
Covert Hepatic Encephalopathy 186
Overt Hepatic Encephalopathy 187
Laboratory Tests 188
Treatment 189
Chapter 14 - Primary biliary cirrhosis 193
Key Points 193
Epidemiology 193
Genetics 194
Immunologic Abnormalities 194
Pathogenesis 195
Pathology 197
Clinical Features 199
Diagnosis 202
Treatment 203
Chapter 15 - Primary sclerosing cholangitis 208
Key Points 208
Overview 208
Terminology and Diagnostic Criteria 208
Clinical Features 209
Diseases Associated with Primary Sclerosing Cholangitis 211
Epidemiology 212
Etiology and Pathogenesis 213
Natural History 214
Treatment 215
Complications and Their Treatment 216
Acknowledgment 218
Chapter 16 - Hemochromatosis 219
Key Points 219
Epidemiology 219
Genetics 219
Classification 220
Pathophysiology 221
Clinical Features 222
Natural History and Prognosis 224
Diagnosis 224
Differential Diagnosis 227
Treatment 227
Screening 228
Chapter 17 - Wilson disease and related disorders 230
Key Points 230
Copper Metabolism (Figs 17.1 and 17.2) 230
Genetics 231
Pathogenesis 233
Clinical Features 233
Diagnosis 236
Treatment 238
Other Copper-Related Disorders 243
Chapter 18 - Alpha-1 antitrypsin deficiency and other metabolic liver diseases 245
Key Points 245
Overview 245
Alpha-1 Antitrypsin Deficiency (α-1 ATD) 246
Hereditary Tyrosinemia 248
Gaucher’s Disease 250
Glycogen Storage Disease (GSD) 251
Cystic Fibrosis (CF) 252
Porphyria 254
Other Inborn Errors of Metabolism 256
Chapter 19 - Budd–Chiari syndrome and other vascular disorders 259
Key Points 259
Budd–Chiari Syndrome 259
Portal Vein Thrombosis 263
Sinusoidal Obstruction Syndrome 265
Chapter 20 - The liver in heart failure 268
Key Points 268
Overview 268
Hepatic Circulation 268
Liver Architecture 269
Pathophysiology 270
Pathology 271
Etiology (Table 20.1) 274
Frequency 275
Clinical Features 275
Laboratory Features 277
Radiologic Features 279
Treatment 280
Prognosis 280
Chapter 21 - The liver in pregnancy 282
Key Points 282
Overview 282
Approach to the Pregnant Patient 283
Liver Disorders Unique to Pregnancy 285
Pregnancy in Patients with Chronic Liver Disease 291
Viral Hepatitis and Herpes Simplex Virus Infections in Pregnant Women (see also Chapters 3 and 4) 293
Budd–Chiari Syndrome (see also Chapter 19) 295
Cholelithiasis and Cholecystitis in Pregnant Women (see also Chapter 32) 295
Chapter 22 - The liver in systemic disease 297
Key Points 297
Cardiac Disease (see Chapter 20) 297
Connective Tissue Diseases 299
Endocrine and Metabolic Disorders 301
Granulomatous Disease and Sarcoidosis (see Chapter 26) 301
Lymphoma and Hematologic Diseases 302
Infections (see Chapter 29) 303
Gastrointestinal and Nutritional Disorders 304
Amyloidosis 306
Chapter 23 - Pediatric liver disease 308
Key Points 308
Consequences of Physiologic Immaturity of the Liver 308
Hyperbilirubinemia 309
Hepatomegaly 312
Acute Liver Disease 316
Systemic Diseases Affecting the Liver (see Chapter 22) 317
Chapter 24 - Liver disease in the elderly 320
Key Points 320
Cellular and Biochemical Aspects 320
Pathophysiology of the Aging Liver 321
Hepatic Diseases in the Elderly 322
Chapter 25 - Hepatobiliary complications of HIV 332
Key Points 332
Viral Hepatitis and Other Viral Infections 332
Other Infections (see also Chapter 29) 336
Malignant Diseases 337
Nonalcoholic Fatty Liver Disease 338
Antiretroviral-Induced Hepatotoxicity 338
AIDS-Related Biliary Tract Diseases 339
Chapter 26 - Granulomatous liver disease 342
Key Points 342
Pathogenesis of Granulomas 342
Causes of Hepatic Granulomas 343
Clinical Features 343
Specific Types of Granulomatous Liver Disease 346
Therapy 351
Chapter 27 - Hepatic tumors 352
Key Points 352
Benign Tumors of the Liver 352
Malignant Tumors of the Liver 355
Diagnostic Approach to Liver Masses or Tumors 360
Chapter 28 - Hepatic abscesses and cysts 363
Key Points 363
Amebic Liver Abscess 363
Pyogenic Liver Abscess 369
Hepatic Cysts 372
Hydatid Disease of the Liver (Fig. 28.3) 373
Diagnostic Approach to Hepatic Abscesses and Cysts 377
Chapter 29 - Other infections involving the liver 380
Key Points 380
Bacterial Infections Involving the Liver 380
Spirochetal Infections of the Liver 384
Parasitic Diseases that Involve the Liver (Table 29.1) 385
Fungal Liver Disease 400
Chapter 30 - Surgery in the patient with liver disease and postoperative jaundice 403
Key Points 403
Effects of Anesthesia and Surgery on the Liver 403
Estimation of Operative Risk in Patients with Liver Disease 405
Obstructive Jaundice (see Chapters 33 and 34) 411
Hepatic Resection (see Chapter 27) 412
Preoperative Evaluation and Preparation 413
Postoperative Jaundice 416
Chapter 31 - Liver transplantation 420
Key Points 420
Overview 420
Selection of Candidates 421
Donor Selection 425
Major Diseases Considered for Transplantation 426
Exceptional Conditions in Transplant Listing 428
Immunosuppression 430
Post-transplant Complications 431
Chapter 32 - Cholelithiasis and cholecystitis 434
Key Points 434
Classification of Gallstones 434
Pathogenesis 435
Diagnosis 436
Natural History 436
Surgical Treatment 438
Medical Treatment 438
Acute Cholecystitis 439
Acute Acalculous Cholecystitis 441
Postcholecystectomy Problems 442
Biliary Sludge 442
Other Less Common Syndromes Associated with Gallstones 443
Chapter 33 - Diseases of the bile ducts 445
Key Points 445
Bile Duct Stones 445
Postcholecystectomy Problems 451
Postoperative Bile Duct Injuries and Leaks 452
Recurrent Pyogenic Cholangitis 454
Choledochal Cysts 455
Chapter 34 - Tumors of the biliary tract 460
Key Points 460
Benign Tumors of the Gallbladder 460
Benign Tumors of the Bile Duct 461
Carcinoma of the Gallbladder 461
Carcinoma of the Bile Duct (Cholangiocarcinoma) 466
Index 475