Menu Expand
Diagnosis and Management of Chronic Liver Diseases, An Issue of Medical Clinics, E-Book

Diagnosis and Management of Chronic Liver Diseases, An Issue of Medical Clinics, E-Book

Anne M. Larson

(2014)

Additional Information

Abstract

Chronic liver diseases progressively destruct liver tissue, leading to fibrosis and cirrhosis. Liver diseases can be caused by viral, autoimmune, or toxic (drugs/alcohol). Most conditions can be managed pharmacologically for indefinite periods of time. The articles in this issue will review best practices for managing and treating patients who present with these chronic problems, like hepatitis, nonalcoholic fatty liver, end stage liver disease, and drug-induced injuries.

Table of Contents

Section Title Page Action Price
Front Cover Cover
Diagnosis andManagement of Chronic Liver Diseases\r i
Copyright\r ii
Medical Clinics Of North America\r v
Contributors vii
Contents ix
Foreword xiii
Preface xv
Evaluation of Abnormal Liver Tests 1
Key points 1
Introduction 1
Markers of hepatocellular injury 2
Aminotransferases 2
Cholestasis 5
Alkaline phosphatase 5
γ-glutamyltransferase 9
5′ nucleotidase 9
Tests of liver metabolism: total bilirubin 9
Tests of liver synthetic function 12
Noninvasive markers of fibrosis 12
Approach to patient evaluation and diagnosis 12
Summary 14
Acknowledgments 14
References 15
An Overview of Emerging Therapies for the Treatment of Chronic Hepatitis C 17
Key points 17
Hepatitis C life cycle and therapeutic targets 18
Protease (NS3/4A) inhibitors 18
Telaprevir 20
Phase 2 studies of telaprevir for treatment-naive patients 20
PROVE 1 20
PROVE 2 20
Phase 2 studies of telaprevir for treatment-experienced patients 21
PROVE 3 21
Alternative telaprevir dosing regimens 21
Phase 3 studies of telaprevir 22
Telaprevir for Treatment-naive Patients 22
ADVANCE 22
ILLUMINATE 23
Telaprevir for Treatment-experienced Patients Who Failed to Achieve SVR with Previous Peg-IFN-α and Ribavirin Therapy 23
REALIZE 23
Telaprevir long-term study 24
EXTEND 24
Boceprevir 24
Phase 2 study of boceprevir for treatment-naive patients 25
SPRINT 1 25
Phase 3 studies of boceprevir 25
Boceprevir for Treatment-naive Patients 25
SPRINT 2 25
Boceprevir for Treatment-experienced Patients Who Had Partial or Relapse Responses to Treatment with Previous Peg-IFN-α and ... 26
RESPOND 2 26
Predictors of SVR in SPRINT-2 and RESPOND-2 27
Viral resistance to linear NS3 protease inhibitors telaprevir and boceprevir 27
Second-generation NS3 protease inhibitors 28
NS5B polymerase inhibitors 28
NIs 28
NNIs 30
NS5A inhibitors 31
Strategies to prevent resistance to DAAs 31
Combination therapies 32
Other antiviral therapeutics 33
Pegylated IFN-λ 33
Cyclophilin Inhibitors 33
Caspase inhibitors 34
Therapeutic vaccine GI-5005 34
Matrix metalloprotease inhibitors 35
Summary 35
References 35
Chronic Hepatitis B Virus Infection 39
Key points 39
Introduction 39
Epidemiology of HBV and screening for patients with chronic HBV infection 39
Prevalence of HBV Worldwide and Whom to Screen for HBV in Developed Countries 39
Risk of Developing Chronic HBV After Acute Infection 40
Natural History of Chronic HBV 40
HBV Genotypes 44
Management of chronic HBV 44
Routine Monitoring of Patients with Chronic HBV 45
Use of Liver Biopsy 46
Selection of Treatment Candidates and Criteria 47
Choice of Antiviral Medications for Chronic HBV 47
Length of Antiviral Treatment in Patients on Oral Antiviral Medications 48
Special considerations 48
HBV/HDV Coinfection 48
HBV/HIV Coinfection 49
HBV/HCV Coinfection 49
Reactivation of HBV with Cancer Chemotherapy or Immunosuppressive Therapy 49
Management of HBV After Liver Transplantation 50
Screening for HCC 50
The Health Care Worker with Chronic HBV Infection 50
Summary 51
References 51
Review of Treatment Options for Nonalcoholic Fatty Liver Disease 55
Key points 55
Introduction 55
Epidemiology 56
Definition and natural history 57
Associations and pathogenesis 57
Clinical manifestations and diagnosis 58
Treatment 59
Lifestyle modifications 60
Bariatric surgery 62
Pharmacologic agents 63
Weight Loss Medications 63
Insulin Sensitizing Agents 63
Lipid-Lowering Agents 64
Antioxidants 64
Cytoprotective Agents 65
New Therapeutics of Interest 65
Summary 66
References 66
Cholestatic Liver Disease 73
Key points 73
Introduction 73
Diagnosis and management 73
Symptoms 73
Diagnosis 74
Differential Diagnosis 75
Management 78
Primary Biliary Cirrhosis 78
Primary Sclerosing Cholangitis 78
Pruritus 78
Fatigue 79
Osteoporosis 79
Vitamin Deficiency 80
Dyslipidemia 80
Portal Hypertension 80
Malignancy 81
Summary 81
References 81
Metal Storage Disorders 87
Key points 87
Introduction 87
Hereditary hemochromatosis 88
Diagnosis 88
Clinical features 89
Biochemical testing 89
Genetic testing 89
Hepatic iron concentration 90
Treatment 91
Survival and Screening 92
Wilson disease 93
Diagnosis 93
Clinical presentation 93
Laboratory testing 94
Liver biopsy 95
Genetic testing 95
Treatment 96
Transplant and Survival 97
References 97
Hepatocellular Carcinoma and Other Liver Lesions 103
Key points 103
Introduction 103
Risk factors 104
Surveillance 104
Diagnosis and staging 105
Symptoms 106
Differential diagnosis 107
Malignant Lesions 107
Benign Lesions 107
Management and treatment 109
Early-stage HCC 109
Intermediate-stage HCC 110
Advanced-stage HCC 112
Multidisciplinary Management 112
Summary and future considerations 112
References 113
Management of End-stage Liver Disease 119
Key points 119
Introduction 119
Ascites 120
Evaluation of Ascites 120
History and physical examination 120
Diagnostic and therapeutic paracentesis 120
Initial evaluation of cause of ascites 120
Albumin and total protein 120
Cell count and cultures 122
Other tests 122
Persistent ascites caused by cirrhosis 122
Basic Management of Ascites 122
Treatment of the underlying disorder 122
Dietary sodium restriction 122
Fluid restriction 123
Diuretics 123
Medications to be avoided 123
Management of tense ascites 123
Management of Refractory Ascites 123
Serial large-volume therapeutic paracenteses 123
Albumin infusions with therapeutic paracentesis 124
Transjugular intrahepatic portosystemic shunt 124
Contraindications 124
Outcome after TIPS 124
Peritoneovenous shunts 124
Complications Associated with Ascites 125
Spontaneous Bacterial Peritonitis 125
Indications for testing 125
Diagnostic criteria 125
Distinguishing from secondary bacterial peritonitis 126
Criteria for treatment 127
Treatment regimens 127
Adjunctive IV albumin 128
Secondary prophylaxis of SBP 128
Primary prophylaxis of SBP 129
Primary and secondary SBP prophylaxis 129
Gastrointestinal hemorrhage 129
Infection prophylaxis after gastrointestinal hemorrhage 129
Dilutional Hyponatremia 130
Hepatorenal Syndrome 130
Diagnostic criteria for HRS 131
Umbilical Hernia 132
Hepatic Hydrothorax 132
Varices 132
Pathophysiology and Portal Dynamics 132
Hepatic Venous Pressure Gradient 132
Indications and Methods for Variceal Screening 133
Variceal screening 133
Special circumstances 133
Preprimary and Primary Prophylaxis of Variceal Bleeding 133
Absence of varices 133
Small esophageal varices 133
Large esophageal varices 133
Treatment of Acute Variceal Bleeding 134
General management 134
Pharmacologic therapy 135
When to Consider Liver Transplant During the Management of Chronic Liver Disease 153
Key points 153
Introduction 153
Keeping an eye on transplant timing during long-term management of cirrhosis 154
Goals and success of liver transplantation 155
Disparities in the use of liver transplantation 156
Indications for liver transplantation 156
Absolute contraindications to liver transplantation 156
Cardiac and Pulmonary Diseases 156
Sepsis or Active Infection 158
Extrahepatic Malignancy 158
AIDS-Defining Illness or Poorly Controlled Human Immunodeficiency Virus 158
Inadequate Social Support 158
Active Substance Use 158
Relative contraindications to liver transplantation 158
Advanced Age 158
Obesity 158
HIV Infection 159
Malnutrition 159
History of Poor Medical Adherence 159
Importance of timing of initial referral 159
Timing Based on Severity of End-Stage Liver Disease 159
Model for End-Stage Liver Disease Score 159
Child-Turcotte-Pugh Score 161
Evidence of Decompensated Cirrhosis 162
Timing based on the specific underlying liver disease 162
Hepatocellular Carcinoma 162
Cholangiocarcinoma 163
Primary Biliary Cirrhosis and Primary Sclerosing Cholangitis 163
Roles for the referring physician in optimizing patients for transplant referral 163
Summary 164
References 165
Index 169