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Hepatitis C
, HCV Infection
See Also
Hepatitis C Antiviral Regimen
Viral Hepatitis
Bloodborne Pathogen Exposure
Epidemiology
Mortality from Hepatitis C in the United States is more than any other infectious disease
Effective treatment exists for those diagnosed, but many are undiagnosed
Only 52% of estimated patients with Hepatitis C in U.S. have been diagnosed
Only 37% of Hepatitis C patients have been diagnosed
Worldwide, only 5% have been diagnosed, and <1% have been treated
Chhatwai (2019) Aliment Pharmacol Ther 50(1): 66-74 [PubMed]
Prevalence
U.S. Population: 1.8% (4 to 6.5 million)
Chronic hepatitis
Prevalence
is estimated at 3.7 million (2016)
Prevalence
is underestimated
Undiagnosed patients infected in the 1960s and 1970s
Opioid
epidemic quadrupled acute infection rate ages 18-39 years from 2010 to 2018
World
Prevalence
estimated at >185 million
Associated with 350,000 deaths per year
Intravenous Drug Abuse
: 97% (some communities)
Pathophysiology
Incubation 7-8 weeks
HCV RNA found in blood within 3 weeks post-exposure
Transmission by
Blood Product
s and blood exposure
Intravenous Drug Abuse
(43-60% of acute cases in U.S.)
Intravenous Immunoglobulin
Transfusion
Accounts for 85% transfusion associated hepatitis
Clotting Factor
transfusion before 1987
Blood Product Transfusion
before 1992
Risk from transfusion low after July 1992
Now <1 case per 1,000,000 units transfused (2015)
Tattoo
needles
Organ transplant (before July 1992)
Longterm
Hemodialysis
Vertical transmission from mother to child
Delivery method does not alter transmission rate
Average rate: 6%
HIV coinfection: 17%
Needle Stick
injury (4-10% rate of
Infectivity
)
Seroconversion in 2200 healthcare workers per year
No apparent
Parenteral
risk factor in 40% of cases
Transmission by other body fluid is less common
Transmission to simple household contacts is rare
No association with
Lactation
Sexual transmission is much less common
Prevalence
1.5% in longterm partners
Higher risk behaviors that raise transmission (blood to blood transmission)
Multiple partners
Early sex
Non-
Condom
use
Sex with associated
Trauma
or open lesions
Comorbid
Sexually Transmitted Disease
Men who have Sex with Men
(esp. if HIV positive)
Anal intercourse
Sex during
Menses
Shared sexual paraphernalia
Pathophysiology
Similar to
Flavivirus
with RNA genome
Similar viruses
Yellow Fever
virus
Dengue
Virus
Findings
Signs and Symptoms
Acute infection
See
Viral Hepatitis
Asymptomatic in up to 70-80% of cases
Symptoms in up to 35% of acute HCV Infection cases (onset 2 to 12 weeks after exposure)
Malaise
Weakness
Anorexia
Minor
Fatigue
Jaundice
(uncommon in acute infection)
Right Upper Quadrant Abdominal Pain
or ache
Nausea
Arthralgia
s
Chronic disease
Most patients are asymptomatic
Observe for signs of
Cirrhosis
Differential Diagnosis
Acute Hepatitis Causes
History
Screening Indications
Universal screening for Hepatitis C age 18 to 79 years old at least once, regardless of risk factors (U.S., 2019)
Screen all pregnant patients
Screen once all patients born between 1945 and 1965 for Hepatitic C
Screen periodically (up to annually) for continued high risk behavior
Intravenous Drug Abuse
HIV positive
Men who have Sex with Men
(unprotected)
Other screening indications
Received blood
Clotting Factor
concentrate before 1987
Received
Blood Transfusion
or transplant before 1993
Received blood from donor later found with HCV
Received
Hemodialysis
Symptoms or signs of liver disease, or persistently elevated serum transaminases
Mother with HCV at the time of delivery
Labs
Diagnosis
See
Hepatitis C Serology
Hepatitis C Antibody
Detection
Detectable 4 to 10 weeks after exposure
Positive in 97% of HCV Infections at 6 months
Screening:
EIA for Anti-HCV
Antibody
Third generation enzyme linked immunoabsorbent assay
Test Sensitivity
and
Test Specificity
: 99%
Negative
Consider
False Negative
if
Immunocompromised
Repeat in 12 weeks if HCV exposure in prior 6 months
Alternatively, HCV RNA may be obtained every 4-8 weeks for 6 months
Positive
Confirm with HCV RNA (see below)
Screening: OraQuick HCV Rapid
Antibody
Test
CLIA Waved point-of-care test
Test Sensitivity
: 94.1%
Test Specificity
: 99.5%
Negative Predictive Value
: 99.9%
Positive Predictive Value
: 72.7%
Confirmation of positive xHCV:
RT-PCR for HCV RNA
HCV RNA indicates acute infection (present as early as 2 weeks after exposure)
Start with qualitative PCR (more sensitive)
Positive EIA xHCV with negative PCR HCV RNA suggests resolved
Repeat in 1-2 months if negative
Also indicated before initiating HCV therapy
Viral
Genotype
Indicated before initiating HCV therapy
Of 6 HCV
Genotype
s, types Ia, Ib, 2 and 3 account for 97% of U.S. HCV Infections
HCV
Genotype
s 2 and 3 have better prognosis than HCV
Genotype
1
Labs
Assessment of liver disease
Liver Function Test
s
Serum Albumin
ProTime
(PT) with INR
Partial Thromboplastin Time
(PTT)
Liver
Transaminase (Indicate hepatocellular necrosis)
Serum AST
Serum ALT
Increases by 8 to 10 weeks (range 2 to 21 weeks, mean 7 weeks) from onset
Peak at 10 to 20 times normal upper limit
Normal in up to one third of patients
Comorbid Infections
Human Immunodeficiency Virus
Test (
HIV Test
)
Anti-HAV (
Hepatitis A Virus
Antibody
)
Hepatitis B Surface Antigen
(
HBsAg
)
Other tests
Serum Iron
(for
Hemochromatosis
)
Renal Function
Tests
Serum Creatinine
Blood Urea Nitrogen
(BUN)
Labs
Post-exposure to Hepatitis C
Virus
Indications
Blood-borne Exposure to Hepatitis C positive source (xHCV positive with detectable HCV RNA)
Protocol
Baseline (at time of exposure)
Hepatitis C Antibody
Hepatitis C RNA
Alanine
Transaminase (ALT)
Week 4-6 post-exposure
Hepatitis C RNA
Month 4-6 post-exposure
Hepatitis C Antibody
Hepatitis C RNA
Alanine
Transaminase (ALT)
Evaluation
Grading
See
Metavir Scoring System
(
Liver Fibrosis
,
Cirrhosis
)
Imaging (and advanced labs) to evaluate for fibrosis or
Cirrhosis
See
Cirrhosis
for interpretation
Transient Elastography and AST to
Platelet
Ratio Index
Fibrosis-4
Fibrosure
Management
Gene
ral
See
Prevention of Liver Disease Progression
Avoid
Alcohol
Alcohol
and Hepatitis C work synergistically
Alcohol
decreases response to
Interferon
therapy
Avoid
Hepatotoxin
s
Chemical Dependency
treatment for injection drug use (if indicated)
Avoid iron supplements
Maintain a
Low Fat Diet
Maintain a target
Body Mass Index
<25 kg/m2
Target a
Low Sodium Diet
<2000 mg/day
Vaccination
(decreases Hepatitis C progression risk)
Hepatitis A Vaccine
Hepatitis B Vaccine
Pneumococcal Vaccine
and
Prevnar
Vaccine
Prevent transmission
Do not share razors or
ToothBrush
es
Cover skin lesions
Do not donate
Blood Product
s
Use
Condom
protection for intercourse (esp. for multiple partners,
Men who have Sex with Men
)
Management
Antiviral Agent
s
See
Hepatitis C Antiviral Regimen
Consider early treatment for
Acute Hepatitis
C (started within 4 weeks of onset)
Improves prognosis and decreases risk of chronic infection
Wiegand (2006) Hepatology 43(2): 250-6 [PubMed]
Management
HCV-Related
Cirrhosis
Refer for consideration of
Liver Transplant
ation (see below)
Hepatocellular Carcinoma
monitoring
Obtain
RUQ Ultrasound
and a-fetoprotein every 6-12 months
Esophageal Varices
monitoring
Obtain upper endoscopy every 1-2 years
Management
Liver Transplant
ation
Hepatitis C is most common cause of
Liver Transplant
Post-transplant survival similar to other liver failure
One year survival post-transplant: 84%
Five year survival post-transplant: 68%
Ten year survival post-transplant: 60%
Predictors of poorer outcome
Female liver donor
Recipient over age 52 years
Preoperative
Serum Creatinine
>1 mg/dl
More urgent UNOS status
Increased
Serum AST
and
Serum ALT
levels
References
Ghobrial (2001) Ann Surg 234:384-94 [PubMed]
Complications
Cirrhosis
(20 to 30% in 25 to 30 years)
Individualized risk can be calculated (see below)
Decompensated
Cirrhosis
(
Ascites
,
Hepatic Encephalopathy
,
Portal Hypertension
,
Varices
)
One Year: 3.9%
Five Years: 18%
Ten Years: 29%
Hepatocellular Carcinoma
Annual risk: 2-4% if
Cirrhosis
present
Five Years: 7%
Ten Years: 14%
Other associated conditions (Extrahepatic Manifestations)
Diabetes Mellitus
(four fold increased risk)
Membranoproliferative
Glomerulonephritis
Idiopathic Pulmonary Fibrosis
Thyroid
Disorders (
Hypothyroidism
,
Hyperthyroidism
,
Thyroiditis
)
Vascular Disease
Cardiovascular Disease (
Coronary Artery Disease
)
Cerebrovascular Disease
Rheumatologic and Autoimmune
Sjogren's Syndrome
Rheumatoid Arthritis
Cryoglobulinemic
Vasculitis
Dermatologic conditions
Porphyria cutanea tarda
Lichen Planus
Cutaneous necrotizing
Vasculitis
Raynaud Phenomenon
Necrolytic Acral Erythema
Malignancy
B-Cell
Non-Hodgkin Lymphoma
Monoclonal Gammopathy
Course
Progression after acute HCV Infection
Spontaneous resolution: 15-45% of cases
HCV RNA undetectable at 6 months after acute HCV
Decreased chance of spontaneous clearance in
HIV Infection
Factors favoring spontaneous clearance and resolution
Younger age
Jaundice
Increase
Alanine
transaminase level
HBsAg
positive
Female gender
HCV
Genotype
1
Specific host genes (e.g. IL28 gene)
Chronic Hepatitis: 50 to 85% of cases
HCV RNA present >6 months after acute HCV Infection
Cirrhosis
develops in 20% of chronic HCV after 20-30 years, with a 75% mortality
Chronic HCV mortality is secondary to
Cirrhosis
, end-stage liver disease and hepatocellular cancer
Survival
One Year: 96%
Five Years: 91%
Ten Years: 79%
Risk Factors for Progression to fibrosis and
Cirrhosis
Age over 40 to years at time of infection
Duration of infection
Median duration of infection to
Cirrhosis
: 30 years
In up to one third,
Cirrhosis
delayed for >50 years
Male gender
Excessive
Alcohol
intake
Marked risk at >50 grams/day
Moderate risk
Men: >40 grams/day
Women: >20 grams/day (2 beers, 1 pint wine)
Other risk factors
HIV Infection
Hepatitis B
Virus
Infection
Immunosuppression
Obesity
Hepatotoxic Medication
s
Nonalcoholic Steatohepatitis
Resources
IDSA HCV Management Guidelines
http://www.hcvguidelines.org
Probablility of
Cirrhosis
in Patients with Hepatitis C
http://www.aafp.org/afp/20031101/poc.html
References
Gross (1998) Mayo Clin Proc 73(4):355-60 [PubMed]
Maness (2021) Am Fam Physician 104(6): 626-35 [PubMed]
Morton (1998) Ann Emerg Med 31:381-90 [PubMed]
Heathcote (2000) N Engl J Med 343:1673-80 [PubMed]
Ward (2004) Am Fam Physician 69(6):1429-40 [PubMed]
Wilkins (2015) Am Fam Physician 91(12): 835-42 [PubMed]
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