Hepatitis C virus (HCV) is a bloodborne virus that causes liver inflammation. Many infected individuals show no symptoms at first, but without treatment, the infection can become chronic and lead to cirrhosis or liver cancer over time.
The good news is that modern oral antiviral treatments can cure over 95% of patients within a short duration, with minimal side effects—far better than past treatments.
This article explains everything you need to know about hepatitis C: from how it spreads, symptoms, testing, and treatment options to prevention strategies, based on the latest clinical guidelines from Thailand and international liver associations.
Hepatitis C virus (HCV) is an enveloped, single-stranded RNA virus belonging to the Flaviviridae family. It causes liver inflammation in both acute and chronic stages, and may lead to serious complications such as liver cirrhosis or liver cancer if left untreated.
Most individuals infected with hepatitis C are asymptomatic in the early stages, which makes the infection difficult to detect. It is often discovered incidentally during routine blood tests, preoperative screenings, or blood donation assessments.
HCV is primarily transmitted through blood-to-blood contact. Common routes include sharing needles, receiving unscreened blood transfusions, or undergoing unsafe medical procedures. It is not spread through casual contact such as hugging, kissing, or sharing utensils in daily life.
Hepatitis C virus (HCV) has six major genotypes, labeled Genotype 1 through 6. Each genotype differs in geographical distribution and treatment response.
Today, most patients can be treated effectively with newer DAA regimens that are pangenotypic, meaning they work across all major genotypes. Examples include sofosbuvir/velpatasvir and glecaprevir/pibrentasvir.
Nevertheless, genotyping may still be necessary in certain cases—especially in patients with cirrhosis, chronic kidney disease, or prior treatment failure—to help tailor the most appropriate treatment plan.
There are several types of hepatitis viruses: A (HAV), B (HBV), C (HCV), D (HDV), and E (HEV). Each differs in transmission method, clinical course, and treatment approach.
A key difference is that there is currently no vaccine for HCV, whereas effective vaccines are available for HAV and HBV. HCV is also one of the leading causes of liver transplantation worldwide due to its chronic progression.
Hepatitis C virus (HCV) is primarily transmitted through blood-to-blood contact. Infection occurs when blood from an infected person enters the bloodstream of another individual. Common modes of transmission include:
Sexual transmission is possible, though less common, and is more likely in the presence of open sores, high-risk behaviors, or co-infection with HIV.
HCV is not transmitted through saliva, tears, sweat, food, or casual contact. Everyday interactions such as hugging, kissing, or sharing meals pose no risk unless blood is involved.
Although hepatitis C is primarily transmitted through blood exposure, several behaviors can significantly increase the risk of acquiring the virus, often unknowingly:
Casual contact—such as hugging, sharing utensils, or living in the same household—does not pose a risk for hepatitis C infection.
Most people infected with hepatitis C have no noticeable symptoms in the early stages, making the infection difficult to detect. Symptoms can be classified into two phases:
About 20–30% of patients may experience:
However, over 70% of individuals show no symptoms or only mild, nonspecific signs.
If the infection persists beyond six months without spontaneous clearance, it becomes chronic. Symptoms may take years or even decades to appear:
Some individuals with chronic infection remain asymptomatic until significant liver damage has occurred.
Without timely diagnosis and proper treatment, chronic hepatitis C infection can lead to serious complications affecting both the liver and other organ systems.
This is a condition where healthy liver tissue is progressively replaced by scar tissue (fibrosis), impairing liver function. Common signs include:
Chronic hepatitis C is a major risk factor for liver cancer, especially in patients with cirrhosis. Those left untreated have a significantly increased lifetime risk of developing HCC.
Beyond the liver, HCV can be linked to systemic issues such as:
Because hepatitis C is often asymptomatic in its early stages, screening plays a critical role in identifying undiagnosed infections.
Current guidelines from the World Health Organization (WHO), U.S. Centers for Disease Control and Prevention (CDC), and various liver societies recommend testing the following groups:
HCV testing is simple and typically requires only a single blood draw. If the result is positive, further testing will confirm the infection and guide treatment decisions.
Diagnosing hepatitis C involves a two-step process: initial screening and confirmation of active infection
This test detects antibodies to the hepatitis C virus in the blood. A positive result indicates that the person has been exposed to HCV, but does not confirm whether the infection is still active.
If Anti-HCV is positive, a follow-up test—either HCV RNA or PCR—is needed to check for the actual presence of the virus.
Detection of HCV RNA confirms an active (ongoing) infection.
Test Type |
What it detects |
Meaning of a positive result |
Anti-HCV |
Antibodies to HCV |
Past or current exposure to HCV |
HCV RNA / PCR |
Viral genetic material |
Ongoing infection is present |
If active infection is confirmed, additional assessments such as liver enzymes (ALT, AST), FibroScan, and treatment planning will follow.
For most hepatitis C tests, such as Anti-HCV or HCV RNA (PCR), fasting is not required. These are standard blood tests that are not affected by food or drink.
However, if your doctor has ordered additional tests—such as fasting blood sugar, cholesterol, or a full liver panel— you may be instructed to fast for 8 to 12 hours beforehand.
The best approach is to check with your healthcare provider or lab ahead of time to confirm any pre-test instructions.
FibroScan, also known as Transient Elastography, is a non-invasive technology that uses low-frequency sound waves to measure liver stiffness. It helps assess the extent of liver fibrosis or cirrhosis without the need for a traditional liver biopsy.
The device sends sound waves through the skin over the right upper abdomen. The speed at which the waves bounce back is measured—faster waves indicate stiffer (more fibrotic) liver tissue. Results are shown in kilopascals (kPa).
Historically, hepatitis C treatment involved injectable interferon combined with oral ribavirin. This approach had limited effectiveness, significant side effects, and required long durations (6–12 months).
Today, treatment has shifted to Direct-Acting Antivirals (DAAs)—oral medications that directly inhibit the virus, delivering superior outcomes.
Treatment Aspect |
Interferon/Ribavirin |
New DAAs |
Medication form |
Injection + oral |
Oral only |
Treatment duration |
24–48 weeks |
8–12 weeks (sometimes shorter) |
Cure rate (SVR) |
50–70% |
Over 95% |
Side effects |
Fever, chills, depression |
Minimal (e.g., mild fatigue) |
Suitability |
Requires strong health |
Safe for most patient groups |
Modern DAAs are now the standard of care, especially pangenotypic options like sofosbuvir/velpatasvir or glecaprevir/pibrentasvir—effective and convenient for a broad range of patients.
Direct-Acting Antivirals (DAAs) are medications that target specific proteins or enzymes critical to the hepatitis C virus lifecycle. They disrupt the virus’s ability to replicate and produce new viral particles.
These combinations are effective across all major HCV genotypes (1–6) and achieve cure rates above 95%.
Treatment duration for hepatitis C using Direct-Acting Antivirals (DAAs) typically ranges from 8 to 12 weeks, depending on factors such as:
Patient Group |
Treatment Duration (Weeks) |
No cirrhosis, treatment-naïve |
8 weeks |
Compensated cirrhosis |
12 weeks |
Failed prior interferon-based therapy |
≥12 weeks (based on regimen) |
Certain cases—such as co-infections or special populations—may require adjustments in regimen and duration. Final decisions are based on guidelines from ThaiLiver, AASLD, or EASL.
SVR, or Sustained Virologic Response, is the primary goal of hepatitis C treatment. It is defined as having no detectable HCV RNA in the blood 12 weeks after completing antiviral therapy—indicating a clinical cure with minimal risk of relapse.
Today’s newer DAAs allow 95–99% of patients to achieve SVR, with minimal side effects and without injections.
Even after achieving viral clearance (SVR), post-treatment follow-up remains important to prevent complications and detect possible reinfection—especially in high-risk individuals.
Patients diagnosed with hepatitis C should seek care at facilities equipped with specialists in gastroenterology or hepatology, and access to standardized lab testing and follow-up systems.
The cost of hepatitis C treatment varies depending on the healthcare facility, type of medication, and the patient’s insurance coverage.
In general, expenses fall into three main categories:
Although there is currently no vaccine for hepatitis C, the infection can be prevented by avoiding high-risk behaviors and practicing strict hygiene measures.
Currently, there is no approved vaccine for hepatitis C available for human use. Despite ongoing research, no candidate has yet demonstrated sufficient efficacy in clinical trials.
Although there is no vaccine for hepatitis C, it is recommended that individuals with HCV receive vaccines for hepatitis A (HAV) and hepatitis B (HBV).
Co-infection with HAV or HBV can worsen liver inflammation and significantly increase the risk of complications like acute liver failure.
Pregnant women infected with hepatitis C should be co-managed by an obstetrician and a liver specialist. While HCV typically does not harm fetal development, there is an estimated 5–6% risk of mother-to-child transmission.
Hepatitis C in children and adolescents is less common than in adults but may result from vertical transmission or past blood exposure. While general care principles are similar to adults, there are important differences in medication choice and monitoring.
Although Direct-Acting Antivirals (DAAs) can achieve a clinical cure (SVR),
clearing hepatitis C once does not provide lifelong immunity.
Therefore, reinfection is possible if the individual is exposed to the virus again.
Hepatitis C virus (HCV) often causes no symptoms in its early stages, leading many individuals to remain undiagnosed. Without treatment, it can progress to chronic infection and cause severe complications such as cirrhosis, liver cancer, and liver failure.
A: No. HCV is not transmitted via saliva or shared utensils. It spreads only through direct blood-to-blood contact.
A: No. Individuals with current or past HCV infection should not donate blood or organs to prevent transmission.
A: Repeat HCV RNA testing at 12 weeks post-treatment to confirm SVR. If cirrhosis is present, continue ultrasound and AFP every 6 months.
A: Risk is very low without direct blood contact. Still, avoid sharing sharp personal items like nail clippers or razors.
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