Hepatitis B virus mutant strains
Hello, doctor.
I have been undergoing blood tests for nearly eight months, and my liver enzymes have changed from GOT 90, GPT 148 to GOT 120, GPT 256.
During this time, the doctor said the ultrasound was normal.
Finally, I tested positive for Hepatitis B DNA (HBV-DNA), and the doctor confirmed it is a mutant strain of the Hepatitis B virus.
The doctor prescribed Tenofovir (Zeffix 100mg/tab), to be taken once a day, but this medication is not covered by health insurance and must be paid out of pocket.
Why is that? The doctor assured me that taking this medication would definitely lower my liver enzymes, but after two weeks of taking it, my liver enzymes have not decreased; in fact, they have increased.
Why is this happening? This has made me lose confidence in the doctor's expertise.
Will my condition improve?
Guozi, 30~39 year old female. Ask Date: 2004/08/31
Dr. Xu Jinchuan reply Gastroenterology and Hepatology
Hello! 1.
According to the National Health Insurance Administration's criteria for reimbursement of treatment for Hepatitis B and C, it is stipulated that HBsAg (positive) must be present for more than six months and HBeAg (positive) for more than three months, with ALT levels at or above five times the upper limit of normal (ALT ≥ 5X), and without decompensated liver function.
Under these conditions, full reimbursement is possible.
However, if your condition is due to a mutation of Hepatitis B, reimbursement from the National Health Insurance requires a liver biopsy, and a report from the biopsy is necessary (this was approved on August 1 of this year).
Therefore, if you do not wish to undergo a liver biopsy, you will need to pay out of pocket.
2.
Generally, it takes 4 to 5 weeks of taking Tenofovir (干安能) for liver function to show improvement.
You have only been on it for two weeks, so it is too early to see any effects; further observation is needed.
Reply Date: 2004/08/31
More Info
Understanding Hepatitis B Mutant Strains: Treatment Challenges and Concerns
Hepatitis B virus (HBV) infection is a significant global health issue, with millions of people affected worldwide. The emergence of mutant strains of HBV presents unique challenges in treatment and management. Your situation, characterized by elevated liver enzymes and the identification of a mutant strain, raises several important considerations regarding treatment efficacy and the potential for disease progression.
Firstly, it is essential to understand that the treatment of chronic hepatitis B typically involves antiviral medications aimed at suppressing viral replication. The most commonly used antiviral agents include nucleos(t)ide analogs such as Lamivudine, Adefovir, Entecavir, and Tenofovir. These medications can effectively reduce viral load and improve liver function in many patients. However, the presence of mutant strains can complicate treatment. Mutant strains may exhibit resistance to certain antiviral medications, leading to suboptimal responses and continued liver inflammation.
In your case, the use of Zeffix (Lamivudine) has not resulted in the expected decrease in liver enzyme levels. This could be due to several factors. One possibility is that the specific mutant strain of HBV you are infected with has developed resistance to Lamivudine. Resistance mutations can occur when the virus replicates in the presence of antiviral drugs, allowing it to survive and continue to replicate despite treatment. This phenomenon is particularly common with Lamivudine, which is why it is often not the first choice for treatment in patients with known resistance.
Another factor to consider is the timing of the treatment. Antiviral medications may take time to show their effects, and liver enzyme levels can fluctuate due to various reasons, including ongoing liver inflammation or other underlying conditions. It is also important to note that the initial rise in liver enzymes after starting treatment does not always indicate treatment failure; it may reflect a transient response as the liver begins to heal.
Regarding your concerns about the cost of the medication and the lack of insurance coverage, this is a common issue faced by many patients with chronic hepatitis B. The criteria for insurance coverage can vary significantly based on the specific health care system and the guidelines established for treatment eligibility. In many cases, antiviral medications are covered when certain clinical criteria are met, such as elevated liver enzymes or significant liver fibrosis. If your condition does not meet these criteria, you may be required to pay out-of-pocket for your medications.
It is understandable to feel frustrated and lose confidence in your healthcare provider when treatment does not yield the expected results. However, it is crucial to maintain open communication with your physician. Discuss your concerns about the treatment plan, the potential for resistance, and the possibility of switching to a different antiviral agent, such as Tenofovir, which has a higher barrier to resistance and is often more effective against mutant strains of HBV.
In conclusion, managing hepatitis B, particularly with mutant strains, requires a comprehensive approach that includes regular monitoring of liver function, viral load, and potential resistance patterns. If your current treatment is not effective, it may be beneficial to seek a second opinion from a hepatologist or a specialist in infectious diseases who has experience with hepatitis B management. They can provide further insights into your treatment options and help you navigate the complexities of your condition. Remember, the goal of treatment is not only to reduce liver enzymes but also to prevent long-term complications such as liver cirrhosis and hepatocellular carcinoma.
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