Hi, amanat-
The amount of fibrosis (scarring) that occurs in the liver as a result of HCV is best determined by needle biopsy. A needle is inserted through the skin and a small sample of tissue is then examined under a microscope.
Using the Metavir scale, a pathologist will determine the amount of cellular inflammation as well as fibrosis. The pathologist will report fibrosis on a scale of F0 through F4 with F4 indicating cirrhosis.
I don’t know what diagnostic resources are available to you in Pakistan. The liver biopsy is an invasive surgical procedure, and is considered the ‘gold standard’ for this purpose.
Other options are blood tests:
Fibrosure
http://www.ncbi.nlm.nih.gov/pubmed/15723588
Fibrospect
http://www.ncbi.nlm.nih.gov/pubmed/16970596
However, while these are both non-invasive, they are not as accurate as liver biopsy. Another option in some countries is Echosens Fibroscan:
http://www.hivandhepatitis.com/hep_c/news/2007/121107_d.html
Fibroscan measures liver stiffness via sound waves, and approximates the degree of fibrosis. Be sure to discuss these options with your doctor, and see what fits your needs.
Good luck,
--Bill
Thanks for ur reply. will u please tell me how i can get information about the stage of my disease. my liver condition and chances of recovery.
Once again thank u very much for this kindness
Yes, we understand; cost is often a consideration in HCV management. Many people here in the U.S. purchase health insurance; but those that can not afford insurance can not afford treatment either. A standard course of HCV therapy (peginterferon/ribavirin, lab costs, doctor visits) here in the U.S. costs in excess of USD $ 60,000 (PKR 5,121,000.00).
Depending on your previous response profile, Infergen might be an option; for true null responders there are few viable options at this time.
Good luck and take care-
Bill
Thanks A lot all of u who take my problem seriously . my virus type is 3a and viral load is 122662IU/ml(306655 copies/ml). I am in pakistan where new research and medicine are not available to common people . one year before a doctor says that he will import a mediciene name Infergen 15mg from america for me it costs 433 us dollar which was out of my range. will u please help me what shoud i do now
Bad info by doctors should be a crime, its a good thing you are coming here to ask questions.
Yes find a gastroenterologist who has experience with hep c, there are some great drugs coming down the pike and people who want to help. Keep looking for the right information and the right people to lead you there.
"now doctor says that there is no treatment for my disease". At least half the people who try treatment who are genotype 1 are non responders.
GOOD NEWS!!!
Luckily your doctor is absolutely wrong!!!
Many people on this forum have treated multiple times before clearing the virus.
Get a referral to see an experienced gastroenterologist who has successfully treated many hep c patients and is current with the latest developments with treating hep c patients. They will help you.
I feel sorry for the docs other patients as he is giving out false information.
Hectorsf
If you are a genotype 3, unfortunately the new drugs (protease inhibitors) expected to be released sometime soon are ineffective on genotype 3. On the other hand, the polymerase inhibitors currently being used in trials have shown to be effective with all genotypes so don't give up hope. They are working on drugs that will cure you.
Trinity
Read about the new drugs that should be out by the summertime hopefully. Hoping they will give you a much better chance.
Telapravir & Bocepravir are their names.