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Dear Bandit,

Dr. Berkson's treatment, as I understand it, does make some people feel better when they are symptomatic with joint and muscle aches and pains.

What it exactly does, I do not know. What I DO know is that it does nothing for the eradication of the virus. If it has an anti-fibrotic effect, I have not heard that claim.

The treatment that your husband HAS had very likely improved the condition of his liverr and may even have reduced the fibrosis a bit.

It sounds to me that the problem is that he has lost hope due to the negativity of the doctor and has accepted that he is going to die in the next few years.

That is sad because it is probably untrue from a medical perspective, but it certainly will reduce his overall quality of life if he believes it.

So, I would recommend a second opinion from a doctor who is not associated with the first one (they tend to travel in like- minded flocks in the same practice.)

Your best bet is a university hepatology site.

Your husband is no where near cirrhosis at a stage 2. If he does not drink alcohol, smoke, expose himself to chemicals and noxious fumes, he will probably outlive us all. But, he needs to hear it from an expert that he trusts and respects. That would be my first step if I were in your shoes.

I cannot see Dr. Berkson doing any harm at a stage 2 and if your husband respects and trusts him, it might also do him some good.
The psychological benefits might outweigh the medical ones, but that is still worth an awful lot and should not be discounted.

I hope this helps.



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[This message has been edited by thanbey (edited 05-11-2001).]

Sean has made some very sound points.

Here is a an "ask the experts" response from Jenny Heathcote of University of Toronto, a well respected hepatologist. Some of the key points might interest you. I have no knowledge of Dr. Berksons's treatment other than what I have already posted above.

best wishes,


A 40-year-old white man presented with chronic hepatitis C and mildly elevated aminotransferases 1 year ago. At that time, biopsy showed mild disease activity with periportal fibrosis (grade 2, stage 2). After 1 year of combination therapy with interferon and ribavirin, he had normalization of serum aminotransferases and no associated side effects. Virus is still present, although at a reduced titer. Should this patient be maintained on low-dose combination therapy?

from Jenny Heathcote, MD, 05/10/01
This patient has chronic hepatitis C with mild inflammation and scarring on his liver biopsy. He is a nonresponder to the current "standard" of care for treating hepatitis C virus (HCV) infection.[1] Fortunately, he suffered few side effects from this treatment. Because the patient's viral load is lower at the end of antiviral therapy than it was at baseline, the question arises as to whether the patient would benefit from further therapy.
Currently, there is one well-conducted, relatively small study[2] that supports the concept of continuing antiviral therapy in the presence of persisting viremia. In a series of 53 patients whose liver histology was found to improve at the end of a 6-month course of interferon monotherapy despite remaining viremic (albeit at lower titer), antiviral therapy was continued for an additional 6 months in half of patients. Liver histology continued to improve during that latter 6 months of treatment for this group of patients when compared with that of those whose treatment had been stopped. However, no long-term follow-up biopsies were performed, so we do not know if "catch-up" occurred upon cessation of therapy in those who were treated for 12 months but who remained viremic.

This well-conducted study has prompted the initiation of the Hepatitis C Antiviral Long-term Treatment Against Cirrhosis (HALT-C) trial to evaluate long-term interferon (pegylated) monotherapy in nonresponders to previous antiviral therapy who had severe "background" liver disease. The results of this National Institutes of Health-supported study will not be available for many years. It was not considered appropriate to subject individuals to long-term interferon treatment combined with ribavirin "combination" therapy.

There are, nevertheless, several recommendations for those patients with chronic hepatitis C who are nonresponders to current antiviral therapy. Alcohol intake should be maintained at a minimum because even "social" drinking is associated with enhanced hepatic fibrosis if continued for long periods.[3] And, more recently, it has been recognized that central obesity is associated with more progressive liver disease.[4] Patients are advised to undergo vaccination against hepatitis A and B if they are not already immune. It is important to reassure individuals that the natural progression (with the avoidance of the risk factors discussed) of chronic hepatitis C is very slow. Such individuals should be encouraged to enter trials of therapy involving new agents; otherwise, ongoing treatment is not recommended.

Fortunately, this patient has only mild-to-moderately severe chronic hepatitis C and is unlikely to progress rapidly to more severe disease. It may be advisable to repeat his liver biopsy in 3 years unless at that point in time we have reliable markers of liver fibrosis not requiring biopsy.[5]

EASL International Consensus Conference on Hepatitis C; February 26-28, 1999; Paris, France.

Consensus Statement. European Association for the Study of the Liver. J Hepatol. 1999;30:956-961.

Shiffman ML, Hofmann CM, Contos MJ, et al. A randomized, controlled trial of maintenance interferon therapy for patients with chronic hepatitis C virus and persistent viremia. Gastroenterology. 1999;117:1164-1172.

Poynard T, Bedossa P, Opolon P. Natural history of liver fibrosis progression in patients with chronic hepatitis C. The OBSVIRC, METAVIR, CLINIVIR, and DOSVIRC groups. Lancet. 1997;349:825-832.

Hourigan LF, Macdonald GA, Purdie D, et al. Fibrosis in chronic hepatitis C correlates significantly with body mass index and steatosis. Hepatology. 1999;29:1215-1219.

Imbert-Bismut F, Ratziu V, Pieroni L, et al. Biochemical markers of liver fibrosis in patients with hepatitis C virus infection: a prospective study. Lancet. 2001;357:1069-1075.


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