June 1998 - hepc.bull

Canada's Hepatitis C Newsletter

 

HeCSC VICTORIA VOLUNTEERS NEEDED

Volunteers are needed for fundraising for the Victoria Chapter of HeCSC. If you are interested, please contact Judith Fry at 592-0252.

Volunteers are needed to make ribbons. Please call Judith Fry at 592-0252.


If you would like to volunteer for the Fun Run, please call the office (388-4311) and leave a message for Fatima Jones. We need muffins, bought or home- made, and we need people to man the tables.

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Eur J Gastroenterol Hepatol 1998 Feb;10(2):125-131

Effects of interferon therapy on fibrosis serum markers in HCV- positive chronic liver disease.

Mazzoran L, Tamaro G, Mangiarotti MA, Marchi P, Baracetti S, Gerini U, Fanni-Cannelles M, Zorat F, Pozzato G

Istituto di Medicina Clinica, University School of Medicine, Trieste, Italy.

OBJECTIVE: To evaluate serum levels of prolyl- hydroxylase and helical domain of Type IV collagen, markers of hepatic fibrogenesis, in patients with HCV- positive chronic liver disease and the effects of interferon therapy on these markers.

DESIGN: Prolyl-hydroxylase and Type IV collagen were determined before therapy and each month during the treatment and follow-up.

METHODS: Fifty-seven HCV-positive patients were studied. All the subjects received alpha2a recombinant interferon, 6 MU subcutaneously three times a week for 4 weeks, followed by 3 MU thrice weekly for 5 months. After cessation of treatment, each patient was followed for 12 months. Prolyl-hydroxylase and helical domain of Type IV collagen were measured by using immunoenzymatic methods. HCV-RNA and HCV genotype were determined according to the method of Okamoto.

RESULTS: In the patients prolyl-hydroxylase (39.8+/- 8.9 ng/ml) was not different from controls (39.1+/-5.9 ng/ml). On the contrary, the patients showed a mean Type IV collagen (133.6+/-93.3 ng/ml) significantly (P < 0.01) higher than controls (100.2+/-10.5 ng/ml). A good relationship between the degree of liver fibrosis and the Type IV collagen serum level was found (r = 0.68; P < 0.005). In both responders and non- responders the Type IV collagen levels decreased during interferon therapy. During the follow-up, in responders the Type IV collagen did not show modifications, while in non-responders/relapsers it returned rapidly to the pretreatment levels (139.1+/- 100.7 ng/ml).

CONCLUSION: In HCV-positive chronic liver disease, prolylhydroxylase is not a good marker of hepatic fibrosis, while Type IV collagen is a useful tool for evaluating fibrogenic activity. Interferon seems to be able to reduce the liver fibrosis even without the inhibition of viral replication and independently from liver necrosis. [Editor: Emphasis mine]

PMID: 9581987, UI: 98241143

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A Call for Participants in an Herbal Study

by Darlene Morrow


Alta Natural Herbs and Supplements Ltd. along with the RA Co. Ltd, Tbilisi, Republic of Georgia, plan to introduce and market HEPATICO. HEPATICO is an herbal preparation (oral) made from the extracts of wildcrafted herbs (nettle, plantain and immortelle in a base of milk thistle) collected in the Mingrelian and Zemo-svanetian mountains of the Republic of Georgia.

This herbal remedy has undergone extensive preclinical and clinical investigations in the Republic of Georgia since 1992. At present, there are 17 abstracts being translated from Russian into English. This research looks at the treatment of acute and chronic forms of hepatitis and cirrhosis. The translation of these documents should be completed in the next month and copies will be sent to me. When I receive them, I will update everyone on what I find.

FROM THE COMPANY’S PRESS RELEASE:

“HEPATICO is a non-toxic, safe oral dietary supplement and herbal remedy that restores the liver and normalizes its functions. Clinical investigations with HEPATICO have shown that patients (children and adults) ill with acute Hepatitis A, or C were cured in 7 to 10 days, while patients (children and adults) suffering from chronic forms recover in 14 to 28 days. Favorable therapeutic results with HEPATICO were observed in patients with cirrhosis. Recovery from cirrhosis took place in 1 to 7 months depending on the complexity and stage of the disease.”

I am strongly opposed to the use of the word “cure.” The cure claim is based on the normalisation of the liver enzymes, alkaline phosphatase, bilirubin, cholesterol and bile acids. As we all know, this by no means suggests that the HCV is no longer present. What it does suggest is that there is no active liver damage going on at that particular time. Liver enzymes normally fluctuate. How long was the follow up? Neither PCR nor liver biopsies were performed to further validate their claims.

However, they further claim: “Immunological indicators have been studied. The immunological examinations were conducted one day prior to the administration of HEPATICO and two weeks after the treatment regimen ended. The following immunological indicators were determined: the content of leukocytes, lymphocytes, and the content of basis populations and subpopulations of lymphocytes by the method of flour cytometry of the T- cell (CD3), T-Helpers/Inducers (CD4), T- suppressors/cytotoxic lymphocytes (CD8), B- lymphocytes (CD72), natural killer cells (CD16), HLA-DR lymphocytes, the ratio Tx/Tc (the immunoregulatory indicator—IRI), the level of serum immunoglobulins (lg) of the 3 classes IgA, IgM and IgG and the content of marker proteins. The researchers concluded that HEPATICO has a positive effect on patients with various forms of hepatitis as evidenced by its positive effect on the majority of the measured immunological indicators.”

The company would like to continue to study the effects of HEPATICO. They would like about 100 participants for a short one month study. They expect rapid results. These results will be measured by pre and post liver function tests. HEPATICO will be supplied at no cost to participants.

The participants must have their physician’s permission. Your physician would be responsible for monitoring your blood tests and providing feedback to Alta Natural.

The company would like very much to work together with the physicians. Alta Natural Herbs has 2 Russian physicians on staff: Dr. David Khoupenia and Dr. Tamar Jvania. Both received their medical training/education at Pirogov Medical University in Moscow. At present they are not licensed to practice medicine in Canada. As Medical Directors of Alta Natural, they would like to encourage and invite other medical professionals to tour their facility and discuss the existing research.

The company is based in Richmond, BC at 1148-20800 Westminster Hwy. Please contact either Dr. David Khoupenia, or Mr. Greg Shafransky or Mr. Vernon McKay at 604/303-1131 for more information. Their email address is: Alta Natural

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Am J Gastroenterol 1997 Jul;92(7):1081-1091

Diagnosis and treatment of gastrointestinal bleeding secondary to portal hypertension.

American College of Gastroenterology Practice Parameters Committee.

Guidelines for clinical practice are intended to suggest preferable approaches to particular medical problems as established by interpretation and collation of scientifically valid research, derived from extensive review of published literature. When data are not available that will withstand objective scrutiny, a recommendation may be made based on a consensus of experts. Guidelines are intended to apply to the clinical situation for all physicians without regard to specialty. Guidelines are intended to be flexible, not necessarily indicating the only acceptable approach, and should be distinguished from standards of care, which are inflexible and rarely violated. Given the wide range of choices in any health care problem, the physician should select the course best suited to the individual patient and the clinical situation presented. These guidelines are developed under the auspices of the American College of Gastroenterology and its practice parameters committee. These guidelines are also approved by the governing boards of American College of Gastroenterology and Practice Parameters Committee. Expert opinion is solicited from the outset for the document. Guidelines are reviewed in depth by the committee, with participation from experienced clinicians and others in related fields. The final recommendations are based on the data available at the time of the production of the document and may be updated with pertinent scientific developments at a later time.

The following guidelines are intended for adults and not for pediatric patients.

OBJECTIVE: To develop practice guidelines for the management of gastrointestinal bleeding in adult patients with cirrhosis and portal hypertension.

METHOD: Randomized controlled trials published through October of 1993 were evaluated by members of the American College of Gastroenterology Practice Parameters Committee. Each paper was reviewed by three members of the committee and rated for quality of design by predetermined criteria. Meta- analysis of the studies for each treatment were evaluated for both outcome and quality of design and formed the basis for recommendations for treatment. Randomized controlled trials published between October of 1993 and August of 1995 have been added to update and modify the recommendations. The reader is referred to an excellent article by D'Amico et al. (The treatment of portal hypertension: A meta-analytic review. Hepatology 1995;22:332-354), which presents most of the meta-analyses reviewed by this committee.

CONCLUSIONS: Once esophageal varices have been established by endoscopy as the site of bleeding, either sclerotherapy or endoscopic variceal ligation should be performed to control the bleeding episodes. Concomitant use of vasoactive drugs lowers portal pressure, potentially offers the endoscopist a clearer field in which to work, and is the only noninvasive treatment for nonesophagogastric variceal sites of bleeding related to portal hypertension. For patients failing medical therapy, the transjugular intrahepatic portasystemic shunt procedure is a reasonable alternative to an emergency surgically created shunt. Nonselective beta-adrenergic blockers are the only proven therapy for prevention of first variceal hemorrhage. Both nonselective beta-adrenergic blockers and endoscopic variceal ligation (which has replaced sclerotherapy for this indication) are effective in reducing the risk of recurrent variceal bleeding. For patients failing these approaches, selective or total shunts or, in selected patients, liver transplantation are appropriate rescue procedures.

PMID: 9219775, MUID: 97363482

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HOW HEP C IS TREATED IN EUROPE

by Joan King-Diemecke

According to an article appearing in the March 1998 issue of the Journal of Viral Hepatitis, more than three hundred European doctors filled out a questionnaire with respect to their medical practices regarding hepatitis C virus (HCV) infection. The survey found that there was general agreement concerning the necessity of screening patients for HCV in cases of a history of blood transfusion, haemodialysis, haemophilia or intravenous drug addiction (90% of positive answers), but there were differing opinions as to whether or not to test for possible cases of vertical (mother to child) and nosocomial (occupational, such as nurses) transmission of HCV.

To prevent sexual and vertical transmission, 22% of the doctors were in favour of barrier methods (condoms, etc.), and 34% were against; 49% encouraged breast-feeding for babies born to HCV- positive mothers, and 14% were against. A great majority (70%) of those surveyed were in favour of taking preventative measures in the home.

Testing practices varied, 60% using RIBA (recombinant immunoblot assay). PCR was ordered by 77% when ALTs were elevated and by 89% when ALTs were normal. Biopsies were requested by 90% of the doctors and ultrasounds were prescribed by 91% in cases of elevated ALTs. However, in cases of normal ALTs, only 40% ordered biopsies and 70% ordered ultrasound testing.

Only thirty per cent of those surveyed counseled their patients to stop drinking alcohol and 60% advised moderation.

Two-thirds of the responders did not take into account biopsy or PCR results before starting antiviral therapy (such as Interferon) . Eighty per cent of the participants reported that they gave their patients interferon (IFN) for 12 months. For most of the items studied, there was a large variation of answers.

Those who ran the survey concluded that preventive and medical practices towards HCV are not homogeneous throughout the EU and suggested the need for a European consensus conference in this regard.

Based on :

J Viral Hepat 1998 Mar;5(2):131-141

Medical practices regarding hepatitis C virus infection in Europe.

Nalpas B, Delaroques-Astagneau E, Bihan CL, Drucker J, Desenclos JC Reseau National de Sante Publique, St Maurice, France.

PMID: 9572038, UI: 98233565


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U ASK

Natalie Rock RN, BS Hepatology Clinical Research Nurse,

Dept of Medicine UBC, Vancouver Hospital Div. Gastroenterology

Question: When is my hair going to stop falling out?

Hair loss, although not common, does occur with interferon treatment. Often it is mild and not apparent to others, but occasionally it may be more marked. Growth of hair requires nutrients, particularly protein, but loss of hair can occur for many reasons including some immune abnormalities. It takes a while for hair to grow out from the follicle once the reason depressing hair growth has been removed. Thus, it usually takes 3 to 4 weeks after the stopping of interferon before new hair starts to grow out. From then on the hair growth generally returns to normal. There is, however, individual variation in the rate of hair growth. It will take some months before full- length hair has returned.

Question: What does it mean when you are told that you have the virus (determined through a PCR) but that it is dormant? What course of action should be taken, are there regular tests one should have, and is there anything one can do to lower the risk of the virus becoming active?

It is uncommon for viruses to cause chronic disease. Most viruses, such as measles, chickenpox etc., are eradicated from the body in a short time. Herpes, HIV, and hepatitis C are, however, chronic viruses that stay in the body and inside cells permanently. The activity of the disease caused by the virus varies, however; at times the disease is active, at times not. Herpes virus, for example, causes the so- called "cold sores." Cold sores are not always present—indeed they may only occur infrequently—but the virus is always present and if one did a biopsy at the site where the cold sore occurs the virus may be seen inside the cells but there is no inflammation or activity. The reason for this is not understood. Since the disease (inflammation, ulceration) may be the body's response rather than the activity of the virus, it may be that the disease activity is related to the "host" (or patient) rather than the virus. There may be a number of factors that influence the body's response, including immune activity, the presence of other infections, stress, and so forth. Hepatitis C is like herpes in that at times there appears to be no inflammation in the liver although the virus may be identified in the blood or in the liver. In essence, the virus is “'dormant” although it would be better to say that there is no "disease activity." This period of inactivity is extremely variable: in some people it may last many years, in others only brief periods of time, and in some people not at all.

Studies of patients whose disease is inactive have suggested that it is best not to treat, since treating may alter the state of inactivity and actually create active disease. Thus it is the present recommendation that patients be checked every 6 to 12 months and if there is evidence of disease activity (elevated enzymes) treatment should be considered at that time. It has been shown that alcohol in some way makes the hepatitis C virus more active and so alcohol use is discouraged. General good health and good nutrition is important. Patients should be vaccinated against hepatitis A since this disease combines with hepatitis C to induce a more fulminant disease.

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Independent and combined action of hepatitis C virus infection and alcohol consumption on the risk of symptomatic liver cirrhosis.

By Howard J. Worman, M. D. Corrao, G., and Arico, S. .

Hepatology 1998. 27:914-919.

Alcohol abuse and hepatitis C virus (HCV) infection are the two major risk factors for the development of cirrhosis in the Western Hemisphere. This report examined these two risk factors in two case-control studies from Italy. The cases were 285 patients with cirrhosis admitted for the first time to a hospital for worsening liver disease. The controls were 417 patients admitted during the same time period for acute diseases not related to alcohol. The odds ratio of developing symptomatic cirrhosis was 9.2 in subjects who drank no alcohol and had HCV infection compared to subjects who had zero lifetime daily alcohol consumption and no evidence of HCV infection. For heavy lifetime alcohol users (greater than 175 g/day), the odds ratio for developing symptomatic cirrhosis was 15 in those without HCV infection and 147 in those with HCV infection.

An additive relative risk for developing symptomatic cirrhosis was also seen with lower levels of daily alcohol consumption in individuals with chronic HCV infection. These results show that alcohol abuse and chronic HCV infection are independent risk factors for developing cirrhosis. These two risk factors together greatly compound the odds of developing cirrhosis, especially at high levels of alcohol use.

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Stuffed Cabbage

2 cups cooked wild rice

1 cup diced onion

4 cloves of garlic, thinly sliced

raisins

apple cider (for sautéing)

one small head cabbage

tangy tomato sauce (recipe below)

In apple cider, sauté onion and garlic until onion is soft. Add rice, raisins and some more cider. Heat gently for a few minutes to let flavours meld.

Take cabbage and core and plunge into hot water for a few (5?) minutes to loosen leaves. Peel off a dozen or so leaves.

Put a layer of sauce in the bottom of the pan. Roll the cabbage leaves around the rice mixture by putting a tablespoon or so of the mixture in the middle of the cabbage leaf, fold up the sides and roll. Put the rolled cabbage on the sauce; layer as needed by putting sauce on top of the cabbage, adding more rolls, and end with sauce. Cover and bake 30 minutes in a 350 degree oven.

Tangy Tomato Sauce

1 28-oz can crushed tomatoes

1 cup diced onion

4 or more cloves minced garlic

1 tbs. apple cider

1 tbs. lemon juice

Sauté onion and garlic. Add crushed tomatoes. Simmer 5 minutes. Add apple cider and lemon juice. Simmer 5 more minutes. It's done!

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KUDOS

by Darlene Morrow

I would like to thank Dr. Anderson and all the office staff for their continued help and collaboration on some of the articles that appear in the hepcBC.bull.

Natalie Rock is extremely busy and dedicated to helping those with HCV, among others. She patiently answers endless questions and encourages phone calls for any items that require clarification. Many a time she has sent me her column for the newsletter at 11 p.m. Other times she will submit them on a Saturday.

We all owe them a tremendous debt of gratitude for their untiring efforts to promote education about HCV.

Thank you!

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AN OPEN LETTER TO THE HONOURABLE ALLAN ROCK AND ALL MEMBERS OF THE FEDERAL GOVERNMENT RE: THE TAINTED BLOOD TRAGEDY!

Dear Mr. Rock,

As a victim of tainted blood I have watched the shenanigans in Ottawa with a mixture of disbelief, disgust, contempt and as much anger as I can muster given the precarious state of my health.

In my opinion, you, the Prime Minister and members of the Liberal government, have become past masters at the art of obfuscation. You are right when you state that there is risk in any medical procedure. I accepted that risk when I had my heart valve replaced in 1983 and re-replaced in 1996. What I cannot, and will not, accept is the fact that my life is in jeopardy due to money-saving decisions made by faceless bureaucrats who are now deemed not to be responsible or accountable.

To suggest that compensating all the victims of tainted blood will bankrupt the health system and lead to a flood of claims is obfuscation and arrant nonsense. Does it bankrupt the system when we give billions of dollars to countries like Indonesia? Does it bankrupt the system when we aid our fellow Canadians affected by floods, ice storms, and so forth? I think not. About the only thing bankrupt in this whole sorry mess is, in my opinion, the morality of the federal and many provincial governments.

All decent people must feel for those who suffer from "medical misfortune," but to refer to the tainted blood tragedy as a "medical misfortune" is another example of obfuscation. The list of dates when our government could have acted goes back to the 1960's but I refer only to the decision made on July 13, 1981, by so-called "regulators" and officials of the Red Cross, not to buy a readily available surrogate test. In my opinion this decision alone condemned hundreds, perhaps even thousands, of Canadians, including me, to death. And I thought the death penalty had been abolished in Canada.

"Window of Opportunity"? My how you Liberals love that phrase. To use it in the context of the tainted blood tragedy is another example of obfuscation. I put it to you, Sir, that there is no "window," but a bloody great chasm as wide as the Grand Canyon, and you and your lackeys are teetering on the brink, and, in my opinion, unless you listen to the wishes of the vast majority of the Candian people who are your employers, you will all be pushed over the edge in the next election.

"Precedent"? This is a word you Liberals appear to hate as much as you love "Window of Opportunity." Again I put it to you, Sir, that by using the dates 1986 to 1990 you have created two dangerous precedents that could have an enormous impact on Canada. You have made the United States not only arbiter of the Canadian health system but also of Canadian law. We are sick and tired of hearing about the United States. A country where the number of citizens who cannot afford health insurance exceeds the population of Canada is no example by which to judge our health care system. You did not wait for the United States to act when you brought in gun control against the wishes of vast numbers of law-abiding citizens.

Now you are faced with an issue where the vast majority of Canadians believe the victims of tainted blood should be compensated and those responsible be brought to account. And what is your response? To go against the wishes of the people and continue defending the indefensible. If one of our ships is in a collision the captain has to answer to a court martial and is held responsible for his actions. Yet in the civil arm of government, individuals or groups of individuals can cause untold harm to their fellow citizens by their actions or lack of action, yet walk away scot free. Why is there this double standard? Why are those who fail to carry out their duties in a responsible manner never held accountable?

In my opinion those who are responsible for the blood tragedy should be made to answer for their actions or lack thereof as has happened in other countries.

Ron Thiel

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ROCK HARD IN OTTAWA - ODE TO A ROCK HEAD

Like the Rock of Gibraltar

He stands firm and square

Allan Rock will not alter

So try if you dare

He's made his stand

And stuck to his guns

By treating Hep-C’ers

Like miserable bums


And if you don't like it

Well, that's just sour grapes

But remember ----- Gibraltar

Is crawling with apes.

Ron.T.

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CLASS ACTION SUITS:

BRITISH COLUMBIA

Camp Church and Associates

Sharon Matthews / Kim Graham

4th Floor, Randall Building

Vancouver, B.C. V6B 1Z5

1-(800) 689-2322

Grant Kovacs Norell



Bruce Lemer

Grosvenor Building

930-1040 West Georgia Street

Vancouver, BC, V6E 4H1

Phone: (604) 609-6699 Fax: (604) 609-6688



Before August 1, 1986

Klein Lyons

David A Klein

805 West Broadway, Suite 500

Vancouver, B.C. V5Z 1K1

(604)874-7171 or 1-(800) 468-4466

(604)874-7180 (FAX)


also:

Dempster, Dermody, Riley and Buntain

William Dermody

4 Hughson Street South, 2nd Floor

Hamilton, Ontario L8N 3Z1

(905) 572- 6688


The toll free number to get you in touch with the Hepatitis C Counsel is 1-(800)-229-LEAD (5323).

ONTARIO AND OTHER PROVINCES

Pre 1986/post 1990

Mr. David Harvey

Goodman & Carr

200 King Street West

Suite 2300

Toronto, Ontario, M5H 3W5

Phone: (416) 595-2300

Fax: (416) 595-0527


TRACEBACK PROCEDURES:

This information is for anyone who has received blood transfusions in Canada, if they wish to find out if their donors were Hep C positive.

TRACEBACK INQUIRIES

Contact:

Dr. Lisa Jeppesen, Dr. P Doyle, or Glenda

The Canadian Red Cross Society

4750 Oak Street

Vancouver, BC, V6H 2N9

1-(888) 332-5663 (local 207)



Class Action/ Compensation

If you would like more information about class action/compensation, you can contact:

Tricia Plunkett. Tel. (250) 479-5369


Meetings will be set up so that we can share our experiences dealing with lawyers, the results of our own investigations, and so that we can decide what is in our own best interest as far as legal steps to take.

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RUN FOR LIFE!

Hepatitis C Society 5K Fun Run

June 28, 1998 at 9:00am

Location: Cordova Bay - Lochside Park- Lochside Trail, Dooley Road, Hunt Road back to to Lochside Park via Lochside Trail.

Course: Flat trail, country roads.

Catagories: Men's and Women's winners.

Awards: Trophies for overall Male and Female winners.

Prizes: Draw prizes after the race.

T-Shirts: First 200 get t-shirts before race. Later registration get shirts after race.

Entry Fee: $15.00 up to June 14th. $20.00 late registration up to June 28th deadline.

Registration: Drop off at Victoria Running Room, 1008 Douglas Street.

Race Kit Pick-Up: 10:00am to 5:00pm on June 27th.

For More Information: Call Victoria Running Room at 383-4224

OR

Hepatitis C Society at 388-4311.

**Proceeds go to the Hepatitis C Society of Canada**



Joan King-Diemecke

joan_king@bc.sympatico.ca



[Editors: Darlene Morrow, David Mazoff & Joan Diemecke].
Copyright © 1998, 1997 by [HeCSC- Victoria Chapter and HepC BC].
Revised: May 26, 1998.