FAQs About Treating Hepatitis C
Treatment for hepatitis C has changed dramatically in recent years. Piedmont Healthcare Hepatologist Raymond Rubin, MD, answers questions he hears often from his patients about treating – and curing – the disease.
1. Q: What’s the difference between the hepatitis C infection and the disease?
A: In the old days, when I was going to start someone on interferon and ribavirin, our practice would have a class every other week for the patients who were about to get started to show them, of course, how to give themselves an injection. But most of the session was devoted to side effect management. We would see these patients very frequently when they were on treatment. We would handle a lot of telephone calls and office visits with patients who were having all kinds of side effects.
On the other hand, now, I have a brief review with patients of the potential side effects and I’ll tell them that about 20% of people who take this medication could experience headache, fatigue, insomnia, or some GI distress; serious side effects are exceptionally rare and needing to stop the medication is exceptionally rare. Other than that, there isn’t a ton of prep. I usually review with them how often they need to get their blood tested during the treatment, and also more importantly, how to tell that they’re cured once the treatment has stopped.
3. Q: What do you wish your patients knew about hepatitis C?
A: First and foremost, if you’re a baby boomer, get tested for hepatitis C. Most people with hepatitis C don’t know they have it, and most of those people were born between 1945 and 1965. And hepatitis C rarely has symptoms, so you really won’t know you have it until you’re either tested, or you experience symptoms of severe liver disease. Testing and finding out early so you can treat it is a better way to go.
I also wish my patients knew that hepatitis C can cause severe complications, like cirrhosis and end-stage liver disease. Now that it’s curable and the treatment is so much easier, it’s worth talking to your doctor about getting treated.
Lastly, I want all my patients to know that hepatitis C is curable. It’s incredible.
4. Q: What’s the hardest part of treating hepatitis C for you?
A: It's difficult to find all the patients with hepatitis C who haven't been tested yet, and it's challenging to get these expensive medications paid for by insurance. One really hard part of treating hepatitis C, honestly, is that there’s only one of me! Now that there’s a cure and the treatment is so much more tolerable, there’s no shortage of people getting treated. But the shortage is in people who know how to take care of these patients. Practitioners need to recognize that a subset of these patients either already have cirrhosis or may develop cirrhosis and it’s important to refer these patients to a hepatitis specialist, called a hepatologist. Those doctors are very savvy and know how to best treat hep C.
THIS CONTENT DOES NOT PROVIDE MEDICAL ADVICE. This content is provided for informational purposes and reflects the opinions of the author. It is not a substitute for professional medical advice, diagnosis or treatment. Always seek the advice of a qualified healthcare professional regarding your health. If you think you may have a medical emergency, contact your doctor immediately or call 911.
Rubin, MD, is a hepatologist who spent three years conducting research for new
hepatitis C treatments. He is now Chief Scientific Officer of Piedmont
Transplant Institute. View his Healthgrades profile >
Healthgrades Operating Company, Inc. All rights reserved. May not be reproduced
or reprinted without permission from Healthgrades Operating Company, Inc. Use
of this information is governed by the Healthgrades User Agreement.