Psychological relief is the most important benefit of a hepatitis C cure for patients

Roger Pebody
Published:
13 September 2018

When asked to describe what their hepatitis C cure meant to them, Australians who had recently completed treatment emphasised an improved sense of psychological wellbeing, according to a qualitative study recently published in Hepatology, Medicine and Policy.

They described their relief about no longer fearing the development of liver disease or cancer, or of infecting others. Interviewees who had a history of injecting drug use understood their cure as a way to break the connection with their past.

Jacqueline Richmond of La Trobe University and colleagues recruited people who had achieved a sustained virological response 12 weeks after completing treatment (SVR12) in order to be interviewed about their experience of treatment and of cure. All participants were recruited from clinics in Melbourne, Australia between October 2016 and April 2017. The interviews were conducted during an early phase of the roll-out of direct acting antiviral (DAA) treatment in Australia; those interviewed are therefore likely to be ‘early adopters’ who may have been more motivated and enthusiastic than some other people who are eligible for treatment.

Twenty people took part in semi-structured interviews. They were evenly split between men and women; most had been diagnosed for over a decade; four had cirrhosis or other indications of severe liver disease; and seven had previously tried interferon-based therapy.

The most frequently identified outcome of achieving a ‘cure’ was being relieved of the psychological burden of living with hepatitis C. Most participants had not experienced physical symptoms, so the mental burden of hepatitis C was more important than the physical burden.

People had less uncertainty and fear in relation to the future. A woman who had been diagnosed in 1990 commented:

“It hasn’t changed my life that much because I never really had any symptoms… The biggest change is just…emotionally…you go from being someone with a chronic disease that has the potential to cut your life short to being free.”

While they were living with hepatitis C, they were never sure whether to attribute illnesses or fatigue to hepatitis C, another illness, or ageing.

“The fact that that’s not there anymore, like if I get sick or I’m ill means all I’ve got is that. I’ve just got the flu ... It’s not that it’s my liver’s fricking packing up on me or something.”

Being cured helped people feel ‘normal’ again. In particular, they did not feel ‘dirty’ or ‘infectious’.

“I love not being infectious…That for me has probably been the biggest thing – not having to feel guilty every time I had a blood test done that I might infect somebody, going to the dentist is nowhere near as stressful.”

“At my house, with toothbrushes and razors and stuff, it’s been something that I’ve had to be really, really vigilant with, with children in the house and with my partner… It’s really nice to know that I don’t have that in me anymore, and there aren’t those risks there of passing it on to anyone else.”

Many participants had acquired hepatitis C through injecting drug use, something that some individuals still felt guilt and shame around long after they had stopped injecting. Having hepatitis C had been an ongoing marker of their history of drug use breaking that connection was transformative. A man who had been diagnosed in 2003 said:

“It’s like the last mark… is now gone. All the rest is just memories that I don’t have to think about.”

One woman spoke about no longer worrying about her daughter’s friends finding out about it. However, not everyone agreed that this history could so easily be erased:

“I still feel guilty about it…about having used drugs when I was younger, about having contracted the hepatitis C… It’s just a bit of a mental scar that I suppose I’m going to carry for a long time.”

While many participants had not felt they had physical symptoms before commencing treatment, some described experiencing improved physical health as a result of being cured.

“I don’t know how much of that is psychological. I don’t think it’s all psychological. I’m sure there is a physical element … I have more energy, I am sleeping better, just a whole range of things.”

For some, the physical effects of living with hepatitis C only became apparent once they had been cured. 

However, those who had significant liver damage would continue to need to attend a clinic for regular monitoring. They said this would be an ongoing reminder of the virus.

Participants were keen to encourage other people with hepatitis C to find out about treatment with DAAs.

“I have told a few people and other people have asked me… I recommend it.”

“I would urge anybody with hep C to very much be confident about getting onto this drug to cure themselves.”

They said that it was important to distinguish DAAs from interferon-based treatment, emphasising the reduced burden of side-effects and DAAs being simpler to take.

However, stigma associated with having injected drugs discouraged one interviewee from discussing his treatment more openly.

“One part of me wants to sort of yell it at the top of my voice and say, look, this is an amazing, miraculous cure out there. Please, anyone that’s got hep C, go and get involved with it. But then the other part of me, sort of I suppose the conservative – but… I still feel guilty about it.”

Another participant continued to inject drugs and worked as a peer educator. While she often discussed her experience of treatment, she noted that many injectors saw hepatitis C treatment as something to do after they finished injecting drugs.

“I am finding that just even talking to the community on the street, it’s just like - yeah, big deal, there’s a treatment, but I’m not done with the life at the moment here, you know. And they do see it as something to happen when they’ve done with their using life.”

The authors conclude: "Future engagement strategies targeting people with hepatitis C who are not currently accessing DAA treatment need to use the lived experience of being cured, particularly the significant psychological impact." This should be promoted alongside the benefits to physical health, they say.

Reference

Richmond JA et al. Achieving a hepatitis C cure: a qualitative exploration of the experiences and meanings of achieving a hepatitis C cure using the direct acting antivirals in Australia. Hepatology, Medicine and Policy 3:8, 2018. (Full text freely available.)