Understanding quality of life for people living with HIV
There was a time when HIV care focused solely on suppressing the virus. As HIV care has evolved, the focus has moved away from surviving HIV to living and ageing well with HIV, with improved quality of life (QoL) being the desired goal.
To help support people living with HIV to live long, happy, healthy lives, it’s important to understand the challenges people face and how they impact their quality of life.
Positive Perspectives is a global study that shines light on the experiences and aspirations of 2,389 people living with HIV aged 18–84 from 25 countries. It investigates how people living with HIV rate their health and how living with HIV impacts their lives and affects their outlook for the future. The study also examines their experiences with antiretrovial therapy (ART) and the interactions and relationships people living with HIV have with healthcare professionals.
*Defined in Positive Perspectives as taking five or more pills a day or taking medicines for five or more health conditions.
QoL and the ‘fourth 90’
Thanks to innovations in antiretroviral treatment, HIV is now a long-term, treatable health condition.
While there is still more work to be done to ensure universal access to ART, significant progress has been made in reaching the UNAIDS 90–90–90 targets set for 2020:
Improving long-term QoL is becoming a critical priority in the care of people living with HIV, a target that has become known as the ‘fourth 90’.
Erika Castellanos explains why focussing on QoL is essential for people living with HIV.
What does this mean for people living with HIV?
The results from Positive Perspectives confirm the importance of a holistic approach to HIV care.
Empowered people living with HIV who are involved in open and active dialogue and joint decision-making with their healthcare providers were more likely to report undetectable viral load and, more importantly, improved aspects of their QoL.
Taking multiple medications
were concerned about taking more medicines as they grow older<sup>1</sup>
were worried about long-term effects of HIV medicines<sup>1</sup>
would like to be more involved in decisions about their HIV treatment<sup>2</sup>
Approximately 1/3 were uncomfortable discussing their concerns about ART side-effects with their healthcare providers<sup>2</sup>
Undetectable = Untransmittable (U=U)
Just over one-third of people living with HIV in the study reported they were not told about U=U by their healthcare providers<sup>3</sup>
of people who reported being informed about U=U by their healthcare providers reported optimal treatment adherence<sup>3</sup>
HIV and women
of women living with HIV were more likely than men living with HIV (41% 609/1,486) to report suboptimal health<sup>4</sup>
Despite over two-thirds desiring greater involvement in their care, a significantly higher proportion of women living with HIV were uncomfortable discussing treatment issues with healthcare providers<sup>4</sup>
Ageing well with HIV
Almost one-quarter of people living with HIV aged 50 and over reported poor physical, mental, sexual and overall health<sup>5</sup>
reported barriers to raising concerns with their healthcare providers<sup>6</sup>