As the number of young people living with HIV increases
internationally, new and innovative ways to talk about sex, disclosure, and
health need to be developed for HIV-positive adolescents.
According to a panel presenting at the Eighteenth International
AIDS Conference in Vienna, the needs of adolescents living with HIV
are much more sensitive and varied than those of adults, as they must
simultaneously deal with 'adult' issues like disclosure, practicing safe sex,
and adhering to treatment, while also addressing issues traditionally
associated with adolescence, such as body image, first sexual experience, peer
pressure and forming personal identity.
Jasna Loos of the Institute
of Tropical Medicine in Belgium presented the findings of a formative
needs assessment conducted amongst HIV-positive young people in Kenya and Uganda. Considering the categories
of body image, sexual identity, increased importance to peers, envisioning the
future, and independence
– all central themes within adolescent development
– Loos
noted that HIV-positive young people concurrently felt empowered and excited about growing
older, while also being weary of the potential restrictions and increased
responsibility resulting from their HIV status.
Disclosure proved to be a “pivotal step in their lives”, often
resulting in positive life changes
With regards to body image,
respondents felt that puberty and growth offered a new start and chance to
transform from a social outsider to that of a social insider, as those
previously sickly in appearance and smaller than their peers grew into healthy
adults. Peer influence was central to understanding sexuality, sexual norms
and identity, with positive adolescents attempting to mirror so-called 'normal'
behaviour. Due to notions of AIDS as a deadly virus, Loos notes that many
adolescents “lived in the moment” and wanted to get “the most out of a life
with HIV”. In reality, this often resulted in early first sexual experience, as
young people “did not want to die without having sex”.
Loos notes that, as yet, there are few evidence-based
interventions to help positive adolescents in coping with such issues. Based on
the findings of the study, she suggests that sexual and reproductive health be
fully integrated with HIV services, specifically by building upon existing
resources; that providers focus on a holistic approach and do not rely on
'one-size-fits-all' programmes; and that service providers focus on building
trust with adolescents.
Sabrina Bakeera-Kitaka from Kampala’s
Mulago Hospital discussed adolescents’
experiences in disclosing status to their peers, friends and family. A study
conducted at Mulago assessed the experiences of ten men and ten women who
were taking ART, and followed them through the process of disclosure. Partner
disclosure proved to be most challenging for the participants, who cited fear
of rejection, and loss of respect and care, if their status became known.
Participants also said that they did not want to disclose to their family
members in order to protect them from “distressing information”. Generally,
however, disclosure proved to be a “pivotal step in their lives”, often
resulting in positive life changes including increased care and support, both
financial and emotional.
In addition to psychosocial and behavioural concerns, a
recent study conducted at the Family Care Center at Harlem Hospital in New York City
looked at the effects that the virus has on neurocognitive functions among
HIV-positive adolescents living in a poor, urban area. While several other studies
have focused on neurocognitive and behavioural effects from viral infection,
questions have arisen as to whether these effects stem from HIV and
opportunistic infections specifically or, rather, are a result of social
factors affecting those most affected by the virus
– such as poverty, poor
education, and single-parent households. Affected neurocognitive functions
include fine motor strength, language, executive skills and memory, academic
achievement, and general cognitive ability.
The Harlem study attempted
to consider the “neighborhood question” by assessing neuropsychological test
results, ART regimen, CD4 count and demographic information amongst adolescent
patients. While all study participants displayed some sort of learning or
behavioural disorder, the study found that “environmental influences on
neurocognitive functioning may be negligible given the impact of advanced HIV
infection and psychiatric illness.” As such, high rates of psychiatric illness
among HIV-positive adolescents require increased prevention and intervention
strategies.
Interestingly, panelists noted that differing experiences for
adolescents generally depended on whether an individual was infected
through neonatal or postnatal exposure. However, this is currently an anecdotal
observation, and requires further exploration before conclusions can be made.
Treatment adherence also poses a significant challenge for adolescents living
with the virus, regardless of how they became infected. Ana-Maria Schweitzer of
the Baylor College of Medicine, highlighting her work in Romania, noted
that 60% of adolescents will struggle with adherence at some point. In her
study, adherence was affected by misconceptions surrounding the need for good
adherence, as well as by fears of unwanted disclosure and frustrations stemming
from a sense of limited freedom associated with a treatment regimen.
Of central concern to young people living with HIV is the question
of transition in treatment throughout the adolescent years. Bakeera-Kitaka’s Mulago Hospital
currently houses a 'transition clinic', which attempts to facilitate patients’
movement from child to adult care. This programme has seen the majority of
patients successfully making the transition from one to the other. However, more
research and discussion is needed to understand best practices in this regard.