Abstract

BackgroundLittle is known on outcomes after transition to adult care among adolescents with perinatal HIV infection. Though there is data from other chronic pediatric diseases suggesting increased morbidity and mortality following transfer to adult care, this has not well been studied among the first wave of survivors of perinatal HIV infection. The primary objective of this study was to determine outcomes after transition to adult care among a cohort of HIV-infected adolescents in Québec, Canada. Secondary objectives were to document participant experiences with the transition process, identify barriers to successful transition, and potential changes to improve the transition process.MethodsClinic records were reviewed to identify all perinatally-infected youth who transitioned from the Centre Maternel et Infantile sur le Sida pediatric HIV clinic (Montreal) at age 18 to an adult care provider between 1999 and 2012. Transitioned patients were contacted using last available patient or parental listed phone number on hospital record, internet based telephone directory, or social media. A standardized questionnaire was administered by telephone or in-person interview, and copies of current medical records obtained from treating physicians.ResultsForty-five patients were transferred between 1999 and 2012, among whom 25 consented to the study, eight were lost to follow-up, eight refused participation, and four were deceased. Overall 76 % of patients remained engaged in care, defined by at least one physician visit within 6 months of the interview. Over 50 % reported difficulty with adherence to their current drug regimens. At one-year post-transfer, there was a decrease in the proportion of patients with CD4 count >500 cells/mm3 from 64 to 29 %, and a statistically significant decrease in absolute CD4 count (mean 370 vs 524 cells/mm3, p = 0.04.). The majority (92 %) of participants felt that 18 was too young an age to transfer to adult care, and provided suggestions for improving the transition process.ConclusionsThis group of perinatally-infected youth remained engaged in care after transition, however difficulties with adherence and assuming responsibility for their own care were identified as issues in their post-transition care. The high rate of mortality among them and the changes to their health status post-transition suggest that further work is necessary to document the health outcomes of this group in larger, more diverse cohort settings.

Highlights

  • Little is known on outcomes after transition to adult care among adolescents with perinatal human immunodeficiency virus type 1 (HIV) infection

  • Though there is a wealth of information from other chronic pediatric diseases that illustrates that the transition process is often associated with increased morbidity, mortality, poorer social and educational outcomes, and high rates of loss to follow-up and non-retention in care [5,6,7], adolescents with HIV have unique characteristics when compared to other pediatric populations, which make it difficult to extrapolate data from transition studies of other chronic diseases [8]

  • While the normal transition process is marked by a sense of loss and grief that occurs when going from one life stage to another, this change may be experienced more intensely for young adults living with HIV, as many have already suffered the loss of important caregivers in their lives, including the death of one or more parent [9]

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Summary

Introduction

Little is known on outcomes after transition to adult care among adolescents with perinatal HIV infection. Though there is data from other chronic pediatric diseases suggesting increased morbidity and mortality following transfer to adult care, this has not well been studied among the first wave of survivors of perinatal HIV infection. Though there is a wealth of information from other chronic pediatric diseases that illustrates that the transition process is often associated with increased morbidity, mortality, poorer social and educational outcomes, and high rates of loss to follow-up and non-retention in care [5,6,7], adolescents with HIV have unique characteristics when compared to other pediatric populations, which make it difficult to extrapolate data from transition studies of other chronic diseases [8]. A similar study among 20–24 year olds in the UK found a significantly higher mortality rate compared to HIV uninfected youth [16]

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