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“We did not know what was wrong”—Barriers along the care cascade among hospitalized adolescents with HIV in Gaborone, Botswana

  • Leslie A. Enane ,

    Roles Conceptualization, Formal analysis, Methodology, Supervision, Writing – original draft, Writing – review & editing

    lenane@iu.edu

    Affiliations Division of Infectious Diseases, The Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America, Department of Pediatrics, The Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America, Ryan White Center for Pediatric Infectious Disease and Global Health, Indiana University School of Medicine, Indianapolis, Indiana, United States of America, Botswana-UPenn Partnership, Gaborone, Botswana

  • Keboletse Mokete,

    Roles Investigation, Writing – review & editing

    Affiliation Botswana-Baylor Children’s Clinical Centre of Excellence, Gaborone, Botswana

  • Dipesalema Joel,

    Roles Conceptualization, Supervision, Writing – review & editing

    Affiliations Botswana-Baylor Children’s Clinical Centre of Excellence, Gaborone, Botswana, Faculty of Medicine, University of Botswana, Gaborone, Botswana

  • Rahul Daimari,

    Roles Writing – review & editing

    Affiliation Faculty of Medicine, University of Botswana, Gaborone, Botswana

  • Ontibile Tshume,

    Roles Project administration, Writing – review & editing

    Affiliation Botswana-Baylor Children’s Clinical Centre of Excellence, Gaborone, Botswana

  • Gabriel Anabwani,

    Roles Conceptualization, Supervision, Writing – review & editing

    Affiliations Botswana-Baylor Children’s Clinical Centre of Excellence, Gaborone, Botswana, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, United States of America

  • Loeto Mazhani,

    Roles Conceptualization, Supervision, Writing – review & editing

    Affiliation Faculty of Medicine, University of Botswana, Gaborone, Botswana

  • Andrew P. Steenhoff,

    Roles Conceptualization, Supervision, Writing – review & editing

    Affiliations Division of Infectious Diseases, The Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America, Department of Pediatrics, The Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America, Botswana-UPenn Partnership, Gaborone, Botswana, Center for Global Health, The Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America

  • Elizabeth D. Lowenthal

    Roles Conceptualization, Formal analysis, Funding acquisition, Methodology, Supervision, Writing – review & editing

    Affiliations Department of Pediatrics, The Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America, Botswana-UPenn Partnership, Gaborone, Botswana, Center for Global Health, The Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America, Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America

“We did not know what was wrong”—Barriers along the care cascade among hospitalized adolescents with HIV in Gaborone, Botswana

  • Leslie A. Enane, 
  • Keboletse Mokete, 
  • Dipesalema Joel, 
  • Rahul Daimari, 
  • Ontibile Tshume, 
  • Gabriel Anabwani, 
  • Loeto Mazhani, 
  • Andrew P. Steenhoff, 
  • Elizabeth D. Lowenthal
PLOS
x

Abstract

High mortality among adolescents with HIV reflects delays and failures in the care cascade. We sought to elucidate critical missed opportunities and barriers to care among adolescents hospitalized with HIV at Botswana’s tertiary referral hospital. We enrolled all HIV-infected adolescents (aged 10–19 years) hospitalized with any diagnosis other than pregnancy from July 2015 to January 2016. Medical records were reviewed for clinical variables and past engagement in care. Semi-structured interviews of the adolescents (when feasible) and their caregivers explored delays and barriers to care. Twenty-one eligible adolescents were identified and 15 were enrolled. All but one were WHO Clinical Stage 3 or 4. Barriers to diagnosis included lack of awareness about perinatal HIV infection, illness or death of the mother, and fear of discrimination. Barriers to adherence to antiretroviral therapy included nondisclosure, isolation, and mental health concerns. The number of hospitalized HIV-infected adolescents was lower than expected. However, among those hospitalized, the lack of timely diagnosis and subsequent gaps in the care cascade elucidated opportunities to improve outcomes and quality of life for this vulnerable group.

Introduction

Worldwide, adolescent AIDS-related deaths are increasing, despite improvements in access to antiretroviral therapy (ART) [1]. From 2005–2012, while AIDS-related deaths declined by 30% in all other age groups, AIDS-related deaths in adolescents increased by 50% [2]. HIV/AIDS is a leading cause of death among adolescents globally, particularly in sub-Saharan Africa [3].

Mortality increases are particularly striking among 10–14 year-old adolescents with HIV, reflecting failures to diagnose perinatally infected children and to successfully engage them in care early in the course of their illnesses. Gaps have been described throughout the adolescent HIV care cascade—at HIV diagnosis, linkage to and retention in care, and ART adherence and suppression of viral load [4]. There is an urgent need to identify strategies to help adolescents make the same morbidity and mortality gains seen in other age groups.

Botswana is among the countries with the highest HIV prevalence in the world, with 21.9% of the adult population living with HIV [5]. Botswana has been a pioneer in responding to the HIV/AIDS epidemic; Botswana introduced PMTCT services in 1999, and in 2002 was the first sub-Saharan African country to provide universal free ART to citizens [6]. Botswana is now approaching 90-90-90 targets; however, successes are not shared equally across age groups. While it is estimated that 84% of Botswana’s adults living with HIV are receiving ART, only 60% of Botswana’s children (under 15 years) living with HIV are on ART [5]. Age-disaggregated outcome data are not available for the approximately 17,000 adolescents living with HIV in Botswana [5].

By investigating delays in the HIV care cascade among hospitalized adolescents with HIV in this high-prevalence setting, we aimed to examine the full spectrum of missed opportunities for HIV care in those most vulnerable to poor outcomes.

Methods

Setting

This study was conducted between July 2015 and January 2016 at Princess Marina Hospital (PMH) in Gaborone, Botswana, the country’s main government referral hospital. PMH is located adjacent to the Botswana-Baylor Children’s Clinical Centre of Excellence, which has provided comprehensive HIV care to thousands of children and adolescents since 2003, and provides adolescent-centered services, such as a Teen Club support group. HIV testing is indicated for all hospitalized children and adolescents with unknown HIV status, per Botswana National HIV & AIDS Guidelines [7].

Data collection

The study nurse and other research team members consulted with ward medical teams to identify all adolescents (ages 10 to 19) with HIV hospitalized at PMH for any admission diagnosis other than pregnancy over a 6-month period. Adolescents admitted for any admission diagnosis to the medical, pediatric, surgical, oncology, or intensive care wards were included. Pregnant patients were excluded because the intent was to understand reasons for delayed access to care, and pregnant patients with HIV represent mainly those with more recent behaviorally-acquired infections in this context [5,8]. Prenatal care (PNC) uptake is high and 92.8% of mothers in Botswana’s PNC program were tested for HIV in their last pregnancy [8]. Furthermore, hospitalizations of pregnant adolescents in this setting are primarily for labor and delivery, or obstetric complications, rather than complications of HIV, which were our primary interest. Adolescent HIV deaths are roughly equal among males and females, and highest among 10–14 year-olds, arguing against pregnancy being a major driver of adolescent HIV deaths [2,9].

We developed semi-structured interview guides which begin with open-ended questions querying the adolescents’ prior engagement in care (S1 File). Sequential questions determined if critical failures or delays occurred in the diagnosis and treatment cascade. Probes investigated barriers to care at each stage of the cascade where critical challenges or failures occurred. The acceptability of specific proposed interventions to improve care at each stage was explored. Separate interview guides were used for disclosed and non-disclosed adolescents, and for caregivers. Guides for non-disclosed adolescents did not mention HIV, but asked generally about barriers to medical care for adolescents, as well as any challenges with adherence to medicines and clinic visits.

Eligible adolescents and their caregivers were approached with information about the study and to request informed consent/assent. Strict precautions were taken to prevent inadvertent disclosure of HIV status throughout the informed consent process and study procedures. This included avoidance of inadvertent disclosure to young adolescents who were not aware of their own status by avoiding use of the term HIV in any assent documents or in the interview guide for non-disclosed adolescents. Adolescents were presumed to be non-disclosed unless their primary caregiver confirmed that the adolescent was aware that he or she had HIV infection. Caregivers and adolescents (when medically stable) were interviewed separately in a confidential setting near the hospital ward. Interviews were conducted in Setswana by a bilingual research nurse with extensive experience caring for children and adolescents with HIV and training in interview techniques. Clinical and demographic variables were abstracted from medical records onto paper forms, and uploaded into a secure REDCap database [10]. A master list of study numbers and identifying information was kept separate from the de-identified study data used for analysis. Study materials were kept in a locked cabinet in a secured office where only the study team had access.

Data analysis

Clinical and demographic data were analyzed using standard descriptive statistics, using Stata/SE 14.1 (StataCorp, College Station, Texas, USA). Interviews were audio-recorded, transcribed, and translated into English. The first and senior authors reviewed all transcripts and relayed queries to the study nurse, who contacted participants with follow-up questions when clarification was needed. Transcripts were coded and analyzed through thematic analysis. Initial codes were organized according to stage of the care cascade addressed by the participants, as well as hypothesized factors impacting the care cascade. Through reading and re-reading of the data, the coding structure was augmented with themes that emerged from the data [11,12]. NVivo 11 analysis software (QSR International Pty Ltd, Melbourne, Australia) was used to organize and analyze the data.

Ethics statement

All procedures performed were in accordance with the principles expressed in the 1964 Helsinki Declaration. Written informed consent was obtained from all adolescents over age 18, and from parents/guardians of adolescent minors. Written assent was obtained from adolescent minor participants. Adolescents who were too ill to participate in assent procedures were included if their primary caregiver consented to review of the adolescent’s chart, and to be interviewed about the adolescent’s past engagement in care. The study protocol was approved by the institutional review boards of the University of Botswana, Princess Marina Hospital, the University of Pennsylvania, Children’s Hospital of Philadelphia, and the Health Research Development Committee at the Botswana Ministry of Health.

Results

Over the 6-month study period, 21 adolescents meeting inclusion/exclusion criteria were hospitalized at PMH. Fifteen were enrolled in the study. One eligible adolescent died before enrollment and caregiver consent was withdrawn after another died. Two minors did not have a caregiver present who could consent to their participation and two declined consent/assent. Of all eligible adolescents, 4/21 (19.0%) died; among the adolescents enrolled in our study, 2/15 (13.3%) died during the hospitalization. Interviews were conducted with 13 adolescents and 15 adult caregivers, of whom 9 were mothers, 4 were sisters, one was an aunt, and one was a grandmother to the hospitalized adolescent.

The median age of the adolescents was 14.1 years (interquartile range [IQR 12.7–17.6]). Nine (60%) adolescents were 12–14 years old (Table 1). Median age at HIV diagnosis was 7.5 years (IQR 1.5–12.1 years). All were thought to be perinatally infected, given the age at diagnosis, clinical course, and family history. Two-thirds of patients were diagnosed with HIV after the age of 5 years (10/15, 66.7%), and a third after the age of 10 years (5/15, 33.3%). Of 10 patients with available labs from time of diagnosis, 3 (30.0%) had advanced immunodeficiency, and 7 (70.0%) had severe immunodeficiency [13]. 14/15 (93.3%) of patients were WHO Clinical Stage 3 or 4 [13].

Diagnoses made on admission or during hospitalization were categorized by systems (Table 2). The majority of adolescents (9/15, 60.0%) were hospitalized for AIDS-related diagnoses. Pulmonary tuberculosis (TB) (5/15, 33.3%), anemia (5/15, 33.3%), severe malnutrition (4/15, 26.7%), and oncologic diagnoses (3/15, 20.0%) were noted in multiple patients. Two patients were admitted for elective surgical procedures, one of which was probably HIV-related (tenotomy needed due to early life encephalopathy).

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Table 2. Diagnoses given on admission or during hospitalization per medical teama.

https://doi.org/10.1371/journal.pone.0195372.t002

Only the two patients admitted for elective surgical procedures were diagnosed in infancy. All other adolescents had experienced delays in HIV diagnosis (Table 3). While delays were common, only one patient was diagnosed during the current hospitalization, at the age of 12. Significant challenges to retention in care were identified, with 3/14 previously diagnosed adolescents having been out of care as much as several years. Of 13 patients on ART, 6 reported significant adherence difficulties.

Specific barriers and missed opportunities for care were explored for each stage of the cascade where adolescents experienced significant delays or challenges (Table 4). Many barriers presented significant challenges at multiple stages of the cascade. Barriers related to diagnosis and adherence were most common and are presented in-depth.

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Table 4. Key themes relating to missed opportunities, barriers to care, and areas for intervention along the HIV care cascadea.

https://doi.org/10.1371/journal.pone.0195372.t004

Missed opportunities for diagnosis

Presenting frequently to clinics or hospitals without receiving an HIV test was reported by many. Chronic illnesses included cough, pneumonia, TB, diarrhea, ear infections, rashes, oral ulcers, and wasting. In a few cases, the child had to withdraw from school due to severe illness, but had not yet been tested for HIV. In some, failure to diagnose the mother may have contributed to delayed diagnosis of the child.

Barriers to HIV diagnosis, linkage, and retention in care

Lack of awareness.

Caregivers frequently discussed their past lack of knowledge of the possibility of undiagnosed perinatal HIV infection in their children, or remarked that they “did not believe” that the child could be infected. Some noted that the child “grew up well-nourished” or “was doing fine” prior to becoming ill. When the child did become ill, multiple caregivers remarked that “it never crossed [their] mind” or that they “never thought [that the child could have HIV].” In some cases, the mother herself had not yet been diagnosed—one mother reported, “even myself I had not tested.”

Illness or death of the mother.

Severe illness or death of the child’s mother was a common contributor to delayed diagnosis or failure to retain a child in care when “there was no one to bring [the child] to clinic”. Challenges in adherence and retention for mothers–“her mother stopped treatment and is now very sick”–contributed to delays in children’s care. In these situations, other family members needed to take on the medical care of the child, including the decision to test for HIV.

Lack of disclosure to other family members.

Lack of disclosure of the child’s status to other family members was an important barrier to diagnosis and retention in care, particularly if the mother was ill, or if the child was living with family members who were not aware of the child’s status. Two adolescents had several-year gaps in care after diagnosis, due to severe illness of the mother and lack of disclosure of the child’s status to other family members who potentially could have brought the child for care.

I was very sick and bedridden. I had once come to clinic after he was diagnosed, for initiation [of ART], but I stopped as there was no one to bring him. I had not told anyone about my child’s status at home, for fear of being discriminated against, even though they knew my status.

Mother of a 13 year-old male

Stigma and fear of discrimination.

Stigma and fear of discrimination were barriers to diagnosis and care at all stages of the cascade. Caregivers expressed fear of discrimination, even from close family members, as in the preceding example. They reported that stigma was also acutely experienced by adolescents, particularly in their interactions with peers.

It hurts him; he does not like it. Especially when you speak with a raised voice, telling him he has the sickness, his perception is maybe other people are listening.

Sister of a 17 year-old male

We need to meet with health professionals to continue talking about this illness, so that the child understands that this is an illness like any other; she does not differ from others.

Sister of a 19 year-old female

Adherence challenges

Adherence challenges were commonly described among adolescents on ART. Key barriers to adherence included: lack of disclosure of HIV status to the adolescent or family members, stigma, isolation, and mental health concerns including para-suicidal behavior. (A sister of a 19 year-old female reported, “sometimes she will even be refusing to go to the clinic, saying she wants to be left to die.”) For those adolescents who had been told their HIV status, adolescents and caregivers spoke of both the challenges and breakthroughs for these youth in “accepting themselves,” or coming to terms with the diagnosis.

Potential interventions

Participants were asked about specific proposed interventions at each stage along the cascade where challenges were faced (Table 4). Peer support was currently available to some, but not all, of the disclosed adolescents, and was seen as a particularly vital intervention to support adolescent mental health, confidence, education about HIV, and adherence. Adolescents described the peer group setting as a means to escape isolation and stigma—to “be in the same air together”–to “be free with each other.” As one 12 year-old male stated, “[the groups help us] to understand that whether you are on medications or not you are still the same.” Unfortunately, many adolescents were not able to benefit from a peer group due to being unaware of their HIV status or receiving care at sites lacking peer groups.

Regular reminders from personal contacts were seen by some as helpful, though others felt that visit reminders were unnecessary for themselves. Similarly, cell phone reminders (of medication schedule or of clinic visits) were generally not perceived as being as helpful as phone calls from clinic staff in the case of missed appointments or concerning lab results. Such outreach was seen as evidence of a strong relationship of the clinic staff to the adolescent. Multiple caregivers noted, “it shows that they care.”

Family therapy interventions were generally viewed favorably. Several caregivers noted that the involvement of other family members could provide additional encouragement and support to the adolescent. A few caregivers and adolescents expressed concerns relating to disclosure of the adolescent’s status to close family members–“I just don’t want them to know.” Family interventions may be challenged by limited disclosure within the family.

Caregivers and adolescents offered additional unprompted insights into key facilitators to adolescent care, including adolescent disclosure support, family disclosure and involvement, and adolescent mental health services and counseling (Table 4). The need for additional adolescent counseling was noted by multiple caregivers, as they described significant isolation and mental health concerns among their adolescents. The importance of disclosure to the adolescent as well as to trusted family members were recognized as being critical to the discussed interventions.

Discussion

Significant delay in HIV diagnosis emerged as the most consistent challenge in the care cascade in this study of hospitalized adolescents with HIV infection. The median age at HIV diagnosis (7.5 years) is older than it was once thought that children could survive with HIV untreated [14], and a third were diagnosed in adolescence. While long-term survival of perinatally infected adolescents is increasingly recognized among clinicians and researchers, most laypeople may not know that these children could potentially survive into adolescence untreated [15]. Few of these adolescents were born in the pre-ART era, when more than half died in the first 2 years of life [16]. Many improvements in pediatric HIV diagnosis have occurred since the time these adolescents were infants, with widespread availability of early infant diagnostic services and improved implementation of “opt out” testing. However, there has been insufficient emphasis on HIV diagnosis of young children in healthcare settings outside of the PMTCT context [17]. Most adolescents in this study presented to clinics or were hospitalized on several occasions, before being tested for HIV. For some, HIV testing was reportedly not offered despite their manifestations of HIV-related illnesses. For others, there was hesitancy on the part of the caregivers to test. Clinical and public health leaders in high HIV-burden settings should eliminate barriers to universal pediatric testing. This should include efforts to increase awareness among health care workers and lay people about the possibility of survival into older childhood and adolescence with perinatally acquired HIV. Other efforts to increase uptake of pediatric HIV testing in clinical settings, and to support caregivers through counselling and stigma-reduction interventions, should be pursued.

Late presentation of perinatal HIV infection is associated with profound immunosuppression and advanced disease [14]. Perinatally infected adolescents who do not initiate treatment until after long-standing, advanced immunosuppression are medically vulnerable [18]. Prolonged untreated HIV infection contributes to chronic inflammation, impaired immune recovery, neurologic and developmental pathology, and the development of opportunistic infections and malignancies. The fact that HIV is the leading cause of death among 10–14 year-olds worldwide suggests that we have failed to find and adequately treat far too many children before they develop profound illness [19]. The high mortality (19.0%) among adolescents with HIV in our cohort is consistent with that observed among children and adults hospitalized with HIV globally and in the African region [20]. There are very limited data around causes of hospitalization and mortality for adolescents with HIV infection; in our series, AIDS-related diagnoses were frequent, as has been observed among children and adults with HIV globally in the ART era [20].

Once diagnosed and linked to care, disengagement of children and adolescents is a complex challenge. A few adolescents in this series had become disengaged soon after diagnosis, and were out of care for years prior to hospitalization with advanced illness. The challenge of early disengagement from HIV care has been described in children in Botswana, and in studies of youth and adults elsewhere in sub-Saharan Africa [2124]. Prior research has demonstrated the negative impacts of stigma, discrimination, and fear of disclosure on adult retention in HIV care [25]. In this series, maternal illness, stigma, and lack of disclosure to close family members influenced poor retention. Further research is needed to define barriers and facilitators to long-term retention for children and adolescents in high-prevalence settings. In addition, interventions to minimize disengagement of children and adolescents and to track and re-engage those who are lost to follow-up should be included in HIV care programs.

Stigma played a central role in breakdowns in the care cascade, and impacted adolescent care through pervasive effects on disclosure to the adolescent and to family. Family relationships, engagement with care, experience of isolation, and adherence to ART were also directly impacted by stigma. While stigma significantly complicates care for all persons living with HIV, perinatally infected adolescents have a particularly unique and challenging experience of stigma [26,27]. These adolescents transition from dependence on caregivers (who may themselves be facing severe illness, mental health issues, poverty, stigma, and isolation); to learning their status; coping with illness or death of family members; navigating peer relationships; and developing autonomy in care; all while undergoing the developmental transition of adolescence and into young adulthood. Interventions to reduce stigma and to mitigate the experience of stigma for adolescents—by strengthening family, peer, and community support—are urgently needed, and will be critical to improving adolescent HIV outcomes in the care cascade [2629].

Problems adhering to ART were common in this study of hospitalized adolescents, and daunting adherence challenges in this age group are well documented [18,30,31]. It is important to recognize that in Gaborone, where pioneering adolescent-centered services are available to support adherence, adherence nevertheless remains a critical and complex challenge. Participants in this series were enthusiastic about participation in a peer group to reduce social isolation and improve HIV education and ART adherence. Many of the adolescents in this series were not receiving adolescent-centered services, such as engagement in a peer support group, either because their status was not yet disclosed to them, or because they were enrolled at clinics that did not provide these and other youth-friendly care services. Indeed adolescent-centered HIV care services remain an exception to the rule, and are not widely available in most settings [18]. For those engaged at clinics providing such services, some continued to have complex difficulties adhering to therapy, including mental health needs requiring ongoing counseling and support. The current evidence base for interventions to improve adolescent adherence is severely limited [32]. Studies of developmentally-appropriate approaches to improve adolescent adherence to ART are critically needed.

Despite the gaps in care and advanced illness experienced by the adolescents in this series, the number of adolescents identified at the tertiary referral hospital in Botswana over a 6-month period was unexpectedly small. This finding contrasts with alarming recent estimates that 100 adolescents are dying daily from HIV in sub-Saharan Africa [33]. While the HIV prevalence in Botswana is high, with its small population, the approximately 17,000 HIV-infected adolescents in Botswana make up less than 1% of the global population of adolescents with HIV, and an even smaller proportion of global adolescent HIV deaths, with fewer than 500 deaths annually [5]. PMH serves as both the major referral hospital for the country and the primary hospital for the capital city. However, our study may under-represent the adolescent epidemic in Botswana if adolescents with HIV were predominantly admitted to primary hospitals other than PMH or died in the communities. It’s worth noting that chronically ill patients in Botswana may be brought back to their ancestral villages for end-of-life care [34]. It is also possible that the low number of admissions reflects some relative successes of the pediatric HIV treatment program in Botswana, which may not be representative of the broader adolescent HIV epidemic in sub-Saharan Africa.

A further limitation of our study was our reliance on interviews for self-report of adherence challenges, and for recollection of delays and challenges earlier in the adolescent’s history. Recall bias may have minimized some barriers while over-emphasizing others. The breadth of our semi-structured interview was designed to ascertain the full scale of missed opportunities and challenges along the HIV care cascade for adolescents. However, this did not allow for exhaustive exploration of all specific barriers or potential interventions. For example, targeted interventions to support family disclosure and to mitigate mental health concerns were discussed with all participants, but not comprehensively evaluated by this study. Finally, by excluding pregnant adolescents whom we presumed would be admitted primarily for obstetric care and more likely to have behaviorally acquired HIV, we were not able to evaluate gaps in the care cascade prior to hospitalization with any HIV-related complications in this group. These are important areas for future investigations.

Conclusion

These data highlight the failure of timely diagnosis of pediatric HIV infection among adolescents at the highest risk of poor HIV treatment outcomes. More work is still needed to address pervasive stigma, to study interventions for adherence and retention, to support disclosure to both adolescents and their close family members when needed, and to raise awareness of late presentation of perinatal HIV infection. Greater access to disclosure support, peer groups, adherence support, and mental health care is needed.

Supporting information

S1 File. Interview guides.

Interview guides used for caregivers, disclosed adolescents, and non-disclosed adolescents.

https://doi.org/10.1371/journal.pone.0195372.s001

(PDF)

Acknowledgments

The authors wish to express their gratitude and appreciation for the patients, caregivers, and hospital staff who made this study possible. This work is dedicated to the memory of Dr. Melissa Ketunuti.

References

  1. 1. UNAIDS. All In to #EndAdolescentAIDS. UNAIDS; 2015 Jan.
  2. 2. United Nations Children’s Fund, UNICEF. Towards an AIDS-Free Generation: Children and AIDS: Sixth Stocktaking Report, 2013. New York, NY: UNICEF; 2013 Nov pp. 1–88.
  3. 3. WHO. Health for the World’s Adolescents: A second chance in the second decade [Internet]. Geneva, Switzerland: World Health Organization; 10 May 2014 [cited 29 Nov 2017]. http://www.who.int/maternal_child_adolescent/documents/second-decade/en/
  4. 4. Wood SM, Dowshen N, Lowenthal E. Time to Improve the Global Human Immunodeficiency Virus/AIDS Care Continuum for Adolescents: A Generation at Stake. JAMA Pediatr. 2015;169: 619–620. pmid:25985061
  5. 5. UNAIDS. UNAIDS Estimates 2017. [Internet]. [cited 30 Nov 2017]. http://aidsinfo.unaids.org
  6. 6. Farahani M, Vable A, Lebelonyane R, Seipone K, Anderson M, Avalos A, et al. Outcomes of the Botswana national HIV/AIDS treatment programme from 2002 to 2010: a longitudinal analysis. The Lancet Global Health. Elsevier; 2014;2: e44–50.
  7. 7. Botswana Ministry of Health. Botswana National HIV & AIDS Treatment Guidelines. 2012;: 1–197.
  8. 8. Statistics Botswana. Botswana AIDS Impact Survey IV(BAIS IV) 2013: Summary Results [Internet]. Gaborone: Statistics Botswana; 2013 Nov. http://www.statsbots.org.bw/sites/default/files/publications/Botswana%20AIDS%20Impact%20Survey%20Summary%20%20Apr%202014.pdf
  9. 9. UNICEF. For Every Child, End AIDS: Seventh Stocktaking Report, 2016. New York, NY: UNICEF; 2016 pp. 1–92.
  10. 10. Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, Conde JG. Research electronic data capture (REDCap)—A metadata-driven methodology and workflow process for providing translational research informatics support. Journal of Biomedical Informatics. Elsevier Inc; 2009;42: 377–381. pmid:18929686
  11. 11. Fereday J, Muir-Cochrane E. Demonstrating rigor using thematic analysis: A hybrid approach of inductive and deductive coding and theme development. International Journal of Qualitative Methods. 2008;5: 80–92.
  12. 12. Kondracki NL, Wellman NS, Amundson DR. Content analysis: review of methods and their applications in nutrition education. J Nutr Educ Behav. 2002;34: 224–230. pmid:12217266
  13. 13. WHO. WHO case definitions of HIV for surveillance and revised clinical staging and immunological classification of HIV-related disease in adults and children. Geneva, Switzerland: World Health Organization; 2007 Sep pp. 1–52.
  14. 14. Ferrand RA, Luethy R, Bwakura F, Mujuru H, Miller RF, Corbett EL. HIV Infection Presenting in Older Children and Adolescents: A Case Series from Harare, Zimbabwe. Clinical Infectious Diseases. 2007;44: 874–878. pmid:17304463
  15. 15. Buzdugan R, Watadzaushe C, Dirawo J, Mundida O, Langhaug L, Willis N, et al. Positive attitudes to pediatric HIV testing: findings from a nationally representative survey from Zimbabwe. Vermund SH, editor. PLoS ONE. Public Library of Science; 2012;7: e53213–8. pmid:23285268
  16. 16. Newell M-L, Coovadia H, Cortina-Borja M, Rollins N, Gaillard P, Dabis F. Mortality of infected and uninfected infants born to HIV-infected mothers in Africa: a pooled analysis. The Lancet. 2004;364: 1236–1243.
  17. 17. Cohn J, Whitehouse K, Tuttle J, Lueck K, Tran T. Paediatric HIV testing beyond the context of prevention of mother-to-child transmission: a systematic review and meta-analysis. The Lancet HIV. Elsevier; 2016;0.
  18. 18. Lowenthal ED, Bakeera-Kitaka S, Marukutira T, Chapman J, Goldrath K, Ferrand RA. Perinatally acquired HIV infection in adolescents from sub-Saharan Africa: a review of emerging challenges. The Lancet Infectious Diseases. 2014;14: 627–639. pmid:24406145
  19. 19. Mokdad AH, Forouzanfar MH, Daoud F, Mokdad AA, El Bcheraoui C, Moradi-Lakeh M, et al. Global burden of diseases, injuries, and risk factors for young people’s health during 1990–2013: a systematic analysis for the Global Burden of Disease Study 2013. The Lancet. 2016;387: 2383–2401.
  20. 20. Ford N, Shubber Z, Meintjes G, Grinsztejn B, Eholie S, Mills EJ, et al. Causes of hospital admission among people living with HIV worldwide: a systematic review and meta-analysis. The Lancet. World Health Organization. Published by Elsevier Ltd/Inc/BV. All rights reserved; 2015;2: e438–44.
  21. 21. Lamb MR, Fayorsey R, Nuwagaba-Biribonwoha H, Viola V, Mutabazi V, Alwar T, et al. High attrition before and after ART initiation among youth (15–24 years of age) enrolled in HIV care. AIDS. 2014;28: 559–568. pmid:24076661
  22. 22. Ojwang VO, Penner J, Blat C, Agot K, Bukusi EA, Cohen CR. Loss to follow-up among youth accessing outpatient HIV care and treatment services in Kisumu, Kenya. AIDS Care. 4 ed. 2015;28: 500–507. pmid:26565428
  23. 23. Arnesen R, Moll AP, Shenoi SV. Predictors of loss to follow-up among patients on ART at a rural hospital in KwaZulu-Natal, South Africa. Perno CF, editor. PLoS ONE. Public Library of Science; 2017;12: e0177168–12. pmid:28542309
  24. 24. Machine EM, Gillespie SL, Homedes N, Selwyn BJ, Ross MW, Anabwani G, et al. Lost to follow-up: failure to engage children in care in the first three months of diagnosis. AIDS Care. 2016;: 1–9. pmid:27160542
  25. 25. Hall BJ, Sou K-L, Beanland R, Lacky M, Tso LS, Ma Q, et al. Barriers and Facilitators to Interventions Improving Retention in HIV Care: A Qualitative Evidence Meta-Synthesis. AIDS and Behavior. Springer US; 2016;: 1–13. pmid:27582088
  26. 26. Williams S, Renju J, Ghilardi L, Wringe A. Scaling a waterfall: a meta-ethnography of adolescent progression through the stages of HIV care in sub-Saharan Africa. Journal of the International AIDS Society. Taylor & Francis; 2017;20: 1–17. pmid:28953326
  27. 27. Wolf HT, Halpern-Felsher BL, Bukusi EA, Agot KE, Cohen CR, Auerswald CL. “It is all about the fear of being discriminated [against]…the person suffering from HIV will not be accepted”: a qualitative study exploring the reasons for loss to follow-up among HIV-positive youth in Kisumu, Kenya. BMC Public Health. BioMed Central; 2014;14: 1565–11. pmid:25377362
  28. 28. Reif LK, Bertrand R, Benedict C, Lamb MR, Rouzier V, Verdier R, et al. Impact of a youth-friendly HIV clinic: 10 years of adolescent outcomes in Port-au-Prince, Haiti. Journal of the International AIDS Society. 2016;19: 1–10. pmid:27389256
  29. 29. Teasdale CA, Alwar T, Chege D, Fayorsey R, Hawken MP, Abrams EJ. Impact of Youth and Adolescent Friendly Services on Retention of 10–24-Year-Olds in HIV Care and Treatment Programs in Nyanza, Kenya. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2016;71: e56–e59. pmid:26505330
  30. 30. Vreeman RC, Nyandiko WM, Liu H, Tu W, Scanlon ML, Slaven JE, et al. Comprehensive Evaluation of Caregiver-Reported Antiretroviral Therapy Adherence for HIV-Infected Children. AIDS and Behavior. 2015;19: 626–634. pmid:25613594
  31. 31. Yang E, Mphele S, Moshashane N, Bula B, Chapman J, Okatch H, et al. Distinctive barriers to antiretroviral therapy adherence among non-adherent adolescents living with HIV in Botswana. AIDS Care. 2018;30: 224–231. pmid:28643572
  32. 32. Shaw S, Amico KR. Antiretroviral Therapy Adherence Enhancing Interventions for Adolescents and Young Adults 13–24 Years of Age: A Review of the Evidence Base. J Acquir Immune Defic Syndr. 2016;72: 387–399. pmid:26959190
  33. 33. UNAIDS. Estimates. 2016.
  34. 34. Livingston J. Debility and the Moral Imagination in Botswana (African Systems of Thought Series). Bloomington: Indiana University Press; 2005.