First name
Jessica
Last name
Eby

Title

INVESTIGATING OUTCOMES OF ADOLESCENTS AND YOUNG ADULTS (10-24 YEARS OF AGE) LOST TO FOLLOW-UP FROM TUBERCULOSIS TREATMENT IN GABORONE, BOTSWANA.

Year of Publication

2019

Date Published

2019 Jun 17

ISSN Number

1532-0987

Abstract

<p>This retrospective study investigated outcomes among lost to follow-up (LTFU) adolescents and young adults (AYAs: 10-24 years of age) with tuberculosis (TB) registered from 2008 to 2014 in Gaborone, using surveillance data. Of 68 LTFU AYAs, 16 repeated treatment; 8 completed and 6 were again LTFU. Of 4 confirmed deaths, 3 had TB/HIV coinfection. Approaches to improve AYA retention in TB care are needed.</p>

DOI

10.1097/INF.0000000000002369

Alternate Title

Pediatr. Infect. Dis. J.

PMID

31220045

Title

Psychosocial assessments for HIV+ African adolescents: establishing construct validity and exploring under-appreciated correlates of adherence.

Year of Publication

2014

Number of Pages

e109302

Date Published

2014

ISSN Number

1932-6203

Abstract

<p><strong>STUDY OBJECTIVES: </strong>Psychosocial factors such as outcome expectancy, perceived stigma, socio-emotional support, consideration of future consequences, and psychological reactance likely influence adolescent adherence to antiretroviral treatments. Culturally-adapted and validated tools for measuring these factors in African adolescents are lacking. We aimed to identify culturally-specific factors of importance to establishing local construct validity in Botswana.</p>

<p><strong>METHODS: </strong>Using in-depth interviews of 34 HIV+ adolescents, we explored how the psychosocial factors listed above are perceived in this cultural context. We evaluated six scales that have been validated in other contexts. We also probed for additional factors that the adolescents considered important to their HIV medication adherence. Analyses were conducted with an analytic framework approach using NVivo9 software.</p>

<p><strong>RESULTS: </strong>While the construct validity of some Western-derived assessment tools was confirmed, other tools were poorly representative of their constructs in this cultural context. Tools chosen to evaluate HIV-related outcome expectancy and perceived stigma were well-understood and relevant to the adolescents. Feedback from the adolescents suggested that tools to measure all other constructs need major modifications to obtain construct validity in Botswana. The scale regarding future consequences was poorly understood and contained several items that lacked relevance for the Batswana adolescents. They thought psychological reactance played an important role in adherence, but did not relate well to many components of the reactance scale. Measurement of socio-emotional support needs to focus on the adolescent-parent relationship, rather than peer-support in this cultural context. Denial of being HIV-infected was an unexpectedly common theme. Ambivalence about taking medicines was also expressed.</p>

<p><strong>DISCUSSION: </strong>In-depth interviews of Batswana adolescents confirmed the construct validity of some Western-developed psychosocial assessment tools, but demonstrated limitations in others. Previously underappreciated factors related to HIV medication adherence, such as denial and ambivalence, should be further explored.</p>

DOI

10.1371/journal.pone.0109302

Alternate Title

PLoS ONE

PMID

25279938

Title

Antiretroviral treatment in HIV-1 infected pediatric patients: focus on efavirenz.

Year of Publication

2014

Number of Pages

29-42

Date Published

2014 May 29

ISSN Number

1179-9927

Abstract

<p>Efavirenz is a non-nucleoside reverse transcriptase inhibitor (NNRTI), used for the treatment of human immunodeficiency virus (HIV)-1 infection. Approved by the US Food and Drug Administration in 1998, its indication was recently extended to include children as young as 3 months of age. The World Health Organization and many national guidelines consider efavirenz to be the preferred NNRTI for first-line treatment of children over the age of 3 years. Clinical outcomes of patients on three-drug antiretroviral regimens which include efavirenz are as good as or better than those for patients on all other currently approved HIV medications. Efavirenz is dosed once daily and has pediatric-friendly formulations. It is usually well tolerated, with central nervous system side effects being of greatest concern. Efavirenz increases the risk of neural tube defects in nonhuman primates and therefore its use during the first trimester of pregnancy is limited in some settings. With minimal interactions with antituberculous drugs, efavirenz is preferred for use among patients with HIV/tuberculosis coinfection. Efavirenz can be rendered inactive by a single point mutation in the reverse transcriptase enzyme. Newer NNRTI drugs such as etravirine, not yet approved for use in children under the age of 6 years, may maintain their activity following development of efavirenz resistance. This review highlights key points from the existing literature regarding the use of efavirenz in children and suggests directions for future investigation.</p>

DOI

10.2147/PHMT.S47794

Alternate Title

Pediatric Health Med Ther

PMID

25937791

Title

The adherence-outcome relationship is not altered by diary-driven adjustments of microelectronic monitor data.

Year of Publication

2015

Number of Pages

1313-20

Date Published

2015 Dec

ISSN Number

1099-1557

Abstract

<p><strong>PURPOSE: </strong>The purpose of this study was to determine whether diary-driven adjustment of Medication Event Monitoring System (MEMS) data based on Supporting Information strengthens the relationship between measured antiretroviral medication adherence and plasma HIV viral load (VL).</p>

<p><strong>METHODS: </strong>HIV+ adolescents on antiretroviral treatment were monitored with MEMS for 30 days preceding a VL measurement. The primary outcome was VL ≥ 400 copies/mL. Handwritten diaries were used to comprehensively record deviations from recommended use (bottle opened but dose not taken or bottle not opened and dose taken). Data were adjusted ("cleaned") based on diary events. Data were "capped" at the prescribed number of doses/day. Receiver operator characteristic analysis compared the relationships between (i) raw MEMS data, (ii) diary-cleaned, (iii) capped, or (iv) cleaned and capped MEMS data and VL.</p>

<p><strong>RESULTS: </strong>Over 30 days preceding VL measurements, 273 adolescents had 465 diary events. Capping resulted in fewer patients classified as 95% adherent (65.2%) compared with raw data (71.4%), p &lt; 0.001. Adherence was highly associated with VL (OR 1.05, p &lt; 0.001). The area under the receiver operating characteristic curve for continuous adherence compared with VL was 0.89 (95%CI: 0.82-0.95). Neither diary-cleaning, capping, nor cleaning and capping MEMS data significantly altered the association between adherence and VL (p = 0.14, 0.40, and 0.19, respectively).</p>

<p><strong>CONCLUSION: </strong>Medication Event Monitoring System data-cleaning based on diary entries did not affect the adherence-VL relationship. Copyright © 2015 John Wiley &amp; Sons, Ltd.</p>

DOI

10.1002/pds.3887

Alternate Title

Pharmacoepidemiol Drug Saf

PMID

26456482

Title

Brief Report: Apparent Antiretroviral Over-adherence by Pill Count is Associated with HIV Treatment Failure in Adolescents.

Year of Publication

2016

Date Published

2016 Mar 16

ISSN Number

1944-7884

Abstract

<p>Pill counts with calculated adherence percentages are used in many settings to monitor adherence, but can be undermined by patients discarding pills to hide non-adherence. Pill counts suggesting that &gt;100% of prescribed doses were taken can signal "pill dumping." We defined "over-adherence" (OA) among a cohort of 300 HIV-infected adolescents as having &gt;1/3 of pill counts with &gt;100% adherence during a year of follow-up. Apparent over-adherence was more common in those with virologic failure than those with suppressed viral loads (33% vs 13%, chi p=0.001). Pill count adherence repeatedly &gt;100% may identify HIV-infected adolescents at increased risk of treatment failure.</p>

DOI

10.1097/QAI.0000000000000994

Alternate Title

J. Acquir. Immune Defic. Syndr.

PMID

26990822

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