Dual Analysis of Loss to Follow-up for Perinatally HIV-Infected Adolescents Receiving Combination Antiretroviral Therapy in Asia
BACKGROUND: Perinatally HIV-infected adolescents (PHIVA) are an expanding population vulnerable to loss to follow-up (LTFU). Understanding the epidemiology and factors for LTFU is complicated by varying LTFU definitions.
SETTING: Asian regional cohort incorporating 16 pediatric HIV services across 6 countries.
METHODS: Data from PHIVA (aged 10-19 years) who received combination antiretroviral therapy 2007-2016 were used to analyze LTFU through (1) an International epidemiology Databases to Evaluate AIDS (IeDEA) method that determined LTFU as >90 days late for an estimated next scheduled appointment without returning to care and (2) the absence of patient-level data for >365 days before the last data transfer from clinic sites. Descriptive analyses and competing-risk survival and regression analyses were used to evaluate LTFU epidemiology and associated factors when analyzed using each method.
RESULTS: Of 3509 included PHIVA, 275 (7.8%) met IeDEA and 149 (4.3%) met 365-day absence LTFU criteria. Cumulative incidence of LTFU was 19.9% and 11.8% using IeDEA and 365-day absence criteria, respectively. Risk factors for LTFU across both criteria included the following: age at combination antiretroviral therapy initiation <5 years compared with age ≥5 years, rural clinic settings compared with urban clinic settings, and high viral loads compared with undetectable viral loads. Age 10-14 years compared with age 15-19 years was another risk factor identified using 365-day absence criteria but not IeDEA LTFU criteria.
CONCLUSIONS: Between 12% and 20% of PHIVA were determined LTFU with treatment fatigue and rural treatment settings consistent risk factors. Better tracking of adolescents is required to provide a definitive understanding of LTFU and optimize evidence-based models of care.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2019 |
---|---|
Erschienen: |
2019 |
Enthalten in: |
Zur Gesamtaufnahme - volume:82 |
---|---|
Enthalten in: |
Journal of acquired immune deficiency syndromes (1999) - 82(2019), 5 vom: 15. Dez., Seite 431-438 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Bartlett, Adam W [VerfasserIn] |
---|
Links: |
---|
Themen: |
Anti-Retroviral Agents |
---|
Anmerkungen: |
Date Completed 02.06.2020 Date Revised 15.12.2020 published: Print Citation Status MEDLINE |
---|
doi: |
10.1097/QAI.0000000000002184 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM30318079X |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM30318079X | ||
003 | DE-627 | ||
005 | 20231225112305.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2019 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1097/QAI.0000000000002184 |2 doi | |
028 | 5 | 2 | |a pubmed24n1010.xml |
035 | |a (DE-627)NLM30318079X | ||
035 | |a (NLM)31714422 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Bartlett, Adam W |e verfasserin |4 aut | |
245 | 1 | 0 | |a Dual Analysis of Loss to Follow-up for Perinatally HIV-Infected Adolescents Receiving Combination Antiretroviral Therapy in Asia |
264 | 1 | |c 2019 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 02.06.2020 | ||
500 | |a Date Revised 15.12.2020 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a BACKGROUND: Perinatally HIV-infected adolescents (PHIVA) are an expanding population vulnerable to loss to follow-up (LTFU). Understanding the epidemiology and factors for LTFU is complicated by varying LTFU definitions | ||
520 | |a SETTING: Asian regional cohort incorporating 16 pediatric HIV services across 6 countries | ||
520 | |a METHODS: Data from PHIVA (aged 10-19 years) who received combination antiretroviral therapy 2007-2016 were used to analyze LTFU through (1) an International epidemiology Databases to Evaluate AIDS (IeDEA) method that determined LTFU as >90 days late for an estimated next scheduled appointment without returning to care and (2) the absence of patient-level data for >365 days before the last data transfer from clinic sites. Descriptive analyses and competing-risk survival and regression analyses were used to evaluate LTFU epidemiology and associated factors when analyzed using each method | ||
520 | |a RESULTS: Of 3509 included PHIVA, 275 (7.8%) met IeDEA and 149 (4.3%) met 365-day absence LTFU criteria. Cumulative incidence of LTFU was 19.9% and 11.8% using IeDEA and 365-day absence criteria, respectively. Risk factors for LTFU across both criteria included the following: age at combination antiretroviral therapy initiation <5 years compared with age ≥5 years, rural clinic settings compared with urban clinic settings, and high viral loads compared with undetectable viral loads. Age 10-14 years compared with age 15-19 years was another risk factor identified using 365-day absence criteria but not IeDEA LTFU criteria | ||
520 | |a CONCLUSIONS: Between 12% and 20% of PHIVA were determined LTFU with treatment fatigue and rural treatment settings consistent risk factors. Better tracking of adolescents is required to provide a definitive understanding of LTFU and optimize evidence-based models of care | ||
650 | 4 | |a Comparative Study | |
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, N.I.H., Extramural | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 7 | |a Anti-Retroviral Agents |2 NLM | |
700 | 1 | |a Lumbiganon, Pagakrong |e verfasserin |4 aut | |
700 | 1 | |a Jamal Mohamed, Thahira A |e verfasserin |4 aut | |
700 | 1 | |a Lapphra, Keswadee |e verfasserin |4 aut | |
700 | 1 | |a Muktiarti, Dina |e verfasserin |4 aut | |
700 | 1 | |a Du, Quy Tuan |e verfasserin |4 aut | |
700 | 1 | |a Hansudewechakul, Rawiwan |e verfasserin |4 aut | |
700 | 1 | |a Ly, Penh Sun |e verfasserin |4 aut | |
700 | 1 | |a Truong, Khanh Huu |e verfasserin |4 aut | |
700 | 1 | |a Van Nguyen, Lam |e verfasserin |4 aut | |
700 | 1 | |a Puthanakit, Thanyawee |e verfasserin |4 aut | |
700 | 1 | |a Sudjaritruk, Tavitiya |e verfasserin |4 aut | |
700 | 1 | |a Chokephaibulkit, Kulkanya |e verfasserin |4 aut | |
700 | 1 | |a Do, Viet Chau |e verfasserin |4 aut | |
700 | 1 | |a Kumarasamy, Nagalingeswaran |e verfasserin |4 aut | |
700 | 1 | |a Nik Yusoff, Nik Khairulddin |e verfasserin |4 aut | |
700 | 1 | |a Kurniati, Nia |e verfasserin |4 aut | |
700 | 1 | |a Fong, Moy Siew |e verfasserin |4 aut | |
700 | 1 | |a Wati, Dewi Kumara |e verfasserin |4 aut | |
700 | 1 | |a Nallusamy, Revathy |e verfasserin |4 aut | |
700 | 1 | |a Sohn, Annette H |e verfasserin |4 aut | |
700 | 1 | |a Kariminia, Azar |e verfasserin |4 aut | |
700 | 0 | |a TREAT Asia Pediatric HIV Observational Database of IeDEA Asia-Pacific |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Journal of acquired immune deficiency syndromes (1999) |d 1999 |g 82(2019), 5 vom: 15. Dez., Seite 431-438 |w (DE-627)NLM101679912 |x 1944-7884 |7 nnns |
773 | 1 | 8 | |g volume:82 |g year:2019 |g number:5 |g day:15 |g month:12 |g pages:431-438 |
856 | 4 | 0 | |u http://dx.doi.org/10.1097/QAI.0000000000002184 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 82 |j 2019 |e 5 |b 15 |c 12 |h 431-438 |