Dual Analysis of Loss to Follow-up for Perinatally HIV-Infected Adolescents Receiving Combination Antiretroviral Therapy in Asia

被引:2
作者
Bartlett, Adam W. [1 ]
Lumbiganon, Pagakrong [2 ,23 ]
Mohamed, Thahira A. Jamal [3 ]
Lapphra, Keswadee [4 ]
Muktiarti, Dina [5 ]
Quy Tuan Du [6 ]
Hansudewechakul, Rawiwan [7 ]
Ly, Penh Sun [8 ]
Khanh Huu Truong [6 ]
Lam Van Nguyen [9 ]
Puthanakit, Thanyawee [10 ,11 ,26 ]
Sudjaritruk, Tavitiya [12 ,13 ]
Chokephaibulkit, Kulkanya [4 ]
Do, Viet Chau [14 ]
Kumarasamy, Nagalingeswaran [15 ]
Yusoff, Nik Khairulddin Nik [16 ]
Kurniati, Nia [5 ]
Fong, Moy Siew [17 ]
Wati, Dewi Kumara [18 ]
Nallusamy, Revathy [19 ]
Sohn, Annette H. [20 ]
Kariminia, Azar [1 ]
Khol, V. [8 ]
Tucker, J. [21 ]
Ezhilarasi, C. [15 ]
Kinikar, A. [22 ]
Mave, V. [22 ]
Nimkar, S. [22 ]
Vedaswari, D. [18 ]
Ramajaya, I. B. [18 ]
Fong, S. M. [17 ]
Lim, M. [17 ]
Daut, F. [17 ]
Mohamad, P. [16 ]
Mohamed, T. J.
Drawis, M. R. [3 ]
Chan, K. C. [19 ]
Sirisanthana, V. [12 ,13 ]
Aurpibul, L.
Ounchanum, P. [7 ]
Denjanta, S. [7 ]
Kongphonoi, A. [7 ]
Kosalaraksa, P. [23 ]
Tharnprisan, P. [23 ]
Udomphanit, T. [23 ]
Jourdain, G. [24 ,25 ]
Anugulruengkit, S. [11 ,26 ]
Jantarabenjakul, W. [11 ,26 ]
Nadsasarn, R. [11 ,26 ]
Phongsamart, W. [4 ]
机构
[1] UNSW Australia, Kirby Inst, Sydney, NSW, Australia
[2] Khon Kaen Univ, Fac Med, Dept Pediat, Khon Kaen, Thailand
[3] Hosp Kuala Lumpur, Inst Pediat, Kuala Lumpur, Malaysia
[4] Mahidol Univ, Siriraj Hosp, Fac Med, Dept Pediat, Bangkok, Thailand
[5] Univ Indonesia, Cipto Mangunkusumo Fac Med, Jakarta, Indonesia
[6] Childrens Hosp 1, Ho Chi Minh City, Vietnam
[7] Chiangrai Prachanukroh Hosp, Chiang Rai, Thailand
[8] Natl Ctr HIV AIDS Dermatol & STDs, Phnom Penh, Cambodia
[9] Natl Hosp Pediat, Hanoi, Vietnam
[10] Thai Red Cross AIDS Res Ctr, HIV Netherlands Australia Thailand Res Collaborat, Bangkok, Thailand
[11] Chulalongkorn Univ, Fac Med, Dept Pediat, Bangkok, Thailand
[12] Chiang Mai Univ, Fac Med, Dept Pediat, Chiang Mai, Thailand
[13] Chiang Mai Univ, Res Inst Hlth Sci, Chiang Mai, Thailand
[14] Childrens Hosp 2, Ho Chi Minh City, Vietnam
[15] VHS, VHS Infect Dis Med Ctr, Chennai Antiviral Res & Treatment Clin Res Site C, Chennai, Tamil Nadu, India
[16] Hosp Raja Perempuan Zainab II, Kelantan, Malaysia
[17] Hosp Likas, Kota Kinabalu, Sabah, Malaysia
[18] Udayana Univ, Sanglah Hosp, Bali, Indonesia
[19] Penang Hosp, George Town, Penang, Malaysia
[20] Fdn AIDS Res, TREAT Asia AmfAR, Bangkok, Thailand
[21] New Hope Cambodian Children, Phnom Penh, Cambodia
[22] BJ Med Coll & Sassoon Gen Hosp, Pune, Maharashtra, India
[23] Khon Kaen Univ, Dept Pediat, Div Infect Dis, Fac Med, Khon Kaen, Thailand
[24] PHPT IRD UMI 174 Inst Rech Dev, Chiang Mai, Thailand
[25] Chiang Mai Univ, Chiang Mai, Thailand
[26] Chulalongkorn Univ, Res Unit Pediat & Infect Dis, Bangkok, Thailand
[27] Worldwide Orphans Fdn, Ho Chi Minh City, Vietnam
基金
美国国家卫生研究院;
关键词
HIV; adolescent; loss to follow-up;
D O I
10.1097/QAI.0000000000002184
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
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收藏
页码:431 / 438
页数:8
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