Clinical outcomes after an unstructured treatment interruption in children and adolescents with perinatally acquired HIV infection

被引:31
|
作者
Saitoh, Akihiko [1 ]
Foca, Marc [3 ]
Viani, Rolando M. [1 ]
Heffernan-Vacca, Susan [3 ]
Vaida, Florin [2 ]
Lujan-Zilbermann, Jorge [4 ]
Emmanuel, Patricia J. [4 ]
Deville, Jaime G. [5 ]
Spector, Stephen A. [1 ]
机构
[1] Univ Calif San Diego, Dept Pediat, Div Infect Dis, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Family & Prevent Med, Div Biostat & Bioinformat, La Jolla, CA 92093 USA
[3] Columbia Univ, Dept Pediat, Div Infect Dis, New York, NY 10027 USA
[4] Univ S Florida, Coll Med, Dept Pediat, Div Infect Dis, Tampa, FL 33612 USA
[5] Univ Calif Los Angeles, Sch Med, Dept Pediat, Div Infect Dis, Los Angeles, CA 90024 USA
关键词
treatment interruption; HIV-1; children; adolescent; nadir CD4(+) T-cell percentage; medication fatigue;
D O I
10.1542/peds.2007-1086
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
OBJECTIVE. An unstructured treatment interruption in children with perinatally acquired HIV infection is an issue with unresolved significance. The objective of this study was to investigate the actual prevalence and clinical outcomes of a treatment interruption in children and adolescents with perinatally acquired HIV-1 infection. METHODS. Clinical data were analyzed for 72 children and adolescents who had HIV-1 infection and stopped their medications at 4 academic centers in the United States between January 2000 and September 2004. RESULTS. Among 405 patients with perinatal HIV-1 infection, 72 (17.8%) experienced a treatment interruption during the observation period. The mean age of patients at the time of the treatment interruption was 12.8 years, and the mean length of the treatment interruption was 14 months. Medication fatigue was the most common reason for a treatment interruption. The CD4(+) T-cell percentage nadir before the treatment interruption did not predict CD4(+) T-cell percentage declines during the treatment interruption; however, the CD4(+) T-cell percentage gain from nadir to the time of the treatment interruption predicted CD4(+) T-cell percentage declines during the treatment interruption. During the median follow-up of 19 months (range: 6-48 months), 48 (67%) patients resumed antiretroviral medications. As expected, there was a continuous CD4(+) T-cell percentage decrease and plasma HIV-1 RNA increase during the observation period. Overall, 7 (10%) patients were admitted to the hospital; 2 (3%) patients experienced an AIDS-defining illness. CONCLUSIONS. An unstructured treatment interruption seems to be a major issue for youth with perinatally acquired HIV-1 infection. Patients who experienced the greatest rise in CD4(+) T-cell percentage on treatment had the largest CD4(+) T-cell percentage decline after the treatment interruption. Close monitoring is required when a treatment interruption occurs in children and adolescents with HIV infection.
引用
收藏
页码:E513 / E521
页数:9
相关论文
共 50 条
  • [21] Adults with Perinatally Acquired HIV; Emerging Clinical Outcomes and Data Gaps
    Henderson, Merle
    Fidler, Sarah
    Foster, Caroline
    TROPICAL MEDICINE AND INFECTIOUS DISEASE, 2024, 9 (04)
  • [22] An Updated Systematic Review of Neuroimaging Studies of Children and Adolescents with Perinatally Acquired HIV
    Kayla A. Musielak
    Jodene Goldenring Fine
    Journal of Pediatric Neuropsychology, 2016, 2 (1-2) : 34 - 49
  • [23] Use and Outcomes of Antiretroviral Monotherapy and Treatment Interruption in Adolescents With Perinatal HIV Infection in Asia
    Bartlett, Adam W.
    Lumbiganon, Pagakrong
    Kurniati, Nia
    Sudjaritruk, Tavitiya
    Mohamed, Thahira J.
    Hansudewechakul, Rawiwan
    Ly, Penh S.
    Truong, Khanh H.
    Puthanakit, Thanyawee
    Nguyen, Lam, V
    Chokephaibulkit, Kulkanya
    Do, Viet C.
    Kumarasamy, Nagalingeswaran
    Yusoff, Nik Khairulddin Nik
    Fong, Moy S.
    Watu, Dewi K.
    Nallusamy, Revathy
    Sohn, Annette H.
    Law, Matthew G.
    Ly, P. S.
    Khol, V
    Tucker, J.
    Kumarasamy, N.
    Chandrasekaran, E.
    Wati, D. K.
    Vedaswari, D.
    Ramajaya, I. B.
    Kurniati, N.
    Muktiarti, D.
    Fong, S. M.
    Lim, M.
    Daut, F.
    Yusoff, N. K. Nik
    Mohamad, P.
    Mohamed, T. J.
    Drawis, M. R.
    Nallusamy, R.
    Chan, K. C.
    Sudjaritruk, T.
    Sirisanthana, V
    Aurpibul, L.
    Hansudewechakul, R.
    Ounchanum, P.
    Denjanta, S.
    Kongphonoi, A.
    Lumbiganon, P.
    Kosalaraksa, P.
    Tharnprisan, P.
    Udomphanit, T.
    Jourdain, G.
    JOURNAL OF ADOLESCENT HEALTH, 2019, 65 (05) : 651 - 659
  • [24] Serological response to 13-valent pneumococcal conjugate vaccine in children and adolescents with perinatally acquired HIV infection
    Bamford, Alasdair
    Kelleher, Peter
    Lyall, Hermione
    Haston, Mitch
    Zancolli, Marta
    Goldblatt, David
    Kampmann, Beate
    AIDS, 2014, 28 (14) : 2033 - 2043
  • [25] CONTROLLING PERINATALLY ACQUIRED HIV-INFECTION
    ROGERS, MF
    WESTERN JOURNAL OF MEDICINE, 1987, 147 (01): : 109 - 110
  • [26] Impact of the frequency of plasma viral load monitoring on treatment outcomes among children with perinatally acquired HIV
    Sudjaritruk, Tavitiya
    Boettiger, David C.
    Nguyen, Lam Van
    Mohamed, Thahira J.
    Wati, Dewi K.
    Bunupuradah, Torsak
    Hansudewechakul, Rawiwan
    Ly, Penh S.
    Lumbiganon, Pagakrong
    Nallusamy, Revathy A.
    Fong, Moy S.
    Chokephaibulkit, Kulkanya
    Yusoff, Nik K. Nik
    Truong, Khanh H.
    Do, Viet C.
    Sohn, Annette H.
    Sirisanthana, Virat
    JOURNAL OF THE INTERNATIONAL AIDS SOCIETY, 2019, 22 (06)
  • [27] PERINATALLY ACQUIRED HIV-INFECTION IN CHILDREN - EARLY TREATMENT WITH AZIDOTHYMIDINE AND PREVENTION OF SECONDARY INFECTIOUS COMPLICATIONS
    MICHEL, G
    VALLEE, D
    THURET, I
    CHAMBOST, H
    TAMALET, C
    DEBOISSE, P
    LECLAIRE, M
    FARNARIER, C
    KAPLANSKI, S
    PERRIMOND, H
    PEDIATRIE, 1992, 47 (11): : 773 - 778
  • [28] Age-related viral suppression in adolescents living with perinatally acquired HIV infection
    Raghunanan, S.
    Foster, C.
    HIV MEDICINE, 2017, 18 : 12 - 13
  • [29] RESPONSES TO COMMON VACCINES IN ADOLESCENTS WITH HIV ACQUIRED PERINATALLY
    Rosso, R.
    De Hoffer, L.
    Parisini, A.
    Nicolini, L. A.
    Secondo, G.
    Taramasso, L.
    Nicco, E.
    Di Biagio, A.
    Viscoli, C.
    INFECTION, 2011, 39 : S69 - S70
  • [30] PERINATALLY ACQUIRED HIV AND EMOTIONAL DISORDERS IN CHILDREN
    Laura, M.
    Wilkinson, P.
    ACTA PAEDIATRICA, 2010, 99 : 89 - 89