Extending Visit Intervals for Clinically Stable Patients on Antiretroviral Therapy: Multicohort Analysis of HIV Programs in Southern Africa.
Adolescent
Adult
Africa, Southern
Anti-Retroviral Agents
/ therapeutic use
CD4 Lymphocyte Count
Cohort Studies
Delivery of Health Care
/ organization & administration
Drug Monitoring
Female
HIV Infections
/ drug therapy
Humans
Male
Middle Aged
Regression Analysis
Survival Analysis
Treatment Outcome
Viral Load
Young Adult
Journal
Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005
Informations de publication
Date de publication:
01 08 2019
01 08 2019
Historique:
entrez:
27
6
2019
pubmed:
27
6
2019
medline:
25
2
2020
Statut:
ppublish
Résumé
The World Health Organization recommends differentiated antiretroviral therapy (ART) delivery with longer visit intervals for clinically stable patients. We examined time trends in visit frequency and associations between criteria for clinical stability and visit frequency in ART programs in Southern Africa. We included adults on ART from 4 programs with viral-load monitoring, 2 programs with CD4 monitoring, and 4 programs with clinical monitoring of ART. We classified patients as clinically stable based on virological (viral load <1000 copies/mL), immunological (CD4 >200 cells/µL), or clinical (no current tuberculosis) criteria. We used Poisson regression and survival models to examine associations between criteria for clinical stability and the rate of clinic visits. We included 180,837 patients. There were trends toward fewer visits in more recent years and with longer ART duration. In all ART programs, clinically stable patients were seen less frequently than patients receiving failing ART, but the strength of the association varied. Adjusted incidence rate ratios comparing visit rates for stable patients with patients on failing ART were 0.82 (95% confidence interval: 0.73 to 0.90) for patients classified based on the virological criterion, 0.81 (0.69 to 0.93) for patients classified based on the clinical criterion, and 0.90 (0.85 to 0.96) for patients classified based on the immunological criterion for stability. Differences in visit rates between stable patients and patients failing ART were variable and modest overall. Larger differences were seen in programs using virological criteria for clinical stability than in programs using immunological criteria. Greater access to routine viral-load monitoring may increase scale-up of differentiated ART delivery.
Sections du résumé
BACKGROUND
The World Health Organization recommends differentiated antiretroviral therapy (ART) delivery with longer visit intervals for clinically stable patients. We examined time trends in visit frequency and associations between criteria for clinical stability and visit frequency in ART programs in Southern Africa.
METHODS
We included adults on ART from 4 programs with viral-load monitoring, 2 programs with CD4 monitoring, and 4 programs with clinical monitoring of ART. We classified patients as clinically stable based on virological (viral load <1000 copies/mL), immunological (CD4 >200 cells/µL), or clinical (no current tuberculosis) criteria. We used Poisson regression and survival models to examine associations between criteria for clinical stability and the rate of clinic visits.
RESULTS
We included 180,837 patients. There were trends toward fewer visits in more recent years and with longer ART duration. In all ART programs, clinically stable patients were seen less frequently than patients receiving failing ART, but the strength of the association varied. Adjusted incidence rate ratios comparing visit rates for stable patients with patients on failing ART were 0.82 (95% confidence interval: 0.73 to 0.90) for patients classified based on the virological criterion, 0.81 (0.69 to 0.93) for patients classified based on the clinical criterion, and 0.90 (0.85 to 0.96) for patients classified based on the immunological criterion for stability.
CONCLUSION
Differences in visit rates between stable patients and patients failing ART were variable and modest overall. Larger differences were seen in programs using virological criteria for clinical stability than in programs using immunological criteria. Greater access to routine viral-load monitoring may increase scale-up of differentiated ART delivery.
Identifiants
pubmed: 31242142
doi: 10.1097/QAI.0000000000002060
pii: 00126334-201908010-00012
pmc: PMC6597180
mid: NIHMS1525564
doi:
Substances chimiques
Anti-Retroviral Agents
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
439-447Subventions
Organisme : World Health Organization
ID : 001
Pays : International
Organisme : NIAID NIH HHS
ID : U01 AI069924
Pays : United States
Références
J Int AIDS Soc. 2017 Nov;20 Suppl 7:
pubmed: 29130601
J Acquir Immune Defic Syndr. 2014 Sep 1;67(1):45-51
pubmed: 24872139
Trop Med Int Health. 2016 Sep;21(9):1124-30
pubmed: 27371814
J Acquir Immune Defic Syndr. 2016 Jan 1;71(1):e16-23
pubmed: 26473798
J Acquir Immune Defic Syndr. 2018 Aug 15;78 Suppl 2:S124-S127
pubmed: 29994834
Int J Epidemiol. 2012 Oct;41(5):1256-64
pubmed: 21593078
Stat Med. 2002 Aug 15;21(15):2175-97
pubmed: 12210632
J Int AIDS Soc. 2018 Mar;21(3):
pubmed: 29537628
J Int AIDS Soc. 2017 Jul 21;20(Suppl 4):21648
pubmed: 28770597
Lancet HIV. 2015 Jul;2(7):e271-8
pubmed: 26423252
BMC Health Serv Res. 2014 Aug 19;14:352
pubmed: 25138583
PLoS One. 2018 Jun 11;13(6):e0198686
pubmed: 29889862
Clin Infect Dis. 2016 Apr 15;62(8):1043-8
pubmed: 26743094
Trop Med Int Health. 2015 Apr;20(4):430-47
pubmed: 25583302
Clin Infect Dis. 2018 Jan 6;66(2):237-243
pubmed: 29020295
Clin Infect Dis. 2018 Sep 28;67(8):1269-1277
pubmed: 29635466
J Int AIDS Soc. 2017 Jul 21;20(Suppl 4):21647
pubmed: 28770599
Nature. 2015 Dec 3;528(7580):S68-76
pubmed: 26633768
J Int AIDS Soc. 2017 Jul 21;20(Suppl 4):21650
pubmed: 28770594
Clin Infect Dis. 2018 Mar 5;66(6):893-903
pubmed: 29373672
AIDS. 2014 Mar;28 Suppl 2:S161-9
pubmed: 24849476