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Southern African Journal of HIV Medicine
              ISSN: (Online) 2078-6751, (Print) 1608-9693
                                                       Page 1 of 6  Original Research


                               Feasibility of implementing same-day

                       antiretroviral therapy initiation during routine

                            care in Ekurhuleni District, South Africa:

                               Retention and viral load suppression






               Authors:                 Background: Same-day initiation (SDI) of antiretroviral therapy (ART) has been advocated as
               Nolundi Mshweshwe-       an approach to increase linkage to care and overall  ART initiation. Clinical trials have
               Pakela   1
               Bhakti Hansoti           demonstrated impressive benefits. However, questions regarding patient preparedness and
                        2,3
               Tonderai Mabuto          retention in care remain for routine implementation of this approach.
                          1,4
               Deanna Kerrigan   5
               Griffiths Kubeka         Objectives: In this study, we sought to describe SDI of ART during routine care delivery and
                         1
               Elizabeth Hahn   3       compare time to ART initiation on longitudinal care outcomes.
               Salome Charalambous
                             1,4
               Christopher J. Hoffmann 1,6,7    Method: We performed a retrospective chart review of 100 consecutive individuals, newly
                                        diagnosed with HIV, from 10 health facilities across Ekurhuleni, from January to July 2017.
               Affiliations:            Records were reviewed for a period of 1 year post-diagnosis.  Abstracted data included
               1 Implementation Research
               Division, The Aurum Institute,   demographics, time to  ART initiation, clinic visits and laboratory test results (including
               Johannesburg, South Africa  viral load testing).
               2 Department of Emergency   Results: A total of 993 patient records were reviewed, of which 826 were included in the
               Medicine, Johns Hopkins   analysis. The majority of patients (752, 91%) had ART initiation recorded, of which 654 (79%)
               School of Medicine,      had  ART initiated within 30 days, and 224 (27%) had SDI. Uptake of SDI of  ART was
               Baltimore, United States of   higher  among women (36% vs. 10.4%;  p < 0.001) and in younger patients (33.7% in those
               America
                                        < 29 years; p < 0.01). Retention in care at 6 months was achieved in 477 (58%) patients. Of those
               3 Department of International   with 6-month viral loads, 350/430 (73%) had a viral load < 400 c/m. Retention in care and
               Health, Johns Hopkins    viral suppression were similar among those with SDI of ART and later ART initiation.
               Bloomberg School of Public
               Health, Baltimore,       Conclusion: Same-day initiation of ART was successfully delivered with similar retention
               United States of America  and viral load outcomes as subsequent initiation, providing re-assurance for scale-up of this
                                        strategy in routine care.
               4 School of Public Health,
               University of the        Keywords: HIV testing; primary care; SDI; ARV initiation; implementation.
               Witwatersrand,
               Johannesburg, South Africa
                                       Introduction
               5 Department of Sociology,
               American University,    Timely linkage to antiretroviral therapy (ART) is pivotal to decreasing human
               Washington, United States of   immunodeficiency virus (HIV) transmission and reducing HIV-associated morbidity and
               America
                                               1
                                       mortality.  Increasing evidence indicates that same-day initiation (SDI) of ART can increase
               6 Department of Medicine,   overall linkage to care (LTC) and the proportion of patients with viral load suppression. 2,3,4,5,6,7
               Johns Hopkins University   Randomised studies from South Africa, Haiti and Lesotho have demonstrated the feasibility,
               School of Medicine,     acceptability and improved retention over 6 months with SDI of ART when compared with
               Baltimore, United States of   standard practices in research settings. 5,8,9  In response to clinical trial evidence of the benefits
               America
                                       of  SDI of ART,  the  South African Department of  Health announced  a policy of  universal
               7 Department of Health,   testing and treatment  (UTT) in public health facilities in September 2016 and endorsed
                                                 10
               Behavior, and Society, Johns   SDI of ART.  The UTT directorate specified: ‘ART should be started as soon as the patient is
               Hopkins Bloomberg School   ready and  within 2  weeks’, with immediate (same-day) initiation prioritised for pregnant
               of Public Health, Baltimore,   or breastfeeding women.  Same-day initiation of ART was further highlighted as a priority
                                                            10
               United States of America
                                       in  a 2017 South  African Department of Health circular. 10,11  and in the 2017 World
                                       Health Organization rapid ART initiation guidelines. 12
               Read online:            Corresponding author: Christopher Hoffmann, [email protected]
               Read online:
                        Scan this QR
                        Scan this QR   Dates: Received: 10 Mar. 2020 | Accepted: 07 May 2020 | Published: 20 Aug. 2020
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                                       Copyright: © 2020. The Authors. Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License.
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