Immediate Blood Draw for CD4+ Cell Count Is Associated with Linkage to Care in Durban, South Africa : Findings from Pathways to Engagement in HIV Care

BACKGROUND: Timely linkage to care by newly-diagnosed HIV+ individuals remains a significant challenge to achieving UNAIDS 90-90-90 goals. Current World Health Organization (WHO) guidelines recommend initiating anti-retroviral treatment (ART) regardless of CD4+ count, with priority given to those with CD4+ <350 cells/μl. We evaluated the impact of not having a day-of-diagnosis CD4+ count blood draw, as recommended by South African guidelines, on time to linkage, using data from a prospective cohort study.

METHODS: Individuals (N = 2773) were interviewed prior to HIV counseling and testing at three public sector primary care clinics in the greater Durban area; 785 were newly-diagnosed and eligible for the cohort study; 459 (58.5%) joined and were followed for eight months with three structured assessments. Linkage to care, defined as returning to clinic for CD4+ count results, and day-of-diagnosis blood draw were self-reported.

RESULTS: Overall, 72.5% did not have a day-of-diagnosis CD4+ count blood draw, and 19.2% of these never returned. Compared with a day-of-diagnosis blood draw, the adjusted hazard ratio of linkage (AHRlinkage) associated with not having day-of-diagnosis blood draw was 0.66 (95%CI: 0.51, 0.85). By 4 months, 54.8% of those without day-of-diagnosis blood draw vs. 75.2% with one were linked to care (chi-squared p = 0.004). Of those who deferred blood draw, 48.3% cited clinic-related and 51.7% cited personal reasons. AHRlinkage was 0.60 (95%CI: 0.44, 0.82) for clinic-related and 0.53 (95%CI: 0.38, 0.75) for personal reasons relative to having day-of-diagnosis blood draw.

CONCLUSIONS: Newly-diagnosed HIV+ individuals who did not undergo CD4+ count blood draw on the day they were diagnosed-regardless of the reason for deferring-had delayed linkage to care relative to those with same-day blood draw. To enhance prompt linkage to care even when test and treat protocols are implemented, all diagnostic testing required before ART initiation should be performed on the same day as HIV testing/diagnosis. This may require modifying clinic procedures to enable overnight blood storage if same-day draws cannot be performed, and providing additional counseling to encourage newly-diagnosed individuals to complete day-of-diagnosis testing. Tracking HIV+ individuals via clinic registries should commence immediately from diagnosis to reduce these early losses to care.

Medienart:

E-Artikel

Erscheinungsjahr:

2016

Erschienen:

2016

Enthalten in:

Zur Gesamtaufnahme - volume:11

Enthalten in:

PloS one - 11(2016), 10 vom: 27., Seite e0162085

Sprache:

Englisch

Beteiligte Personen:

Hoffman, Susie [VerfasserIn]
Exner, Theresa M [VerfasserIn]
Lince-Deroche, Naomi [VerfasserIn]
Leu, Cheng-Shiun [VerfasserIn]
Phillip, Jessica L [VerfasserIn]
Kelvin, Elizabeth A [VerfasserIn]
Gandhi, Anisha D [VerfasserIn]
Levin, Bruce [VerfasserIn]
Singh, Dinesh [VerfasserIn]
Mantell, Joanne E [VerfasserIn]
Blanchard, Kelly [VerfasserIn]
Ramjee, Gita [VerfasserIn]

Links:

Volltext

Themen:

Anti-Retroviral Agents
Journal Article

Anmerkungen:

Date Completed 20.06.2017

Date Revised 19.12.2018

published: Electronic-eCollection

Citation Status MEDLINE

doi:

10.1371/journal.pone.0162085

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM265014964