Better outcomes from accelerated HIV diagnosis

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A programme to accelerate the process of HIV diagnosis, preparation and starting antiretroviral therapy (ART) in South Africa led to a higher proportion of people initiating treatment and better health outcomes, according to results from the RapIT trial presented at the Conference on Retroviruses and Opportunistic Infections (CROI 2016).

Recent findings from the START and Temprano trials have shown that starting HIV treatment early, while the CD4 cell remains above 500 cells/mm3, reduces the occurrence of Aids-related events, serious non-Aids-related illness and death. Recognising this, the World Health Organisation now recommends that everyone diagnosed with HIV should start treatment.

Yet despite these new guidelines, most people with HIV in South Africa start treatment too late. One reason for not promptly initiating ART is that the process is long and cumbersome, explained Sydney Rosen of Boston University School of Public Health.

In a typical scenario, a person would take an HIV test, give a blood sample for CD4 cell measurement and complete a tuberculosis (TB) screen during their first visit. On their second visit, they would obtain CD4 and TB results and start TB treatment if needed. The third, fourth and fifth visits would be devoted to counselling and education about the importance of adherence. Finally, on the sixth visit, the person would undergo a physical examination and receive antiretrovirals.

“Each visit requires time, money and motivation on the patient’s part and many do not make it through the process,” Rosen said. This complex process is a legacy of expensive, scarce and toxic drugs used in the past and the belief that people need time, counselling and education to become ready for lifelong therapy, she suggested, stating “we made them come back essentially to demonstrate their worthiness for treatment.”

As a result, in 2012-2013 more than half of people with HIV in South Africa started therapy after their CD4 count had fallen below 200 cells/mm3, and 25 to 40% of those determined to be eligible for treatment did not start within six months.

The RapIT randomised, controlled trial was designed to assess the outcomes of same-day treatment initiation. The RapIT protocol condenses all the steps of the testing, counselling and medication dispensing process, making it faster and easier for people to start ART. The aim was to have all steps completed during a single clinic visit, ideally on the same day a person tests HIV positive.

At last year’s International AIDS Society conference, researchers reported findings from San Francisco’s RAPID programme, which found that offering ART on the same day as HIV diagnosis led to a high rate of treatment uptake and more rapid viral load suppression. The RapIT trial aimed to show whether a similar accelerated process would work in a comparatively resource-limited setting.

Between April 2013 and September 2014, RapIT enrolled 463 people at two sites in Johannesburg, one a primary health clinic and the other a hospital-based HIV clinic. More than half were women – though pregnant women were excluded – and the median age was approximately 35 years. About 40% had tested positive for HIV the same day while the rest had been recently diagnosed and were providing a blood sample for CD4 testing or receiving their first CD4 results. Participants who were deemed eligible for ART were randomly assigned to follow either the rapid procedure (n = 187) or the standard multi-visit procedure (n = 190). Most were started on a standard first-line ART regimen unless this was contraindicated. Drug resistance testing was not done before dispensing therapy, following the standard of care in South Africa.

In the rapid arm, 97% of participants initiated ART within 90 days of enrolment, compared with 72% in the standard procedure arm. Only five people in the rapid arm did not start treatment, and four of these were lost during the TB workup. More than 70% in the rapid arm started ART the same day, and the median time between study enrolment and dispensing of antiretrovirals was 2.4 hours.

Among the participants who started ART within 90 days, 64% in the rapid arm and 51% in the standard arm remained on treatment and reached an undetectable viral load by 10 months. The rapid procedure increased ART initiation by 36% and viral suppression by 26%.

Among the remaining participants, 34% in the rapid arm and 21% in the standard arm started ART but did not achieve viral suppression. Seventeen per cent and 8%, respectively, initiated but did not stay on treatment – higher in the rapid arm because more people in the standard arm never started in the first place. Thus, most loss to care happened before starting treatment in the standard arm but after ART initiation in the rapid arm.

Looking at factors that influenced outcomes, about equal numbers of participants in the rapid and standard arms stayed on treatment and achieved viral suppression in the hospital clinic (63 vs 61%), but at the primary health clinic the rapid arm did considerably better (64 vs 43%), suggesting the latter had more room for improvement, Rosen suggested.

Improved outcomes in the rapid versus standard arm were evident for women under age 35 (60 vs 47%) and especially for men under 35 (71 vs 38%), though the difference was not significant for older women or men. The rapid procedure was both acceptable to patients and feasible to implement, Rosen said, and a cost-effectiveness is underway.

“RapIT demonstrated that it is possible to initiate nearly all eligible patients on ART (and 3/4 on the same day) and improve overall health outcomes,” the researchers concluded. “(The) largest effect (was) seen in younger people and primary health clinics.” While loss to follow-up after ART initiation was higher in the rapid arm, this was “not enough to offset the benefits,” they said, adding that adherence support after starting ART remains a priority.

Very high rates of patient attrition from HIV care between HIV testing and ART initiation have been documented in sub-Saharan Africa. Our objective was to estimate the effect of accelerated initiation procedures on uptake of ART and viral suppression.
We conducted a randomized controlled trial (RapIT Trial, NCT01710397) of immediate ART initiation in two public sector clinics in South Africa (a primary health clinic (PHC) and a hospital-based HIV clinic). Adult (≥18), non-pregnant patients receiving a positive HIV test or first CD4 count were randomized to standard or rapid initiation. On the day of HIV test or first CD4 count, rapid arm patients received a point-of-care (POC) CD4 count (Alere Pima) if needed; those ART eligible received a POC TB test (Xpert MTB/RIF) if symptomatic, rapid POC blood tests (Roche Reflotron), physical exam, education, counseling, and ARV dispensing. Patients in the control arm followed standard clinic procedures (3-5 additional clinic visits over 2-6 weeks prior to ARV dispensing). Follow up was by passive medical record review. Primary outcomes were initiation of ART ≤ 90 days and viral suppression, defined as initiated, retained in care, and suppressed (≤400 copies/ml), ≤ 10 months of study enrollment.
Of 600 patients screened, 377 were eligible for ART and for the study (56% female, median age 35, median CD4 count 210 cells/mm3). In the rapid arm 182/187 (97%) initiated ART ≤ 90 days, compared to 136/190 (72%) in the standard arm (RR 1.36; 1.24-1.49). In the rapid arm, 119/187 (64%) initiated and were suppressed at 10 months, compared to 96/190 (51%) in the standard arm (RR 1.26; 1.05-1.50). Adjustment for sex and baseline CD4 count did not affect results. Effects were larger for the PHC than for the hospital-based HIV clinic, for unemployed than for employed patients, and for patients under age 35 than for patients over 35. 72% of rapid arm patients initiated on the same day as HIV test or first CD4 count (Figure 1). All rapid arm patients in the rapid arm who did not start ART ≤ 180 days were delayed due to TB treatment. Time used for treatment initiation in the rapid arm averaged 2.8 hours.
Offering same-day ART initiation to adult patients in South Africa increased uptake of ART by 36% and viral suppression by 26%. It is feasible and acceptable in public sector clinics, and not all POC instruments will be essential in the future. It should be considered for adoption in high-volume clinics in the public sector in Africa.

Aidsmap material
CROI 2016 abstract

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