- Research article
- Open Access
- Open Peer Review
Impact of peer support on virologic failure in HIV-infected patients on antiretroviral therapy - a cluster randomized controlled trial in Vietnam
BMC Infectious Diseasesvolume 16, Article number: 759 (2016)
The effect of peer support on virologic and immunologic treatment outcomes among HIVinfected patients receiving antiretroviral therapy (ART) was assessed in a cluster randomized controlled trial in Vietnam.
Seventy-one clusters (communes) were randomized in intervention or control, and a total of 640 patients initiating ART were enrolled. The intervention group received peer support with weekly home-visits. Both groups received first-line ART regimens according to the National Treatment Guidelines. Viral load (VL) (ExaVir™ Load) and CD4 counts were analyzed every 6 months. The primary endpoint was virologic failure (VL >1000 copies/ml). Patients were followed up for 24 months. Intention-to-treat analysis was used. Cluster longitudinal and survival analyses were used to study time to virologic failure and CD4 trends.
Of 640 patients, 71% were males, mean age 32 years, 83% started with stavudine/lamivudine/nevirapine regimen. After a mean of 20.8 months, 78% completed the study, and the median CD4 increase was 286 cells/μl. Cumulative virologic failure risk was 7.2%. There was no significant difference between intervention and control groups in risk for and time to virologic failure and in CD4 trends. Risk factors for virologic failure were ART-non-naïve status [aHR 6.9;(95% CI 3.2–14.6); p < 0.01]; baseline VL ≥100,000 copies/ml [aHR 2.3;(95% CI 1.2–4.3); p < 0.05] and incomplete adherence (self-reported missing more than one dose during 24 months) [aHR 3.1;(95% CI 1.1–8.9); p < 0.05]. Risk factors associated with slower increase of CD4 counts were: baseline VL ≥100,000 copies/ml [adj.sq.Coeff (95% CI): −0.9 (−1.5;−0.3); p < 0.01] and baseline CD4 count <100 cells/μl [adj.sq.Coeff (95% CI): −5.7 (−6.3;−5.4); p < 0.01]. Having an HIV-infected family member was also significantly associated with gain in CD4 counts [adj.sq.Coeff (95% CI): 1.3 (0.8;1.9); p < 0.01].
There was a low virologic failure risk during the first 2 years of ART follow-up in a rural low-income setting in Vietnam. Peer support did not show any impact on virologic and immunologic outcomes after 2 years of follow up.
Globally, the number of HIV-infected people receiving antiretroviral therapy (ART) was about 14.9 million by end of 2014, most of them living in low- and middle-income countries [1–3]. To ensure the sustainability of ART programs in resource-limited settings, it is essential to find effective ways to maintain patients on first-line regimens as long as possible as adherence to ART has a major influence on treatment failure and the development of HIV drug resistance [1, 4–6]. However, the provision of ART in low-resource settings remains challenging due to the shortage of human resources . The World Health Organization (WHO) and the United States President’s Emergency Plan for AIDS Relief (PEPFAR) advocated a strategy to mobilize the involvement of people living with HIV (PLHIV) through task shifting among health workforce team . WHO/UNAIDS proposed the “Treatment 2.0” initiative that aimed to reach and sustain universal access to treatment and capitalize on the preventive benefit of ART through five high-priority goals: 1) optimize drug regimens; 2) provide point of care diagnosis; 3) reduce costs; 4) adapt delivery systems and 5) mobilize communities [3, 8].
In sub-Saharan Africa, peer support and home-based care have become part of the HIV comprehensive care and treatment package [9–11], in which the role of peer support is acknowledged as an essential activity for treatment success . A recent randomized controlled trial (RCT) in Uganda showed that community-based peer health worker intervention had an effect on reducing virologic failure risk after 96 weeks of treatment . A meta-analysis review indicates that peer education programs in developing countries are moderately effective at improving behavioral outcomes but show no significant impact on biological outcomes . On the other hand, in most Asian countries, where the HIV epidemic is in a concentrated stage targeting the high risk population such as injecting drug users (IDUs) and sex workers, the adherence support may pose different challenges . Hence the impact of peer support in Asian countries on virologic failure has not been proven.
In Vietnam, the ART programs have been rapidly scaling up with the support from PEPFAR and Global Fund to fight AIDS, Tuberculosis and Malaria (GFATM). By the end of 2010, more than 82,700 people had access to free ART (70% coverage) . According to the revised National Guidelines , VL testing is indicated only for assessing patients suspected of failing the first-line treatment [18, 19]. A qualitative study conducted among 48 PLHIV about adherence obstacles encountered during ART, methods that patients used to enhance adherence, treatment support structures, and attitudes toward home delivery of ART showed that stigma was identified as a strong barrier to ART adherence and that patients seeked more community-based support, preferably from PLHIV who had received sufficient training. Home delivery of ART medications was seen as undesirable by PLHIV, who feared that it might increase stigma and discrimination . We have shown that the community-based peer support had an impact on reducing stigma and discrimination, increasing the access to counseling and testing, improving the quality of life, and enhancing adherence to ART among ART patients presenting at clinical stages 3 and 4 at baseline. However, communitybased peer support had no impact on quality of life among ART patients enrolled at clinical stages 1 and 2 . However, the impact of peer support on treatment outcomes, especially on virologic failure, has not yet been assessed.
We conducted this study with the aim of testing the hypothesis that peer support intervention has an impact on virologic and immunologic responses in HIV-infected patients initiated on first-line ART regimens in a rural resource-limited setting in Quang Ninh, Vietnam. This approach will result in evidence-based ART strategies for large populations in low income and low prevalence settings, which will have an impact on HIV treatment guidelines globally.
Quang Ninh province is located along northeastern Vietnam with a population of 1.1 million and an area of 6100 km2. Quang Ninh has 14 cities/districts, in which Ha Long City is the biggest (20 communes, 221,000 habitants). It is also home to the famous World Heritage Site, Ha Long Bay. Coal mining, fisheries, and tourism are the main industries.
HIV prevalence in Quang Ninh was about 1%, of which 55% of PLHIV were IDUs (reported by Provincial AIDS Committee-2006). Patients were recruited from four outpatient clinics (OPC): Ha Long CDC-LifeGap clinic, located in the provincial hospital in Ha Long City and supported by PEPFAR which has more resources, and three Global Fund supported clinics (Uong Bi, Ha Long Health Center and Yen Hung). These were the only clinics in the districts and hence there was a low risk for selection bias from both patients and the project.
The cluster randomized controlled trial “Directly Observed Therapy for Antiretrovirals” (DOTARV), registration number NCT01433601 was carried out in 4 districts/cities (Ha Long, Uong Bi, Dong Trieu, Yen Hung). The reasons for choosing these 4 districts/cities were: (i) community based care was not available, (ii) these were adjacent districts, and (iii) each had high HIV prevalence. To minimize contamination (that the effect of peer support to patients in the intervention group would also influence the control groups due to personal relationships among patients in intervention and control group), the unit of randomization and analysis was the cluster (commune).
Participant recruitment and study procedures
This trial was conducted between July 2007 through November 2011, with 2 years of patient recruitment and 2 years of follow-up.
According to the National Guidelines (2005) , HIV-infected individuals were eligible to be registered for free at an ART clinic if they: i) were confirmed HIV positive, ii) possessed valid civil registration information (home address and telephone), iii) had a family member who could act as a supporter, and iv) agreed to enroll and to be followed up in the ART program. Each clinic was staffed with two medical doctors, one adherence counselor, one reception nurse, one phlebotomy nurse, one pharmacist, and one volunteer who was a person living with HIV (PLHIV). The staff were trained on basic and advanced HIV care and treatment and certified by Ministry of Health.
All registered patients received a set standard of care, co-trimoxazole prophylaxis, and were assessed at baseline for socio-economic situations. They were also evaluated clinically, undergoing WHO HIV clinical staging, as well as screening for tuberculosis (TB), viral hepatitis B and C, and opportunistic infections (OIs). Their CD4 counts were taken, and those who were eligible for ART (clinical stage 4 with CD4 count <200 cells/μl or clinical stage 3 with CD4 count <350 cells/μl) were put on the waiting list for ART and selected on a “first come, first served” basis. Patients diagnosed with OIs were treated by OI medications. If TB was diagnosed, patients were referred to the provincial TB hospital in Ha Long City. They were initiated on ART after receiving two months of intensive TB treatment. Every month, a range of 15 to 20 patients per clinic, from both groups, were selected, based on the “first come, first served” recruitment list, to attend a pre-ART readiness training on both an individual and group basis. Each clinic received a quota of patients that were planned to initiate ART stipulated by the local health authorities. The training included HIV basics, stigma and discrimination, positive living, transmission prevention, ART regimens and treatment adherence. A family member also attended the training and became an adherence supporter for the patient. ARV drugs were provided in pre-packed dosage form for convenience and to promote adherence. The first-line ARV regimens included two nucleoside reverse transcriptase inhibitors (NRTIs): stavudine (d4T) or zidovudine (AZT) plus lamivudine (3TC) combined with one non-nucleoside reverse transcriptase inhibitor NNRTI: nevirapine (NVP) or efavirenz (EFV). All care and medications were provided free of charge.
Patients who participated in the study were selected from the pre-ART waiting list. All patients fulfilling the criteria and planned for ART were asked for their consent to take part in the trial. The patients were informed about the trial by study doctors. The patients, if they agreed to participate, signed the informed consent form. Study doctors would assign patients to either the intervention group or the control group based on the commune where they were living from one of a total of 71 communes in 4 districts. The ratio for intervention: control communes was 36:35 (1:1). The clusters in all four districts were randomized by a statistician who was not involved in the study and were matched according to the following criteria (i) urban vs. rural (official registration, based on population density), (ii) vicinity to the clinic (more or less than 5 km), and (iii) population (more or less than 25,000). The randomization of matched clusters was through a computer software by a statistician not directly involved in the project with no local acquaintance. This study followed an open label cluster randomized controlled trial design.
Inclusion criteria were (i) confirmed HIV-infected, (ii) reported as ART-naïve, (iii) resident in any of the four study districts, (iv) age 18 years or older, (v) eligible for ART according to the National Guidelines (2005), CD4 count <200 cells/μl or clinical stage 4, or clinical stage 3 with CD4 count <350 cells/μl, (vi) willing to submit to follow ups and to receive adherence support by a peer-supporter, and (vii) signed a written informed consent.
Exclusion criteria were (i) pregnancy or (ii) mental illness.
Intervention strategy: peer-support
The peer-support intervention strategy was home-based adherence counseling conducted by peer supporters who were HIV-infected individuals on ART and nominated by fellow patients and health care staff at each clinic site. The qualifications needed for peer-supporters were (i) social ability, (ii) good ART adherence for at least 6 months, (iii) high school graduation, (iv) willingness to participate in the study and (v) passed the qualifying test after the training. The OPC’s and local health authorities proposed candidates that fulfilled the selection criteria’s. The proportion of the peer-supporters to the number of recruited patients living in each district was about 1:20, meaning that one supporter would support a maximum of 20 patients. The peer-supporters received 1-week’s training conducted by project researchers on basic HIV care and support, communication and counseling skills, and the process for completing the adherence checklist form. Two 1-week refresher trainings were provided yearly throughout the study.
The standard support performed by peer-supporters included home-based visits and completion of the adherence checklist form, in which patients were asked about their wellbeing, OI and adverse drug reaction (ADR) signs and symptoms, the times at which they took the pills, any doses missed for last 4 days, barriers to adherence, and pill count. If an incomplete adherence was reported, the peer supporter would counsel and discuss with the patients and family supporters how to improve the adherence.
The initial schedule of support was twice a week in the first 2 months, then once a week when patients’ adherence passed assessments. Additional visits were provided if patients were sick or had a serious ADR or a history of poor adherence. A telephone call was used to arrange a 15- to 30-min appointment place in advance between peer supporters and patients to minimize wasting time or to ensure confidentiality for patients who feared disclosure of their HIV status to others in their surroundings. Due to the associated stigma, the supporters did not wear a work outfit for home visits to minimize the patient’s fear of stigma developing from others in their surroundings. Before being recruited for the study, patients were made aware that being a part of the study would require them to disclose their HIV status. They were warned about the possibility of stigmatization. If patients were not comfortable with that possibility or if they experienced any harm during the study, patients would choose not to be a part of the study. This was monitored during the OPC visits. To ensure satisfactory work by the peer supporters, bi-weekly supervision of peer-support activities was conducted by a peer-support group leader in each district. Monthly supervision meetings of peer-support activities were performed by project researchers.
Patients in both intervention and control groups received a set standard of care and treatment according to the National Guidelines  including pre-ART initiation, which consisted of three ART adherence training sessions in both individual and group settings. Health checks, blood sampling and drug dispensations were carried out on a monthly basis at the OPC. Selfreported adherence for the last-4-day period was assessed quarterly by an adherence counseling staff member. CD4 counts were run at baseline and every 6 months by using the Partec CyFlow® system in Uong Bi hospital and the Becton Dickinson® system in Quang Ninh provincial hospital.
Viral load and CD4 count screening
The Exavir™ Load, an enzyme-linked immune-sorbent assay (ELISA)-based VL quantification test (Cavidi AB, Uppsala, Sweden [23, 24]), was used in Vietnam for the first time to monitor the virologic outcomes for all participants every 6 months for 24 months of the study. The detection limits range from 200 to 410,000 copies/ml . Details on the laboratory procedures of ExaVir Load assay were reported in an earlier publication .
CD4 counts were run at baseline and every 6 months by the Partec CyFlow® in Uong Bi hospital and the Becton Dickinson® in Quang Ninh provincial hospital.
In both the intervention and control groups, patients were assessed by health care staff at the clinic for adherence every 3 months using an adherence checklist modified from the contextualized Adult AIDS Clinical Trials Group (AACTG) adherence instrument . In this checklist, patients self-reported any OI and ADR symptoms, whether they had missed any doses during the last 4 days, or if they had incorrectly measured their pill-count.
Incomplete adherence was defined as the patient stating in the 3-month adherence checklist form that he or she missed more than one dose (2 or more; either in morning or evening) of ARV during the 24 months of their follow-up time.
Complete adherence was defined as the patient self-reporting in the 3-month adherence checklist form that he or she did not miss any dose or just one dose (either in the morning or evening) of ARV drugs during the 24 months of their follow-up time.
Virologic failure was defined as either (i) primary virologic failure if VL >1000 copies/ml after 6 months of ART initiation or (ii) secondary virologic failure if VL was undetectable (<200 copies/ml) after 6 months of ART initiation and then became >1000 copies/ml at any time point during the follow-up. Virologic failure patients were reported to the attending medical doctors and adherence counselors in their respective clinics. Then a follow-up VL test was repeated after at least one month but within 3 months of the initial virologic failure. If VL remained >1000 copies/ml, the patient was then reported to an OPC doctor and flagged for a confirmatory PCR VL. According to VGHADT (2009) , patients were eligible for switching to second-line therapy if they meet the criteria of clinical or immunologic failure and, if available, they have been confirmed to have a PCR VL >5000 copies/ml. Additionally, patients with detectable viral load in the intervention group received an intensive adherence counseling support by the peer supporters through the provision of two to three home visits per week.
Death events were ascertained by a medical doctor confirmation or, in the intervention group, by a peer-supporter through telephone calls or home visits. In cases of a missing follow-up, event of death was confirmed through telephone calls to family members and home visits by peer supporters.
Lost-to-follow-up was defined as: when the patient was either arrested or placed in a compulsory drug rehabilitation center for 24 months due to active heroin use, thus disabling follow-up during the study period; or when the patient did not show up at the OPC for 3 consecutive visits; or if the patient voluntarily withdrew from the study. Patients in both groups were called to determine the reason of their lost-to-follow-up.
Transferred patients were defined as those who were confirmed as being registered with another OPC which was outside of our four study sites.
Changed-regimen was defined as a patient who had to change one of the three ARV drugs in the regimen for any clinical reason (ADRs or TB co-infection treatment) during ART.
The primary endpoint was the risk of virologic failure during 24 months of follow-up.
The secondary endpoint was the time course of CD4 cell counts over the period of 24 months of follow up.
Data were collected as follows: i) socio-economic situation at baseline, ii) clinical and laboratory data at baseline and follow-up visits every 6 months, (iii) self-reported adherence form was administered by health staff every 3 months, and (iv) ART adherence forms completed by peer supporters.
Patients were allocated to the intervention group according to a randomization of clusters (communes) where patients lived. Sample size for cluster randomized trial was calculated by using formulas in . Assuming the baseline figure for virologic failure risk in the intervention group equal to 5%, and equal to 15% in the control group, a power of 80%, the significance level of the two-sided alpha 0.05, a randomization ratio of 1 (intervention):1 (control), an estimation of intraclass coefficient equal to 0.1, a number of clusters in each group equal to 35 and adding 30% for lost-to-follow-up, the minimum needed sample size was 638 patients (about 319 patients per study arm).
Intention-to-treat analysis was used to calculate virologic failure risk.
Mean, median and standard deviation were used for summarizing numerical variables, frequencies, and percentages for the categorical variables.
Chi-square tests were performed to compare intervention and control groups for demographic and clinical characteristics at baseline.
Crude relative risks (RR) at 6, 12, 18, and 24 months were calculated to assess the relationship between virologic failure and intervention/control groups at different time points.
Kaplan-Meier curves were produced, together with a log-rank test, to compare time to virologic failure between control and intervention group. Cox proportional hazards frailty model, adjusting for potential confounders, was used to analyze the hazard rate among the intervention and control groups, taking into account the clustered nature of the data. Schoenfeld residuals were used for checking the proportional hazard assumptions; no timedependent variables were considered.
The final model was selected using a forward- stepwise selection with a p-value cut-off for entering the model equal to 0.1. A likelihood-ratio test was used for testing the null hypothesis of no variance of the frailty effects.
CD4 count trends over time were analyzed using a mixed-effects model with a polynomial function of time in the fixed component. Due to the hierarchical structure of the data, random effects of clusters (communes, individual and measurement) were incorporated into the model. Square-root transformation was used for the CD4 count approximating a normal distribution .
Once the data was collected, the models were adjusted for the following variables: randomized groups (control vs intervention); age (≥35 vs <35 years); gender (male vs female); WHO clinical stage (stage 1 and 2 vs stage 3 and 4); baseline VL (≥100,000 copies/ml vs <100,000 copies/ml) and baseline CD4 counts (≥100 cells/μl vs <100 cells/μl); ART-naïve status (yes vs no); history of IDU (yes vs no); TB history (yes vs no); history of OIs (yes vs no); having an HIV-infected family member (yes vs no); receiving ART in Halong CDC clinic (yes vs no), changed ART regimen (yes vs no); and incomplete adherence (yes vs no). Since there was a significant difference between the groups receiving ART in Halong CDC clinic, it was especially important to adjust for this difference.
The above mentioned demographic and clinical characteristics at baseline were tested as independent variables both in the survival and mixed effects models. P-values less than 0.05 were considered significant in the final model. The statistical analyses were performed using STATA version 12.0 (College Station, StataCorp LP, TX, USA).
Results recruitment of the cohort
During the period of July 2007 through November 2009, a total of 640 HIV-infected participants (332 intervention patients and 308 control patients) were enrolled from 59 communes (30 intervention communes and 29 control communes). As 12 of the communes had no participants, these were removed from the analysis. Ha Long City had the majority of patients (418; 65%), then Uong Bi (87; 14%), Dong Trieu (71; 11%) and Yen Hung (64; 10%). The distribution of patients in the four study clinics were: Ha Long CDC Life-Gap clinic (307; 48%); The Uong Bi Hospital clinic included patients from Dong Trieu district (181; 28%); Ha Long Health Center clinic (106; 17%) and Yen Hung clinic (46; 7%). On average, each commune had 11 patients. However, the number of patients was not distributed equally among communes: the Cao Xanh commune in Ha Long City has the highest number of patients (46) while 12 communes had only 1 patient each and another 12 had no patients enrolled in the study (Table 1). A sensitivity analysis was done and found that the inclusion of the 12 communes with 1 patient each did not invalidate the findings of the study (data not shown).
After conducting a one-week pilot training session, we selected 14 qualified peer supporters (8 females, 6 males), aged between 25 and 44 years. The number of supporters was proportional to the number of intervention patients in each district/city. Seven peer supporters were based in Ha Long (191 patients), 3 in Uong Bi (51 patients), 2 in Dong Trieu (56 patients) and 2 in Yen Hung (34 patients). Each peer supporter was responsible for visiting between 10 and 20 patients.
By the end of the study, mean follow-up time was 20.4 ± 7.2 months (20.5 ± 7.2 and 20.4 ± 7.3 months for intervention and control groups, respectively), 78% (501/640) of patients remained on ART, 11% (70/640) were dead, 10% (64/640) were lost-to-follow-up and 1% (5/640) had transferred to other clinics. Among the lost-to-follow-up patients, 17 (27%) had voluntarily withdrawn, 7 (11%) did not show up for three consecutive visits and 40 (62%) were arrested and put in rehabilitation centers due to injecting heroin. Eleven patients were arrested during the ART treatment, however, they had continuous access to ART and then resumed their ART at the clinics after being released from the rehabilitation center, therefore they were not considered lost-to-follow-up. The distribution of retention in care, dead, lostto-follow-up, and transferred patients were equally distributed in both intervention and control groups (Fig. 1).
Table 2 described the characteristics of the cohort divided by control and intervention groups at baseline with no significant differences observed between the two groups, apart from in those patients from the Ha Long CDC clinic.
At month 24, clinical outcomes improved, as mean body weight increased from 50.2 ± 7.3 kg at baseline to 53.7 ± 7.9 kg at month 24 (p < 0.001). However, there was no significant difference in gaining weights between the intervention and control groups (50.2 ± 6.8 vs 50.3 ± 7.7 kg at baseline, respectively; p = 0.86 and 53.5 ± 7.0 vs 53.9 ± 8.8 kg at month 24, respectively; p =0.66). There were 163 (25%) patients who had to change their treatment regimens due to ADRs, of which the most common reasons for changing the regimens were peripheral neuropathy (104; 64%), rash (25; 15%), hepatitis (15; 9%) or TB treatment (9; 6%). However, there was no significant difference between the intervention and control groups (89; 27% vs 74; 24%, p = 0.47). Fifty-four patients (8.5%) developed at least one OI or TB after 6 months of ART (8% in the intervention group and 9% in the control). Six (1%) patients switched to second-line regimens (3 in the intervention group and 3 in the control); all of these switched after treatment and at least 18 months after having confirmatory PCR VL >5000 copies/ml. The overall mortality risk was 11% with no significant difference between the intervention and control group (results not shown). Based on the monitoring during OPC visits no case of peer-support induced stigmatization was detected during the study.
After 24 months of ART initiation, a total of 46 patients (7.2%) experienced virologic failure. There was no significant difference regarding virologic failure risks between the intervention (cumulative virologic failure at 24 months equal to 23/332; 6.9%) and control groups (23/308, 7.5%) at any time point (6, 12, 18, or 24 months) (Table 3). Of the 46 virologic failure cases, 22 (48%) were primary virologic failure. The Kaplan-Meier curves showed no significant difference in time to virologic failure between the intervention and control group (Log-rank p-value = 0.77) (Fig. 2).
The adjusted results from the Cox proportional hazards frailty model showed that the significant risk factors for developing virologic failure were ART-non-naïve status [aHR 7.0;(95% CI 3.3–14.7); p < 0.01]; baseline VL ≥100,000 copies/ml [aHR 2.3;(95% CI: 1.2–4.3); p < 0.05], and incomplete adherence [aHR 3.1;(95% CI: 1.1–8.9); p < 0.05] (Table 4).
There was no significant effect of intervention on time to virologic failure.
After excluding the 35 ART-non-naïve patients, the statistical analysis among only 605 naïve patients (316 in the intervention group and 289 in the control group) also showed no significant difference in virologic failure risks between intervention and control group [6.3% vs 5.2%; respectively, RR = 1.22; (95% CI: 0.63–2.37); p = 0.56] (data not shown).
The median CD4 counts increased rapidly from 83 cells/μl (IQR 29–176) at baseline to 202 cells/μl (IQR 121–311) at month 6, to 260 cells/μl (IQR 168–400) at month 12, to 305 cells/μl (IQR 220–463) at month 18 and to 371 cells/μl (IQR 249–534) at month 24 (Fig. 3). The increase of median CD4 count from baseline to month 24 was 286 cells/μl (292 cells/μl in the intervention group and 279 cells/μl in the control group).
Patients with baseline VL ≥100,000 copies/ml [adj.sq.coeff. (95% CI): −0.9 (−1.5;−0.3); p < 0.01] and baseline CD4 count <100 cells/μl [adj.sq.coeff. (95% CI): −5.7 (−6.3;−5.1); p < 0.01] had a significantly lower increase of CD4 count compared to the other patients. On the other hand, patients with an HIV-infected family member had a significantly higher increase in CD4 count compared to those who did not have an HIV-infected family member [adj.sq.coeff. (95% CI): 1.3 (0.8;1.9); p < 0.01] (Tables 4 and 5).
The results showed no significant effect of the intervention on the evolution of CD4 count trend between the intervention and control groups.
Discussion virologic failure, mortality and retention rates
To our knowledge, this is the first randomized controlled trial study in Vietnam to assess the impact of peer support on virologic and CD4 outcomes among HIV-infected patients starting ART. Our study showed a comparably low virologic failure risk, low mortality and high retention rate after 24 months of follow-up. This indicates that a well-funded and organized ART program implemented through PEPFAR and Global Fund in Vietnam can be rolled out successfully in remote and resource-limited settings.
After 24 months follow-up, the virologic failure risk in our study (7.2%) was lower than anticipated when the study was planned and compared to other countries (15 to 20%) [30–33]. This, in retrospect, may have made the study underpowered. Among the 46 virologic failure cases in our study, 22 (48%) were secondary virologic failure (10 in the intervention group and 12 in the control group). In Sub-Saharan African countries, findings from systematic reviews showed an overall virologic failure risk (VL >1000 copies/ml) was 24% within 12 months of ART  and 15% after 24 months of ART , the highest risk (43%) was seen in a Rwanda .
In our study, the proportion of virologically suppressed patients on ART at 24 months was 94% which is higher than those reported from other resource-constrained settings including Uganda (86%) , Malawi (84%)  and Cameroon (52%) . Studies in Vietnam reported that the proportion of patients with viral suppression among IDU populations were 73%  and 70% in Ho Chi Minh City . In neighboring Cambodia, 88% (306/346) of patients had achieved VL <400 copies/ml  and in Thailand, 15% (55/345) had virologic failure (>400 copies/ml) at 24 months . However, most of these studies reported ontreatment results that were analyzed in a cross-sectional fashion and included both ARTnaïve and non-naïve patients. The good treatment outcome in our study may be explained by several factors including that the vast majority of patients were ART-naïve and the VL results were reported to the treating doctors since knowledge about viremia may result in intensification of the adherence support, both for intervention and control group patients.
Despite the fact that the majority of the patients were severely immune-suppressed with low CD4 counts at baseline and half were reported to be at clinical stage 3 or 4, our study showed a lower mortality risk (11% or 6.4/100 person-years) compared to other studies in resourcelimited countries [36–38, 42–44]. However, the mortality risk of this study was higher than that of studies in middle- and high-income countries [45–47]. The survival and causes of death among patients in our cohort was previously reported .
The retention rate of patients on ART was 78% after 24 months with no significant difference between the intervention and control groups (p = 0.7). High retention rates in care indicate not only an improved health care system and ART programs in Vietnam, but also effective care and support activities in the community to motivate and engage patients in care. A recent study in Vietnam conducted among 4531 adults and 313 children showed that 81.2 and 84.4%, respectively, were still on ART after 12 months . This result was similar with the retention rate in Thailand (80.8% after 5 years) , Cambodia (80% after 4 years)  and higher compared to studies in sub-Saharan Africa with 24 months of follow-up: Uganda (72%)  and Malawi (66%) . Other studies also showed that engagement of HIV care is associated with improved clinical, virologic and immunologic parameters and survival outcomes [50, 51]. Therefore, retaining HIV-infected patients in care has become a public health issue to ensure the success and sustainability of ART programs .
As shown in our study, CD4 counts responded well after 24 months of ART (overall increase of 286 cells/μl). This finding is in line with other studies that show how CD4 cell counts increased quickly, in particular after 6 months of ART [38, 53]. However, there was no significant difference between the intervention and control groups in CD4 trends after the adjustment (p = 0.69). Factors that predict the increase of CD4 counts were the VL at baseline ≥100,000 copies/ml, a baseline of CD4 counts <100 cells/μl, and having an HIV-infected family member. In a study in Thailand, CD4 count at baseline and changes in CD4 count were important in predicting CD4 counts ≤200 cells/μl .
In our study, after 24 months we found 45 patients (7%) had immunologic failure, of whom 23 (6.9%) were in the intervention group and 22 (7.1%) in the control group (no significant difference, p >0.05). Also, there was a high discordance (71%) between immunologic and virologic failure. Only 13 patients (29%) had both immunologic failure and virologic failure (p <0.001).
Factors associated with virologic failure
Our study showed that ART-non-naïve status, high baseline VL (≥100,000 copies/ml) and incomplete adherence (missing more than one dose during 24 months) were risk factors for virologic failure. High VL (>100,000 copies/ml) at baseline can be a predictor for the slower increase of CD4 counts and mortality . Therefore, our findings were in line with other studies that high VL at baseline is a predictor for virologic failure and mortality during ART [18, 55, 56]. Contrarily, studies in Thailand shows low baseline CD4 count and race/ethnicity were independent predictors of virologic response, however baseline VL and gender were not . Also, univariate analysis showed having a child was significantly associated with lower virologic failure risk .
Impact of peer support intervention
The study results might answer the research question in that there was no significant difference between the intervention and control groups in both cumulative virologic failure risk and time to virologic failure after 2 years of follow-up. This result could be explained in several ways. While the simplest explanation is that peer support inherently does not affect treatment outcomes, we cannot exclude the possibility that our sample sizes may simply have been insufficiently large. With a larger study, we might have been able to gain enough statistical power to discern a difference between the intervention and control groups. Also, the adherence is self-reported, and may have been affected by observer bias. Also, the ART program in Vietnam has been well funded and implemented through international donors including PEPFAR and Global Fund. Before ART was initiated, each patient had to be assessed for ART readiness, name a supporting family member and attend three adherence counseling sessions according to the National Guidelines . Furthermore, the eventual effect of the intervention might also be masked by a “ceiling effect” in which the control group also received a sufficient baseline adherence support. Free ARV may have also contributed to this “ceiling effect”. The baseline support may have been at such a high level that additional support did not affect treatment outcomes.
In addition, patient support could have originated from a number of different sources that may have contaminated the study including the OPCs and the community-based programs. Quang Ninh province, with a comparably high HIV prevalence, was receiving PEPFAR support in order to set up “comprehensive care, treatment and support” programs with NGOs, which were very active during the time of the project implementation. The availability of community-based activities provided by “the Bright Future” and other community outreach groups might have constituted a “contamination” where patients in the intervention group could meet and share adherence experiences with patients in the control group.
Furthermore, IDU in both the control and intervention groups had incentives to remain on the treatment regimens. Active IDUs may get arrested and placed into a drug rehabilitation centers. The risk of this may be increased if they fail to follow the treatment schedule, and thereby get attention from authorities. IDUs also received further counseling at the OPC and, for those in the intervention group, from the peer supporters.
In our study, 400 (63%) patients lived with their parents and other family members who might also play an important role as “internal supporters” to support patients in taking ARVs. Vietnamese culture strongly values the care of the extended family members, so most patients had good support for adherence from their families.
In our study, we only reported data to the 24-month-follow-up; hence the sustained or longterm effect of the adherence support intervention cannot be excluded. It should be noted that as patients started their ARV and improved their health, their perceived need for peer support may have declined. It was also apparent from discussion with peer supporters and patients that the personal relationship between the patient and supporter was crucial for long term peer support and follow up. Many patients saw the benefit and developed a close bound to their peer supporter, sometimes too close from the peer supporter’s point of view. In other cases, the patients perceived the support as an annoyance. A recent study in Uganda has also shown that peer health care intervention had no impact on cumulative risk of virologic failure and virologic outcomes on short-term ART and suggested that it might be best suited for patients who have taken ART for longer periods, especially as it may mitigate the effects of “treatment fatigue” as patients tire of continually taking ART . Therefore, to assess the sustained effect of the peer support intervention in our cohort, further research to continue following up patients with VL and CD4 count monitoring up to at least 48 months is needed.
Despite the results showing peer support had no significant effect on virologic failure, it is nevertheless clear that good outcomes can be achieved in resource-limited communities. The support the patients received may still be considered a global standard of care.
This is the first cluster randomized controlled trial on HIV conducted in a rural setting in Vietnam. We had some limitations and constraints in logistics, in recruiting patients, collecting data, and analysis due to a lack of precedence to follow. It took 2 years for recruiting enough patients instead of 10 months that we had originally planned. There were 35 (6%) patients who were ART-non-naïve. However, as the study was intention-to-treat and the non-naïve status was revealed after enrollment, these cases were still included in the study and the results might not represent whole treatment-naïve population. Patients in both groups may receive other community-based supports that might be a “contamination”. In addition, patients in the intervention group could meet and share adherence experiences with patients in the control group at the clinic (i.e., there were 2 couples of whom the men in the intervention group married women in control group). Some patients were willing to move or even travel long distances in order to receive treatment from a certain clinic. This devotion to obtaining ARV could have contributed to the high adherence in both groups. The CD4 counts were done in two different hospital laboratories which may bias the estimation of immunologic failure. As the clusters were randomized before the recruitment of patients and the selection process of the patients should have randomized the individual clusters, the difference in the number of patients in each arm is unlikely to lead to bias. A limitation in our study was that the adherence data collected from peer supporters during their patient encounters in the intervention group wasn’t included in the analyses.
ART programs in resource-limited rural settings like Quang Ninh, Vietnam can provide an effective care and treatment with a low virologic failure risk if the patients are well-prepared for ART and followed up regularly by an out-patient clinic. Peer support to improve adherence did not show any impact on virologic failure and CD4 trends during first 2 years of ART. High VL at baseline is a predictor for virologic failure and CD4 trends.
WHO (2015) http://www.who.int/hiv/en/. Assessed 7 July 2015.
UNAIDS (2013) Global report on the global AIDS epidemic - 2013 Available at: http://www.unaids.org/sites/default/files/media_asset/UNAIDS_Global_Report_2013_en_1.pdf. Accessed 7 July 2015.
UNAIDS (2015) Global AIDS Response Progress Reporting 2015: Available at: http://www.unaids.org/sites/default/files/media_asset/JC2702_GARPR2015guidelines_en.pdf. Accessed 7 July 2015.
Gardner EMB, William J, Steiner JF, Anderson PL, Bangsberg DR. Antiretroviral medication adherence and the development of class-specific antiretroviral resistance. AIDS. 2009;23(9):1035–46.
Bangsberg DRHF, Charlebois ED, Zolopa AR, Holodniy M, Sheiner L, Bamberger JD, Chesney MA, Moss A. Adherence to protease inhibitors, HIV-1 viral load, and development of drug resistance in an indigent population. AIDS. 2000;14(4):357–66.
Ziad El-Khatib AME, Ledwaba J, Mohapi L, Laher F, Karstaedt A, Charalambous S, Petzold M, Katzenstein D, Morris L. Viremia and drug resistance among HIV-1 patients on antiretroviral treatment – a cross-sectional study in Soweto, South Africa. AIDS. 2010;17:1679–87.
WHO. Global recommendations and guidelines on taks shifting. 2007. Geneva. Available at http://www.who.int/healthsystems/TTR-TaskShifting.pdf. Accessed 7 July 2015.
WHO (2012) Treatment 2.0 http://files.unaids.org/en/media/unaids/contentassets/documents/unaidspublication/2011/20110824_JC2208_outlook_treatment2.0_en.pdf. Accessed 12 Dec 2016.
Filler SJ, Berruti AA, Menzies N, Berzon R, Ellerbrock TV, et al. Characteristics of HIV Care and Treatment in PEPFAR-Supported Sites. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2011;57:e1–6. doi:10.1097/QAI.1090b1013e3182158980.
Weidle PJ, Wamai N, Solberg P, Liechty C, Sendagala S, et al. Adherence to antiretroviral therapy in a home-based AIDS care programme in rural Uganda. Lancet. 2006;368:1587–94.
Koenig SP, Léandre F, Farmer PE. Scaling-up HIV treatment programmes in resource-limited settings: the rural Haiti experience. AIDS. 2004;18:S21–5.
Gusdal AK, Obua C, Andualem T, Wahlström R, Chalker J, et al. Peer counselors’ role in supporting patients’ adherence to ART in Ethiopia and Uganda. AIDS Care. 2011;23:657–62.
Chang LW, Kagaayi J, Nakigozi G, Ssempijja V, Packer AH, et al. Effect of peer health workers on AIDS care in Rakai, Uganda: a cluster-randomized trial. PLoS One. 2010;5:e10923.
Medley A, Kennedy C, O’Reilly K, Sweat M. Effectiveness of peer education interventions for HIV prevention in developing countries: a systematic review and meta-analysis. AIDS Educ Prev. 2009;21:181–206.
Knodel J, Hak S, Khuon C, So D, McAndrew J. Parents and family members in the era of ART: evidence from Cambodia and Thailand. AIDS Care. 2011;23:1264–73.
VAAC. Vietnam AIDS Response Progress Report 2014. Hanoi December 2013. http://www.unaids.org/sites/default/files/country/documents//VNM_narrative_report_2014.pdf. Accessed 12 Dec 2016.
MoH (2009) Vietnam National Guidelines for HIV/AIDS Diagnosis and Treatment - (in Vietnamese, published with Decision No. 3003/QD-BYT dated 19/8/2009 of the Minister of Health) https://aidsfree.usaid.gov/sites/default/files/hts_policy_vietnam.pdf. Accessed 12 Dec 2016.
Trinh TT, Montague BT, Flanigan TP, Gerard HM. HIV suppression among patients on treatment in Vietnam: a review of HIV viral load testing in a public urban clinic in Ho Chi Minh City. AIDS Research and Treatment. 2011;2011.
Huong DTM, Bannister W, Phong PT, Kirk O, Peters L. Factors associated with HIV-1 virological failure in an outpatient clinic for HIV-infected people in Haiphong, Vietnam. Int J STD AIDS. 2011;22:659–64.
Van Tam V, Pharris A, Thorson A, Alfven T, Larsson M. “It is not that I forget, it’s just that I don’t want other people to know”: barriers to and strategies for adherence to antiretroviral therapy among HIV patients in Northern Vietnam. AIDS Care. 2011;23:139–45.
Vu T, Larsson M, Pharris A, Diedrichs B, Nguyen H, et al. Peer support and improved quality of life among persons living with HIV on antiretroviral treatment: A randomised controlled trial from north-eastern Vietnam. Health and Quality of Life Outcomes. 2012;10:53.
Vietnam Ministry of Health. Vietnam National Guidelines for HIV/AIDS Diagnosis and Treatment. In Vietnamese. Published with the Decision No. 3003/QD-BYT dated 19/08/2009 of the Minister of Health 2011. http://www.vaac.gov.vn/Cms_Data/Contents/Vaac/Folders/DocumentLaw/Vanban/~contents/8YUJW54X7VRF64XS/4139-Q-BYT.pdf. Accessed 12 December 2016.
Greengrass VL, Plate MM, Steele PM, Denholm JT, Cherry CL, et al. Evaluation of the Cavidi ExaVir Load Assay (Version 3) for Plasma Human Immunodeficiency Virus Type 1 Load Monitoring. J Clin Microbiol. 2009;47:3011–3.
Iqbal HS, Balakrishnan P, Cecelia AJ, Solomon S, Kumarasamy N, et al. Use of an HIV-1 reverse-transcriptase enzyme-activity assay to measure HIV-1 viral load as a potential alternative to nucleic acid-based assay for monitoring antiretroviral therapy in resource-limited settings. J Med Microbiol. 2007;56:1611–4.
CAVIDI Instruction for use of ExaVir™ Load Analyzer Version 3.0, issued Dec 2006, revised Mar 2009 http://www.cavidi.se/wp-content/uploads/2014/06/ExaVir_Load_Instructions.pdf. Assessed 12 Dec 2016.
Cuong DD., Agneskog E, Chuc NTK, Santacatterina M, Sönnerborg A, Larsson M (2012) Monitoring the efficacy of antiretroviral therapy by a simple reverse transcriptase assay in HIV-infected adults in rural Vietnam. Future Virol (manuscript accepted on 24 July 2012).
Chesney MA, Ickovics JR, Chambers DB, Gifford AL, Neidig J, et al. Selfreported adherence to antiretroviral medications among participants in HIV clinical trials: the AACTG adherence instruments. AIDS Care. 2000;12:255–66.
Hemming K, Marsh J, A menu-driven facility for sample-size calculations in cluster randomized controlled trials. Stata Journal, Stata Press; 2013.
Diddle P HP, Liang K, Zeger S. Analysis of Longitudinal Data. Biometrics 2nd edition; 2002.
Fox MP, van Cutsem G, Giddy J, Maskew M, Keiser O, et al. Rates and Predictors of Failure of First-line Antiretroviral Therapy and Switch to Second-line ART in South Africa. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2012; Publish Ahead of Print.
Castelnuovo B, Sempa J, Agnes KN, Kamya MR, Manabe YC. Evaluation of WHO Criteria for Viral Failure in Patients on Antiretroviral Treatment in ResourceLimited Settings. AIDS Research and Treatment 2011.
Steven J, Reynolds GN, Newell K, Ndyanabo A, Galiwongo R, Boaz I, Quinn TC, Gray R, Wawer M, Serwadda D. Failure of immunologic criteria to appropriately identify antiretroviral treatment failure in Uganda. AIDS. 2009;23:697–700.
Meya D, Spacek L, Tibenderana H, John L, Namugga I, et al. Development and evaluation of a clinical algorithm to monitor patients on antiretrovirals in resource-limited settings using adherence, clinical and CD4 cell count criteria. J Int AIDS Soc. 2009;12:3.
Barth RE, van der Loeff MF, Schuurman R, Hoepelman AI, Wensing AM. Virological follow-up of adult patients in antiretroviral treatment programmes in subSaharan Africa: a systematic review. Lancet Infect Dis. 2010;10:155–66.
Fischer A, Karasi JC, Kibibi D, Omes C, Lambert C, et al. Antiviral efficacy and resistance in patients on antiretroviral therapy in Kigali, Rwanda: the real-life situation in 2002. HIV Medicine. 2006;7:64–6.
Chang LW, Alamo S, Guma S, Christopher J, Suntoke T, et al. Two-year virologic outcomes of an alternative AIDS care model: evaluation of a peer health worker and nurse-staffed community-based program in Uganda. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2009;50:276–82.
Ferradini L, Jeannin A, Pinoges L, Izopet J, Odhiambo D, et al. Scaling up of highly active antiretroviral therapy in a rural district of Malawi: an effectiveness assessment. Lancet. 2006;367:1335–42.
Laurent C, Kouanfack C, Laborde-Balen G, Aghokeng AF, Mbougua JBT, et al. Monitoring of HIV viral loads, CD4 cell counts, and clinical assessments versus clinical monitoring alone for antiretroviral therapy in rural district hospitals in Cameroon (Stratall ANRS 12110/ESTHER): a randomised non-inferiority trial. Lancet Infect Dis. 2011;11:825–33.
Jordan MR, La H, Nguyen HD, Sheehan H, Lien TTM, et al. Correlates of HIV-1 viral suppression in a cohort of HIV-positive drug users receiving antiretroviral therapy in Hanoi, Vietnam. Int J STD AIDS. 2009;20:418–22.
Ferradini LLD, Prak N, Ngeth C, Fernandez M, Pinoges L, Puertas G, Taburet AM, Ly N, Rouzioux C, Balkan S, Quillet C, Delfraissy JF. Positive outcomes of HAART at 24 months in HIV-infected patients in Cambodia. AIDS. 2007;12:2293–301.
Tsuchiya NPP, Yasuda T, Mukoyama Y, Rojanawiwat A, Matsubayashi T, Saeng-aroon S, Auwanit W, Matsuyama A, Sawanpanyalert P, Ariyosh. Demographic, socioeconomic, behavioral and clinical factors predicting virologic failure with generic fixeddose combination antiretroviral therapy before universal health insurance coverage in northern Thailand. Southeast Asian J Trop Med Public Health. 2009;40:71–82.
Zhang F, Dou Z, Ma Y, Zhang Y, Zhao Y, et al. Effect of earlier initiation of antiretroviral treatment and increased treatment coverage on HIV-related mortality in China: a national observational cohort study. Lancet Infect Dis. 2011;11:516–24.
Pujades-Rodríguez M, Schramm B, Som L, Nerrienet E, Narom P, et al. Immunovirological outcomes and resistance patterns at 4 years of antiretroviral therapy use in HIV-infected patients in Cambodia. Tropical Med Int Health. 2011;16:205–13.
Huet C, Ouedraogo A, Konaté I, Traore I, Rouet F, Kaboré A, Sanon A, Mayaud P, Van de Perre P, Nagot N. Long-term virological, immunological and mortality outcomes in a cohort of HIV-infected female sex workers treated with highly active antiretroviral therapy in Africa. BMC Public Health. 2011;11:700.
Fregonese F, Collins IJ, Jourdain G, LeCoeur S, Cressey TR, et al. Predictors of 5years mortality in HIV-infected adults starting highly active antiretroviral therapy (HAART) in Thailand. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2012; Publish Ahead of Print.
Group‡ TPLTOIPIptftCoOHEREC. Trends in virological and clinical outcomes in individuals with HIV-1 infection and virological failure of drugs from three antiretroviral drug classes: a cohort study. Lancet Infect Dis. 2012;12:119–27.
Collaboration TATiLICA-L. Mortality of HIV-1-infected patients in the first year of antiretroviral therapy: comparison between low-income and high-income countries. Lancet. 2006;367:817–24.
Cuong DD, Thorson A, Sönnerborg A, Hoa NP, Chuc NTK, et al. Survival and causes of death among HIV-infected patients starting antiretroviral therapy in northeastern Vietnam. Scand J Infect Dis. 2012;44:201–8.
Do TN, Nguyen TMT, Do MH, Masaya K, Dang TB, et al. Combining cohort analysis and monitoring of HIV early-warning indicators of drug resistance to assess antiretroviral therapy services in Vietnam. Clin Infect Dis. 2012;54:S306–12.
Fleishman JA, Yehia BR, Moore RD, Korthuis PT, Gebo KA, et al. Establishment, Retention, and Loss to Follow-Up in Outpatient HIV Care. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2012; Publish Ahead of Print.
Avnish Tripathi EY, Gibson JJ, Duffus WA. The impact of retention in early HIV medical care on viro-immunological parameters and survival: a statewide study. AIDS Res Hum Retrovir. 2011;27:751–8.
Horstmann E, Brown J, Islam F, Buck J, Agins BD. Retaining HIV-infected patients in care: where are we? Where do we go from here? Clin Infect Dis. 2010;50:752–61.
Dragsted UB, Mocroft A, Vella S, Viard J-P, Hansen A-BE, et al. Predictors of immunological failure after initial response to highly active antiretroviral therapy in HIV-1-infected adults: a EuroSIDA study. J Infect Dis. 2004;190:148–55.
Srasuebkul P, Ungsedhapand C, Ruxrungtham K, Boyd MA, Phanuphak P, et al. Predictive factors for immunological and virological endpoints in Thai patients receiving combination antiretroviral treatment. HIV Medicine. 2007;8:46–54.
Egger M, May M, Chêne G, Phillips AN, Ledergerber B, et al. Prognosis of HIV1-infected patients starting highly active antiretroviral therapy: a collaborative analysis of prospective studies. Lancet. 2002;360:119–29.
Lohse N, Obel N, Kronborg G, Laursen A, Pedersen C, et al. Declining risk of triple-class antiretroviral drug failure in Danish HIV-infected individuals. AIDS. 2005;19:815822.
We would like to thank the Swedish International Development Cooperation Agency (SIDA), the CHAIN EU FP7, Global Fund, CDC-Lifegap Project, and Health System Research Project of Hanoi Medical University in Vietnam for providing financial and technical supports. We are also grateful to Ms. Iram Bilal, Dr Nguyen Phuong Hoa, Ms. Nguyen Binh Minh, Dr. Tran Thanh Do, Dr. Nguyen Phuong Thanh, Dr Hoang Thi Thao, Dr. Nguyen Thi Tuyet Mai, Ms. Pham Thi Tuoi and all colleagues, health staff, external supporters, and patients in the DOTARV Project.
Swedish International Development Cooperation Agency (SIDA) and the CHAIN EU FP7.
Availability of data and materials
The data can be provided from the main author upon request.
Dr. DDC has participated in development of study design, the field coordination, data collection, data analysis, and manuscript writing; he is the first author. Prof. AS has participated in development study design and manuscript writing. Dr. VVT has participated in development of study design, the field coordination, data collection, and manuscript writing. Dr. ZE-K has participated in data analysis and manuscript writing. MS and GM are statisticians and have supported data analysis and manuscript writing. Prof. NTKC was the coordinator and participated in development of the study design, the field coordination, data collection, and manuscript writing. Prof. VD has participated in development study design and manuscript writing. Prof. AT has participated in development study design and manuscript writing. NKL has participated in data analysis and manuscript writing. Prof. PNA has participated in study design and manuscript writing. Associate Prof. ML has participated in grant writing, overall project coordination, study design, data collection, data analysis, and manuscript writing. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethical approval and consent to participate
The study was approved by the Institutional Review Boards of Hanoi Medical University, Ministry of Health, Vietnam (numbers 26/IRB, 66/HMURB, 59/HMURB and 98/HMURB) of Hanoi Medical University) and the Regional Board for Ethics Review from Karolinska Institutet in Stockholm, Sweden (number 2006/1367-31/4). Before conducting the study, written informed consent was obtained and all identifying information (names, initials, etc.) were then omitted to ensure the confidentiality. Patients in the intervention group were informed about the study and that they would be visited by a peer supporter and that the home visits might disclose their HIV status. Biological samples were collected and used only after written consent. All blood samples were coded to protect the identity of patients and to ensure confidentiality.
Both intervention and control groups received equal care and treatment and those who did not fulfill the inclusion criteria’s for the study were managed with a set standard of care and treatment according to the National Guidelines [17, 22]. Peer-supporters received ART at the study clinics and were treated in the same way as other HIV patients according to the National Guidelines. Moreover, peer-supporters’ viral loads (ExaVir™ Load) were also measured every 6 months, and they were compensated by receiving a salary and being refunded transportation fees each month. Data were accessible only to the research team, data manager, and coordinator of the project.