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. 2024 Dec 19;4(12):e0004072. doi: 10.1371/journal.pgph.0004072

Improving HIV testing and retention among adolescents and youths: Lessons from a quasi-experimental study of the Red-Carpet Program in Malawi

Rachel Chamanga 1,*, Tessa Musukwa 1, Cosima Lenz 2, Louiser Kalitera 1, Geoffrey Singini 1, Felix Gent 1, Harrid Nkhoma 1, Godfrey Woelk 2, Judith Kose 3,4, Thulani Maphosa 1
Editor: Rashmi Josephine Rodrigues5
PMCID: PMC11658608  PMID: 39700233

Abstract

Adolescents and youth living with HIV (AYLHIV) often face significant challenges in HIV care. Elizabeth Glaser Pediatric AIDS Foundation in Malawi implemented the Red-Carpet Program (RCP) to provide fast-tracked services for AYLHIV in care.This study aimed to assess the effect of RCP on Provider-Initiated HIV testing, linkage to care and antiretroviral therapy (ART), and retention in care among AYLHIV in Blantyre, Malawi. This quasi-experimental study compared outcomes among newly identified AYLHIV enrolled in four intervention health facilities implementing RCP with those of three non-intervention facilities between July 2020 and March 2021. Non-intervention sites were selected by matching based on patient volumes and baseline retention rates prior to the intervention ensuring comparability with the intervention sites. Proportions and Chi-square tests were used to compare outcomes between the two groups. Kaplan-Meier curves were employed to assess longitudinal outcomes, and Cox regression analysis was used to estimate the hazard of non-retention in care. Data were collected from 475 AYLHIV from RCP sites and 248 AYLHIV from non-intervention sites. In the non-intervention sites, 87% of AYLHIV were female, compared to 78% in the RCP sites. A higher proportion of adolescents (67%) underwent provider-initiated HIV testing at intervention site s than at non-intervention sites (51%), p<0.01. Retention in care was higher in RCP sites, with 67% of AYLHIV in care at 12 months post-initiation compared with 56% in non-intervention sites, p = 0.005. AYLHIV from intervention sites were less likely to experience non-retention than those from non-intervention sites (adjusted Hazard Ratio: 0.47, 95% CI: 0.28–0.80). The implementation of the RCP facilitated higher rates of provider-initiated HIV testing among adolescents and youth. Furthermore, RCP demonstrated the potential to improve retention in care The RCP offers promise for enhancing outcomes among this vulnerable population, emphasizing the need for tailored HIV interventions for adolescents and youth.

Introduction

Globally, approximately 2.1 million adolescents and youth navigate the formidable challenges of HIV/AIDS [1]. Within this vulnerable population, adolescents and youth aged 10–24 years living with HIV often have disproportionately inferior outcomes across the HIV care continuum [2]. Compared to adults, they exhibit lower awareness of their HIV status, face substantial hurdles in initiating essential antiretroviral therapy (ART), and exhibit suboptimal viral suppression rates and retention in care [3–5].

The journey of adolescents and youths living with HIV has, in part, been compounded by the historical focus of HIV testing and treatment services on adults, inadvertently neglecting the distinctive requirements of this critical demographic [6]. Adolescence, marked by constant life transitions, experimentation, and engaging in risky behaviours, also face unique factors such as challenges with inconsistent support from caregivers that impact their adherence to ART medication[7]. Non-adherence leads to treatment defaults, virologic failure, and viral rebound, even after initial viral suppression [8–10].

Recognizing the pressing need for tailored, youth-responsive interventions designed to address the unique hurdles confronting adolescents living with HIV, the Elizabeth Glaser Pediatric AIDS Foundation (EGPAF)–Malawi, in collaboration with ViiV Healthcare and the Malawi Ministry of Health, embraced the evidence-based Red-Carpet Program (RCP) that had been conducted by EGPAF in Kenya [11,12]. The RCP’s primary focus in Malawi was to enhance HIV testing, linkage to care, and retention in care among adolescents and youth living with HIV, through a youth-centric approach.

Malawi, with its high HIV prevalence rate (8.9%), has witnessed the highest incidence of infections among adolescents and youth aged 15–24 years, with young women being particularly vulnerable due to early sexual debut and entering into relationships with significantly older male partners [13–15]. Paradoxically, despite their heightened risk, young people, especially males, exhibit a reluctance to be tested for HIV [16]. The proportion of those who had never had an HIV test was higher in males aged 15–19 years, with 65% reporting never having an HIV test, compared to 51% in females of the same age group [17]. This gender disparity could be attributed to the traditional male aversion to healthcare-seeking behaviour and the misperception of lower infection risk, unlike females who often access healthcare facilities for reproductive services and testing [16,18,19]. Other influential factors affecting HIV testing engagement include having accurate knowledge about HIV infection, attainment of secondary school education, and household characteristics, such as the educational status of caregivers [16].

Additionally, even among those who undergo HIV testing and are enrolled in care, viral suppression rates remain low, with national estimates as low as 66% [13]. This is in contrast to the 84% suppression rate observed in adults aged 15–49 years in Malawi [13]. Furthermore, retention in care among adolescents and youth ‘ lags behind that of adults, accentuating the urgency of tailored interventions [20].

The introduction of the RCP in Malawi represents a dedicated endeavour to address the distinctive difficulties faced by adolescents and youth living with HIV, with a special emphasis on leveraging a peer-led approach to identify and retain adolescents and youth in care [11,12]. However, while peer-led initiatives have shown promise in improving HIV testing and ART outcomes, the available evidence remains mixed and limited, especially within the context of sub-Saharan Africa [21–23].

In this context, our evaluation aimed to provide an assessment of the RCP effect on adolescents living with HIV in Blantyre, Malawi. We examined HIV testing outcomes, linkage to ART, and retention in care at 6- and 12-months post ART initiation. This investigation is a significant step toward improving the understanding of how peer-led initiatives can enhance HIV care outcomes for adolescents and youth, who continue to be disproportionally impacted by the epidemic.

Methodology

Study design

This study employed a quasi-experimental program evaluation approach using secondary data collected from adolescents and youth who underwent HIV testing and were newly initiated into ART care between July 2020 and March 2021.

Study setting

The research was conducted in Blantyre, Malawi, at seven primary health facilities, including four intervention sites participating in the RCP and three non-intervention sites selected based on their similarity in key characteristics to the intervention sites. The characteristics which we matched on between intervention and non-intervention sites included: being a primary care facility in urban settings; having the same volume of newly diagnosed AYLHV and those in HIV care; and having similar baseline retention rates before implementation of the intervention (within ± 5%) We matched on baseline retention rates which are retention rates of the AYLHIV before implementing the program. We matched on this to ensure that there was no bias amongst the facilities with other facilities doing better in retention than others before the intervention.

Intervention

The Red-Carpet Program, implemented by EGPAF Malawi in collaboration with the Malawi Ministry of Health, introduced a novel approach utilizing Youth Champions (YCs) to support adolescent and youth clients at RCP facilities. YCs, aged 18–25 years, were peer navigators and treatment supporters recruited from among adolescents and youth living with HIV. YCs were volunteers, but received a stipend for their role. Eligibility to become a YC included being fully disclosed to and open to discussing their status and experiences, demonstrating adherence, achieving viral suppression, and having received at a minimum, a secondary school diploma. YCs were strategically stationed at various entry points across the facilities, such as outpatient departments, sexually transmitted infections clinics, antenatal care clinics, HIV testing and screening clinics, family planning clinics, maternity wards, and ART clinics. With the aid of standardized scripts co-developed with young people, YCs engaged with adolescents and youth seeking care at the facility, providing support for HIV testing, counselling, ART initiation, and enrolment in RCP. They also guided those testing negative for risk reduction and prevention support, including pre-exposure prophylaxis. Additionally, YCs offered psychosocial support, adherence support, and retention activities, which encompassed appointment reminders, tracing clients who missed appointments, and conducting home visits for AYLHIV, facing care-related challenges.

Study population

This study included newly initiated HIV-positive males and females aged 10–24 years who initiated ART between July 2020 and March 2021. At the intervention sites, we included all AYLHIV newly initiated on ART and exposed to the intervention through registration in the Red-Carpet enrolment register; we excluded newly initiated AYLHIV who had not been exposed to the Red Carpet intervention or those newly initiated AYLHIV who had transfer-into the facility. At the non-intervention sites, all newly initiated AYLHIV on ART, as documented in the ART registry during the same period, were included in the study; we excluded newly initiated AYLHIV who had transferred into the facility.

Data collection & data analysis

Trained data abstractors collected data from multiple registers, including the HIV testing register, ART register and HIV viral load register. Individual-level data from the electronic medical records (EMR) were also obtained. The data abstractors obtained this data between 20 Oct 21 to 07 Nov 21. The data abstractors obtained de-identified data of the AYLHIV. Data were entered into tablets using the Open Data Kit (ODK) electronic data-collection tool. The abstracted data comprised of age, sex, date of HIV diagnosis, date of ART initiation, ART regimen, date of ART clinic attendance, and HIV treatment outcomes. Treatment outcomes were defined as a) died–documented as deceased; b) alive and active in care—attended the clinic at the last scheduled visit; c) defaulted–missed treatment collection or a clinical appointment for 2 or more months after ARVs are expected to have run out with no record of death; d)documented to have transferred out–moved to receive services at another facility. Primary outcomes included the proportion of AYLHIV accessing provider-initiated HIV testing (PITC), linkage to care on the same day, and retention in care 6 and 12 months after ART initiation. Quantitative analysis was conducted using STATA v17, involving descriptive analysis, chi-square tests, Kaplan-Meier curves, and Cox regression analysis.

Survival analysis was utilized for two assessments. In the first analysis (Analysis A), we analysed AYLHIV defaulted from care and those who had died as having the outcome of interest, patients who transferred out were treated as intention-to-treat where they contributed their time to the study during analysis but were censored. The second analysis (Analysis B), only that were alive in care were considered to be “retained in care at the facility;” those that had “died”, “defaulted” or “transferred out” were considered as having the outcome of interest.

Ethical considerations

This evaluation was approved by the Malawi National Health Science Research Committee (NHSRC) and the US-based ADVARA Institutional Review Boards under the “Evaluation of Outcomes achieved through integrated HIV/AIDS and TB Prevention, Care and Treatment Programs in Malawi” protocol, which allows for retrospective data review of program data. The protocol was reviewed and approved in accordance with the U.S. Centre for Disease Non-intervention and Prevention (CDC) human research protection procedures, with no direct interaction with human subjects or access to identifiable data or specimens for research purposes. Informed consent or assent was waived by the National Health Research Sciences Committee and ADVARA Institutional Review Board.

Results

During the study period, 8% (499/6,336) of AYLHIV tested for HIV at RCP sites and 6% (251/4,534) of those tested at control sites tested positive for HIV. Linkage to ART for newly diagnosed AYLHIV was 98% (490/499) at RCP sites compared to 96% (241/251) at control sites. Complete individual data were extracted for 723 newly initiated AYLHIV receiving antiretroviral therapy (ART) (475/499 [95%] AYLHIV from intervention and 248/251 [99%] from non-intervention sites). The total person time for follow up in the study was 627.02 person-days; with 417.14 person-days in the intervention sites and 209.88 person-days in the non-intervention sites.

Table 1 provides an overview of the demographic and clinical characteristics of the AYHLIV included in the study, differentiating between the intervention and non-intervention groups. The overwhelming majority of these AYHLIV cases were female, accounting for 80% of the total cohort; of these female AYLHIV, 35.6% were pregnant. The intervention sites exhibited a higher proportion of males compared to the non-intervention sites (22.1% vs. 13.3%, p<0.01). The age distribution of participants in both groups was not significantly different, with a median age at ART initiation of 21 years (Interquartile Range [IQR] 19–23) across both non-intervention and intervention sites. Notably, all AYLHIV attending both types of sites were initiated on a dolutegravir-based regimen, ensuring consistency in the treatment protocols. The mean time to ART initiation was 0.19 days in intervention sites and 0.25 days in non-intervention sites.

Table 1. Demographic and clinical characteristics of adolescents and youths newly initiated into care comparing non-intervention and intervention sites.

Variable Description Total
N = 723
Non-intervention
N = 248
Intervention
N = 475
P-value
N (%) N (%) N (%)
Sex Males 138 (19.1) 33 (13.3) 105 (22.1) <0.01
Females pregnant 208 (28.8) 58 (23.4) 150 (31.6)
Female non-pregnant 377 (52.1) 157 (63.3) 220 (46.3)
Age at ART initiation
10–14 27 (3.7) 5 (2.0) 22 (4.6) 0.17
15–19 168 (23.3) 62 (25.0) 106 (22.3)
20–24 528 (73.0) 181 (73.0) 347 (73.1)
WHO staging WHO Stage I/II 697(96.4) 242 (97.6) 455 (95.8) 0.44
WHO Stage III/IV 26(3.6) 6 (2.4) 20 (4.2)
Reason for HIV testing a Provider-initiated (PITC) 339 (65.2) 67 (51.5) 272 (69.7) <0.01
Family referral slip (Active Index Testing) 122 (23.5) 48 (36.9) 74 (19.0)
Other (Voluntary) 59 (11.3) 15(11.6) 44 (11.3)
Previous HIV test a** Negative 360 (69.2) 79 (60.8) 281(72.0) 0.01
Positive 51(9.8) 11 (8.5) 40 (10.3)
Never tested 108(20.8) 40 (30.7) 68 (17.4)
Initiation on ART a Newly tested 468 (90.2) 119 (91.5) 350 (89.7) 0.55
Previously tested positive 51 (9.8) 11 (8.5) 40 (10.3)
Initiated ART on same day Yes 697 (96.4) 236 (95.2) 461(97.1) 0.19
No 26 (3.6) 12 (4.8) 14 (2.9)
Viral load suppressed * Yes 156 (85.7) 56 (86.2) 100 (85.5) 0.89
No 26 (14.3) 9 (13.8) 17 (14.5)

*Those who had viral load results: Intervention sites, n = 117, non-intervention sites n = 65.

** 2 had inconclusive results.

a The numbers do not add to the totals due to missing data. There were 118 missing in non-intervention and 85 missing in intervention sites.

The study revealed a substantial disparity in prior HIV-testing experiences between the intervention and non-intervention sites. A higher proportion of AYLHIV at the intervention facilities had undergone provider-initiated HIV testing than those at non-intervention sites (69.7% vs. 51.5%, p<0.01). Approximately 21% of AYLHIV that were newly initiated on ART had never been tested previously, with a significantly higher proportion observed in the non-intervention sites (30.7% vs. 17.4%, p = 0.01). Furthermore, the data indicated that the majority of newly initiated AYLHIV had tested negative previously, with the intervention sites outperforming the non-intervention sites in this regard by 72.0% and 60.8%, respectively (p = 0.01).

At the time of data collection, all 723 AYLHIV had been on ART for more than six months, rendering them eligible for viral load assessments. However, viral load samples were collected for only a portion of the cohort, with viral load results accessible for only 25.1% (182) of the study population. The overall suppression rate was 86% among this group with viral load testing done. There was no discernible distinction in suppression rates between the non-intervention and intervention sites, with rates of 87% and 86%, respectively (p = 0.89).

At 6-months post-ART initiation, the proportion of AYHLIV retained at the facility was 77.3% in the intervention sites and 68.7% in the non-intervention sites (p-value 0.012) (Table 2). However, these differences became more pronounced at the 12-month interval, with retention dropping to 66.7% at the intervention sites and 56.4% at the non-intervention sites (p-value 0.005). At the end of the first year post-ART initiation, 63.1% of the AYLHIV were successfully retained at the clinic where they had initiated ART;25.0% had transferred to other facilities, 11.6% had defaulted from care, and 0.3% had died.

Table 2. Cumulative retention into care at 6 and 12 months by demographic characteristics.

Variable Description Total aRetained in care at 6 months aRetained in care at 12 months
Non-intervention Intervention Non-intervention Intervention Non-intervention Intervention
N N N (%) N (%) N (%) N (%)
Sex Males 33 105 23 (69.7) 80 (76.2) 21(63.6)* 64 (60.9)
Females pregnant 58 150 44 (75.8) 124 (82.7) 41 (70.7) 109(72.7)
Female Non-pregnant 157 220 104(66.2) 163(74.1) 78 (49.7) 144(65.4)
Age at ART start 10–14 5 22 5 (100.0) 17(77.3) 4(80.0) 15(68.1)
15–19 62 106 42 (67.7) 76(71.7) 32(51.6) 61(57.5)
20–24 181 347 124(67.9) 274(78.9) 104(57.4) 241(69.4)
WHO staging WHO Stage I or II 242 455 165(68.1) 350(76.9) 134 (55.4)* 304(66.8)
WHO Stage III or IV 6 20 6(100.0) 17(85.0) 6(100.0) 13(65.0)
Reason for HIV test Provider-initiated 67 272 47(70.1) 214(78.6) 43(64.2) 181(66.5)
Family referral slip (Active Index Testing) 48 74 35(72.9) 60(81.0) 29(60.4) 53(71.6)
Other (Voluntary) 15 44 9(60.0) 32(72.7) 6(40.0) 33(75.0)
Previous HIV test Negative 79 281 59(74.6) 224(79.7) 51(64.5) 200(71.2)
Positive 11 40 5(45.4) 25(62.5) 5(45.4) 20(50.0)
Never tested 40 68 27(67.5) 56(82.3) 22(55.0) 46(67.6)
Method into ART Newly tested 119 350 86(72.9) 281(80.2)* 73(61.3) 247(70.5)*
Previously tested positive 11 40 5(45.4) 25(62.5) 5(45.4) 20(50.0)
Viral load suppressed Yes 57 100 57(100.0)* 100(100.0) 52(91.2) 95(95.0)
No 9 17 8(88.9) 17(100.0) 8(88.9) 16(94.1)
Total 248 475 171(68.7) 367) (77.3) 140 (56.4) 317 (66.7)

a Retained into care were only those who were “Alive and on ART”, this excluded deaths, transfer outs and defaulters. *p value of Chi-square test was ≤ 0.05.

Breaking down these figures by site type, in the intervention sites, 66.7% of AYLHIV were still actively receiving ART, 12.4% had defaulted, 0.4% had died, and 20.5% had transferred to alternative care settings. In contrast, the non-intervention sites exhibited a slightly lower proportion of AYLHIV who were alive on ART (56.4%), with 10.1% experiencing defaults, 0.0% having died, and 33.5% having transferred out. Notably, approximately 60% of those who transferred out of the study population were non-pregnant women, with 66% of this subgroup falling within the 20–24 years age category.

Analysis of retention rates within intervention and non-intervention sites across various demographic groups including age, sex, and WHO staging revealed interesting patterns. At the intervention sites, insignificant differences were observed in retention rates across the age, sex, and WHO staging. However, significant variations in retention rates were observed within the non-intervention sites: Females who were not pregnant exhibited the lowest retention rate at 49.7%, in contrast to males (63.6%) and pregnant females (70.7%) at the non-intervention sites at the 12-month mark (p = 0.01). In contrast, in the intervention sites, the proportion of females who were not pregnant and retained into care was notably higher, hovering around 65.4%, with males having the lowest proportion of being retained into care at 60.9% and pregnant females having the highest proportion at 72.7%; the differences between males and females were not significant (p = 0.13).

Furthermore, older adolescents aged 15–19 years displayed a lower proportion of retention in care compared to other age groups (10–14 and 20–24 years) at the 12-month juncture, although this difference did not reach statistical significance [(57.5% vs. 68.1% vs. 69.4%; p = 0.07 in intervention sites) (51.6% vs. 80.0% vs. 57.4% in non-intervention sites, p = 0.41)]. However, those with advanced WHO stage III or IV experienced higher proportions of retention than those with WHO stage I or II at the 12-month mark in the non-intervention sites (100.0% vs. 55.1%; p = 0.03), while this difference was less pronounced in the intervention sites (65.0% vs. 66.8%, p = 0.86).

Adolescents and youth who had previously tested positive for HIV exhibited lower proportions of active care engagement than those who were newly diagnosed at the 12-month mark in intervention sites (50.0% vs. 70.5%; p<0.01). A similar trend was noted in the non-intervention sites, where 45.4% of previously diagnosed individuals were in care compared to 61.3%, although this difference was not statistically significant (p = 0.30). Moreover, a lower proportion of AYLHIV with an unsuppressed viral load was engaged in active care compared to those with suppressed viral loads at the 6-month point in the non-intervention sites (88.9% vs. 100.0%; p = 0.01).

In Fig 1A and 1B, Kaplan-Meier curves illustrate the comparative retention outcomes between the intervention and non-intervention groups stratified by whether patient transfer is censored or included as outcome. Analysis A (when patients who transfer out are censored at time of transfer), no appreciable difference in retention was observed when comparing the non-intervention and intervention sites, as evidenced by a log-rank test p-value of 0.85. However, in Analysis B (when those who transferred out are included as outcome of interest), retention is significantly different between the non-intervention and intervention sites, with a log-rank test p-value of 0.005.

Fig 1. Kaplan Meier curve describing retention in care for non-intervention vs intervention sites.

Fig 1

Table 3 further illuminates the differences in hazard ratios of the risk of being lost to care between non-intervention and intervention sites, adjusting for age and sex. In Analysis A, there is no significant difference in the hazard of being lost in care, with an adjusted hazard ratio (aHR) of 0.95 (95% confidence interval [CI]: 0.37–2.42).However, Analysis B shows a substantially decreased hazard of being lost to care in the intervention sites when compared to the non-intervention sites, as evidenced by an aHR of 0.47 (95% CI: 0.28–0.80).

Table 3. Cox Proportional Hazard of lost to care; non-intervention and intervention sites.

Analysis A Analysis B
Variable Description Crude (95% CI) Adjusted (95% CI) Crude (95% CI) Adjusted (95% CI)
Intervention Non-intervention 1.00 1.0 1.0 1.0
Intervention 1.09 (0.43–2.72) 0.95(0.37–2.42) 0.48 (0.28–0.81) 0.47 (0.28–0.80)
Sex Females 1.00 1.0 1.0 1.0
Males 1.88 (0.76–4.67) 1.86(0.72-4-79) 1.01 (0.53–1.92) 1.22 (0.63–2.33)
Age at ART start 10–14 1.00 1.0 1.0 1.0
15–19 0.45 (0.05–4.39) 0.57 (0.06–5.79) 2.42 (0.31–18.45) 2.29 (0.29–17.7)
20–24 0.71 (0.09–5.41) 0.89(0.11–7.06) 2.06 (0.28–15.02) 1.99 (0.27–14.7)

Discussion

In this quasi-experimental evaluation of the Red-Carpet Program in Malawi, we demonstrated significant improvements in Provider Initiated Testing and Counselling (PITC) services, specifically tailored to adolescents and youth in the intervention sites compared to the non-intervention sites. These findings align with other studies conducted in Kenya, which have shown enhanced HIV-testing outcomes among adolescents and youth in similar program settings [11].

The Red Carpet Program strategically addresses critical issues related to implementing adolescent-friendly services, fostering increased screening and testing among eligible adolescents and youth seeking care at health facilities [12]. This was evidenced by the identification of more male adolescents living with HIV, and a reduction in the proportion of adolescents and youths who had never undergone HIV testing in intervention sites. This trend echoes the positive outcomes observed in a study conducted in Malawi, where the establishment of adolescent-friendly clinics, known as "Girl Power" clinics, led to a 23% increase in HIV testing among adolescents and young women when compared to the standard of care [24].

Moreover, similar increases in HIV testing willingness and uptake among adolescents and youth have been reported in other settings utilizing peer-interventions, as reported in a study in Ethiopia that assessed peer-led HIV behavior education in schools, which resulted in an increase in knowledge and increased interest in seeking HIV testing among students in the intervention group [21]. However, the fidelity of implementing adolescent-friendly services remains a concern, with studies showing that only 40% of expected facilities provide such services [25]. Ensuring the widespread availability and accessibility of youth-responsive services in all health facilities is a challenge that adolescent programs continue to face [25].

Despite promising advancements in HIV testing, the overall retention rates at 12 months post-ART initiation (63.1%) are lower than those reported in other studies [26–28]. For instance, a study in South Africa documented retention rates of 90.5% and 85.4% 6- and 12-months after post-ART initiation, respectively [27]. Similarly, a cohort study in Namibia reported 6- and 12-month retention rates of 97.7% and 94%, respectively [28]. In contrast, lower retention rates of 49% at 1-year post-ART initiation were reported in Mozambique [8], and Uganda observed a 65% retention rate among adolescents in care after 5 years of follow-up [29]. These discrepancies may be attributed to various factors, including the local context and rigor of program implementation.

A nuanced examination revealed higher proportions of AYLHIV who were alive and receiving ART at intervention facilities than at non-intervention sites at both 6 and 12 months, specifically when calculated using cumulative retention. However, these differences were not apparent when the transfer-outs were censored in the survival analysis. This discrepancy in outcomes aligns with findings from other studies that reported variations in retention outcomes depending on whether transfer-outs were included or excluded from the analysis [30]. Our study had a relatively higher proportion of participants classified as transfer-outs (25%), which exceeds the percentages reported in other studies, which tend to be approximately 16% [20,31]. Most of these transfers occurred in non-intervention sites, which could have been because the RCP intervention reduced patient desire to transfer out. Interventions that are focused on adolescents in Malawi have been shown to provide greater retention into care [32]. The transfers mirrored a prevalent pattern where female adolescents and young adults, particularly those who are not pregnant, exhibit a higher likelihood of being lost to care or transferring due to their inherent mobility and potential migration (for example, a non-pregnant female AYLHIV who gets married may move to her spouses location) [31,33].This was however in contrast with findings from South Africa, where pregnant adolescents and young females demonstrated lower retention rates than their non-pregnant counterparts [26]. Similarly, a study from Malawi focusing on women receiving Option B+ treatment reported higher rates of attrition among pregnant or breastfeeding women than among those who were not pregnant. However further research is required to understand the reasons why transfer-outs are more prevalent in AYLHIV in Malawi.

Furthermore, our study identified that adolescents and youths who had previously tested positive for HIV but had not yet started ART exhibited lower retention than those newly diagnosed in the non-intervention sites. This delay in ART initiation could be attributed to factors such as denial of HIV status, fear of stigma, lack of disclosure of HIV status, concerns about side effects, long waiting times at ART clinics, and transportation challenges [33]. These issues continue to influence adolescents and youth and affect their retention of care.

Finally, our study revealed that AYLHIV in WHO Clinical Stage III or IV had higher retention rates than those in WHO Clinical Stage I or II at non-intervention sites. This aligns with the findings of other studies, in which advanced WHO staging was not associated with attrition [29]. Those with advanced HIV disease may be more motivated to seek care because of their health condition, which leads to closer follow-up and better retention [26,29].

This study has some limitations, including gaps in updating electronic medical records (EMRs) which could lead to delays in reported outcomes. The study also utilised a quasi-experimental design where the selection of control and intervention sites was not randomised and thus it is difficult strongly make causal associations. We also incurred missing data for some of the key variables such as viral load which may have affected calculation of the outcomes.

Conclusion

In conclusion, our study highlights the impact of the RCP in increasing provider-initiated HIV testing and enhancing retention rates among adolescents and youth in Malawi. However, while retention was better at intervention sites, retention at care at 12-months post ART initiation was not optimal in either group. Notably, this study revealed the vulnerability for poor retention of non-pregnant females, those in WHO stage I or II, and individuals who previously tested positive for HIV but did not initiate ART, underlining the pressing need for tailored interventions. These findings underscore the importance of ongoing efforts to deliver effective adolescent-friendly services, promote early ART initiation, and address the unique challenges faced by adolescents in their fight against HIV/AIDS.

Supporting information

S1 Data. Study data set.

(XLSX)

pgph.0004072.s001.xlsx (524.2KB, xlsx)

Data Availability

All data are in the manuscript and/or supporting information files.

Funding Statement

The authors declare that this work was supported by ViiV Health Care under the Viiv Malawi Grant 519 (Viiv RC 2020-21 – Malawi – 519). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. No additional external funding was received for this study. The authors have no financial relationships or competing interests that could be perceived as influencing the results or interpretation of this research. Its contents are solely the authors' responsibility and do not necessarily represent the official views of Viiv Health Care.

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PLOS Glob Public Health. doi: 10.1371/journal.pgph.0004072.r002

Decision Letter 0

Rashmi Josephine Rodrigues

19 Jun 2024

PGPH-D-24-00709

Improving HIV Testing and Retention among Adolescents: Lessons from the Red-Carpet Program in Malawi

PLOS Global Public Health

Dear Dr. Chamanga,

Thank you for submitting your manuscript to PLOS Global Public Health. After careful consideration, we feel that it has merit but does not fully meet PLOS Global Public Health’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

==============================

EDITOR:

Overall the manuscript is well written. However, I request you to kindly address the following-

1. The manuscript refers to both adolescents and young adults, hence please consider adding ' in the title. 

2. The word 'impact' is used in the last paragraph of the introduction. Kindly replace with effect as impact is a long term effect and this study assesses outcomes at 6 and 12 months post ART initiation.

Kindly clarify if all the AYLHIV in records at the intervention and nonintervention sites were included. If all were included, a sample size calculation is not necessary.

3. It is unclear what 'baseline retention rates' in the inclusion of sites means. 

Also non-intervention sites were selected based on numbers of adolescents in care and retention rates at would it not affect the outcome studied? Selecting sites based on similar rates of diagnosis would be more appropriate. 

4. Were all AYLHIV during the study period at each site included? If not what were the exclusion criteria e.g., incomplete records, those diagnosed at the facility but belonging to a different region.

5. Were AYLHIV who missed the last visit </=2 months ago included in alive and active in care? Usually what is the practice regarding dispensing medications in Malawi?- is this monthly or once in 2 months?

6. Is there a better term for Defaulted? Health programmes tend to use the tearm lost-to-foloow-up instead of default. Kindly consider changing this- unless ofcourse the National Program in Malawi uses the tearm 'default'. Also, does default include AYLHIV who returned to care with more than 2 months of missing follow-ups?

7. Please indicate the total person-time follow-up in the study and in the intervention and non-intervention arms. Also, would be good to have mean/median time to treatment initiation.

8. Kindly discuss limitations of the methodology in a bit more detail- the quasiexperimental design, the selection of nonintervention sites, quality of records and the data at all sites to name a few. On the other hand, small sample size is generally not included under limitations, especially, if all records were included. Reasons why all records were not included could be a limitation.

9. Minor language edits necessary e.g., "AYLHIV patients", 63.1% of the "patients with AYLHIV" and "the overall retention rates at 12 months after post-ART".  Also kindly use standard teminilogy through-out the document,

==============================

Please submit your revised manuscript by Jul 19 2024 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at globalpubhealth@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pgph/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

We look forward to receiving your revised manuscript.

Kind regards,

Rashmi Josephine Rodrigues, M.D., Ph.D.

Academic Editor

PLOS Global Public Health

Journal Requirements:

1. Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

2. Please provide separate figure files in .tif or .eps format only and remove any figures embedded in your manuscript file. Please also ensure all files are under our size limit of 10MB.

For more information about figure files please see our guidelines:

https://journals.plos.org/globalpublichealth/s/figures 

https://journals.plos.org/globalpublichealth/s/figures#loc-file-requirement

3. In the online submission form, you indicated that "The data set is readily available on request by the journal". 

All PLOS journals now require all data underlying the findings described in their manuscript to be freely available to other researchers, either 

1. In a public repository, 

2. Within the manuscript itself, or 

3. Uploaded as supplementary information.

This policy applies to all data except where public deposition would breach compliance with the protocol approved by your research ethics board. If your data cannot be made publicly available for ethical or legal reasons (e.g., public availability would compromise patient privacy), please explain your reasons by return email and your exemption request will be escalated to the editor for approval. Your exemption request will be handled independently and will not hold up the peer review process, but will need to be resolved should your manuscript be accepted for publication. One of the Editorial team will then be in touch if there are any issues.

Additional Editor Comments (if provided):

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Does this manuscript meet PLOS Global Public Health’s publication criteria? Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe methodologically and ethically rigorous research with conclusions that are appropriately drawn based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

**********

3. Have the authors made all data underlying the findings in their manuscript fully available (please refer to the Data Availability Statement at the start of the manuscript PDF file)?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception. The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS Global Public Health does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: While their research methodology is robust and their findings significant, the article requires minor corrections. Overall, this study serves as a crucial contribution to the field, highlighting the urgent need for action in addressing the strategies to improve HIV screening and retention in care to achieve the 95*95*95 targget by 2025. Thank you for the opportunity to review this enlightening article.

Reviewer #2: At the outset, I must congratulate the authors of the study and the EGPAF team at Malawi for the wonderful work you all are doing at the helm of the HIV epidemic. I must definitely appreciate the efforts taking in improving the AYLHIV outcomes, a very important subgroup of the PLHIV who require extra care and effort which the RCP is an embodiment of.

Strengths of the Study:

1. Well structured study with good methodological explanation.

2. An important separation with use of two groups for Analysis based on the transferred out individuals which could act as a large confounding group in evaluation of your study.

3. Intelligently written and well presented study.

Suggestions:

I had a few semantic errors which I have brought to your notice:

Line 52 - Would suggest use of p =0.012, instead of just 0.012.

Line 148 - Would suggest use of d) for the 4th treatment outcome " transferred out"

Table 1 : How has the missing data been analysed? included or not included in analysis?

Line 219 - Would suggest WHO Staging instead of WHO Stagingg.

Recommendations:

1. Would consider further research and analysis into the transferred out, to understand the underlying factors which contribute to the same since it is a large percent of the cohort which was censored.

2. Would advocate for the low viral load testing done in your participants as it has significantly reduced the numbers and hence the outcome. To consider ways to boost viral load testing more robustly with use of YCs or an intervention which is deemed fit by you all.

3. The full title and short title uses keywords like adolescents which by WHO definition would be just 10-19years, but the median age of ART initiation was 21 years which is more in the bracket of young adult. However there are multiple papers which believe comprehensive adolescent care should include upto 24 years and hence the same must be highlighted in your paper as a need for inclusion of the age group. I think it is important to reflect the same in the title like use of AYLHIV in the title.

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

Do you want your identity to be public for this peer review? If you choose “no”, your identity will remain anonymous but your review may still be made public.

For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: Claudia Merlin Tony

Reviewer #2: Yes: Nikith Austin D'Souza

**********

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

Attachment

Submitted filename: PLOS_ review.docx

pgph.0004072.s003.docx (12.5KB, docx)
PLOS Glob Public Health. doi: 10.1371/journal.pgph.0004072.r004

Decision Letter 1

Rashmi Josephine Rodrigues

28 Oct 2024

PGPH-D-24-00709R1

Improving HIV Testing and Retention among Adolescents and Youth: Lessons from the quasi-experimental study of the Red-Carpet Program in Malawi

PLOS Global Public Health

Dear Dr. Chamanga,

Thank you for submitting your manuscript to PLOS Global Public Health. After careful consideration, we feel that it has merit but does not fully meet PLOS Global Public Health’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Kindly address the comments by the reviewer in the attached documents as well as the sanitised copy of the manuscript.

Please submit your revised manuscript by Nov 27 2024 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at globalpubhealth@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pgph/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

We look forward to receiving your revised manuscript.

Kind regards,

Rashmi Josephine Rodrigues, M.D., Ph.D.

Academic Editor

PLOS Global Public Health

Journal Requirements:

Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

Additional Editor Comments (if provided):

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: (No Response)

Reviewer #2: All comments have been addressed

**********

2. Does this manuscript meet PLOS Global Public Health’s publication criteria? Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe methodologically and ethically rigorous research with conclusions that are appropriately drawn based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available (please refer to the Data Availability Statement at the start of the manuscript PDF file)?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception. The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS Global Public Health does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: (No Response)

Reviewer #2: Queries have been addressed adequately!

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

Do you want your identity to be public for this peer review? If you choose “no”, your identity will remain anonymous but your review may still be made public.

For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: Yes: Nikith Austin DSouza

**********

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

Attachment

Submitted filename: PLOS_rev_8Oct24.pdf

pgph.0004072.s005.pdf (18.3KB, pdf)
PLOS Glob Public Health. doi: 10.1371/journal.pgph.0004072.r006

Decision Letter 2

Rashmi Josephine Rodrigues

28 Nov 2024

Improving HIV Testing and Retention among Adolescents and Youth: Lessons from the quasi-experimental study of the Red-Carpet Program in Malawi

PGPH-D-24-00709R2

Dear Dr Chamanga,

We are pleased to inform you that your manuscript 'Improving HIV Testing and Retention among Adolescents and Youth: Lessons from the quasi-experimental study of the Red-Carpet Program in Malawi' has been provisionally accepted for publication in PLOS Global Public Health.

Before your manuscript can be formally accepted you will need to complete some formatting changes, which you will receive in a follow up email. A member of our team will be in touch with a set of requests.

Please note that your manuscript will not be scheduled for publication until you have made the required changes, so a swift response is appreciated.

IMPORTANT: The editorial review process is now complete. PLOS will only permit corrections to spelling, formatting or significant scientific errors from this point onwards. Requests for major changes, or any which affect the scientific understanding of your work, will cause delays to the publication date of your manuscript.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they'll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact globalpubhealth@plos.org.

Thank you again for supporting Open Access publishing; we are looking forward to publishing your work in PLOS Global Public Health.

Best regards,

Rashmi Josephine Rodrigues, M.D., Ph.D.

Academic Editor

PLOS Global Public Health

***********************************************************

Reviewer Comments (if any, and for reference):

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

**********

2. Does this manuscript meet PLOS Global Public Health’s publication criteria? Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe methodologically and ethically rigorous research with conclusions that are appropriately drawn based on the data presented.

Reviewer #1: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available (please refer to the Data Availability Statement at the start of the manuscript PDF file)?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception. The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS Global Public Health does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Kind Madam/Sir,

I hope this message finds you well. I have thoroughly reviewed your article titled " Improving HIV Testing and Retention among Adolescents and Youth: Lessons from the quasi- experimental study of the Red-Carpet Program in Malawi" and wanted to share my feedback with you.

Strengths: The appropriate changes are made as suggested. Overall, your article presents a valuable contribution to HIV management. The thorough analysis and the innovative approach to methodology are commendable. Your insights have the potential to significantly influence future research in this area.

Thank you once again for the opportunity to review your work. All the best on your future endeavors.

Best regards

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Reviewer #1: Yes: Claudia Merlin

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Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Data. Study data set.

    (XLSX)

    pgph.0004072.s001.xlsx (524.2KB, xlsx)
    Attachment

    Submitted filename: Manuscript Coverletter Apr 2024.doc

    pgph.0004072.s002.doc (35.5KB, doc)
    Attachment

    Submitted filename: PLOS_ review.docx

    pgph.0004072.s003.docx (12.5KB, docx)
    Attachment

    Submitted filename: Rebuttal letter_26_July_24.docx

    pgph.0004072.s004.docx (61.9KB, docx)
    Attachment

    Submitted filename: PLOS_rev_8Oct24.pdf

    pgph.0004072.s005.pdf (18.3KB, pdf)
    Attachment

    Submitted filename: Rebuttal letter_6_Nov_24.pdf

    pgph.0004072.s006.pdf (56.5KB, pdf)

    Data Availability Statement

    All data are in the manuscript and/or supporting information files.


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