Skip to main content
Journal of the International AIDS Society logoLink to Journal of the International AIDS Society
. 2020 Jun 30;23(Suppl 3):e25522. doi: 10.1002/jia2.25522

Cost‐effectiveness of couples’ voluntary HIV counselling and testing in six African countries: a modelling study guided by an HIV prevention cascade framework

Kristin M Wall 1,2,, Mubiana Inambao 1,3, William Kilembe 1, Etienne Karita 1, Elwyn Chomba 4, Bellington Vwalika 1,5, Joseph Mulenga 1, Rachel Parker 1, Tyronza Sharkey 1, Amanda Tichacek 1, Eric Hunter 1,6,7, Robert Yohnka 1, Gordon Streeb 8, Phaedra S Corso 9, Susan Allen 1
PMCID: PMC7325504  PMID: 32602618

Abstract

Introduction

Couples’ voluntary HIV counselling and testing (CVCT) is a high‐impact HIV prevention intervention in Rwanda and Zambia. Our objective was to model the cost‐per‐HIV infection averted by CVCT in six African countries guided by an HIV prevention cascade framework. The HIV prevention cascade as yet to be applied to evaluating CVCT effectiveness or cost‐effectiveness.

Methods

We defined a priority population for CVCT in Africa as heterosexual adults in stable couples. Based on our previous experience nationalizing CVCT in Rwanda and scaling‐up CVCT in 73 clinics in Zambia, we estimated HIV prevention cascade domains of motivation for use, access and effectiveness of CVCT as model parameters. Costs‐per‐couple tested were also estimated based on our previous studies. We used these parameters as well as country‐specific inputs to model the impact of CVCT over a five‐year time horizon in a previously developed and tested deterministic compartmental model. We consider six countries across Africa with varied HIV epidemics (South Africa, Zimbabwe, Kenya, Tanzania, Ivory Coast and Sierra Leone). Outcomes of interest were the proportion of HIV infections averted by CVCT, nationwide CVCT implementation costs and costs‐per‐HIV infection averted by CVCT. We applied 3%/year discounting to costs and outcomes. Univariate and Monte Carlo multivariate sensitivity analyses were conducted.

Results

We estimated that CVCT could avert between 54% (Sierra Leone) and 62% (South Africa) of adult HIV infections. Average costs‐per‐HIV infection averted were lowest in Zimbabwe ($550) and highest in South Africa ($1272). Nationwide implementations would cost between 7% (Kenya) and 21% (Ivory Coast) of a country’s President’s Emergency Plan for AIDS Relief (PEPFAR) budget over five years. In sensitivity analyses, model outputs were most sensitive to estimates of cost‐per‐couple tested; the proportion of adults in heterosexual couples and HIV prevention cascade domains of CVCT motivation and access.

Conclusions

Our model indicates that nationalized CVCT could prevent over half of adult HIV infections for 7% to 21% of the modelled countries’ five‐year PEPFAR budgets. While other studies have indicated that CVCT motivation is high given locally relevant promotional and educational efforts, without required indicators, targets and dedicated budgets, access remains low.

Keywords: Africa, cost‐effectiveness, costs and cost analysis, couples, HIV, HIV prevention cascade, prevention and control

1. INTRODUCTION

Incident HIV infections in sub‐Saharan Africa have fallen 13% over recent years due to global prevention efforts [1]. However, this decline in new infections is slowing, gaps in the scale‐up of treatment and prevention services persist, and flatlined funds are not projected to meet 2030 Sustainable Development Goals [1, 2]. Now more than ever, maximizing the value of limited funding is critical, and evaluating the cost‐effectiveness of HIV prevention and treatment strategies is essential for improved resource allocation [1, 3]. The HIV prevention cascade, which evaluates domains of intervention motivation for use, access and effectiveness among a priority population, provides a useful framework to evaluate and advocate for prevention interventions [4] and has been used to evaluate interventions such as pre‐exposure prophylaxis (PrEP), voluntary medical male circumcision (VMMC) and prevention of mother‐to‐child transmission (PMTCT) [5, 6, 7, 8].

The HIV prevention cascade has yet to be described or evaluated for couples’ voluntary HIV counselling and testing (CVCT), an evidence‐based intervention in which couples receive joint pre‐test counselling, testing and post‐test counselling with counsellor‐facilitated serostatus disclosure [9, 10]. CVCT decreases sexual and perinatal HIV incidence [11, 12, 13, 14, 15, 16] by educating and placing joint responsibility on the dyad to increase uptake of condoms, VMMC, family planning, antiretroviral therapy (ART) and PMTCT [13, 14, 15, 17]. The priority population for CVCT is stable couples. With the exception of South Africa, most African adults are in cohabiting sexual unions [18], and the majority of HIV transmissions in sub‐Saharan Africa occur in heterosexual HIV discordant or concordant HIV‐negative couples [19]. Despite World Health Organization (WHO) [9] and the US Centers for Disease Control and Prevention (CDC) [10] CVCT recommendations, only a small percentage of African adults have been tested with partners.

Building on our technical support for the nationalization of CVCT in antenatal clinics (ANC) in Rwanda, where >80% of couples are now tested [20], we recently reported the cost‐effectiveness of a CVCT demonstration project serving 207,428 Zambian couples in 73 government clinics [21]. Receiving CVCT was associated with a 79% reduction in seroincidence among discordant couples using ART, 63% among discordant couples not using ART and 47% among concordant‐negative couples. The cost‐per‐HIV infection averted (CHIA) for CVCT was $659. We then built and validated a deterministic compartmental model which incorporated key domains from the HIV prevention cascade framework and reported the CHIA for nationalizing CVCT in Zambia ($394 CHIA) [21].

In the present analysis, we adapt this model to estimate the proportion of adult HIV infections averted, total costs and CHIA for nationalizing CVCT in six countries across sub‐Saharan Africa.

2. METHODS

2.1. Ethics approval

This retrospective costing and modelling study used de‐identified data from the publicly available sources cited. The Institutional Research Board at Emory University waived informed consent requirements.

2.2. Deterministic compartmental model

Our CVCT CHIA model details are published [21]. In summary, a deterministic compartmental model with one‐year time steps based on a series of differential equations was developed in Excel which allows heterosexual adult couples who are either concordant HIV‐negative or discordant, and on ART or off ART, to transition between states of HIV status and/or ART use over time. Our previous model structure [21] has been adapted here to incorporate HIV prevention cascade domains of motivation and access, which the previous model did not include.

Our model uses HIV seroincidence rates in uncounselled (“pre‐CVCT”) serodiscordant and concordant‐negative couples (which is assumed to be a function of all current prevention programmes taking place in country) and applies the estimated effectiveness of CVCT among couples depending on their joint HIV serostatus and ART use. These effectiveness estimates are applied each year, and couples move from concordant negative to discordant and from discordant to concordant positive accordingly. Estimated “pre‐CVCT” ART use and ART initiation in the year following CVCT are also model parameters, with an additional proportion of HIV‐positive individuals taking up ART each year. Estimated costs‐per‐couple tested are based on our programmatic experience. The model outputs HIV infections averted by CVCT (by subtracting the cumulative infections that are projected to occur post‐CVCT from those occurring pre‐CVCT), total incremental financial costs to implement CVCT and incremental CHIA by CVCT [21]. As evidence suggests that the HIV prevention impact of CVCT is sustainable for at least five years [22, 23, 24, 25], we chose a five‐year time horizon.

In the model, we conceptualize the expansion of CVCT in four phases: initiation, expansion, maturation and maintenance which are described in more detail below. These phases are defined by a changing set of estimated values for the HIV prevention cascade domains of motivation and access among the priority population for CVCT (Figure 1) and cost‐per‐couple tested.

Figure 1.

Figure 1

Generic HIV prevention cascade for CVCT. CVCT, couples’ voluntary HIV counselling and testing.

Using this model, we previously estimated the cost‐effectiveness of nationalizing CVCT in Zambia by applying the actual financial expenditures and CVCT effectiveness observed when scaling‐up services in 73 government clinics in Lusaka, Copperbelt and Southern Provinces which reached 207,428 couples. We conducted sensitivity analyses to evaluate the effect of possible differential loss to follow‐up, informative censoring using inverse probability of censoring weighting [26, 27], and inverse probability of treatment weighting to evaluate the possibility of confounding when using observational data to estimate intervention effects. We found that our model was robust in these sensitivity analyses [21]. Additionally, to internally validate the model, we used logical testing by varying transition probabilities and setting costs and outcomes to 0 separately, which resulted in logical expected values.

2.3. Base‐case model parameters applied to all countries

Base‐case estimates for CVCT HIV prevention impact were derived from our CVCT implementation in 73 Zambian government clinics [21] (Table 1). Briefly, from September 2010 to March 2016, CVCT services were implemented including joint pre‐test counselling; rapid HIV testing; joint post‐test counselling; provision of condoms and referrals as needed for ART, VMMC and family planning. History of prior HIV testing and self‐reported ART use were documented. HIV antibody‐negative individuals had repeat tests one month after CVCT. Discordant couples returned for quarterly retesting and counselling, and concordant HIV‐negative couples returned for annual retesting and counselling [28]. Promotions utilized influential community health workers and mass media [28, 29].

Table 1.

Base‐case model parameters applied to all countries

  Value and source
CVCT effective use (HIV prevention impact)
Among concordant HIV‐negative couples 47% [21]
Among discordant couples not on ART 63% [21]
Among discordant couples on ART 79% [21]
ART use
Immediate increase in uptake after CVCT 38% [21]
Additional uptake per year 5% [21]
CVCT motivation among the priority population
Initiation phase 20% of couples [20, 21]
Expansion phase 38% of couples [20, 21]
Maturation phase 66% of couples [20, 21]
Maintenance phase 15% of couples [20, 21]
CVCT access among those motivated
Initiation phase 50% of motivated couples [20, 21]
Expansion Phase 56% of motivated couples [20, 21]
Maturation phase 60% of motivated couples [20, 21]
Maintenance phase 70% of motivated couples [20, 21]

ART, antiretroviral treatment; CVCT, couples’ voluntary HIV counselling and testing; USD, United States Dollar.

During the implementation, the impact of CVCT was assessed over longitudinal follow‐up. HIV seroincidence rates for discordant and concordant HIV‐negative couples were calculated as incident infections divided by HIV‐negative person‐years (PY) of follow‐up, stratified by whether couples had (“post‐CVCT”) or had not (“pre‐CVCT”) received CVCT. As shown in Table 1, in concordant‐negative couples, we observed a 47% reduction in HIV seroincidence pre‐CVCT (1.1/100PY) versus post‐CVCT (0.6/100PY). In serodiscordant couples in which the HIV+ partner was not on ART, we observed a 63% reduction in incidence (13.0/100PY pre‐CVCT versus 4.8/100PY post‐CVCT). Finally, in serodiscordant couples in which the HIV+ partner was on ART, we observed a 79% reduction in incidence (8.5/100PY pre‐CVCT versus 1.8/100PY post‐CVCT) [21]. We also use the increase in ART uptake reported in the previously published manuscript (38% of non‐users initiated ART after CVCT with 5%/year additional uptake thereafter) [21]. Self‐reported ART initiation is not assumed to imply adherence/suppressive ART.

Base‐case estimates for cost‐per‐couple tested, motivation for CVCT, and access to CVCT were derived from both the Zambian implementation study described and our years of experience supporting nationalization of CVCT in Rwanda [20, 21]. We derived incremental financial costs from the donor’s perspective from a primary costing study of actual expenditures to implement CVCT in government clinics following Global Heath Cost Consortium guidance [30]. Cost data were reported by activity were recorded by study staff during programme implementation and entered in AccPac (Sage Group). Based on our experiences in Rwanda and Zambia [20, 21], motivation for CVCT, and access to CVCT varied over time and are used to define implementation phases as shown in Table 1: initiation phase (advocacy, training and promotions to motivate 20% of couples, 50% of whom have CVCT access); expansion phase (continued advocacy and training, increased community and politico‐administrative involvement, CVCT certification for a majority of providers and active promotions to motivate 38% of couples, 56% of whom have CVCT access); maturation phase (an established programme with CVCT integrated into existing services including ANC, individual HIV counselling and testing, ART, VMMC and family planning services and 66% of couples are motivated, 60% of whom have CVCT access); and finally the maintenance phase (for hard‐to‐reach residual and new couples where only 15% are motivated, of whom 70% have CVCT access). Thus, 80% of couples are assumed to be reached with testing, as seen in Rwandan ANC [20].

2.4. Country‐specific parameters

South Africa, Zimbabwe, Kenya, Tanzania, Ivory Coast and Sierra Leone have diverse HIV epidemics and published data available for the model inputs (Table 2). Country‐specific model parameters include: (1) proportion of adults in cohabiting heterosexual couples, (2) couple HIV serostatus distribution, (3) ART use, (4) HIV seroincidence in uncounselled (pre‐ CVCT) concordant‐negative couples, (5) HIV seroincidence in uncounselled discordant couples not on ART, (6) HIV seroincidence in uncounselled discordant couples on ART and (7) estimated cost‐per‐couple tested. Published estimates of HIV seroincidence in uncounselled concordant‐negative couples [31, 32, 33, 34] and uncounselled discordant non‐ART using couples [31, 32, 33, 34, 35] are limited to Eastern Africa. Given limited data for Southern African countries, model inputs 4, 5 and 6 (Table 2) were estimated from Zambia data [21]. As no published data are available for HIV seroincidence in uncounselled ART‐using discordant couples in Eastern and Western Africa, we used 5/100PY reflecting the broadly lower incidence in Eastern/Western versus Southern Africa [36]. Finally, since the primary cost driver for CVCT is salaries for counselling, testing and promotions [20, 21], we derived a conversion factor using country‐specific nurse salaries (USD 2015) applied to cost‐per‐couple tested estimates calculated from our Zambian implementation ($75 initiation phase, $50 expansion phase, $25 maturation phase, $30 maintenance phase [21]) to generate cost‐per‐couple tested estimates for each country.

Table 2.

Country‐specific base‐case model parameters

Model input Southern Africa Eastern Africa Western Africa
South Africa Zimbabwe Kenya Tanzania Ivory Coast Sierra Leone
Value   Value   Value   Value   Value   Value  
1
Adult population (ages 15 to 64) 37,904,001 [37] 7 892 000 [37] 2 974 500 [37] 3 001 700 [37] 1 383 900 [37] 428 200 [37]
Adult population in stable couples (%) 35% [18] 58% [18] 57% [18] 57% [18] 59% [18] 62% [18]
2
Discordant couples among all stable couples (%) 16% [18] 9% [18] 6% [18] 5% [18] 5% [18] 3% [18]
Concordant‐negative couples among all stable couples (%) 70% [18] 80% [18] 91% [18] 91% [18] 93% [18] 97% [18]
3
Adults on ART of all estimated positive adults (%) 62% [38] 89% [38] 69% [38] 72% [38] 55% [38] 43% [38]
4
Uncounselled seroincidence among concordant‐negative couples (per 100 PY) 1/100 PY [21] 1/100 PY [21] 0.5/100 PY [31, 32, 33, 34] 0.5/100 PY [31, 32, 33, 34] 0.5/100 PY a 0.5/100 PY a
5
Uncounselled seroincidence among non‐ART using discordant couples (per 100 PY) 13/100 PY [21] 13/100 PY [21] 10/100 PY [31, 32, 33, 34, 35, 39] 10/100 PY [31, 32, 33, 34, 35, 39] 10/100 PY a 10/100 PY a
6
Uncounselled seroincidence among ART using discordant couples (per 100 PY) 8/100 PY [21] 8/100 PY [21] 5/100 PY a 5/100 PY a 5/100 PY a 5/100 PY a
7
Cost‐per‐couple tested (2015 USD)   [21, 40]   [21, 40]   [21, 40]   [21, 40]   [21, 40]   [21, 40]
Initiation phase $229   $84   $59   $73   $103   $71  
Expansion phase $153   $56   $39   $49   $69   $47  
Maturation phase $76   $28   $20   $24   $34   $24  
Maintenance phase $92   $34   $24   $29   $41   $28  

“Uncounselled” indicates pre‐couples’ voluntary HIV counselling and testing. Demographic Health Survey defines stable couples as partners consensually living together in a union within a household. Most recent Demographic Health Survey data used. ART, antiretroviral treatment; PY, person year.

a

Estimated based on lower HIV incidence in Eastern and Western Africa versus Southern Africa [36].

2.5. Base‐case analyses

The estimated proportion of adult HIV infections averted, total CVCT implementation costs, CHIA and proportion of President’s Emergency Plan for AIDS Relief (PEPFAR) budgets required for nationwide implementation in each selected country are outcomes of interest. These are presented alongside per capita gross domestic products (GDPs) for context. All outcomes and costs were discounted at 3%/year as recommended by the US Public Health Service Task Force [41]. We adhered to Consolidated Health Economic Evaluation Reporting Standards [42] for cost‐effectiveness analyses.

2.6. One‐way and probabilistic sensitivity analyses

We conducted one‐way sensitivity analyses for all model inputs by varying each parameter ±20%. Inputs which most influenced model outputs are reported. Because key model parameters of cost‐per‐couple tested and CVCT effectiveness were derived from just two countries, we also conducted probabilistic Monte Carlo simulation multivariate sensitivity analyses for each parameter of interest (±50% of base‐case estimates using a uniform distribution) with 1000 draws in Excel. Average outcomes and standard deviations from simulated results are reported. A uniform distribution was chosen to fix a functional form on the parameter estimates and to reflect a large degree of uncertainty around the selected parameters.

3. RESULTS

The total cost for nationwide CVCT implementation and cumulative infections averted are also shown in Table 3. Estimated average CHIA ranged from $1272 in South Africa to $550 in Zimbabwe. Our model estimated that CVCT could prevent between 54% and 62% of HIV infections. The proportion of the 2018 PEPFAR budget required for CVCT nationalization over five years ranged from 7% in Kenya to 21% in Ivory Coast. For context, per capita GDP for each country is shown.

Table 3.

Proportion of adult infections averted, overall CHIA and total cost for CVCT in six African countries (primary base‐case analyses)

Southern Africa Total cost of CVCT Cumulative HIV infections averted Average CHIA a Proportion of infections averted, % 2018 PEPFAR Budget [43] Cost of CVCT as % of PEPFAR budget for five years, % Per capita GDP
South Africa $532,704,861 418,855 $1272 62 $575,258,390 19 $13,054
Zimbabwe $67,053,208 121,984 $550 58 $145,546,200 9 $2,224
East‐Central Africa
Kenya $176,419,535 231,312 $763 57 $505,480,000 7 $3,384
Tanzania $219,582,392 219,486 $1000 56 $512,422,250 9 $3,094
Western Africa
Ivory Coast $145,955,594 119,508 $1221 57 $140,508,601 21 $3,771
Sierra Leone $33,113,126 34,803 $951 54 Unknown $1,547

No PEPFAR budget reported for Sierra Leone. Per capita GDP (2017 estimates in 2015 USD): https://www.cia.gov/library/publications/the‐world‐factbook/rankorder/2004rank.html. CHIA, cost per HIV infection averted; CVCT, Couples' HIV voluntary counselling and testing; PEPFAR: President's Emergency Plan for AIDS Relief.

a

Weighted average across all implementation phases.

Figure 2 presents country‐specific CHIA estimates by implementation phase. During the initiation phase, the CHIA ranged from $2503 in South Africa to $1080 in Zimbabwe. During the expansion phase, the CHIA ranged from $720 to $1672. During the maturation phase, the CHIA ranged from $360 to $831. Finally, during the maintenance phase, the CHIA ranged from $437 to $1005.

Figure 2.

Figure 2

Modelled cost‐per‐HIV infection averted by phase of CVCT implementation in six sub‐Saharan African countries. CVCT, couples' HIV voluntary counselling and testing.

3.1. Sensitivity analyses

One‐way sensitivity (Table 4 presents representative findings from South Africa) analyses indicated our model was relatively robust to parameter assumptions, with resulting CHIA still relatively low compared to other HIV prevention interventions (discussed below). Our model was most sensitive to the costs‐per‐couple tested (varying input parameters by ±20% resulted in total CVCT costs which were ±20% different from base‐case). Our model was also sensitive to varying the proportion of adults in heterosexual couples (a higher proportion of adults in heterosexual couples lead to a proportional increase in HIV infections averted and total CVCT costs). Similarly, our model was sensitive to the proportion of couples motivated for and with access to CVCT (with increasing motivation and access was associated with proportional changes in increased infections averted and costs).

Table 4.

Parameters and results of one‐way sensitivity analyses: Illustrative example of South Africa

Sensitivity analysis parameters Infections averted % change a Total cost of CVCT % change a CHIA % change a
Discount rate
2% 3% 5% 2%
4% −3% −5% −2%
Cost/couple tested (by implementation phase)
$183; $122; $61; $74 0% −20% −20%
$274; $184; $91; $110 0% 20% 20%
Proportion adults in heterosexual couples
28% −20% −20% 0%
42% 20% 20% 0%
Proportion couples motivated for CVCT (by implementation phase)
40%; 40%; 53%; 12% −20% −20% 0%
60%; 60%; 79%; 18% 20% 20% 0%
Proportion couples with access to CVCT (by implementation phase)
16%; 32%; 48%; 56% −20% −20% 0%
24%; 48%; 72%; 84% 20% 20% 0%
Proportion concordant negative
56% −9% 0% 10%
84% 10% 0% −9%
Proportion discordant
13% −9% 0% 10%
19% 11% 0% −10%
HIV seroincidence rates before CVCT (per 100 PY)
Among concordant HIV‐negative couples
0.80 −9% 0% 10%
1.20 9% 0% −8%
Among ART using HIV discordant couples
6.40 −6% 0% 6%
9.60 6% 0% −6%
Among non‐ ART using HIV discordant couples
10.40 −4% 0% 4%
15.60 4% 0% −4%
CVCT prevention impact
Among concordant HIV‐negative couples
38% −7% 0% 8%
56% 7% 0% −7%
Among ART using HIV discordant couples
63% −10% 0% 11%
95% 11% 0% −10%
Among non‐ART using HIV discordant couples
50% −2% 0% 2%
76% 2% 0% −2%
ART use
Among HIV‐positive adults before CVCT
50% 2% 0% −2%
74% −3% 0% 3%
Among HIV‐positive adults after CVCT
61% −1% 0% 1%
92% 1% 0% −1%
Proportion initiating ART each year after CVCT
4% 0% 0% 0%
6% 0% 0% 0%

ART, antiretroviral treatment; CHIA, cost‐per‐HIV infection averted; CVCT, couples’ voluntary HIV counselling and testing; PY, person‐years.

a

% Change relative to base‐case primary analyses.

Additionally, our model was relatively sensitive (with results varying roughly ±10% relative to base‐case) to the proportion of concordant negative and discordant couples in the population (with higher proportions of at‐risk couples leading to increased infections averted and therefore lower CHIAs).

A higher pre‐CVCT seroincidence rate in concordant‐negative couples and higher CVCT effectiveness in concordant‐negative couples both increased HIV infections averted. Finally, increasing CVCT effectiveness in ART using discordant couples by ±20% varied total infections averted by roughly ±10% (with higher prevention impact leading to increased infections averted and improved cost‐effectiveness).

Examining the country‐specific parameters specifically, differences in model outcomes across countries are influenced by differences in seroincidence rates pre‐CVCT (with higher uncounselled seroincidence rates being associated with higher numbers of infections averted and improved cost‐effectiveness) and the proportion of couples who were discordant (with higher discordancy associated with higher numbers of infections averted and improved cost‐effectiveness).

Probabilistic multivariate sensitivity analyses (Table 5) also highlighted that total CVCT costs were sensitive to cost‐per‐couple tested, with coefficients of variation of 15% to 16%. Our model was less susceptible to variation in CVCT impact, with coefficients of variation of 10% to 12%.

Table 5.

Probabilistic sensitivity analysis results

Varying costs‐per‐couple tested by ±50% (uniform distribution) of the base‐case estimates a
Southern Africa Total cost of CVCT SD CV Average CHIA SD CV
South Africa 527,493,591 80,271,276 15% $1280 $198 15%
Zimbabwe 67,478,299 9,792,498 15% $466 $73 16%
East‐Central Africa
Kenya 175,560,051 28,074,065 16% $765 $116 15%
Tanzania 219,184,615 33,759,017 15% $997 $158 16%
Western Africa
Ivory Coast 145,820,457 22,312,561 15% $1217 $191 16%
Sierra Leone 33,384,147 4,850,786 15% $953 $145 15%
Varying CVCT impacts by ±50% (uniform distribution) of the base‐case estimates b
Southern Africa Cumulative HIV infections averted SD CV Average CHIA SD CV
South Africa 420,653 45,818 11% $1304 $146 11%
Zimbabwe 116,862 14,257 12% $570 $68 12%
East‐Central Africa
Kenya 232,821 25,860 11% $788 $86 11%
Tanzania 220,013 25,895 12% $1043 $120 12%
Western Africa
Ivory Coast 118,752 12,769 11% $1269 $131 10%
Sierra Leone 34,876 4091 12% $998 $120 12%

CHIA, cost per HIV infection averted; CV, coefficient of variation is the standard deviation divided by the mean estimate; CVCT, couples voluntary HIV counselling and testing; SD, standard deviation.

a

No impact on cumulative HIV infections averted;

b

no impact on total cost of CVCT.

4. DISCUSSION

Our model estimated that CVCT could prevent over half of adult HIV infections for 7% to 21% of selected countries’ five‐year PEPFAR budgets. Applying an HIV prevention cascade framework [5] is helpful to evaluate CVCT. In the countries under study, the priority population for CVCT, stable couples, comprises 35% to 62% of the adult population. Key barriers and solutions related to this priority population’s motivation to use CVCT, CVCT access and effective use are summarized in Table 6 and discussed in detail below.

Table 6.

CVCT HIV prevention cascade domains with key barriers and solutions

Motivation Access Effective use
Reasons for gap
Lack of knowledge and low risk perception Lack of availability or easy access in government facilities

Inconsistent condom use, continued outside partner risk

Lack of ART uptake

Lack of men's ability to attend regular clinic hours, opportunity costs Lack of trained government providers
Concerns about CVCT consequences Perceived cost/affordability Non‐linkage to ART programmes
Evidence‐based ways to close the gap
Interventions

Incentives/transport reimbursement

Partner tracing, male‐focused sessions, 'expert couple' and influential community leader promotions

Informational messaging highlighting partner safety, U = U, and addressing common concerns

Convenient service delivery hours and platforms

Provider training and reimbursement (possibly during off‐hours)

Ongoing condom and behavioural counselling, targeted safe conception and alcohol counselling

Integration with ART (for treatment and prevention) programmes

Platforms to deliver interventions
Clinics, community health workers, influential peers and mass media Clinic‐based services, mobile testing, home‐based testing, self‐testing Clinic‐based services, mobile testing, home‐based testing, self‐testing
Policies to support interventions
Budgets for training messaging, demand creation and incentives Budgets, required reporting indicators and targets for CVCT Budgets for integrated services, ongoing M&E
Training and reimbursement of providers  

ART, antiretroviral treatment; CVCT, couples voluntary HIV counselling and testing; M&E, monitoring and evaluation.

4.1. Motivation

Sensitivity analyses indicated countries with a higher proportion of heterosexual couples motivated to uptake CVCT prevented more infections. Motivation for CVCT has been high across studies in diverse populations including heterosexual couples in Mozambique [44, 45], Tanzania [46, 47], South Africa [48, 49], Uganda [50], Thailand [51], Iran [52] and men who have sex with men (MSM) in South Africa [53] and the US [54, 55]. Although promising, these are relatively small‐scale efforts: knowledge of CVCT remains low in many settings and education and demand creation are essential to increase broad motivation [28, 29, 56]. Key barriers to motivation include lack of community knowledge of HIV serodiscordance and HIV risk. For example we found that only 30% of couples seeking CVCT in Durban knew about serodiscordance [49]. Other barriers to motivation include opportunity costs, men’s inability to attend regular clinic hours, limited knowledge that CVCT services exist, and concerns about consequences like relationship dissolution [28, 29, 56, 57].

Reports highlight successful strategies to overcome these barriers and increase motivation including use transport reimbursement [57]; nonmonetary incentives in Zambia [58] and rural Zimbabwe [59]; invitations plus facilitated contact tracing to support partner attendance in Malawi [60]; male‐focused interactive sessions with testimonies from ‘expert couples’ who received CVCT in rural Uganda [50]; and CVCT invitations and promotions delivered by influential community leaders and via mass media in Zambia and Rwanda [28, 29, 56]. Additionally, the desire to keep one’s partners safe from transmission is a motivating factor for ART and PrEP use [61, 62], and “undetectable = untransmittable” messaging may reduce stigma and motivate couples to uptake CVCT and ART to achieve viral suppression [63]. Finally, messaging should emphasize that outcomes of intimate partner violence (IPV), relationship dissolution or emotional distress are rare and CVCT typically strengthens relationships [16, 17, 54, 60, 64, 65]. To broadly increase CVCT motivation, budgets for training, demand creation and incentives (all included in our modelled CVCT costs) will be required.

4.2. Access

Sensitivity analyses indicated that countries with a higher proportion of heterosexual couples with CVCT access will prevent more infections at a higher cost. The PEPFAR 2020 Country Operation Plan [43] highlights family HIV testing and emphasizes that HIV prevention among pregnant, postpartum and breastfeeding women should include “couples‐based services to promote scaled‐up testing and treatment of male partners.” However, as CVCT is not broadly offered as standard of care in the selected countries, nor it is a required indicator for reporting [66], access remains low across Africa. As with most interventions, a main barrier to access is the cost of wide‐spread implementation. As expected, higher costs‐per‐couple tested increase total CVCT costs. Economies of scale are incorporated into estimated cost‐per‐couple tested (over time, costs to test couples decrease, with the exception of the final “hard‐to‐reach” couples).

Our experience in Zambia reflected the initiation and expansion phases [21]. Government clinic staff were paid during their off‐duty hours. Unfortunately, the amount of funding available was insufficient to maintain momentum. In contrast, Rwanda succeeded in increasing access and nationalizing CVCT in ANC between 2008 and 2013 (after which CVCT become a social norm and demand creation was no longer needed) [20]. Based on the estimated impact of CVCT in Rwanda from observational epidemiological studies [11, 23, 24], the Rwandan government health insurance and performance‐based financing plans now reimburse the costs of CVCT, and additional funding for off‐duty staff is no longer required. Reaching Rwanda’s success will require investment. As many demonstration projects correspond to the more expensive initiation phase, implementers may fail to see that continuous investment is necessary to achieve social diffusion, incorporate CVCT into daily clinical practice and adapt data recording and reporting tools to achieve sustained access [57].

In addition to clinic‐based CVCT, mobile testing in Rwanda [29]; home‐based couples’ testing in Tanzania [67], Kenya [68] and Malawi [69]; and self‐testing to increase CVCT in Kenya [70] have been studied. An improved understanding of differences in CVCT access and costs (as well as motivation) for different modalities is warranted.

4.3. Effective use

CVCT decreases sexual and perinatal HIV incidence [11, 12, 13, 14, 15, 16] by educating and placing joint responsibility on the dyad to increase uptake of condoms, VMMC, family planning, ART and PMTCT [13, 14, 15, 17]. CVCT effectiveness must be monitored to understand facilitators and barriers to achieving reductions in HIV incidence. Our previous analyses found factors associated with inconsistent condom use, non‐ART initiation or continued outside partner risk in discordant couples post‐CVCT included alcohol use and fertility intentions [71]. To improve effective use of CVCT for all couples, targeted safe conception or alcohol counselling may be warranted. Importantly, as seen in sensitivity analyses, a higher prevention impact in concordant‐negative couples increased CVCT cost‐effectiveness. It has been argued that CVCT may have a sizable impact on the epidemic through HIV prevention in concordant‐negative couples (via reduction in outside relationship risk) since they comprise the majority of the population [72, 73].

For the smaller though higher‐risk population of discordant couples, “Test‐and‐Treat” will continue to expand. Unfortunately, many country’s HIV incidence rates have not decreased as substantially as predicted in the test‐and‐treat era, and several large cluster‐randomized trials have failed to clearly demonstrate the population‐level prevention impact of universal test‐and‐treat policies [74]. Where CVCT increases ART uptake and adherence in serodiscordant couples, it may bolster the effectiveness of test‐and‐treat. Additionally, to achieve the PEPFAR 2020 priority of PrEP for discordant couples [43], CVCT can effectively identify discordant couple candidates. Although PrEP is not currently available in most countries outside of relatively small demonstration and research projects, CVCT counselling can be updated to include PrEP as it becomes available.

Finally, an improved understanding of the effectiveness of CVCT in home‐based settings, mobile‐testing and via self‐testing is needed with regular monitoring and evaluation of these delivery platforms. With self‐testing in particular, how well couples disclose, understand their respective results and adopt appropriate risk reduction without facilitated joint post‐test counselling merits further investigation [75, 76, 77, 78].

4.4. Comparative cost‐effectiveness

We found CVCT CHIA estimates to be similar to interventions largely considered cost‐effective including individual voluntary HIV counselling and testing (estimated in a previous systematic review of studies in sub‐Saharan Africa at $1315 [79] and $483 for an individual and couples testing intervention in Kenya [79, 80]) and family planning for PMTCT via prevention of unintended pregnancy ($663) [79]. A recent systematic review of 60 studies from African countries reported median CHIA estimates for VMMC ($2965), ART for PMTCT ($1144), treatment‐as‐prevention interventions ($7903) and PrEP ($13,267) [81].

4.5. Limitations

As in all models, we attempt to simplify a complex reality, and outputs are dependent on assumptions. Extensive sensitivity analyses quantify the impact of these assumptions. Our model seeks to isolate the impact of CVCT on HIV infections averted given constant pre‐CVCT and post‐CVCT HIV incidence. We do not attempt to predict the course of the epidemic in the selected countries over time by considering myriad other prevention or treatment interventions. More detailed models isolating the prevention impact of CVCT attributable to condom use, VMMC uptake, improved ART uptake and adherence, and/or reductions in concurrent relationships are warranted. While deterministic compartmental models are well‐suited to examine average characteristics in a population and are thus appropriate for our goal, they do not evaluate individual‐level effects as do agent‐based models. Finally, while some studies of HIV prevention interventions translate infections averted into disability‐adjusted life‐years averted or quality‐adjusted life‐years gained, a recent systematic review did not find standard conversions applicable across country settings [81]. While such cost‐utility estimates are often applied to determine if an intervention is cost‐effective [82], this threshold is often questioned by experts since it does not consider intervention affordability [83, 84]. While cost‐utility analyses are useful for comparing interventions with different natural units, given dedicated HIV prevention budgets and the common use of CHIA estimates in other studies [81], we feel that CHIA is a more useful comparative measure.

5. CONCLUSIONS

Our model indicated that nationalized CVCT could prevent over half of adult HIV infections for 7% to 21% of the modelled countries’ five‐year PEPFAR budgets. Unfortunately, WHO CVCT guidelines have yet to be broadly implemented. While studies indicate that CVCT motivation is high given locally relevant promotional and educational efforts, access remains low without dedicated budgets or required indicators.

COMPETING INTEREST

The authors have no conflicts of interest.

AUTHORS’ CONTRIBUTIONS

KMW contributed to the analysis and interpretation of data; drafted the article and revised it critically for important intellectual content; and gave final approval of the version to be published. MI contributed to the conception and design of the study, revised the article critically for important intellectual content and gave final approval of the version to be published. WK contributed to the conception and design of the study, revised the article critically for important intellectual content and gave final approval of the version to be published. EK contributed to the conception and design of the study, revised the article critically for important intellectual content and gave final approval of the version to be published. EC contributed to the conception and design of the study, revised the article critically for important intellectual content and gave final approval of the version to be published. BV contributed to the conception and design of the study, revised the article critically for important intellectual content and gave final approval of the version to be published. JM contributed to the conception and design of the study, revised the article critically for important intellectual content and gave final approval of the version to be published. RP contributed to the analysis and interpretation of data; revised the article critically for important intellectual content and gave final approval of the version to be published. TS contributed to the analysis and interpretation of data; revised the article critically for important intellectual content and gave final approval of the version to be published. AT contributed to the study conception and design, revised the article critically for important intellectual content and gave final approval of the version to be published. EH contributed to the analysis and interpretation of data; revised the article critically for important intellectual content and gave final approval of the version to be published. RY contributed to the analysis and interpretation of data; revised the article critically for important intellectual content and gave final approval of the version to be published. GS contributed to the analysis and interpretation of data; revised the article critically for important intellectual content and gave final approval of the version to be published. PC contributed to the analysis and interpretation of data; revised the article critically for important intellectual content and gave final approval of the version to be published. SA contributed to the study design and conception, contributed to the analysis and interpretation of data; revised the article critically for important intellectual content and gave final approval of the version to be published.

Acknowledgements

Funding

This work was supported by Arise—Enhancing HIV Prevention Programs for At‐Risk Populations, through financial support provided by the Canadian Government through Foreign Affairs, Trade and Development Canada (DFATD, formerly CIDA, http://www.international.gc.ca/international/index.aspx?lang=eng) with technical support from PATH [CID.1450‐08863‐SUB to SA]. Arise implements innovative HIV prevention initiatives for vulnerable communities, with a focus on determining cost‐effectiveness through rigorous evaluations. This study was also supported by the United Kingdom Department for International Development (DFID, https://www.gov.uk/government/organisations/department‐for‐international‐development) [UK202340‐102 to SA]; the International AIDS Vaccine Initiative (https://www.iavi.org/;) with the generous support of the American people through the United States Agency for International Development (USAID, https://www.usaid.gov/;); National Institutes of Health (https://www.nih.gov/;) grants [R01 MH66767 to SA, R01 HD40125 to SA and R01 MH95503 to SA, K01 MH107320 to KMW, R01 AI051231 to SA]; the AIDS International Training and Research Program Fogarty International Center [D43 TW001042 to SA] and the Emory Center for AIDS Research [P30 AI050409]. The contents are the responsibility of the authors and do not necessarily reflect the views of sponsors, who had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript. The corresponding author had full access to all the data in the study and had final responsibility for the decision to submit for publication.

Wall, K. M. , Inambao, M. , Kilembe, W. , Karita, E. , Chomba, E. , Vwalika, B. , Mulenga, J. , Parker, R. , Sharkey, T. , Tichacek, A. , Hunter, E. , Yohnka, R. , Streeb, G. , Corso, P. S. and Allen, S. Cost‐effectiveness of couples’ voluntary HIV counselling and testing in six African countries: a modelling study guided by an HIV prevention cascade framework. J Int AIDS Soc. 2020; 23(S3):e25522

REFERENCES

  • 1. UNAIDS . Global AIDS Update 2019. 2019. [cited 2020 Feb 25]. Available from: https://www.unaids.org/en/resources/documents/2019/2019‐global‐AIDS‐update
  • 2. Global Burden of Disease Health Financing Collaborator Network . Spending on health and HIV/AIDS: domestic health spending and development assistance in 188 countries, 1995–2015. Lancet. 2018;391(10132):1799–829. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Granich R, Gupta S, Montaner J, Williams B, Zuniga JM. Pattern, determinants, and impact of HIV spending on care and treatment in 38 high‐burden low‐ and middle‐income countries. J Int Assoc Provid AIDS Care. 2016;15(2):91–100. [DOI] [PubMed] [Google Scholar]
  • 4. Schaefer R, Gregson S, Fearon E, Hensen B, Hallett TB, Hargreaves JR. HIV prevention cascades: a unifying framework to replicate the successes of treatment cascades. Lancet HIV. 2019;6(1):e60–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Moorhouse L, Schaefer R, Thomas R, Nyamukapa C, Skovdal M, Hallett TB, et al. Application of the HIV prevention cascade to identify, develop and evaluate interventions to improve use of prevention methods: examples from a study in east Zimbabwe. J Int AIDS Soc. 2019;22:e25309. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Hensen B, Fearon E, Schaap AB, Lewis JJ, Weiss HA, Tembo M, et al. Application of an HIV prevention cascade to identify gaps in increasing coverage of voluntary medical male circumcision services in 42 rural Zambian communities. AIDS Behav. 2019;23(5):1095–103. [DOI] [PubMed] [Google Scholar]
  • 7. Bhattacharjee P, Musyoki HK, Becker M, Musimbi J, Kaosa S, Kioko J, et al. HIV prevention programme cascades: insights from HIV programme monitoring for female sex workers in Kenya. J Int AIDS Soc. 2019;22:e25311. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Garnett GP, Krishnaratne S, Harris KL, Hallett TB, Santos M, Enstone JE, et al. Cost‐effectiveness of interventions to prevent HIV acquisition In: Holmes KK, Bertozzi S, Bloom BR, Jha P, editors. Major infectious diseases. 3rd edition. Washington (DC): The International Bank for Reconstruction and Development / The World Bank; 2017. Nov. [PubMed] [Google Scholar]
  • 9. WHO . Guidance on couples HIV testing and counselling including antiretroviral therapy for treatment and prevention in serodiscordant couples: recommendations for a public health approach. 2012. [cited 2020 March 5]. Available from: http://apps.who.int/iris/bitstream/10665/44646/1/9789241501972_eng.pdf [PubMed]
  • 10. CDC . Testing together. 2020. [cited 2020 March 5]. Available from: https://www.cdc.gov/hiv/effective‐interventions/diagnose/testing‐together/index.html
  • 11. Allen S. Confidential HIV testing and condom promotion in Africa. Impact on HIV and gonorrhea rates. JAMA. 1992;268(23):3338–43. [PubMed] [Google Scholar]
  • 12. Fideli US, Allen SA, Musonda R, Trask S, Hahn BH, Weiss H, et al. Virologic and immunologic determinants of heterosexual transmission of human immunodeficiency virus type 1 in Africa. AIDS Res Hum Retroviruses. 2001;17(10):901–10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Painter TM. Voluntary counseling and testing for couples: a high‐leverage intervention for HIV/AIDS prevention in sub‐Saharan Africa. Soc Sci Med. 2001;53(11):1397–411. [DOI] [PubMed] [Google Scholar]
  • 14. McKenna SL, Muyinda GK, Roth D, Mwali M, Ng'andu N, Myrick A, et al. Rapid HIV testing and counseling for voluntary testing centers in Africa. AIDS. 1997;11 Suppl 1:S103–10. [PubMed] [Google Scholar]
  • 15. Were WA, Mermin JH, Wamai N, Awor AC, Bechange S, Moss S, et al. Undiagnosed HIV infection and couple HIV discordance among household members of HIV‐infected people receiving antiretroviral therapy in Uganda. J Acquir Immune Defic Syndr. 2006;43(1):91–5. [DOI] [PubMed] [Google Scholar]
  • 16. Roth DL, Stewart KE, Clay OJ, van der Straten A, Karita E, Allen S. Sexual practices of HIV discordant and concordant couples in Rwanda: effects of a testing and counselling programme for men. Int J STD AIDS. 2001;12(3):181–8. [DOI] [PubMed] [Google Scholar]
  • 17. Becker S, Mlay R, Schwandt HM, Lyamuya E. Comparing couples’ and individual voluntary counseling and testing for HIV at antenatal clinics in Tanzania: a randomized trial. AIDS Behav. 2010;14(3):558–66. [DOI] [PubMed] [Google Scholar]
  • 18. Demographic and Health Surveys. 2020. [cited 2020 Feb 25]. Available from: http://www.measuredhs.com/;
  • 19. Chemaitelly H, Awad SF, Shelton JD, Abu‐Raddad LJ. Sources of HIV incidence among stable couples in sub‐Saharan Africa. J Int AIDS Soc. 2014;17:18765. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20. Karita E, Nsanzimana S, Ndagije F, Wall KM, Mukamuyango J, Mugwaneza P, et al. Implementation and operational research: evolution of couples' voluntary counseling and testing for HIV in Rwanda: from research to public health practice. J Acquir Immune Defic Syndr. 2016;73(3):e51–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Wall KM, Inambao M, Kilembe W, Karita E, Vwalika B, Mulenga J, et al. HIV testing and counselling couples together for affordable HIV prevention in Africa. Int J Epidemiol. 2019;48(1):217–27. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Dunkle KL, Greenberg L, Lanterman A, Stephenson R, Allen S. Source of new infections in generalised HIV epidemics – Authors' reply. Lancet. 2008;372(9646):1300–1. [DOI] [PubMed] [Google Scholar]
  • 23. Allen S, Meinzen‐Derr J, Kautzman M, Zulu I, Trask S, Fideli U, et al. Sexual behavior of HIV discordant couples after HIV counseling and testing. AIDS. 2003;17(5):733–40. [DOI] [PubMed] [Google Scholar]
  • 24. Allen S, Tice J, Van de Perre P, Serufilira A, Hudes E, Nsengumuremyi F, et al. Effect of serotesting with counselling on condom use and seroconversion among HIV discordant couples in Africa. BMJ. 1992;304(6842):1605–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Wall KM, Kilembe W, Vwalika B, Haddad LB, Lakhi S, Onwubiko U, et al. Sustained effect of couples' HIV counselling and testing on risk reduction among Zambian HIV serodiscordant couples. Sex Transmit Infect. 2017;93(4):259–66. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. Jiménez‐Moro JL, Gómez J.Inverse probability of censoring weighting for selective crossover in oncology clinical trials. Paper SP02 2014 [cited 2018 April 26]. Available from: https://www.lexjansen.com/phuse/2014/sp/SP02.pdf
  • 27. Howe CJ, Cole SR, Lau B, Napravnik S, Eron JJ. Selection bias due to loss to follow up in cohort studies. Epidemiology. 2016;27(1):91–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28. Wall KM, Kilembe W, Nizam A, Vwalika C, Kautzman M, Chomba E, et al. Promotion of couples' voluntary HIV counselling and testing in Lusaka, Zambia by influence network leaders and agents. BMJ Open. 2012;2:e001171. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Wall K, Karita E, Nizam A, Bekan B, Sardar G, Casanova D, et al. Influence network effectiveness in promoting couples' HIV voluntary counseling and testing in Kigali, Rwanda. AIDS. 2012;26(2):217–27. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Global Health Cost Consortium . Analyzing and presenting results: Principles 15–17. 2020. [cited 2020 February 11]. Available from: https://ghcosting.org/pages/standards/principles/analysing_and_presenting_results
  • 31. Carpenter LM, Kamali A, Ruberantwari A, Malamba SS, Whitworth JAG. Rates of HIV‐1 transmission within marriage in rural Uganda in relation to the HIV sero‐status of the partners. AIDS. 1999;13(9):1083–9. [DOI] [PubMed] [Google Scholar]
  • 32. Hugonnet S, Mosha F, Todd J, Mugeye K, Klokke A, Ndeki L, et al. Incidence of HIV infection in stable sexual partnerships: a retrospective cohort study of 1802 couples in Mwanza Region, Tanzania. J Acquir Immune Defic Syndr. 2002;30(1):73–80. [DOI] [PubMed] [Google Scholar]
  • 33. Serwadda D, Gray RH, Wawer MJ, Stallings RY, Sewankambo NK, Konde‐Lule Bongs Lainjo JK, et al. The social dynamics of HIV transmission as reflected through discordant couples in rural Uganda. AIDS. 1995;9(7):745–50. [DOI] [PubMed] [Google Scholar]
  • 34. Quinn TC, Wawer MJ, Sewankambo N, Serwadda D, Li C, Wabwire‐Mangen F, et al. Viral load and heterosexual transmission of human immunodeficiency virus type 1. Rakai Project Study. Group. N Engl J Med. 2000;342(13):921–9. [DOI] [PubMed] [Google Scholar]
  • 35. Chemaitelly H, Awad SF, Abu‐Raddad LJ. The risk of HIV transmission within HIV‐1 sero‐discordant couples appears to vary across sub‐Saharan Africa. Epidemics. 2014;6:1–9. [DOI] [PubMed] [Google Scholar]
  • 36. Kamali A, Price MA, Lakhi S, Karita E, Inambao M, Sanders EJ, et al. Creating an African HIV clinical research and prevention trials network: HIV prevalence, incidence and transmission. PLoS ONE. 2015;10:e0116100. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. The World Bank . Indicators. 2019. [cited 2020 Feb 25]. Available from: https://data.worldbank.org/indicator/SP.POP.1564.TO?view=chart
  • 38. UNAIDS . AIDSInfo: people living with HIV receiving ART. 2018. [cited 2020 Feb 25]. Available from: http://www.unaids.org/en/dataanalysis/datatools/aidsinfo/;
  • 39. Awad SF, Chemaitelly H, Abu‐Raddad LJ. Estimating the annual risk of HIV transmission within HIV sero‐discordant couples in sub‐Saharan Africa. Int J Infect Dis. 2018;66:131–34. [DOI] [PubMed] [Google Scholar]
  • 40. PayScale. 2020. [cited 2020 Apr 9]. Available from: https://www.payscale.com/;
  • 41. Weinstein MC. Recommendations of the panel on cost‐effectiveness in health and medicine. JAMA. 1996;276(15):1253–8. [PubMed] [Google Scholar]
  • 42. Husereau D, Drummond M, Petrou S, Carswell C, Moher D, Greenberg D, et al. Consolidated health economic evaluation reporting standards (CHEERS) statement. Int J Technol Assess Health Care. 2013;29(2):117–22. [DOI] [PubMed] [Google Scholar]
  • 43. PEPFAR . PEPFAR 2020 Country Operational Plan Guidance for all PEPFAR Countries. 2019. [cited 2020 Mar 1]. Available from: https://www.state.gov/wp‐content/uploads/2019/11/2019‐11‐25‐COP20‐Guidance‐Full‐Consolidated_Public‐2‐1.pdf
  • 44. Audet CM, Blevins M, Chire YM, Aliyu MH, Vaz LME, Antonio E, et al. Engagement of men in antenatal care services: increased HIV testing and treatment uptake in a community participatory action program in mozambique. AIDS Behav. 2016;20(9):2090–100. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45. Audet CM, Graves E, Barreto E, De Schacht C, Gong W, Shepherd BE, et al. Partners‐based HIV treatment for seroconcordant couples attending antenatal and postnatal care in rural Mozambique: a cluster randomized trial protocol. Contemp Clin Trials. 2018;71:63–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46. Becker S, Mlay R, Schwandt HM, Lyamuya E. Comparing couples' and individual voluntary counseling and testing for HIV at antenatal clinics in Tanzania: a randomized trial. AIDS Behav. 2010;14(3):558–66. [DOI] [PubMed] [Google Scholar]
  • 47. Theuring S, Mbezi P, Luvanda H, Jordan‐Harder B, Kunz A, Harms G. Male involvement in PMTCT services in Mbeya Region, Tanzania. AIDS Behav. 2009;13 Suppl 1:92–102. [DOI] [PubMed] [Google Scholar]
  • 48. Kilembe W, Wall KM, Mokgoro M, Mwaanga A, Dissen E, Kamusoko M, et al. Implementation of couples' voluntary HIV counseling and testing services in Durban, South Africa. BMC Public Health. 2015;15:601. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49. Kilembe W, Wall KM, Mokgoro M, Mwaanga A, Dissen E, Kamusoko M, et al. Knowledge of HIV serodiscordance, transmission, and prevention among couples in Durban, South Africa. PLoS ONE. 2015;10:e0124548. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50. Matovu JKB, Todd J, Wanyenze RK, Kairania R, Serwadda D, Wabwire‐Mangen F. Evaluation of a demand‐creation intervention for couples’ HIV testing services among married or cohabiting individuals in Rakai, Uganda: a cluster‐randomized intervention trial. BMC Infect Dis. 2016;16(1):379. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51. Lolekha R, Kullerk N, Wolfe MI, Klumthanom K, Singhagowin T, Pattanasin S, et al. Assessment of a couples HIV counseling and testing program for pregnant women and their partners in antenatal care (ANC) in 7 provinces, Thailand. BMC Int Health Human Rights. 2014;14:39. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52. Ayatollahi J, Ayatollahi J, Nasab Sarab MA, Sharifi M. Acceptability of HIV/AIDS testing among pre‐marital couples in Iran (2012). Niger Med J. 2014;55(4):294–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53. Stephenson R,Rentsch C, Sullivan P, McAdams‐Mahmoud A, Jobson G, Struthers H, et al. Attitudes toward couples‐based HIV counseling and testing among MSM in Cape Town, South Africa. AIDS Behav. 2013;17 Suppl 1:S43–50. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54. Sullivan PS, White D, Rosenberg ES, Barnes J, Jones J, Dasgupta S, et al. Safety and acceptability of couples HIV testing and counseling for US men who have sex with men: a randomized prevention study. J Int Assoc Provid AIDS Care. 2014;13(2):135–44. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55. Wall KM, Canary L, Workowski K, Lockard A, Jones J, Sullivan P, et al. Acceptability of couples' voluntary HIV testing among HIV‐infected patients in care and their HIV‐negative partners in the United States. Open AIDS J. 2016;10:1–13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56. Kelley AL, Hagaman AK, Wall KM, Karita E, Kilembe W, Bayingana R, et al. Promotion of couples' voluntary HIV counseling and testing: a comparison of influence networks in Rwanda and Zambia. BMC Public Health. 2016;16:744. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57. Inambao M, Kilembe W, Canary LA, Czaicki NL, Kakungu‐Simpungwe M, Chavuma R, et al. Transitioning couple's voluntary HIV counseling and testing (CVCT) from stand‐alone weekend services into routine antenatal and VCT services in government clinics in Zambia's two largest cities. PLoS ONE. 2017;12:e0185142. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58. Czaicki NL, Davitte J, Siangonya B, Kastner R, Ahmed N, Khu NH, et al. Predictors of first follow‐up HIV testing for couples' voluntary HIV counseling and testing in Ndola, Zambia. J Acquir Immune Defic Syndr. 2014;66(1):e1–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59. Sibanda EL, Tumushime M, Mufuka J, Mavedzenge SN, Gudukeya S, Bautista‐Arredondo S, et al. Effect of non‐monetary incentives on uptake of couples' counselling and testing among clients attending mobile HIV services in rural Zimbabwe: a cluster‐randomised trial. Lancet Glob Health. 2017;5(9):e907–15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60. Rosenberg NE, Mtande TK, Saidi F, Stanley C, Jere E, Paile L, et al. Recruiting male partners for couple HIV testing and counselling in Malawi's option B+ programme: an unblinded randomised controlled trial. Lancet HIV. 2015;2(11):e483–91. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61. Patel RC, Stanford‐Moore G, Odoyo J, Pyra M, Wakhungu I, Anand K, et al. "Since both of us are using antiretrovirals, we have been supportive to each other": facilitators and barriers of pre‐exposure prophylaxis use in heterosexual HIV serodiscordant couples in Kisumu, Kenya. J Int AIDS Soc. 2016;19(1):21134. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62. Patel RC, Leddy AM, Odoyo J, Anand K, Stanford‐Moore G, Wakhungu I, et al. What motivates serodiscordant couples to prevent HIV transmission within their relationships: findings from a PrEP implementation study in Kenya. Cult Health Sex. 2018;20(6):625–39. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63. UNAIDS . Undetectable = Untransmittable. 2018. [cited 2020 March 5]. Available from: https://www.unaids.org/sites/default/files/media_asset/undetectable‐untransmittable_en.pdf
  • 64. Semrau K, Kuhn L, Vwalika C, Kasonde P, Sinkala M, Kankasa C, et al. Women in couples antenatal HIV counseling and testing are not more likely to report adverse social events. AIDS (London, England). 2005;19(6):603–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65. Desgrees‐du‐Lou A, Orne‐Gliemann J. Couple‐centred testing and counselling for HIV serodiscordant heterosexual couples in sub‐Saharan Africa. Reprod Health Matters. 2008;16(32):151–61. [DOI] [PubMed] [Google Scholar]
  • 66. PEPFAR . Monitoring, evaluation, and reporting indicator reference guide. 2019. [cited 2020 Mar 5]. Available from: https://www.state.gov/wp‐content/uploads/2019/10/PEPFAR‐MER‐Indicator‐Reference‐Guide‐Version‐2.4‐FY20.pdf
  • 67. Njau B, Watt MH, Ostermann J, Manongi R, Sikkema KJ. Perceived acceptability of home‐based couples voluntary HIV counseling and testing in Northern Tanzania. AIDS care. 2012;24(4):413–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68. Krakowiak D, Kinuthia J, Osoti AO, Asila V, Gone MA, Mark J, et al. Home‐based HIV testing among pregnant couples increases partner testing and identification of serodiscordant partnerships. J Acquir Immune Defic Syndr. 2016;72:S167–73. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69. Becker S, Taulo FO, Hindin MJ, Chipeta EK, Loll D, Tsui A. Pilot study of home‐based delivery of HIV testing and counseling and contraceptive services to couples in Malawi. BMC Public Health. 2014;14:1309. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70. Masters SH, Agot K, Obonyo B, Napierala Mavedzenge S, Maman S, Thirumurthy H. Promoting partner testing and couples testing through secondary distribution of HIV self‐tests: a randomized clinical trial. PLoS Med. 2016;13:e1002166. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71. Joseph Davey DL, Wall KM, Kilembe W, Naw HK, Brill I, Vwalika B, et al. HIV incidence and predictors of HIV acquisition from an outside partner in serodiscordant couples in Lusaka, Zambia. J Acquir Immune Defic Syndr. 2017;76(2):123–31. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72. Over M.Opportunities for presidential leadership on AIDS: from an “Emergency Plan” to a sustainable policy. 2009. [cited 2020 March 5]. Available from: http://citeseerx.ist.psu.edu/viewdoc/download?doi=10.1.1.178.8723&rep=rep1&type=pdf
  • 73. Chemaitelly H, Awad SF, Shelton JD, Abu‐Raddad LJ. Sources of HIV incidence among stable couples in sub‐Saharan Africa. J Int AIDS Soc. 2014;17(1):18765. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74. Abdool Karim SS. HIV‐1 Epidemic control ‐ insights from test‐and‐treat trials. N Engl J Med. 2019;381(3):286–8. [DOI] [PubMed] [Google Scholar]
  • 75. Anglewicz P, Chintsanya J. Disclosure of HIV status between spouses in rural Malawi. AIDS Care. 2011;23(8):998–1005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76. Nyandat J, van Rensburg G. Non‐disclosure of HIV‐positive status to a partner and mother‐to‐child transmission of HIV: evidence from a case‐control study conducted in a rural county in Kenya. South Afr J HIV Med. 2017;18(1):691. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77. Maeri I, El Ayadi A, Getahun M, Charlebois E, Akatukwasa C, Tumwebaze D, et al. “How can I tell?” Consequences of HIV status disclosure among couples in eastern African communities in the context of an ongoing HIV “test‐and‐treat” trial. AIDS Care. 2016;28 Sup3:59–66. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 78. King R, Wamai N, Khana K, Johansson E, Lindkvist P, Bunnell R. “Maybe his blood is still strong”: a qualitative study among HIV‐sero‐discordant couples on ART in rural Uganda. BMC Public Health. 2012;12(1):801. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79. Galarraga O, Colchero MA, Wamai RG, Bertozzi SM. HIV prevention cost‐effectiveness: a systematic review. BMC Public Health. 2009;9 Suppl 1:S5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80. John FN, Farquhar C, Kiarie JN, Kabura MN, John‐Stewart GC. Cost effectiveness of couple counselling to enhance infant HIV‐1 prevention. Int J STD AIDS. 2008;19(6):406–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81. Sarkar S, Corso P, Ebrahim‐Zadeh S, Kim P, Charania S, Wall K. Cost‐effectiveness of HIV prevention interventions in Sub‐Saharan Africa: a systematic review. EClinicalMedicine. 2019;10:10–31. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82. WHO . Cost effectiveness and strategic planning (WHO‐CHOICE). 2013. Available from: https://www.who.int/choice/cost‐effectiveness/en/;. Accessed May 1, 2020.
  • 83. Bertram MY, Lauer JA, De Joncheere K, Edejer T, Hutubessy R, Kieny M‐P, et al. Cost‐effectiveness thresholds: pros and cons. Bull World Health Organ. 2016;94(12):925–30. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84. Woods B, Revill P, Sculpher M, Claxton K. Country‐level cost‐effectiveness thresholds: initial estimates and the need for further research. Value Health. 2016;19(8):929–35. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of the International AIDS Society are provided here courtesy of Wiley

RESOURCES