HIV Infections, Pregnancy Related
Conditions
Keywords
PrEP
Brief summary
In a region with 15-20% HIV prevalence, an estimated 20% of HIV-uninfected women could have HIV exposures in pregnancy. In a theoretical scenario of perfect PrEP coverage, all women at risk receive PrEP while no women not at HIV risk receive PrEP (Figure 4). With mandatory PrEP given to all women (similar to the approaches used for malaria prophylaxis), all women at risk would be covered but many women not at risk receive unnecessary PrEP. Our premise is that a targeted PrEP model may be closer to perfect coverage than a universal offer/self-select model. Implementing targeted PrEP through strategies that include facilitation of partner testing with self-tests could add HIV prevention benefit by increasing partner HIV diagnosis and treatment similar to the initiation of PrEP among pregnant women. By implementing these strategies and measuring uptake, use, and HIV incidence, we can inform the best health systems model for PrEP delivery in pregnancy.
Detailed description
Women living in regions with high HIV prevalence are at high risk of HIV acquisition in pregnancy and postpartum because they infrequently use condoms, do not know their partner's HIV status, and have biologic changes or changes in their partner's sexual partnerships that increase susceptibility. Oral pre-exposure antiretroviral prophylaxis (PrEP) may be an attractive strategy for HIV prevention in pregnancy/postpartum; however, it is important to ensure PrEP reaches women who are at risk for acquiring HIV during pregnancy while avoiding unnecessary PrEP use during pregnancy. Clinicians and women are using PrEP in pregnancy; in qualitative studies, women, health workers and policy-makers support use of PrEP in pregnancy but advocate for models of PrEP delivery that ensure women at risk receive PrEP while minimizing unnecessary PrEP use in women not at risk. Targeting PrEP to women at greatest risk of HIV may maximize benefits, minimize potential risks, and optimize cost-effectiveness. This cluster-randomized clinical trial (RCT) in 20 Maternal Child Health (MCH) clinics in western Kenya (10 clinics per arm, up to 250 women per clinic, up to 5000 women overall), will compare 2 models of PrEP delivery in pregnancy. Clinics will offer universal availability of PrEP (and women self-select whether to use) or targeted offer of PrEP (i.e., offer to women identified as high risk through a standardized risk assessment and partner self-testing, and then women identified as high-risk select whether to use). Leveraging the pre-existing MCH clinic visit schedule will enable programmatically relevant assessment of PrEP uptake, use, and HIV incidence. The outcome of the study will be a model of PrEP delivery in pregnancy that optimizes effectiveness, safety, and cost-effectiveness. Our team has expertise in maternal-child HIV (John-Stewart, Kinuthia), PrEP clinical trials and implementation science (Baeten, Richardson), partner self-testing (Thirumurthy), economics and qualitative research (Barnabas, O'Malley). AIM 1a. In a cluster-RCT, compare universal PrEP (offer to all; women self-select PrEP) to targeted PrEP (limit the offer to women identified as high risk through a standardized risk assessment and partner self-testing) for outcomes reflecting the balance of PrEP effectiveness and avoiding unnecessary PrEP exposure to women at low or no risk of HIV: HIV incidence at 9 months postpartum among all women (including those who did and did not receive PrEP) and proportion of women exposed to PrEP. AIM 1b. To compare trial arms for proportion of women 'appropriately' on PrEP (risk factors), PrEP adherence (drug levels) and duration, partners with known HIV status, partners on ART; infant outcomes (growth, birth outcomes, HIV status). AIM 2. To estimate the incremental cost-effectiveness of targeted PrEP compared to universal PrEP for women during pregnancy and postpartum, per HIV infection and disability-adjusted life-year (DALY) averted. AIM 3. To qualitatively assess barriers and facilitators to uptake, adherence, acceptability, and feasibility in universal and targeted PrEP models at the organizational, provider, and individual woman level.
Interventions
Counseling at universal sites, will use a standardized counseling script to state that PrEP is available for women at risk for HIV, explain that HIV prevalence in the region is high, and will note that women with HIV positive partners or who don't know their partner's status may be at risk. Counseling will specify that women may have their own reasons to feel at risk or to want PrEP. Following standardized counseling, women will select PrEP at the same visit or will be allowed to deliberate on the decision and come back at the next visit with a decision. Women will be informed that it is advisable to use PrEP if they know their partner is HIV positive or if they do not know their partner's status and will be encouraged to bring untested partners to clinic if status is unknown.
Following enrollment, the targeted PrEP clinics will provide two inter-related innovations over two ANC visits. In the targeted PrEP clinics, any of the following three criteria can trigger enhanced PrEP counseling. A participant that meets any one of these criteria will receive PrEP counseling during the study visit where the criteria is met: 1. Risk Score \>6 (Risk score includes male partner status known/unknown, syphilis infection, and lifetime number of male partners) or any National AIDS and STI Control Programme (NASCOP) risk factors 2. participant declines partner self-tests regardless of partner HIV status, and/or 3. their partner declines self-testing or tests positive.
Sponsors
Study design
Intervention model description
We will select 20 clinics from Western Kenya. Ten clinics will be randomized to universal PrEP and ten to targeted PrEP (Table 2). To ensure balance between study arms in terms of key site characteristics, sites will be categorized on HIV prevalence and ANC volume, and restricted randomization will be used for site (cluster) allocation to intervention and control arms (68).
Eligibility
Inclusion criteria
* Eligibility for enrollment will include age ≥15 years * Pregnant at any gestational age * Tuberculosis negative * Plans to reside in area for at least one year postpartum * Plans to receive postnatal and infant care at the study facility * Not currently enrolled in any other studies.
Exclusion criteria
* HIV+ at time of enrollment
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Maternal HIV Incidence | 6 weeks, 6 months, 9 months postpartum | Maternal HIV Incidence |
| Appropriate PrEP Decision | Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30). | Scored 1 for high risk women using PrEP and low risk women not using PrEP; 0 for high risk women NOT on PrEP and low risk women using PrEP |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| PrEP Duration | Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30). | Number of months on PrEP |
| Partner With Known HIV Status | At 9 months postpartum | Participants report of partner's HIV status |
| Infant Birthweight | time of delivery | Infant Birthweight |
| PrEP Use | Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30). | PrEP Utilization by participants |
| PrEP Acceptance | Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30). | PrEP accepted by participants |
| Preterm Birth | At birth | Birth \<37 weeks gestation |
| Infant Growth | 9 months of age | Infant height, weight, and age (Weight-for-Age \[WAZ\], Height-for-Age \[HAZ\], Weight-for-Height \[WHZ\] Z-scores). A Z-score of 0 represents the population mean. Indicators of infant malnutrition are defined as Underweight- WAZ Z-score\<-2; Stunting-HAZ Z-Score \<-2; Wasting- WHZ Z-Score \<-2. |
| PrEP Adherence | Enrollment to 9 months postpartum | Sequential dried blood spots, PrEP adherence by DBS dichotomous by pregnancy or postpartum thresholds equivalent to \ 7 doses per week (≥650 fmol/punch during pregnancy or ≥950 fmol/punch postpartum) based on the thresholds established by the 2009 IMPAACT directly observed PrEP PK study. |
Other
| Measure | Time frame | Description |
|---|---|---|
| PrEP Adherence by Self-report | Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30). | Any missed doses in the last month reported by participants |
| Partner on ART if HIV Positive | Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30). | Participant report of partner ART use if partner is HIV positive |
Countries
Kenya
Participant flow
Pre-assignment details
Enrollment ended on July 31, 2019. At that time 4,447 women had enrolled (consented) into the PrIMA study out of an anticipated 4,500.
Participants by arm
| Arm | Count |
|---|---|
| Universal PrEP Counselling All enrolled women receiving antenatal care at facilities assigned to Universal PrEP arm will receive standardized HIV risk counseling and then self-select whether they want to use PrEP.
Universal PrEP Counseling: Counseling at universal sites, will use a standardized counseling script to state that PrEP is available for women at risk for HIV, explain that HIV prevalence in the region is high, and will note that women with HIV positive partners or who don't know their partner's status may be at risk. Counseling will specify that women may have their own reasons to feel at risk or to want PrEP. Following standardized counseling, women will select PrEP at the same visit or will be allowed to deliberate on the decision and come back at the next visit with a decision. Women will be informed that it is advisable to use PrEP if they know their partner is HIV positive or if they do not know their partner's status and will be encouraged to bring untested partners to clinic if status is unknown. | 2,250 |
| Targeted PrEP Clinics All enrolled women receiving antenatal care at facilities assigned to the Targeted PrEP arm will be assessed for HIV-risk prior to receiving targeted PrEP counseling.
Targeted PrEP Counseling: Following enrollment, the targeted PrEP clinics will provide two inter-related innovations over two ANC visits. In the targeted PrEP clinics, any of the following three criteria can trigger enhanced PrEP counseling. A participant that meets any one of these criteria will receive PrEP counseling during the study visit where the criteria is met:
1. Risk Score \>6 (Risk score includes male partner status known/unknown, syphilis infection, and lifetime number of male partners) or any National AIDS and STI Control Programme (NASCOP) risk factors
2. participant declines partner self-tests regardless of partner HIV status, and/or
3. their partner declines self-testing or tests positive. | 2,197 |
| Total | 4,447 |
Baseline characteristics
| Characteristic | Targeted PrEP Clinics | Universal PrEP Counselling | Total |
|---|---|---|---|
| Age, Continuous | 24.1 years | 23.9 years | 24.0 years |
| Age, Customized 25-35 | 850 Participants | 830 Participants | 1680 Participants |
| Age, Customized <25 years of age | 1238 Participants | 1307 Participants | 2545 Participants |
| Age, Customized 35+ | 108 Participants | 112 Participants | 220 Participants |
| Age, Customized Age missing | 1 Participants | 1 Participants | 2 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 2197 Participants | 2250 Participants | 4447 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 0 Participants | 0 Participants | 0 Participants |
| Region of Enrollment Kenya | 2197 participants | 2250 participants | 4447 participants |
| Sex: Female, Male Female | 2197 Participants | 2250 Participants | 4447 Participants |
| Sex: Female, Male Male | 0 Participants | 0 Participants | 0 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 2 / 2,250 | 2 / 2,197 |
| other Total, other adverse events | 7 / 2,250 | 7 / 2,197 |
| serious Total, serious adverse events | 132 / 2,250 | 118 / 2,197 |
Outcome results
Appropriate PrEP Decision
Scored 1 for high risk women using PrEP and low risk women not using PrEP; 0 for high risk women NOT on PrEP and low risk women using PrEP
Time frame: Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Universal PrEP Counselling | Appropriate PrEP Decision | 1535 Participants |
| Targeted PrEP Clinics | Appropriate PrEP Decision | 1299 Participants |
Maternal HIV Incidence
Maternal HIV Incidence
Time frame: 6 weeks, 6 months, 9 months postpartum
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Universal PrEP Counselling | Maternal HIV Incidence | 0.38 incidence/100 Person years |
| Targeted PrEP Clinics | Maternal HIV Incidence | 0.31 incidence/100 Person years |
Infant Birthweight
Infant Birthweight
Time frame: time of delivery
Population: This analysis is restricted to mothers with live born infants with birth weight data available in their clinical records.
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Universal PrEP Counselling | Infant Birthweight | 3.5 kg |
| Targeted PrEP Clinics | Infant Birthweight | 3.5 kg |
Infant Growth
Infant height, weight, and age (Weight-for-Age \[WAZ\], Height-for-Age \[HAZ\], Weight-for-Height \[WHZ\] Z-scores). A Z-score of 0 represents the population mean. Indicators of infant malnutrition are defined as Underweight- WAZ Z-score\<-2; Stunting-HAZ Z-Score \<-2; Wasting- WHZ Z-Score \<-2.
Time frame: 9 months of age
Population: Length measurements could not be ascertained from all infants
| Arm | Measure | Group | Value (MEDIAN) |
|---|---|---|---|
| Universal PrEP Counselling | Infant Growth | Infant WAZ at 9mo PP | 0.12 z-score |
| Universal PrEP Counselling | Infant Growth | Infant HAZ at 9mo PP | -0.35 z-score |
| Universal PrEP Counselling | Infant Growth | Infant WHZ at 9mo PP | 0.42 z-score |
| Targeted PrEP Clinics | Infant Growth | Infant WAZ at 9mo PP | -0.01 z-score |
| Targeted PrEP Clinics | Infant Growth | Infant HAZ at 9mo PP | -0.47 z-score |
| Targeted PrEP Clinics | Infant Growth | Infant WHZ at 9mo PP | 0.29 z-score |
Partner With Known HIV Status
Participants report of partner's HIV status
Time frame: At 9 months postpartum
Population: This analysis is restricted to participants who reported having a partner at 9-months postpartum.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Universal PrEP Counselling | Partner With Known HIV Status | 1680 Participants |
| Targeted PrEP Clinics | Partner With Known HIV Status | 1648 Participants |
PrEP Acceptance
PrEP accepted by participants
Time frame: Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Universal PrEP Counselling | PrEP Acceptance | 441 Participants |
| Targeted PrEP Clinics | PrEP Acceptance | 387 Participants |
PrEP Adherence
Sequential dried blood spots, PrEP adherence by DBS dichotomous by pregnancy or postpartum thresholds equivalent to \ 7 doses per week (≥650 fmol/punch during pregnancy or ≥950 fmol/punch postpartum) based on the thresholds established by the 2009 IMPAACT directly observed PrEP PK study.
Time frame: Enrollment to 9 months postpartum
Population: Of the 186 participants sampled for this analyses, 427 DBS samples were analyzed (232 universal arm, 195 targeted arm).
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Universal PrEP Counselling | PrEP Adherence | 7 Samples w/ adherence at ~7dose/week |
| Targeted PrEP Clinics | PrEP Adherence | 9 Samples w/ adherence at ~7dose/week |
PrEP Duration
Number of months on PrEP
Time frame: Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).
Population: This analysis is restricted to participants who initiated PrEP during the study period.
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Universal PrEP Counselling | PrEP Duration | 8.6 months |
| Targeted PrEP Clinics | PrEP Duration | 9.0 months |
PrEP Use
PrEP Utilization by participants
Time frame: Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Universal PrEP Counselling | PrEP Use | 397 Participants |
| Targeted PrEP Clinics | PrEP Use | 323 Participants |
Preterm Birth
Birth \<37 weeks gestation
Time frame: At birth
Population: This analysis is restricted to participants who reported a live birth and had gestational age at birth data available.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Universal PrEP Counselling | Preterm Birth | 506 Participants |
| Targeted PrEP Clinics | Preterm Birth | 309 Participants |
Partner on ART if HIV Positive
Participant report of partner ART use if partner is HIV positive
Time frame: Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).
Population: This analysis is restricted to participants with a partner known to be living with HIV.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Universal PrEP Counselling | Partner on ART if HIV Positive | 37 Participants |
| Targeted PrEP Clinics | Partner on ART if HIV Positive | 31 Participants |
PrEP Adherence by Self-report
Any missed doses in the last month reported by participants
Time frame: Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Universal PrEP Counselling | PrEP Adherence by Self-report | 184 Participants |
| Targeted PrEP Clinics | PrEP Adherence by Self-report | 120 Participants |