Introduction Despite early adoption of the WHO guidelines to deliver lifelong antiretroviral (ARV) regimen to pregnant women on HIV diagnosis, the HIV prevention of mother to child transmission programme in Papua New Guinea remains suboptimal. An unacceptable number of babies are infected with HIV and mothers not retained in treatment. This study aimed to describe the characteristics of this programme and to investigate the factors associated with programme performance outcomes. Methods We conducted a retrospective analysis of clinical records of HIV-positive pregnant women at two hospitals providing prevention of mother to child transmission services. All women enrolled in the prevention of mother to child transmission programme during the study period (June 2012-June 2015) were eligible for inclusion. Using logistic regression, we examined the factors associated with maternal loss to follow-up (LTFU) before birth and before infant registration in a paediatric ARV programme. Results 763 of women had records eligible for inclusion. Demographic and clinical differences existed between women at the two sites. Almost half (45.1%) of the women knew their HIV-positive status prior to the current pregnancy. Multivariate analysis showed that women more likely to be LTFU by the time of birth were younger (adjusted OR (AOR)=2.92, 95% CI 1.16 to 7.63), were newly diagnosed with HIV in the current/most recent pregnancy (AOR=3.50, 95% CI 1.62 to 7.59) and were in an HIV serodiscordant relationship (AOR=2.94, 95% CI 1.11 to 7.84). Factors associated with maternal LTFU before infant registration included being primipara at the time of enrolment (AOR=3.13, 95% CI 1.44 to 6.80) and being newly diagnosed in that current/most recent pregnancy (AOR=2.49, 95% CI 1.31 to 4.73). 6.6% (50 of 763) of exposed infants had a positive HIV DNA test. Conclusions Our study highlighted predictors of LTFU among women. Understanding these correlates at different stages of the programme offers important insights for targets and timing of greater support for retention in care.
The two sites were selected as they were both in high-burden HIV provinces, were the longest running sites for prevention of mother to child transmission in the country, and were well supported through donor funding and non-governmental organisations, such as the Clinton Health Access Initiative. Port Moresby is the national capital city, on the southern coast of the country, and is a melting pot of people from across the country. It is one of only three cities in the country. Goroka is a town and the provincial capital of the Eastern Highlands Province, in the lower highlands region of the country. The geographical, sociocultural and economic contexts of these two sites are diverse. Unlike Port Moresby, Goroka is much smaller and people access the town from across the province, travelling by foot and road. Travel between these two sites is only possible by air. HIV testing is available at numerous ANC clinics in each province; however, there is only one prevention of mother to child transmission clinic in each province. The implementation model for the prevention of mother to child transmission programme differed between the two sites. In Port Moresby, prevention of mother to child transmission services were integrated in antenatal, delivery and postnatal care services for the first 6 weeks. After the 6-week postnatal period, HIV-exposed infants were referred for enrolment in the paediatric HIV clinic for ongoing HIV prophylaxis, confirmatory HIV testing and treatment as required, while mothers were referred to the adult ART outpatient clinic. The adult and paediatric HIV clinics were not co-located and operated on different days, and clinical records were not linked manually or electronically. In Goroka, prevention of mother to child transmission services were integrated in antenatal, delivery and postnatal care, and the mother-infant pair is cared for by the same clinical team until the confirmatory HIV test for the infant was conducted at 18 months. Despite its co-location infants were still enrolled in the paediatric HIV clinic at 6 weeks. At 18 months after birth, the mother was transferred (back) to the adult ART clinic, while the HIV-infected infant/s remained in the clinic for ongoing clinical care and management. All healthcare was provided by staff who were employed as government healthcare workers or were supported and funded by the Clinton Health Access Initiative, funded by the Australian government. The clinical audit used a ‘capture all’ approach, documenting all women with HIV enrolled in the prevention of mother to child transmission programme for the 3-year time period spanning June 2012 (when Option B+ was formally adopted in PNG) until June 2015. Data sources included paper-based antenatal records of HIV-positive women and their infants’ medical records at either the same prevention of mother to child transmission clinic (Goroka) or the paediatric HIV clinic elsewhere in the hospital (Port Moresby). For all available records, two research midwives manually extracted data related to patient demographics, pregnancy care, HIV and other sexually transmitted infection testing, prevention of mother to child transmission enrolment, ART initiation and clinic appointments, and these were recorded on preprinted study clinical research forms. Infants’ HIV DNA test results were obtained from infant records. Infant records in Goroka were physically co-located with the mothers. In Port Moresby, mother-infant pairs were linked manually by extracting the name of the mother, the birth date of the infant on her ANC record, and if recorded the sex of the newborn. Staff at the paediatric HIV clinic then identified infant records to link the mother-infant pairs. Research midwives cross-checked each other’s completed data forms to ensure all forms were completed as accurately as possible. After reviewing each form for validity and completeness, de-identified data were double-entered into a purposely developed study database and stored on a password-protected computer at the Papua New Guinea Institute of Medical Research. All electronic data were merged into a single study database and analysed using STATA V.13.1. At enrolment into the prevention of mother to child transmission programme, sociodemographic, obstetric and HIV-related characteristics were recorded and laboratory assessments conducted. In our analysis we only included the first pregnancy when assessing maternal characteristics and outcomes. However, for infant characteristics and outcomes, all live births were included. LTFU was measured and defined at two timepoints. First, pregnant women enrolled in the prevention of mother to child transmission programme were categorised as ‘lost to follow-up before delivery’ if they did not return to the health facility for delivery, and could include scheduled antenatal prevention of mother to child transmission visits. Second, pregnant enrolled women in the prevention of mother to child transmission programme were defined as ‘lost to follow-up before infant registration’ if they did not register the newborn child at the respective clinics for prevention of mother to child transmission services and were lost from the programme either during antenatal, peripartum or early postnatal services. Although the study sponsor originally sought to have the audit measure maternal LTFU at 2 years after lifetime ART initiation in the prevention of mother to child transmission programme (Option B+), this was not possible. In PNG, paper-based adult ART records were used and there was no system that linked women in prevention from mother to child transmission programmes to adult ART service records. At the time the audit was undertaken, only two ART sites in Port Moresby were using an electronic database, which was manually updated into a national database by staff at the National Department of Health every few months. Enrolment of a child into paediatric HIV programmes shows ongoing engagement in HIV care. The fact that so many women did not enrol their children in these clinics shows disengagement. Like prevention of mother to child transmission programmes, there is only one paediatric HIV clinic in each province. Descriptive analyses were conducted to describe the women enrolled in the prevention of mother to child transmission programmes at the sites and the HIV outcomes of their infants. χ2 tests, two-sample t-tests and Wilcoxon rank-sum tests were performed to examine differences in sociodemographic and other behavioural characteristics of women and infants in the sites. Multivariate logistic regression analysis was undertaken to investigate factors associated with maternal LTFU before birth and the mean time before the infant was registered in a paediatric ART programme. Based on findings from previous research24 and data available from this study, we selected variables that might influence the outcome of interest (maternal LTFU) to be included in the predictive models. For the analysis of factors associated with maternal LTFU before birth, we used Firth’s logistic regression25 26 to account for bias due to rare event data, which are known to produce substantial bias estimates with conventional logistic regression.27 Assumption of rare event data was made based on few outcome events per variable (EPV) guideline with at least five EPV in models used for confounding adjustment.28 Infant HIV testing and results were quantified and described. This was a retrospective cohort study and women were no longer attending the ANC. Consent from the participating hospitals was granted to access clinical records on the condition that no identifiable information, including names, was recorded on the clinical research forms. We did not invite patient and public involvement in the design of the study due to the nature of the study, being a retrospective clinical audit commissioned by UNICEF. All study results were disseminated to stakeholders at the conclusion of the study.