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      Implementation and Operational Research: The Impact of Option B+ on the Antenatal PMTCT Cascade in Lilongwe, Malawi

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          Abstract

          Objective:

          In 2011, Malawi implemented Option B+ (B+), lifelong antiretroviral therapy (ART) for pregnant and breastfeeding women. We aimed to describe changes in service uptake and outcomes along the antenatal prevention of mother-to-child transmission (PMTCT) cascade post-B+ implementation.

          Design:

          Pre/post study using routinely collected program data from 2 large Lilongwe-based health centers.

          Methods:

          We compared the testing of HIV-infected pregnant women at antenatal care, enrollment into PMTCT services, receipt of ART, and 6-month ART outcomes pre-B+ (October 2009–March 2011) and post-B+ (October 2011–March 2013).

          Results:

          A total of 13,926 (pre) and 14,532 (post) women presented to antenatal care. Post-B+, a smaller proportion were HIV-tested (99.3% vs. 87.7% post-B+; P < 0.0001). There were 1654 (pre) and 1535 (post) HIV-infected women identified, with a larger proportion already known to be HIV-infected (18.1% vs. 41.2% post-B+; P < 0.0001) and on ART post-B+ (18.7% vs. 30.2% post-B+; P < 0.0001). A significantly greater proportion enrolled into the PMTCT program (68.3% vs. 92.6% post-B+; P < 0.0001) and was retained through delivery post-B+ (51.1% vs. 65% post-B+; P < 0.0001). Among those not on ART at enrollment, there was no change in the proportion newly initiating ART/antiretrovirals (79% vs. 81.9% post-B+; P = 0.11), although median days to initiation of ART decreased [48 days (19, 130) vs. 0 days (0, 15.5) post-B+; P < 0.0001]. Among those newly initiating ART, a smaller proportion was alive on ART 6 months after initiation (89.3% vs. 78.8% post-B+; P = 0.0004).

          Conclusions:

          Although several improvements in PMTCT program performance were noted with implementation of B+, challenges remain at several critical steps along the cascade requiring innovative solutions to ensure an AIDS-free generation.

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          Most cited references17

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          Missed opportunities to prevent mother-to-child-transmission: systematic review and meta-analysis.

          To determine magnitude and reasons of loss to program and poor antiretroviral prophylaxis coverage in prevention of mother-to-child transmission (PMTCT) programs in sub-Saharan Africa. Systematic review and meta-analysis. We searched PubMed and Embase databases for PMTCT studies in sub-Saharan Africa published between January 2002 and March 2012. Outcomes were the percentage of pregnant women tested for HIV, initiating antiretroviral prophylaxis, having a CD4 cell count measured, and initiating antiretroviral combination therapy (cART) if eligible. In children outcomes were early infant diagnosis for HIV, and cART initiation. We combined data using random-effects meta-analysis and identified predictors of uptake of interventions. Forty-four studies from 15 countries including 75,172 HIV-infected pregnant women were analyzed. HIV-testing uptake at antenatal care services was 94% [95% confidence intervals (CIs) 92-95%] for opt-out and 58% (95% CI 40-75%) for opt-in testing. Coverage with any antiretroviral prophylaxis was 70% (95% CI 64-76%) and 62% (95% CI 50-73%) of pregnant women eligible for cART received treatment. Sixty-four percent (95% CI 48-81%) of HIV exposed infants had early diagnosis performed and 55% (95% CI 36-74%) were tested between 12 and 18 months. Uptake of PMTCT interventions was improved if cART was provided at the antenatal clinic and if the male partner was involved. In sub-Saharan Africa, uptake of PMTCT interventions and early infant diagnosis is unsatisfactory. An integrated family-centered approach seems to improve retention.
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            Impact of an Innovative Approach to Prevent Mother-to-Child Transmission of HIV — Malawi, July 2011–September 2012

            Antiretroviral medications can reduce rates of mother-to-child transmission of human immunodeficiency virus (HIV) to less than 5% (1). However, in 2011, only 57% of HIV-infected pregnant women in low- and middle-income countries received a World Health Organization (WHO)–recommended regimen for prevention of mother-to-child transmission (PMTCT), and an estimated 300,000 infants acquired HIV infection from their mothers in sub-Saharan Africa; 15,700 (5.2%) of these infants were born in Malawi (2). An important barrier to PMTCT in Malawi is the limited laboratory capacity for CD4 cell count, which is recommended by WHO to determine which antiretroviral medications to start (3). In the third quarter of 2011, the Malawi Ministry of Health (MOH) implemented an innovative approach (called “Option B+”), in which all HIV-infected pregnant and breastfeeding women are eligible for lifelong antiretroviral therapy (ART) regardless of CD4 count (4). Since that time, several countries (including Rwanda, Uganda, and Haiti) have adopted the Option B+ policy, and WHO was prompted to release a technical update in April 2012 describing the advantages and challenges of this approach as well as the need to evaluate country experiences with Option B+ (5). Using data collected through routine program supervision, this report is the first to summarize Malawi’s experience implementing Option B+ under the direction of the MOH and supported by the Office of the Global AIDS Coordinator (OGAC) through the President’s Emergency Plan for AIDS Relief (PEPFAR). In Malawi, the number of pregnant and breastfeeding women started on ART per quarter increased by 748%, from 1,257 in the second quarter of 2011 (before Option B+ implementation) to 10,663 in the third quarter of 2012 (1 year after implementation). Of the 2,949 women who started ART under Option B+ in the third quarter of 2011 and did not transfer care, 2,267 (77%) continue to receive ART at 12 months; this retention rate is similar to the rate for all adults in the national program. Option B+ is an important innovation that could accelerate progress in Malawi and other countries toward the goal of eliminating mother-to-child transmission of HIV worldwide. Antiretroviral medications can be provided to improve a patient’s own health, prevent vertical HIV transmission from mother to infant, and/or prevent horizontal transmission to an uninfected sex partner. In most resource-limited settings, ART eligibility is based on CD4 cell count or clinical staging. For pregnant women with CD4 ≤350 cells/mm3 or at WHO clinical stage 3 or 4, the 2010 WHO PMTCT recommendations include lifelong ART. For HIV-infected pregnant women not eligible for ART, either of two prophylaxis options (called “Option A” and “Option B”) is recommended. Option A involves prophylaxis with a single drug, zidovudine (AZT), during pregnancy, and additional antiretroviral medications during labor, delivery, and the postpartum period. Option B involves triple-drug ART during pregnancy and breastfeeding. Both options include additional antiretroviral medications for infants (1). In Malawi, the MOH determined the health sector did not have the laboratory and infrastructure capacity to provide universal access to CD4 cell count testing needed to successfully implement either of the two recommended options. Instead, they proposed a modified Option B (called “Option B+”), in which all confirmed HIV-infected pregnant and breastfeeding women are offered lifelong ART regardless of CD4 count or clinical stage. This policy streamlined the process of ART initiation and had the potential to improve maternal health, facilitate access to PMTCT and ART, reduce HIV transmission risk to uninfected male partners, and provide protection against vertical HIV transmission in future pregnancies (4,6). Implementation of Option B+ also required integration of ART into all antenatal care (ANC) settings, training of nearly all health-care workers in a new integrated curriculum, and a change in the adult first-line ART regimen to one that included the antiretroviral medication efavirenz.* Implementation was facilitated by existing task-shifting policies that allow clinical officers, medical assistants, and nurses to start ART (4). Every integrated PMTCT/ART site in Malawi is visited quarterly by members of a nationally coordinated supervision team composed of MOH service providers, supervisors, supporting partners, and CDC-Malawi staff. Direct supervision of every site in every quarter is the key feature of the national HIV program. Innovative patient registers have been created to permit longitudinal follow-up and cohort analyses for patients receiving antenatal and HIV care. Data collected during these supervision visits include the number of persons started on ART, the reason for starting ART, and, of those started on ART in previous quarters, the number of patients retained in care. These facility-level aggregated data are returned to the central-level MOH, entered into a database, cleaned, and then analyzed to produce MOH’s Quarterly HIV Programme Reports,† on which this report is based. Implementation of Option B+ required training of 4,839 health-care workers and resulted in decentralization of ART to all health centers with ANC, with an increase from 303 ART sites in June 2011 to 641 integrated PMTCT/ART sites in September 2012 (Figure 1). After implementation of Option B+ began in July 2011, the total number of all persons started on ART per quarter increased by 61%, from 18,442 in the second quarter of 2011 to 29,707 in the third quarter 2012. Implementation of Option B+ resulted in a 748% increase in the number of pregnant and breastfeeding women starting ART, from 1,257 in the second quarter of 2011 (representing 5% of all new ART initiations) to 10,663 in the third quarter of 2012 (35% of all new ART initiations) (Figure 2). Of the women starting ART in the third quarter of 2011 (the first quarter of Option B+ implementation) who did not transfer care during follow up, 77% continue to receive ART at 12 months (Figure 3). This rate is similar to the 80% 12-month ART retention rate observed among adults who initiated ART in the second quarter of 2011 (the last quarter before Option B+ implementation). Editorial Note In June 2011, PEPFAR (under the leadership of OGAC) and the Joint United Nations Program on HIV/AIDS launched a global plan to virtually eliminate mother-to-child transmission of HIV with the goal of reducing new HIV infections in children by 90% by 2015.§ In Malawi, under the new policy, the number of pregnant and breastfeeding women started on ART has increased and the retention rate has remained similar to the rate for adults continuing to receive ART at 12 months before Option B+ implementation. Option B+ is an important innovation that could accelerate progress in Malawi and other countries toward the goal of eliminating mother-to-child transmission of HIV worldwide. Barriers to ART provision for pregnant women in resource-limited settings include the need for CD4 cell count, distance between ANC sites where HIV diagnosis is made and ART sites where treatment is started, transportation costs, and human resource constraints that lead to long waiting times and scheduling difficulties (3). The removal of the barrier of CD4 cell count, decentralization of ART into all ANC sites, and the training of nearly all nurses and clinical officers on the new integrated PMTCT/ART guidelines facilitated the increase in the number of pregnant and breastfeeding women started on ART. Implementation of Option B+ in Malawi enabled women to receive ART and ANC services in the same clinic and from the same provider without adversely affecting retention in care. The seven-fold increase in the number of pregnant and breastfeeding women started on ART per quarter during the first year of Option B+ has multiple potential benefits to mothers, their partners, and their children. For women, ART provides protection for their own health and, therefore, with expansion of ART coverage, a substantial reduction in mortality through the postpartum period can be expected (7,8). For HIV-uninfected sexual partners, ART offers protection from HIV transmission. In Malawi, one third of HIV-infected women are estimated to be in stable relationships with HIV-uninfected partners; studies suggest a substantial reduction in HIV transmission within these relationships in the setting of effective ART (6,9). For children of current and future pregnancies, ART provides protection from HIV infection during pregnancy and breastfeeding. The mother-to-child transmission rate for women on ART is expected to be reduced, from approximately 40% without intervention to less than 5%. With PEPFAR funding, CDC is supporting a nationally representative prospective evaluation to estimate the mother-to-child transmission rate in Malawi (1). Important challenges and questions remain. Evaluations to assess the cost-effectiveness of this approach are needed, and although 12-month retention rates are reassuring, lifelong ART adherence will need to be maintained. Although high-quality HIV testing is accepted by nearly all women at ANC in resource-limited settings, the Malawi MOH estimates that failure to ascertain maternal HIV status at ANC is now responsible for 54% of new infant infections in Malawi, likely as a result of irregular availability of test kits and poor quality assurance of rapid testing at ANC sites. (10; Frank Chimbwandira, Malawi MOH, personal communication, 2012). With PEPFAR funding, CDC is supporting birth defects surveillance in Malawi and elsewhere because limited data currently are available on the possible adverse effects of efavirenz-based ART regimens on infants exposed in early gestation (5). The success of Option B+ in increasing ART coverage demonstrates the combined effect of streamlined ART initiation, decentralized and integrated service delivery, policy changes to allow nurses to start ART, and direct supervision of every site. Continued progress in Malawi demands consistent provision of high-quality HIV testing in ANC and continuing efforts to ensure lifelong ART adherence among women started on ART through Option B+. What is already known on this topic? Mother-to-child transmission of human immunodeficiency virus (HIV) can be reduced to less than 5% with antiretroviral medications. However many HIV-infected pregnant and breastfeeding women in sub-Saharan Africa still do not receive services to prevent transmission to their infants. An important barrier is the limited laboratory capacity for CD4 cell count, which is recommended by the World Health Organization to determine which antiretroviral medications to start in pregnant and breastfeeding women. What is added by this report? In 2011, Malawi implemented a new policy (Option B+) to provide all HIV-infected pregnant and breastfeeding women with lifelong antiretroviral therapy (ART) regardless of CD4 count. The number of pregnant and breastfeeding women started on ART increased by 748%, from 1,257 in the second quarter of 2011 (before Option B+ implementation) to 10,663 in the third quarter of 2012 (1 year after implementation). What are the implications for public health practice? Option B+ is an important innovation that could accelerate progress in Malawi and other countries toward the goal of eliminating mother-to-child transmission of HIV worldwide.
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              The Tingathe programme: a pilot intervention using community health workers to create a continuum of care in the prevention of mother to child transmission of HIV (PMTCT) cascade of services in Malawi

              Introduction Loss to follow-up is a major challenge in the prevention of mother to child transmission of HIV (PMTCT) programme in Malawi with reported loss to follow-up of greater than 70%. Tingathe-PMTCT is a pilot intervention that utilizes dedicated community health workers (CHWs) to create a complete continuum of care within the PMTCT cascade, improving service utilization and retention of mothers and infants. We describe the impact of the intervention on longitudinal care starting with diagnosis of the mother at antenatal care (ANC) through final diagnosis of the infant. Methods PMTCT service utilization, programme retention and outcomes were evaluated for pregnant women living with HIV and their exposed infants enrolled in the Tingathe-PMTCT programme between March 2009 and March 2011. Multivariate logistic regression was done to evaluate maternal factors associated with failure to complete the cascade. Results Over 24 months, 1688 pregnant women living with HIV were enrolled. Median maternal age was 27 years (IQR, 23.8 to 30.8); 333 (19.7%) were already on ART. Among the remaining women, 1328/1355 (98%) received a CD4 test, with 1243/1328 (93.6%) receiving results. Of the 499 eligible for ART, 363 (72.8%) were successfully initiated. Prior to, delivery there were 93 (5.7%) maternal/foetal deaths, 137 (8.1%) women transferred/moved, 51 (3.0%) were lost and 58 (3.4%) refused ongoing PMTCT services. Of the 1318 live births to date, 1264 (95.9%) of the mothers and 1285 (97.5%) of the infants received ARV prophylaxis; 1064 (80.7%) infants were tested for HIV by PCR and started on cotrimoxazole. Median age at PCR was 1.7 months (IQR, 1.5 to 2.5). Overall transmission at first PCR was 43/1047 (4.1%). Of the 43 infants with positive PCR results, 36 (83.7%) were enrolled in ART clinic and 33 (76.7%) were initiated on ART. Conclusions Case management and support by dedicated CHWs can create a continuum of longitudinal care in the PMTCT cascade and result in improved outcomes.
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                Author and article information

                Journal
                J Acquir Immune Defic Syndr
                J. Acquir. Immune Defic. Syndr
                qai
                Journal of Acquired Immune Deficiency Syndromes (1999)
                JAIDS Journal of Acquired Immune Deficiency Syndromes
                1525-4135
                1944-7884
                15 April 2015
                11 March 2015
                : 68
                : 5
                : e77-e83
                Affiliations
                [* ]Baylor International Pediatric AIDS Initiative at Texas Children's Hospital, Houston, TX;
                []Baylor College of Medicine-Abbott Fund Children's Clinical Center of Excellence, Lilongwe, Malawi;
                []University of North Carolina School of Medicine, Chapel Hill, NC;
                [§ ]UNC Project, Lilongwe, Malawi;
                []Department of Medicine, Baylor College of Medicine, Houston, TX;
                []Department of Pediatrics, Epidemiology Center, Baylor College of Medicine, Houston, TX;
                [# ]Department of HIV and AIDS, Ministry of Health, Lilongwe, Malawi;
                [** ]ICAP-Columbia University, Mailman School of Public Health, New York, NY; and
                [†† ]College of Physicians and Surgeons, Columbia University, New York, NY.
                Author notes
                Correspondence to: Maria H. Kim, MD, Private Bag B-397, Baylor College of Medicine Children's Foundation Malawi, Lilongwe 3, Malawi (e-mail: mhkim@ 123456bcm.edu ).
                Article
                QAIV14728 00019
                10.1097/QAI.0000000000000517
                4359035
                25585302
                e9fd1603-d4f7-46c9-9d85-f6fb4399a7dc
                Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved.

                This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially.

                History
                : 08 August 2014
                : 11 November 2014
                Categories
                Epidemiology and Prevention
                Custom metadata
                ONLINE-ONLY
                TRUE

                hiv,pmtct,option b+,retention,malawi,africa
                hiv, pmtct, option b+, retention, malawi, africa

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