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      Scaling Down to Scale Up: A Health Economic Analysis of Integrating Point-of-Care Syphilis Testing into Antenatal Care in Zambia during Pilot and National Rollout Implementation

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          Abstract

          Maternal syphilis results in an estimated 500,000 stillbirths and neonatal deaths annually in Sub-Saharan Africa. Despite the existence of national guidelines for antenatal syphilis screening, syphilis testing is often limited by inadequate laboratory and staff services. Recent availability of inexpensive rapid point-of-care syphilis tests (RST) can improve access to antenatal syphilis screening. A 2010 pilot in Zambia explored the feasibility of integrating RST within prevention of mother-to-child-transmission of HIV services. Following successful demonstration, the Zambian Ministry of Health adopted RSTs into national policy in 2011. Cost data from the pilot and 2012 preliminary national rollout were extracted from project records, antenatal registers, clinic staff interviews, and facility observations, with the aim of assessing the cost and quality implications of scaling up a successful pilot into a national rollout. Start-up, capital, and recurrent cost inputs were collected, including costs of extensive supervision and quality monitoring during the pilot. Costs were analysed from a provider’s perspective, incremental to existing antenatal services. Total and unit costs were calculated and a multivariate sensitivity analysis was performed. Our accompanying qualitative study by Ansbro et al. (2015) elucidated quality assurance and supervisory system challenges experienced during rollout, which helped explain key cost drivers. The average unit cost per woman screened during rollout ($11.16) was more than triple the pilot unit cost ($3.19). While quality assurance costs were much lower during rollout, the increased unit costs can be attributed to several factors, including higher RST prices and lower RST coverage during rollout, which reduced economies of scale. Pilot and rollout cost drivers differed due to implementation decisions related to training, supervision, and quality assurance. This study explored the cost of integrating RST into antenatal care in pilot and national rollout settings, and highlighted important differences in costs that may be observed when moving from pilot to scale-up.

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          Rapid tests for sexually transmitted infections (STIs): the way forward.

          In the developing world, laboratory services for sexually transmitted infections (STIs) are either not available, or where limited services are available, patients may not be able to pay for or physically access those services. Despite the existence of national policy for antenatal screening to prevent congenital syphilis and substantial evidence that antenatal screening is cost-effective, implementation of syphilis screening programmes remains unacceptably low because of lack of screening tools that can be used in primary health care settings. The World Health Organization Sexually Transmitted Diseases Diagnostics Initiative (SDI) has developed the ASSURED criteria as a benchmark to decide if tests address disease control needs: Affordable, Sensitive, Specific, User-friendly, Rapid and robust, Equipment-free and Deliverable to end-users. Rapid syphilis tests that can be used with whole blood approach the ASSURED criteria and can now be deployed in areas where no previous screening has been possible. Although rapid tests for chlamydia and gonorrhoea lack sensitivity, more tests are in development. The way forward for STI diagnostics requires a continuing quest for ASSURED tests, the development of a road map for test introduction, sustainable programmes for quality assurance, and the creation of a robust infrastructure linked to HIV prevention that ensures sustainability of STI control efforts that includes viral STIs.
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            Point-of-Care Tests to Strengthen Health Systems and Save Newborn Lives: The Case of Syphilis

            Rosanna Peeling and colleagues describe their experience of introducing point-of-care testing to screen for syphilis in pregnant women living in low- and middle-income countries.
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              Allowing for differential timing in cost analyses: discounting and annualization.

              There are differences in timing related to when costs of certain inputs are incurred and when they are used over the lifetime of a programme. This paper looks at the issues related to the comparison of cost data over time focusing on discounting and annualization adjustments, which are used by economists to calculate financial and economic costs. The process of discounting is used to deal with the notion of time preference. Time preference implies that future costs are worth less, and hence discounted more, to reflect individual and societal preferences to have resources and money now rather than in the future. While discounting is appropriate in many situations, it is also useful to compute an annual equivalent cost when recurrent costs of an intervention are incurred, or are expected to be incurred, in subsequent years. This approach has the added benefit of illustrating how capital items are actually used during the lifetime of an intervention. This paper presents methods to both discount and annualize costs, and discusses rules-of-thumb to decide when to make these adjustments.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                13 May 2015
                2015
                : 10
                : 5
                : e0125675
                Affiliations
                [1 ]Department of Epidemiology & Biostatistics, George Washington University School of Public Health, Washington, DC, United States of America
                [2 ]Department of Clinical Research, London School of Hygiene and Tropical Medicine, London, United Kingdom
                [3 ]Elizabeth Glaser Pediatric AIDS Foundation, Lusaka, Zambia
                [4 ]Department of Global Health and Development, London School of Hygiene and Tropical Medicine, London, United Kingdom
                [5 ]HIV/AIDS STI Programme, Ministry of Health, Lusaka, Zambia
                [6 ]Elizabeth Glaser Pediatric AIDS Foundation, Washington, DC, United States of America
                Johns Hopkins University, UNITED STATES
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: FTP RWP CF EMA S. Strasser. Performed the experiments: KDS S. Sweeney ATN CF EMA GTM MMG. Analyzed the data: KDS S. Sweeney CF ATN EMA. Contributed reagents/materials/analysis tools: FTP. Wrote the paper: KDS EMA FTP CF S. Sweeney. Reivew, revisions, and final manuscript approval: KDS EMA S. Strasser S. Sweeney GTM MMG CF ATN RWP FTP.

                [¤a]

                Current address: Department of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America

                [¤b]

                Current address: AME International, Vienna, Austria

                [¤c]

                Current address: ICAP program, Mailman School of Public Health, Columbia University, New York, New York, United States of America

                Article
                PONE-D-14-42724
                10.1371/journal.pone.0125675
                4430530
                25970443
                f8cc96b4-b4e5-4c2c-8642-d9f9b997036b
                Copyright @ 2015

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

                History
                : 24 September 2014
                : 25 March 2015
                Page count
                Figures: 2, Tables: 6, Pages: 19
                Funding
                The pilot study was funded from UNICEF/UNDP/World Bank/World Health Organization Special Programme for Research and Training in Tropical Diseases through a grant from the Bill & Melinda Gates Foundation (grant no. OPP 47697). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Custom metadata
                All data are available in the Supporting Information files or within the mansuscript.

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