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Essential medicines for reproductive health: developing evidence based interagency list

机译:生殖健康基本药物:建立基于证据的机构间清单

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id="__p1" class="p p-first">Objectives: Although poor reproductive health constitutes a significant proportion of the disease burden in developing countries, essential medicines for reproductive health are often not available to the population. The objective was to analyze the guiding principles for developing national Essential Medicines Lists (EML). The second objective was to compare the reproductive health medicines included on these EMLs to the 2002 WHO/UNFPA list of essential drugs and commodities for reproductive health. Another objective was to compare the medicines included in existing international lists of medicines for reproductive health. id="__p2">Methods: The authors calculated the average number of medicines per clinical groups included in 112 national EMLs and compared these average numbers with the number of medicines per clinical group included on the WHO/UNFPA List. Additionally, they compared the content of the lists of medicines for reproductive health developed by various international agencies. id="__p3">Results: In 2003, the review of the 112 EMLs highlighted that medicines for reproductive health were not consistently included. The review of the international lists identified inconsistencies in their recommendations. The reviews’ outcomes became the catalyst for collaboration among international agencies in the development of the first harmonized Interagency List of Essential Medicines for Reproductive Health. Additionally, WHO, UNFPA and PATH published guidelines to support the inclusion of essential medicines for reproductive health in national medicine policies and EMLs. The Interagency List became a key advocacy tool for countries to review their EMLs. id="__p4">In 2009, a UNFPA/WHO assessment on access to reproductive health medicines in six countries demonstrated that the major challenge was that the Interagency List had not been updated recently and was inconsistently used. id="__p5" class="p p-last">Conclusion: The addition of cost-effective medicines for reproductive health to EMLs can result in enhanced equity in access to and cost containment of these medicines, and improve quality of care. Action is required to ensure their inclusion in national budget lines, supply chains, policies and programmatic guidance.
机译:目标:尽管生殖健康不佳在发展中国家疾病负担中占很大比例,但人们往往无法获得基本的生殖健康药物。目的是分析制定国家基本药物清单(EML)的指导原则。第二个目标是将这些EML中包含的生殖健康药物与2002年WHO / UNFPA生殖健康基本药物和商品清单进行比较。另一个目的是比较现有的国际生殖健康药物清单中包含的药物。 id =“ __ p2”>方法:作者计算了112个国家EML中每个临床组的平均药物数量,并将这些平均数量与WHO / UNFPA清单中每个临床组的药物数量。此外,他们还比较了各个国际机构制定的生殖健康药物清单的内容。 id =“ __ p3”>结果:2003年,对112种EML进行了审查,结果表明,生殖健康药物并未得到一贯纳入。对国际清单的审查发现了其建议中的不一致之处。审查的结果成为国际机构之间在制定第一个统一的生殖健康基本药物机构间清单的过程中促进合作的催化剂。此外,世卫组织,人口基金和PATH出版了指导方针,以支持将生殖健康基本药物纳入国家医学政策和EML。 《机构间清单》成为各国审查其EML的主要宣传工具。 id =“ __ p4”> 2009年,人口基金/世卫组织对六个国家获取生殖健康药物的评估表明,主要挑战是《机构间清单》。 id =“ __ p5” class =“ p p-last”>结论:EML中添加具有成本效益的生殖健康药物可以提高获取和成本公平性控制这些药物,提高护理质量。需要采取行动确保将其纳入国家预算项目,供应链,政策和计划指南中。

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