The Indonesian national family planning program: progress and remaining challenges in implementing a rights-based approach

IF 1.2 Q4 HEALTH POLICY & SERVICES
Budi Utomo, Sukma Rahayu, Elvira Liyanto, N. Romadlona, Dewi Nuryana, Riznawaty Imma Aryanty, Melania Hidayat, Anggraini Sariastuti, Maria Gayatri, R. Magnani
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Abstract

Purpose Indonesia subscribes to rights-based principles of family planning. However, a chasm between principles and practice has long been noted on a global basis, and progress has not been well-documented. This paper aims to assess the extent to which the Indonesian national family planning program has evolved in a manner that is consistent with rights-based principles. Design/methodology/approach The primary source of data was five Indonesian Demographic Health Surveys undertaken from 1997 to 2017. The analyses were organized around three major categories of family planning-related human rights. Trend analysis and logistic regression were used in analyzing the data. Findings Indonesian women have considerable autonomy in family planning decision, reporting that family planning decisions were mainly made by themselves or jointly with their spouse. Although contraceptive method awareness and demand for family planning are high, Indonesia fares poorly with regard to informed choice in contraceptive method selection. Access to family planning services is comparatively high as judged by contraceptive prevalence, family planning demand satisfaction and unmet need for family planning. However, significant geographic and socioeconomic inequity were observed on many indicators, with eastern Indonesian provinces consistently lagging behind. Research limitations/implications This paper focuses on married couple, as Indonesia has a restrictive policy to limiting access and information of family planning for other groups, unmarried youth in particular. Originality/value This paper makes an important contribution to document how effectively the prohuman rights policy orientation toward family planning has been translated into services.
印度尼西亚国家计划生育计划:在实施基于权利的方法方面取得的进展和依然面临的挑战
目的 印度尼西亚赞同基于权利的计划生育原则。然而,长期以来,全球范围内一直存在原则与实践之间的鸿沟,进展情况也没有得到很好的记录。本文旨在评估印尼国家计划生育计划在多大程度上符合以权利为本的原则。 设计/方法/途径 主要数据来源于 1997 年至 2017 年期间进行的五次印度尼西亚人口健康调查。分析围绕计划生育相关人权的三大类进行。在分析数据时使用了趋势分析和逻辑回归。 调查结果 印度尼西亚妇女在计划生育决策方面拥有相当大的自主权,她们表示计划生育决策主要由自己或与配偶共同做出。虽然对避孕方法的认识和对计划生育的需求很高,但印尼在避孕方法选择的知情选择方面表现不佳。从避孕普及率、计划生育需求满意度和未满足的计划生育需求来看,计划生育服务的普及率相对较高。然而,在许多指标上都发现了明显的地域和社会经济不平等,印尼东部省份一直处于落后状态。 研究局限性/意义 本文重点关注已婚夫妇,因为印尼的限制性政策限制了其他群体,尤其是未婚青年获得 计划生育的机会和信息。 独创性/价值 本文在记录支持人权的计划生育政策导向如何有效转化为服务方面做出了重要贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.90
自引率
7.10%
发文量
48
期刊介绍: nternational Journal of Human Rights in Healthcare (IJHRH) is an international, peer reviewed journal with a unique practical approach to promoting race equality, inclusion and human rights in health and social care. The journal publishes scholarly and double blind peer-reviewed papers of the highest standard, including case studies and book reviews. IJHRH aims include: -To explore what is currently known about discrimination and disadvantage with a particular focus on health and social care -Push the barriers of the human rights discourse by identifying new avenues for healthcare practice and policy internationally -Create bridges between policymakers, practitioners and researchers -Identify and understand the social determinants of health equity and practical interventions to overcome barriers at national and international levels. The journal welcomes papers which use varied approaches, including discussion of theory, comparative studies, systematic evaluation of interventions, analysis of qualitative data and study of health and social care institutions and the political process. Papers published in IJHRH: -Clearly demonstrate the implications of the research -Provide evidence-rich information -Provoke reflection and support critical analysis of both challenges and strengths -Share examples of best practice and ‘what works’, including user perspectives IJHRH is a hugely valuable source of information for researchers, academics, students, practitioners, managers, policy-makers, commissioning bodies, social workers, psychologists, nurses, voluntary sector workers, service users and carers internationally.
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