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Immigrant parents’ experiences of accessing child healthcare services in a host country: A qualitative thematic synthesis

机译:移民父母在东道国访问儿童医疗保健服务的经历:定性专题合成

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Abstract Aim To explore voluntary immigrant parents’ experiences of child healthcare services in host countries. Design Thomas and Harden's qualitative thematic synthesis method. Data Sources Five electronic databases (CINAHL, Medline, PubMed, Psych INFO and Web of Science), were systematically searched from January 2000 ‐ October 2018. Review methods Included studies focused on voluntary migrant/immigrant parents’ experiences of child healthcare services. Data were abstracted independently by two authors. Critical Appraisal Skills Programme tools were applied, and qualitative thematic synthesis was performed. Findings Nine studies were eligible for inclusion. Five descriptive themes were identified: (a) seeking information and reassurance, (b) seeking information from "people like me”, (c) comparison between child healthcare services in home and host countries, (d) effective communication, and (e) cultural isolation and perceived discrimination. Three analytical themes emerged: navigation of parenting in a health context in a new environment; trust; and balance. Conclusions Many immigrant families reported positive experiences, others felt patronized and disrespected, leading to a lack of trust and making them less willing to access universal child health care. Trusted advocates, who are culturally competent, have a role in helping immigrant parents navigate the child healthcare system and negotiate with healthcare professionals. Health registration of children of immigrants may encourage the uptake of universal healthcare services. More research is required into the specific health needs of voluntary immigrants. Impact Less is known about the experiences of voluntary immigrants than those of refugees/asylum seekers in accessing child healthcare. Navigating health systems is difficult. This can be due to language difficulties, differences in systems of healthcare, and differences in culture/health beliefs. When both parties have some understanding of the others’ healthcare practices and beliefs, balance can be found; helping the families to positively compare healthcare and incentivising them to engage in universal child healthcare.
机译:摘要旨在探讨志愿移民父母在东道国儿童医疗保健服务的经验。设计托马斯和硬铭的定性专题合成方法。数据来源五届2000年10月 - 2018年10月系统地搜查了数据来源五个电子数据库(Cinahl,Medline,PubMed,PeSCOM,Scent),Schity Info和Web)。审查方法包括关于志愿移民/移民父母的儿童医疗保健服务的经验。数据由两位作者独立抽象。批判性评估技能计划工具进行了应用,并且进行了定性专题合成。调查结果九项研究有资格包含。确定了五个描述性主题:(a)寻求信息和保证,(b)寻求来自家庭和东道国儿童医疗保健服务的“像我这样的人”的信息,(d)有效沟通,(e)文化孤立与感知歧视他们不愿意进入普遍儿童保健。有信任的倡导者在文化上有能力,在帮助移民父母中致力于浏览儿童医疗保健系统并与医疗专业人士谈判。移民儿童的健康登记可能会鼓励对普遍医疗保健服务的吸收。需要更多的研究是志愿移民的特定健康需求。对较少的影响是已知的志愿移民的经验比难民/寻求庇护者在获取儿童医疗保健方面的经验。导航卫生系统很难。这可能是由于语言困难,医疗保健系统的差异以及文化/健康信念的差异。当双方都有一些了解其他人的医疗保健行为和信仰时,可以找到平衡;帮助家庭积极比较医疗保健并激励他们从事普遍儿童医疗保健。

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