Sandelowski Margarete, Barroso Julie
University of North Carolina at Chapel Hill, School of Nursing, NC 27599, USA.
J Obstet Gynecol Neonatal Nurs. 2005 May-Jun;34(3):307-18. doi: 10.1177/0884217505276291.
To integrate the findings of qualitative studies of expectant parents receiving positive prenatal diagnosis.
Seventeen published and unpublished reports appearing between 1984 and 2001 and retrieved between December of 2002 and March of 2003. The electronic databases searched include Academic Search Elite, AIDS Information Online (AIDSLINE), Anthropological Index Online, Anthropological Literature, Black Studies, Cumulative Index to Nursing and Allied Health Literature (CINAHL), Digital Dissertations, Dissertation Abstracts Index (DAI), Educational Resource Information Center (ERIC), MEDLINE, PsycInfo, Public Affairs Information Service (PAIS), PubMed, Social Science Abstracts (SocSci Abstracts), Social Science Citation Index, Social Work Abstracts, Sociological Abstracts (Sociofile), Women's Resources International, and Women's Studies.
Qualitative studies involving expectant parents living in the United States of any race, ethnicity, nationality, or class who learned during any time in pregnancy of any fetal impairment by any means of diagnosis were eligible for inclusion.
Metasummary techniques, including the calculation of frequency effect sizes, were used to aggregate the findings. Metasynthesis techniques, including constant comparison analysis and the reciprocal translation of concepts, were used to interpret the findings.
The topical emphasis in the findings is on the termination of pregnancy following positive diagnosis. The thematic emphasis is on the dilemmas of choice and decision making. Positive prenatal diagnosis was for couples an experience of chosen losses and lost choices. Couples managed information to minimize stigmatization and cognitive dissonance.
Existing guidelines for caring for couples after perinatal losses must accommodate the chosen loss experientially defining positive prenatal diagnosis.
整合对接受产前阳性诊断的准父母进行定性研究的结果。
1984年至2001年间发表和未发表的17份报告,于2002年12月至2003年3月间检索获得。检索的电子数据库包括学术搜索精英版、艾滋病信息在线(AIDSLINE)、在线人类学索引、人类学文献、黑人研究、护理及相关健康文献累积索引(CINAHL)、数字学位论文、学位论文摘要索引(DAI)、教育资源信息中心(ERIC)、医学文献数据库(MEDLINE)、心理学文摘数据库(PsycInfo)、公共事务信息服务(PAIS)、医学期刊数据库(PubMed)、社会科学文摘(SocSci Abstracts)、社会科学引文索引、社会工作文摘、社会学文摘(Sociofile)、国际妇女资源库和妇女研究数据库。
涉及居住在美国的任何种族、族裔、国籍或阶层的准父母的定性研究,这些准父母在孕期的任何时间通过任何诊断手段得知胎儿有任何损伤,均符合纳入标准。
采用元总结技术,包括计算频率效应量,对研究结果进行汇总。采用元综合技术,包括持续比较分析和概念的相互翻译,对研究结果进行解读。
研究结果在主题上强调阳性诊断后的妊娠终止。在专题上强调选择和决策的困境。对夫妇来说,产前阳性诊断是一种有选择的损失和失去选择的经历。夫妇们管理信息以尽量减少污名化和认知失调。
现有的围产期损失后照顾夫妇的指南必须考虑到有选择的损失,这在经验上界定了产前阳性诊断。