Improving the consent process for pregnant mothers at risk of preterm delivery

改善有早产风险的孕妇的同意程序

• 批准号: 8918710
• 负责人: Frank Xavier Placencia
• 金额: $ 12.38万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-09-01 至 2019-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8918710
• 关键词: Address; Affect; Caregivers; Caring; Child; Clinical; Consent; Counseling; Data; Decision Making; Development; Discipline of obstetrics; Education; Educational Models; Environment; Environment Design; Ethical Theory; Ethicists; Ethics; Family; Fetal Development; Fetus; Future; Goals; Health; Hospitals; Infant; Infant Health; Informed Consent; Knowledge; Life; Long-Term Care; Long-Term Effects; Medical; Mentors; Modeling; Mothers; Nature; Neonatal; Outcome; Parents; Patients; Perinatal; Physicians; Pregnancy; Pregnant Women; Premature Birth; Premature Infant; Process; Qualifying; Reporting; Research; Research Design; Research Institute; Research Personnel; Resuscitation; Risk; Series; Shapes; Staging; Surveys; career development; congenital anomaly; end of life; evidence base; high risk infant; improved; interest; life-sustaining therapy; patient population; post intervention; pregnant; premature; prenatal; programs; prospective; satisfaction; skills

DESCRIPTION (provided by applicant): Candidate and environment: Dr. Placencia is an accomplished investigator in neonatal ethics. His long term goal is to become an independent investigator who uses empiric evidence to change, modify, or support the normative ethical standards. He has identified a mentor who pioneered this approach, the support of a premiere research institute and clinical environment, and designed a career development program to augment his research skills and expertise in ethics. With these critical components, he will be uniquely qualified to achieve his goals. Objective: Develop an ethical model for parental perinatal decision making about the care of high-risk infants, and develop a clinical model by which parental decision making may be improved. Study Design: SA 1: Develop an evidence based critical appraisal of the Best Interests Standard (BIS). SA 1.1: Survey parents of high risk infants to determine what information they want regarding the familial impact of providing long term care, how such information would have shaped their decision-making, and whether it would have been appropriate for them to consider these effects? SA 1.2: Defend an empirically and ethically justified critical appraisal of the BIS by incorporating data gathered in our previou surveys on the conceptualization of the BIS and in SA1.1. SA 2: Develop, assess, and disseminate a data-driven, ethically justified model for prenatal education of pregnant women and their partners on the consequences to the infant of premature delivery. SA 2.1: Create of a series of educational videos for pregnant women at 18-30 weeks gestation and their partners, describing the current stage of fetal development and what to expect if the fetus delivers premature. SA 2.2: Determine the efficacy of the video on parental knowledge via pre- and post- assessments. SA 2.3: Assess maternal satisfaction with educational impact via post intervention survey. SA 2.4: Assess impact on decision making regarding resuscitation or life sustaining therapy (LST) amongst patients who deliver prematurely at 22-26 weeks. SA 2.5: Assess physicians' satisfaction with educational impact for parents of infants born between 22-34 weeks and impact on decisions regarding resuscitation or LST for infants born at 22-26 weeks. Future RO1: SA 3: Adaption of our model of prenatal education for non-academic obstetric settings. Future RO1: SA 4: Expand the study of the video's impact on parental decision making. Future RO1: SA 5: Adaption of the model for parents of infants with known congenital anomalies.

描述（由申请人提供）：候选人和环境：Placencia博士是一位有成就的新生儿伦理学研究者。他的长期目标是成为一名独立的研究者，利用经验证据来改变、修改或支持规范性的伦理标准。他已经确定了一位开创这种方法的导师，一个一流的研究机构和临床环境的支持，并设计了一个职业发展计划，以增强他的研究技能和伦理方面的专业知识。有了这些关键因素，他将是唯一有资格实现他的目标的人。目的：建立高危儿围生期父母护理决策的伦理模型，并建立改善父母决策的临床模型。研究设计：SA 1：对最佳利益标准（BIS）进行基于证据的批判性评估。SA 1.1：调查高危父母