Peay Holly L, Gwaltney Angela You, Moultrie Rebecca, Cope Heidi, Boyea Beth Lincoln-, Porter Katherine Ackerman, Duparc Martin, Alexander Amir A, Biesecker Barbara B, Isiaq Aminah, Check Jennifer, Gehtland Lisa, Bailey Donald B, King Nancy M P
Genomics, Bioinformatics, and Translational Research Center, RTI International, Research Triangle Park, NC, Unites States.
Department of Biostatistics and Data Science, Wake Forest School of Medicine, Winston Salem, NC, United States.
Front Genet. 2022 May 12;13:891592. doi: 10.3389/fgene.2022.891592. eCollection 2022.
A challenge in implementing population-based DNA screening is providing sufficient information, that is, understandable and acceptable, and that supports informed decision making. Early Check is an expanded newborn screening study offered to mothers/guardians whose infants have standard newborn screening in North Carolina. We developed electronic education and consent to meet the objectives of feasibility, acceptability, trustworthiness, and supporting informed decisions. We used two methods to evaluate Early Check among mothers of participating infants who received normal results: an online survey and interviews conducted via telephone. Survey and interview domains included motivations for enrollment, acceptability of materials and processes, attitudes toward screening, knowledge recall, and trust. Quantitative analyses included descriptive statistics and assessment of factors associated with knowledge recall and trust. Qualitative data were coded, and an inductive approach was used to identify themes across interviews. Survey respondents ( = 1,823) rated the following as the most important reasons for enrolling their infants: finding out if the baby has the conditions screened (43.0%), and that no additional blood samples were required (20.1%). Interview respondents ( = 24) reported the value of early knowledge, early intervention, and ease of participation as motivators. Survey respondents rated the study information as having high utility for decision making (mean 4.7 to 4.8 out of 5) and 98.2% agreed that they had sufficient information. Knowledge recall was relatively high (71.8-92.5% correct), as was trust in Early Check information (96.2% strongly agree/agree). Attitudes about Early Check screening were positive (mean 0.1 to 0.6 on a scale of 0-4, with lower scores indicating more positive attitudes) and participants did not regret participation (e.g., 98.6% strongly agreed/agreed Early Check was the right decision). Interview respondents further reported positive attitudes about Early Check materials and processes. Early Check provides a model for education and consent in large-scale DNA screening. We found evidence of high acceptability, trustworthiness and knowledge recall, and positive attitudes among respondents. Population-targeted programs need to uphold practices that result in accessible information for those from diverse backgrounds. Additional research on those who do not select screening, although ethically and practically challenging, is important to inform population-based DNA screening practices.
实施基于人群的DNA筛查面临的一项挑战是提供足够的信息,即易于理解且可接受的信息,并支持明智的决策。早期检查是一项针对在北卡罗来纳州接受标准新生儿筛查的婴儿的母亲/监护人开展的扩展新生儿筛查研究。我们开发了电子教育和知情同意程序,以实现可行性、可接受性、可信度以及支持明智决策的目标。我们采用两种方法对参与研究且婴儿检查结果正常的母亲进行早期检查评估:在线调查和电话访谈。调查和访谈的领域包括参与动机、材料和流程的可接受性、对筛查的态度、知识记忆以及信任度。定量分析包括描述性统计以及对与知识记忆和信任度相关因素的评估。对定性数据进行编码,并采用归纳法确定访谈中的主题。调查受访者(n = 1823)将以下内容列为让婴儿参与研究的最重要原因:了解婴儿是否患有所筛查的疾病(43.0%),以及无需采集额外血样(20.1%)。访谈受访者(n = 24)表示,早期知晓、早期干预和参与的便利性是参与的动机。调查受访者认为研究信息对决策非常有用(平均分为4.7至4.8分,满分5分),98.2%的受访者同意他们已获得足够的信息。知识记忆相对较高(正确率为71.8 - 92.5%),对早期检查信息的信任度也较高(96.2%的受访者强烈同意/同意)。对早期检查筛查的态度是积极的(在0 - 4分的量表上平均分为0.1至0.6分,分数越低表明态度越积极),参与者不后悔参与(例如,98.6%的受访者强烈同意/同意早期检查是正确的决定)。访谈受访者进一步表示对早期检查的材料和流程持积极态度。早期检查为大规模DNA筛查中的教育和知情同意提供了一个模式。我们发现有证据表明受访者具有较高的可接受性、可信度和知识记忆,以及积极的态度。针对人群的项目需要坚持为不同背景的人提供可获取信息的做法。对那些未选择筛查的人群进行更多研究,尽管在伦理和实际操作上具有挑战性,但对于为基于人群的DNA筛查实践提供信息很重要。