孕妇和临床医生对无创产前检查的看法:系统综述和定性荟萃综合。

Q1 Medicine Ontario Health Technology Assessment Series Pub Date : 2019-02-19 eCollection Date: 2019-01-01
Meredith Vanstone, Alexandra Cernat, Umair Majid, Forum Trivedi, Chanté De Freitas
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引用次数: 0

摘要

背景:孕妇有携带受染色体异常影响的胎儿的风险。为孕妇提供产前筛查以评估其风险。近年来,临床上引入了无创产前检测(NIPT),它利用母体血液中循环的无细胞胎儿DNA来量化染色体异常的风险。目前,NIPT是为染色体异常高风险妊娠提供公共资助的,如果风险中等的孕妇选择自掏腰包,他们可以使用NIPT。方法:我们对初级实证定性研究进行了系统回顾,该研究描述了孕妇、其家人、临床医生和其他有NIPT相关生活经验的人的经历和观点。我们对这些群体的信仰、经历、偏好和观点感兴趣。我们使用定性荟萃综合的综合技术分析了36项定性和混合方法研究中的可用证据。结果:大多数人(孕妇、临床医生和其他有相关生活经验的人)表示,NIPT为孕妇及其伴侣提供了重要信息。大多数人都非常热衷于扩大NIPT的使用范围,因为它可以在怀孕早期提供染色体异常的信息,具有相对较高的准确性,并且没有与手术相关的妊娠损失风险。然而,许多团体警告说,扩大NIPT的使用范围可能会导致这种检测的常规化,对孕妇、他们的家人、医疗保健系统、残疾人和整个社会造成潜在伤害。扩大后勤、财务、情感和信息访问可能被视为一种好处,但也可能对各种群体造成伤害。其中许多挑战与历史上对其他形式产前检测的批评相呼应,其中一些问题因NIPT的特殊特征而减轻或加剧。结论:无创产前检测为孕妇提供了显著的益处,但也可能与知情决策、不公平使用、检测的社会压力以及对残疾人的支持减少等潜在危害有关。
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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Perspectives of Pregnant People and Clinicians on Noninvasive Prenatal Testing: A Systematic Review and Qualitative Meta-synthesis.

Background: Pregnant people have a risk of carrying a fetus affected by a chromosomal anomaly. Prenatal screening is offered to pregnant people to assess their risk. In recent years, noninvasive prenatal testing (NIPT) has been introduced clinically, which uses the presence of circulating cell-free fetal DNA in the maternal blood to quantify the risk of a chromosomal anomaly. At present, NIPT is publicly funded for pregnancies at high risk of a chromosomal anomaly, and available to pregnant people at average risk if they choose to pay out of pocket.

Methods: We performed a systematic review of primary, empirical qualitative research that describes the experiences and perspectives of pregnant people, their families, clinicians, and others with lived experience relevant to NIPT. We were interested in the beliefs, experiences, preferences, and perspectives of these groups. We analyzed the evidence available in 36 qualitative and mixed-methods studies using the integrative technique of qualitative meta-synthesis.

Results: Most people (pregnant people, clinicians, and others with relevant lived experience) said that NIPT offered important information to pregnant people and their partners. Most people were very enthusiastic about widening access to NIPT because it can provide information about chromosomal anomalies quite early in pregnancy, with relatively high accuracy, and without risk of procedure-related pregnancy loss. However, many groups cautioned that widening access to NIPT may result in routinization of this test, causing potential harm to pregnant people, their families, the health care system, people living with disabilities, and society as a whole. Widened logistical, financial, emotional, and informational access may be perceived as a benefit, but it can also confer harm on various groups. Many of these challenges echo historical critiques of other forms of prenatal testing, with some issues mitigated or exacerbated by the particular features of NIPT.

Conclusions: Noninvasive prenatal testing offers significant benefit for pregnant people but may also be associated with potential harms related to informed decision-making, inequitable use, social pressure to test, and reduced support for people with disabilities.

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来源期刊
Ontario Health Technology Assessment Series
Ontario Health Technology Assessment Series Medicine-Medicine (miscellaneous)
CiteScore
4.60
自引率
0.00%
发文量
0
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