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多中心试验中豁免产前同意的受试者的围产期结局。

Perinatal Outcomes of Subjects Enrolled in a Multicenter Trial with a Waiver of Antenatal Consent.

机构信息

Neonatal Research Institute, Sharp Mary Birch Hospital for Women & Newborns, San Diego, California.

Department of Biostatistics, The UAB School of Public Health, Birmingham, Alabama.

出版信息

Am J Perinatol. 2022 Jun;39(8):904-908. doi: 10.1055/s-0040-1719184. Epub 2020 Nov 3.

Abstract

OBJECTIVE

This study aimed to determine whether outcomes differed between infants enrolled in the PREMOD2 trial and those otherwise eligible but not enrolled, and whether the use of waiver effected these differences.

STUDY DESIGN

The multicenter PREMOD2 (PREmature infants receiving Milking Or Delayed cord clamping) trial was approved for waiver of antenatal consent by six of the nine sites institutional review boards, while three sites exclusively used antenatal consent. Every randomized subject delivered at a site with a waiver of consent was approached for postnatal consent to allow for data collection. Four of those six sites IRBs required the study team to attempt antenatal consent when possible. Three sites exclusively used antenatal consent.

RESULTS

Enrolled subjects had higher Apgar scores, less use of positive pressure ventilation, a lower rate of bronchopulmonary dysplasia, and a less frequent occurrence of the combined outcome of severe intraventricular hemorrhage or death. A significantly greater number of infants were enrolled at sites with an option of waiver of consent (66 vs. 26%, risk ratio = 2.54,  < 0.001). At sites with an option of either approaching families before delivery or after delivery with a waiver of antenatal consent, those approached prior to delivery refused consent 40% (range 15-74% across six sites) of the time.

CONCLUSION

PREMOD2 trial demonstrated analytical validity limitations because of the variable mix of antenatal consent and waiver of consent. A waiver of antenatal consent for minimal risk interventional trials conducted during the intrapartum period will be more successful in enrolling a representative sample of low and high-risk infants if investigators are able to enroll all eligible subjects.

CLINICAL TRIAL REGISTRATION

ClinicalTrials.gov identifier: NCT03019367.

KEY POINTS

· Waiver of consent is when informed consent cannot be obtained prior to delivery.. · Cord milking is a procedure in which blood is pushed (stripped) two to four times towards the newborn.. · Delayed clamping means the umbilical cord is not clamped immediately after birth..

摘要

目的

本研究旨在确定参加 PREMOD2 试验的婴儿与其他符合条件但未参加试验的婴儿的结局是否存在差异,以及是否使用豁免对这些差异产生影响。

研究设计

多中心 PREMOD2(早产婴儿接受挤奶或延迟脐带夹闭)试验获得了 9 个研究中心中 6 个机构审查委员会的产前同意豁免批准,而 3 个中心仅使用产前同意。在使用豁免的研究中心中,每一位随机分娩的婴儿都被要求在产后同意参与研究,以收集数据。这 6 个中心中有 4 个要求研究团队在可能的情况下尝试进行产前同意。3 个中心仅使用产前同意。

结果

纳入的婴儿具有更高的 Apgar 评分,较少使用正压通气,支气管肺发育不良的发生率更低,且严重脑室内出血或死亡的联合结局发生频率更低。在可以选择豁免同意的中心,入组婴儿的数量明显更多(66% vs. 26%,风险比=2.54,<0.001)。在可以选择在分娩前或分娩后通过豁免获得同意的中心中,在分娩前与家属接触的中心中,40%的家庭(6 个中心的比例范围为 15%-74%)拒绝了同意。

结论

PROMOD2 试验因产前同意和豁免同意的混合方式而存在分析有效性的局限性。如果研究人员能够招募所有符合条件的婴儿,那么在分娩期间进行的低风险干预性试验中,选择豁免产前同意的方式将更有可能成功招募到具有代表性的低危和高危婴儿样本。

临床试验注册

ClinicalTrials.gov 标识符:NCT03019367。

关键点

· 豁免同意是指在分娩前无法获得知情同意的情况下。· 脐带挤奶是一种将血液(挤出)向新生儿方向推送两到四次的过程。· 延迟夹闭是指脐带在出生后不立即夹闭。

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