Natale Joanne E, Lebet Ruth, Joseph Jill G, Ulysse Christine, Ascenzi Judith, Wypij David, Curley Martha A Q
Department of Pediatrics, University of California, Davis, CA.
Department of Family and Community Health, School of Nursing, University of Pennsylvania, Philadelphia, PA.
J Pediatr. 2017 May;184:204-208.e1. doi: 10.1016/j.jpeds.2017.02.006. Epub 2017 Mar 2.
To evaluate whether race or ethnicity was independently associated with parental refusal of consent for their child's participation in a multisite pediatric critical care clinical trial.
We performed a secondary analyses of data from Randomized Evaluation of Sedation Titration for Respiratory Failure (RESTORE), a 31-center cluster randomized trial of sedation management in critically ill children with acute respiratory failure supported on mechanical ventilation. Multivariable logistic regression modeling estimated associations between patient race and ethnicity and parental refusal of study consent.
Among the 3438 children meeting enrollment criteria and approached for consent, 2954 had documented race/ethnicity of non-Hispanic White (White), non-Hispanic Black (Black), or Hispanic of any race. Inability to approach for consent was more common for parents of Black (19.5%) compared with White (11.7%) or Hispanic children (13.2%). Among those offered consent, parents of Black (29.5%) and Hispanic children (25.9%) more frequently refused consent than parents of White children (18.2%, P < .0167 for each). Compared with parents of White children, parents of Black (OR 2.15, 95% CI 1.56-2.95, P < .001) and Hispanic (OR 1.44, 95% CI 1.10-1.88, P = .01) children were more likely to refuse consent. Parents of children offered participation in the intervention arm were more likely to refuse consent than parents in the control arm (OR 2.15, 95% CI 1.37-3.36, P < .001).
Parents of Black and Hispanic children were less likely to be approached for, and more frequently declined consent for, their child's participation in a multisite critical care clinical trial. Ameliorating this racial disparity may improve the validity and generalizability of study findings.
ClinicalTrials.gov: NCT00814099.
评估种族或族裔是否与父母拒绝同意其子女参与一项多中心儿科重症监护临床试验独立相关。
我们对呼吸衰竭镇静滴定随机评估(RESTORE)的数据进行了二次分析,RESTORE是一项在31个中心进行的关于机械通气支持的急性呼吸衰竭危重症儿童镇静管理的整群随机试验。多变量逻辑回归模型估计了患者种族和族裔与父母拒绝研究同意之间的关联。
在3438名符合入选标准并被征求同意的儿童中,2954名记录了种族/族裔为非西班牙裔白人(白人)、非西班牙裔黑人(黑人)或任何种族的西班牙裔。与白人(11.7%)或西班牙裔儿童(13.2%)的父母相比,黑人儿童的父母(19.5%)更常出现无法征求同意的情况。在那些被提供同意的人中,黑人儿童(29.5%)和西班牙裔儿童(25.9%)的父母比白人儿童的父母(18.2%,两者P均<0.0167)更频繁地拒绝同意(参与试验)。与白人儿童的父母相比,黑人儿童(比值比2.15,95%置信区间1.56 - 2.95,P<0.001)和西班牙裔儿童(比值比1.44,95%置信区间1.10 - 1.88,P = 0.01)的父母更有可能拒绝同意。被提供参与干预组的儿童的父母比对照组的父母更有可能拒绝同意(比值比2.15,95%置信区间1.37 - 3.36,P<0.001)。
黑人及西班牙裔儿童的父母被征求其子女参与多中心重症监护临床试验同意的可能性较小,且更频繁地拒绝同意。改善这种种族差异可能会提高研究结果的有效性和普遍性。
ClinicalTrials.gov:NCT00814099 。