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Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial.
Pereira, Stacey; Smith, Hadley Stevens; Frankel, Leslie A; Christensen, Kurt D; Islam, Rubaiya; Robinson, Jill Oliver; Genetti, Casie A; Blout Zawatsky, Carrie L; Zettler, Bethany; Parad, Richard B; Waisbren, Susan E; Beggs, Alan H; Green, Robert C; Holm, Ingrid A; McGuire, Amy L.
Affiliation
  • Pereira S; Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas.
  • Smith HS; Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas.
  • Frankel LA; Department of Psychological, Health, and Learning Sciences, University of Houston, Houston, Texas.
  • Christensen KD; Department of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, Massachusetts.
  • Islam R; Department of Population Medicine, Harvard Medical School, Boston, Massachusetts.
  • Robinson JO; Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Genetti CA; Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas.
  • Blout Zawatsky CL; Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas.
  • Zettler B; Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts.
  • Parad RB; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts.
  • Waisbren SE; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
  • Beggs AH; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
  • Green RC; Department of Pediatric Newborn Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
  • Holm IA; Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts.
  • McGuire AL; Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
JAMA Pediatr ; 175(11): 1132-1141, 2021 11 01.
Article in En | MEDLINE | ID: mdl-34424265
ABSTRACT
Importance Newborn genomic sequencing (nGS) may provide health benefits throughout the life span, but there are concerns that it could also have an unfavorable (ie, negative) psychosocial effect on families.

Objective:

To assess the psychosocial effect of nGS on families from the BabySeq Project, a randomized clinical trial evaluating the effect of nGS on the clinical care of newborns from well-baby nurseries and intensive care units. Design, Setting, and

Participants:

In this randomized clinical trial conducted from May 14, 2015, to May 21, 2019, at well-baby nurseries and intensive care units at 3 Boston, Massachusetts, area hospitals, 519 parents of 325 infants completed surveys at enrollment, immediately after disclosure of nGS results, and 3 and 10 months after results disclosure. Statistical analysis was performed on a per-protocol basis from January 16, 2019, to December 1, 2019. Intervention Newborns were randomized to receive either standard newborn screening and a family history report (control group) or the same plus an nGS report of childhood-onset conditions and highly actionable adult-onset conditions (nGS group). Main Outcomes and

Measures:

Mean responses were compared between groups and, within the nGS group, between parents of children who received a monogenic disease risk finding and those who did not in 3 domains of psychosocial impact parent-child relationship (Mother-to-Infant Bonding Scale), parents' relationship (Kansas Marital Satisfaction Scale), and parents' psychological distress (Edinburgh Postnatal Depression Scale anxiety subscale).

Results:

A total of 519 parents (275 women [53.0%]; mean [SD] age, 35.1 [4.5] years) were included in this study. Although mean scores differed for some outcomes at singular time points, generalized estimating equations models did not show meaningful differences in parent-child relationship (between-group difference in adjusted mean [SE] Mother-to-Infant Bonding Scale scores postdisclosure, 0.04 [0.15]; 3 months, -0.18 [0.18]; 10 months, -0.07 [0.20]; joint P = .57) or parents' psychological distress (between-group ratio of adjusted mean [SE] Edinburgh Postnatal Depression Scale anxiety subscale scores postdisclosure, 1.04 [0.08]; 3 months, 1.07 [0.11]; joint P = .80) response patterns between study groups over time for any measures analyzed in these 2 domains. Response patterns on one parents' relationship measure differed between groups over time (between-group difference in adjusted mean [SE] Kansas Marital Satisfaction Scale scores postdisclosure, -0.19 [0.07]; 3 months, -0.04 [0.07]; and 10 months, -0.01 [0.08]; joint P = .02), but the effect decreased over time and no difference was observed on the conflict measure responses over time. We found no evidence of persistent negative psychosocial effect in any domain. Conclusions and Relevance In this randomized clinical trial of nGS, there was no persistent negative psychosocial effect on families among those who received nGS nor among those who received a monogenic disease risk finding for their infant. Trial Registration ClinicalTrials.gov Identifier NCT02422511.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parents / Neonatal Screening / Exome Sequencing Type of study: Clinical_trials / Guideline / Prognostic_studies / Qualitative_research Limits: Adult / Female / Humans / Male / Newborn Language: En Journal: JAMA Pediatr Year: 2021 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parents / Neonatal Screening / Exome Sequencing Type of study: Clinical_trials / Guideline / Prognostic_studies / Qualitative_research Limits: Adult / Female / Humans / Male / Newborn Language: En Journal: JAMA Pediatr Year: 2021 Type: Article