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Parents’ Psychological and Decision-Making Outcomes following Prenatal Diagnosis with Complex Congenital Heart Defect: An Exploratory Study

Background. Parents with a fetus diagnosed with a complex congenital heart defect (CHD) are at high risk of negative psychological outcomes. Purpose. To explore whether parents’ psychological and decision-making outcomes differed based on their treatment decision and fetus/neonate survival status. M...

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Autores principales: Thorpe, Alistair, Delaney, Rebecca K., Pinto, Nelangi M., Ozanne, Elissa M., Pershing, Mandy L., Hansen, Lisa M., Lambert, Linda M., Fagerlin, Angela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619352/
https://www.ncbi.nlm.nih.gov/pubmed/37920604
http://dx.doi.org/10.1177/23814683231204551
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author Thorpe, Alistair
Delaney, Rebecca K.
Pinto, Nelangi M.
Ozanne, Elissa M.
Pershing, Mandy L.
Hansen, Lisa M.
Lambert, Linda M.
Fagerlin, Angela
author_facet Thorpe, Alistair
Delaney, Rebecca K.
Pinto, Nelangi M.
Ozanne, Elissa M.
Pershing, Mandy L.
Hansen, Lisa M.
Lambert, Linda M.
Fagerlin, Angela
author_sort Thorpe, Alistair
collection PubMed
description Background. Parents with a fetus diagnosed with a complex congenital heart defect (CHD) are at high risk of negative psychological outcomes. Purpose. To explore whether parents’ psychological and decision-making outcomes differed based on their treatment decision and fetus/neonate survival status. Methods. We prospectively enrolled parents with a fetus diagnosed with a complex, life-threatening CHD from September 2018 to December 2020. We tested whether parents’ psychological and decision-making outcomes 3 months posttreatment differed by treatment choice and survival status. Results. Our sample included 23 parents (average Age([years]): 27 ± 4, range = 21–37). Most were women (n = 18), non-Hispanic White (n = 20), and married (n = 21). Most parents chose surgery (n = 16), with 11 children surviving to the time of the survey; remaining parents (n = 7) chose comfort-directed care. Parents who chose comfort-directed care reported higher distress ( [Formula: see text]  = 1.51, s = 0.75 v. [Formula: see text]  = 0.74, s = 0.55; Mdifference = 0.77, 95% confidence interval [CI], 0.05–1.48) and perinatal grief ( [Formula: see text]  = 91.86, s = 22.96 v. [Formula: see text]  = 63.38, s = 20.15; Mdifference = 27.18, 95% CI, 6.20–48.16) than parents who chose surgery, regardless of survival status. Parents who chose comfort-directed care reported higher depression ( [Formula: see text]  = 1.64, s = 0.95 v. [Formula: see text]  = 0.65, s = 0.49; Mdifference = 0.99, 95% CI, 0.10–1.88) than parents whose child survived following surgery. Parents choosing comfort-directed care reported higher regret ( [Formula: see text]  = 26.43, s = 8.02 v. [Formula: see text]  = 5.00, s = 7.07; Mdifference = 21.43, 95% CI, 11.59–31.27) and decisional conflict ( [Formula: see text]  = 20.98, s = 10.00 v. [Formula: see text]  = 3.44, s = 4.74; Mdifference = 17.54, 95% CI; 7.75–27.34) than parents whose child had not survived following surgery. Parents whose child survived following surgery reported lower grief (Mdifference = −19.71; 95% CI, −39.41 to −0.01) than parents whose child had not. Conclusions. The results highlight the potential for interventions and care tailored to parents’ treatment decisions and outcomes to support parental coping and well-being. HIGHLIGHTS: Question: Do the psychological and decision-making outcomes of parents differ based on their treatment decision and survival outcome following prenatal diagnosis with complex CHD? Findings: In this exploratory study, parents who decided to pursue comfort-directed care after a prenatal diagnosis reported higher levels of psychological distress and grief as well as higher decisional conflict and regret than parents who decided to pursue surgery. Meaning: The findings from this exploratory study highlight potential differences in parents’ psychological and decision-making outcomes following a diagnosis of complex CHD for their fetus, which appear to relate to the treatment approach and the treatment outcome and may require tailoring of psychological and decision support.
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spelling pubmed-106193522023-11-02 Parents’ Psychological and Decision-Making Outcomes following Prenatal Diagnosis with Complex Congenital Heart Defect: An Exploratory Study Thorpe, Alistair Delaney, Rebecca K. Pinto, Nelangi M. Ozanne, Elissa M. Pershing, Mandy L. Hansen, Lisa M. Lambert, Linda M. Fagerlin, Angela MDM Policy Pract Original Research Article Background. Parents with a fetus diagnosed with a complex congenital heart defect (CHD) are at high risk of negative psychological outcomes. Purpose. To explore whether parents’ psychological and decision-making outcomes differed based on their treatment decision and fetus/neonate survival status. Methods. We prospectively enrolled parents with a fetus diagnosed with a complex, life-threatening CHD from September 2018 to December 2020. We tested whether parents’ psychological and decision-making outcomes 3 months posttreatment differed by treatment choice and survival status. Results. Our sample included 23 parents (average Age([years]): 27 ± 4, range = 21–37). Most were women (n = 18), non-Hispanic White (n = 20), and married (n = 21). Most parents chose surgery (n = 16), with 11 children surviving to the time of the survey; remaining parents (n = 7) chose comfort-directed care. Parents who chose comfort-directed care reported higher distress ( [Formula: see text]  = 1.51, s = 0.75 v. [Formula: see text]  = 0.74, s = 0.55; Mdifference = 0.77, 95% confidence interval [CI], 0.05–1.48) and perinatal grief ( [Formula: see text]  = 91.86, s = 22.96 v. [Formula: see text]  = 63.38, s = 20.15; Mdifference = 27.18, 95% CI, 6.20–48.16) than parents who chose surgery, regardless of survival status. Parents who chose comfort-directed care reported higher depression ( [Formula: see text]  = 1.64, s = 0.95 v. [Formula: see text]  = 0.65, s = 0.49; Mdifference = 0.99, 95% CI, 0.10–1.88) than parents whose child survived following surgery. Parents choosing comfort-directed care reported higher regret ( [Formula: see text]  = 26.43, s = 8.02 v. [Formula: see text]  = 5.00, s = 7.07; Mdifference = 21.43, 95% CI, 11.59–31.27) and decisional conflict ( [Formula: see text]  = 20.98, s = 10.00 v. [Formula: see text]  = 3.44, s = 4.74; Mdifference = 17.54, 95% CI; 7.75–27.34) than parents whose child had not survived following surgery. Parents whose child survived following surgery reported lower grief (Mdifference = −19.71; 95% CI, −39.41 to −0.01) than parents whose child had not. Conclusions. The results highlight the potential for interventions and care tailored to parents’ treatment decisions and outcomes to support parental coping and well-being. HIGHLIGHTS: Question: Do the psychological and decision-making outcomes of parents differ based on their treatment decision and survival outcome following prenatal diagnosis with complex CHD? Findings: In this exploratory study, parents who decided to pursue comfort-directed care after a prenatal diagnosis reported higher levels of psychological distress and grief as well as higher decisional conflict and regret than parents who decided to pursue surgery. Meaning: The findings from this exploratory study highlight potential differences in parents’ psychological and decision-making outcomes following a diagnosis of complex CHD for their fetus, which appear to relate to the treatment approach and the treatment outcome and may require tailoring of psychological and decision support. SAGE Publications 2023-10-31 /pmc/articles/PMC10619352/ /pubmed/37920604 http://dx.doi.org/10.1177/23814683231204551 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Article
Thorpe, Alistair
Delaney, Rebecca K.
Pinto, Nelangi M.
Ozanne, Elissa M.
Pershing, Mandy L.
Hansen, Lisa M.
Lambert, Linda M.
Fagerlin, Angela
Parents’ Psychological and Decision-Making Outcomes following Prenatal Diagnosis with Complex Congenital Heart Defect: An Exploratory Study
title Parents’ Psychological and Decision-Making Outcomes following Prenatal Diagnosis with Complex Congenital Heart Defect: An Exploratory Study
title_full Parents’ Psychological and Decision-Making Outcomes following Prenatal Diagnosis with Complex Congenital Heart Defect: An Exploratory Study
title_fullStr Parents’ Psychological and Decision-Making Outcomes following Prenatal Diagnosis with Complex Congenital Heart Defect: An Exploratory Study
title_full_unstemmed Parents’ Psychological and Decision-Making Outcomes following Prenatal Diagnosis with Complex Congenital Heart Defect: An Exploratory Study
title_short Parents’ Psychological and Decision-Making Outcomes following Prenatal Diagnosis with Complex Congenital Heart Defect: An Exploratory Study
title_sort parents’ psychological and decision-making outcomes following prenatal diagnosis with complex congenital heart defect: an exploratory study
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619352/
https://www.ncbi.nlm.nih.gov/pubmed/37920604
http://dx.doi.org/10.1177/23814683231204551
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