“We needed this”: perspectives of parents and healthcare professionals involved in a pilot newborn screening program for spinal muscular atrophy

Background: Newborn screening (NBS) for spinal muscular atrophy (SMA) is a recognised model through which health outcomes can be improved. However, perspectives of parents and healthcare professionals (HCPs) involved in such programs are largely unknown. Methods: A pilot program for SMA ran from Aug...

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Main Authors: Didu S.T. Kariyawasam, MBBS, Arlene M. D'Silva, PhD, Janine Vetsch, PhD, Claire E. Wakefield, PhD, Veronica Wiley, PhD, Michelle A. Farrar, PhD
Format: Article
Language:English
Published: Elsevier 2021-03-01
Series:EClinicalMedicine
Online Access:http://www.sciencedirect.com/science/article/pii/S2589537021000225
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spelling doaj-a2e8d88161e14f1aa806a635dccb2c592021-03-27T04:28:43ZengElsevierEClinicalMedicine2589-53702021-03-0133100742“We needed this”: perspectives of parents and healthcare professionals involved in a pilot newborn screening program for spinal muscular atrophyDidu S.T. Kariyawasam, MBBS0Arlene M. D'Silva, PhD1Janine Vetsch, PhD2Claire E. Wakefield, PhD3Veronica Wiley, PhD4Michelle A. Farrar, PhD5Department of Neurology, Sydney Children's Hospital, Randwick, Sydney, New South Wales, Australia; School of Women's and Children's Health, University of New South Wales Medicine, UNSW Sydney, New South Wales, AustraliaCorrespondence: Dr Arlene D'Silva, School of Women's and Children's Health, University of New South Wales Medicine, New South Wales 2031, Australia. T: 02 9382 5517.; School of Women's and Children's Health, University of New South Wales Medicine, UNSW Sydney, New South Wales, AustraliaSchool of Women's and Children's Health, University of New South Wales Medicine, UNSW Sydney, New South Wales, Australia; Kids Cancer Centre, Sydney Children's Hospital, Randwick, AustraliaSchool of Women's and Children's Health, University of New South Wales Medicine, UNSW Sydney, New South Wales, Australia; Kids Cancer Centre, Sydney Children's Hospital, Randwick, AustraliaNSW Newborn Screening Program, Children's Hospital Westmead, Westmead, New South Wales, Australia; Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, AustraliaDepartment of Neurology, Sydney Children's Hospital, Randwick, Sydney, New South Wales, Australia; School of Women's and Children's Health, University of New South Wales Medicine, UNSW Sydney, New South Wales, AustraliaBackground: Newborn screening (NBS) for spinal muscular atrophy (SMA) is a recognised model through which health outcomes can be improved. However, perspectives of parents and healthcare professionals (HCPs) involved in such programs are largely unknown. Methods: A pilot program for SMA ran from August 2018-July 2020. Using a mixed-methods convergent methodology, we used a self-administered questionnaire to understand parents’ perceptions and psychological impact of the program from diagnosis to treatment. We thematically analysed successes/challenges encountered by HCPs and recommendations for service improvement from both participant groups. Findings: 202,388 infants were screened for SMA and the perceptions of 44 parents and HCPs affected by a positive result in eighteen newborns was ascertained. Parents (n=29, 100%) were satisfied with NBS for SMA. Although screen-positive result was distressing for all parents, quality of life improved over time [CarerQoL-7D baseline median score 4 (SD=1.4) vs six-month median score 8 (SD=1.3), p<0.001)]. Challenges for HCPs included managing the time-critical nature of the pathway whilst remaining cognisant of limitations associated with the predictive screening test. Interpretation: Interpretation: NBS for SMA fulfils criteria for population-wide screening. Net benefits are acknowledged by stakeholders to optimise lifelong outcomes. Harms including psychological distress associated with a screen-positive result may be managed by targeted psychosocial support, information provision and a personalised model of care together strengthening healthcare systems. Funding: The NSW Pilot NBS study was funded by Luminesce Alliance. Dr Kariyawasam received funding from the RTP Scholarship, University of New South Wales and The Freedman Family Foundation Scholarship, Sydney Children's Hospital Foundation.http://www.sciencedirect.com/science/article/pii/S2589537021000225
collection DOAJ
language English
format Article
sources DOAJ
author Didu S.T. Kariyawasam, MBBS
Arlene M. D'Silva, PhD
Janine Vetsch, PhD
Claire E. Wakefield, PhD
Veronica Wiley, PhD
Michelle A. Farrar, PhD
spellingShingle Didu S.T. Kariyawasam, MBBS
Arlene M. D'Silva, PhD
Janine Vetsch, PhD
Claire E. Wakefield, PhD
Veronica Wiley, PhD
Michelle A. Farrar, PhD
“We needed this”: perspectives of parents and healthcare professionals involved in a pilot newborn screening program for spinal muscular atrophy
EClinicalMedicine
author_facet Didu S.T. Kariyawasam, MBBS
Arlene M. D'Silva, PhD
Janine Vetsch, PhD
Claire E. Wakefield, PhD
Veronica Wiley, PhD
Michelle A. Farrar, PhD
author_sort Didu S.T. Kariyawasam, MBBS
title “We needed this”: perspectives of parents and healthcare professionals involved in a pilot newborn screening program for spinal muscular atrophy
title_short “We needed this”: perspectives of parents and healthcare professionals involved in a pilot newborn screening program for spinal muscular atrophy
title_full “We needed this”: perspectives of parents and healthcare professionals involved in a pilot newborn screening program for spinal muscular atrophy
title_fullStr “We needed this”: perspectives of parents and healthcare professionals involved in a pilot newborn screening program for spinal muscular atrophy
title_full_unstemmed “We needed this”: perspectives of parents and healthcare professionals involved in a pilot newborn screening program for spinal muscular atrophy
title_sort “we needed this”: perspectives of parents and healthcare professionals involved in a pilot newborn screening program for spinal muscular atrophy
publisher Elsevier
series EClinicalMedicine
issn 2589-5370
publishDate 2021-03-01
description Background: Newborn screening (NBS) for spinal muscular atrophy (SMA) is a recognised model through which health outcomes can be improved. However, perspectives of parents and healthcare professionals (HCPs) involved in such programs are largely unknown. Methods: A pilot program for SMA ran from August 2018-July 2020. Using a mixed-methods convergent methodology, we used a self-administered questionnaire to understand parents’ perceptions and psychological impact of the program from diagnosis to treatment. We thematically analysed successes/challenges encountered by HCPs and recommendations for service improvement from both participant groups. Findings: 202,388 infants were screened for SMA and the perceptions of 44 parents and HCPs affected by a positive result in eighteen newborns was ascertained. Parents (n=29, 100%) were satisfied with NBS for SMA. Although screen-positive result was distressing for all parents, quality of life improved over time [CarerQoL-7D baseline median score 4 (SD=1.4) vs six-month median score 8 (SD=1.3), p<0.001)]. Challenges for HCPs included managing the time-critical nature of the pathway whilst remaining cognisant of limitations associated with the predictive screening test. Interpretation: Interpretation: NBS for SMA fulfils criteria for population-wide screening. Net benefits are acknowledged by stakeholders to optimise lifelong outcomes. Harms including psychological distress associated with a screen-positive result may be managed by targeted psychosocial support, information provision and a personalised model of care together strengthening healthcare systems. Funding: The NSW Pilot NBS study was funded by Luminesce Alliance. Dr Kariyawasam received funding from the RTP Scholarship, University of New South Wales and The Freedman Family Foundation Scholarship, Sydney Children's Hospital Foundation.
url http://www.sciencedirect.com/science/article/pii/S2589537021000225
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