“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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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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