Literature DB >> 27685758

Physician driven variation in the care of children with spinal muscular atrophy type 1.

Maryam Oskoui1,2, Pamela Ng3, Stephen Liben1, David Zielinski1.   

Abstract

BACKGROUND: Increasing numbers of families are requesting active supportive management for their child with spinal muscular atrophy type 1 (SMA1), leading to longer survival and greater prevalence of affected children. Strong opinions exist among physicians for and against the provision of care measures prolonging life.
OBJECTIVE: To describe current practice in the care of SMA1 in Canada, and explore the factors underlying inter-physician variability.
METHODS: A cross-sectional survey of Canadian hospital-based pediatric neurologists and pediatric respirologists was performed in 2015. Odds ratios and 95% confidence intervals were calculated to compare proportions between groups.
RESULTS: There was a 54% completion rate (99 physicians). Over half of participants believed that a disease modifying therapy was likely within 10 years. Quebec respirologists were 50 times less likely to offer long-term non-invasive ventilation (NIV) than respirologists in other provinces (OR 50.6, 95% CI 2.4-1075.3), and 20 times less likely to discuss tracheostomy with families (OR 20.4, 95% CI 2.0-211.8). High raters of perceived happiness of affected children were more likely to find NIV an acceptable measure for acute (OR 6.7, 95% CI 1.7-26.0) and chronic (OR 13.7, 95% CI 4.0-46.4) respiratory failure and prophylactic use (OR 5.8, 95% CI 2.2-15.6).
CONCLUSION: Physician knowledge, opinions, subjective perception of child happiness, and regional factors, all influence physicians' practices and the shared decision-making process. Parents may not be informed or offered all the services available to their child. Knowledge translation initiatives are needed to enhance SMA1 care. Pediatr Pulmonol. 2017;52:662-668.
© 2016 Wiley Periodicals, Inc. © 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  neuromuscular diseases; quality of life; respiratory support; spinal muscular atrophy

Mesh:

Year:  2016        PMID: 27685758     DOI: 10.1002/ppul.23616

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  8 in total

1.  Decisions around Long-term Ventilation for Children. Perspectives of Directors of Pediatric Home Ventilation Programs.

Authors:  Jeffrey D Edwards; Marilyn C Morris; Judith E Nelson; Howard B Panitch; Rachel L Miller
Journal:  Ann Am Thorac Soc       Date:  2017-10

2.  Decisions for Long-Term Ventilation for Children. Perspectives of Family Members.

Authors:  Jeffrey D Edwards; Howard B Panitch; Judith E Nelson; Rachel L Miller; Marilyn C Morris
Journal:  Ann Am Thorac Soc       Date:  2020-01

3.  Indirect estimation of the prevalence of spinal muscular atrophy Type I, II, and III in the United States.

Authors:  Cathy Lally; Cynthia Jones; Wildon Farwell; Sandra P Reyna; Suzanne F Cook; W Dana Flanders
Journal:  Orphanet J Rare Dis       Date:  2017-11-28       Impact factor: 4.123

Review 4.  Emerging therapies and challenges in spinal muscular atrophy.

Authors:  Michelle A Farrar; Susanna B Park; Steve Vucic; Kate A Carey; Bradley J Turner; Thomas H Gillingwater; Kathryn J Swoboda; Matthew C Kiernan
Journal:  Ann Neurol       Date:  2017-02-17       Impact factor: 10.422

5.  Financial, opportunity and psychosocial costs of spinal muscular atrophy: an exploratory qualitative analysis of Australian carer perspectives.

Authors:  Michelle A Farrar; Kate A Carey; Sarah-Grace Paguinto; Georgina Chambers; Nadine A Kasparian
Journal:  BMJ Open       Date:  2018-05-24       Impact factor: 2.692

6.  An Integrated Safety Analysis of Infants and Children with Symptomatic Spinal Muscular Atrophy (SMA) Treated with Nusinersen in Seven Clinical Trials.

Authors:  Basil T Darras; Michelle A Farrar; Eugenio Mercuri; Richard S Finkel; Richard Foster; Steven G Hughes; Ishir Bhan; Wildon Farwell; Sarah Gheuens
Journal:  CNS Drugs       Date:  2019-09       Impact factor: 5.749

Review 7.  Changes in Ventilatory Support Requirements of Spinal Muscular Atrophy (SMA) Patients Post Gene-Based Therapies.

Authors:  Panagiota Panagiotou; Christina Kanaka-Gantenbein; Athanasios G Kaditis
Journal:  Children (Basel)       Date:  2022-08-11

8.  Burden of Spinal Muscular Atrophy (SMA) on Patients and Caregivers in Canada.

Authors:  H J McMillan; B Gerber; T Cowling; W Khuu; M Mayer; J W Wu; B Maturi; K Klein-Panneton; C Cabalteja; H Lochmüller
Journal:  J Neuromuscul Dis       Date:  2021
  8 in total

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