Management of children with spinal muscular atrophy type 1 in Australia. Issue 10 (8th July 2013)

• Record Type: Journal Article
• Authors: Tassie, Benjamin; Isaacs, David; Kilham, Henry; Kerridge, Ian
• Is Part Of: Journal of paediatrics and child health. Volume 49:Issue 10(2013:Oct.)
• Page Start: 815
• Page End: 819
• Publication Date: 2013-07-08
• Subjects: Children -- Health and hygiene -- Periodicals; Pediatrics -- Periodicals; 618.92
• DOI: 10.1111/jpc.12291
• Languages: English
• ISSNs: 1034-4810

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="jpc12291-sec-0001" sec-type="section"> <title>Aims</title> <p>The study aims to: (i) estimate the prevalence of spinal muscular atrophy type 1 (SMA 1); (ii) describe what practices characterise end‐of‐life care of patients with SMA 1; and (iii) ascertain whether a consistent approach to the management of these patients exists in Australia.</p> </sec> <sec id="jpc12291-sec-0002" sec-type="section"> <title>Methods</title> <p>An audit of the Australasian pathology laboratories offering the diagnostic <italic>SMN1</italic> deletion test was conducted for patients diagnosed with SMA in Australia for 2010 and 2011. In addition, a retrospective clinical audit was conducted in eight major Australian paediatric hospitals of the end‐of‐life care provided to children with confirmed SMA 1 from 2005 to 2010.</p> </sec> <sec id="jpc12291-sec-0003" sec-type="section"> <title>Results</title> <p>Thirty‐five children were included in the clinical audit, accounting for an estimated 61% of children diagnosed with SMA 1 from 2005 to 2010. Twenty‐six per cent were ventilated invasively, only two of whom were intubated after the diagnosis was confirmed. No children were ventilated long term (>90 days) or had a tracheostomy performed. Nasogastric tube feeding was a common measure to support adequate nutritional intake. Total parenteral nutrition, gastrostomy and fundoplication were not provided for any children. Conflict over end‐of‐life care decisions was documented in one instance, without the involvement of a guardianship tribunal.</p> </sec> <sec id="jpc12291-sec-0004" sec-type="section"> <title>Conclusion</title> <p>There appears to be a consistent approach in the management of children with SMA 1 in Australia, which can be characterised as 'actively managed dying'. This study could contribute to the development of Australian consensus guidelines for the management of these children. These results also highlight a number of ethical issues related to the management of children with SMA 1.</p> </sec> </abstract>