Symptom management and psychological support for families are the cornerstones of end-of-life care for children with spinal muscular atrophy type 1
Creator
Pede CD; Agosto C; Tommasi V; Gregorio A; Benini F
Identifier
10.1111/apa.14086
Publisher
Acta Paediatrica
Date
2017
Subject
Dyspnoea; End Of Life; Paediatric Palliative Care; Pain Relief; Spinal Muscular Atrophy Type 1
Description
AIM: This study described end-of-life care for children affected by spinal muscular atrophy type 1 (SMA1), which is characterised by progressive muscle weakness and develops in the first six months of life. METHODS: We retrospectively analysed 17 children (13 boys) who attended the University of Padua's paediatric palliative care centre in Italy from March 2000 to March 2015. All the children received supportive care without proactive respiratory intervention to prolong survival. RESULTS: The median age at admission was 3.57 months and the median age at death was 6.80 months. The most frequent symptoms were dyspnoea and pain. In the last 72 hours of life 15/17 children required more intense doses of morphine and, or, benzodiazepines for intractable dyspnoea and pain, but deep palliative sedation was not needed. Airway suction to manage secretions and nasogastric tubes were required in all cases. The place of death was previously planned by the parents in all cases - home, hospital or hospice - and 15/17 deaths occurred in that place. We also interviewed 16 of the 17 parents after their child died. CONCLUSION: Our study found that symptom management and psychological support for families were the cornerstones of end-of-life care for children with SMA1. This article is protected by copyright. All rights reserved.
Rights
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Citation List Month
November 2017 List
Notes
1651-2227 Pede, Chiara Di Agosto, Caterina Tommasi, Valentina De Gregorio, Alessandra De Benini, Franca Journal Article Norway Acta Paediatr. 2017 Sep 23. doi: 10.1111/apa.14086.