Palliative Care in SMA Type 1: A Prospective Multicenter French Study Based on Parents' Reports.

SMA caregivers ethics palliative care standard of care

Journal

Frontiers in pediatrics
ISSN: 2296-2360
Titre abrégé: Front Pediatr
Pays: Switzerland
ID NLM: 101615492

Informations de publication

Date de publication:
2020
Historique:
received: 09 10 2019
accepted: 07 01 2020
entrez: 6 3 2020
pubmed: 7 3 2020
medline: 7 3 2020
Statut: epublish

Résumé

Spinal muscular atrophy type 1 (SMA-1) is a severe neurodegenerative disorder, which in the absence of curative treatment, leads to death before 1 year of age in most cases. Caring for these short-lived and severely impaired infants requires palliative management. New drugs (nusinersen) have recently been developed that may modify SMA-1 natural history and thus raise ethical concerns about the appropriate level of care for patients. The national Hospital Clinical Research Program (PHRC) called "Assessment of clinical practices of palliative care in children with Spinal Muscular Atrophy Type 1 (SMA-1)" was a multicenter prospective study conducted in France between 2012 and 2016 to report palliative practices in SMA-1 in real life through prospective caregivers' reports about their infants' management. Thirty-nine patients were included in the prospective PHRC (17 centers). We also studied retrospective data regarding management of 43 other SMA-1 patients (18 centers) over the same period, including seven treated with nusinersen, in comparison with historical data from 222 patients previously published over two periods of 10 years (1989-2009). In the latest period studied, median age at diagnosis was 3 months [0.6-10.4]. Seventy-seven patients died at a median 6 months of age[1-27]: 32% at home and 8% in an intensive care unit. Eighty-five percent of patients received enteral nutrition, some through a gastrostomy (6%). Sixteen percent had a non-invasive ventilation (NIV). Seventy-seven percent received sedative treatment at the time of death. Over time, palliative management occurred more frequently at home with increased levels of technical supportive care (enteral nutrition, oxygenotherapy, and analgesic and sedative treatments). No statistical difference was found between the prospective and retrospective patients for the last period. However, significant differences were found between patients treated with nusinersen vs. those untreated. Our data confirm that palliative care is essential in management of SMA-1 patients and that parents are extensively involved in everyday patient care. Our data suggest that nusinersen treatment was accompanied by significantly more invasive supportive care, indicating that a re-examination of standard clinical practices should explicitly consider what treatment pathways are in infants' and caregivers' best interest. This study was registered on clinicaltrials.gov under the reference NCT01862042 (https://clinicaltrials.gov/ct2/show/study/NCT01862042?cond=SMA1&rank=8).

Identifiants

pubmed: 32133329
doi: 10.3389/fped.2020.00004
pmc: PMC7039815
doi:

Banques de données

ClinicalTrials.gov
['NCT01862042']

Types de publication

Journal Article

Langues

eng

Pagination

4

Informations de copyright

Copyright © 2020 Hully, Barnerias, Chabalier, Le Guen, Germa, Deladriere, Vanhulle, Cuisset, Chabrol, Cances, Vuillerot, Espil, Mayer, Nougues, Sabouraud, Lefranc, Laugel, Rivier, Louvier, Durigneux, Napuri, Sarret, Renouil, Masurel, Viallard and Desguerre.

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Auteurs

Marie Hully (M)

Pediatric Neurology Department, Necker-Enfants Malades Hospital, APHP, Paris, France.
Physical Rehabilitation Department, Necker-Enfants Malades Hospital, APHP, Paris, France.

Christine Barnerias (C)

Pediatric Neurology Department, Necker-Enfants Malades Hospital, APHP, Paris, France.

Delphine Chabalier (D)

Pediatric Neurology Department, Necker-Enfants Malades Hospital, APHP, Paris, France.

Sophie Le Guen (S)

Clinical Research Department, Necker-Enfants Malades Hospital, APHP, Paris, France.

Virginie Germa (V)

Physical Rehabilitation Department, Necker-Enfants Malades Hospital, APHP, Paris, France.

Elodie Deladriere (E)

Physical Rehabilitation Department, Necker-Enfants Malades Hospital, APHP, Paris, France.

Catherine Vanhulle (C)

Neonatal Department, Charles Nicolle Hospital, Rouen, France.

Jean-Marie Cuisset (JM)

Pediatric Neurology Department and Neuromuscular Diseases Reference Center, CHU, Lille, France.

Brigitte Chabrol (B)

Pediatric Neurology Department, La Timone Hospital, APHM, Marseille, France.

Claude Cances (C)

Pediatric Neurology Department, Enfants Hospital, Toulouse, France.

Carole Vuillerot (C)

Pediatric Physical Rehabilitation Department, Femme Mère Enfants Hospital, Bron, France.

Caroline Espil (C)

Pediatric Neurology Department, Pellegrin Hospital, Bordeaux, France.

Michele Mayer (M)

Pediatric Neurology Department, Armand Trousseau Hospital, APHP, Paris, France.

Marie-Christine Nougues (MC)

Pediatric Neurology Department, Armand Trousseau Hospital, APHP, Paris, France.

Pascal Sabouraud (P)

Pediatric Department, American Memorial Hospital, Reims, France.

Jeremie Lefranc (J)

Pediatric Neurology Department, Morvan Hospital, Brest, France.

Vincent Laugel (V)

Pediatric Neurology Department, Hautepierre Hospital, Strasbourg, France.

Francois Rivier (F)

Pediatric Neurology Department & Neuromuscular Diseases Reference Center AOC, CHU Montpellier, PhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.

Ulrike Walther Louvier (UW)

Pediatric Neurology Department & Neuromuscular Diseases Reference Center AOC, CHU Montpellier, Montpellier, France.

Julien Durigneux (J)

Pediatric Neurology Department, University Hospital, Angers, France.

Sylvia Napuri (S)

Pediatric Department, South Hospital, Rennes, France.

Catherine Sarret (C)

Pediatric Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.

Michel Renouil (M)

Pediatric Department, St-Pierre Hospital, Saint-Denis, France.

Alice Masurel (A)

Genetic Department, Children Hospital, CHU Dijon, Dijon, France.

Marcel-Louis Viallard (ML)

Palliative Care Team, Necker-Enfants Malades Hospital, APHP, Paris, France.
Research Team "ETRES", UMR des Cordeliers, Université de Paris, Paris, France.

Isabelle Desguerre (I)

Pediatric Neurology Department, Necker-Enfants Malades Hospital, APHP, Paris, France.

Classifications MeSH