Evidence map›Paper›PMID 32133329›Full record

ArticleFrontiers in pediatrics2020

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

Marie Hully, Christine Barnerias, Delphine Chabalier, Sophie Le Guen, Virginie Germa, Elodie Deladriere, Catherine Vanhulle, Jean-Marie Cuisset, Brigitte Chabrol, Claude Cances and 16 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in pediatrics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01862042 (Evaluation of Palliative and Supportive Care for Spinal Muscular Atrophy), which is not on this map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01862042 nacompletednot on this map

Evaluation of Palliative and Supportive Care for Spinal Muscular Atrophy (SMA) Type 1 Patients

TypeinterventionalSponsorAssistance Publique - Hôpitaux de ParisRan2012 to 2018Enrolled39ConditionsSpinal Muscular Atrophy 1ArmsFollow-up diary and questionnaire
3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Observational
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Revisiting the role of mitochondria in spinal muscular atrophy.Cellular and molecular life sciences : CMLS · 2021
    Review
  12. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors at 19 institutions in 2 countries.

Marie HullyPediatric Neurology Department, Necker-Enfants Malades Hospital, APHP, Paris, France.
Christine BarneriasPediatric Neurology Department, Necker-Enfants Malades Hospital, APHP, Paris, France.
Delphine ChabalierPediatric Neurology Department, Necker-Enfants Malades Hospital, APHP, Paris, France.
Sophie Le GuenClinical Research Department, Necker-Enfants Malades Hospital, APHP, Paris, France.
Virginie GermaPhysical Rehabilitation Department, Necker-Enfants Malades Hospital, APHP, Paris, France.
Elodie DeladrierePhysical Rehabilitation Department, Necker-Enfants Malades Hospital, APHP, Paris, France.
Catherine VanhulleNeonatal Department, Charles Nicolle Hospital, Rouen, France.
Jean-Marie CuissetPediatric Neurology Department and Neuromuscular Diseases Reference Center, CHU, Lille, France.
Brigitte ChabrolPediatric Neurology Department, La Timone Hospital, APHM, Marseille, France.
Claude CancesPediatric Neurology Department, Enfants Hospital, Toulouse, France.
Carole VuillerotPediatric Physical Rehabilitation Department, Femme Mère Enfants Hospital, Bron, France.
Caroline EspilPediatric Neurology Department, Pellegrin Hospital, Bordeaux, France.
Michele MayerPediatric Neurology Department, Armand Trousseau Hospital, APHP, Paris, France.
Marie-Christine NouguesPediatric Neurology Department, Armand Trousseau Hospital, APHP, Paris, France.
Pascal SabouraudPediatric Department, American Memorial Hospital, Reims, France.
Jeremie LefrancPediatric Neurology Department, Morvan Hospital, Brest, France.
Vincent LaugelPediatric Neurology Department, Hautepierre Hospital, Strasbourg, France.
Francois RivierPediatric Neurology Department & Neuromuscular Diseases Reference Center AOC, CHU Montpellier, PhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.
Ulrike Walther LouvierPediatric Neurology Department & Neuromuscular Diseases Reference Center AOC, CHU Montpellier, Montpellier, France.
Julien DurigneuxPediatric Neurology Department, University Hospital, Angers, France.
Sylvia NapuriPediatric Department, South Hospital, Rennes, France.
Catherine SarretPediatric Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Michel RenouilPediatric Department, St-Pierre Hospital, Saint-Denis, France.
Alice MasurelGenetic Department, Children Hospital, CHU Dijon, Dijon, France.
Marcel-Louis ViallardPalliative Care Team, Necker-Enfants Malades Hospital, APHP, Paris, France.
Isabelle DesguerrePediatric Neurology Department, Necker-Enfants Malades Hospital, APHP, Paris, France.
Assistance Publique – Hôpitaux de Paris · FRHôpital Necker-Enfants Malades · FRCentre de Recherche des Cordeliers · FRCentre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier Saint-Denis · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre Hospitalier Universitaire de Lille · FRCentre Hospitalier Universitaire de Montpellier · FRCentre Hospitalier Universitaire Dijon Bourgogne · FRHôpital Armand-Trousseau · FRHôpital Charles-Nicolle · FRHôpital de la Timone · FRHôpital des Enfants · FRHôpital d'Hautepierre · FRHôpital Femme Mère Enfant · FRHôpital Pellegrin · FRInserm · FRSorbonne Université · FRUniversité d'Angers · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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).

Indexed as

caregiversethicspalliative careSMAstandard of care

Identifiers

PMID32133329
PMCPMC7039815
OpenAlexW3008837820

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.