Suppr超能文献

1型脊髓性肌萎缩症的姑息治疗:一项基于家长报告的前瞻性多中心法国研究。

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

作者信息

Hully Marie, Barnerias Christine, Chabalier Delphine, Le Guen Sophie, Germa Virginie, Deladriere Elodie, Vanhulle Catherine, Cuisset Jean-Marie, Chabrol Brigitte, Cances Claude, Vuillerot Carole, Espil Caroline, Mayer Michele, Nougues Marie-Christine, Sabouraud Pascal, Lefranc Jeremie, Laugel Vincent, Rivier Francois, Louvier Ulrike Walther, Durigneux Julien, Napuri Sylvia, Sarret Catherine, Renouil Michel, Masurel Alice, Viallard Marcel-Louis, Desguerre Isabelle

机构信息

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

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

出版信息

Front Pediatr. 2020 Feb 18;8:4. doi: 10.3389/fped.2020.00004. eCollection 2020.

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).

摘要

1型脊髓性肌萎缩症(SMA - 1)是一种严重的神经退行性疾病,在缺乏治愈性治疗的情况下,大多数病例会在1岁前死亡。照顾这些寿命短暂且严重受损的婴儿需要姑息治疗。最近研发出了新药(诺西那生钠),这可能会改变SMA - 1的自然病程,从而引发了关于对患者适当护理水平的伦理问题。名为“1型脊髓性肌萎缩症(SMA - 1)患儿姑息治疗临床实践评估”的国家医院临床研究项目(PHRC)是一项于2012年至2016年在法国进行的多中心前瞻性研究,旨在通过照护者对其婴儿管理情况的前瞻性报告,汇报SMA - 1在现实生活中的姑息治疗实践。39例患者被纳入前瞻性PHRC研究(17个中心)。我们还研究了同期另外43例SMA - 1患者(18个中心)的回顾性管理数据,其中包括7例接受诺西那生钠治疗的患者,并与之前两个10年期(1989 - 2009年)发表的222例患者的历史数据进行了比较。在研究的最近阶段,诊断时的中位年龄为3个月[0.6 - 10.4]。77例患者在中位年龄6个月时死亡[1 - 27]:32%在家中死亡,8%在重症监护病房死亡。85%的患者接受肠内营养,部分通过胃造口术(6%)。16%的患者进行无创通气(NIV)。77%的患者在死亡时接受了镇静治疗。随着时间的推移,姑息治疗在家中进行得更为频繁,技术支持性护理水平有所提高(肠内营养、氧疗以及镇痛和镇静治疗)。在最后阶段,前瞻性和回顾性患者之间未发现统计学差异。然而,接受诺西那生钠治疗的患者与未接受治疗的患者之间存在显著差异。我们的数据证实,姑息治疗在SMA - 1患者的管理中至关重要,并且家长广泛参与日常患者护理。我们的数据表明,诺西那生钠治疗伴随着明显更多的侵入性支持性护理,这表明对标准临床实践的重新审视应明确考虑何种治疗途径最符合婴儿和照护者的最大利益。本研究已在clinicaltrials.gov上注册,注册号为NCT01862042(https://clinicaltrials.gov/ct2/show/study/NCT01862042?cond=SMA1&rank=8)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb8/7039815/798e8d305336/fped-08-00004-g0001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验