• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

杜氏肌营养不良症患者的长期通气:医生的观念与实践

Long-term ventilation for patients with Duchenne muscular dystrophy : physicians' beliefs and practices.

作者信息

Gibson B

机构信息

Department of Physical Therapy, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.

出版信息

Chest. 2001 Mar;119(3):940-6. doi: 10.1378/chest.119.3.940.

DOI:10.1378/chest.119.3.940
PMID:11243978
Abstract

STUDY OBJECTIVES

Although long-term ventilation (LTV) has been shown to extend the lives of individuals with Duchenne muscular dystrophy (DMD), initiating LTV is still considered controversial. The purpose of the study was to describe the LTV-related attitudes and practices of Canadian physicians who follow up patients with DMD.

DESIGN

The study consisted of a mail questionnaire supplemented by face-to-face interviews.

PARTICIPANTS

Forty-five physicians who follow up patients with DMD through Canadian neuromuscular clinics.

MEASUREMENTS

A mail questionnaire of 66 closed-ended questions related to practice and attitudes was completed by all respondents. Qualitative semistructured interviews were conducted with six volunteer physicians, and were audiotaped and transcribed.

RESULTS

The results indicated that 25.0% of physicians do not discuss LTV with all of their DMD patients. The most frequently cited reason for advising against LTV was poor patient quality of life (52.6%). Three themes emerged from the qualitative data: mentioning and discussing LTV are discrete events with different purposes, nighttime and full-time LTV decisions are approached differently, and physicians modify their discussions to influence outcome.

CONCLUSIONS

The study demonstrated considerable agreement among the physicians regarding disclosure practices. Concerns are raised by the number of physicians who do not disclose to all patients and families and the role of quality-of-life judgments in decision making. It is suggested that because of their subjective nature, quality-of-life judgments should not be made without the participation of the patient and family, and that an initial disclosure is the minimum requirement of informed consent/decision making.

摘要

研究目的

尽管长期通气(LTV)已被证明可延长杜氏肌营养不良症(DMD)患者的生命,但启动LTV仍存在争议。本研究的目的是描述随访DMD患者的加拿大医生与LTV相关的态度和做法。

设计

本研究包括一份邮寄问卷,并辅以面对面访谈。

参与者

通过加拿大神经肌肉诊所随访DMD患者的45名医生。

测量方法

所有受访者均完成了一份包含66个与实践和态度相关的封闭式问题的邮寄问卷。对6名志愿医生进行了定性半结构化访谈,并进行了录音和转录。

结果

结果表明,25.0%的医生没有与他们所有的DMD患者讨论LTV。反对LTV的最常见原因是患者生活质量差(52.6%)。定性数据中出现了三个主题:提及和讨论LTV是具有不同目的的离散事件,夜间和全日制LTV决策的处理方式不同,医生会调整他们的讨论以影响结果。

结论

该研究表明医生们在披露做法上有相当大的共识。未向所有患者和家属披露信息的医生数量以及生活质量判断在决策中的作用令人担忧。建议由于生活质量判断具有主观性,不应在患者和家属未参与的情况下做出,并且初始披露是知情同意/决策的最低要求。

相似文献

1
Long-term ventilation for patients with Duchenne muscular dystrophy : physicians' beliefs and practices.杜氏肌营养不良症患者的长期通气:医生的观念与实践
Chest. 2001 Mar;119(3):940-6. doi: 10.1378/chest.119.3.940.
2
Swiss physicians' practices of long-term mechanical ventilatory support of patients with Duchenne Muscular Dystrophy.瑞士医生对杜氏肌营养不良症患者进行长期机械通气支持的做法。
Swiss Med Wkly. 2005 Oct 1;135(39-40):599-604. doi: 10.4414/smw.2005.11130.
3
UK physicians' attitudes and practices in long-term non-invasive ventilation of Duchenne Muscular Dystrophy.英国医生在杜氏肌营养不良症长期无创通气方面的态度和做法。
Pediatr Rehabil. 2006 Oct-Dec;9(4):351-64. doi: 10.1080/13638490600622613.
4
Duchenne muscular dystrophy: Canadian paediatric neuromuscular physicians survey.杜氏肌营养不良症:加拿大儿科神经肌肉医师调查。
Can J Neurol Sci. 2010 Mar;37(2):195-205. doi: 10.1017/s0317167100009926.
5
[Survey for assessing how Duchenne muscular dystrophy is explained to children with the disorder].[关于评估如何向患有杜氏肌营养不良症的儿童解释该疾病的调查]
No To Hattatsu. 2013 Jan;45(1):11-6.
6
Decisions around Long-term Ventilation for Children. Perspectives of Directors of Pediatric Home Ventilation Programs.儿童长期通气决策。儿科家庭通气项目主任的观点。
Ann Am Thorac Soc. 2017 Oct;14(10):1539-1547. doi: 10.1513/AnnalsATS.201612-1002OC.
7
European Cross-Sectional Survey of Current Care Practices for Duchenne Muscular Dystrophy Reveals Regional and Age-Dependent Differences.欧洲横断面调查揭示了杜氏肌营养不良症现行治疗实践中的区域性和年龄依赖性差异。
J Neuromuscul Dis. 2016 Nov 29;3(4):517-527. doi: 10.3233/JND-160185.
8
Alzheimer's disease diagnosis disclosure in Brazil: a survey of specialized physicians' current practice and attitudes.巴西阿尔茨海默病诊断结果的披露:对专科医生当前实践和态度的调查。
Int Psychogeriatr. 2008 Jun;20(3):471-81. doi: 10.1017/S1041610207005819. Epub 2007 Sep 6.
9
Cardiopulmonary support in duchenne muscular dystrophy.杜氏肌营养不良症的心肺支持
Lung. 2006 Jul-Aug;184(4):205-15. doi: 10.1007/s00408-005-2584-x.
10
"Watching time tick by…": Decision making for Duchenne muscular dystrophy trials.“看着时间流逝……”:杜氏肌营养不良症试验的决策制定
Contemp Clin Trials. 2016 Jan;46:1-6. doi: 10.1016/j.cct.2015.11.006. Epub 2015 Nov 9.

引用本文的文献

1
An algorithm for discontinuing mechanical ventilation in boys with x-linked myotubular myopathy after positive response to gene therapy: the ASPIRO experience.一种在接受基因治疗后出现阳性反应的 X 连锁肌管肌病男孩中停止机械通气的算法:ASPIRO 经验。
Respir Res. 2024 Sep 16;25(1):342. doi: 10.1186/s12931-024-02966-0.
2
The factorial survey as an approach to investigate clinical decision-making: examining influences on a clinician's decision to initiate life-sustaining clinical technology for a child with spinal muscular atrophy type 1.作为一种调查临床决策方法的析因调查:考察对临床医生为1型脊髓性肌萎缩症患儿启动维持生命临床技术决策的影响。
Front Pediatr. 2023 Oct 24;11:1252440. doi: 10.3389/fped.2023.1252440. eCollection 2023.
3
The quality of life in children with spinal muscular atrophy: a case-control study.脊髓性肌萎缩症患儿的生活质量:一项病例对照研究。
BMC Pediatr. 2022 Dec 12;22(1):708. doi: 10.1186/s12887-022-03751-y.
4
Mortality and respiratory support in X-linked myotubular myopathy: a RECENSUS retrospective analysis.X 连锁肌小管肌病的死亡率和呼吸支持:REENSUS 回顾性分析。
Arch Dis Child. 2020 Apr;105(4):332-338. doi: 10.1136/archdischild-2019-317910. Epub 2019 Sep 4.
5
Fluid flow and particle transport in mechanically ventilated airways. Part II: particle transport.机械通气气道中的流体流动与颗粒传输。第二部分:颗粒传输。
Med Biol Eng Comput. 2016 Jul;54(7):1097-109. doi: 10.1007/s11517-015-1408-2. Epub 2015 Nov 5.
6
Communication regarding breathing support options for youth with Duchenne muscular dystrophy.关于杜兴氏肌营养不良症青少年呼吸支持方案的沟通。
Paediatr Child Health. 2011 Aug;16(7):395-8. doi: 10.1093/pch/16.7.395.
7
Ethical challenges in home mechanical ventilation: a secondary analysis.家庭机械通气中的伦理挑战:二次分析。
Nurs Ethics. 2012 Mar;19(2):233-44. doi: 10.1177/0969733011414967. Epub 2011 Dec 19.
8
Home mechanical ventilation: a Canadian Thoracic Society clinical practice guideline.家庭机械通气:加拿大胸科学会临床实践指南。
Can Respir J. 2011 Jul-Aug;18(4):197-215. doi: 10.1155/2011/139769.
9
A systematic review of quality of life in adults with muscle disease.肌肉疾病成人生活质量的系统评价。
J Neurol. 2011 Sep;258(9):1581-92. doi: 10.1007/s00415-011-6062-5. Epub 2011 May 20.
10
Widening gap in age at muscular dystrophy-associated death between blacks and whites, 1986-2005.1986 年至 2005 年间,黑人和白人的肌营养不良相关死亡率的年龄差距扩大。
Neurology. 2010 Sep 14;75(11):982-9. doi: 10.1212/WNL.0b013e3181f25e5b.