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1
Carers' experiences of dysphagia in people treated for head and neck cancer: a qualitative study.头颈癌患者吞咽困难的照护者体验:一项定性研究
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2
The experience of food, eating and meals following radiotherapy for head and neck cancer: a qualitative study.头颈部癌症放射治疗后食物、进食和用餐体验:一项定性研究。
J Clin Nurs. 2013 Apr;22(7-8):1034-43. doi: 10.1111/jocn.12151.
3
Recognizing new perspectives in eating difficulties following stroke: a concept analysis.认识到中风后饮食困难的新视角:概念分析。
Disabil Rehabil. 2013 Aug;35(17):1491-500. doi: 10.3109/09638288.2012.736012. Epub 2012 Nov 19.
4
Dysphagia, nutrition, and hydration in ischemic stroke patients at admission and discharge from acute care.缺血性脑卒中患者入院和出院时的吞咽障碍、营养和水合作用。
Dysphagia. 2013 Mar;28(1):69-76. doi: 10.1007/s00455-012-9414-0. Epub 2012 Jun 9.
5
Long-term functional outcomes and patient perspective following altered fractionation radiotherapy with concomitant boost for oropharyngeal cancer.头颈部肿瘤调强放疗同期加量后长期的功能预后和患者角度分析
Dysphagia. 2012 Dec;27(4):481-90. doi: 10.1007/s00455-012-9394-0. Epub 2012 Feb 24.
6
Association between severity of dysphagia and survival in patients with head and neck cancer.头颈部癌症患者吞咽困难严重程度与生存的关系。
Head Neck. 2012 Jun;34(6):776-84. doi: 10.1002/hed.21819. Epub 2011 Aug 30.
7
Consequence of dysphagia in the hospitalized patient: impact on prognosis and hospital resources.住院患者吞咽困难的后果:对预后和医院资源的影响。
Arch Otolaryngol Head Neck Surg. 2010 Aug;136(8):784-9. doi: 10.1001/archoto.2010.129.
8
Relatives' experiences of family members' eating difficulties.亲属对家庭成员饮食困难的经历。
Scand J Occup Ther. 2009 Mar;16(1):25-32. doi: 10.1080/11038120802257195.
9
Preparing family caregivers for death and bereavement. Insights from caregivers of terminally ill patients.让家庭护理者做好面对死亡和丧亲之痛的准备。绝症患者护理者的见解。
J Pain Symptom Manage. 2009 Jan;37(1):3-12. doi: 10.1016/j.jpainsymman.2007.12.010. Epub 2008 Jun 6.
10
Validation of the Caregiver Mealtime and Dysphagia Questionnaire (CMDQ).照顾者用餐时间与吞咽困难问卷(CMDQ)的验证
Dysphagia. 2008 Mar;23(1):47-58. doi: 10.1007/s00455-007-9094-3. Epub 2007 Nov 14.

吞咽困难患者照料者生活质量问卷(QOLC-M)的编制

Development of Quality of Life Due to Dysphagia Questionnaire for Caregivers of Individuals with Dysphagia (QOLC-M).

作者信息

Jain Harshitha, Jagtap Mansi

机构信息

Bharati Vidyapeeth (Deemed to be University), School of Audiology and Speech Language Pathology, Dhankawadi Campus, Katraj, Pune, Maharashtra 411043 India.

出版信息

Indian J Otolaryngol Head Neck Surg. 2022 Dec;74(Suppl 3):5645-5656. doi: 10.1007/s12070-021-02931-z. Epub 2021 Nov 13.

DOI:10.1007/s12070-021-02931-z
PMID:36742933
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9895363/
Abstract

Caregivers play an important role in providing care for patients with dysphagia and experience various psychosocial issues, but these areas remain unexplored. There is paucity of tools to assess quality of life of caregivers of individuals with dysphagia attending to these cases. Hence, a need was felt to carry out the present study to develop a tool to assess quality of life for caregivers of individuals with dysphagia. Construction of questionnaire was done in Marathi language and validated by native Marathi speakers and face validity by experts. The questionnaire was administered on 30 caregivers of individuals with dysphagia.A detailed case history, demographic information of the caregivers was noted and questionnaire was administered on the caregivers using interview method. The data was subjected to measures of internal consistency and reliability. Statistical analysis revealed a high item to total correlation (0.6-0.92).Internal consistency was found to be high (α = 0.95) while Intraclass Correlation Coefficient (ICC) was administered for reliability revealing high reliability (ICC = 0.85).The analysis of responses of the caregivers on the statements revealed moderate to high scores for many statements indicating impact of dysphagia on activities of daily living, social aspects, feelings and attitudes and problems faced during feeding. QOLC-M was found to be a tool with high reliability and internal consistency. It could identify the impact of dysphagia on caregiver's QOL highlighting specific problems faced by them.

摘要

照顾者在为吞咽困难患者提供护理方面发挥着重要作用,并且会经历各种心理社会问题,但这些领域仍未得到探索。目前缺乏评估照顾吞咽困难患者的照顾者生活质量的工具。因此,人们觉得有必要开展本研究,以开发一种评估吞咽困难患者照顾者生活质量的工具。问卷用马拉地语编制,并由母语为马拉地语的人进行验证,同时由专家进行表面效度评估。该问卷对30名吞咽困难患者的照顾者进行了施测。记录了详细的病例史、照顾者的人口统计学信息,并采用访谈法对照顾者进行问卷施测。对数据进行了内部一致性和信度测量。统计分析显示项目与总分的相关性较高(0.6 - 0.92)。发现内部一致性较高(α = 0.95),同时采用组内相关系数(ICC)评估信度,结果显示信度较高(ICC = 0.85)。对照顾者对各项陈述的回答分析表明,许多陈述的得分从中度到高度,表明吞咽困难对日常生活活动、社会方面、情感和态度以及喂食过程中面临的问题产生了影响。吞咽困难照顾者生活质量问卷(QOLC - M)被发现是一种具有高信度和内部一致性的工具。它可以确定吞咽困难对照顾者生活质量的影响,突出他们所面临的具体问题。