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本文引用的文献

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Self-report of medical diagnosis of chronic kidney disease: prevalence and characteristics in the Brazilian adult population, National Health Survey 2013 and 2019.自我报告的慢性肾脏病医学诊断:2013 年和 2019 年巴西成年人群中的流行情况和特征,全国健康调查。
Epidemiol Serv Saude. 2022;31(spe1):e2021385. doi: 10.1590/SS2237-9622202200017.especial.
2
Indigenous Peoples' perspectives of living with chronic kidney disease: systematic review of qualitative studies.原住民对慢性肾病生活的看法:定性研究的系统综述
Kidney Int. 2022 Oct;102(4):720-727. doi: 10.1016/j.kint.2022.05.030. Epub 2022 Jul 2.
3
Components of quality of life in hemodialysis patients from family caregivers' perspective: a qualitative study.从家庭照顾者角度出发的血液透析患者生活质量构成要素:一项定性研究。
BMC Nephrol. 2021 Nov 13;22(1):379. doi: 10.1186/s12882-021-02584-8.
4
The psychosocial needs and quality of life of family caregivers of patients with organ transplant.器官移植患者家庭照顾者的心理社会需求与生活质量
J Res Nurs. 2019 Aug;24(5):344-355. doi: 10.1177/1744987119845029. Epub 2019 Aug 8.
5
Ethical Challenges in Dialysis and Transplantation: Perspectives From the Developing World.透析和移植中的伦理挑战:发展中国家的观点。
Semin Nephrol. 2021 May;41(3):211-219. doi: 10.1016/j.semnephrol.2021.05.002.
6
Qualitative Methods in Health Care Research.医疗保健研究中的定性方法
Int J Prev Med. 2021 Feb 24;12:20. doi: 10.4103/ijpvm.IJPVM_321_19. eCollection 2021.
7
Exploring the challenges and needs of home caregivers of hemodialysis patients in the Philippines: A mixed methods study.探索菲律宾血液透析患者家庭护理者的挑战和需求:混合方法研究。
Nurs Forum. 2021 Oct;56(4):823-833. doi: 10.1111/nuf.12618. Epub 2021 Jun 2.
8
Effect of main family caregiver's anxiety and depression on mortality of patients with moderate-severe stroke.主要照顾者的焦虑和抑郁对中重度脑卒中患者死亡率的影响。
Sci Rep. 2021 Feb 2;11(1):2747. doi: 10.1038/s41598-021-81596-8.
9
Association between sleep disorder and quality of life in patients with type 2 diabetes: a cross-sectional study.2 型糖尿病患者睡眠障碍与生活质量的关系:一项横断面研究。
BMC Endocr Disord. 2020 Jun 30;20(1):98. doi: 10.1186/s12902-020-00579-4.
10
The application and tailoring of Colaizzi's phenomenological approach in a hospital setting.在医院环境中应用和定制科莱齐的现象学方法。
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家庭照顾者与血液透析患者共同生活的经历:一项描述性现象学研究

Family Caregivers' Experiences of Living with Hemodialysis Patients: A Descriptive Phenomenology.

作者信息

Solaimanimoghaddam Rasool, Beydokhti Tahereh Baloochi, Firouzkohi Mohammad Reza

机构信息

Social Determinants of Health Research Center, Birjand University of Medical Sciences, Birjand, Iran.

Medical-Surgical Nursing Department, School of Nursing, Gonabad University of Medical Sciences, Gonabad, Iran.

出版信息

Iran J Nurs Midwifery Res. 2024 Sep 4;29(5):535-541. doi: 10.4103/ijnmr.ijnmr_276_22. eCollection 2024 Sep-Oct.

DOI:10.4103/ijnmr.ijnmr_276_22
PMID:39478713
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11521120/
Abstract

BACKGROUND

Several challenges are experienced by caregivers of patients with chronic kidney disease undergoing hemodialysis treatment. These difficulties pertain to the patients, their hemodialysis treatment, and other caregiving responsibilities and concerns. Given the adverse effects of caring for individuals with such conditions on the lives of caregivers, this study aims to investigate the experiences of hemodialysis patients' family caregivers.

MATERIALS AND METHODS

A qualitative study with a descriptive, phenomenological approach was conducted in the hemodialysis department of a teaching hospital in Birjand, Iran, in 2022. Fourteen participants were selected through purposive sampling. The data were collected through semistructured interviews and analyzed using Colaizzi's method.

RESULTS

The participants were caregivers of dialysis patients who had a 6-month history of caring for patients and were first-degree relatives of the patient. A total of 278 initial codes emerged, which were categorized into three overarching themes and eight subthemes based on the research purpose and question. The overarching themes comprised caregiver time and cost strain, social challenges faced by the caregiver, and life challenges faced by the caregiver.

CONCLUSIONS

Caregivers of patients with chronic kidney disease face problems in multiple dimensions and are susceptible to developing new problems. The majority of caregivers in this study were extremely vulnerable women; if they experience difficulties, the family's foundation will be weakened. Therefore, caregivers should be included in patients' treatment plans. The expression of caregivers' experiences can help solve the problems they are facing and also helps hospital managers and health planners better plan to solve problems.

摘要

背景

接受血液透析治疗的慢性肾病患者的照料者面临着诸多挑战。这些困难涉及患者本身、他们的血液透析治疗以及其他照料职责和担忧。鉴于照料此类患者对照料者生活产生的不利影响,本研究旨在调查血液透析患者家庭照料者的经历。

材料与方法

2022年在伊朗比尔詹德一家教学医院的血液透析科进行了一项采用描述性现象学方法的定性研究。通过目的抽样选取了14名参与者。通过半结构化访谈收集数据,并使用科莱齐方法进行分析。

结果

参与者是透析患者的照料者,他们有6个月的患者照料史,且是患者的一级亲属。总共出现了278个初始编码,根据研究目的和问题将其分为三个总体主题和八个子主题。总体主题包括照料者的时间和经济压力、照料者面临的社会挑战以及照料者面临的生活挑战。

结论

慢性肾病患者的照料者在多个维度面临问题,且容易出现新问题。本研究中的大多数照料者是极度脆弱的女性;如果她们遇到困难,家庭基础将被削弱。因此,应将照料者纳入患者的治疗计划。照料者经历的表达有助于解决他们面临的问题,也有助于医院管理者和卫生规划者更好地规划解决问题的方案。