肝豆状核变性病人主要照顾者获益感现状及影响因素研究

    The current status and influencing factors of the benefit finding among the main caregivers of patients with Wilson Disease

    • 摘要:
      目的: 调查肝豆状核变性(WD)病人主要照顾者获益感现状并分析其影响因素。
      方法: 2024年1-5月,采取横断面研究方法,便利抽取安徽中医药大学第一附属医院脑病科272例WD病人及其主要照顾者进行问卷调查,收集病人及照顾者的一般人口学资料、照顾者获益感问卷评分、照顾者反应评估量表评分及智谋量表评分。
      结果: 肝豆状核变性病人主要照顾者获益感总分(105.22 ± 17.06)分,且各维度与照顾积极反应中的自尊维度、智谋总分、个人智谋以及社会智谋之间呈正相关(r = 0.393~0.512、r = 0.317~0.466、r = 0.286~0.441、r = 0.291~0.401,P < 0.01),与照顾消极反应中的健康问题维度和经济问题维度呈负相关(r = –0.327~–0.416、r = –0.334~–0.457,P < 0.01)。多重线性回归显示,照顾者自尊(B = 1.271,95%CI:0.933~1.610)、经济问题(B = –1.337,95%CI:–1.745~–0.929)、智谋水平(B = 0.241,95%CI:0.167~0.315)及是否有照顾经历(B = –4.727,95%CI:–7.740~–1.714)是肝豆状核变性病人主要照顾者获益感的主要影响因素(均P < 0.01),解释总变异的47.0%。
      结论: 肝豆状核变性病人主要照顾者获益感处于中等水平,医护人员应及早识别肝豆状核变性病人主要照顾者的心理状况,且重点关注有经济困难、无照顾经历、自尊和智谋水平较低的照顾者,并实施个体化干预,从而提高其获益感水平。

       

      Abstract:
      Objective To investigate the current status of the benefit finding among the main caregivers of patients with Wilson disease (WD), and analyze its influencing factors.
      Methods From January to May 24, a cross-sectional study method was adopted. A total of 272 WD patients and their main caregivers in the Department of Neurology of the First Affiliated Hospital of Anhui University of Chinese Medicine were conveniently selected for questionnaire surveys. The general demographic data of patients and caregivers, scores of the Caregiver Benefit Perception Questionnaire, scores of the Caregiver Response Assessment Scale, and scores of the Wisdom Scale were collected.
      Results The total score of benefit finding among the main caregivers of patients with Wilson disease was (105.22 ± 17.06) points. Each dimension of the benefit finding showed a positive correlation with the self-esteem dimension, total score of resourcefulness, personal resourcefulness and social resourcefulness of positive caregiving responses (r = 0.393 to 0.512, r = 0.317 to 0.466, r = 0.286 to 0.441, r = 0.291 to 0.401, P < 0.01), and a negative correlation with the health problems and financial problems dimensions of negative caregiving responses (r = –0.327 to –0.416, r = –0.334 to –0.457, P < 0.01). The results of multiple linear regression analysis showed that the self-esteem of caregiver (B = 1.271, 95%CI: 0.933 to 1.610), financial problems (B = –1.337, 95%CI: –1.745 to –0.929), resourcefulness level (B = 0.241, 95%CI: 0.167 to 0.315) and caregiving experience (B = –4.727, 95%CI: –7.740 to –1.714) were the main influencing factors of caregiver benefit for patients with Wilson Disease (all P < 0.01), explaining 47.0% of the total variation.
      Conclusions The benefit finding among the primary caregivers of patients with Wilson Disease is at a moderate level. Medical staff should identify the psychological status of primary caregivers of patients with Wilson Disease as early as possible, and focus on caregivers with economic difficulties, no caregiving experience, low self-esteem and resourcefulness level and implement personalized interventions to improve their benefit finding.

       

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