Tuğba Bilgehan, Bahar İnkaya
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引用次数: 3

摘要

姑息病人护理人员的护理负担及其影响因素目的:姑息病人及其生活空间较大的护理人员受到身体、心理、社会、物质和精神等多方面的影响。这项研究是一项研究人员对姑息性患者护理负担和因素的横断面研究。方法:本研究由98名护理人员进行,他们在2018年11月1日至2019年6月15日期间为在Pursaklar州立医院姑息病房住院的患者提供了至少一个月的护理。数据收集采用“社会形态数据表”和“护理人员压力量表(BVSÖ)”。在评估数据时;使用百分比、平均值、单向方差、独立样本t检验和Mann-Whitney U检验。统计学显著性水平p<0.05。结果:得出的结论是,59.2%的照顾者是女性,69%是已婚,93.9%在提供照顾时有困难,89.8%在提供照顾的同时得到支持。参与者的护理人员压力量表总分平均值为8.94±2.03,观察到87.7%的人有主观护理负担。护理负担和年龄(p=0.032)、月收入(p=0.020)、与护理者的亲密程度(p=0.001)、对患者的护理持续时间(p=0.009)。接受支持(p=0.018)、提供护理的困难区域(p=0.023)和日常护理的持续时间(p=0.000)之间存在统计学上显著的关系。结论:在本研究中,检查了照顾姑息性患者的个人的护理负担,确定主观护理负担较高。建议根据姑息治疗患者的需求为其主要护理人员提供心理和社会支持,并提高卫生专业人员对这一问题的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PALYATİF HASTALARINA BAKIM VEREN BİREYLERİN BAKIM YÜKÜ VE ETKİLEYEN FAKTÖRLER
Care Burden of Caregivers of Palliative Patients and the Influencing Factors Aim: Palliative patients and caregivers of a large living space of their time are affected from many aspects including physical, psychological, social, material and spiritual. This study is a researcher-cross-sectional study of caregiver care burden and factors for palliative patients. Methods: This study was conducted with 98 caregivers who provided care for at least one month to patients hospitalized in the palliative ward of Pursaklar State Hospital between November 01, 2018 and June 15, 2019. "Sociodemographic Data Form" and "Caregiver Stress Scale (BVSÖ)" were used for data collection. In evaluating the data; Percentages, means, One Way Anova, Independent Sample t Test and Mann Whitney U test were used. For statistical significance level p <0.05 was accepted. Results : It was concluded that 59.2% of the caregivers were female, 69% were married, 93.9% had difficulties while providing care, and 89.8% received support while providing care. The total score average of the Caregiver Stress Scale of the participants was 8.94 ± 2.03, and it was observed that 87.7% had a subjective care burden. Care burden and age (p = 0.032), monthly income (p = 0.020), degree of closeness to the caregiver (p = 0.001), duration of care for the patient (p = 0.009), There is a statistically significant relationship between receiving support (p = 0.018), the area of difficulty in providing care (p = 0.023), and the duration of daily care (p = 0.000). Conclusion: In this study, which examined the care burden of individuals caring for palliative patients, it was determined that the subjective care burden was high. Providing psychological and social support for primary caregivers for palliative patients according to their needs, and raising awareness on this issue among health professionals may be recommended.
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