• Title/Summary/Keyword: 간병인

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Development of EEG-based Serving Robot Care Service for Multi-person Room Patients (다인실환자를 위한 EEG기반 서빙로봇 간병서비스 개발)

  • Lee, So-Yeon;Choi, Bongjun;Moon, Mikyeong
    • Proceedings of the Korean Society of Computer Information Conference
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    • 2022.07a
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    • pp.649-650
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    • 2022
  • 간병 서비스를 제공하는 데에 있어 가장 중요한 것은 간병인의 스트레스 관리 및 체력 관리이다. 그러나 요양 시설의 수요 증가량에 비해 간병인의 공급량은 줄어들고 있으며 고령화로 인해 노인이 노인을 간병하는 노노간병 사례가 증가하고 있다. 1인당 부양하는 환자 수의 증가와 간병인의 연령이 평균적으로 높아지면서 간병 스트레스 및 간병 살인 문제가 빈번하게 발생하고 있다. 본 논문에서는 환자의 EEG를 실시간으로 분석해 환자에게 필요한 것을 전달해주는 서빙로봇 간병서비스 개발 내용에 대해 기술하고 있다. 이 시스템을 통해 장시간 노동에 따른 간병인의 간병 스트레스와 간병 부담을 덜어줄 수 있을 것으로 기대한다.

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편견과 차별을 넘어서 -간병인 구하기 힘들어-

  • 김영미
    • RED RIBBON
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    • s.55
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    • pp.12-13
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    • 2003
  • 에이즈환자라고 하면 간병인을 구하기도 어려웠다. 감염인이라는 사실을 알리지 않고 간병인을 구했다가도 감염인인 것을 알고는 그만 두는 것도 문제였다. 비감염인이면서 감염인을 간병하겠다고 나서는 사람이 간혹 있을라치면 그 때는 간병비가 비감염인 간병보다 $50\%$정도 더 요구되었다.

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Nursing in Family and Welfare: Political Meanings of the 'Pflegeversicherung' (가족내 간병과 간병보험의 복지정책적 함의)

  • 이진숙
    • Korea journal of population studies
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    • v.24 no.1
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    • pp.183-202
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    • 2001
  • Traditionally the women have had responsibility for homework, blinding-up of the children and caring of the aged in the family. But in models society the women would like to take jobs much more than in the past, and therefore women who have jobs are in the condition of mental and physical stress very heavily. So it is urgently needed of the social-political arrangements for caring-worker in the family (generally the women). This paper examines this problem, especially problem of the nursing of the aged in the family, and compares the political arrangements between in Korea and Germany.

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Relationship between Job Stress and Mental Health of Caretakers (간병인의 직무스트레스와 정신건강과의 상관관계)

  • Ro, Hyo-Lyun;Kim, Sung-Joong;Lee, Moon-Hwan
    • The Journal of the Korea Contents Association
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    • v.9 no.11
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    • pp.297-308
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    • 2009
  • The purpose of this study is to explore the relationship between job stress and mental health of caretakers by SCL-90-R. This study are to offer basic information for patients the quality of service interventions. The sample for the study consisted of 247 caretakers who work in Busan. The results of this study are as follows: 1) Caretakers' mental health and job stress was not serious level. 2) There was an important factor in job stress, which was suitable pay. 3) Caretakers' job stress was positively related to mental health. There is a statistical correlation between the relationship with mental health and job stress. 4) Caretakers' mental health was affected by job stress level. Therefore, We need training and program that focuses on management job stress in caretakers.

Factors Influencing Caregiver Burden During Rehabilitation of Stroke Patients (뇌졸중 환자 재활 시 간병인 부담에 영향을 미치는 요인)

  • Yu-Mi, Kim;Seung-Min, Baek;Yong-Il, Na;Yong-Soon, Yoon
    • Journal of Industrial Convergence
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    • v.20 no.11
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    • pp.27-34
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    • 2022
  • In this study, we aimed to determine which medical conditions of the stroke patients admitted for rehabilitation more than four weeks after onset affect caregiver burden. Participants diagnosed with stroke and their respective primary caregivers were enrolled and assessed after an 8-week follow-up period. The areas of evaluation for stroke patients included neurologic state, cognition, performance in daily life movements, gait, and balance, and caregivers were evaluated in the area of burden. The evaluation was conducted at the start of the rehabilitation course and eight weeks later. Patient caregivers were found to be under mild to moderate burden while providing care throughout the hospitalization period. The patient's neurologic state and cognition were correlated with caregiver burden. In the all patient and the subacute stroke patient group, multiple regression analysis confirmed that the neurologic state and balance stability were factors that influenced caregiver burden. Hence, we suggest that improvement in the patient's balance stability be emphasized during the course of rehabilitation to mitigate caregiver burden.

Symptom Features of Terminally Ill Cancer Patients and Depression of Family Caregivers

  • Kim, Hyo Min;Koh, Su-Jin;Hwang, In Cheol;Choi, Youn Seon;Hwang, Sun Wook;Lee, Yong Joo;Kim, Young Sung
    • Journal of Hospice and Palliative Care
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    • v.20 no.3
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    • pp.188-193
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    • 2017
  • Purpose: There has been very little study on the associations between patient's symptoms themselves and family caregiver (FC)'s depression in the palliative phase. This cross-sectional study was to investigate the relationship between symptom features of terminally ill cancer patients and their FC's depression. Methods: We performed a multicenter survey using the MD Anderson symptom inventory and the Hospital Anxiety and Depression Scale. A total of 293 patient-FC pairs were recruited from seven tertiary medical centers. A multivariate regression analysis was applied for identifying the relevant factors associated with FC depression and for estimating adjusted depression score of FCs. Results: Among various psychosocial factors, low FC quality of life, low social support, spouse, and more caregiving time were significantly associated with FCs' depression. According to the presence of FCs' depression, there were significant differences in some symptom characteristics of patients. Even after adjusting for the relevant confounders, depression scores were lower in FCs caring for patients who had negative symptoms (loss of appetite, P=0.005; drowsiness, P=0.024; and dry mouth, P=0.043) than in FCs caring for patients who had not. FCs caring for patients with severe appetite loss had lower depression scores than those with not severe one (P=0.039). Conclusion: Our result suggests that patient's symptom characteristics might be helpful when evaluating a FC's depression.

A Study of the Acculturation Meaning among Chinese-Chosun Residential Care Attendants in Long-Term Care Setting (조선족 간병인의 문화적응 경험에 관한 연구: 노인 간병서비스를 제공하는 조선족 여성을 중심으로)

  • Hong, Sae-Young;Kim, Gum-Ja
    • 한국노년학
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    • v.30 no.4
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    • pp.1263-1280
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    • 2010
  • The present study describes the acculturation meaning of 12 Chinese-Chosun residential care attendants(RCAs) who are currently working in long-term care settings for Korean older adults. Using a qualitative research method, the findings show that the acculturation process of Chinese-Chosun RCAs consists of three stages: entrance, conflict, and adaptation. In the initial stage, the assets of the social and cultural networks among their friends and relatives, who already settled down or employed as RCAs, provided more opportunities for being employed as a RCA. However, most Chinese-Chosun RCAs experienced a number of conflicts while they adapted to mainstream society and perform caregiving tasks. They perceived discrimination, heavy workload, prejudice, and homesick. Nevertheless, they appeared to adapt effectively to Korean society and working environments because they were aware of the various benefits of working as a RCA such as higher wage and more job openings compared to other jobs, a rapport with the patients and patients' families, flexible work hours, and pride as a caregiver. This type of qualitative groundwork will be an important precursor to the design, implementation, and evaluation of acculturation research for minority immigrant workers in the Korean social welfare system.

Survey on the Care Burden and Quality of Life in Family Caregivers of Patients Using Home Mechanical Ventilator in Yeongnam Region, Korea (영남권역에서 가정용 인공호흡기를 사용하는 환자 가족간병인의 간병 부담과 삶의 질)

  • Son, Ju-Hyun;Moon, Myung-Hoon;Cho, Mi-Kyung;Yun, Ra-Yu;Huh, Sung-Chul;Min, Ji-Hong;Moon, Jung-In;Kim, Soo-Yeon
    • The Journal of Korean society of community based occupational therapy
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    • v.10 no.1
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    • pp.39-49
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    • 2020
  • Objective : The aim of this study was to investigate the care burden and life quality in family caregivers of community-dwelling patients using home mechanical ventilator(HMV) in Yeognam region. Methods : Survey performed to family caregivers of the patients using HMV in Yeognam region, Korea. The questionnaire is composed with patient care and the burden on caring. Korean version of Short Form Zarit Burden Interview(K-ZBI-12) and 3-Level version of EuroQol-5 Dimension applying Korean weight(KEQ-5D-3L) were also investigated. Statistical significance was accepted for p<.05. Results : A total 98 out of 150 questionnaires were analyzed. The K-ZBI-12(33.08±10.34) had a correlation with KEQ-5D-3L(0.71±0.25) negatively(p=.038). Patients' age, duration of HMV, financial burden and professional caregivers' care time had correlations with K-ZBI-12 positively(p<.05). KEQ-5D-3L correlated duration of HMV negatively(p=.017). Invasive ventilator group had lower KEQ-5D-3L than the non-invasive ventilator group(p=.008). K-ZBI-12 was lower in more than one caregiver care of patients than in one(p=.001). Conclusion : This study revealed high care burden and low quality of life in family caregivers of the patients with HMV in Yeongnam region, Korea. Efforts are needed to continually identify the needs of patients and their families, and the socioeconomic support and medical services associated with HMV.

간병서비스 지원 프로그램

  • Kim, Gyeong-Seon
    • RED RIBBON
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    • s.75
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    • pp.10-11
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    • 2007
  • 대한에이즈예방협회에서는 HIV/AIDS 감염인 지원사업의 일환으로 간병지원 서비스를 제공하고 있습니다. 지난 분기에 발행된 '레드리본'에서는 재가복지를 필요로 하는 감염인들에게 제공될 수 있도록 재가복지 서비스에 대한 전반적인 소개를 하였습니다. 연속기획으로 이번 호에서는 '간병지원 서비스'에 대한 전반적인 소개를 통해 간병서비스가 필요한 감염인 및 관련단체들에게 유익한 정보가 되길 바라는 마음입니다.

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An Investigation of Caretakers Needs for Changes in Electric Wheelchairs (간병인의 전동휠체어 사용에 대한 만족도 조사)

  • Lee, Jung Ah;Lee, Bum-Suk;Choi, Hyun;Yoo, Sung Moon;Yang, Sung Pil;Bae, Jae Hyuk;Pak, Han Ram
    • Journal of rehabilitation welfare engineering & assistive technology
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    • v.10 no.3
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    • pp.177-184
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    • 2016
  • The purpose of this study was to investigate caretakers' demands and request in electric wheelchairs. The survey included the usability questionnaire (safety, operability, satisfactions) which were selected by opinions of caretakers and specialist of rehabilitation for electric wheelchairs. The survey also included questionnaires consisting of such questions as to demographic information, care experience, care time, and care burden, and demand for folding electric wheelchairs. Participants were fifty caretakers of electric wheelchair users. Caretakers' average age was 54.54years, and the average duration of their care experience was 80.98 months with average care time 9.80 hours per day. In safety and operability, most of participants were mostly satisfied. However, in satisfaction of weight and clean of electric wheelchairs was dissatisfied. They reported that the biggest problem of electric wheelchairs were too heav and difficult to control and that the greatest difficulty in helping electric wheelchair users was helping them with transfer to and from the wheelchair. They also need their prefer to develop folding electric wheelchairs. In this study, caretakers emphasized necessity of development light, easy to storage and clean electric wheelchairs. In conclusion, it is required to develop folding electric wheelchairs to reflect caretaker's opinions.