• 제목/요약/키워드: Patient caring

검색결과 202건 처리시간 0.02초

뇌졸중환자의 일상생활 수행능력에 따른 가족의 부담감 (The Degree of Burden of Family Caregivers as Related to the Level of ADL of Patients with Strokes)

  • 김현미;박점희;장군자
    • 지역사회간호학회지
    • /
    • 제9권2호
    • /
    • pp.362-373
    • /
    • 1998
  • This study was designed and undertaken to identify the degree of burden of family caregivers for patients who had a stroke as the burden is related to the ADL of the patients. The data were collected from October 3rd, 1997 to March 20th, 1998. The subjects in this study were 126 caregivers as family members and 126 patients with strokes who were hospitalized in two oriental medicine hospitals and four general hospitals located in Taegue and Pusan City. The questionnaires consisted of questions regarding burden(25 items) of caregivers and ADL (25 items) of patients with strokes. Data were analyzed using percentages, mean, t - test and ANOV A done with the SPSS program. The results of this study were as follows: 1. The score for family caregiver's burden was higher than the middle score. 2. The family caregivers' age had statistically significant differences in the degree of burden. 3. The age and sex of patients affected the burden of caregivers significantly. That is, caregivers felt more of a burden when caring for the patient group in their sixties than in any other age group and female patients created more of a burden than male patients. 4. There was a statistically significant difference in the degree of caregiver burden according to the level of patient ADL.

  • PDF

암성 통증관리 교육이 암 환자의 통증과 통증관리 염려에 미치는 효과 (The Effect of Cancer Pain Management Education on the Pain and the Concerns of Pain Management in Cancer Patients)

  • 신순복;이명화
    • 재활간호학회지
    • /
    • 제6권1호
    • /
    • pp.90-103
    • /
    • 2003
  • Pain management is a major issue in caring of cancer patients. Because pain management cancer patient of does not control effectively, it is important to educate reporting pain and using analgesics for having cancer patient's concerns and anxiety. The purpose of this study was to identify the effect of cancer pain management education on the pain and concerns of pain management in cancer patients. This study was a quasi-experimental as nonequivalent control pretest-post test design. The subjects of this study consisted of 50 (experimental group 25, control group 25) patients hospitalized in K university hospital in Busan. The data were collected from December 1, 2001 to April 12, 2002. The measurement tool for the concerns of pain management had used questionnaires interpretated by Kim(1999) developed by based Ward(1993) and pain nominal scale. The collected data were analyzed frequency, percentage, mean, SD, $X^2$-test, t-test, ANCOVA. The results of this study were as follows: 1. The 1st hypothesis : "The experimental group which had received the cancer pain management education were lower than the control group in the score of pain" was not supported (p>0.05). 2. The 2nd hypothesis : "The experimental group which had received the cancer pain management education were lower than the control group in concerns of pain management" was supported (F=5.285, p<0.01). In conclusion, the cancer pain management education can know what was effective to decrease in the concerns of pain management in cancer patients. Therefore, Pain Management Education must be positively utilized in clinical situation.

  • PDF

간병요양중인 산재환자의 일상생활수행능력 및 간병인에 대한 만족도 (Survey of ADL of Industrial Accident Disabled and the Caregiver Satisfaction Degree)

  • 최정명;오진주;김춘미;이현주
    • 한국직업건강간호학회지
    • /
    • 제17권1호
    • /
    • pp.5-13
    • /
    • 2008
  • Purpose: The purpose of this study is to identify Activities of Daily Living(ADL) of industrial accident disabled with a caregiver and to evaluate the degree of satisfaction with services according to kinds of caregiver, professional or non-professional. Method: Data was collected from 178 patients in three workers' accident medical corporations of H, A and D cities from July to August, 2006. Five inspectors interviewed with the disabled by visiting the hospital. Collected data was analyzed for the frequency, percentages, t-test, etc. Results: The average score of ADL which ranged from 1 to 7 was 3.6. The 51.5 percent of caregivers for industrial accident disabled were non-professional and the 48.5 percent of caregivers were professional. 50.9 percent of the reason for the family caregivers was because of economical one. The caregiver satisfaction degree was 3.7 out of 4. The satisfaction degree with the professional caregivers was significantly higher than that with non-professional family caregivers for their excellent knowledge and techniques. Conclusion: A nursing expenses for the industrial accident disabled was intended to provide appropriate nursing services for the patient and so, it should not be a kind of income. So, the system for caring services should be investigated and the qualification of caregivers should be classified according to the health condition of the patient or ADL.

  • PDF

요양보호사의 감정노동과 소진이 노인 돌봄 태도에 미치는 융복합적 영향요인 (The Effect of Attitudes toward the geriatric of Caregivers on their Emotional Work and Burnout)

  • 이소영;홍주영
    • 융합정보논문지
    • /
    • 제9권7호
    • /
    • pp.41-47
    • /
    • 2019
  • 본 연구는 요양보호사의 감정노동과 소진이 노인 돌봄 태도에 미치는 영향요인 파악하기 위한 서술적 조사이다. 2018년 12월 1일부터 30일까지 D시, K도에서 6개월 이상 노인 돌봄으로 근무한 요양보호사 142명으로 구조화된 설문지로 자가기입방식의 설문 조사를 시행하였다. 수집된 자료는 SPSS 21.0을 이용하여 t-test, ANOVA, Pearson 상관분석 및 다중회귀분석을 시행하였다. 본 연구결과는 요양보호사의 노인 돌봄 태도에 영향을 미치는 변수로 감정노동의 주의 정도, 건강상태, 근무형태이며, 설명력은 31%였다. 즉, 요양보호사는 노인의 행동을 그대로 이해하며 받아들여야 하는 감정표현의 주의 정도에 관한 요구가 높을수록, 자가건강상태가 좋지 않을수록, 근무형태가 불안정할수록 노인 돌봄 태도에 부정적인 영향을 미치는 것으로 확인되었다. 따라서 요양보호사의 노인 돌봄 태도를 높이기 위하여 요양보호사의 안정적인 근무 환경과 더불어 사회적 인식 개선을 위한 교육프로그램의 적용이 필요하다.

Practical Considerations in Providing End-of-Life Care for Dying Patients and Their Family in the Era of COVID-19

  • Kim, Yejin;Yoo, Shin Hye;Shin, Jeong Mi;Han, Hyoung Suk;Hong, Jinui;Kim, Hyun Jee;Choi, Wonho;Kim, Min Sun;Park, Hye Yoon;Keam, Bhumsuk
    • Journal of Hospice and Palliative Care
    • /
    • 제24권2호
    • /
    • pp.130-134
    • /
    • 2021
  • In the era of coronavirus disease 2019 (COVID-19), social distancing and strict visitation policies at hospitals have made it difficult for medical staff to provide high-quality end-of-life (EOL) care to dying patients and their families. There are various issues related to EOL care, including psychological problems of patients and their families, difficulties in EOL decision-making, the complicated grief of the bereaved family, moral distress, and exhaustion of medical staff. In relation to these issues, we aimed to discuss practical considerations in providing high-quality EOL care in the COVID-19 pandemic. First, medical staff should discuss advance care planning as early as possible and use the parallel planning strategy. Second, medical staff should play a role in facilitating patient-family communication. Third, medical staff should actively and proactively evaluate and alleviate dying patients' symptoms using non-verbal communication. Lastly, medical staff should provide care for family members of the dying patient, who may be particularly vulnerable to post-bereavement problems in the COVID-19 era. Establishing a system of screening high-risk individuals for complicated grief and connecting them to bereavement support services might be considered. Despite the challenging and limited environment, providing EOL care is essential for patients to die with dignity in peace and for the remaining family to return to life after the loved one's death. Efforts considering the practical issues faced by all medical staff and healthcare institutions caring for dying patients should be made.

중증 만성폐쇄성 폐질환 환자로 살아가기 -살얼음판 위를 걸어가는 삶- (Living as Severe COPD Patient - Life of Stepping on the Thin Ice)

  • 김성렬;김윤옥;권경민
    • 성인간호학회지
    • /
    • 제22권6호
    • /
    • pp.663-675
    • /
    • 2010
  • Purpose: The purpose of this study was to explore the life experiences of patients with a severe Chronic Obstructive Pulmonary Disease (COPD). Methods: The data were collected through in-depth interviews of six patients suffering from severe COPD. The interviewed data were audio-recorded and transcribed verbatim and checked for accuracy. The Giorgi method of phenomenology was used for analyzing data. Results: Eight themes forming the, units of meaning, were: Repeated and Unpredictable Suffering of Dyspnea, Confidence Loss/Exhaustion Life due to non-efficient breathing, Gradually Deprived Liberty, Absolute Being to Sustaining my life, Source of Burden but Significant Person I am in the Family, Endless Tug-of-War-Capability/Endeavor to Breath, Longing for my Life, and Dead-end of breathing. Conclusion: The study results provide an in-depth understanding of life experiences of patients suffering from severe COPD. The findings will be useful to nurses caring for this population.

의료기관 가정간호 환자의 주 간호자가 인식한 재가복지서비스 요구 및 영향요인 (Influencing Factors on the Need of Community Care Services in the Family Caregivers of Hospital?based Home Care Patients)

  • 장미영;이가언
    • 지역사회간호학회지
    • /
    • 제20권4호
    • /
    • pp.443-452
    • /
    • 2009
  • Purpose: The purpose of this study were to examine the need of community care services and the influencing factors of the need in the family care givers of hospital-based home care patients. Methods: Data were collected from 256 family caregivers, who were recruited from 10 hospitals in a metropolitan city. A structured questionnaire on the characteristics of caregivers, resources, and patients was administered. Also, questions on the need of community care services were added. Logistic regression analysis was used to identify the influencing factors of the need for community care services. Results: The participant needed more transportation service, lease of health care devices, visiting bath, caring, visiting hair dressing than that of housekeeping, short-term care, and day care service. Various variables from the three factors were found to be influenced on the need of community care services. Conclusion: The accessibility of the higher need of community care services should be increased for hospital-based home care users. Also, the factors of Family care giver, Resource, and Patient might be considered to provide community care services of hospital-based home care users.

  • PDF

돌봄 제공자가 없는 노인에 대한 태도, 경험, 공감이 간호실천에 미치는 영향 (The Influence of Attitude, Experience and Empathy on the Nursing Care of the Elderly Who Have No Caregiver)

  • 서남숙;문지선;홍소형;박양희
    • 보건의료산업학회지
    • /
    • 제10권2호
    • /
    • pp.179-191
    • /
    • 2016
  • Objectives : The purpose of this study was to identify the factors influencing nursing care behavior for hospitalized elderly patients who have no family caregiver. Methods : Participants were 170 nurses working in general hospitals in G city. Data were collected from November to December, 2015 and analyzed by exploratory factor analysis, t-test, ANOVA, Pearson's correlation coefficient, and multiple regression with the SPSS/WIN 20.0 program. Results : There were significant correlations among experience, empathy, and nursing care behavior. Experience and empathy were significant factors influencing nursing care behavior and explained 29.4% of the variance in the score; in particular, empathy had a positive effect on nursing care behavior. Conclusions : The results show that theempathy of nurses' is the most important factor in caring for elderly patients who have no family caregiver. Nurse education programs should be developed that increase the empathy of nurses to improve the quality of nursing care for the elderly.

간호사의 직무스트레스와 노인에 대한 지식, 태도 및 케어실천행위 (The Relations of Nurses' Job Stress and Knowledge, Attitude and Care Behavior for Elderly Patients)

  • 윤숙희
    • 간호행정학회지
    • /
    • 제15권4호
    • /
    • pp.593-600
    • /
    • 2009
  • Purpose: This study was to examine the relation of nurses' job stress and knowledge, attitude and care behavior for elderly patient in hospitals. Method: One hundred ninety one nurses caring the elderly patients in hospitals in Ilsan, Busan and Gyeongsangnam-do were subjects. The data was collected between Sept. 21 and 31, 2009. Data was analyzed using t-test, ANOVA, Pearson correlation with SPSS/Win 17.0 and the fitness of pathway models with AMOS 5.0. Results: The mean scores of job stress and knowledge were in middle range, and attitude and care behavior were in a little higher range. The fitness of hypothetical model was excellent. Job stress had direct effects on attitude and care behavior, knowledge had direct effect on attitude and attitude had direct effect on care behavior. But the pathways related to job stress and attitude and job stress and care behavior were not significant. In modified model deleted the pathway between job stress and attitude, the pathway related to job stress and behavior also was not significant. Conclusion: Education related to the elderly for nurses to improve care behavior is needed continuously.

  • PDF

중환자실 환자의 억제대 경험과정 (ICU Patients' Experience Process of Physical Restraint)

  • 김미영
    • 성인간호학회지
    • /
    • 제19권4호
    • /
    • pp.583-592
    • /
    • 2007
  • Purpose: The purposes of this study were to explore and describe the use of restraint on patients and to generate a grounded theory of how the use of restraint affects patients who have been restrained. Methods: Interview data from seven patients with physical restraint was analyzed using the Strauss and Corbin's grounded theory method. Data were collected and analyzed simultaneously. Unstructured and in-depth interviews were conducted retrospectively with patients recalling their memories of ICU following their transfer to general unit. Results: 'Safety belt' was emerged as a core category and it reflected that physical restraint provided a sense of security to patients. On the basis of core category, a model of the experience process of restrained patients in ICU was developed. The experience process were categorized into four stages: resistance, fear, resignation, and agreement. Stages of these proceeds appeared to have been influenced by the nurses' attitude and caring behavior such as the frequency of nurse-patient interaction, repetition of explanation, and empathetic understanding. Conclusion: These findings indicate that patients have mixed feelings towards restraint use, although negative feelings were stronger than positive ones. The result of this study will help nurses make effective nursing intervention.

  • PDF