• 대한간호학회지
• /
• 제28권2호
• /
• pp.479-489
• /
• 1998

This work was done for 9 patients having experience of a herb medical treatment after being diagnosed as CVA during a year from January, 1996 to December, 1996 by using an ethnographic research method. The summarized results of this research are following. Ⅰ. THE EXPERIENCE OF THE ILLNESS First, the falling-ill phase is the time that they have the first stroke of paralysis and the decision pattern of medical institution' comes out. The emotional experience in the period is something like 'flustration', 'anxiety', 'despair', and 'expectation'. Second, the active-treatment phase is the time that the patients as well as their family or care giver not only show the positive attitude and actively participate in the illness treatment but also show a lot of interest in medical institutions and activities of health recovery. There is a primary factor of the continuation of treatment as an experience of treatment and being crushed and sensitivity as an experience of the illness. Third, the rehabilitation phase is the time that the patients or their family become tired and insensitive to the treatment and recuperation, and then reduce the treatment activity. There is a primary influence factor of the discontinuance of treatment as an experience of treatment and physical experience and emotional experience as an experience of the illness. The physical experience is divided into 'personal-hygiene care', and 'the sphere of activity' The emotional experiences are 'blaming someone', 'contempt' and 'despair' as a negative experience and 'hope' as a positive experience. Ⅱ. COPING STRATEGY There are a physical coping, an emotional and mental coping, a social coping, and a spiritual coping as a coping strategy used for the patients to overcome their illness and adjust themselves to their altered life. First, the physical coping comes out as 8 categories, 'using an auxiliary tool', 'doing exercise', 'protecting', 'improving their diet', 'taking care of something', 'using subsidiary medicines', 'trying a folk remedy', and 'having interest in their health'. Second, for the emotional and mental coping, there are 'accepting' and 'trying' as a positive coping and a failure of control as a negative coping. Third, the social coping is appeared as 'being supported'. Fourth, the spiritual coping is recognized as' recourse to God' and 'preparation of death'. After all, the elderly CVA patients in an agricultural area choose the act of treatment based on the traditional belief and the relationship with a caretaker. A personal health can be maintained by taking care of themselves and controling their mind, and the overcome of the illness is decided on the basis of traditional concepts and cultural principles in which the patients as well as the family, neigbors and take carers should work out together and cooperate with each other in order to achieve that.

• Journal of Hospice and Palliative Care
• /
• 제16권4호
• /
• pp.264-273
• /
• 2013

목적: 본 연구는 암환자를 돌보는 간호사들을 대상으로 간호사의 영성, 죽음불안 및 소진 정도를 확인하고, 세 변수들간의 관계를 파악하고자 한 서술적 조사 연구이다. 방법: 대상자는 서울에 소재하는 일개 암 전문 종합병원에서 근무하는 간호사 210명을 대상으로 하였다. 자료는 2012년 4월부터 6월까지 수집하였으며, 수집한자료는 SPSS 19.0 program을 사용하여 t-test, one-way ANOVA, Scheff'e test, Pearson's correlation coefficient로 분석하였다. 결과: 영성은 6점 만점에 평균 3.51점이었으며, 하위영역별로는 삶의 의미와 목적, 관계성, 내적 자원, 초월성 순으로 높았다. 죽음불안은 5점 만점에 평균 3.22점이었으며, 하위영역별로는 죽음의 부인, 짧은 시간 지각, 죽음에 대한 두려움, 죽음 연관 문제에 대한 두려움 순으로 높았다. 소진 정도는 7점 만점에 평균 4.10점이었으며, 하위영역별로는 정서적 소모, 비 인간화, 개인적 성취감 감소 순으로 높았다. 영성은 죽음불안(r=-0.327, P=0.01)과 소진 정도(r=-0.690, P=0.01)에 역상관관계가 있었으며, 소진은 죽음불안(r=0.550, P=0.01)과 정상관 관계가 있었다. 결론: 본 연구 결과를 바탕으로 간호사들의 영성을 높이고, 그들의 죽음불안과 소진 정도를 낮출 수 있는 영적 중재를 제공하는 것을 제안한다.

• 한국보건간호학회지
• /
• 제4권1호
• /
• pp.5-16
• /
• 1990

'What is nursing' this question could always be arised and such a question could bring forth the new possibility to definete the nursing concept more clearly. At the middle of 19th Centry, Mrs. Nightingale defined the concept of nursing as follows; 'Nursing is a kind of treatment act to aid the patient so that the health of patients may be recovered naturally, as keeping the most comfortable circumstances.' But after then, the role and function of nurses about purpose and method of nursing has continuously been studied, as the social circumstance has been changed. The fact that care provider and client have the same concept about nursing is very important at the first step of assessment. But at the present time, the care provider and client have not same concept yet, so the difference of unrsing concept between care provider and client is analyzed in this study. This study would be belived to be helpful for the advance of nursing in the future. In this study, 20 questionare from nursing objectives developed by Abdellah(basic care needs, sustenal care needs, remedial care needs and restorative care needs) are used for adult. The data of this study by the 6 point rating scale are analyzed by SAS as follows; 1. Respondent's view is that nursing is necessary in case of group(school or company) rather than private and in case of abnormal conditions rather than normal conditions. 2. Every questionares of nursing objectives are divided into 4 points of view such as basic care needs, sustenal care needs, remedial care needs and restorative care needs are examined. The evaluation by 6 point rating scale revealed that $5.08\pm0.65$ point in basic care needs $4.93\pm0.68$ point in sustenal care needs $4.91\pm0.80$ point in remedial care needs and $4.61\pm0.91$ point in restorative care needs. While basic care needs and substenal care needs that need more physical care show high points, remedial care needs and restorative care needs that need more psychological, social and spiritual care show low points. 3. It was checked whether there is any significant difference between above 4 point of views in nursing objectives and qeneral characteristics or not. As a result, there is significant difference between 4 point of view and ages, educational level, marriage, composition of children. And also there is significant difference between religion and basic care needs, remedial care needs and restorative care needs. But there is no significant difference between any point of view and sex, occupation, experience of admission and experience of family admission. As this study is based on the data gethered from a restricted area, the result can not represent the opinion of all the clients. Therefore the same kind of study should be carried out on many areas repeatedly and also it should be tried to extract objective concept. And also periodical study is needed to observe the changing process of nursing concept.

• Journal of Hospice and Palliative Care
• /
• 제10권1호
• /
• pp.21-28
• /
• 2007

본 고에서는 보다 수준 높은 호스피스 케어를 위해서는 고통에 대한 포괄적인 이해와 영적 접근에 대한 의식확장이 전제되어야 한다는 가정 하에 관련된 문헌을 살펴보았다. 최근 건강관련분야 특히 만성적 건강문제에 접근하는 기본 패러다임으로 총체적 모델에 대한 관심이 증대하고 있는데 이는 인간에 대한 존엄과 인간을 몸과 마음 그리고 영적인 요소가 하나로 통합된 존재로 보는 이론체계를 수용한다. 따라서 전인적, 총체적으로 인간을 이해하는 것은 죽음을 앞둔 대상자의 건강과 관련된 의사결정과 치유과정에 필수적인 요소라 할 수 있으며 이 때 제기될 수 있는 윤리적 관점은 또다른 차원의 문제인 것이다. 인간은 죽음을 체험하면서 궁극적인 고통과 대면하게 되는데 이러한 문제를 해결하기 위해서는 의료적 조치인 이성의 힘만이 아니라 절대자인 신(God : 하느님 : 우주)과의 관계 안에서의 모색이 연결되어져야 할 것이라고 본다. 죽음의 고통을 겪고 있는 대상자들은 의료인의 따뜻한 마음과 전인적인 포용력을 요구하는 인간적인 특성을 소지하고 있다. 호스피스에 관심을 갖는 의료인들은 인간의 마음 속 깊은 곳에 자리하고 있는 종교심 또는 영적 영역의 장을 인정하고 애정어린 몸짓으로 대상자의 고통에 함께 함으로써 보다 수준 높은 호스피스 케어가 이루어질 수 있으므로 그들의 곁에 있다는 것을 느끼게 해주는 한편 고통에 대한 의식을 확장하고 발전시키고자 하는 신념을 소지할 필요가 있다.

• Journal of Hospice and Palliative Care
• /
• 제13권2호
• /
• pp.76-80
• /
• 2010

목적: 본 연구에서는 제주지역내의 보건소, 지역 암센터와 말기암환자 전문의료기관 등에서 실시하고 있는 재가암환자 관리 사업의 객관적 현황을 파악하여 각 기관별의 재가암 관리를 위한 역할을 정립하고자 한다. 방법: 제주지역에서 재가암환자 관리를 실시하고 있는 각 기관을 대상으로 재가암환자 관리 사업의 시작연도와 현재 실시하고 있는 사업과 부족한 부분 등을 알아보고, 각 기관과의 연관사업 등을 파악하였다. 결과: 제주지역내의 재가암환자 관리는 6개의 보건소와 1개의 지역 암센터, 1개의 말기암환자 전문의료기관이 활동 중에 있으며, 제공되는 서비스는 약간의 차이는 있으나, 신체적, 정서적, 영적, 교육 정보적 서비스를 실시하고 있으나 보건소의 경우, 통증완화를 위한 마약성 진통제의 사용이 부족한 실정이었다. 결론: 본 연구는 재가암환자 관리 사업에서 말기암환자 전문의료기관과 보건소에서 급성기의 경우와 재가암환자 관리를 위한 인력의 교육을 위한 교육은 지역 암센터와 연계하여 재가암환자에 대한 체계적인 관리와 역할 분담을 정립시켜야 할 것으로 생각된다.

• 간호행정학회지
• /
• 제6권1호
• /
• pp.55-81
• /
• 2000

This study examined nursing care in a Newborn Intensive Care Unit (NICU) by reviewing nursing activities for the newborns. Through direct observation, time used for nursing care according to the nursing activity, shift, day of the week, and position of the nurses was measured. This study was done on November 15, 21, 24, 1999 at a university medical center hospital and included eight nurses and 179 newborns as the study subjects. The data were collected from the medical records, and by using a nursing activity record for the NICU, and a nursing activity time record for the NICU. The first step in the data collection process was to develop a list of nursing activities which was done through a literature review, examination of medical affairs and duty records. Content validity was measured by a panel of three professors who were experienced clinicians. In the second step two pre-training sessions were held with three sophomore student nurses who then measured the time for each nursing activity using a stopwatch. The data were analyzed using frequencies for nursing activities, averages, percentages and ANOVA for differences between shift and between days of the week, and percentages and t-test for differences according to position of the nurse. The results are as follows: 1) The total number of activities was 156, direct or indirect nursing activities. Direct nursing activity classified according to physical, educational, emotional/social/economic/spiritual needs. There were 109 direct nursing activities in 16 fields. 2) The order of nursing activities, according to time required, was record keeping, nutritional care, measurement/observation, medication, hygiene care, examination and specimen collection, and checking supplies, and according to frequency, measurement/ examination, record keeping, nutrition care, hygiene care, elimination care and medication. 3) According to shift, direct care during the night shift at 313.4 minutes was the longest time and indirect nursing care during the night shift at 252.2 minutes was the highest time. 4) For days of the week, Monday had the highest time for direct care 275.8 minutes (34.6%) and Wednessday had the highest time for indirect nursing care 269.6 minutes (36.1%). 5) For nursing time according to position of nurse, general nurses had the highest for direct care (330.7 minutes), nurse managers for indirect nursing activities (239.0 minutes) and general nurses for individual private time (63.9 minutes). The results of this study show that the major nursing time consuming activities included record keeping, nutrition care and measurement/examination. For newborns, time needs to be allowed for care to be sensitive, sophisticated and specialized rather than concentrated on indirect nursing tasks such as record keeping. Therefore, it is imperative to develop computerized systems that support a systematic approach to record keeping which is more efficient. Moreover, nursing needs according to shift, day or position of nurse can be utilized in assessing nursing resources through a computerized process.

• Journal of Hospice and Palliative Care
• /
• 제10권4호
• /
• pp.195-201
• /
• 2007

목적: 본 연구에서는 전국의 시 군 구 보건소 재가 암환자 관리사업의 객관적 실태분석의 일환으로 재가 암환자 관리 사업의 주 대상자인 재가 암환자를 대상으로 개발된 조사도구를 이용하여 그들의 재가 암환자 관리 요구도와 제공정도를 파악하는데 목적이 있다. 방법: 재가암환자 관리사업의 요구도 및 제공정도로 구성된 설문지를 개발 조사하고 수집된 자료는 SPSS WIN 12.0을 이용하여 빈도와 백분율을 중심으로 분석하였다. 결과: 현재 재가 암환자 관리사업을 통해 제공되고 있는 서비스를 신체적, 정서적, 영적, 교육정보적 서비스로 나누어 재가 암환자들을 대상으로 조사한 결과 요구도와 제공정도는 정서적 서비스에서 가장 높고 다음으로 교육 정보적 서비스, 영적 서비스, 신체적 서비스 순으로 조사되었다. 각 서비스별 주요 항목을 살펴보면 신체적 서비스의 경우 통증조절은 요구도에 비해 그 제공정도가 낮았고 반면 배설장애조절과 개인위생은 요구도에 비해 그 제공정도가 높은 것으로 나타났다. 또한 정서적 서비스의 경우 전반적으로 요구도와 제공정도가 높았고 영적 서비스의 경우 요구도에 알맞게 서비스가 제공되고 있는 것으로 나타났다. 결론: 본 연구는 보건소 재가암환자 관리사업에 대한 환자의 서비스 요구도와 실제 제공받은 서비스 정도를 분석한 연구로서 향후 재가 암환자의 요구도에 근거한 효율적 프로그램 개발의 기초자료로 활용이 가능할 것으로 사료된다.

• Journal of Hospice and Palliative Care
• /
• 제16권2호
• /
• pp.98-107
• /
• 2013

목적: 본 연구는 우리나라의 가정 호스피스 기관의 서비스 실태와 문제점을 파악함으로써 가정 호스피스의 개념을 재정립하고, 가정 호스피스의 표준 설정과 제도화, 다양한 호스피스 유형들의 연계 체계 구축의 기초자료로 활용하고자 시도되었다. 방법: 2011년 5월을 기준으로 확인된 호스피스 기관 166개 중 의학적 돌봄을 포함하는 가정 호스피스를 운영한다고 응답한 29개 기관 전수의 질문지가 자료 분석에 사용되었다. 결과: 대상 기관 중 호스피스 입원 병실이 있는 경우는 51.7%, 순수 가정형은 34.5%이었다. 팀 구성원은 간호사와 자원봉사자가 각각 62.0%, 62.1%, 팀 구성원의 방문은 간호사와 자원봉사자가 각각 평균 8.84회와 6.0회, 팀 회의는 월평균 2.65회, 비용은 대부분 무료로, 필요한 재원을 마련하는 방법에는 개인의 기부가 가장 많았다. 하루 평균 방문 환자 수는 평균 2.46명, 비암성 환자는 6.9%의 기관만이 돌보고 있었다. 58.6% 기관에서 협력의뢰를 위한 공식적인 체계를 구축하고 있었으며, 방문 범위는 44.8%에서 거리나 시간에 제한을 두고 있었다. 제공되는 서비스는 가족 상담과 서비스 연계가 가장 많았고, 가정 호스피스 의뢰방법은 환자 및 가족의 직접 의뢰가 51.7%로 가장 많았다. 대부분은 서비스 제공을 위한 기본 의료장비 및 물품을 갖추고 있는 반면 특수 장비는 부족하였다. 호스피스 전용병상이 있는 경우는 대부분 정부 및 공공기관의 후원으로 이루어지고 서비스 측면에서는 팀 회의, 통증조절, 증상조절이 잘 이루어지고 있었다. 기관운영 장애요인으로는 재정문제, 인력부족, 호스피스 인식 부족의 순위를 보였으며, 이를 위해 가장 먼저 해결해야 할 과제로는 '수가제도화'라고 주장하였다. 결론: 현재 우리나라의 가정 호스피스는 호스피스 본연의 목적을 달성하기에는 많은 제한이 있으므로 빠른 제도화와 서비스 표준 확립이 이루어져야 할 것이다.

• 가정과삶의질연구
• /
• 제23권4호
• /
• pp.1-15
• /
• 2005

Korean society is experiencing rapid changes which are certain to shape the lives of the older people and their families. So, the purpose of this study was to improve the quality of the elderly welfare service in Korea. Even though the interest about the elderly welfare in Korea is rapidly on the increase, the reality of Korean Society still leaves much to be desired, quantitatively as well as qualitatively. Pay attent to this point, now going to grasp the situation of not the handicapped elder people but the general elder people actual life condition and demand for welfare. So this study focused on the demand of not out-of home service but in-home care service. It was based on the data from by Korea National Statistical Office, having observed 6,139 elderly people. The results were as follows. They hope to get the elderly welfare services about health examination service, nursing survice, supporting service for household. That was, the most of them wanted in-home care service than out-of home care service. To ensure effective care to the elderly, it needed development and settlement of welfare service in face of their daily living. And, even though they recognized that they should cover the elderly life expenses themselves, the rate was hit that indicated their adult children as a parents supporter. This means that we should consider not only to the elder people but also to the family which contained the old people as the elderly welfare service. As a remedy, we can find the cooperation between elder welfare service at the social welfare organization and counsel, education at the family strengthen center. To improve the quality of the elderly welfare service in Korea, the elderly welfare service should focus not only on the physical and spiritual health maintenance but also active understanding living environment and growing ability to arbitrate between individual and living.

• 근관절건강학회지
• /
• 제19권2호
• /
• pp.197-209
• /
• 2012

Purpose: This study was aimed to revise Personal Power of Health Care (PPHC) scale which was developed to measure the personal power and competence for health care. Methods: Research phases designed for this study were literature review, scale development, and discussion with experts and pre-test for content validity, and survey for construct validity and reliability. The scale was composed of 25 items with 7 dimensions and tested to 592 adults ranged from 20 to 59 aged living in S and W city. Results: From factor analysis, 7 dimensions were identified and named as follows: Health-perception, Health problem identifying and solving, Socio-economical involvement, Sociocultural relationship, Self-regulation, Spiritual wellbeing, and Health policy participation. The total explained variance was 54.69%. The reliability was .817 of Cronbach's alpha. The PCHC scale was significantly different from gender, religion, education level, monthly income, and presence of family disease, but not different from age and job. Also, there were significant correlations among Health Promotion Lifestyles Profile II, WHO QOL-BREF and self-efficacy. Conclusion: This PCHC scale is reliable and valid to measure personal competence of health care.