• 제목/요약/키워드: Home cancer patient

검색결과 86건 처리시간 0.033초

보건소 재가암환자관리사업 대상자의 서비스 요구도 분석 (Needs Assessment for the Beneficiaries of Home-Based Cancer Patients Management Project)

  • 이주형;박정임;강지훈;염정호;고대하;권근상
    • 농촌의학ㆍ지역보건
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    • 제36권4호
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    • pp.238-250
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    • 2011
  • 지속적인 암환자 및 암 관련 의료비용 급증은 환자 개인의 고통 및 경제적 부담으로 작용할 뿐만아니라 사회적인 부담이 되고 있다. 이에 재가암 환자에 대한 통증관리 등의 서비스 제공은 의료 비용을 절감하는데 효과가 있을 것으로 여겨지고 있다. 따라서 재가암환자에 대한 적절한 의료 및 복지 서비스 등을 제공하기 위한 자료로 활용하고자 재가암환자관리사업 수혜자의 서비스 요구도에 대하여 각 보건소의 재가암환자관리사업 담당자가 재가암환자관리사업 수혜자 방문시 면접조사방법으로 조사하였고, 불충분응답자 15명을 제외한 661명을 최종 분석대상으로 하였다. 재가암환자의 서비스 요구도에 대한 요인분석 결과 5가지 영역으로 분류할 수 있었고, 요인별 신뢰도는 0.593~0.890이었다. 요구도의 순위는 사회적 지지, 정보 및 교육제공, 심리적 문제해결, 신체증상해결, 가사도움 순으로 조사되었다. 대상자를 암 치료 및 진행 정도에 따라 말기암 환자, 치료중인 암환자, 암 완치자로 분류하였을 때, 말기암환자의 요구도가 가장 높게 나타났으며, 사회적지지, 심리적 문제 해결, 정보 및 교육 순서로 요구도가 높았다. 나머지 그룹에서는 사회적지지, 정보 및 교육, 심리적 문제 해결 순으로 말기 암환자와 차이를 보였다. 뿐만 아니라, 연령별, 거주 지역별, 종교 유무에 따른 서비스 요구도에 차이가 관찰되었고, 이를 바탕으로 현재 제공되고 있는 재가암환자관리의 효율적인 추진을 위해 대상자 분류, 연령별 및 거주 지역별 특성에 따른 서비스가 제공될 수 있도록 해야 할 것이다.

보건소 재기 암환자 관리사업에 대한 환자의 요구도 및 제공정도 (A Study on Demand and the Supply for Home-based Cancer Patient Management Projects of Public Health Centers)

  • 조현;손주영;허점도;진은희
    • Journal of Hospice and Palliative Care
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    • 제10권4호
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    • pp.195-201
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    • 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.

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재가 비암 환자의 생의 말기 단계별 신체적, 영적 간호요구도 - 간호요구의 중요도와 난이도를 중심으로 - (Physical and Psychospiritual Care Need by End-of-life Stages among Non-cancer Patient at Home: Based on the Importance and Difficulty of Care Need)

  • 이종은;김순례
    • 지역사회간호학회지
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    • 제23권2호
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    • pp.127-133
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    • 2012
  • Purpose: This study was conducted to assess needs at each end-of-life care stage and to analyze importance and difficulty of care needs for home care nursing among non-cancer patients. Methods: We used a retrospective design. Total eligible patients were 117 at the ages of 40 and over, who continuously received home care nursing throughout beginning, stable, and near death stages, and finally died at home from January 1, 2006 to December 31, 2006. Descriptive statistics, Cochran's Q test, Friedman's test were used for data analysis. Results: In the area of physical care, the care need for 'assistance for activities in daily life' was significantly highest in the beginning stage. The care need for 'aggravation or adverse changes in physical symptoms' was significantly increased in the near death stage. In the area of psychospiritual care, 'family's psychological burden' was revealed as having the highest rate of care needs in the every stage. Conclusion: Future intervention should consider assessing care needs in end-of-life care for non-cancer patients who are provided with home care nursing.

암성 통증 조절을 위한 자가통증조절장치를 이용한 몰핀의 지속적 피하투여 -증례 보고- (Continuous Subcutaneous Administration of Morphine Using Patient Controlled Analgesia Device for Control of Cancer Pain)

  • 이경호;이철;김원태
    • The Korean Journal of Pain
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    • 제11권2호
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    • pp.321-325
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    • 1998
  • Most of the patients with pain resulting from advanced cancer need opioid for adequate analgesia. Various Methods of drug administration to control the pain have been developed. One of them, continuous administration of intravenous morphine is used for more effective pain control in the patient with severe pain that cannot be satisfactorily controlled by other Methods of morphine administration. But this is not a suitable method at home because of the possibility of serious infectious complications and the difficulty in managing intravenous access by untrained personnel. Continuous subcutaneous adminstration of drugs can not only overcome such disadvantages of continuous intravenous infusion but also get almost the same effect of pain control as continuous intravenous infusion, and allows opportunity to move freely and return home, improving quality of life. We used continuous subcutaneous morphine and metoclopramide in the patients with cancer pain via a portable PCA device, and accomplished satisfactory pain relief without significant side effect.

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지역사회 재가 암환자 가족의 사회적 지지 스트레스, 건강상태 및 삶의 질과의 관계 (The Relationship of Social Support, Stress, Health Status and Quality of Life in Caregivers of Home-stay Cancer Patient in a Comminity)

  • 김분한;김태수;김의숙;정연
    • Journal of Hospice and Palliative Care
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    • 제3권2호
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    • pp.144-151
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    • 2000
  • 본 연구는 지역사회의 재가 암환자와 그 가족의 삶의 질을 증진하기위하여, 사회적 지지, 스트레스 건강상태 및 삶의 질 정도와 이들간의 관련성을 탐색하기 위하여 시도하였다. 본 연구의 대상자는 일 지역사회의 22개동 전역에 걸쳐 거주하는 암환자 가족 중 암환자를 주로 돌보는 사람이었으며, 대상자의 특성과 제변수를 측정할 수 있는 설문지를 이용하여 면접과 전화를 이용하여 자료를 수집하였다. 수집된 자료는 Window SFSS-PC를 이용하여, 빈도와 백분율, 기술통계 및 t-test와 ANOVA, Pearson's correlation coefficient를 검정하였다. 연구 분석 결과 암환자를 돌보는 가족원들이 지각한 사회적 지지는 가족지지망이 평균 3.24로 간호사 지지(평균 3.03)보다 높게 나타났다. 스트레스 정도는 평균 3.52로 측정변수들 중 가장 높게 나타났으며, 건강상태(신체적 불편감)은 평균 2.98로 심각하지 않은 것으로 나타났다. 삶의 질 정도는 평균 2.34로 측정변수들 중 가장 낮아 보통정도 이하로 가장 낮은 것으로 나타났다. 또한 암환자를 돌보는 가족원의 나이가 많을수록 건강문제 경험 정도는 높아지는 경향을 보였으며, 교육정도가 낮을수록 건강문제 경험 정도는 높아지는 경향을 보였다. 암환자 가족원들의 가족지지망 정도가 높을수록 간호사지지 정도도 높게 지각하는 것으로 나타났으며, 스트레스 정도가 높을수록 건강상태도 좋지 않은 것으로 나타났다. 또한 스트레스가 높고 건강상태가 좋지 않을수록 삶의 질 정도가 낮았다. 그러므로 암환자를 돌보는 가족원의 건강상태를 유지하고, 삶의 질을 높이기 위해서는 환자를 돌보면서 경험하게 되는 스트레스를 감소시키거나 또는 스트레스를 덜 인지할 수 있고 스트레스에 대한 대처를 증진시킬 수 있는 방안을 강구해야 할 것이다.

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방문간호를 통한 암환자의 위기중재 효과에 관한 연구 (The Effect of Crisis Intervention by the Visiting Nurse with Patients with Cancer)

  • 김조자;유지수;박지원
    • 대한간호학회지
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    • 제19권1호
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    • pp.63-80
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    • 1989
  • This study was undertaken at Yonsei University Medical Center to identify the crisis responses and nursing problems of patients who had been diagnosed with cancer, and changing patterns of grieving over time periods, and to analyse the effectiveness of follow up care through home visiting nursing. This study was carried out in three stages. The 1st study data were collected from a total of 205 patients who had been diagnosed with cancer from Sept.1 to Dec. 31, 1987 using a cross-sectional method. The 2nd study data were collected three times from 30 patients with cancer at 4 weeks intervals from March 1 to June 31, 1988 using a longitudinal method. The 3rd study data were collected from two different groups from March 1 to June 31, 1988. One was an experimental group who was visited by nurses and the other one was a control group not visited by nurses. The subjects of the 3rd study consisted of 60 patients with cancer and a Quasi-experimental research design was used. The results were as follows ; 1. The patients did not experience one stage at a time among the five stages of grieing, denial anger, bargaining, depression and acceptance, as identified by Kubler Ross. They experienced a combination of stages, especially of the bargaining and the depression stages. This stages did not change with the passing of time. 2. The patients expressed more physical and socioecounomical problems than emotional problems. And they used more problem coping methods than emotional coping methods. 3. Follow up care through home visiting nursing positively influenced the patient's quality of life, especially their physical well-being and symptom control The patients responded positively to the home visiting nursing, stating that it was helpful In them. It was concluded that the development of a home visiting nursing program is needed for the effective home care of patients with cancer.

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Providing End-of-Life Care in the Community: What Are the Challenges in Malaysia?

  • Leong, Yoke Yeng;Hamzah, Ednin;McCarthy, Sylvia;Lim, Zee Nee
    • Journal of Hospice and Palliative Care
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    • 제25권3호
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    • pp.133-137
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    • 2022
  • A 72-year-old woman with metastatic lung cancer to bone and brain and with left external iliac vein thrombosis was under the care of a community palliative care provider. She experienced an acute pain crisis due to acute limb ischemia of the left lower limb. Goals-of-care discussions were held with the patient and her family; she prioritized symptom control and end-of-life care at home. The family and patient were aware of her short prognosis. Her complex pain was managed by the community palliative team, and her family was empowered to give subcutaneous injections. We illustrate a case showing the importance of community health services with palliative care support in providing symptom management and support to patient and family caregivers throughout the course of a life-limiting illness. It also highlights family caregivers' potential psychological distress in delivering subcutaneous injections in terminal care for a patient at home.

재가암 환자 통합건강증진 프로그램 개발 및 효과 (Development and Effect of the Integrated Health Promotion Program for Cancer Survivors Living at Home)

  • 윤희상;황은아
    • 지역사회간호학회지
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    • 제32권1호
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    • pp.51-63
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    • 2021
  • Purpose: This study aimed to develop an integrated health promotion program for cancer survivors residing in the community based on the shared care model, and evaluate its effectiveness. Methods: A quasi-experimental trial was conducted. The participants consisted of 35 cancer survivors with completed intensive cancer therapy at the cancer hospital. The intervention group (n=20) and the control group (n=15) were recruited from among a district home cancer patient registrations. The intervention group participated in an integrated health promotion program based on the MAPP (Mobilizing for Action through Planning and Partnership) development process. The program consisted of physical, psycho-social and body image units. The participants were assessed before the program, and immediately after the program. Data were collected between July 1 and September 2, 2018 using FACT-G quality of life (QOL), distress thermometer (DT), and resilience. The data were analyzed by performing a χ2 test, Fisher's exact test, Mann-Whitney test, and ranked ANCOVA using SPSS. Results: The intervention group reported a higher QOL overall and significantly higher social/family well-being than the control group. Distress was significantly lower in intervention group than in the control group. Resilience had no significant difference between the two groups. Conclusion: These findings indicate that the integrated health promotion program base on the shared care model and MAPP development process could be effective intervention for improving social/family well-being and the QOL, and reducing distress of cancer survivors at home. Community health center nurses need to provide intervention to support self-care competency for cancer survivors' comprehensive care with physical, psycho-social, and body image to help them adjust their life to a moderate risk group in the community.

말기암환자에서 가정호스피스완화 돌봄 경험 (Experience of Home-Based Hospice Care of Terminal-Cancer Patients)

  • 김분한;강화정
    • Journal of Hospice and Palliative Care
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    • 제17권4호
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    • pp.223-231
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    • 2014
  • 목적: 본 연구의 목적은 말기암환자로서 가정호스피스 돌봄을 받고 있는 대상자의 삶의 경험에서 얻어지는 현상을 이해하고 경험의 본질을 이해하고자 함이다. 방법: 가정호스피스 돌봄을 받고 있는 말기암환자 10명으로부터 심층면담을 통해 자료를 수집하였고 Colaizzi의 현상학적 방법을 사용하여 분석하였다. 결과: 의미 있는 진술에서 구성된 의미가 도출되고, 구성된 의미에서 주제 및 주제모음을 확인하여 범주화 한 결과, '삶의 질 저하', '남은 삶의 수용', '신앙으로 준비된 죽음', '고마움', '부정적 대처'의 범주가 도출되었다. 결론: 가정호스피스 돌봄을 받고 있는 말기암환자들의 삶의 경험을 이해하고, 호스피스 간호를 통해 대상자가 부정적인 삶의 경험을 극복하고, 긍정적인 삶의 경험을 할 수 있도록 체계화된 호스피스 간호의 제공이 필요하다.

가정간호 서비스 질 평가를 위한 도구개발연구 (A basic research for evaluation of a Home Care Nursing Delivery System)

  • 김모임;조원정;김의숙;김성규;장순복;유호신
    • 가정간호학회지
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    • 제6권
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    • pp.33-45
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    • 1999
  • The purpose of this study was to develop a basic framework and criteria for evaluation of quality care provided to patients with the attributes of disease in the home care nursing field, and to provide measurement tools for home health care in the future. The study design was a developmental study for evaluation of hospital-based HCN(home care nursing) in Korea. The study process was as follows: a home care nursing study team of College of Nursing. Yonsei University reviewed the nursing records of 47 patients who were enrolled at Yonsei University Medical Center Home Care Center in March, 1995. Twenty-five patients were insured at that time, were selected from 47 patients receiving home care service for study feasibility with six disease groups; Caesarean Section (C/S), simple nephrectomy, Liver cirrhosis(LC), chronic obstructive pulmonary disease(COPD), Lung cancer or cerebrovascular accident(CVA). In this study, the following items were selected : First step : Preliminary study 1. Criteria and items were selected on the basis of related literature on each disease area. 2. Items were identified by home care nurses. 3. A physician in charge reviewed the criteria and content of selected items. 4. Items were revised through preliminary study offered to both HCN patients and discharged patients from the home care center. Second step : Pretest 1. To verify the content of the items, a pretest was conducted with 18 patients of which there were three patients in each of the six selected disease groups. Third step : Test of reliability and validity of tools 1. Using the collected data from 25 patients with either cis, Simple nephrectomy, LC, COPD, Lung cancer, or CVA. the final items were revised through a panel discussion among experts in medical care who were researchers, doctors, or nurses. 2. Reliability and validity of the completed tool were verified with both inpatients and HCN patients in each of field for researches. The study results are as follows: 1. Standard for discharge with HCN referral The referral standard for home care, which included criteria for discharge with HCN referral and criteria leaving the hospital were established. These were developed through content analysis from the results of an open-ended questionnaire to related doctors concerning characteristic for discharge with HCN referral for each of the disease groups. The final criteria was decided by discussion among the researchers. 2. Instrument for measurement of health statusPatient health status was measured pre and post home care by direct observation and interview with an open-ended questionnaire which consisted of 61 items based on Gorden's nursing diagnosis classification. These included seven items on health knowledge and health management, eight items on nutrition and metabolism, three items on elimination, five items on activity and exercise, seven items on perception and cognition, three items on sleep and rest, three items on self-perception, three items on role and interpersonal relations, five items on sexuality and reproduction, five items on coping and stress, four items on value and religion, three items on family. and three items on facilities and environment. 3. Instrument for measurement of self-care The instrument for self-care measurement was classified with scales according to the attributes of the disease. Each scale measured understanding level and practice level by a Yes or No scale. Understanding level was measured by interview but practice level was measured by both observation and interview. Items for self-care measurement included 14 for patients with a CVA, five for women who had a cis, ten for patients with lung cancer, 12 for patients with COPD, five for patients with a simple nephrectomy, and 11 for patients with LC. 4. Record for follow-up management This included (1) OPD visit sheet, (2) ER visit form, (3) complications problem form, (4) readmission sheet. and (5) visit note for others medical centers which included visit date, reason for visit, patient name, caregivers, sex, age, time and cost required for visit, and traffic expenses, that is, there were open-end items that investigated OPD visits, emergency room visits, the problem and solution of complications, readmissions and visits to other medical institution to measure health problems and expenditures during the follow up period. 5. Instrument to measure patients satisfaction The satisfaction measurement instrument by Reisseer(1975) was referred to for the development of a tool to measure patient home care satisfaction. The instrument was an open-ended questionnaire which consisted of 11 domains; treatment, nursing care, information, time consumption, accessibility, rapidity, treatment skill, service relevance, attitude, satisfaction factors, dissatisfaction factors, overall satisfaction about nursing care, and others. In conclusion, Five evaluation instruments were developed for home care nursing. These were (1)standard for discharge with HCN referral. (2)instrument for measurement of health status, (3)instrument for measurement of self-care. (4)record for follow-up management, and (5)instrument to measure patient satisfaction. Also, the five instruments can be used to evaluate the effectiveness of the service to assure quality. Further research is needed to increase the reliability and validity of instrument through a community-based HCN evaluation.

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