• 제목/요약/키워드: 암 환자 가족

검색결과 198건 처리시간 0.024초

두경부암 환자의 기능상태, 우울과 가족지지 (Functional Status, Depression, and Family Support in Head and Neck Cancer Patients)

  • 박용경
    • 종양간호연구
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    • 제5권1호
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    • pp.31-39
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    • 2005
  • Purpose: This study was to identify the levels of functional status, depression, family support and their relationship among those variables in head and neck cancer patients. Method: The subjects were 100 patients with head and neck cancer patients who visited at outpatients clinic in one university hospital in Taegu. The instrument used for this study were Functional Status in Head & Neck Cancer - Self Report Scale developed by Baker(1995), Self-Rating Depression Scale by Zung(1965) and Family support assessment tool by Kang hyun-suk(1984). The data were analysed percentage, mean, t-test, ANOVA and pearson's corelation using SAS program. Result: There was significantly negative correlation between functional status and depression(r=-.71) and between depression and family support(r=-.56). The relationship of functional status and family support was significant as r= .33. Conclusion: It was found that functional status, depression and family support of head and neck cancer patient were closely related each other. Therefore it is necessary to design nursing intervention to enhance family support or decrease depression for improving quality of life in head and neck cancer patient.

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유방암 환자의 수술 후 심리사회적 적응, 부부친밀도 및 가족지지 (Psychosocial Adjustment, Marital Intimacy and Family Support of Post-mastectomy Patients)

  • 조옥희;유양숙
    • 종양간호연구
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    • 제9권2호
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    • pp.129-135
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    • 2009
  • Purpose: This study was to explore the psychosocial adjustment, marital intimacy and family support of post-mastectomy patients. Methods: The subjects were 90 post-mastectomy patients (stage I or II) who were eligible and agreed to participate in the study. The data collection period was from March to May, 2008. Subjects completed a survey including demographics, psychosocial adjustment scale by Lee (a 4-point Likert scale), marital intimacy scale by Kim (a 4-point Likert scale), and family support by Shim (a 5-point Likert scale). Data were analyzed using SAS (ver 9.0) program and frequency, mean (SD), t-test, ANOVA and Pearson correlation coefficients were used. Results: The mean scores of the psychosocial adjustment and marital intimacy were 2.8 (${\pm}0.4$) and 2.5 (${\pm}0.5$). Also, the mean score of the family support was 3.6 (${\pm}0.7$). Regarding the correlation between the psychosocial adjustment, marital intimacy and family support, there was a positive correlation. Conclusion: These results showed that subjects who had higher marital intimacy and family support showed better in psychosocial adjustment. To improve psychosocial adjustment of post-mastectomy patients for breast cancer more effectively, there is an necessity to provide various strategic supports and intervention for effective communication with spouse and family.

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암 환자 가족의 호스피스 요구 조사 도구개발 (Development of Needs Assessment Instrument for Hospice Care in Families of the Patients with Cancer)

  • 강경아;김신정
    • Journal of Korean Biological Nursing Science
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    • 제7권1호
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    • pp.57-68
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    • 2005
  • Purpose : The purpose of this study was to develop a tool to assess the need for hospice care in families of patients with cancer. Method : Research design was a methodological study. The tool was developed in 3 stages : first, preliminary items were developed based on a questionnaire about the needs for hospice care that was given to 8 families of patients with cancer; second, a panel of specialists reduced the number of preliminary items using 2 validity tests on the contents. Finally, reliability and validity were tested by a sample of 98 families who have a patient with cancer from April 2003 to July 2004. Result: Cronbach's alpha coefficient for internal consistency was .94 for the final total 22 items. Using the factor analysis, 4 factors with eigenvalue of more than 1.0 were extracted and these factors explained 65% of the total variance. The four factors were labeled as 'control of terminal physical problems', 'emotional care', 'spiritual care for preparing for death', and 'family support'. The final items of the tool developed on the need of hospice care consisted of 22 items. Conclusion : The instrument, for accessing the need for hospice care in families of patients with cancer, developed in this study was identified as a tool with a high degree of reliability and validity. In this sense, this tool can be effectively utilized for implementing and improving hospice care for patients with terminal cancer.

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BRCA 돌연변인 검사 중 유방암 환자 가족의 커뮤니케이션 패턴 (Communication Patterns in Korean Families during BRCA Genetic Testing for Breast Cancer)

  • ;정명희;최경숙
    • 종양간호연구
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    • 제11권3호
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    • pp.200-209
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    • 2011
  • Purpose: The purpose of this micro-ethnography is to examine whether science and societal changes impact family communication patterns among a convenience sample of 16 Korean women. Methods: The authors observed family communication in the context of a new breast cancer genetic screening and diagnostic testing program to detect BRCA gene mutations in Korean women at highest risk. Results: Analysis of in-depth interviews and field notes taken during participant observation illustrated that communication patterns in families vary according to a woman's position in the family. If a grandmother tests positive for a gene mutation, her daughters make decisions on her behalf; they open and maintain the communication channel among family members. If a housewife is diagnosed with cancer and a genetic mutation, she immediately consults her husband and her sisters. The husband creates an open communication channel between his wife, his parents and his siblings. As a result, a woman's cancer is a concern for the whole family not merely a woman's secret or crisis. Conclusion: Cultural differences are important to consider when designing new genetic service programs in different countries.

유방암 환자와 배우자의 갈등해결방식과 부부친밀도 및 가족기능 (Conflict Resolution Styles, Marital Intimacy and Family Functions of Breast Cancer Patients and Their Spouses)

  • 유양숙;황경혜;조옥희
    • 성인간호학회지
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    • 제25권1호
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    • pp.33-40
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    • 2013
  • Purpose: The purpose of this study was to explore conflict resolution styles, marital intimacy and family functions among breast cancer patients and their spouses. Methods: The subjects were total 126 participants. Breast cancer patients who completed chemotherapy and or radiation along with their spouses. Data were collected using questionnaires with questions about conflict resolution styles, marital intimacy and family functions. Results: There were no differences between breast cancer patients and their spouses in verbal aggression, avoidance of conflict resolution styles and family functions. As patients reported using positive conflict resolution styles the spouse-perceived marital intimacy and family functions were higher. Those patients who perceived marital intimacy as lower they also reported more verbal aggression and avoidance. As breast cancer patients perceived family functions increasing, their spouses perception of both intimacy and family function increased. Conclusion: As these results, it should be considered as basic data to develop family intervention programs such as positive communication and effective stress management and improving of conflict resolution, intimacy and family functions among breast cancer patients and their spouses.

말기 암환자 가족의 돌봄 경험 (Experiences of Family Caregivers of Patients with Terminal Cancer)

  • 최은숙;김금순
    • 대한간호학회지
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    • 제42권2호
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    • pp.280-290
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    • 2012
  • Purpose: This study done to identify the experiences of families caring for patients with terminal cancer. The question was, "What is the caregiving experience of a family who has a member with terminal cancer?" Methods: Grounded Theory was applied and in-depth interviews were done with 11 family members. Interviews were recorded with the interviewees' consent and were transcribed and analyzed. Participants' relationships to patients were 6 spouses, 4 daughters, and 1 mother. The ages of the participants were between 32 and 62, with an average of 47.5. Results: The study showed "enduring with bonds" as the main category and the main factor affecting this category was the "patients' diagnosis of terminal cancer." The caregiving experience was divided into four stages: shock, confusion, struggle, and acceptance. Mediating factors were relationship with the patient, intimacy with the patient, social support, communication, and trust. Conclusively, participants underwent internal maturity, and changes occurred in family and social and personal life. Conclusion: The families took care of the patients with responsibility and love. The study results should help with the understanding of a family with a member with terminal cancer and should be used to develop nursing, mediating, and consulting programs for these caregivers.

암환자를 돌보는 가족원의 스트레스, 대처방식과 소진의 관계 (Relationships between Stress, Ways of Coping and Burnout of Family Caregivers of Cancer Patients)

  • 홍민주;태영숙;노미영
    • 종양간호연구
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    • 제12권1호
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    • pp.92-99
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    • 2012
  • Purpose: The study was to examine the relationships between stress, ways of coping and burnout among family caregivers of cancer patients. Methods: Data were collected by self-reported questionnaires from 207 family caregivers of cancer patients at one university hospital and one general hospital in Busan, Korea. The instruments included a Stress Scale, a Ways of Coping Scale and a Burnout Scale. The collected data were analyzed using frequency, percentage, t-test, ANOVA, Scheffe's test, and Pearson's correlation coefficients with the SPSS WIN 19.0 program. Results: Stress was found to have significant relationships with age, relation to the patient, education, monthly income, degree of care-giving, financial burden and activities of daily living of patient. In active coping, there were significant differences according to education and religion. Passive coping was significantly related to gender. In burnout, there were significant differences according to age, relation to the patient, education, occupational status, monthly income, degree of care-giving, financial burden and activities of daily living of patient. Stress and burnout showed a positive correlation, while there was a negative correlation between burnout and active coping. Conclusion: These results suggest that promoting active coping would better support family caregivers of cancer patients in managing burnout effectively.

골육종과 폐선암을 동반한 리-프라우메니 증후군: 증례 보고 (Osteosarcoma with Adenocarcinoma of Lung in Li-Fraumeni Syndrome: A Case Report)

  • 오창선;이진호;정성택;나보람
    • 대한골관절종양학회지
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    • 제20권2호
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    • pp.99-103
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    • 2014
  • Li-Fraumeni syndrome은 소아나 청장년층에서 다양한 형태의 종양을 유발할 수 있는 상염색체 우성 유전 질병이다. 이는 종양억제 유전자인 TP53 의 변형에 의해 발생하게 된다. 이 질환은 매우 드물며, 진단되지 못하고 간과되는 경향이 많다. 이에 저자들은 17세, 폐선암을 동반한 근위 경골 골육종 환자에서 가족력을 통해 이 질환을 의심하고, 유전자 검사를 통하여 확진한 증례를 보고하고자 한다.

말기 암 환자에서 임상변수를 이용한 생존 기간 예측 (Prediction of Life Expectancy for Terminally Ill Cancer Patients Based on Clinical Parameters)

  • 염창환;최윤선;홍영선;박용규;이혜리
    • Journal of Hospice and Palliative Care
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    • 제5권2호
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    • pp.111-124
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    • 2002
  • 목적 : 의학의 발달로 인간의 생존 기간이 길어졌지만, 암 발생율과 사망율은 오히려 증가하고 있어 그로 인해 말기 암 환자는 계속 늘어나고 있는 실정이다. 말기 암 환자를 진료하는 데 있어서 환자의 생존 기간을 예측하는 것은 중요한 문제로 만약 환자의 생존 기간을 예측할 수 있다면 남은 시간에 따라 환자, 가족, 의료진은 치료의 선택에 큰 차이를 보일 것이다. 이에 저자 등은 말기 암 환자에서 사망 위험도를 높이는 예후 인자를 알아내고 이들 예후 인자의 개수에 따른 생존 기간을 예측하여 말기 암 환자의 진료에 도움이 되고자 하였다. 방법 : 2000년 7월 1일부터 2001년 8월 31일 사이에 국민건강보험공단 일산병원 가정의학과에 말기 암으로 입원한 환자 157명을 대상으로 입원당시 환자의 임상변수 31가지를 조사하였다. 그리고 환자의 의무기록과 조사된 환자의 신상기록을 가지고 2001년 10월 31일까지의 환자의 생존 여부를 확인하였다. Kaplan-Meier 방법과 로그순위 검정(log-rank test)을 이용하여 임상변수에 따른 생존 기간에 차이가 있는지를 알아보았다. Cox의 비례위험함수 모형(Cox's proportional hazard model)을 이용하여 임상변수 중 사망 위험도를 높이는 유의한 변수를 얻은 후 이를 예후 인자로 삼고, 이것을 와이블 비례위험함수 모형(Weibull proportional hazard function model)을 이용하여 예후 인자들의 유무에 따른 생존 기간의 평균, 중앙값 제 1사분위수 그리고 제 3사분위수를 계산하여 생존기간을 예측하였다. 결과 : 말기 암 환자 157명 중 성별은 남자가 79명(50.3%), 여자가 78명(49.7%)이었고, 평균 연령은 남자가 $65.1{\pm}13.0$세, 여자는 $64.3{\pm}13.7$세였다. 암의 종류를 보면 위암이 36명(22.9%)으로 제일 많았고, 폐암이 27명(17.2%), 대장암이 20명(12.7%) 순이었다. 의식변화, 식욕부진, 저혈압, 수행능력 저하, 백혈구 증가증, 중성구 증가증, 크레아티닌 증가, 저알부민혈증, 고빌리루빈혈증, 간효소(SGPT)치 증가, 프로트롬빈 시간(PT) 연장, 활성부분 트롬보플라스틴 시간(aPTT) 연장, 저나트륨혈증, 고칼륨혈증 등을 보이는 환자는 통계학적으로 유의하게 생존 기간이 짧았다. 이중 Cox의 비례위험함수 모형을 통해 수행능력 저하, 중성구 증가증, PT 연장, aPTT 연장인 경우가 환자의 사망위험도를 높이는 유의한 예후 인자로 나왔다. 생존 기간의 중앙값은 4가지 인자가 모두 있는 경우는 3.0일, 3가지만 있는 경우는 $5.7{\sim}8.2$일, 2가지만 있는 경우는 $11.4{\sim}20.0$일, 1가지만 있는 경우는 $27.9{\sim}40.0$일, 4가지 모두 없는 경우는 77일로 나왔다. 결론 : 말기 암 환자에서 수행능력 저하, 중성구 증가증, PT 연장, aPTT 연장이 사망위험도를 높이는 예후 인자임을 알 수 있었다. 이들 4개 인자를 통해 말기 암 환자에서 생존 기간을 예측할 수 있을 것으로 사료된다.

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중소도시 일 유방클리닉 방문 여성의 유방암 검진현황 -의무기록을 이용한 후향적 조사연구- (The status of breast cancer screening of women at a breast clinic in a small city in Korea -Using medical records-)

  • 이혜원;김영미
    • 디지털융복합연구
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    • 제19권10호
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    • pp.491-500
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    • 2021
  • 유방암 환자의 제 특성을 파악하여, 유방암 조기 검진의 중요성과 젊은 유방암의 심각성을 알리기 위해 시행하였다. 2010년 5월 1일부터 2020년 4월 30일까지(10년간) 일 유방 클리닉에 내원한 환자 23,200명 중 유방암으로 진단받은 483명의 의무기록을 이용한 후향적 조사연구이다. 유방암으로 진단받은 483명의 나이는 40대(36.0%)가 가장 많았으며, 30대(25.9%)가 다음으로 많았다. 유방암 가족력이 있는 경우가 5.4%, 폐경 상태는 29.2%였으며, 내원 동기로는 종괴가 54.2%로 가장 많았고, 유방 검진 경험은 출산 경험자가 비출산자보다 많았으며, 20-30대에서 유방검사 경험이 가장 적었다. 젊은 여성을 대상으로 유방암 검진의 중요성을 교육할 필요가 있으며, 유방암의 국가암검진 연령에 대한 재검토를 제언한다.