• 제목/요약/키워드: Stroke Patient's Caregiver

검색결과 28건 처리시간 0.021초

Subjective and Objective Caregiver Burden in Parkinson's Disease

  • Kim, Keum-Soon;Kim, Bog-Ja;Kim, Kyung-Hee;Choe, Myoung-Ae;Yi, Myung-Sun;Hah, Yang-Sook;Chung, Sun-Ju;Kwon, So-Hi
    • 대한간호학회지
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    • 제37권2호
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    • pp.242-248
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    • 2007
  • Purpose. Parkinson's disease (PD) is a common neurodegenerative disorder characterized by motor disabilities and increasing dependence on others for daily life activities with consequent impact on patients' and caregivers' quality of life. The aim of this study was to elucidate the burden on primary caregivers of patients with PD, and identify related factors. Methods. A cross-sectional descriptive study. Seventy-six primary caregivers of PD patients in a neurology out-patient clinic, Seoul, Korea completed structured questionnaires, of which 68 were analyzed. The structured self-report questionnaire included (1) demographic information on the caregivers, (2) information regarding the disease characteristics of the patients, and (3) the subjective and objective caregiver burdens as assessed on Montgomery, Gonyea, & Hooyman's scale. Results. The mean age of the caregivers was 54.56 years, and spouses represented the largest proportion (47.0%). Caregivers of PD patients experienced high levels of burden (mean scores on the subjective and objective burdens were 45.22 and 34.90, respectively), which were comparable to the caregiver burdens in stroke, and higher than the caregiver burdens in general chronic disease. Older caregivers and spousal caregivers experienced significantly higher burdens (p=.004 and p=.019, respectively). A greater motor disability and higher modified Hoehn and Yahr grade were related to higher caregiver burden (p=.001 and p=.018, respectively). Conclusion. Caring for PD patients is associated with a high level of caregiver burden. Therefore, healthcare professionals should identify the burden of caregivers who look after PD patients and develop comprehensive management strategies both for patients and their caregivers.

뇌졸중환자 가족간병원의 스트레스에 관한 연구 (A Study on the Stress of the Family Caregivers for Patients with Stroke)

  • 권원안;김한수
    • The Journal of Korean Physical Therapy
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    • 제20권2호
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    • pp.25-32
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    • 2008
  • Purpose: The purpose of this study was to provide the basic data to decrease the stress of the family caregivers. Methods: The questionnaire was administrated to the family caregivers of 156 patients with stroke who consented to be interviewed. Among 156 caregivers, we analyzed 120 caregivers. We evaluated on the stress of the family caregivers. Results: First, the general characteristics of patient with CVA were high at 82.55% in male, 55.83% in infarction, 53.33% in the left hemiplegia, 47.50% in sixties, 80.83% in 1 recurrence rate, 27.50% in 1-2 years of disease period. Second, the general characteristics of family caregivers were high in above sixties, female in gender, existence in religion, married in marital status, high school in educational level, below 1 million-won in monthly income, spouse in relationship with patient, below 1 years in total caring period. Third, it showed that stress of family caregivers above 3.0 score has 8 items. Forth, the patient's characteristic that have the influence on the stress was significant in the period of disease(p<0.05). Finally, the characteristics of family caregivers that have the influence on the stress were the monthly income, caring period(p<0.05). Conclusion: These findings indicated that the stress of the family caregivers was correlated with the time in hospital, the income and nursing period.

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재활전문병원에 입원중인 뇌졸중 환자 주 돌봄 제공자의 스트레스 영향요인 (Influencing Factors on Stress in Caregivers of Stroke Patients Being Admitted in Rehabilitation Centers)

  • 김남희;태영숙;최윤숙;배주희
    • 한국산학기술학회논문지
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    • 제17권2호
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    • pp.188-201
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    • 2016
  • 본 연구의 목적은 재활전문병원에 입원중인 뇌졸중 환자 주 돌봄 제공자의 스트레스 영향요인을 파악하기 위하여 시도된 설명적 상관관계 연구이다. B시에 소재한 3개의 재활전문병원 주 돌봄 제공자 200명에 대한 자료를 2015년 9월 1일부터 9월 30일까지 수집하여 SPSS Win 18.0 프로그램을 이용하여 분석하였다. 연구도구는 Connor-Davidson Resilience Scale, Caregiving Mastery Subscale, MOS(Medical Outcomes Study), Burden Interview(BI)를 사용하여 측정하였다. 스트레스에 가장 큰 영향을 미치는 요인은 사회적지지로 전체의 9.3%의 설명력을 보였고, 다음으로 환자를 돌봄 기간, 종교 유무, 경제적 상태, 주 돌봄 제공자 연령, 회복 탄력성, 주 돌봄 제공자 건강상태, 환자 의식상태, 환자연령을 포함하여 주 돌봄 제공자의 스트레스는 총 30%의 설명력을 나타냈다. 따라서 이러한 결과를 바탕으로 재활전문병원에 입원중인 주 돌봄 제공자의 스트레스를 감소시킬 수 있는 사회적지지 프로그램의 개발이 필요하며, 스트레스에 영향을 준 제 특성요인들을 고려하여 스트레스 중재프로그램을 개발할 필요가 있을 것이다.

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
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    • 제9권2호
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    • pp.362-373
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    • 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.

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뇌졸중 환자를 돌보는 중·고령층 여성 간병인의 신체통증 영향 요인 (Factors of Bodily Pain Among Stroke Patient's Female Caregivers in Their Middle to Older Age)

  • 문종훈;박인혜
    • 재활치료과학
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    • 제8권1호
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    • pp.63-71
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    • 2019
  • 목적: 본 연구는 뇌졸중 환자를 돌보는 중 고령층 여성 간병인의 신체통증 영향 요인을 탐색하고 하였다. 연구방법: 본 연구는 대구 및 경북 지역에 위치한 병원 5곳에서 뇌졸중 환자 75명과 이들을 간병하는 중 고령층 여성 간병인 75명을 대상으로 수행하였다. 측정은 뇌졸중환자의 일반적 특성, 인지기능, 상지기능, 일상생활능력을 평가하였고, 간병인은 일반적 특성과 신체통증이 평가되었다. 신체통증 영향 요인을 알아보기 위하여 위계적 다중회귀분석(stepwise multiple regression analysis)을 이용하였고 상관관계를 확인하기 위하여 피어슨 상관분석(Pearson correlation analysis)을 이용하였다. 결과: 중 고령층 여성 간병인의 신체통증 영향 요인은 현재 자신이 돌보고 있는 뇌졸중 환자의 일상생활능력(${\beta}=-.489$, p<.001)과 간병경력(${\beta}=-.309$, p=.003)으로 나타났다($R^2=.276$). 상관분석결과, 뇌졸중 환자의 일상생활능력, 상지기능, 인지기능은 유의한 연관성을 나타냈다(r=.434~.751, p<.001). 결론: 본 연구의 결과는 중 고령층 여성 간병인의 신체통증 감소를 위해 현재 자신이 돌보는 뇌졸중 환자의 기능수준과 간병경력이 중요한 변수임을 증명한다.

Factors Influencing Discharge Destination and Length of Stay in Stroke Patients in Restorative Rehabilitation Institution

  • Gyu-Bum Lee;Jee-Sun Lee;Jeong Soo Kim
    • 한국전문물리치료학회지
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    • 제31권1호
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    • pp.48-54
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    • 2024
  • Background: Promoting patients' safe return home at discharge and reducing length of stay in hospital is key for Restorative Rehabilitation Institution (RMI). Objects: This study was designed to identify the factors influencing the return to home and length of stay among various factors. Methods: A total of 120 stroke patients (76 males and 44 females) who were hospitalized in an adult inpatient unit of a RMI for more than 2 months were retrospectively analyzed for this study (multivariate logistic regression analyses, p < 0.001). As predictor variables for assessing the return to home and length of stay, demographic data (sex, age, duration between onset and admission, length of stay, caregiver after discharge, occupation after discharge, reason for discharge, and household type after discharge) were collected. Additionally, following measurements were selectively collected from patient's medical records: scores of Mini-Mental State Examination Korean version (K-MMSE), modified Barthel Index Korean version (K-MBI), Berg Balance Scale and Functional Ambulation Category were obtained at admission and discharge. Results: The K-MMSE at admission and K-MBI at discharge were found to be the predictors of return to home. Additionally, K-MBI at admission influenced the length of stay. Conclusion: This study suggests cognitive functioning at admission and the level of activities of daily living at discharge predicted the return to home and length of stay.

보호자 교육과 경험학습 훈련이 실어증 환자의 의사소통 개선에 미치는 효과 (Effects of Communication Improvement on Caregivers Education and Training on Aphasia)

  • 박희준;장현진
    • 재활치료과학
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    • 제8권2호
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    • pp.79-88
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    • 2019
  • 목적 : 경험학습모델에 따라 하나의 체계적 프로그램으로 결합하였는데 이 접근법의 목표는 환자와 보호자들의 이해를 돕고 필요한 것을 인지시키는 것에 초점을 두었다. 이러한 선행연구들의 결과를 근거로 본 연구자는 환자와 대화상대자 사이의 의사소통 개선을 위한 보호자 교육과 경험학습모델에 근거한 그룹훈련의 장점을 알아보고자 하였다. 연구방법 : 이 연구에서는 부산광역시 소재에 있는 종합병원에 입원한 40~50세의 비유창성 실어증 환자 6명(구어 실행증 2명, 브로카실어증 3명, 명칭 실어증 1명)과 보호자들을 연구 대상으로 선정하였다. 명확한 정보교환 의사소통은 보호자가 촉진전략을 사용하여 환자의 메시지를 파악하였는지 알아보고 사회적 상호작용 의사소통은 보호자의 긍정적인 행동과 방해하는 행동의 빈도 변화를 파악하였다. 보호자의 행동 변화는 훈련 전의 부정적 행동들이 훈련 후 어떠한 행동으로 변화하였는지 알아보고 설문지를 통해 환자와 보호자들의 만족도를 알아보았다. 결과 : 첫째, 보호자 교육과 경험학습에 근거한 그룹훈련이 명확한 정보교환 의사소통을 향상 시켰다. 둘째, 보호자 교육과 경험학습에 근거한 그룹훈련이 사회적 상호작용 의사소통을 향상 시켰다. 셋째, 보호자 교육과 경험학습에 근거한 그룹훈련이 보호자의 행동을 변화시켰다. 넷째, 보호자 교육과 경험학습에 근거한 그룹훈련이 환자와 보호자들의 만족도를 향상 시켰다. 결론 : 본 연구를 바탕으로 하여 국내에서는 그동안 거의 고려되지 않았던 실어증 환자의 보호자 교육에 대한 중요성을 깨닫고, 국외에서 이미 활용 중인 여러 유형의 프로그램을 표방하여 우리나라의 문화와 재활 환경에 맞는 다양한 보호자 교육의 내용을 계획할 필요가 있다.

뇌졸중환자의 희망 (The Hope of the Stroke Patients)

  • 김이순
    • 대한간호학회지
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    • 제27권1호
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    • pp.212-227
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    • 1997
  • Cerebrovascular diseases in Korea is an important health problem since mortality and mobidity have been increased rapidly. It marked the 2nd cause of specific death rates in 1993. The stroke causes physical function disorder due to hemiparalysis and emotional disorder, and stroke patients experience helplessness, powerlessness. sense of alienation and loss of hope. These feelings make the rehabilitation difficult because they lose the will of life. The subjects of the study were seven citizens who live in Pusan, are over 50 years old and belong to low income-level. The data were collected from Jan. to Sep. 1995. The researcher as a caregiver and volunteer made confidence of them and asked for their agreement on the purpose of the study. The subjects expressed their experience as openheartedly as possible. The analysis of the data was made through the phenomenological analytic method suggested by Giorgi, which is as follows ; as an unit of description which include the subject' expressions and the researcher's observation, it is examined the theme that express the hope experience with the subject's language(underlining), and the focal meanings are identified. The focal meaning is the crystalization of the theme, which is written in the language of the researcher. After intergrating the focal meaning and make the situated structural description as the meaning of the hope experience identified on each subject's point. After intergrating the situated structural description and make the general structural description as the meaning of the hope experience identified on total subject's point then the systemizing of the structure of the hope experienced phenomena and the flowing of the conciousness was researched. The conclusions of this study was as follows : The ten sources of hope which the subjects experienced were sorted as under 〈mutual relations to others : spouse, children, relatives, fellow believer. health professioner. associate patient group〉, 〈spiritual dependence〉. 〈recovery of physical function〉. 〈rumination of the past life〉, 〈expectation of the future〉. 〈economic power〉, 〈belief〉, 〈ability〉. 〈spontaneous participation〉 and 〈recovery of roles〉. Their hope was spoken out by the following two kinds of linguistics. First. the hope was expressed in the affirmative expression as follows : 〈 to be dependable〉, 〈to make efforts〉, 〈to keep under control〉, 〈to desire〉, 〈to be pleasant〉, 〈to be peaceful〉, 〈to be grateful〉, 〈to give help〉, 〈self-confidence. Courage〉, 〈to be happy〉, 〈to satisfy oneself〉, 〈to share with others〉, 〈to understand〉 and 〈to be affected, be impressed〉 Second, the hope was expressed in the negative on pression as under : 〈to be distressed〉, 〈to be uneasy〉, 〈to be sorry, be unsatisfied〉 〈despair〉, 〈to abandon〉, 〈to be fearful〉, 〈to suffer〉, 〈to bear a burden〉 〈to be confused〉, 〈to be solitary〉, 〈chest trouble〉, 〈to feel heavy〉 〈grief〉, 〈to be daunted〉, 〈to get angry〉, 〈to be uncomfortable〉, 〈to have something regretable〉 and 〈to feel guilty〉. And their hope was expressed by the following four behavioral expressions : 〈physical sphere〉, 〈psychological sphere〉, 〈social support sphere〉 and 〈spiritual sphere〉. The reaction patterns of their hope experience appeared in the following 4 coping method : 〈conquest type〉, 〈dependence type〉, 〈adaptation type〉 and 〈fate type〉. Finally, in the hope structure the sense of certainty don't always coexict with the sense of uncertainty, When the stroke patients try to search for the best quality of life, the senses of certainty and uncertainty make a continual cyclic system in the hope structure.

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