• Child Health Nursing Research
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• 제2권1호
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• pp.93-111
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• 1996

The purpose of the study is to identify the lived experience of mothers who have children with cerebral palsy in order to understand their agony. Moreover, the result of study was to find some nursing intervention for disabled children and their mothers. For this purpose, ten mothers who are willing to cooperate with this research were selected at random from those who have children with the cerebral palsy, currently using the municipal facilities for the handicapped with cerebral malfunction. Data collection was done from October 4, 1994 th December 31, 1994. The data were collected by asking the mothers mentioned above with some unstructured open-ended questions, recorded on the tapes with permission by the interviewee in order to prevent missing of the interviewed contents. These collected data have been substantiated and properly analyzed on the basis of phenomenological approach initiated by Colaizzi's method. The results and validity are proved to be credible by means of the individual checking of the interviewed mothers. The results of this study are as follows : 1. When the mother is first informed of the diagnosis of cerebral palsy on her child, she usually misses the crucial timing needed for proper treatment of the child's disorder because she is notified through the doctor's indifference and his apparently inactive, matter-of-fact attitude. At first she suspects the doctor's diagnosis and tries to attribute it to the unknown cause from a certain genetic problem and then she quickly wants to deny the whole situation that her child is really suffering from the cerebral palsy. The reality is too much for her to accept as it is and she would not believe her child is abnormal. Therefore, she even attempts depend on the power of God for its solution. 2. The mother, who goes thorough this kind of uncommon experiences, is totally devoted to the treatment and care of the child and completely ignores her own life and happiness. At the same time, she feels sorry for her other normal children she believes having not enough care and concern. Also, she feels sorry for the sick child when the child's brothers or sisters show special concern for the patient out of sympathy. It is sorry and not satisfied for her that the child is growing with abnormality and neighbor other around have inappropriate attitudes. Likewise, she is discontent with her husband's lack of concern about the child's treatment. She believes that the health care system in this society isn't fulfilling its due purpose. In the state of her utmost distress and anxiety, she always feels the need of competent consultants, and is angry about that her child is treated as an abnormal being, she is trying to hide the child from other people and to make him or her disappear, if possible. Although she doesn't have harmonious relation with her husband, she id happy when he shows his affection for the child and she feels relieved and thankful when the relatives don't mention about the child's condition Since the child's overall status of health is continuously in unstable conditions, requiring her all-time readiness for an emergency, she feels guilty of her child's illness toward the fEmily members as if it was her own fault to have borne such an abnormal child and she feels responsible for the child morally and financially if necessary Because her life is centered on taking care of the child, she cannot afford to enjoy her own life and happiness. She is a lonely mother, fatigued, with no proper relationship with other people around her. With this sense of guilt and responsibility as a mother of an unusual disease, she has no choice but to grieve her destiny from which she is not allowed to escape. 3. Nevertheless, the mother with the child suffering from the cerebral palsy does not easily give up the hope of getting her child cured and she believes that in the long run, though slower than hoped, her abnormal son or daughter will be eventually cured to become a normal sibling someday. This kind of hope is sustained by the mother's strong faith coming from observing the progress of other similar children getting better. Sometimes she is encouraged to have this faith by other mothers who share the same painful experiences, believing that her child will improve even more rapidly than others with the same palsy. Full of hope, she painstakingly waits for the child's healing. Moreover, she plans to have another child. she thinks that the patient child's brothers and sisters only can truly understand and look after the patients. However, when she notices that the progress of other children under the treatment does not look so hopeful, she is distressed by the thoughts that her child may never get well. Too, she is worried that the patient's brother or sister will be born as the same invalid with the cerebral disease. She is discouraged to have another baby as much as she is encouraged to. She is also troubled by the thought that in case she has another baby, she will have to be forced. to neglect the patient child, especially when she does have an extra hand or some reliable person to help her with taking care of the patient.

• 호스피스학술지
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• 제2권2호
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• pp.28-48
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• 2002

The advances of medical technologies have not only prolonged human life span, but also extended suffering period for the patients with incurable medical diseases. Hospice movement was developed to help these patients keep dignity and lives peaceful at the end of their life. Since many patients prefer to spend the last moment of life at home with their family, hospice home care has become very popular worldwide. The purpose of this study for a promotion and development of hospice home care in Korea, and features basic research on medical profession's knowledge and attitudes to hospice home care. This study which was used for the research questionnaires developed by the researcher that were answered by 100 physicians and 127 nurses in a general hospital. Data were collected from April 22, 2002 to May 10, 2002. The SPSS was used to make a comparative analysis of the frequency, percentile, ANOVA, and x2-test. The results of the study were as follows; 1.The medical profession showed high level of knowledge of the definition and philosophy of hospice. However, the physician group of the examinees showed insufficient knowledge of the fact that hospice care includes bereavement care, while the nurse group's response to the same question showed a significant difference(x2=10.752, p=.001). 2.For whom the hospice home care is provided, 95.6% of the respondents showed very high level of knowledge as answering that the incurable terminal illness patients and their families are the beneficiaries of hospice care. The respondents counted nurses, volunteers, pastors, physicians and social workers, consecutively, as hospice care providers. More nurse were positive toward pastors than physicians in regarding as a hospice care provider by a significant difference(x2=11.634, p=.001). 3.For when to referral hospice home care to the patients, only 34.2% answered that patients with less than 6 months of survival time are advised to receive hospice care, reflecting very low level of knowledge. 23.0% of the physicians and 48.0% of the nurses answered that hospice care should be provided when death is imminent, making a significant difference between the two groups(x2=6.413, p=.000). 4.To promote hospice activities, 87.2% pointed out that it is crucial to make general people, including those engaging in the medical field, more aware of hospice. 79.7% answered that a national hospice management should be developed, marking a significant difference between the physician group and nurse group(x2=10.485, p=.001). 5.Advantages of hospice home care are 87.2% responded that patients can have better rest at home receiving hospice home care. Economical merit was brought forward as one of the advantages also, where there was a significant difference between the physicians group and nurse group(x2=7.009, p=.008). 6.The medical professions' attitude to hospice home care are 92.8% of the physicians answered that they would advise incurable terminally ill patients to be discharged from hospital, with 44.3% of them advising the patients to receive hospice home care after leaving the hospital. From the nurses' point of view, 20.9% of the terminally ill patients are being referred to hospice home care after discharge, which makes a significant difference from the physicians' response(x2=19.121, p=.001). 7. 30.6% of physicians have referred terminally ill patients to hospice home care, 75.9% of whom were satisfied with their decision. Those physicians who have never referred their patients to hospice home care either did not know how to do it(66.7%) or were afraid of losing trust by giving the patients an impression of giving up(27.3%). 94.9% of the physicians responded that they would refer their last stage patients to a doctor who is involving palliative care. 8.Only 36.2% of nurses have suggested to physicians that refer the terminally ill patients discharged from the hospital to hospice home care. Once suggested, 95.8% of the physicians have accepted the suggestion. Nurses were reluctant to suggest hospice home care to the physicians, as 48.8% of the nurses said they did not want to. From the result of this study the following conclusion can be drawn, the medical profession's awareness of general hospice care has been increased greatly compared to the results of the previously performed studies. However, this study result also shows that their knowledge of hospice home care is not good enough yet. There is a need for high recommended that medical education institute and develop regular courses on various types of hospice care. Medical field training courses for physicians and nurses will be very helpful as well. It is also important to train hospice experts such as palliative physicians and develop a national hospice management urgently in order to improve the hospice care in Korea.

• 한국방사선학회논문지
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• 제17권2호
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• pp.257-265
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• 2023

본 연구의 목적은 코로나에 대한 일반적 특성에 따른 매년 백신접종 의향 여부, 백신접종 경험에 따른 매년 백신접종 의향 여부, 백신접종 관련 지식/태도에 따른 매년 백신접종 의향 여부, 매년 백신접종 의향에 부정적인 응답의 인자들을 파악함으로써 매년 예방접종 의향에 미치는 요인을 파악하기 위하여 2021년 1월경에 1개 K 대학병원을 대상으로 규격화한 설문을 통해 조사하였다. 통계분석은 일반적 특성, 백신접종 경험에 따른 제 변수 및 백신접종 관련 지식/태도에 따라 향후 COVID-19 백신접종을 매년 실시하라는 정책이 나오면 접종에 대한 의향은 빈도와 백분율을 산출하고 카이제곱 검정(-test) 시행하였고, 카이제곱 검정에서 유의했지만, 기대도수가 5보다 작은 범주가 25% 이상이면 피셔 정확 검정(Fisher's exact test)으로 비율 차이 검정을 하였다. 단순 분석에 유의한 변수들을 이용한 다중 로지스틱 회귀분석을 통해 향후 백신 예방접종 여부의 예측모형과 각 독립 변수들이 미치는 효과 크기를 추정하였다. 단순 로지스틱 회귀분석에서 매년 백신접종 의향에 맞지 않겠다고 응답한 이유는 백신접종을 한 이유가 '나의 감염을 예방하기 위하여' 응답한 경우보다 '가족과 병원 내원객의 감염 예방하기 위하여'의 응답한 경우가 11.0배 높았고 '지역사회와 국가의 집단면역 형성을 위하여' 응답한 경우가 3.67배 높았다. 1, 2차 예방접종 후 경험한 이상 반응에서 접종 부위 통증 경험한 경우가 8.42배 높았고, 붓거나 발적 경험을 한 경우 4.00배, 관절통을 겪은 경우가 5.69배 피로감을 느낀 경우가 5.57배 높게 매년 접종 의향이 없었다. 또한 백신접종에 대한 불안 정도를 느낄수록 매년 백신을 맞지 않겠다는 의향이 2.94배씩 높았다.

• 한국산학기술학회논문지
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• 제13권6호
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• pp.2607-2616
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• 2012

본 연구에서는 의료기관의 환자안전문화를 이해하고, 의사들의 환자안전문화에 대한 인식분석을 위한 기초자료로 활용하고자 시도하였다. G시에 소재한 상급종합병원 의사를 대상으로 2011년 8월 1일 부터 9월 5일까지 설문조사하여 194부를 최종분석 하였다. 연구결과는 첫째, 대상자와 병동 및 병원안전문화 간의 관계는 직원배치가 성별, 연령별, 병원 근무년수, 환자 접촉여부, 1주 근무시간에 따라 인식의 차이가 있으며, 조직학습과 병동내 팀워크는 1주 근무시간에 따라, 병동 안전문화 모든 하부영역은 진료과별로 유의하게 나타났다. 둘째, 대상자와 의료사고보고체계, 환자 안전도 평가 및 전반적 의식수준과의 관계에서는 사고에 대한 피드백과 의사소통, 사고빈도보고, 전반적 안전의식이 진료과별로 유의하였으며, 전반적 안전의식은 환자접촉과 1주 근무시간에 따라 유의한 결과를 나타냈다. 셋째, 병동 및 병원 안전문화 인식 하부영역과 전반적 인식, 환자안전도 평가는 모두 정의 상관관계가 있는 것으로 나타났다. 의료사고 보고체계와는 직속상관/관리자의 태도와 병원경영진의 태도를 제외한 모든 영역에서 정의 상관관계가 있는 것으로 나타났다. 넷째, 환자안전도 영향을 미치는 환자안전문화 하부영역은 조직학습, 의사소통의 개방성, 전반적 안전인식, 부서간의 협조체계, 피드백과 의사소통, 비처벌적 대응에서 유의한 결과를 나타냈다. 결론적으로, 의사들의 병동 및 병원 환자안전문화 수준을 높이고 의료사고보고체계를 충실하게 하기 위해서는 적절한 직원배치와 근무시간을 바탕으로 병동 내 조직적 학습을 통한 팀워크을 활성화 시키고, 부서간 팀원간의 개방적 의사소통과 사고에 대한 피드백을 제공하여 환자 안전에 대한 병원경영진의 적극적인 지원과 진료과별 협조체계 구축이 필요하다.

• Journal of Preventive Medicine and Public Health
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• 제1권1호
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• pp.25-36
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• 1968

Introduction In order to improve medical education through the introduction of a concept of comprehensive health care of a community, an area surrounding the University Campus was chosen for the Community Health Service Project. It has been on operation for last 4 years with its major emphasis on family planning services, and maternal and child health care. The major objectives of this survey at the area are to obtain: 1) The demographic data, 2) The health need and trend of medical care, 3) The attitude and practice in maternity care to be used for further improvement of the planning and the services of the project. Population and Survey Method Out of three Dongs of the Community Health Service Area, only two Dongs namely Changchun and Yonhee were selected for the survey. Total number of households and population in the area studied was 3,683 and 21,857 respectively. An interview was performed with questionnaire schedule which was recorded by interviewers. This includes the degree of utilization of health services provided by the Community Health Service Program such as family planning, prenatal care during their last pregnancy, delivery history and complications of the delivery as well as the incidence of illnesses in general. Prior to the interview, all interviewers were trained for interviewing technique for two days. The survey was carried out during the period from October December 1967. Results 1) Demographic Data : 41.3% of the population studied were children under age 15 and only 3.5% were over 60 years of age. Crude birth rate and crude death rate of this area studied during the period of November 1966-October 1967 were 20.5 and 7.7 respectively. Infant mortality rate during the same period was 35.9. 50.4% of the 2,832 households fell into the category of middle class, 39.8% to the lower class and 9.5% to the upper class in economic condition. 19.8% of 2,832 householders had no formal education, 22.7% primary school, and 57.5% middle or higher school education. 2) Health Status and Utilization of the Community Health Service: Those who suffered from many illnesses during the month of October, 1967 were 690(4.6% of 14,891 persons). Classification of these patients into the type of disease shown respiratory diseases 27.4%, gastrointestinal diseases 18.1%, tuberculosis 10.9%, skin and genitourethral diseases 4.5% and gynecologic patients 4.5%. Only 55.9% of the patients received medical care at hospital or doctor's clinic. But among TB and gynecologic patients, 70.7% and 72.4% were treated at medical facilities. 10.6% of 2,832 householders interviewed has ever utilized the Community Health Service Program provided by the Yonsei Medical School, Classifying these clients into the type of service, 35.9% utilized the wellbaby clinic, 31.0% the family planning clinic, 14.7% the home delivery care, and the rest utilized other services such as the premarital guidance cinlic and the sanitary inspection service. 3) Maternity Care: 23.6% of 2,151 deliveries were done at medical facilities such as hospital, private clinic, while 76.4% were done at home. Acceptance rate of prenatal care was 32.6% as whole, but 49.6 of 774 women who had the prenatal care service had their deliveries at medical facility. 45.1% of total deliveries were attended by medical and or paramedical personnel. 75.8% of the deliveries of those received prenatal care were attended by medical and or paramedical personnel while only 27.8% of the deliveries of those who did not have prenatal care attended by medical and or paramedical personnel. 49.8% of deliveries of the upper class, 29.8% of the middle class and 9.9% of the lower class were attended by medical and or paramedical personnel. 6.2, 3.3% and 24.8% of mothers reported about their xeperience of edema, coma and fever during the period of trimester of pregnancy and puerperium. 4) Family Planning: The rate of practice of family planning was 27.9%. 31.7% of them were by IUD, 2.9% by oral pill, 15.2% by sterilization and the rest by traditional methods. Those women who had 3 to 4 children had highest(30.2%). Practice rate among the various methods of family planning, oral pill was the most popular method to whom had 2 or less children. In relation between the practicing rate of family planning and living standard, the upper, middle and lower class practiced 37.5, 29.4 and 19.9% respectively.

• Journal of Hospice and Palliative Care
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• 제1권1호
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• pp.47-55
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• 1998

목적 : 암은 우리나라 사망원인의 첫째이며 말기암환자에서 보이는 신체증상 중 통증은 의료인이 반드시 조절을 해주어야 한다. 암환자의 90%이상에서 통증조절이 가능하며, 말기 암환자의 임종 24시간 전 $33{\sim}60%$에서는 의식이 명료하여 진통제의 경고, 투여가 가능하다. 마지막 24시간 동안의 진통제 사용실태와 내과계와 외과계 의사에따른 통증조절 방법의 차이를 조사함으로서 보다 계획적이고 적극적인 통증 조절 중요성의 중요성을 강조하고자 본 연구를 시행하였다. 방법 : 1994년 7월 1일부터 1995년 6월 30일까지 모대학병원에 입원하여 암으로 사망한 환자 160명을 대상으로 의무기록지, 간호기록지를 조사하는 후향적 코호트 방법을 시행하여 인구통계학적 자료와 사망 24시간전의 의식상태, 통증여부, 암의 종류 등을 조사하였다. 대상자를 내과의사와 외과의사에 의해 치료받은 군으로 나누어 임종전 24시간 동안 투여한 진통제의 용량, 투여방법, 투여종류, 필요시 마타 투여된 진통제의 평균 횟수를 비교 분석하였다. 진통제의 용량은 경구몰핀 등가량으로 환산해서 계산하였다. 결과 : 1) 전체 160명 중 남자가 102명(63.8%)명, 여자는 58명(36.2%) 이었고 평균연령은 56.4세였다. 2) 평균입원 27.8일이었으며 원발부위에 따른 암의 종류는 위암 42명(26.3%), 폐암 29명(18.1%), 간암 29명(18.1%), 췌장암 10명(6.2%), 대장암 9명(5.6%), 자궁경부암 6명(3.7%), 유방암 5명(3.1%)의 순이었다. 3) 160명 중 125명(78.13%)이 통증을 호소했고 진통제를 투여받은 환자는 내과계 103명중 66명(64.08%), 외과계 57명 중 31명(54.39%)이었다. 97명 중 50명(51.55%)에서 경고, 투여가 가능했다. 4) 임종 24시간 전에 86명(53.75%)에서 의식이 명료했다. 5) 규칙적으로 투여된 진통제의 종류는 경구용 모핀이 34명(내과계 24명, 외과계 10명)으로 제일 많았고, 주사용 모르핀이 26명(내과계 20명, 외과계 6명), 경구용 코데인이 8명 (내과 5명, 외과 3명)의 순이었다. 비정기적으로 통증조절을 위해 투여된 약물로는 주사용 모르핀이 16회, 데메롤 근주가 12회, nubain 근주가 9회의 순이었다. 6) 규칙적으로 투여된 진통제의 평균량은 내과계에서 115.41 OME에서 외과계 52.7 OME 보다 많았으나(P<0.05), 환자 요구시마다 투여된(p.r.n.) 진통제의 양은 외과계가 66.64 OME 로서 내과계 23.49 OME 보다 유의하게 많았다(P<0.01). 7) 통증호소시에 투여한 진통제의 횟수에 있어서도 내과계 평균은 0.62회, 외과계는 1.88로 유의한 차이가 있었다(P<0.001). 8) 보조진통제의 사용은 내과계에서 57명(55.34%), 외과계에서 25명(43.86%)이 사용했다. 결론 : 임종 24시간 전에 과반수 이상이 의식이 명료했으며 내과의사가 외과의사보다 적극적으로 통증조절을 하고 있으나 많은 의사들이 규칙적인 통증조절보다는 비정기적인 투약과 진통제의 비경구투여를 선호하였다.