• 제목/요약/키워드: Validity of diagnosis

검색결과 407건 처리시간 0.033초

지게차의 제도적, 기술적, 교육적 요인이 재해감소에 미치는 영향에 관한 연구 (A Study on the Impact of Forklift Institutional, Technical, and Educational Factors on a Disaster Reduction)

  • 박영민;김진억
    • 한국재난정보학회 논문집
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    • 제19권4호
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    • pp.770-778
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    • 2023
  • 연구목적: 지게차 산업재해 감소를 위해 제도적, 기술적, 교육적인 요인들로 구분하여 각 요인이 재해 감소에 영향을 미치는가에 관한 연구가 필요하다. 연구방법: 리커트 5점 척도를 기반으로 한 오프라인 설문지를 바탕으로 SPSS 18 프로그램을 사용하여 기술통계 분석, 타당도 분석, 신뢰도 분석 및 다중 회귀분석을 실시하였다. 연구결과: 다중 회귀분석 결과 재해감소에 대한 독립 변수인 제도적, 기술적, 교육적 요인이 종속변수인 재해 예방 분산의 약 62.5%를 설명하는 것으로 나타났다. 회귀모형 검증은 F=118.775, 유의확률 p<0.01로 통계적으로 유의한 것으로 나타났다. 결론: 첫째, 3톤 미만 전동식 지게차를 검사제도에 포함하여 재해를 예방할 필요가 있다. 둘째, 지게차 충돌 재해를 예방하기 위한 전·후방 카메라 설치와 지게차 라인 빔(Line Beam) 설치를 의무화할 필요가 있다. 셋째, 지게차 관련 특별교육을 매년 시행할 필요가 있고, 운전자 및 인근 근로자를 지게차 특별교육 대상에 포함할 필요가 있다.

고등학교 「식품안전과 건강」 워크북 개발 및 타당도 검증 (Development and Validation of the 'Food Safety and Health' Workbook for High School)

  • 박미정;정난희;유난숙;최성연
    • 한국가정과교육학회지
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    • 제34권1호
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    • pp.59-80
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    • 2022
  • 본 연구는 「식품안전과 건강」과목의 수업과 평가를 지원할 수 있는 워크북을 개발하고 타당도를 검증하는 데 목적이 있다. 워크북 개발은 「식품안전과 건강」교육과정과 식생활 교육자료, 워크북 관련 선행연구를 분석하여 워크북의 개발 방향을 설정하고, 영역별 활동 아이디어를 도출하여 전체 구성을 설계하였다. 이후 초안을 개발하고 3차에 걸쳐서 교차 검토와 식품의약품안전처의 검토와 수정을 반복하여 편집본을 개발하였고, 9인의 전문가와 44인의 가정과교사들에게 타당도 검증을 받아 수정·보완하여 최종적으로 워크북을 완성하였다. 워크북은 4개 영역으로 '식품선택' 영역의 학습 주제 10개 36차시, '식중독과 식품 관리' 영역의 학습 주제 10개 36차시, '식품의 조리' 영역의 학습 주제 11개 43차시, '건강한 식사' 영역의 학습 주제 11개 55차시로 총 42개 학습 주제 170차시로 구성하였다. 워크북은 실천적 문제해결 역량, 생활자립 역량, 창의적사고 역량, 공동체 역량을 고루 배양할 수 있도록 하였으며, 문제를 인식하고 실험을 통해 문제를 해결하거나 발견학습을 통해 학습과제를 수행하고, 실험한 내용에 대해 심화 탐구학습을 진행하며, 평가를 통해 자가진단을 할 수 있도록 맥락적으로 구성하였다. 워크북의 타당도를 검증한 결과 학생 참여형 수업과 평가를 운영하고, 실험·실습을 강화하여 탐구하는 수업 분위기를 형성하는데 매우 적절한 것으로 평가되었다. 본 연구는 고교학점제 시행과 개별 학생의 학습 선택권이 강조되는 시점에서 가정계열 선택과목의 외연을 확장하고, 탐구 중심으로 학생이 주도하는 교실 수업을 구현하는데 기여할 것이다.

퇴원환자의 가정간호요구와 가정간호사업의 효과 분석 - 일 종합병원을 중심으로 (A Study of Home Care Needs of Patients at Discharge and Effects of Home Care -Centered on Patients Discharged from a Rural General Hospilal-)

  • 최연순;김대현;서미혜;김조자;강규숙
    • 대한간호
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    • 제31권4호
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    • pp.77-99
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    • 1992
  • The study was carried out at W. hospital, an affiliated hospital of Y university, involved a total of 163 patients who were discharged from the hospital between May 1990 und March 199J. Data collection was twice, just prior to discharge and a minimum of three months post discharge. Thirty patients who lived within a hour travel time of the hospital received home care during the three months post discharge. Nursing diagnoses and nursing interventions For these patients were analyzed in this study. The results of the study are summarized as follows : 1. Discharge needs for the subjects of the study were analyzed using Gordon's eleven Functional categories and it was found that 48.3% of the total sample had identified nursing needs. Of these, the needs most frequently identified were in the categories of sexuality, 79.3 %, health perception, 68.2 % self concept, 62.5 %, and sleep and rest 62.5 %. Looking ut j he nursing diagnosis that were made for the 30 patients receiving home care, the following diagnoses were the most frequently given; alteration in sexual pattern 79.3%, alterations in health maintenance, 72.6%, alteration in comfort, 68.0%, depression, 64.0%, noncompliance with diet therapy, 6.3.7%, alteration in self concept, 55.6%, and alteration in sleep pattern, 53%. 2. In looking at the effects of home nursing care as demonstrated by changes in the functional categories over the three month period, it was Found that of the 11 functional categories, the need level for health perception, nutrition, activity and self concept decreased slightly over the three month period. On the average sleep patterns improved, but restfulness was slightly less and bowel elimination patterns improved but satisfaction with urinary elimination was slightly less. On the other hand, role enactment, sexuality, stress management and spirituality decreased slightly. The only results that were statistically significant at the 0.05 level were improvement. in digestion and decrease in pain. No statistically significant changes were found in ability related to ADL, the total ADL Score at discharge was $19.78{\pm}8.234, and after 3 months $19.01{\pm}8.12$. Considering that a majority of the patients were over 60 years of age and that many had brain or spinal cord injuries, the fact that their ADL ability did nor deteriorate after discharge can be interpreted as related to a positive impact by the home health care nurses. Similarly there was a slight be not statistically significant decrease in the quality of life scores between the two lest times(l47.83 at discharge and 113.02 at the three month period). Again, when the chronic nature of thee problems facing these patients is considered this maintenance of quality of life can be interpreted as a positive impact by the home health care nurses. 3. One of the home care nursing activities was diagnosis. For this activity it was found that for nine functional health categories(sexuality and spirituality excepted) there were 20 nursing diagnoses. The most frequent were noncompliance, alteration in skin integrity both actual and potential, and impaired physical mobility in that order. 4. Delivery of home health care by the home health nurses included the following nursing activities; assessment, patient education, demonstration of care activities, counselling, direct care to the patient and referrals. Direct care included changing dressings, bladder irrigations, changing Foley catheters, measurement of residual urine, perineal care, position change, back care, oral hygiene, exercise and massage of motion exercises, cleansing enemas, tracheostomy suctioning and tracheostomy care, care of dentures, applications of heat and other similar nursing activities. In conclusion almost 50% of (he sample indicated a need for continued nursing care at the time of discharge and for the patients in the sample who received home care there was a slight decrease in nursing needs but while the patients had chronic and debilitation problems there was ill decrease in ADL abilities or in quality of life. Further study needs Lo be done La increase the reliability and validity of the tool that was used to measure home health care needs. It is also recommended that study by done using a randomized sampling with a control group to compare patients who receive home care with those who do not.

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알쯔하이머병에서 양전자방출단층촬영을 이용한 국소뇌포도당대사의 변화에 관한 연구 (Assessment of Metabolic Impairment in Alzheimer's Disease with [$^{18}F$]FDG PET: Validity and Role of Simplified Tissue Radioactivity Ratio Analysis)

  • 김상은;나덕렬;이정림;최용;이경한;최연성;김도관;김병태;이광호;김승태
    • 대한핵의학회지
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    • 제30권3호
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    • pp.299-314
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    • 1996
  • The purpose of the present study was to validate the use of tissue radioactivity ratios instead of regional metabolic rates for the assessment of regional metabolic changes in Alzheimer's disease(AD) with [$^{18}F$]FDG PET and to examine the correlation of ratio indices with the severity of cognitive impairment in AD. Thirty-seven AD Patients(age $68{\pm}9 yrs$, $mean{\pm}s.d.$; 36 probable and 1 definite AD), 28 patients with dementia of non-Alzheimer type(age $66{\pm}7 yrs$), and 17 healthy controls(age $66{\pm}4 yrs$) underwent [$^{18}F$]FDG PET imaging. Two simplified radioactivity ratio indices were calculated from 37-66 min image: region-to-cerebellar radioactivity ratio(RCR) and a composite radioactivity ratio(a ratio of radioactivity in the most typically affected regions over the least typically affected regions: CRR). Local cerebral metabolic rate for glucose(LCMRglu) was also measured using a three-compartment, five-parameter tracer kinetic model. The ratio indices were significantly lower in AD patients than in controls(RCR in temporoparietal cortex, $0.949{\pm}0.136$ vs. $1.238{\pm}0.129$, p=0.0004; RCR in frontal cortex, $1.027{\pm}0.128$ vs. $1.361{\pm}0.151$, p<0.0001; CRR, $0.886{\pm}0.096$ vs. $1.032{\pm}0.042$. p=0.0024). On the RCR analysis, 86% of AD patients showed a pattern of bilateral temporoparietal hypometabolism with or without frontal involvement; hypometabolism was unilateral in 11% of the patients. When bilateral temporoparietal hypometabolism was considered to be suggestive of AD, the sensitivity and specificity of the RCR analysis for the differential diagnosis of AD were 86% and 73%, respectively. The RCR was correlated significantly with the macroparameter K [$K_1k_3/(k_2+k_3)$] (r=0.775, p<0.0001) and LCMRglu(r=0.633, p=0.0002) measured using the kinetic model. In patients with AD, both average RCR of cortical association areas and CRR were correlated with Mini-Mental Status Examination(r=0.565, p=0.0145; r=0.642, p=0.0031, respectively), Clinical Dementia Rating(r=-0.576, p=0.0124; r=-0.591, p=0.0077), and total score of Mattis Dementia Rating Scale (r=0.574, p=0.0648; r=0.737, p=0.0096). There were also significant correlations between memory and language impairments and corresponding regional RCRs. The results suggest that the [$^{18}F$]FDG PET ratio indices, RCR and CRR, reflect global and regional metabolic rates and correlate with the severity of cognitive impairment in AD. The simplified ratio analysis may be clinically useful for the differential diagnosis and serial monitoring of the disease.

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ASQ :소아과외래에서의 발달지연 선별검사 (The ages and stages questionnaire: screening for developmental delay in the setting of a pediatric outpatient clinic)

  • 김은영;성인경
    • Clinical and Experimental Pediatrics
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    • 제50권11호
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    • pp.1061-1066
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    • 2007
  • 목 적 : 소아의 발달 장애는 조기에 발견하면 조기 치료가 가능하게 되어 치료 효과가 높아지고 후유 장애를 최소화할 수 있다. 발달 장애의 조기 발견을 위하여 기존에 사용해 오던 정식 발달 선별검사는 대부분 시간이 오래 걸리고, 복잡하며, 의료인력이 추가로 필요하기 때문에 바쁜 소아과 외래에서 모든 소아에게 적용하기는 어렵다. 기존의 발달검사 대신에 부모가 작성한 내용을 토대로 평가하는 발달 설문 양식들 중 Ages and Stages Questionnaire (ASQ)는 60개월 이전의 소아의 발달 선별을 목적으로 개발된 검사이다. 본 연구의 목적은 소아과 외래에서 시행하는 발달 지연의 선별 도구로서 ASQ의 타당성을 알아보기 위한 것이다. 방 법 : 가톨릭대학교 의과대학 부속 성모병원 소아과 외래를 방문한 소아의 부모에게 진료 전 대기 시간 동안 한국형 ASQ (K-ASQ)를 완성하도록 하였다. 설문지를 완성한 총 150명 중 만삭 출생아이며 이전에 발달지연의 진단을 받은 적이 없고, 기타 선천성 기형, 경련성 질환을 포함한 신경학적 이상, 유전성 질환의 경력이 없는 소아 67명을 대상으로 하였다. K-ASQ는 각 영역별로 평균에서 2 표준편차(SD) 아래 점수보다 낮으면 "실패"로 판정하며, 한 발달 분야 이상에서 "실패"가 있는 경우를 "선별검사 양성"으로 하였다. 최종 발달평가는 Bayley Scales of Infant Development-II (BSID-II)를 사용하여 판단하였으며, 지능 혹은 운동발달 지수가 평균보다 -1 SD 미만인 경우는 발달지연으로 판정하였다. K-ASQ의 결과를 BSID-II와 비교하여 분석하였다. 결 과 : 1) 대상아의 평균 연령은 $16.4{\pm}7.4$개월($6{\pm}30$개월 범위, 중앙치 14개월)이었다. 10명(14.9%)은 출생 시 부당경량아였으며, 평균 출생체중 $3.1{\pm}0.6kg$, 재태기간 $38.8{\pm}1.4$주이었다. 9명(13.4%)이 쌍생아였고, 33명(49.0%)이 남아였다. 대상 소아들의 모친의 평균 교육 기간은 $13.6{\pm}2.4$년, 53명(79.1%)이 고등학교 졸업 이상의 학력을 가졌고, 21명(31.3%)이 정규직 근무자였다. ASQ 설문지를 완성하는데 평균 $10.2{\pm}3.0$분이 소요되었다. (2) 17명(25.4%)이 ASQ 선별검사 양성이었는데, 그 중 4명은 발달이 지연되었고, 나머지 13명의 발달은 정상이었다. BSID-II로 판정한 발달 지연아 8명 중 4명은 ASQ 선별검사에서 양성이었고, 다른 4명은 선별검사 음성이었다. ASQ 선별검사 음성인 50명 중 4명이 발달지연으로 판단되었다. (3) BSID-II와 비교한 K-ASQ의 민감도(sensitivity)는 50.0%, 특이도(specificity) 78.0%, 양성 예측치 (positive predictive value) 23.5%, 음성 예측치(negative predictive value)는 92.0%로 나타났다. 결 론 : K-ASQ는 높은 음성 예측치를 보여 소아과 외래에서 소아 발달 지연의 선별 도구로서 사용하는 것이 타당한 것으로 판단되었다.

전산화단층촬영에서 촬영 목적 부위와 주변 결정장기에 대한 피폭선량 평가: 선량 권고량 중심으로 (Evaluation of Radiation Exposure Dose for Examination Purposes other than the Critical Organ from Computed Tomography: A base on the Dose Reference Level (DRL))

  • 이서영;김경리;하혜경;임인철;이재승;박형후;곽병준;유윤식
    • 한국방사선학회논문지
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    • 제7권2호
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    • pp.121-129
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    • 2013
  • 최근 다중검출기 CT의 보편화 된 사용으로 환자의 피폭선량이 증가하고 있다. 따라서 광자극발광선량계를 이용해 촬영 목적 부위와 주변 결정장기에 대한 환자의 피폭선량을 측정하고 그에 따른 생물학적 효과를 예측하여 저감화 방안을 제시하고자 하였다. ICRP에서 권고한 표준안을 대상으로 만들어진 인체 모형 표준 팬텀에 교정상수를 부여받은 OSD 선량계를 측정하고자 하는 좌 우 수정체, 갑상선, 촬영의 중심점, 생식선에 부착하여 각 검사 부위별 노출 조건과 동일한 상태에서 환자의 피폭 선량을 모사하였다. OSL 선량계의 평균 교정상수는 $1.0058{\pm}0.0074$이었으며 검사 부위별 주변 결정장기의 등가선량은 좌 우측 수정체의 경우 직접 피폭이 약 50mGy로 최대였으며 간접 피폭되는 경우 0.24mGy, 원거리에서는 0.005mGy미만의 기준 준위 이하로 측정되었다. 갑상선의 경우 두부 검사에서 10.89mGy로 최대였으며 흉부에서 7.75mGy, 복부 및 요추부, 골반부에서는 기준 미만이었다. 생식선의 경우 골반검사에서 21.98mGy로 최대였으며 간접 피폭되는 검사에서 기준 준위 미만에서 6.92mGy까지 피폭되었다. CT 검사에서 DRL에 대한 저감화 방법은 국제기구에서 권고하고 있는 방사선 방어 원칙에 대한 정당한 해석과 제도적 뒷받침이 필요하다. 따라서 환자의 피폭을 최소화하기 위해서는 정당성을 충족하여야 하며 환자의 피폭선량에 미치는 영향들을 체계화하고 조직의 불필요한 피폭을 최소화 하여야 한다.

흉막수에서 Vascular Endothelial Growth Factor의 진단적 의의 (Significance of Vascular Endothelial Growth Factor in Pleural Effusion)

  • 김현구;조원민;류세민;조양현;심재훈;손영상;김학제;최영호
    • Journal of Chest Surgery
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    • 제37권9호
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    • pp.781-786
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    • 2004
  • 흉막수의 원인별 감별진단을 위한 기존의 검사 방법들은 한계가 있었다. 저자들은 VEGF를 이용한 흉막수의 원인별 감별 진단의 유용성과 기존의 검사 수치들과 어떤 상관관계가 있는지 알아보고자 하였다. 대상 및 방법: 흉막수를 가진 총 35명의 환자를 악성종양군(n=10), 양성종양군(n=5), 염증성 질환군(n=10), 그리고 기흉군(n=10)으로 나누어 전향적 연구를 하였다. 각 군으로부터 흉막수를 채취하여 혈구검사, 생화학적 검사(포도당, 단백질, LDH, ADA), 그리고 VEGF를 측정하였다. 결과: 포도당은 염증성 질환군이 양성종양군(60.5$\pm$36.09 mg/dL vs. 162.0$\pm$19.80 mg/dL, p=0.011)과 기흉군(60.5$\pm$36.09 mg/dL vs. 107.3$\pm$15.99 mg/dL, p=0.010)에 비해 낮았고, 양성종양군은 기흉군에 비해 높았다 (162.0$\pm$19.80 mg/dL vs. 107.3 $\pm$ 15.99 mg/dL, p=0.004). ADA는 염증성 질환군이 악성종양군(87.9 $\pm$42.62 IU/L vs. 27.7$\pm$31.04 IU/L, p=0.024)과 기흉군(87.9$\pm$42.62 IU/L vs. 38.5$\pm$33.32 IU/L, p=0.047)에 비해 높았다. VEGF는 기흉군에 비해 악성종양군(82.9$\pm$58.49 pg/dL vs. 364.3$\pm$433.83 pg/dL, p=0.026)과 염증성 질환군(82.9$\pm$58.49 pg/dL vs. 335.8$\pm$383.34 pg/dL, p=0.048)에서 높았다. 악성종양군에서의 VEGF가 양성종양군(364.38$\pm$433.83 pg/dL vs. 53.3$\pm$22.20 pg/dL, p=NS)에 비해 높은 경향을 보였으나 통계적인 의미는 없었다. VEGF전체 값과 다른 검사치들의 전체 값과의 상관관계는 통계적으로 유의하지 않았다. 결론: 흉막수의 원인별 감별진단을 위한 방법 중 농흉에서는 포도당이, 결핵에서는 ADA가 도움이 된다고 할 수 있다. VEGF는 맥관형성과 혈관 투과성이 증가하는 질환인 악성종양과 염증성 질환에서 다른 군에 비해 증가하나 이 두 군 사이를 감별 진단하는 데에는 도움이 되지 못한다고 할 수 있다. 악성종양에서 양성종양에 비해 VEGF가 높은 경향을 보여 좀 더 많은 환자를 대상으로 한 연구가 진행되어야 한다. 또한 VEGF가 다른 기존의 검사수치와 상관관계가 없는 것으로 밝혀져 흉막수의 원인별 감별진단을 위해 앞으로 새로운 검사방법이나, 기존의 검사 수치와 새로운 조합을 하는 데 연구가 진행되어야 한다.

뇌성마비아 어머니의 경험 (Lived experience of mothers who have child with cerebral palsy)

  • 이화자;김이순;이지원;권수자;강인순;안혜경
    • 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.

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두부 손상환자 가족의 간호요구에 대한 연구 (A Study on Needs of the Families of Head Injury Patients)

  • 조규영;박형숙
    • 기본간호학회지
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    • 제6권3호
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    • pp.414-433
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    • 1999
  • The purpose of this study is to identify the needs which are perceived by one of the familiy members who have head injury parients by traffic accidents in the intensive care units. Subjects were 70 families members of head injury patients admitted to 2 general hospitals NICU located Pusan city, 1 general hospital NICU located Ulsan city from December 1. 1998 to February 28. 1999. For this study, 70 family members were interviewed with aid of a Likert scale which was developed by researcher for this study. For development of the survey instrument, literature review and open questionnaire technique with family members and the nurses working in NICU. The 50needs-items were classified into 7 groups according to the homogeneity of the items with the support of literature review. For the content validity, the instrument was reviewed by 1 nursing professor and the internal reliability of this instrument was Cronbach alpha=0.94 which is highly accepted. Data was analyzed by a SPSS computer program. Data analysis included frequency. percentage, mean, standard variance and t-test or ANOVA. The results were as followings : 1. The general characteristics of head injury patients shows that the male was 74.3%, the female was 25.7% and age distribution shows that the fifty-fifty nine years was 30%, the highest. Of religion the buddhism was the most, The diagnosis distribution shows that epidural hematoma was 32.9% and subdural hematoma was 24.3%. The mentalility distribution shows that semicoma was 31.4% and stupor was 31.4%. Hemiplegia was 42.9% 2. The general charaterisrics of the family needs of head injury patients shows that thirty-thirty nine years was 31.4%, the highest. sex distribution shows that the male was 20%, the female was 80%. Of religion the buddism was the most. 3. The family needs of head injury patients was $3.03{\pm}0.42$, needs for the information of a patient's condition was $3.65{\pm}0.48$, the highest. And needs for the information of care and treatment was $3.48{\pm}0.48$, needs to be supplied with comfortable facilities for family was $3.04{\pm}0.66$, needs to be participate in a patient's care was $2.90{\pm}0.55$, needs to be informed about the available resources was $2.83{\pm}0.59$, needs to be supported emotionally for family was $2.79{\pm}0.55$, needs for religious assistance was $2.51{\pm}0.85$. 4. Examining the family needs of head injury patients according to patient's characteristics, mentality, plegia degree and operation were shown be variables to make an effect on the needs for the head injury patients family. At all, according to severity of head. injury, the family needs of head injury patients was high. 5. Examining the family needs of head injury patients according to their general characteristics, we could know that religion, job. income were shown to be variables to make an effect on the family needs. Through the examination it can be seen that the characteristics of head injury patients and the family needs of head injury patients. In conclusion, the family needs of head injury patients was almost same the family needs of ICU patients. Therefore we must involve the family's care of head injury patients and we must provide exact and repeated explanation, education and support the family of head injury patients. As this study was resulted in selecting the families admitted to NICU of some general hospital, we couldn't stretch the result in our favor. Therefore, continuous studies are suggested.

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소아의 위장관 이물에 대한 고찰 (Gastrointestinal Foreign Bodies: Review of 96 Cases)

  • 이민혜;강기수;정혜성;서지현;임재영;박찬후;최명범;우향옥;윤희상
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제5권2호
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    • pp.136-142
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    • 2002
  • 목 적: 위 이하의 소화관에 이물이 존재하는 경우 이물의 종류와 크기에 따라 자연 배출을 기다리거나 제거를 요하는 치료를 할 수 있다. 이에 저자들은 15년간 경상대학교병원 소아과에 상부 소화관 이물로 진단 받은 소아 중 이물이 위 이하의 소화관에 있었던 경우를 자연 배출이 되었던 경우와 내시경적 치료나 수술적 치료가 필요했던 경우의 이물의 위치, 임상 증상, 방사선 소견, 이물을 삼킨 후 내원까지 걸린 시간, 합병증 등을 조사하였다. 방 법: 1987년 2월부터 2002년 2월까지 경상대학교병원 소아과에 이불연하를 주소로 내원한 0~15세 소아 환아 220명 소아 중 이물이 위 이하의 소화관에 위치했던 경우 96례를 대상으로 조사하였다. 결 과: 이물연하를 주소로 내원한 220명 중 내원당시 위나 소장 이하의 부위에 이물이 있었던 경우는 96례였다. 호발 연령은 2~5세였으며, 남아 60명, 여아 36명이었다(남 : 녀=1.66 : 1) 무증상이였던 경우가 62례(64.5%)였고 나머지에서는 구토, 이물감, 복통, 흉통, 보챔 등의 증상이 있었다. 방사선 검사로 이물을 확인할 수 있었던 경우는 81례(86%)였고, 이물의 위치를 확인하지 못하여 바륨 조영술을 시행한 경우가 1례, 내시경적으로 위치를 확인한 경우가 37례였다. 이물이 발견된 위치로는 위가 71례로 가장 많았으며, 소장 및 대장에서 발견되었던 경우는 25례였다. 이물의 종류는 동전(40%)이 가장 많았고, 핀과 같은 날카로운 물질이 27례 있었다 치료로 상부 소화관 내시경으로 제거한 경우가 37례(38.5%)였으며, 4례에서는 전신마취 하에 수술로 제거하였다. 55례에서 자연 배출을 기다렸다. 자연 배출을 지켜본 경우 55례 중 37례가 이불 연하 발생 후 24시간 이내에 내원한 경우로 가장 많았다. 24시간 이후에서 2주 사이에 내원한 경우 위내에 이물이 지속적으로 존재하면 상부 위장관 내시경으로 이물을 제거하였다 이물 연하의 합병증으로는 출혈, 미란, 궤양, 미세천공, 장폐색이 있었으나 빈도는 적었다. 결 론: 본 저자들은 15년 간의 위 이하의 소화관 이불 96례에 대한 고찰한 결과 소아용 위장관 내시경의 발전으로 상부 위장관 이물의 진단과 치료가 용이해졌음을 알 수 있었으나 자연배출을 기다려볼 수 있는 상황에서도 내시경을 이용한 제거가 증가하였는데 이에 대한 타당성에 대한 연구가 필요할 것으로 사료된다.

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