• 제목/요약/키워드: 만성질환아 어머니

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만성질환아 어머니의 희망, 핵심신념, 사회적 지지가 외상 후 성장에 미치는 영향 (Influence of Hope, Core beliefs and Social support on Posttraumatic growth in Mothers of Chronically Ill Children)

  • 김미영;김금순
    • 기본간호학회지
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    • 제19권4호
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    • pp.493-502
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    • 2012
  • Purpose: The purpose of this study was to identify the influence of hope, core beliefs, and social support on the posttraumatic growth of mothers with chronically ill children. Methods: In this study, 94 mothers who gave written consent completed the questionnaires between July 21 and July 31, 2012 when they visited a university hospital in Seoul, Korea. Data were analyzed using t-test, ANOVA, Pearson correlation coefficient and stepwise multiple regression. Results: Hope, core belief and social support had positive correlations with posttraumatic growth. Models including these variables explained 64.8% (F=55.276, p<.001) of the variance for posttraumatic growth. Hope (${\beta}$=.441, p<.001) was the most influential factor. Conclusion: The findings demonstrate that it is essential for nurses to mediate and facilitate posttraumatic growth of mothers caring for chronically ill children. Furthermore, there is an need to develop and implement new strategies in clinical practice that will result in improvements in posttraumatic growth.

만성 알레르기 질환 아동의 어머니-의료진 간 파트너십이 어머니의 아동 상태 관리능력에 미치는 영향 (Effects of the Mother-Medical Staff Partnership on Mothers' Condition Management Ability for Children with Chronic Allergic Diseases)

  • 손해경;송효빈;김동희
    • Child Health Nursing Research
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    • 제24권1호
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    • pp.101-108
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    • 2018
  • Purpose: This study aimed to identify the effects of the mother-medical staff partnership on mothers' condition management ability for children with chronic allergic diseases. Methods: A total of 109 Korean mothers caring for a child with a chronic allergic diseases, identified according to the allergic march, such as food allergy, atopic dermatitis, allergic rhinitis, and allergic asthma, were recruited from the pediatric department of a general hospital in Seoul through convenience sampling. Data were collected using structured self-reported questionnaires from August 1, 2017 to October 31, 2017. and analyzed by descriptive statistics and multiple regression using SPSS version 22.0. Results: The Mother-medical staff partnership had a statistically significant effect on mothers' condition management ability for children with chronic allergic diseases (p<.05). Among the general characteristics, satisfaction with nursing services had a statistically significant effect on mothers' condition management ability (p<.05). Conclusion: In conclusion, strategies to support children with chronic allergic diseases, as well as their caregivers, should consider the mother-medical staff partnership as part of a family-centered approach.

만성질환아 어머니의 아동질병으로 인한 불확실성 경험 (Maternal Uncertainty in Childhood Chronic Illness)

  • 박은숙
    • Child Health Nursing Research
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    • 제4권2호
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    • pp.207-220
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    • 1998
  • The purpose of this study was to build a substantive theory about the experience of the maternal uncertainty in childhood chronic illness. The qualitative research method used was grounded theory. The interviewees were 12 mothers who have cared for a child who had chronic illness. The data were collected through in-depth interviews with audiotape recording done by the investigator over a period of nine months. The data were analyzed simutaneously by a constant comparative method in which new data were continuously coded into categories and properties according to Strauss and Corbin's methodology. The 34 concepts were identified as a result of analyzing the grounded data. Ten categories emerged from the analysis. The categories were lack of clarity, unpredictability, unfamiliarity, negative change, anxiety, devotion normalization and burn-out. Causal conditions included : lack of clarity, unpredictability, unfamiliarity and change ; central phenomena : anxiety, being perplexed ; context. seriousness of illness, support ; intervening condition : belief action/interaction strategies devotion, overprotection ; consequences : normalization, burn-out. These categories were synthesized into the core concept-anxiety. The process of experiencing uncertainty was 1) Entering the world of uncertainty, 2) Struggling in the tunnel of uncertainty, 3) Reconstruction of the situation of uncertainty. Four hypotheses were derived from the analysis : (1) The higher the lack of clarity, unpredictability, unfamiliaity, change, the higher the level of uncertainty (2) The more serious the illness and the less the support, the higher the level of uncertainty. (3) The positive believes will influence the devoted care and normalization of the family life. Through this substantive theory, pediatric nurses can understand the process of experiencing maternal uncertainty in childhood chronic illness. Further research to build substantive theories to explain other uncertainties may contribute to a formal theory of how normalization is achieved in the family with chronically ill child.

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만성질환아 어머니의 삶의 질에 관한 연구 (The Study on the Quality of Life for the Mothers of Hospitalized Chronic Pediatric Patients)

  • 최명애;이현숙;김대희;박명희;윤소영;조연희;방경숙;박연환
    • Child Health Nursing Research
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    • 제6권2호
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    • pp.249-261
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    • 2000
  • The purpose of this study were to identify the quality of life for the mothers of hospitalized chronic pediatric patients, and to explore the factors affecting the QOL of those mothers. The subjects were 201 mothers whose children had hospitalized at one University hospital with chronic diseases. Data were collected from the December, 1997 to December, 1998. We used a revised QOL instrument consisting of 34 items, 5 point likert scale based on the Noh's QOL instrument. The revised QOL consists of six subscales, those are physical status and function, self esteem, emotional status, economic status, relationship with family members, and relationship with neighborhood. Data were analyzed by t-test, ANOVA, Pearson's correlation using SPSS-PC. The results were as follows: 1. The mean score of quality of life for the mothers of chronic pediatric patients was 100.31, and item mean was 2.95. In subscale analysis, item mean of economic status was the lowest, and that of relationship with family members was the highest. 2. Correlations between characteristics of chronic pediatric patients, their mothers and QOL of mothers were as follows; 1) Total QOL of mothers had a significant positive relationship with progressing time relapse after diagnosing and age of mothers. There was a significant negative relationship between the total QOL of mothers and number of hospitalization of their children. 2) QOL on self esteem and economic status had a significant relationship with age of pediatric patients, the time relapse after diagnosis, and age of mothers. Total number of family members and QOL on economic status showed a significant positive relationship. QOL on emotional status, economic status, and relationship with family members of mothers showed negative correlations with the number of hospitalization of their children. 3. Followings were the result of difference in QOL among different demographic cha- racteristics of the subjects. 1) QOL on economic status of mothers was significantly higher when fathers of pediatric patients had jobs. 2) Total QOL score, QOL on emotional status, and QOL on relationship with neighborhood were significantly higher when mothers of pediatric patients had spouses. 3) QOL on self esteem of mothers was significantly higher when mothers had religion. 4. Followings were the result of difference in QOL among different diagnosis of the children. 1) Total QOL score of mothers whose children had congenital heart disease was higher than that of mothers whose children had leukemia and cancer. 2) QOL on emotional status, economic status, and relationship with family members of mothers whose children had congenital heart disease were higher than those of mothers whose children had leukemia, cancer, and epilepsy.

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퇴원에 따른 만성 질환아 어머니의 반응과 환아 돌보기 지지 요구 (The Reaction and the Supporting Need for the Mother in Caring for their Chronicly III Child after Discharge)

  • 채현이
    • 가정∙방문간호학회지
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    • 제8권1호
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    • pp.50-61
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    • 2001
  • With the improvement of current medicine, the number of the chronicly ill children are increasing. The illness of the child drives all of the family to despair. especially it is a burden on the mother who takes care of the ill child. She's faced with many emergencies and feels powerless. The home care for a child is for finding a child's problems early and mediating them. The purpose of this study was to investigate the mother's reaction following their chronicly ill child's discharge and to investigate the supporting needs for caring for an ill child. The subjects of this study were mothers with a chronicly ill child being discharged from a general hospital in Seoul and the data was collected from July 20 to September 30. Data was collected by using questionnaires which were developed by the researcher. (The questionnaires were composed of the average 5 points - Likert's method). The Mother's reaction means that the higher the score, the more negative the mother's thoughts about discharge are. Supporting need for caring for ill an child means that the higher the score, the higher the demand of nursing is. The statistical analysis used the SPSS program for t-test. ANOVA, and Pearson Correlation. The results of this study were as follows: 1. The mother's reaction scores following discharge were the lowest. 19 and the highest 72 so that the total average was 43.15. The answer, 'I worry that my baby will be troubled with illness again after discharge gained the high points (3.94 of 5 points). The answer. 'The discharge of my baby makes me gloomy' gained 2.05-it was the lowest points. Their were significant differences according to religion (p=.006). salary (p=.050). the burden of the medical fee (p = .005) and caregiver (p=.027). 2. Supporting Need for caring for ill an child was the lowest 15 and the highest 67. the total average was 47.87. The answer. 'I'd be glad to get a person whom I could always get counsel about the health of my baby with' scored the high point (average 4.04 of 5). The answer. 'Caring for my baby at home makes me exhausted' gained the lowest point. 2.49. Their were significant differences according to religion (p=.019) and diagnosis (p=.019). 3. The relationship between the reaction of the mother and supporting need for caring for an ill child was a positive correlation (r=0.585). In conclusion. this study revealed that mothers weren't positive about their chronicly ill child's discharge and they wanted to get support for caring for an ill child. Through this study. I proposed that the program to support the chronicly ill child at home and home care by continuous counselling after discharge should be develop.

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만성질환아 어머니의 질병에 대한 불확실성 정도와 양육태도 (Perceived Uncertainty and Rearing Attitude of Mothers with Chronically ILL Children)

  • 박은숙
    • Child Health Nursing Research
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    • 제2권2호
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    • pp.5-18
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    • 1996
  • The purposes of this study were to measure the degree of perceived uncertainty and to identify the rearing attitudes of mothers with chronically ill children, and to examine the relationship between the perceived uncertainty and the rearing attitude of these mothers. The subjects of this study consisted of 133 mothers with chronically ill children, registered at 2 university hospitals in Seoul. Data was collected from April 1 to May 31, 1996. The Parents' Perception of Uncertainty Scale(28-item 4 point scale) and the Maternal Behavior Research Instrument (49-item 5 point scale) were used. Data was analyzed by Cluster analysis, ANOVA MANOVA and t-test. Results of this study are summarized as follows : 1. Mothers perceived their uncertainty to be slightly high (Mn 2.48). The degree of perceived uncertainty by the four components slightly differed unpredictability(2.72), lack in clarity(2.58), vagueness (2.52) and lack of information(2.04) . The degree of perceived uncertainty of mothers with ill children revealed to be influenced significantly by the age of the ill children, duration of illness after the diagnosis, and the experience of hospitalization. 2. Among the rearing attitudes : moderatlely high affective(Mn 3.98) and resrictive(Mn 3.58) attitudes of mothers toward their ill children were identified. Mothers tend to give positive evaluations of their childrens' behaviors (Mn 3.38) and less rejection(Mn 2.81). 3. Mothers' rearing attitude were correlated with the degree of perceived uncertainty in illness ; mothers in the Low Perceived Uncertainty Group (Mn 1.99) revealed the highest affective (Mn 4.08), the lowest resrictive(Mn. 2.72) attitudes and tendency to give positive evaluations of their childrens' behaviors (Mn 3.54) compared to the High Perceived Uncertainty Group(Mn 3.26) and Moderate Perceived Uncertaity Group(Mn 2.57). 4. The degree of perceived uncertainty, the duration of illness after the diagnosis and the experience of hospitalization revealed to be significantly influential to the rearing attitude of mothers with chronically ill children. From the above results, it can be concluded that predicting and controlling mothers' uncertainty are necessary for improved, efficient nursing interventions and normal growth & development of the chronically ill children.

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경련성 질환 환아와 가족 (CHILDREN WITH CHRONIC CONVULSIVE DISORDER AND THEIR FAMILIES)

  • 조수철;김붕년
    • Journal of the Korean Academy of Child and Adolescent Psychiatry
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    • 제13권1호
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    • pp.67-75
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    • 2002
  • 연구목적:만성경련 환아의 가족 구성원들의 정신병리와 환아와의 관계를 평가하기 위해 본 연구를 실시하였다. 환아 어머니의 정신병리와 환아와의 관계 및 부부관계를 조사하였고, 환아 아버지와 타 형제들과 환아와의 관계를 조사하였으며, 부모와 아동사이의 의존성정도와 가족구조를 평가하였다. 연구방법:만성경련질환 환아40명과 성별-나이-학업수준이 일치하는 대조군 30명을 연구대상으로 하였다. 만성환아군은 12개월 이상 약물 치료를 받고 있는 정상지능의 일반학교를 다니는 특발성 경련질환아였고, 대조군은 특별한 신체질환이 없는 중간성적 정도의 초등중학생으로 하였다. $2{\sim}3$차례에 걸친 부모 및 환아 면담을 반구조화된 인터뷰로 실시하였고, 부모와 대조군에게 가정환경척도, 간이정신진단검사, 아동의존척도를 배부하여 평가하도록 하였다. 연구결과:두세 차례에 걸친 가족면담에서, 대조군에 비해 유의하게 높은 부모의 과보호, 형제간 적대감 표출 등의 문제를 환아군에서 확인할 수 있었으며, 부부간의 갈등도 대조군에 비해 유의하게 높았다. 가정환경 척도평가에서 대조군에 비해 감정표현영역, 성취지향성영역, 지적-문화적 태도 영역, 적극적 여가선용 영역에서 유의한 저하를 보였고, 의존성척도에서도 정감적 의존, 의사소통에서의 의존, 여행의 어려움 등이 환아군에서 유의하게 높았다. 환아모의 정신병리도 대조군에 비해 거의 모든 척도에서 유의하게 높았으며, $30{\sim}40$대 도시거주 여성과 비교한 T값을 기준으로 할 때 40%정도가 우울-불안장애의 위험성이 있었다. 결 론:만성경련 환아를 둔 가족내에서, 가족구조상의 문제, 가족내 갈등, 환아에 대한 과보호와 과의존, 모의 정신병리 등이 보다 뚜렷하게 높은 것으로 평가되었으며, 이러한 연구결과는 경련환아의 가족에 대한 적극적인 치료적 중재가 필요함을 시사하는 소견이라고 할 수 있다.

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소아 및 청소년의 실손형 민간의료보험 가입 결정요인 (Determinants of Purchasing Indemnity Private Health Insurance among Adolescents and Children)

  • 유창훈;강성욱;최지헌;권영대
    • 한국콘텐츠학회논문지
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    • 제18권10호
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    • pp.99-110
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    • 2018
  • 최근 자녀의 건강위험에 대한 관심이 높아지면서 소아 및 청소년의 실손형 민간의료보험 가입이 급증하고 있다. 본 연구는 한국의료패널 2009-2015년 자료를 이용하여 소아 및 청소년 4,567명을 대상으로 실손형 민간의료보험 가입의 영향 요인을 분석하였다. 패널로짓을 활용한 분석 결과, 소아 및 청소년의 특성에서는 연령, 출생 순서, 거주지, 장애 여부가, 아버지의 특성에서는 실손형 의료보험 가입, 만성질환 및 장애, 어머니의 특성에서는 자녀와의 연령 차이, 실손형 의료보험 가입, 미충족의료, 가구 특성에서는 1인당 가구소득이 가입에 영향을 미치는 유의한 요인이었다. 만혼과 고령출산, 저출산으로 인한 자녀의 건강위험에 대한 불안감과 의료비 부담을 완화할 수 있도록 소아 및 청소년의 의료보장성 강화정책이 지속적으로 시행될 필요가 있다. 특히 다자녀 가구, 취약계층에 대한 정책적 배려가 필요하다.

만성 틱 장애 뚜렛씨 장애의 임상 특성 (CLINICAL CHARACTERISTICS OF CHRONIC MOTOR TIC DISORDER AND TOURETTE'S DISORDER)

  • 신성웅;임명호;현태영;성양숙;조수철
    • Journal of the Korean Academy of Child and Adolescent Psychiatry
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    • 제12권1호
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    • pp.103-114
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    • 2001
  • 뚜렛씨 장애는 근육틱과 음성틱이 만성적으로 지속되는 질환이다. 만성 틱장애는 근육틱 혹은 음성틱중 하나만 지속적으로 나타나는 질환이다. 본 연구에서는 1998년 4월 1일부터 1999년 4월 1일까지 서울대학교병원 소아정신과 병동에 입원한 만성 틱 장애 아동과 뚜렛씨 장애 아동의 임상적 특징을 조사하고 두 질환 사이의 관계를 비교하고자 시행되었다. 이들의 특성을 확인하기 위해 대조군으로 학습장애 환자를 선정하였다. 조사 결과는 다음과 같다. 첫째, 만성 틱장애(n=13)와 뚜렛씨 장애 환자(n=29)의 평균 발병연령은 각각 $7.3{\pm}2.5$, $7.2{\pm}2.2$세, 입원시 연령은 평균 $11.7{\pm}2.7$, $11.5{\pm}2.6$세, 입원기간은 $5.7{\pm}5.4$, $11.0{\pm}8.7$주였고 두 군 사이에 의미 있는 차이는 없었다. 학습장애의 경우 발병연령($4.2{\pm}1.9$세)이 두 장애보다 빠르고 의료기관을 찾는 시기($9.8{\pm}3.2$세)도 빨랐다. 출생 계절은 틱장애 환자들에서 6월에서 9월 사이가 가장 적었지만 의미 있는 차이는 없었다. 남녀의 성비율은 각각 10:3, 26:3, 11:5였고 의미 있는 차이는 보이지 않았다. 환자가 출생할 때의 아버지와 어머니 연령은 세 군 모두 차이가 없었다. 둘째, 정신과적 가족력이 있는 경우도 세 군 사이에 차이가 없었고 각각 24.1%, 46.2%, 56.3%였다. 발병전 유발 요인이 확인된 경우는 만성틱장애와 뚜렛씨 장애에서 11.1%와 35.7%로서 의미 있는 차이를 보이지는 않았지만 학습장애(56.3%)에 비해서는 적었다. 셋째, 만성 틱장애와 뚜렛씨 장애, 그리고 학습장애 환자의 지능지수는 각각 언어성 지능 $92.3{\pm}10.7$, $94.7{\pm}14.9$, $94.3{\pm}13.8$이었고, 동작성 지능은 $93.0{\pm}20.5$, $97.5{\pm}13.0$, $95.0{\pm}16.9$이었으며, 전체 지능은 $91.9{\pm}20.1$, $95.8{\pm}14.5$, $93.9{\pm}15.1$로서 세 군 사이에 의미 있는 차이는 없었다. 기질적 뇌장애 소견은 CT/MRI 등에서 0%, 27.3%, 6.3%, 뇌파 이상은 8.3%, 17.2%, 12.5%에서 나타났고 차이는 발견하지 못하였다. 넷째, 항도파민 약물에 대한 반응은 만성 틱장애와 뚜렛씨 장애 환자에서 각각 84.6%, 77.0%가 부분관해를 보였고 완전 관해된 경우는 한 명도 없었으며 두 군 사이에 차이가 없었다. 다섯째, 공동 유병현황을 조사한 결과 주의력결핍·과잉운동장애가 학습장애에서 의미 있게 많은 것을 제외하고는 세 군 사이에 통계적으로 의미 있는 차이를 보이지 않았다. 조사 결과 입원한 환자의 경우 만성 틱장애와 뚜렛씨 장애를 가진 환자들은 임상적으로 학습장애를 가진 환자와 많은 부분에서 차이를 보였으나 만성 틱장애와 뚜렛씨 장애를 구분해야 하는 근거를 찾지 못하였다.

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학동기 소아에서 보완대체요법의 이용실태 (A study on the utilization of complementary and alternative medicine for elementary children)

  • 안영준;김은영;문경래
    • Clinical and Experimental Pediatrics
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    • 제52권10호
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    • pp.1103-1108
    • /
    • 2009
  • 목 적:만성질환자가 아닌 일반 학동기 아동을 대상으로 보완대체요법 이용실태를 파악하며 소아청소년과 의사로서 대처 방향을 모색하고자 연구를 실시하였다. 방 법:3개 초등학교 1학년부터 6학년 1,688명의 학부모를 대상으로 설문조사를 시행하였다. 그중 설문지가 회수된 794명(47%)을 분석하였다. 결 과:일반적인 학동기 아동에서 보완대체요법의 이용률은 278명(35%)이었고, 보완대체요법의 종류는 한약제 62.6%, 보조식품 31.3%, 비타민 30.2%, 선식 11.2%, 침술 11.2%, 체 냄, 수지침 순이었다. 보완대체요법의 이용률은 어머니의 학력이 대학 이상 일 때, 종교가 있을 때, 가정 월 총수입이 100만 원 이상일 때 의미 있게 높았으며 이용하게 된 동기는 질병예방목적이 가장 많았고, 주로 주변 사람이나 매체를 통해 이용하였다. 보완대체요법에 대한 만족하지 못하는 경우는 16%였고, 재사용 의향이 없는 경우는 20.5%였고, 환아가 건강할 때 주로 사용하는 경향을 보였다. 환아가 영양결핍, 아토피 피부염, 관절통증, 알레르기비염, 비만, 천식 때 주로 이용하는 경향을 보였다. 결 론:보완대체 의학의 사용이 아이의 건강상태와는 밀접하지 않으며 사용 경로 또한 주변 사람의 권유나 방송 매체 등을 통해 이루어지고, 병원치료와 병행 시 좋을 것이라는 막연한 기대감으로 사용되고 있는 경우가 많아 보완대체요법에 대한 부작용, 효과, 안전성에 대한 연구가 필요하며 만성질환 및 알레르기 질환의 경우 소아청소년과 의사로서 현대의학의 적극적인 치료 및 교육이 필요할 것으로 사료된다.