• Title/Summary/Keyword: 선천심장병

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출생아 100명 중 1명에게 나타나는 선천성 심장병

  • 김남수
    • 가정의 벗
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    • v.37 no.2 s.426
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    • pp.12-13
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    • 2004
  • 출생아 100명중 1명에게 나타난다고 하는 선천성 심장병, 태아 심장 초음파 검사로 심장병이 있는 태아가 태어나지도 못하는 등 많은 문제를 가지고 있습니다. 그러나 치료 기술이 발전하여 조기 진단과 적절한 치료를 받게 되면 정상 수명까지 살 수 있습니다.

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소아심장 검진의 필요성

  • Hong, Chang-Ui
    • 건강소식
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    • v.10 no.11 s.96
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    • pp.24-26
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    • 1986
  • 전 초등학교 아동의 약 0.3%가 선천성 심장병을 가지고 있고, 0.03%가 류마티성 심장병을 가지고 있는 것으로 나와 있다. 그래서 1,000명의 약 3명 정도는 심장병을 가지고 있다. 따라서 모든 학생들에 대하여 심장검진을 해서 심장병이 있고, 없음을 알아야 한다.

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소아심장-집단검사의 필요성

  • Hong, Chang-Ui
    • 건강소식
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    • v.10 no.2 s.87
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    • pp.24-26
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    • 1986
  • 전 초등학교 아동의 0.25%가 선천성 심장병을 가지고 있고, 0.03%가 류마티성 심장병을 가지고 있는 것으로 나와 있다. 그래서 1,000명의 약 3명 정도는 심장병을 가지고 있다. 따라서 모든 학생들에 대하여 심장검진을 해서 심장병이 있고, 없음을 알아야 한다.

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Incidence of congenital heart disease in the western part of Gyeongnam Province in Korea (서부경남 지역의 선천성 심질환의 발생 빈도)

  • Jang, Sun Hwa;Kim, Jae Hui;Yeom, Jung Sook;Park, Eun Sil;Seo, Ji Hyun;Lim, Jae Young;Park, Chan Hoo;Woo, Hyang Ok;Youn, Hee Shang
    • Clinical and Experimental Pediatrics
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    • v.51 no.8
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    • pp.848-855
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    • 2008
  • Purpose : The objective of this study was to ascertain the incidence of congenital heart disease in the western part of Gyeongnam Province in Korea. Methods : We enrolled 849 children (M:F=390:459) who were diagnosed with congenital heart disease (CHD) and received echocardiography during January 1997 to December 2005 in Gyeongsang National University Hospital. The subjects were limited to patients born from 1997 to 2004. The CHDs were classified into acyanotic types and cyanotic type. Further, acyanotic type CHDs were divided into shunt type and valvular types. Results : Numbers of initially diagnosed patients from 1997 to 2004 were as follows: 113, 128, 116, 104, 129, 97, 84, and 78. The median age of initially diagnosed CHD patients was 1 month in the acyanotic type and 0.5 months in cyanotic type. Also, an annual frequency among CHD types and gender ratio were no significant difference in every year. Incidences of CHD from 2000 to 2004 in the western part of Gyeongnam Province were 8.9, 12.7, 10.9, 10.0, and 9.7 per 1,000 live births, respectively. Conclusion : From 1997 to 2001, 100-130, and from 2002 to 2004, less than 100 patients were diagnosed with CHD. This showed a decrease in the numbers of CHD patients in the last three years. However, the Incidence of CHD was 0.89-1.24% during the last five years. Therefore, the decrease in the annual frequency of CHD was due to the recent decline in birth rate in Korea.

Health Management Experiences of Adolescents with Severe Congenital Heart Disease (중증 선천성 심장병 청소년의 건강관리 경험)

  • Hwang, Ji-Hye;Chae, Sun-Mi
    • The Journal of the Korea Contents Association
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    • v.20 no.9
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    • pp.659-671
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    • 2020
  • Severe congenital heart disease (CHD) is a chronic disease requiring continuous and holistic health management to improve patients' quality of life. This study explored the health management experiences of adolescents with severe CHDs in Korea. On the basis of in-depth interviews with nine youths, four categories and 12 subcategories were identified. The participants lacked a full understanding of their health status and the need for appropriate health management for their health status. Nonetheless, they practiced health management to some extent, in ways that were affected by heart function, self-identity, and social support. Although adolescents with severe CHDs were affected by physical limitations and the discriminatory gaze around them, they tried to achieve normalcy through managing information, seeking homogeneity with peers, and fostering positive acceptance about their disease. Regarding demands for health management programs, disease knowledge and mental health content were preferred, and the preferred delivery methods were self-help group camps and smartphone applications. Based on the results of this study, we suggest a health management intervention to promote a healthy transition to adulthood for adolescents with severe CHDs, and that policy-makers should consider measures that would enable a successful transition to adulthood in the future of youth with severe CHDs.

Acoustic variations associated with congenital heart disease (선천성 심장병 환아에서 음향학적 요소의 변동)

  • Oh, Jung Eun;Choi, Yoon Mi;Kim, Sun Jun;Joo, Chan Uhng
    • Clinical and Experimental Pediatrics
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    • v.53 no.2
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    • pp.190-194
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    • 2010
  • Purpose : To investigate the nature of deviant voice physiology in preoperative children with congenital heart disease. Methods : Ninety-four children with congenital heart disease were enrolled. Their cries and related acoustic variables (fundamental frequency, duration, noise to harmonic ratio, jitter and shimmer) were analyzed using a multi-dimensional voice program. Results : The average fundamental frequency showed a significant decrease in patent ductus arteriosus, ventricular septal defect, and tetralogy of Fallot, except in atrial septal defect and pulmonary stenosis. The length of the analyzed sample (duration) did not show a significant difference when compared with the control group. There was a significant increase in jitter percent in ventricular septal defect, patent ductus arteriosus, and atrial septal defect. There was an increase in shimmer in ventricular septal defect, patent ductus arteriosus, and atrial septal defect. The noise-to-harmonic ratio increased in ventricular septal defect, patent ductus arteriosus, and atrial septal defect but there was no significant difference in pulmonary stenosis and tetralogy of Fallot. While analyzing acoustic variables, the voice change was significantly higher, especially in patent ductus arteriosus followed by ventricular septal defect and atrial septal defect. Most of these acoustic variables were deviant in left-to-right shunt lesions in congenital heart disease, especially in patent ductus artriosus. Conclusion : The results of the voice change analysis of preoperative children with congenital heart disease revealed that the acoustic variables differed by each congenital heart disease. Moreover, the acoustic variables were prominently deviant in congenital heart disease with left-to-right shunts.

건강관리 성공사례담 15-심장병

  • Lee, Eun-Hui
    • 건강소식
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    • v.11 no.3 s.100
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    • pp.16-22
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    • 1987
  • 우리는 흔히 ‘살아있음’에 대한 가치를 망각한 채 그날그날을 보내버리고, 어느날 갑자기 우리 앞에 닥친 ‘건강에 대한 위협’이라는 놈 때문에 당황하며 또 더러는 좌절하게 된다. 심한 경우, 우리의 의지 따위(?)와는 관계없이 생명은 “죽음” 앞에 무릎을 꿇고 만다. 불가항력의 경우도 있기는 하지만 대개는 시기를 놓쳐버리는 때가 허다하므로 뒤늦게 후회해 보았댔자 무슨 소용이 있으랴. 어린이 심장병 집단검사만 해도 그렇다. 필요한 일이라는 것은 알지만 실천으로 옮겨지는 예는 드물다. 여기 선천성 심장병의 일종인 “동맥관개존증”이라는 병을 앓고있다가 학교에서 실시한 심전도 집단검사에서 조기발견하여 시기적절하게 치료를 끝내었고, 이제는 건강한 모습으로 미래를 향해 달음박질하는 한소녀를 소개한다. 혹시라도 건강에 관심을 두지 않았던 사람이 있다면 그 귀감이 될 수 있기를 바란다.

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Comparison of Infective Endocarditis between Children and Adults with Congenital Heart Disease: A 16-Year, Single Tertiary Care Center Review (선천성 심장병을 가진 소아와 성인에서 발생한 감염성 심내막염의 비교: 1개 3차 병원의 16년간 경험)

  • Kwon, Jung Eun;Kim, Yeo Hyang
    • Pediatric Infection and Vaccine
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    • v.23 no.3
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    • pp.209-216
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    • 2016
  • Purpose: This study aimed to evaluate and compare the characteristics of infective endocarditis (IE) between children and adults with congenital heart disease (CHD) at a single tertiary care center. Methods: In this retrospective medical record review, we extracted the demographic characteristics, diagnostic variables, and outcomes of patients diagnosed with IE and CHD between 2000 and 2016. Results: We identified a total of 14 pediatric patients (nine male; median age at diagnosis, 3 years). Of the 14 patients, six had a history of previous open heart surgery, while four had undergone tetralogy of Fallot repair, with transannular patch or Rastelli procedure. Among the 10 children with positive blood cultures, the most common isolated organism was Staphylococcus spp. (8/10, 80%). Eleven adult patients had IE and CHD. Among the adult patients, only four were diagnosed with CHD before IE, and ventricular septal defect was the most common CHD. The most common isolated organism was Streptococcus spp. (6/11, 55%). Compared with adult patients, pediatric patients had a higher incidence of previously diagnosed CHD (P=0.001), with Staphylococcus spp. as the causative organism (P=0.027). The median duration between the onset of symptoms and diagnosis of IE was 9 days in children and 42 days in adults (P=0.012). Conclusions: Significant differences with regard to the diagnosis and progress of IE were observed between children and adults. Age-adjusted and systematic reassessment may be necessary for the diagnosis and management of IE.