• Journal of Chest Surgery
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• 제32권5호
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• pp.422-427
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• 1999

배경: 빈맥을 이용하여 심부전을 만드는 방법은 확장성 심근증 모델 중에서 가장 좋은 방법으로 심장에 외과적 손상 혹은 약물의 독성을 최소화할 수 있고 사람의 심부전에 가장 가까우며 조작하기 쉬운 장점이 있다. 새로운 술식의 효과를 검증하기 위하여 심부전이 진행중인 모델에서 동물실험을 시행하는 것은 결과를 얻기 전에 실패할 가능성이 높다. 심부전의 진행을 중지시킨 회복궤도의 변화를 비교하는 방법은 심부전 악화에 의한 사망률을 줄일 수 있는 새로운 방법이지만 빈맥 조작 기술에 따라 저자마다 상당한 차이가 있어 이에대한 자료의 정립이 필요한 실정이다. 대상 및 방법: 21마리의 개(체중 25-35kg)를 대상으로 1)정상의 심장, 2) 심부전 심장, 3) 회복기 4주 4) 회복기 8주 등 4가지로 나누었다. 전신마취하에 우심실첨부에 박동기 전극을 삽입하여 빈맥은 처음 170회/분부터 매주 20회씩 프로그래머를 이용하여 증가시켰다. 4주 후 심부전이 발생하면 8주간의 회복기 동안 회복 궤도를 추적하였다. 심장의 크기와 혈역학적 변화를 관찰하고자 초음파는 2주마다, Swan-Ganz 도자와 열희석법은 4주마다 검사를 실시하여 이완기 말기 좌심실 체적, 수축기말기 좌심실 체적, 심박출율, 중심정맥압, 폐동맥압, 폐동맥 쐐기압, 우심실압, 일회박출량 등을 측정하였으며, 정상과 심부전 심장 상태에서 혈중 카테콜라민을 측정하였다. 그 외 심전도 및 대퇴동맥 도자를 넣어 맥박수, 혈압을 측정하였다. 정상심장, 심부전 심장, 회복기 4주 및 8주에서 측정한 값은 평균$\pm$표준편차로 표시하였다. 결과: 4마리(20%)가 심부전에 의한 합병증으로 사망하였다. 이완기 말기 좌심실 체적은 측정시기에 따라 40.8$\pm$7.4, 82.1$\pm$21.1, 59.9$\pm$7.7, 46.5$\pm$6.5ml로 수축기말기 좌심실 체적과 비슷한 변화양상을 보였으며 심박출율은 50.6$\pm$4.1, 17.5$\pm$5.8, 36.3$\pm$7.3, 41.5$\pm$2.4%였다. 혈압과 맥박은 의의 있는 양상을 보이지 않았으며 중심정맥압, 우심실압, 폐동맥압, 폐동맥 쐐기압 등은 심부전 시에 의의 있는 증가를 보이다가 회복기에는 감소하는 양상을 볼 수 있다. 일회박출량은 21.5$\pm$8.2, 12.3$\pm$3.5, 17.9$\pm$4.6, 15.5$\pm$3.4ml으로 회복기에 심부전 상태로부터 회복하는 경향을 볼 수 있었다. 혈중 카테콜라민은 정상 133.3$\pm$60.0pg/dL에서 심부전 시에는 479.4$\pm$327.3pg/dL로 증가를 보였다(p=0.008). 결론: 빈맥을 이용한 심부전 모델은 외과적손상이 적고, 병의 정도를 임의로 조절할 수 할 수 있는 간편한 방법이다. 회복기에는 심기능 및 심장비대가 회복하는 경향을 보이므로 향후 새로운 술식의 평가를 위하여 회복 궤도를 이용하는 경우 실험 동물의 심부전 악화에 의한 사망율을 줄일 수 있는 새로운 방법이다.

• Journal of Chest Surgery
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• 제12권3호
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• pp.281-288
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• 1979

For years, physicians and anatomists have been interested in the heart that has one functioning ventricle. Various terms have been suggested for this entity including single ventricle, common ventricle, double-inlet left ventricle, cor biatriatum triloculare, and primitive ventricle. In this report, the term "single ventricle" is utilized as suggested by Van Praagh, and is defined as that congenital cardiac anomaly in which a common or separate atrioventricular valves open into a ventricular chamber from which both great arterial trunks emerge. An outlet chamber, or infundibulum, may or may not be present and give rise to the origin of either of the great arteries. This definition excludes the entity of mitral and tricuspid atresia. An 11 year old cyanotic boy was admitted chief complaints of exertional dyspnea and frequent upper respiratory infection since 2 weeks after birth. He was diagnosed as inoperable cyanotic congenital heart disease, and remained without any corrective treatment up to his age of 11 year when he suffered from aggravation of symptoms and signs of congestive heart failure for 2 months before this admission. On 22nd of May 1979, he was admitted for total corrective operation under the impression of tricuspid atresia suggested by a pediatrician. Physical check revealed deep cyanosis with finger and toe clubbing, and grade V systolic ejection murmur with single second heart sound was audible at the left 3rd intercostal space. Development was moderate in height [135 cm] and weight[28Kg]. Routine lab findings were normal except increased hemoglobin [21.1gm%], hematocrit [64 %], and left axis deviation with left ventricular hypertrophy on EKG. Cardiac catheterization and angiography revealed 1-transposition of aorta, pulmonic valvular stenosis, double inlet of a single ventricle with d-loop, and normal atriovisceral relationship [Type III C solitus according to the classification of Van Praagh]. At operation, longitudinal incision at the outflow tract of right ventricle in between the right coronary artery and its branch [LAD from RCA] revealed high far anterior aortic valve which had fibrous continuity with mitral annulus, and pulmonic valve was stenotic up to 4 mm in diameter positioned posterolaterally to the aorta. Ventricular septum was totally defective, and one markedly hypertrophied moderator band originated from crista supraventricularis was connected down to the imaginary septum of the ventricular cavity as a pseudoseptum of the ventricle. Size of the defect was 3X3 cm2 in total. Patch closure of the defect with a Teflon felt of 3.5 x 4 cm2 was done with interrupted multiple sutures after cut off of the moderator band, which was resutured to the artificial septum after reconstruction of the ventricular septum. Pulmonic valvotomy was done from 4 mm to 11 mm in diameter thru another pulmonary arteriotomy incision, and right ventriculotomy wound was closed reconstructing the right ventricular outflow tract with pericardial autograft of 3 x 4 cm2. Atrial septal defect of 2 cm in diameter was closed with 3-0 Erdeck suture, and atrial wall was sutured also when rectal temperature reached from 24`C to 35.5`C. Complete A-V block was managed with temporary external pacemaker with a pacing rate of 110/min. thru myocardial wire, and arterial blood pressure of 80/50 mmHg was maintained with Isuprel or Dopamine dripping under the CVP of 25-cm saline. Consciousness was recovered one hour after the operation when his blood pressure reached 100 /70 mmHg, but vital signs were not stable, and bleeding from the pericardial drainage and complete anuria were persisted until his heart could not capture the pacemaker impulse, and patient died of low output syndrome 320 min after the operation.

• Journal of Chest Surgery
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• 제12권3호
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• pp.289-296
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• 1979

For years, physicians and anatomists have been interested in the heart that has one functioning ventricle. Various terms have been suggested for this entity including single ventricle, common ventricle, double-inlet left ventricle, cor biatriatum triloculare, and primitive ventricle. In this report, the term "single ventricle" is utilized as suggested by Van Praagh, and is defined as that congenital cardiac anomaly in which a common or separate atrioventricular valves open into a ventricular chamber from which both great arterial trunks emerge. An outlet chamber, or infundibulum, may or may not be present and give rise to the origin of either of the great arteries. This definition excludes the entity of mitral and tricuspid atresia. An 11 year old cyanotic boy was admitted chief complaints of exertional dyspnea and frequent upper respiratory infection since 2 weeks after birth. He was diagnosed as inoperable cyanotic congenital heart disease, and remained without any corrective treatment up to his age of 11 year when he suffered from aggravation of symptoms and signs of congestive heart failure for 2 months before this admission. On 22nd of May 1979, he was admitted for total corrective operation under the impression of tricuspid atresia suggested by a pediatrician. Physical check revealed deep cyanosis with finger and toe clubbing, and grade V systolic ejection murmur with single second heart sound was audible at the left 3rd intercostal space. Development was moderate in height [135 cm] and weight[28Kg]. Routine lab findings were normal except increased hemoglobin [21.1gm%], hematocrit [64 %], and left axis deviation with left ventricular hypertrophy on EKG. Cardiac catheterization and angiography revealed 1-transposition of aorta, pulmonic valvular stenosis, double inlet of a single ventricle with d-loop, and normal atriovisceral relationship [Type III C solitus according to the classification of Van Praagh]. At operation, longitudinal incision at the outflow tract of right ventricle in between the right coronary artery and its branch [LAD from RCA] revealed high far anterior aortic valve which had fibrous continuity with mitral annulus, and pulmonic valve was stenotic up to 4 mm in diameter positioned posterolaterally to the aorta. Ventricular septum was totally defective, and one markedly hypertrophied moderator band originated from crista supraventricularis was connected down to the imaginary septum of the ventricular cavity as a pseudoseptum of the ventricle. Size of the defect was 3X3 cm2 in total. Patch closure of the defect with a Teflon felt of 3.5 x 4 cm2 was done with interrupted multiple sutures after cut off of the moderator band, which was resutured to the artificial septum after reconstruction of the ventricular septum. Pulmonic valvotomy was done from 4 mm to 11 mm in diameter thru another pulmonary arteriotomy incision, and right ventriculotomy wound was closed reconstructing the right ventricular outflow tract with pericardial autograft of 3 x 4 cm2. Atrial septal defect of 2 cm in diameter was closed with 3-0 Erdeck suture, and atrial wall was sutured also when rectal temperature reached from 24`C to 35.5`C. Complete A-V block was managed with temporary external pacemaker with a pacing rate of 110/min. thru myocardial wire, and arterial blood pressure of 80/50 mmHg was maintained with Isuprel or Dopamine dripping under the CVP of 25-cm saline. Consciousness was recovered one hour after the operation when his blood pressure reached 100 /70 mmHg, but vital signs were not stable, and bleeding from the pericardial drainage and complete anuria were persisted until his heart could not capture the pacemaker impulse, and patient died of low output syndrome 320 min after the operation.

• Journal of Chest Surgery
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• 제36권7호
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• pp.510-513
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• 2003

우심실 저형성 환자에서 심실중격결손과 대동맥판막 폐쇄부전 및 대동맥판륜 확장증이 동반된 경우는 매우 드물다. 저자들은 우심실 저형성 환자에서 심실중격결손, 대동맥판막 폐쇄부전 및 대동맥판륜 확장증이 동반되어 composite graft를 이용한 근부치환술을 시행한 증례를 보고한다. 환자는 19세 남자로 심장초음파 및 심도자 검사에서 직경 2 cm크기의 막성 심실중격결손과 심한 대동맥판막 폐쇄부전증, 그리고 대동맥판륜 확장증이 동반되어 있었으며 우심실은 bipartite 형태로 심한 저형성을 보였고 Qp/Qs는 1.2였다. 수술소견 상 우관상 및 비관상 판첨 변연부 길이의 현저한 확장, 판첨의 비후와 수축, 그리고 교련부의 융합 및 석회화가 있었다. 수술은 대동맥근부를 통해 자가 심낭 패취를 이용한 심실중격결손 폐쇄술 및 composite graft를 이용한 button Bentall 술식과 우심실 유출로 부위의 비후된 근육을 절제하여 주었다. 환자는 수술 직후 일시적인 심폐기 이탈의 어려움이 있었으며 술 후 14일째 특별한 합병증 없이 퇴원하였다.

• 대한핵의학회지
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• 제20권2호
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• pp.47-52
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• 1986

A noninvasive procedure for diagnosis and quantitation of right-to-left intracardiac shunts will enhance the management of patients with cyanotic congenital heart disease. This study describes an application of radionuclide (RN) angiocardiography for quantitation of right-to-left shunt amount. Gamma variate model was fitted to radionuclide data recorded over the carotid artery. Data analysis was performed retrospectively in 35 patients who underwent cardiac catheterization within a week from the day of RN angiocardiography. Thirty one of the patient had right-to-left shunts and 4 of them had left-to-right shunts. Both the radionuclide and Fick measurements correlated well (r=0.93, 0.93, 0.89, p<0.01 in each measurements). Therefore, RN angiocardiography data may be used for accurate calculation of right-to-left shunts in cyanotic congenital heart disease patients.

• Clinical and Experimental Pediatrics
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• 제52권9호
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• pp.1035-1037
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• 2009

동맥관 개존증은 선천성 심질환 중 비교적 흔한 질환이며, 크기나 중등도에 상관없이 폐쇄가 필요한 질환이다. 경피적 동맥관 폐쇄술은 개흉술에 비하여 합병증의 위험이 적고 경제적으로도 바람직하며, 치료 성적도 우수하여 최근에는 표준적인 치료법으로 받아들여지고 있다. 하지만 원통형 모양의 동맥관 개존증은 흔히 사용하는 분리형 코일이나 ADO로 시술하기에는 여러 가지로 어려운 점이 많다. 저자들은 이러한 형태의 동맥관을 폐쇄하기 위하여 일반적으로 추천되는 것보다 큰 크기의 AVP를 이용하여 원통형 동맥관이 메워지도록 하는 방법을 이용함으로써, 성공적인 동맥관 개존증 폐쇄술을 시행하였기에 이를 보고하는 바이다.

• Journal of Chest Surgery
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• 제33권1호
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• pp.7-19
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• 2000

Background :To assess the accuracy of Electron-Beam Tomography(EBT) in following evaluation of the pulmonary vascular system after a shunt operation in the cyanotic con-genital heart disease with pulmonary stenosis or pulmonary atresia. Material and Method : Sixteen patients(M:F=11:5) who received Blalock-Taussig(n=8) bidirectional cavo-pulmonary shunt(n=10) and unifocalization (n=2) were ncluded in the study. We evaluated the patency of the shunt the morphology of intrapericardial and hilar pulmonary arteries(PA) peripheral pulmonary vascularity by background lung attenuation and the abundance of arterial & venous collateral. Angiography(n=12) and echocardiography(n=20) were used as the gold standard for the comparison of EBT results. Result: EBT was consistent with angiogram/ echo in 100% of the evaluation for the patency of the shunt and in 12(by angiogram 100%) and 19(by echo 95%) for the detection the hypoplasia stenosis or interruption of central PA In measuring of PA EBT and angiogram corrlated(r=0.91) better than EBT-echo(r=0.88) or echo-angiogram(r=0.72) Abundant systemic arterial collateral were noted in 4 and venous collateral in 3 cases. In evaluating the peripheral pulmonary vascularity the homogenous and normal-ranged lung attenuation(m=6) decreased but homo-genous attenuation(n=1) segment-by-sgment heterogeneous attenuation(n=3) homogenous but asymmetrical attenuation(n=3) segment-by-segment heterogeneous attenuation(n=3) homogenous but asymmetrical attenuation(n=3) and venous congestion(n=2) were observed nd 12 of them were compatible with the blood flow pattern revealed by cardiac catheterization. Conclusion: EBT was accurate in the integrated evaluation of the pulmonary vascular system after the shunt including the patency of the shunt operaion the morphology and dimension of the central and hilar PAs and the loco-regional pulmonary flow in the lung parenchyma. It suggests the useful information about the need of secondary shunt operation the proper timing time for total repair and the need of interventional procedure prior to total repair.

• 대한핵의학회지
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• 제14권1호
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• pp.29-36
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• 1980

Most of clinical morbidity in cardiology are associated with abnormalities of the left ventricle. Several methods have been developed to measure the left ventricular function, including cardiac catheterization with cineangiography, echocardiography, and systolic time interval. But these methods have many limitations. ECG gated cardiac blood pool scan provides a safe, noninvasive, repeatable method for determining the left ventricular function. Utilizing the cardiac blood pool scan, we measured the left ventricular function in 165 cardiac patients, and in 26 normal subject. 1. Left ventricular ejection fractions were measured by cardiac blood pool scan, and compared in 20 patients with that measured by x-ray cineangiography. Correlation coefficient was 0.885. 2. Ejection fractions were classified by funtional class made in New York Heart Association. Ejection fractions well represented the functional status. 3. Ejection fractions decreased in cardiomyopathy ($20.1{\pm}4.8%$) and ischemic heart disease ($34.4{\pm}16.7%$). Impaired ejection fractions in myocardial infarction were associated with the extent of infarction. 4. Regional left ventricular wall motion was evaluated from the end-diastolic and end-systolic images. In cardiomyopathy diffuse hypokinesia was noted and in myocardial infarction akinesia was noted on the infarcted areas.

• 대한간호학회지
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• 제30권2호
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• pp.380-390
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• 2000

This study was performed to evaluate the effectiveness of music therapy as one of the psychiatric nursing intervention tools, with addtional information in relieving anxiety during the procedure. Data were collected through nonequivalent pre-and post tests from July 1, 1998 to September 30 1998 in 90 patients (test group A: 28 patients, test group B: 27 patients, control group: 33 patients) who were hospitalized in DongSan Medical Center in order to have cardiac catheterization. The Subjects were informed by educational videos, which were modified according to the sensory information of the 10 study patients. They were based on the informative booklet by Kim keum-soon (1989). The procedural information was also modified according to the hospital`s customs. Provided the music for patients suitable to their tastes, and measured their blood pressure, heart rate, the degree of anxiety using the Spielberger`s measurement device of anxiety, and behavioral response of Finesilver`s. The statistical significance was analyzed using chi-square test and ANOVA. The results of this study were as follows : Hypothesis 1 : There are significant differences in the degree of anxiety among test group A, Test group A was provided only information, Test group B was provided information and the control group was provided neither. Hypothesis 2 : There are significant differences in systolic blood pressure among test group A, test group B, and control group.: non-significant. Hypothesis 3 : There are significant differences in diastolic blood pressure among test group A, test group B, and control group.: significant(F=1.31, p=.27, interaction; F=3.80, p=.00). Hypothesis 4 : There are significant differences in heart rate among test group A, test group B, and control group.: non-significant. Hypothesis 5 : There are significant differences in behavioral responses among test group A, test group B, and control group.: significant(F=10.05, p=.00). Further validation study is required with other subjects and other settings.

• Journal of Chest Surgery
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• 제18권4호
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• pp.635-642
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• 1985

Double outlet left ventricle [DOLV] is a rare cardiac anomaly in which both great arteries arise entirely, or predominantly above the morphologically left ventricle. About 100 cases of DOLV have been reported in the literatures by 1984. We have experienced eight cases of DOLV at Seoul National University Hospital during the period from October 1981 to July 1905. Ages of the patients were ranged from 12 months to 24 years old, and chief complaints on admission were frequent URI and DOE in 5 cases and cyanosis in other 3 cases. In all eight patients, Cardiac catheterization and cineangiography were performed but pre-operative diagnoses were incorrect except one case [VSD in 2 cases, DORV in 2cases, c-TGA in 2 cases and TOF in one case] We have performed total corrective surgery in seven patients. In case I, patch closure of VSD aligning aorta and pulmonary artery with LV, ligation of proximal pulmonary artery and the use of external valved conduit from RV to PA have been employed. In other 6 cases, intraventricular repair using boomerang shaped Dacron patch with correction of associated anomalies were employed. In remaining one patient who had coexistent PDA and coarctation of aorta, we have performed coarctoplasty and PDA ligation initially and the patient is waiting for subsequent total corrective procedure. In seven patients whom we have performed total corrective surgery, there is one hospital mortality due to right heart failure and one complication of complete heart block necessitating permanent pacemaker implantation. All survivors are doing well in follow up period of 9 months to 4 years. To our knowledge, this is the first report of surgical experiences for DOLV in the Korean literature.