Journal of Chest Surgery

The Korean Society for Thoracic and Cardiovascular Surgery (대한심장혈관흉부외과학회)
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Open Heart Surgery of Ventricular Septal Defect in Infancy

영아기 심실중격결손의 개심술

  • 조준용 (경북대학교 의과대학 흉부외과학교실) ;
  • 허동명 (경북대학교 의과대학 흉부외과학교실)
  • Published : 1996.03.01
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Abstract

In selected cases, early corrective surgery is indicated in the management of infants having large ventricular septal defects. The risk of any surgical procedure in infancy is acknowledged to be great and should be avoided whenever possible. However this greater surgical risk is justified when the patient presents with intractable congestive heart failure, severe pulmonary hypertension, marked growth retardation, and recurrent prolonged lower respiratory infections. We analyzed 31 patients with ventricular septal defect in infancy who underwent surgical correction from January 1991 through December 1994. Age ranged from 6 months to 12 months with mean age of 9.2 months. Of the thirty-one patients, 23 patients were male and 8 patients were female. Mean body weight was 7. 4kg. The most common type of ventricular septal defect was perimembraneo s (64.5%). Associated cardiac anomalies were found in 17 patients (55.8%). Mitral regurgitation was the most commonly associated cardiac anomaly (16.1 %) and followed by patent ductus arteriosus (12.9%). When cardiac catheterization data were analysed, the most common range of Qp/qs, RpiRs, Pp/ps were 2.1∼ 3.0, 1-0.25, above 0.70 respectively. Among the indications of surgical correction, there were pulmonary hypertension in 20 patients, congestive heart failure in 3 patients, intractable respiratory infection in 10 patients and growth retardation in 14 patients. The most common surgical approach and method for closure of ventricular septal defect .were right atriotomy (58%) and Dacron patch closure (94%). Postoperative complications occurred in 10 cases (32%) and overall mortality was 12.9% (4 cases). All operative deaths in this series occurred in infants under the age of 8 months and weight of 8 kilograms.

영아기에는 수술에 따른 위험 도가 높기 때문에 가능하면 수술을 피 해야 하지만, 제한된 경우에서 비 교적 큰 심실중격결손을 가진 영아에서도 개심술을 시행하게 된다. 따라서, 난치성 울혈성 심부전, 폐동 맥고혈압, 발육부진, 그리고 반복되는 호흡기 감염이 있는 경우에는 개심술을 시행하게 된다. 저자들은 1991년 1월부터 1994년 12월까지 31례의 영아 심실중격결손환아에서 개심술을 시행하였다. 연령분포는 6개월에서 12개월까지 였고 평균연령은 9.2개 월이 었다. 31례중 남자가 23례 였고, 여자가 8례 였다. 평균 체중은 7.4킬로그램이 었다. 심실중격 결손의 가장 흔한 형 태는 막상주위 형 (64.5%)이었으며, 동반 심기 형은 17례 (55.8%)에서 있었다. 승모판 폐쇄부전이 가장 많았으며 (16.1%), 동맥관개존이 그 다음이 었다 (12.8%). 심 도자검 사결과에서 폐-체 혈류량비, 폐-체 혈압비, 폐-체저 항비는 각각 2.1∼3.0, 0.70이상, 0. 1∼0.25사이 에서 가장 많았다. 수술적응증에서는 폐동맥고혈압이 20례, 울혈성 심부전이 3례, 반복되는 호흡기 감염이 10El,그리고 발육부전이 14례로 나타났다. 가장혼한심장절개법과수술방법은우심방 절개 (58%)와 다크론패취봉합(94%)이 었다. 술후 합병증은 10례 (32%)에서 있었으며, 사망률은 12.9% (4례)이었다 사망례는8개월, 8킬로그램이하의 영아에서 있었다.

Keywords

References

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