Repair of Total Anomalous Pulmonary Venous Return in Infant

1세이하의 총폐정맥 환류이상증의 완전교정

  • 홍유선 (연세대학교 심장혈관센타 심장혈관외과, 연세대학교 의과대학 심장혈관연구소) ;
  • 박영환 (연세대학교 심장혈관센타 심장혈관외과, 연세대학교 의과대학 심장혈관연구소) ;
  • 임상현 (연세대학교 심장혈관센타 심장혈관외과, 연세대학교 의과대학 심장혈관연구소) ;
  • 조범구 (연세대학교 심장혈관센타 심장혈관외과, 연세대학교 의과대학 심장혈관연구소) ;
  • 노환규 (연세대학교 심장혈관센타 심장혈관외과, 연세대학교 의과대학 심장혈관연구소)
  • Published : 1999.11.01

Abstract

Background: Total anomalous pulmonary venous return is a relatively rare disease which has a very high mortality(80% within a year) if not properly corrected surgically. Material and Method: Twenty-six infants with total anomalous pulmonary venous return underwent repair between May, 1991 and February, 1996. Result: There were 19 boys and 7 girls. The mean age at operation was 2.6 months(range: 5 day to 11 month) and the mean body weight was 4.3kg(range:2.8 to 6.7 kg). Preoperative stabilization included ventilator for 5 patients and inotropic support for 6 patients. There were 6 hospital mortalities. Significant risk factors of operative mortality were preoperative ventilator care(p<0.03) and preoperative inotropic support(p<0.05). Age, body weight at operation, pulmonary venous obstruction, high pulmonary arterial pressure, spurasystemic right ventricular pressure or emergency operation did not affected the operative outcome. Postperative pulmonary venous obstruction occurred in three patients 2 or 3 months later, among them one patient was reoperated. The actuarial survival was 76% at 40 months. Conclusion: Although early mortality was high, repair of total anomalous pulmonary venous return should be attempted in early life, but the patients receiving ventilator care or inotropic support need special attention.

Keywords

References

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