右室肺动脉通道重建术在婴幼儿青紫型先心病中的应用

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对2例婴幼儿严重青紫型先心病采用右室肺动脉通道重建术手术姑息治疗,获得成功。现就该手术技术、适应症及特点进行讨论。临床资料 男,女各1例,年龄1312岁,与3612岁,体重8kg与12kg。术前均有严重青紫和阵发性呼吸困难,喜蹲踞,活动耐量差。入院体检心前区隆起,胸骨左缘第3 Two cases of infants with severe cyanotic congenital heart disease using right ventricular pulmonary artery reconstruction surgery palliative care and success. The surgical technique, indications and characteristics are discussed. Clinical data of male and female in 1 case, aged 1312 years, with 3612 years old, weighing 8kg and 12kg. Preoperative severe cyanosis and paroxysmal dyspnea, hi squat, poor tolerance. Admission examination heart area uplift, left sternal third
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