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患儿出生后诊断为复杂紫绀型先天性心脏病:大动脉转位(完全型),室间隔缺损,房间隔缺损,动脉导管未闭,肺动脉高压。出生后病情危重,危及生命,转入中国医科大学附属第一医院新生儿重症监护室,由于患儿主动脉及肺动脉转位,全身供血无氧合,仅靠动脉导管及室间隔缺损分流提供的少量含氧血生存,随时可能缺氧发作危及生命(生后一度需要呼吸机辅助呼吸),长时间等待可能导致严重肺动脉高压失去手术机会。
Children born after the diagnosis of complex cyanotic congenital heart disease: aortic transposition (complete type), ventricular septal defect, atrial septal defect, patent ductus arteriosus, pulmonary hypertension. After the birth of a critical condition, life-threatening, transferred to the First Affiliated Hospital of China Medical University neonatal intensive care unit, due to the aorta and pulmonary artery translocation, systemic oxygen supply without anoxia alone catheter and ventricular septal defect shunt provided A small amount of oxygen-rich blood can endanger life at any time of hypoxia attacks (once the need for ventilator-assisted breathing after birth), a long wait may lead to the loss of surgical opportunities for severe pulmonary hypertension.