Naguib Aymen N, Corridore Marco, Phillips Alistair, Olshove Vincent, Galantowicz Mark, Tobias Joseph D
Department of Anesthesiology, Nationwide Children's Hospital, Columbus, OH, USA The Heart Center, Nationwide Children's Hospital, Columbus, OH, USA.
The Heart Center, Nationwide Children's Hospital, Columbus, OH, USA Department of Cardiothoracic Surgery, Nationwide Children's Hospital, Columbus, OH, USA.
J Intensive Care Med. 2011 Sep-Oct;26(5):330-4. doi: 10.1177/0885066610392673. Epub 2011 Feb 13.
A 1.4-kilogram, male infant was born at 27 weeks gestation at an outside hospital. After birth, the patient's trachea was intubated and surfactant administered. Initial echocardiogram showed a patent ductus arteriosus (PDA) and a ventricular septal defect (VSD), with a possible aberrant vessel arising from the carotid artery. The patient was transferred to our hospital for further management. Repeat echocardiogram showed a right aortic arch with the left common carotid/innominate artery arising from the pulmonary artery. The infant was subsequently brought to the operating room where following sternotomy, the aberrant left innominate artery was reimplanted into the aorta. The origin of the left carotid artery or innominate artery from the pulmonary artery is an extremely rare form of congenital heart disease with a limited number of reports in the literature. The differential pressure gradient between the systemic and pulmonary beds may lead to a steal phenomenon, with shunting of blood from the carotid system into the pulmonary vascular bed, resulting in decreased cerebral blood flow. The left-to-right shunting from the systemic to pulmonary bed may also lead to volume overload of the left side of the heart. In the perioperative care of such patients, control of physiologic factors that control the balance between the pulmonary and systemic vascular resistance is mandatory to ensure that cerebral blood flow is maintained.
一名1.4千克的男婴在外地医院孕27周时出生。出生后,对该患者进行了气管插管并给予了表面活性剂。初始超声心动图显示动脉导管未闭(PDA)和室间隔缺损(VSD),可能有一条异常血管发自颈动脉。患者被转至我院进一步治疗。复查超声心动图显示右位主动脉弓,左颈总动脉/无名动脉发自肺动脉。该婴儿随后被送往手术室,在胸骨切开术后,将异常的左无名动脉重新植入主动脉。左颈动脉或无名动脉发自肺动脉是一种极其罕见的先天性心脏病形式,文献报道数量有限。体循环和肺循环之间的压差可能导致盗血现象,血液从颈动脉系统分流至肺血管床,导致脑血流量减少。从体循环到肺循环的左向右分流也可能导致心脏左侧容量负荷过重。在此类患者的围手术期护理中,控制调节肺循环和体循环血管阻力平衡的生理因素是确保维持脑血流量的必要措施。