急诊开胸治疗先天性大叶性肺气肿——麻醉学问题

Muthukumar Rajagopalan
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摘要

先天性大叶性肺气肿是一种罕见的肺部畸形,通常在新生儿期或婴儿期表现为急性缺氧和呼吸窘迫。它的特征是正常肺的大叶通气过度,随后由于球阀作用导致支气管部分阻塞而出现呼吸窘迫。我们想提出的情况下,3个月大的女性早产(31周)婴儿谁提出了我们的新生儿重症监护病房呼吸窘迫1天。婴儿被诊断为左侧CLE,有严重的纵隔向右侧移位和右位心脏。静脉血气PaCO2 70 mmHg, SpO2 70%,高流量鼻吸氧15 L。我们想强调的麻醉技术气道管理和通气在诱导关键时期,直到开胸肺气肿叶外置。
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Emergency Thoracotomy for Congenital Lobar Emphysema – Anesthesiology Concerns
Congenital lobar emphysema (CLE) is a rare malformation of lungs, which presents usually in neonatal period or infancy as acute hypoxia and respiratory distress. It is characterized by the lobar over aeration of the normal lung followed by respiratory distress due to partial obstruction of bronchus by ball-valve effect. We would like to present the case of a 3-month-old female preterm (31 weeks) baby who presented to our neonatal intensive care unit with respiratory distress for 1 day. The baby was diagnosed with left-sided CLE having severe mediastinal shift to the right side and a dextroposition heart. Her venous blood gas showed PaCO2 of 70 mmHg and SpO2 of 70% with 15 L high-flow nasal oxygen. We would like to highlight the anesthesia techniques of airway management and ventilation during the critical period of induction till thoracotomy and exteriorizing the emphysematous lobe.
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