Acquired interstitial emphysema in a premature patient. Treatment with unilateral angioplasty balloon pulmonary blockage.

D Crehuet Gramatyka, L Sánchez Pulido, C Pérez Costoya, E Enríquez Zarabozo, C Granell Suárez, V Álvarez Muñoz
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Abstract

Introduction: Pulmonary interstitial emphysema is a severe rare complication associated with mechanical ventilation in pre-term patients. It induces alterations both in ventilation and pulmonary perfusion, and it may cause progressive overdistension of the side involved and atelectasis of the contralateral lung. Management is uneasy and requires changing ventilation strategies, with invasive procedures such as blockage and selective pulmonary ventilation being potentially necessary.

Clinical case: Premature female patient born at gestation week 26+0, with an initially good clinical progression and baseline chest X-rays showing no signs of congenital pulmonary injury. On day 20 of life, progressive respiratory deterioration was noted. In the series X-rays and chest CT-scan, a right-sided pulmonary interstitial emphysema with mediastinal displacement and left-sided pulmonary atelectasis, associated with hemodynamic and respiratory instability, was observed. On day 26 of life, in light of the poor clinical progression and the immediate threat of death, decision was made to place a right-sided bronchial blocker with a 3x20 mm angioplasty balloon, after the bronchus had been measured through CT-scan. Following placement, respiratory and ventilation parameters improved immediately. The device was kept inflated for 3 days. 10 days after removing the bronchial blocker, the patient was successfully extubated, and she was discharged after 100 days in hospital, with no respiratory symptoms, and the pre-discharge CT-scan showing no signs of emphysema. After 50 months of follow-up, the patient remains asymptomatic from a respiratory standpoint, and psychomotor development is normal.

Discussion: Selective angioplasty balloon pulmonary blockage has been supported by scientific evidence in extremely premature patients with acquired interstitial emphysema associated with compromised ventilation and atelectasis of the contralateral lung. In our case, it helped save the patient's life with not sequelae being caused.

早产儿获得性间质性肺气肿1例。单侧血管成形术球囊肺阻塞的治疗。
前言:肺间质性肺气肿是早产儿机械通气相关的一种严重的罕见并发症。它会引起通气和肺灌注的改变,并可能导致受累侧进行性过度扩张和对侧肺不张。治疗是不稳定的,需要改变通气策略,有创手术,如阻塞和选择性肺通气是潜在必要的。临床病例:妊娠26+0周出生的早产女性患者,最初临床进展良好,胸部x线基线未见先天性肺损伤迹象。在出生后第20天,注意到进行性呼吸恶化。在一系列x线和胸部ct扫描中,观察到右侧肺间质性肺气肿伴纵隔移位和左侧肺不张,并伴有血流动力学和呼吸不稳定。在生命的第26天,鉴于临床进展不佳和直接的死亡威胁,在通过ct扫描测量支气管后,我们决定放置一个3 × 20 mm血管成形术球囊的右侧支气管阻阻剂。放置后,呼吸和通气参数立即改善。这个装置充气了3天。取出支气管阻滞剂10天后,患者成功拔管,住院100天后出院,无呼吸道症状,出院前ct扫描未见肺气肿征象。经过50个月的随访,从呼吸角度来看,患者仍无症状,精神运动发展正常。讨论:有科学证据支持选择性血管成形术球囊肺阻塞治疗与对侧肺不张和通气受损相关的极早产儿获得性间质性肺气肿。在我们的病例中,它帮助挽救了病人的生命,没有引起后遗症。
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