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Persistent hypoxemia and platypnea-orthodeoxia after left single-lung transplantation: a case report

机译:左单肺移植术后持续性低氧血症和呼吸道正直性低氧血症:一例报告

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Introduction Platypnea-orthodeoxia is a relatively uncommon but striking clinical syndrome characterized by dyspnea and deoxygenation accompanying a change to sitting or standing from a recumbent position. Hypoxemia early after lung transplant can have multiple etiologies. We report a rare case of persistent hypoxemia and platypnea-orthodeoxia after left single-lung transplantation, as a result of right-to-left interatrial shunt through a patent foramen ovale, with subsequent resolution of hypoxemia after percutaneous closure of the patent foramen ovale. Case presentation Our 66-year-old Caucasian male patient exhibited a persistent patent foramen ovale. Persistent patent foramen ovale produces an intermittent intra-atrial right-to-left shunt and occurs in approximately 25 % of the general population. Although the majority of people with patent foramen ovale are asymptomatic, it is believed to act as a pathway for chemicals or thrombi that can result in a variety of clinical manifestations, including stroke, migraine headache, decompression sickness, high-altitude pulmonary edema, and platypnea-orthodeoxia syndrome. Percutaneous closure of the patent foramen ovale has been shown to be effective in the case of right-to-left shunting with normal pulmonary arterial pressure, but the indication remains controversial in other situations where pulmonary pressures are not normal. The most common causes of hypoxemia immediately after lung transplant include: graft dysfunction, reperfusion injury, acute thromboembolic disease, and acute rejection. We report a case of reopening of a patent foramen ovale after left single-lung transplantation with normal pulmonary pressure. Conclusions Our case demonstrates that an open patent foramen ovale leading to massive right-to-left shunting is a possible complication after lung transplant, with significant morbidity, and that it can be treated successfully using a percutaneously placed occlusion device. Through this case report, we aim to improve pre-transplant procedures by demonstrating that a bubble contrast transesophageal echocardiogram can be performed pre-operatively to detect a patent foramen ovale.
机译:引言呼吸道正畸是一种相对不常见但引人注目的临床综合征,其特征在于呼吸困难和脱氧伴随着从仰卧姿势改变为坐姿或站立姿。肺移植后早期的低氧血症可能有多种病因。我们报道了一种罕见的病例,即从左到右的房间隔通过卵圆孔未闭,左单肺移植后出现了持续性低氧血症和支气管扩张症,并通过经皮闭合卵圆孔闭锁解决了低氧血症。病例介绍我们的66岁白人男性患者表现出持续的卵圆孔未闭。持续性卵圆孔未闭,使间房内从右向左分流,约占总人口的25%。尽管大多数患有卵圆孔未闭的人无症状,但据信它可作为化学物质或血栓形成的途径,可导致多种临床表现,包括中风,偏头痛,减压病,高海拔肺水肿和platypnea-orthodesoxia综合征。在正常的肺动脉压下从右向左分流的情况下,经皮闭合卵圆孔闭塞术已被证明是有效的,但在肺压不正常的其他情况下,该适应症仍存在争议。肺移植后立即发生低氧血症的最常见原因包括:移植物功能障碍,再灌注损伤,急性血栓栓塞性疾病和急性排斥反应。我们报告了左单肺移植后肺动脉压力正常后卵圆孔未闭的重新开放的情况。结论我们的病例表明,肺移植后可能出现开放性卵圆孔开放,从右向左大量分流,这是一种可能的并发症,发病率很高,并且可以使用经皮放置的闭塞装置成功治疗。通过该病例报告,我们旨在通过证明可以在手术前进行气泡对比经食管超声心动图检查来检测卵圆孔未闭,从而改善移植前的程序。

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