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用于治疗肺纤维化的单侧肺移植

Unilateral lung transplantation for pulmonary fibrosis.

出版信息

N Engl J Med. 1986 May 1;314(18):1140-5. doi: 10.1056/NEJM198605013141802.

Abstract

Improvements in immunosuppression and surgical techniques have made unilateral lung transplantation feasible in selected patients with end-stage interstitial lung disease. We report two cases of successful unilateral lung transplantation for end-stage respiratory failure due to pulmonary fibrosis. The patients, both oxygen-dependent, had progressive disease refractory to all treatment, with an anticipated life expectancy of less than one year on the basis of the rate of progression of the disease. Both patients were discharged six weeks after transplantation and returned to normal life. They are alive and well at 26 months and 14 months after the procedure. Pulmonary-function studies have shown substantial improvement in their lung volumes and diffusing capacities. For both patients, arterial oxygen tension is now normal and there is no arterial oxygen desaturation with exercise. This experience shows that unilateral lung transplantation, for selected patients with end-stage interstitial lung disease, provides a good functional result. Moreover, it avoids the necessity for cardiac transplantation, as required by the combined heart-lung procedure, and permits the use of the donor heart for another recipient.

摘要

免疫抑制和外科技术的进步使单侧肺移植对于某些终末期间质性肺病患者成为可能。我们报告了两例因肺纤维化导致终末期呼吸衰竭而成功进行单侧肺移植的病例。这两名患者均依赖氧气,病情进展且对所有治疗均无效,根据疾病进展速度预计预期寿命不足一年。两名患者均在移植后六周出院并恢复正常生活。术后26个月和14个月时,他们均存活且状况良好。肺功能研究显示他们的肺容量和弥散能力有显著改善。对于这两名患者,目前动脉血氧张力正常,运动时无动脉血氧饱和度降低。这一经验表明,对于某些终末期间质性肺病患者,单侧肺移植可带来良好的功能结果。此外,它避免了心肺联合手术所需的心脏移植的必要性,并允许将供体心脏用于另一名接受者。

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