肺移植:终末期间质性肺疾病的最后选择

M. Fakhro, S. Lindstedt
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摘要

肺移植(LTx)是一种成熟的、公认的治疗终末期不可逆肺病患者的医疗干预措施。这些疾病包括间质性肺疾病(ILD),其他标准的医疗选择往往已被证明是不够的。LTx术后的生存取决于多种因素,如一般和器官特异性受体状态,以及供体器官状况和手术技术。20世纪80年代和90年代获得的较长生存率确立了医疗领域的LTx。反映了在器官保存、手术技术、免疫抑制剂、受体和供体器官选择以及在受体可能感染的广泛范围内的预防和直接治疗方面取得的进步。尽管LTx是治疗终末期不可逆ILD的黄金标准,特发性肺纤维化(IPF)是最常见的原因,但与LTx中其他患者类别的结果相比,术后结果受到很大影响。本章将提供LTx术后ILD和IFP的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lung Transplantation: A Final Option for End-Stage Interstitial Lung Diseases
Lung transplantation (LTx) is an established, well-recognized medical intervention for treating patients with an end-stage irreversible pulmonary disease. Such diseases include interstitial lung disease (ILD), where other standard medical options often have been proven as insufficient. Post-operative survival after LTx depends on various factors such as the general and organ-specific recipient status in addition to donor organ condition and operative technique. The prolonged survival rates obtained during the 1980s and 1990s have established LTx in the medical field. Reflecting the improvements made in the field of organ preservation, operative technique, immunosuppressants, recipient and donor organ selection and prophylactic as well as direct treatment in the wide spectrum of possible infections in the recipient. Despite LTx being the golden standard for treating end-stage irreversible ILD, with idiopathic pulmonary fibrosis (IPF) as the most common cause, postoperative outcome is greatly hampered compared to the outcome of other patient categories within LTx. This chapter will provide insight in the outcome of ILD and subsequently IFP after LTx.
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