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Improving Outcomes of Liver Transplantation for Polycystic Disease in MELD Era

机译:改善MELD时代多囊性疾病肝移植的效果

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摘要

Background: Liver transplantation (LT) for polycystic liver disease (PLD) has evolved to be an option for treating these patients. Patients with PLD suffer from incapacitating symptoms because of very large liver volumes but liver function is preserved until a late stage. Objective/Methods: Herein, we reviewed the outcome of adult patients with PLD who underwent LT in the US comparing pre-MELD (1990–2001) to MELD era (2002–2009). Results: During this period, only 309 patients underwent LT for PLD. The number of LT for PLD is very low comparing the two eras. The percentage of patients who had combined liver and kidney transplantation (CLKT) for this disease has not changed during MELD era (42.8% vs 38.6%). The waiting time for LT (337 vs 272 days) and CLKT (289 vs 220) has increased in MELD era (p<0.001). In MELD era, 53.4% of LT and 31.2% of CLKT were done as MELD exceptional cases. The allograft and patent survival have significantly improved in MELD era.Conclusion: Patients with PLD had marked improvement of their outcomes after LT in MELD era.
机译:背景:用于多囊性肝病(PLD)的肝移植(LT)已发展成为治疗这些患者的一种选择。 PLD患者由于肝脏体积非常大而无法工作,但肝功能一直保持到晚期。目的/方法:在本文中,我们比较了MELD之前(1990-2001年)与MELD时代(2002-2009年)在美国接受LT的成年PLD患者的结局。结果:在此期间,仅309例接受LT的LT患者。与两个时代相比,PLD的LT数量非常少。在MELD时代,肝肾移植联合治疗(CLKT)的患者百分比没有变化(42.8%vs 38.6%)。在MELD时代,LT(337 vs 272天)和CLKT(289 vs 220)的等待时间增加了(p <0.001)。在MELD时代,作为MELD例外情况,完成了LT的53.4%和CLKT的31.2%。结论:在MELD时代,LT患者术后LT的预后明显改善。

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