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首页> 外文期刊>Transplant international : >Early-onset versus late-onset nonanastomotic biliary strictures post liver transplantation: Risk factors reflect different pathogenesis
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Early-onset versus late-onset nonanastomotic biliary strictures post liver transplantation: Risk factors reflect different pathogenesis

机译:肝移植后早发与晚发非解剖性胆道狭窄:危险因素反映了不同的发病机理

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Nonanastomotic biliary strictures (NAS) cause significant morbidity post liver transplantation. Timing of stricture development varies considerably, but the relationship between timing of stricture onset and aetiology has not been fully elucidated. Database analysis was performed on all adult patients undergoing liver transplantation between 1st January 1990 and 31st May 2008. Diagnosis of NAS required demonstration on at least two radiological studies. Early NAS were defined as developing <1 year post transplant (minimum 1-year follow-up) and late NAS developing >1 year post transplant (minimum 10-year follow- up). Ninety-six of 397 patients developed NAS (24%); 54 were early-onset NAS (56%) and 42 late-onset NAS (44%). Primary sclerosing cholangitis (PSC) was the only risk factor for NAS overall (P = 0.001). However, when patients with PSC were excluded, older donor age was a significant risk for NAS (P = 0.003). Early-onset NAS were associated with advanced donor age (P = 0.02), high MELD score (P = 0.001) and ABO-identical grafts (P = 0.02), whereas late-onset NAS were associated with PSC (P = 0.0008), bilio-enteric anastomosis (P = 0.006) and tacrolimus (P = 0.0001). Advanced donor age is a significant risk for NAS in patients without PSC. Importantly, aetiology of NAS varies depending on time to stricture development, suggesting early-onset and late-onset NAS may have different pathogenesis.
机译:非吻合性胆道狭窄(NAS)导致肝移植后的重大发病。狭窄发生的时间差异很大,但是狭窄发生的时间与病因之间的关系尚未得到充分阐明。在1990年1月1日至2008年5月31日期间对所有接受肝移植的成年患者进行了数据库分析。NAS的诊断需要至少两项放射学研究证实。早期NAS定义为移植后<1年(至少1年的随访),晚期NAS定义为移植后> 1年(至少10年的随访)。 397例患者中有96例患有NAS(占24%); 54例为早期发作的NAS(56%)和42例晚期发作的NAS(44%)。原发性硬化性胆管炎(PSC)是整个NAS的唯一危险因素(P = 0.001)。但是,当排除PSC患者时,较大的供体年龄是NAS的重大风险(P = 0.003)。早发性NAS与较高的供体年龄(P = 0.02),高MELD评分(P = 0.001)和ABO相同的移植物(P = 0.02)相关,而晚发的NAS与PSC相关(P = 0.0008),胆小肠肠吻合术(P = 0.006)和他克莫司(P = 0.0001)。对于没有PSC的患者,较高的供体年龄是NAS的重大风险。重要的是,NAS的病因取决于狭窄发展的时间,这表明早发和晚发NAS可能具有不同的发病机理。

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