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Infections after upper extremity allotransplantation: a worldwide population cohort study, 1998‐2017

机译:上肢分征后感染:全球人口队列研究,1998-2017

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Summary Risk‐to‐benefit analysis of upper extremity allotransplantation (UEA) warrants a careful assessment of immunosuppression‐related complications. This first systematic report of infectious complications after UEA aimed to compare incidence and pattern of infections to that observed after kidney transplantation (KT). We conducted a matched cohort study among UEA and KT recipients from the International Registry on Hand and Composite Tissue Transplantation and the French transplant database DIVAT. All UEA recipients between 1998 and 2016 were matched with KT recipients (1:5) regarding age, sex, cytomegalovirus (CMV) serostatus and induction treatment. Infections were analyzed at three posttransplant periods (early: 0–6?months, intermediate: 7–12?months, late: 12?months). Sixty‐one UEA recipients and 305 KT recipients were included. Incidence of infection was higher after UEA than after KT during the early period (3.27 vs. 1.95 per 1000 transplant‐days, P? = ? 0.01), but not statistically different during the intermediate (0.61 vs. 0.45/1000, P? = ? 0.5) nor the late period (0.15 vs. 0.21/1000, P? = ? 0.11). The distribution of infectious syndromes was significantly different, with mucocutaneous infections predominating after UEA, urinary tract infections and pneumonia predominating after KT. Incidence of infection is high during the first 6?months after UEA. After 1?year, the burden of infections is low, with favorable patterns.
机译:概述上肢同种异体化(UEA)的风险效益分析认证对免疫抑制相关并发症的仔细评估。这是UEA后第一次系统报告感染性并发症的报告旨在比较肾移植(KT)后观察到的感染的发病率和模式。我们在手头和复合组织移植和法国移植数据库划分的国际登记处进行了一项与UEA和KT受援者的匹配队列研究。 1998年至2016年间的所有UEA接受者与KT受者(1:5)与年龄,性别,巨细胞病毒(CMV)血清肿和诱导治疗相匹配。在三个后翻转期(早期:0-6?月份,中级:7-12个月,晚期:& 12?月)分析感染。包括六十一位UEA接受者和305 kt接受者。 UEA后感染的发生率高于早期的KT后(3.27 vs.1.95,每1000个移植天,p?= 0.01),但在中间体期间没有统计学不同(0.61 vs.0.45 / 1000,p?= ?0.5)也不是晚期(0.15与0.21 / 1000,P?= 0.11)。传染性综合征的分布显着不同,含有粘皮肤感染在uea之后占主导地位,尿路感染和肺炎在KT之后主要占主导地位。在UEA后的前6个月,感染发病率很高。 1年后,感染的负担很低,具有良好的模式。

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