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HLA 不相容活体供肾移植后医院再入院:一项多中心研究。

Hospital readmissions following HLA-incompatible live donor kidney transplantation: A multi-center study.

机构信息

Department of Surgery, University of California-San Francisco, San Francisco, CA, USA.

Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Am J Transplant. 2018 Mar;18(3):650-658. doi: 10.1111/ajt.14472. Epub 2017 Sep 23.

DOI:10.1111/ajt.14472
PMID:
28834181
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5820188/
Abstract

Thirty percent of kidney transplant recipients are readmitted in the first month posttransplantation. Those with donor-specific antibody requiring desensitization and incompatible live donor kidney transplantation (ILDKT) constitute a unique subpopulation that might be at higher readmission risk. Drawing on a 22-center cohort, 379 ILDKTs with Medicare primary insurance were matched to compatible transplant-matched controls and to waitlist-only matched controls on panel reactive antibody, age, blood group, renal replacement time, prior kidney transplantation, race, gender, diabetes, and transplant date/waitlisting date. Readmission risk was determined using multilevel, mixed-effects Poisson regression. In the first month, ILDKTs had a 1.28-fold higher readmission risk than compatible controls (95% confidence interval [CI] 1.13-1.46; P < .001). Risk peaked at 6-12 months (relative risk [RR] 1.67, 95% CI 1.49-1.87; P < .001), attenuating by 24-36 months (RR 1.24, 95% CI 1.10-1.40; P < .001). ILDKTs had a 5.86-fold higher readmission risk (95% CI 4.96-6.92; P < .001) in the first month compared to waitlist-only controls. At 12-24 (RR 0.85, 95% CI 0.77-0.95; P = .002) and 24-36 months (RR 0.74, 95% CI 0.66-0.84; P < .001), ILDKTs had a lower risk than waitlist-only controls. These findings of ILDKTs having a higher readmission risk than compatible controls, but a lower readmission risk after the first year than waitlist-only controls should be considered in regulatory/payment schemas and planning clinical care.

摘要

30%的肾移植受者在移植后第一个月内再次入院。那些需要脱敏治疗和不相容活体供肾移植(ILDKT)的供体特异性抗体患者构成了一个独特的亚群,他们可能面临更高的再入院风险。本研究利用 22 个中心的队列,将 379 例接受医疗保险的 ILDKT 与相容的移植匹配对照和仅等待名单匹配对照进行匹配,匹配因素包括 panel reactive antibody、年龄、血型、肾脏替代时间、既往肾移植、种族、性别、糖尿病和移植日期/等待名单日期。使用多层次、混合效应泊松回归确定再入院风险。在第一个月,ILDKT 的再入院风险比相容对照组高 1.28 倍(95%置信区间[CI] 1.13-1.46;P<.001)。风险在 6-12 个月时达到峰值(相对风险[RR] 1.67,95%CI 1.49-1.87;P<.001),在 24-36 个月时减弱(RR 1.24,95%CI 1.10-1.40;P<.001)。与仅等待名单对照相比,ILDKT 在第一个月的再入院风险高 5.86 倍(95%CI 4.96-6.92;P<.001)。在 12-24 个月(RR 0.85,95%CI 0.77-0.95;P=.002)和 24-36 个月(RR 0.74,95%CI 0.66-0.84;P<.001),ILDKT 的再入院风险低于仅等待名单对照。这些发现表明,ILDKT 的再入院风险高于相容对照组,但在第一年之后,ILDKT 的再入院风险低于仅等待名单对照,这应该在监管/支付计划和规划临床护理中得到考虑。

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本文引用的文献

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Transplantation. 2017 Oct;101(10):2520-2526. doi: 10.1097/TP.0000000000001609.
2
Survival Benefit with Kidney Transplants from HLA-Incompatible Live Donors.来自 HLA 不相合活体供者的肾移植的生存获益
N Engl J Med. 2016 Mar 10;374(10):940-50. doi: 10.1056/NEJMoa1508380.
3
Early Changes in Kidney Distribution under the New Allocation System.新分配系统下肾脏分配的早期变化
同种免疫风险分层在肾移植排斥反应中的应用
Transpl Int. 2022 May 20;35:10138. doi: 10.3389/ti.2022.10138. eCollection 2022.
4
B Cell-Derived Extracellular Vesicles Reveal Residual B Cell Activity in Kidney Graft Recipients Undergoing Pre-Transplant Desensitization.B细胞衍生的细胞外囊泡揭示了接受移植前脱敏治疗的肾移植受者中残留的B细胞活性。
Front Med (Lausanne). 2021 Dec 16;8:781239. doi: 10.3389/fmed.2021.781239. eCollection 2021.
5
HLA Desensitization in Solid Organ Transplantation: Anti-CD38 to Across the Immunological Barriers.实体器官移植中的 HLA 脱敏:抗 CD38 跨越免疫屏障。
Front Immunol. 2021 May 20;12:688301. doi: 10.3389/fimmu.2021.688301. eCollection 2021.
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Am J Transplant. 2021 Apr;21(4):1612-1621. doi: 10.1111/ajt.16471. Epub 2021 Feb 27.
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Am J Transplant. 2020 Aug;20(8):2101-2112. doi: 10.1111/ajt.15825. Epub 2020 Mar 12.
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