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高终末期肝病和肝肾综合征模型中活体与死体供肝肝移植的生存获益分析。

Analysis of Survival Benefits of Living Versus Deceased Donor Liver Transplant in High Model for End-Stage Liver Disease and Hepatorenal Syndrome.

机构信息

Department of Surgery, The University of Hong Kong, Hong Kong, China.

Department of Surgery, Queen Mary Hospital, Hong Kong, China.

出版信息

Hepatology. 2021 Jun;73(6):2441-2454. doi: 10.1002/hep.31584. Epub 2021 May 4.

DOI:10.1002/hep.31584
PMID:33006772
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8252626/
Abstract

BACKGROUND AND AIMS

Previous recommendations suggested living donor liver transplantation (LDLT) should not be considered for patients with Model for End-Stage Liver Disease (MELD) > 25 and hepatorenal syndrome (HRS).

APPROACH AND RESULTS

Patients who were listed with MELD > 25 from 2008 to 2017 were analyzed with intention-to-treat (ITT) basis retrospectively. Patients who had a potential live donor were analyzed as ITT-LDLT, whereas those who had none belonged to ITT-deceased donor liver transplantation (DDLT) group. ITT-overall survival (OS) was analyzed from the time of listing. Three hundred twenty-five patients were listed (ITT-LDLT n = 212, ITT-DDLT n = 113). The risk of delist/death was lower in the ITT-LDLT group (43.4% vs. 19.8%, P < 0.001), whereas the transplant rate was higher in the ITT-LDLT group (78.3% vs. 52.2%, P < 0.001). The 5-year ITT-OS was superior in the ITT-LDLT group (72.6% vs. 49.5%, P < 0.001) for patients with MELD > 25 and patients with both MELD > 25 and HRS (56% vs. 33.8%, P < 0.001). Waitlist mortality was the highest early after listing, and the distinct alteration of slope at survival curve showed that the benefits of ITT-LDLT occurred within the first month after listing. Perioperative outcomes and 5-year patient survival were comparable for patients with MELD > 25 (88% vs. 85.4%, P = 0.279) and patients with both MELD > 25 and HRS (77% vs. 76.4%, P = 0.701) after LDLT and DDLT, respectively. The LDLT group has a higher rate of renal recovery by 1 month (77.4% vs. 59.1%, P = 0.003) and 3 months (86.1% vs, 74.5%, P = 0.029), whereas the long-term estimated glomerular filtration rate (eGFR) was similar between the 2 groups. ITT-LDLT reduced the hazard of mortality (hazard ratio = 0.387-0.552) across all MELD strata.

CONCLUSIONS

The ITT-LDLT reduced waitlist mortality and allowed an earlier access to transplant. LDLT in patients with high MELD/HRS was feasible, and they had similar perioperative outcomes and better renal recovery, whereas the long-term survival and eGFR were comparable with DDLT. LDLT should be considered for patients with high MELD/HRS, and the application of LDLT should not be restricted with a MELD cutoff.

摘要

背景与目的

先前的建议认为,对于终末期肝病模型(MELD)评分>25 和肝肾综合征(HRS)的患者,不应该考虑进行活体肝移植(LDLT)。

方法和结果

回顾性地对 2008 年至 2017 年 MELD 评分>25 的患者进行意向治疗(ITT)分析。有潜在活体供者的患者作为 ITT-LDLT 进行分析,而没有供者的患者属于 ITT-尸体供肝移植(DDLT)组。从列入名单之日起分析 ITT 总生存(OS)。共有 325 名患者被列入名单(ITT-LDLT n=212,ITT-DDLT n=113)。ITT-LDLT 组的失访/死亡风险较低(43.4%比 19.8%,P<0.001),而 ITT-LDLT 组的移植率较高(78.3%比 52.2%,P<0.001)。对于 MELD>25 的患者和 MELD>25 且合并 HRS 的患者,ITT-LDLT 组的 5 年 ITT-OS 更优(72.6%比 49.5%,P<0.001)。等待名单死亡率在列入名单后早期最高,生存曲线斜率的明显变化表明,ITT-LDLT 的益处发生在列入名单后的第一个月内。MELD>25(88%比 85.4%,P=0.279)和 MELD>25 合并 HRS(77%比 76.4%,P=0.701)患者在 LDLT 和 DDLT 后 5 年的患者生存率相似。LDLT 组术后 1 个月(77.4%比 59.1%,P=0.003)和 3 个月(86.1%比 74.5%,P=0.029)的肾脏恢复率更高,而两组的长期估计肾小球滤过率(eGFR)相似。ITT-LDLT 降低了所有 MELD 分层的死亡率风险(风险比为 0.387-0.552)。

结论

ITT-LDLT 降低了等待名单死亡率,并允许更早地进行移植。对于 MELD/HRS 较高的患者,LDLT 是可行的,他们具有相似的围手术期结局和更好的肾脏恢复,而长期生存和 eGFR 与 DDLT 相当。对于 MELD/HRS 较高的患者,应考虑 LDLT,并且不应该以 MELD 截断值来限制 LDLT 的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1f/8252626/990130af9766/HEP-73-2441-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1f/8252626/44e3540b8807/HEP-73-2441-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1f/8252626/f34a17dc0d6b/HEP-73-2441-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1f/8252626/990130af9766/HEP-73-2441-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1f/8252626/44e3540b8807/HEP-73-2441-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1f/8252626/f34a17dc0d6b/HEP-73-2441-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1f/8252626/990130af9766/HEP-73-2441-g003.jpg

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