Department of Diagnostic and Interventional Radiology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Department of General Surgery, Unit of Hepatobiliary Surgery, Faculty of Medicine, Cairo University, Cairo, Egypt.
Transpl Int. 2021 Jun;34(6):1134-1149. doi: 10.1111/tri.13839. Epub 2021 Apr 14.
This retrospective cohort study aims to review our 18-year experience with early hepatic artery thrombosis (e-HAT) following living-donor liver transplantation (LDLT), as well as to assess the feasibility, efficacy and potential risks of endovascular management of e-HAT in the first 48 hours (hrs) post-LDLT. Medical records of 730 patients who underwent LDLT were retrospectively reviewed. In all cases who had developed e-HAT, treatment modalities employed and their outcomes were evaluated. Thirty-one patients developed e-HAT(4.2%). Definite technical success and 1-year survival rates of surgical revascularization[11/31 cases(35.5%)] were 72.7% & 72.7%, whereas those of endovascular therapy[27/31 cases(87.1%)] were 70.4% & 59.3%, respectively. Endovascular therapy was carried out in the first 48hrs post-transplant in 9/31 cases(29%) [definite technical success:88.9%, 1-year survival:55.6%]. Four procedure-related complications were reported in 3 of those 9 cases(33.3%). In conclusion, post-LDLT e-HAT can be treated by surgical revascularization or endovascular therapy, with comparable results. Endovascular management of e-HAT in the first 48hrs post-LDLT appears to be feasible and effective, but is associated with a relatively higher risk of procedure-related complications, compared to surgical revascularization. Hence, it can be reserved as a second-line therapeutic option in certain situations where surgical revascularization is considered futile, potentially too complex, or potentially more risky.
本回顾性队列研究旨在回顾我们在活体肝移植(LDLT)后早期肝动脉血栓形成(e-HAT)的 18 年经验,并评估在 LDLT 后 48 小时内对 e-HAT 进行血管内治疗的可行性、疗效和潜在风险。回顾性分析了 730 例接受 LDLT 的患者的病历。对所有发生 e-HAT 的患者,评估了所采用的治疗方式及其结局。31 例患者发生 e-HAT(4.2%)。手术再血管化的明确技术成功率和 1 年生存率[11/31 例(35.5%)]分别为 72.7%和 72.7%,而血管内治疗的分别为 70.4%和 59.3%。9/31 例(29%)在 LDLT 后 48 小时内进行了血管内治疗[明确技术成功率:88.9%,1 年生存率:55.6%]。在这 9 例中有 4 例出现与操作相关的并发症(44.4%)。总之,LDLT 后 e-HAT 可以通过手术再血管化或血管内治疗来治疗,结果相当。与手术再血管化相比,在 LDLT 后 48 小时内对 e-HAT 进行血管内治疗似乎是可行且有效的,但与操作相关的并发症风险较高。因此,在某些情况下,当认为手术再血管化无效、过于复杂或风险较高时,它可以作为二线治疗选择。