Subramaniyam Rekha, Jamir Imtiakum, Kumar Niteen, Agrawal Nitesh, Sood Gaurav, Shriya Aditya, Gupta Anish, Chaudhary Abhideep
Department of HPB Surgery and Liver Transplantation, BLK-Max Super Specialty Hospital, Rajendra Place, New Delhi, India.
Department of Interventional Radiology, BLK-Max Super Speciality Hospital, Rajendra Place, New Delhi, India.
Liver Transpl. 2025 May 8. doi: 10.1097/LVT.0000000000000635.
In living donor liver transplant, graft hyperperfusion can lead to early allograft dysfunction, graft loss, and even mortality. Portal inflow modulation is advocated to prevent hyperperfusion injury. We implemented intraoperative distal splenic artery ligation (SAL) since January 2021 in recipients with one or more of the indications: graft to recipient weight ratio <0.8, graft to spleen volume ratio ≤1, high post-reperfusion portal venous flow (≥250 mL/min/100 g of graft weight), low hepatic artery peak systolic velocity (≤20 cm/s), and/or high post-reperfusion portal venous pressure (≥15 mm Hg). This group was compared with a retrospective splenic artery ligation-not done (non-SAL) group, during July 2019-December 2020, who met any one or more of the above criteria, but had not undergone SAL. Out of 426 patients who underwent living donor liver transplant during the study period, 90 and 42 right lobe adult recipients were included in the SAL and non-SAL groups, respectively. The SAL group had a significant reduction in post-reperfusion portal flow and pressure and also improved hepatic arterial peak systolic velocity compared to the non-SAL group ( p <0.01). Significant reduction in serum total bilirubin and ascitic fluid was observed on post-operative days 1, 3, 5, 7, and 14 in the SAL group ( p <0.01). There was a significant reduction in the incidence of early allograft dysfunction in the SAL group compared to the non-SAL group (8.8% vs. 26.2%, p <0.01). There was a decreased incidence of small for size syndrome (SFSS) ( p <0.05) with no incidence of grade-C SFSS and lower 90-day mortality in the SAL group ( p <0.01). Intraoperative distal SAL significantly reduces portal hyperperfusion, thereby reducing early allograft dysfunction, small for size syndrome, morbidity, and improving 1-year survival.
在活体供肝肝移植中,移植肝高灌注可导致早期移植肝功能障碍、移植肝丢失甚至死亡。提倡进行门静脉血流调节以预防高灌注损伤。自2021年1月起,我们对有以下一项或多项指征的受者实施术中脾动脉远端结扎(SAL):移植肝与受者体重比<0.8、移植肝与脾脏体积比≤1、再灌注后门静脉血流高(≥250 mL/min/100 g移植肝重量)、肝动脉收缩期峰值流速低(≤20 cm/s)和/或再灌注后门静脉压力高(≥15 mmHg)。将该组与2019年7月至2020年12月期间符合上述任何一项或多项标准但未接受SAL的脾动脉结扎未实施(非SAL)回顾性组进行比较。在研究期间接受活体供肝肝移植的426例患者中,SAL组和非SAL组分别纳入了90例和42例右叶成年受者。与非SAL组相比,SAL组再灌注后门静脉血流和压力显著降低,肝动脉收缩期峰值流速也有所改善(p<0.01)。SAL组术后第1、3、5、7和14天血清总胆红素和腹水显著减少(p<0.01)。与非SAL组相比,SAL组早期移植肝功能障碍的发生率显著降低(8.8%对26.2%,p<0.01)。SAL组小体积综合征(SFSS)的发生率降低(p<0.05),C级SFSS无发生,90天死亡率较低(p<0.01)。术中脾动脉远端结扎显著降低门静脉高灌注,从而减少早期移植肝功能障碍、小体积综合征、发病率,并提高1年生存率。