Schleimer Karina, Stippel Dirk L, Kasper Hans-Udo, Tawadros Samir, Suer Christian, Schomäcker Klaus, Hölscher Arnulf, Beckurts K Tobias E
Department of Visceral and Vascular Surgery, University of Cologne, Cologne, Germany.
Transpl Int. 2006 Jul;19(7):581-8. doi: 10.1111/j.1432-2277.2006.00291.x.
Heterotopic auxiliary liver transplantation (HALT) with portal vein arterialization (PVA) was proposed in acute hepatic failure (AHF). However, clinical results of PVA are controversial because of lacking standardized flow-regulation. In rats, we examined HALT with flow-regulated PVA in AHF. Group A: HALT with flow-regulated PVA and 85% resection of the native liver to induce AHF [acute experiments (n = 8), killing after 7 days (n = 8) and after 6 weeks (n = 11)]. Group B: 85% liver-resection (n = 10). The average blood-flow in the arterialized portal vein in HALT achieved normal values (1.7 +/- 0.4 ml/min/g liver-weight). After reperfusion, the diameters of the sinusoids (6.4 +/- 0.6 microm), the postsinusoidal venules (31.1 +/- 3.3 microm) and the intersinusoidal distance (17.9+/-0.7 microm) also achieved normal values. The functional sinusoidal density amounted to 335 +/- 48/cm. The 6-week survival was nine of 11 with excellent liver function (Quick's value: 110% +/- 7.8%). The hepatobiliary radioisotope scanning with (99mTc) ethyl hepatic iminodiacetic acid (EHIDA) showed no significant differences between the native livers and grafts. The hepatocellular morphology was regular, apart from low-grade necroses in two grafts. The grafts' sinusoidal endothelial cells did not show any morphological changes. In group B, however, all rats died from AHF within 6 days. HALT with flow-regulated PVA achieved good results regarding microcirculation, morphology and function and can reliably bridge AHF.
在急性肝衰竭(AHF)中提出了采用门静脉动脉化(PVA)的异位辅助肝移植(HALT)。然而,由于缺乏标准化的血流调节,PVA的临床结果存在争议。在大鼠中,我们研究了在AHF中采用血流调节的PVA的HALT。A组:采用血流调节的PVA进行HALT,并对原肝进行85%切除以诱导AHF[急性实验(n = 8),7天后处死(n = 8)和6周后处死(n = 11)]。B组:85%肝切除(n = 10)。HALT中动脉化门静脉的平均血流量达到正常水平(1.7±0.4 ml/min/g肝重)。再灌注后,肝血窦直径(6.4±0.6微米)、血窦后小静脉直径(31.1±3.