首页> 外文期刊>Journal of Hepatology: The Journal of the European Association for the Study of the Liver >Assessment of chronic rejection in liver graft recipients receiving immunosuppression with low-dose calcineurin inhibitors
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Assessment of chronic rejection in liver graft recipients receiving immunosuppression with low-dose calcineurin inhibitors

机译:接受低剂量钙调磷酸酶抑制剂免疫抑制的肝移植受者的慢性排斥反应评估

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Background & Aims Calcineurin inhibitors represent the cornerstone immunosuppressants after liver transplantation despite their side effects. As liver graft is particularly well tolerated, low doses may be proposed. The aim of this study was to assess the prevalence of chronic rejection in patients with low calcineurin inhibitors regimen and to compare their characteristics with patients under standard doses. Methods All patients with liver transplantation between 1997 and 2004 were divided into two groups. Low-dose patients (n = 57) had tacrolimus baseline levels <5 ng/ml or cyclosporine levels <50 ng/ml at t0 or <100 ng/ml at t + 2 h and were prospectively proposed a liver biopsy, searching for chronic rejection according to Banff criteria. The remaining patients constituted the standard-doses group (n = 40). Results Among the low-dose group, 36 patients in the low-dose group were assessed by biopsy. No chronic rejection was found. Fifty-six percent had only calcineurin inhibitors and 8% received other immunosuppressants only. The median time between liver transplantation and biopsy was 90 months (64-157) and between IS regimen decrease and biopsy was 41 months (11-115). Liver tests were normal in 72% of the patients. Low-dose patients had more often hepatitis B (p = 0.045), less past acute rejection episodes (p = 0.028), and better renal function (p = 0.040). Decrease of calcineurin inhibitors failed in 15% of standard-dose patients without impacting the graft function. In the low-dose group, co-prescription of other immunosuppressants facilitated the decrease (p = 0.051). Conclusions The minimization, or even cessation, of calcineurin inhibitors may be an achievable goal in the long term for most of the liver graft recipients.
机译:背景与目的钙调神经磷酸酶抑制剂尽管有副作用,但却代表了肝移植后的基石免疫抑制剂。由于肝移植的耐受性特别好,因此建议使用低剂量。这项研究的目的是评估在低钙调神经磷酸酶抑制剂治疗方案中慢性排斥反应的患病率,并与标准剂量下的患者进行比较。方法将1997年至2004年的所有肝移植患者分为两组。低剂量患者(n = 57)在t0时他克莫司的基线水平<5 ng / ml或环孢素水平在<0 ng / ml或在t + 2 h时<100 ng / ml,他们被提议进行肝活检,以寻找慢性根据班夫标准拒绝。其余患者为标准剂量组(n = 40)。结果在低剂量组中,对低剂量组中的36例患者进行了活检。未发现慢性排斥反应。 56%的患者仅接受钙调神经磷酸酶抑制剂,而8%的患者仅接受其他免疫抑制剂。肝移植和活检之间的中位时间为90个月(64-157),IS方案减少和活检之间的中位时间为41个月(11-115)。 72%的患者肝脏检查正常。低剂量患者发生乙型肝炎的频率更高(p = 0.045),过去的急性排斥反应较少(p = 0.028),并且肾功能较好(p = 0.040)。在15%的标准剂量患者中,钙调神经磷酸酶抑制剂的减少失败,但不影响移植功能。在低剂量组中,其他免疫抑制剂的共同处方促进了这种降低(p = 0.051)。结论从长远来看,钙调神经磷酸酶抑制剂的减量甚至停止可能是大多数肝移植受者的可实现目标。

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