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首页> 外文期刊>European journal of cardio-thoracic surgery: Official journal of the European Association for Cardio-thoracic Surgery >Preoperative introduction and maintenance immunosuppression therapy of oral-only tacrolimus, mycophenolate mofetil and steroids reduce acute rejection episodes after lung transplantation.
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Preoperative introduction and maintenance immunosuppression therapy of oral-only tacrolimus, mycophenolate mofetil and steroids reduce acute rejection episodes after lung transplantation.

机译:仅口服他克莫司,霉酚酸酯和类固醇的术前引入和维持免疫抑制疗法可减少肺移植后的急性排斥反应。

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OBJECTIVE: Immunosuppression therapy in lung transplantation (LTX) remains unsatisfactory due to a high incidence of infection and frequent acute rejection (AR), leading to early onset of the bronchiolitis obliterans syndrome (BOS). The long-term success of LTX is limited by BOS, associated with marked morbidity and mortality. The strongest risk factor for BOS is frequent AR. Decreasing frequent AR episodes might lead to improved long-term survival following LTX. METHODS: Despite the introduction of many novel agents, the basis of currently applied protocols remains a calcineurin inhibitor, that is, cyclosporine/tacrolimus (TAC). Eighty-two lung recipients received oral-only administered immunosuppression with oral TAC, mycophenolate mofetil (MMF) and intravenous (IV) methylprednisolone as introduction 2h prior to skin incision. Intra-operatively, patients received additional methylprednisolone prior to unclamping the pulmonary arteries. Postoperatively oral TAC/MMF and prednisolone were continued and trough levels closely monitored (target 8-12 ng ml(-1)). Pulmonary function tests were performed frequently and daily after discharge by means of a self-measuring device (daily forced expiratory volume in 1s (FEV(1))) as the major part of a close follow-up and monitoring programme. Trans-bronchial biopsies were rarely performed. Patient data were collected prospectively and stored in transplantation registries. LTX survival was analysed according to the Kaplan-Meier method. RESULTS: The follow-up of the LTX patients through frequent ambulatory care unit visits and close monitoring of the immunosuppressive regimen and the medication response was 100% complete. The mean duration of observation per patient was 1.8 + or - 1.7 years (median 1.4, range: 0.0-6.4 years) and this study included 176.5 patient-related years of follow-up. The 1-, 3- and 5-year survival following LTX was 70%, 60% and 55%, respectively. Eight patients (10%) underwent high-dose intravenous (IV) bolus methylprednisolone treatment and taper for AR. Two additional patients developed BOS more than 4 years following LTX. The AR- and BOS-related mortality was 0% within the 7-year interval of LTX. Alterations in FEV(1) were associated with significant anastomotic airway and infectious complications, requiring frequent bronchoscopic interventions, stenting and laser therapy as well as frequent IV antibiotic treatment. The 30-day and in-hospital mortality of 19.5% was markedly related to primary graft failure and viral infection. Long-term survival was limited predominantly by cytomegalovirus (CMV) infection and sepsis. CONCLUSIONS: Our results suggest that a standard immunosuppressive regimen of TAC and MMF orally administered and introduced prior to skin incision for LTX surgery and maintained long-term might reduce the incidence of acute and chronic rejection. Viral infections and not BOS seemed to be the limiting factor of long-term survival.
机译:目的:由于感染发生率高和频繁的急性排斥反应(AR),导致肺闭塞性细支气管炎综合征(BOS)的早期发作,肺移植(LTX)中的免疫抑制疗法仍然不能令人满意。 LTX的长期成功受到BOS的限制,并伴有明显的发病率和死亡率。 BOS的最强风险因素是频繁的AR。减少频繁的AR发作可能会改善LTX后的长期生存率。方法:尽管引入了许多新型药物,但当前应用方案的基础仍然是钙调神经磷酸酶抑制剂,即环孢素/他克莫司(TAC)。在皮肤切开前2小时,对82位肺接受者进行了口服TAC,霉酚酸酯(MMF)和静脉内(IV)甲基泼尼松龙的口服免疫抑制治疗。术中,患者在放松肺动脉之前接受了其他甲基强的松龙。术后继续口服TAC / MMF和泼尼松龙,并密切监测谷水平(目标8-12 ng ml(-1))。作为密切随访和监测计划的主要部分,经常在出院后每天进行一次肺功能测试(每日用力呼气量为1s(FEV(1)))。很少进行经支气管活检。前瞻性地收集患者数据,并将其存储在移植注册表中。根据Kaplan-Meier方法分析LTX存活率。结果:LTX患者通过频繁的门诊就诊以及对免疫抑制方案的密切监测进行了随访,药物反应100%完成。每位患者的平均观察时间为1.8 +或-1.7年(中位1.4,范围:0.0-6.4年),该研究包括176.5个患者相关的随访年限。 LTX后的1年,3年和5年生存率分别为70%,60%和55%。八名患者(10%)接受了大剂量静脉(IV)甲基强的松龙推注治疗,并逐渐减少了AR。 LTX后超过4年又有2名患者发生BOS。在LTX的7年间隔内,与AR和BOS相关的死亡率为0%。 FEV(1)的改变与明显的吻合口气道和感染并发症相关,需要频繁的支气管镜干预,支架置入和激光治疗以及频繁的静脉抗生素治疗。 30天和医院内的死亡率为19.5%,与原发性移植物衰竭和病毒感染显着相关。长期生存主要受到巨细胞病毒(CMV)感染和败血症的限制。结论:我们的结果表明,在进行LTX手术皮肤切口之前,口服和引入TAC和MMF的标准免疫抑制方案可以降低急性和慢性排斥反应的发生率。病毒感染而非BOS似乎是长期存活的限制因素。

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