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终末期囊性纤维化患者的肺移植和心肺联合移植:斯坦福大学的经验。

Lung and heart-lung transplantation in patients with end-stage cystic fibrosis: the Stanford experience.

作者信息

Vricella Luca A, Karamichalis John M, Ahmad Shahzad, Robbins Robert C, Whyte Richard I, Reitz Bruce A

机构信息

Department of Cardiothoracic Surgery, Stanford University School of Medicine, California 94305-5407, USA.

出版信息

Ann Thorac Surg. 2002 Jul;74(1):13-7; discussion 17-8. doi: 10.1016/s0003-4975(02)03634-2.

Abstract

BACKGROUND

Bilateral lung (BLTx) and heart-lung transplantation have gained wide acceptance as treatment of end-stage lung disease from cystic fibrosis. We reviewed our 13-year experience with thoracic transplantation for cystic fibrosis with an operative approach that favors use of cardiopulmonary bypass for BLTx.

METHODS

Sixty-four patients with cystic fibrosis underwent heart-lung transplantation (n = 22, 34.4%) or BLTx (n = 42, 65.6%) between 1988 and 2000. Mean age and weight at transplantation were 29 +/- 8 years and 51 +/- 11 kg, respectively. Mean follow-up for survivors was 4.4 +/- 3.6 years. Immunosuppression regimen included cyclosporine, tapered corticosteroids, azathioprine, and induction therapy with OKT3 (murine monoclonal antibodies) or rabbit antithymocyte globulin. Cardiopulmonary bypass was used in all but 5 patients (7.8%). However, in 8 (19%) of the 42 patients having BLTx, only the grafting of the second lung was performed with cardiopulmonary bypass.

RESULTS

The operative mortality rate was 1.6%. The actuarial survival rates at 1 year, 3 years, 5 years and 10 years were 93.2%, 77.7%, 61.8%, and 48.1%, respectively, with no significant difference between BLTx and heart-lung transplantation. The major hospital complications were pneumonia (n = 11, 17.2%) and bleeding (n = 8, 12.5%). Clinically significant reperfusion injury was observed in 6 patients, 3 of whom required reintubation. Freedom from acute lung rejection beyond 1 year was 47.7%. One patient underwent late retransplantation, and 4 required bronchial stenting. Obliterative bronchiolitis accounted for eight (50.0%) of 16 late deaths.

CONCLUSIONS

Though postoperative bleeding and pneumonia are still of concern, satisfactory early and intermediate-term results can be expected in patients undergoing BLTx or heart-lung transplantation for cystic fibrosis. Cardiopulmonary bypass can be used for BLTx with no adverse impact on intermediate and long-term outcomes.

摘要

背景

双侧肺移植(BLTx)和心肺移植已被广泛接受为治疗囊性纤维化所致终末期肺病的方法。我们回顾了我们13年来采用有利于在双侧肺移植中使用体外循环的手术方法进行囊性纤维化胸段移植的经验。

方法

1988年至2000年间,64例囊性纤维化患者接受了心肺移植(n = 22,34.4%)或双侧肺移植(n = 42,65.6%)。移植时的平均年龄和体重分别为29±8岁和51±11千克。幸存者的平均随访时间为4.4±3.6年。免疫抑制方案包括环孢素、逐渐减量的皮质类固醇、硫唑嘌呤,以及用OKT3(鼠单克隆抗体)或兔抗胸腺细胞球蛋白进行诱导治疗。除5例患者(7.8%)外,所有患者均使用了体外循环。然而,在42例接受双侧肺移植的患者中,有8例(19%)仅在移植第二侧肺时使用了体外循环。

结果

手术死亡率为1.6%。1年、3年、5年和10年的实际生存率分别为93.2%、77.7%、61.8%和48.1%,双侧肺移植和心肺移植之间无显著差异。主要的医院并发症为肺炎(n = 11,17.2%)和出血(n = 8,12.5%)。6例患者观察到具有临床意义的再灌注损伤,其中3例需要重新插管。1年后无急性肺排斥反应的比例为47.7%。1例患者接受了晚期再次移植,4例需要支气管支架置入。闭塞性细支气管炎占16例晚期死亡病例中的8例(50.0%)。

结论

虽然术后出血和肺炎仍然令人担忧,但对于接受双侧肺移植或心肺移植治疗囊性纤维化的患者,可以预期获得满意的早期和中期结果。体外循环可用于双侧肺移植,对中期和长期结果无不利影响。

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