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囊性纤维化的肺移植:101例单中心连续患者的治疗结果

Lung transplantation for cystic fibrosis: outcome of 101 single-center consecutive patients.

作者信息

Diso D, Anile M, Patella M, Pecoraro Y, Rendina E A, Carillo C, Russo E, Onorati I, Angioletti D, Ruberto F, Mazzesi G, Marullo A G M, Frati G, Venuta F

机构信息

University of Rome Sapienza, Rome, Italy.

出版信息

Transplant Proc. 2013 Jan-Feb;45(1):346-8. doi: 10.1016/j.transproceed.2012.08.010.

DOI:10.1016/j.transproceed.2012.08.010
PMID:23375321
Abstract

Bilateral sequential lung transplantation (BSLT) is nowadays considered a valid therapeutic option for patients with end stage cystic fibrosis. We report our experience with 104 BSLTs in 101 patients. The overall survivals at 1, 3, 5, 10 years were 79%, 65%, 58%, and 42%, respectively. Perioperative mortality was 14.8% (n = 15). The leading causes of perioperative mortality were primary graft dysfunction and sepsis. Three patients were retransplanted owing to obliterative bronchiolitis. In 70 cases (69%), patients displayed ≥ 1 additional risk factors: previous lung resections, colonization by Burkholderia cepacia, diabetes, pneumothorax, or noninvasive ventilatory support. The mean preoperative 1-second forced expiratory volume of 0.69 ± 0.2 L (22%) increased to 85% at 1 year after the operation. The mean time on the waiting list was 12 ± 5 months. The 5 patients treated with extracorporeal membrane oxygenation before urgent transplantation were operated after 3, 5, 6, 30, and 3 days respectively. During the procedure, cardiopulmonary bypass was required in 33 patients (32%). Lung transplantation represents a unique opportunity to ameliorate the quality and improve the survival of patients affected by cystic fibrosis. Timing of referral and patient selection remain crucial for success.

摘要

双侧序贯肺移植(BSLT)如今被认为是终末期囊性纤维化患者的一种有效治疗选择。我们报告了我们在101例患者中进行104例双侧序贯肺移植的经验。1年、3年、5年和10年的总体生存率分别为79%、65%、58%和42%。围手术期死亡率为14.8%(n = 15)。围手术期死亡的主要原因是原发性移植物功能障碍和败血症。3例患者因闭塞性细支气管炎而接受再次移植。在70例(69%)患者中,显示出≥1个其他风险因素:既往肺切除术、洋葱伯克霍尔德菌定植、糖尿病、气胸或无创通气支持。术前平均第1秒用力呼气量为0.69±0.2 L(22%),术后1年增加到85%。平均等待时间为12±5个月。5例在紧急移植前接受体外膜肺氧合治疗的患者分别在3天、5天、6天、30天和3天后接受手术。在手术过程中,33例患者(32%)需要体外循环。肺移植为改善囊性纤维化患者的生活质量和提高生存率提供了一个独特的机会。转诊时机和患者选择对于成功仍然至关重要。

相似文献

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Lung transplantation for cystic fibrosis: outcome of 101 single-center consecutive patients.囊性纤维化的肺移植:101例单中心连续患者的治疗结果
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Lung transplantation for cystic fibrosis: ten years of experience.囊性纤维化的肺移植:十年经验
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Lung transplantation for cystic fibrosis: 6-year follow-up.囊性纤维化的肺移植:6年随访
J Cyst Fibros. 2005 May;4(2):107-14. doi: 10.1016/j.jcf.2005.01.003.
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Lung transplantation for cystic fibrosis.囊性纤维化的肺移植
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Lung transplantation for cystic fibrosis: a single center experience of 100 consecutive cases.肺移植治疗囊性纤维化:100 例连续病例的单中心经验。
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Lung transplantation outcome in cystic fibrosis patients with previous pneumothorax.既往有气胸的囊性纤维化患者的肺移植结局
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Improved results of lung transplantation for patients with cystic fibrosis.囊性纤维化患者肺移植的效果改善。
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Cystic fibrosis. Target population for lung transplantation in North America in the 1990s.囊性纤维化。20世纪90年代北美肺移植的目标人群。
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Drugs R D. 2016 Mar;16(1):1-17. doi: 10.1007/s40268-015-0121-9.
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Lung transplantation for cystic fibrosis: results, indications, complications, and controversies.囊性纤维化的肺移植:结果、适应证、并发症及争议
Semin Respir Crit Care Med. 2015 Apr;36(2):299-320. doi: 10.1055/s-0035-1547347. Epub 2015 Mar 31.
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Extracorporeal membrane oxygenation for pediatric respiratory failure: History, development and current status.
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