Lázaro-Carrasco M T, Morales P, Ferreiro M J, Borro J M, Varela A, Vicente R, Ramos F, Estada J A
Unidad de Trasplante Pulmonar, Clínica Puerta de Hierro, Madrid.
Rev Clin Esp. 1999 May;199(5):280-4.
Retrospective analysis of cystic fibrosis patients who underwent pulmonary transplantation at Clínica Puerta de Hierro, Madrid, and at Hospital La Fe, Valencia. Since the beginning of the programme and until March 1998, a total of 63 patients with cystic fibrosis were studied. Among transplanted patients, 18 were males and 16 females, with a mean age of 18.9 years. All patients underwent sequential bilateral pulmonary transplantation. After transplantation, the most common complication was bacterial pneumonia which affected all patients. Six patients had dehiscence or stenosis of the bronchial suture. Other specific complications of this condition by frequency were intestinal obstruction and diabetes mellitus. Six patients developed obliterans bronchiolitis and one of them underwent a repeat transplantation. Three out of the 34 patients died, and the likelihood of survival after one and three years was 94%. Respiratory function tests and PaO2 peaked at sixth post-transplantation month.
Pulmonary transplantation is a therapeutic option to be considered for the patient with cystic fibrosis and severe involvement of his/her pulmonary disease.
对在马德里的铁之门诊所和巴伦西亚的拉斐医院接受肺移植的囊性纤维化患者进行回顾性分析。自该项目启动至1998年3月,共研究了63例囊性纤维化患者。在接受移植的患者中,男性18例,女性16例,平均年龄18.9岁。所有患者均接受序贯双侧肺移植。移植后,最常见的并发症是细菌性肺炎,所有患者均受影响。6例患者出现支气管缝合处裂开或狭窄。按发生频率排列,该疾病的其他特定并发症为肠梗阻和糖尿病。6例患者发生闭塞性细支气管炎,其中1例接受再次移植。34例患者中有3例死亡,1年和3年后的生存率为94%。呼吸功能测试和动脉血氧分压在移植后第6个月达到峰值。
对于患有囊性纤维化且肺部疾病严重的患者,肺移植是一种可考虑的治疗选择。