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肺移植术后囊性纤维化和非囊性纤维化患者的术后感染

Post-operative infections in cystic fibrosis and non-cystic fibrosis patients after lung transplantation.

作者信息

Bonvillain Ryan W, Valentine Vincent G, Lombard Gisele, LaPlace Stephanie, Dhillon Gundeep, Wang Guoshun

机构信息

Department of Medicine, Louisiana State University Health Sciences Center, New Orleans, Louisiana 70112, USA.

出版信息

J Heart Lung Transplant. 2007 Sep;26(9):890-7. doi: 10.1016/j.healun.2007.07.002.

Abstract

BACKGROUND

Cystic fibrosis (CF) lung disease is the major cause of mortality in CF patients. Lung transplantation remains a valid therapeutic option. It is unknown whether CF patients receiving healthy lungs have an equal susceptibility to infections when compared with non-CF lung transplant patients. Herein we present the largest analyses to date of the post-operative infection profiles of 60 CF and 60 non-CF lung transplant patients.

METHODS

Bilateral allogeneic lung transplantations and post-transplant management were performed according to standard clinical procedures. Post-operative infections were diagnosed by conventional methods based on clinical symptoms and laboratory cultures.

RESULTS

Sixty CF lung-transplant patients developed 278 post-operative respiratory infections, from which 307 pathogens were isolated. Pseudomonas aeruginosa predominantly occupied 60.3%, followed by Mycobacteria spp (7.2%), Aspergillus spp (5.9%) and Staphylococcus spp (5.5%). However, 60 non-CF transplant patients had 154 respiratory infections with 165 pathogens isolated. Pseudomonas aeruginosa was noted in 38.2%, followed by Aspergillus spp (9.7%), Staphylococcus spp (9.7%) and Mycobacteria spp (9.1%). The CF group demonstrated a significantly higher frequency of Pseudomonas respiratory infections than the non-CF group. Interestingly, no significant differences were detected in any infections from other systems including blood, sinuses, skin, wounds, oral cavity, bowel, eyes, peritoneal cavity and urinary tract. Moreover, the CF lung transplant patients had significantly less time free from Pseudomonas infections.

CONCLUSIONS

The normal lungs implanted into CF patients had significantly higher susceptibility to Pseudomonas infections than those into non-CF patients, suggesting that defective innate immunity outside the lungs contributes to CF lung pathogenesis.

摘要

背景

囊性纤维化(CF)肺部疾病是CF患者死亡的主要原因。肺移植仍然是一种有效的治疗选择。与非CF肺移植患者相比,接受健康肺脏的CF患者是否对感染具有相同的易感性尚不清楚。在此,我们展示了迄今为止对60例CF和60例非CF肺移植患者术后感染情况的最大规模分析。

方法

双侧同种异体肺移植及移植后管理按照标准临床程序进行。术后感染通过基于临床症状和实验室培养的传统方法进行诊断。

结果

60例CF肺移植患者发生了278例术后呼吸道感染,从中分离出307种病原体。铜绿假单胞菌占主导地位,为60.3%,其次是分枝杆菌属(7.2%)、曲霉属(5.9%)和葡萄球菌属(5.5%)。然而,60例非CF移植患者发生了154例呼吸道感染,分离出165种病原体。铜绿假单胞菌占38.2%,其次是曲霉属(9.7%)、葡萄球菌属(9.7%)和分枝杆菌属(9.1%)。CF组铜绿假单胞菌呼吸道感染的频率显著高于非CF组。有趣的是,在包括血液、鼻窦、皮肤、伤口、口腔、肠道、眼睛、腹腔和泌尿道等其他系统的任何感染中均未检测到显著差异。此外,CF肺移植患者无铜绿假单胞菌感染的时间明显更短。

结论

植入CF患者的正常肺脏对铜绿假单胞菌感染的易感性明显高于植入非CF患者的肺脏,这表明肺部以外的先天性免疫缺陷促成了CF肺部发病机制。

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