Airway Dehiscence After Lung Transplantation in a Patient With Cystic Fibrosis

被引：0

作者：

Hayes, Don, Jr. ^{[1
,2
]}

Hatton, Kevin W. ^{[3
]}

Feola, David J. ^{[4
]}

Murphy, Brian S. ^{[2
]}

Mullett, Timothy W. ^{[5
]}

机构：

[1] Univ Kentucky, Med Ctr, Lung Transplant Program, Coll Med,Dept Pediat, Lexington, KY 40536 USA

[2] Univ Kentucky, Coll Med, Dept Internal Med, Lexington, KY 40536 USA

[3] Univ Kentucky, Coll Med, Dept Anesthesiol, Lexington, KY 40536 USA

[4] Univ Kentucky, Coll Pharm, Dept Pharm Practice & Sci, Lexington, KY 40536 USA

[5] Univ Kentucky, Coll Med, Dept Surg, Lexington, KY 40536 USA

来源：

RESPIRATORY CARE | 2010年 / 55卷 / 12期

关键词：

anastamosis; anastomotic failure; anastomotic ischemia; dehiscence; cystic fibrosis; CF; lung transplantation; linezolid; resistant; methicillin-resistant Staphylococcus aureus; MRSA; airway-pressure-release ventilation; RESISTANT STAPHYLOCOCCUS-AUREUS; PANRESISTANT BACTERIA; COMPLICATIONS; IMPACT;

D O I：

暂无

中图分类号：

R4 [临床医学];

学科分类号：

1002 ; 100602 ;

摘要：

The presence of resistant pathogens in the lower airways of patients with cystic fibrosis (CF) is not an absolute contraindication for lung transplantation. We describe a case in which a patient with CF died as a result of an anastomotic dehiscence, ischemia, and infection with linezolid-resistant methicillin-resistant Staphylococcus aureus. We review infection issues during the post-lung-transplant period and related anastomotic dehiscence in CF.

引用

页码：1746 / 1750

页数：5

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