Objective: To analyze a single-center experience with infectious compl
ications of single lung transplantation (SLT) with special emphasis on
risk factors for infection in the transplanted and native lung. Desig
n: Consecutive case series. Setting. University teaching hospital. Pat
ients: Fifteen consecutive SLT recipients (mean age, 43 years; 9 men a
nd 6 women). Mean follow-up was 337 days. Results: Fifteen patients ha
d 24 infectious episodes (1.6 per patient) of which 83 percent were li
fe-threatening, 79 percent involved the lung, airway, or pleural space
, and 79 percent occurred in the first 4 months after transplantation.
Despite this high infectious morbidity, there were no infectious deat
hs. The most important infections were bacterial pneumonia (n = 10), c
ytomegalovirus (CMV) pneumonia (n = 5), and bronchial anastomotic infe
ctions (n = 3). Significant risk factors for bacterial pneumonia were
a diagnosis of primary or secondary pulmonary hypertension (p<0.05) an
d the presence of airway complications of stenosis or dehiscence (p<0.
05). No risk factors for overall lung infections were identified. The
native lung was involved in 6 of 16 lung infections and was the exclus
ive site of infection in 4 cases. Underlying disease in the native lun
g may have predisposed to infection at that site by a mechanism of ina
dequate blood flow or impaired ventilation. Three bronchial anastomoti
c infections (Pseudomonas, Candida, Aspergillus) occurred, all with de
hiscence of the anastomosis. These were highly morbid but resolved wit
h antibiotics, stent placement, and surgical retention in two of the t
hree cases. The five episodes of CMV pneumonia caused mild (four patie
nts) or moderate (one patient) dysfunction and responded to antiviral
agents without relapse. Conclusion: The frequency, complexity, and mor
bidity of infections after SLT were great, but most infections were ma
nageable and good outcomes were achieved. A pretransplant diagnosis of
pulmonary hypertension or posttransplant occurrence of bronchial sten
osis or dehiscence were associated with a higher rate of bacterial pne
umonia. The underlying disease in the native lung may predispose to in
fection at that site.