Cc. Chan et al., DIAGNOSTIC YIELD AND THERAPEUTIC IMPACT OF FLEXIBLE BRONCHOSCOPY IN LUNG-TRANSPLANT RECIPIENTS, The Journal of heart and lung transplantation, 15(2), 1996, pp. 196-205
Background: Bronchoalveolar lavage and transbronchial biopsy are often
used for definitive diagnosis of lung rejection and infection in lung
transplant recipients. Although protected specimen brushing is of val
ue in nosocomial bacterial pneumonia, its role in lung transplant reci
pients has not been widely reported. The aim of the study is to review
the diagnostic yield and therapeutic impact of flexible bronchoscopy
with the use of a combination of bronchoalveolar lavage, protected spe
cimen brushing, and transbronchial biopsy in lung transplant recipient
s. Methods: We reviewed flexible bronchoscopy data in 83 lung transpla
nt recipients between February 1990 and March 1995. Only those with br
onchoalveolar lavage, protected specimen brushing, and transbronchial
biopsy were included in the analysis. There were 282 bronchoscopies pe
rformed for clinically suspected lung rejection or infection (clinical
bronchoscopy) and 35 bronchoscopies for follow-up of a previously det
ected histologic abnormality (follow-up bronchoscopy). Results: The to
tal yields for rejection and infection for clinical and follow-up bron
choscopies were 67.4% and 57.9%, respectively. Acute rejection was det
ected with transbronchial biopsy in 26.2% and 34.2% of clinical and fo
llow-up bronchoscopies, respectively. Cytomegalovirus pneumonitis was
detected with transbronchial biopsy in 4.0% and 11.4% of clinical and
follow-up bronchoscopies, respectively. Overall, bacteria was the most
common cause of lower respiratory tract infection. When used together
, protected specimen brushing and bronchoalveolar lavage were compleme
ntary techniques for detection of bacterial lower respiratory tract in
fection with a significantly higher proportion detected with protected
specimen brushing (greater than or equal to 10(3) colony forming unit
s/ml) compared with bronchoalveolar lavage (greater than or equal to 1
0(5) colony forming units/ml) (p < 0.001). Complications were hemorrha
ge (1.9%), pneumothorax (2.5%) and transient hypoxemia (10.5%). The re
sults had an impact on management of rejection and infection in 57.8%
of clinical and 39.5% of follow-up bronchoscopies. Conclusions: We con
clude that bronchoscopy, with the use of a combination of bronchoalveo
lar lavage, protected specimen brushing, and transbronchial biopsy, is
safe with a high diagnostic yield and therapeutic impact for treating
lung transplant recipients.