Jj. Shannon et al., ENDOBRONCHIAL ULTRASOUND-GUIDED NEEDLE ASPIRATION OF MEDIASTINAL ADENOPATHY, American journal of respiratory and critical care medicine, 153(4), 1996, pp. 1424-1430
Citations number
26
Categorie Soggetti
Emergency Medicine & Critical Care","Respiratory System
We conducted a randomized, controlled trial to prospectively confirm t
hat ultrasound-directed transbronchial needle aspiration (USTBNA) resu
lts in: (1) improved sensitivity for detecting lymph nodes involved wi
th neoplasm, and (2) a decreased number of aspirates needed to achieve
a diagnosis as compared with standard transbronchial needle aspiratio
n (TBNA). The study was conducted in a tertiary medical center on pati
ents undergoing fiberoptic bronchoscopy in the evaluation of enlarged
mediastinal lymph nodes. USTBNA or TBNA were followed by rapid, on-sit
e cytopathology examination of the collected specimens. Measurements i
ncluded the (1) age and sex of the patient, prior diagnosis of cancer,
nodal short-axis diameter and node location as determined by computer
ized tomography (CT), and endobronchial abnormalities at bronchoscopy;
(2) number, order, and location of transbronchial aspirates and resul
ts of on-site evaluation; (3) results of surgical exploration in patie
nts with negative transbronchial needle aspiration; (4) sensitivity, s
pecificity, and diagnostic accuracy of USTBNA and TBNA; (5) number of
aspirates required for successful lymph node aspiration as well as for
a diagnosis of cancer for both USTBNA and TBNA; and (6) multiple logi
stic regression analysis to determine the significance of combinations
of clinical predictors and needle-aspirate results. Eighty-two bronch
oscopic examinations were performed on 80 patients. We found no signif
icant difference between USTBNA and TBNA in sensitivity (82.6% versus
90.5%, respectively), specificity (100% for both), or diagnostic accur
acy (86.7% versus 91.7%, respectively). The sensitivity, specificity,
and diagnostic accuracy of USTBNA and TBNA were similarly high, regard
less of node location (paratracheal or subcarinal). A decrease in the
number of aspirates required for lymph node sampling approached statis
tical significance for all USTBNAs as compared with TBNAs (2.03 +/- 0.
19 versus 2.62 +/- 0.25, p = 0.06), but this was not demonstrated for
the number required to confirm cancer (1.95 +/- 0.47 versus 2.68 +/- 0
.21, p = 0.17). The number of aspirates to successful lymph node aspir
ation decreased with USTBNA versus TBNA in paratracheal lymph nodes (2
.00 +/- 0.20 versus 2.91 +/- 0.34, p = 0.03), but not to a diagnosis o
f cancer (1.93 +/- 0.25 versus 3.00 +/- 0.58, p = 0.11). No difference
was seen in the number of aspirates for subcarinal nodes. The number
of TBNA attempts for paratracheal lymph node sampling was inversely co
rrelated with node size (r = 0.48, p = 0.02). No such relation was see
n with USTBNA of paratracheal nodes (r = 0.09, p = 0.66), TBNA of subc
arinal nodes, or USTBNA of subcarinal nodes. A similar relation was se
en between the number of aspirates to a diagnosis of cancer. On multip
le logistic regression analysis, a positive transbronchial aspirate wa
s associated only with a larger lymph node and history of prior cancer
. We conclude that: (1) in the setting of on-site cytopathology, trans
bronchial needle aspiration has a high sensitivity, specificity, and d
iagnostic accuracy in the evaluation of enlarged mediastinal lymph nod
es suspected of harboring malignancy; (2) mediastinal anatomy, includi
ng vascular structures and lymph nodes, is clearly imaged with endobro
nchial ultrasonagraphy; (3) a greater short-axis diameter of the media
stinal lymph node and history of a prior malignancy increase the likel
ihood of a positive transbronchial aspiration; (4) USTBNA exhibits a s
imilarly high diagnostic yield to TBNA in the setting of rapid on-site
cytopathology evaluation; (5) USTBNA decreases the number of aspirate
s required for paratracheal lymph node sampling, which may be particul
arly useful in sampling smaller paratracheal nodes or at institutions
that do not utilize rapid on-site cytopathology evaluation.