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1 ain Erdman ( approximately 25 CFU/animal via bronchoscope).
2 ndobronchial allergen provocations through a bronchoscope.
3 s instilled in the both lung lobes through a bronchoscope.
4 endobronchial allergen provocation through a bronchoscope.
5 soproterenol (2 mg/ml) challenge through the bronchoscope.
6 awake with the aid of a flexible fiberoptic bronchoscope.
7 ar lavage was performed through a fiberoptic bronchoscope.
8 doses of bradykinin, aerosolized through the bronchoscope.
9 ter segmental antigen challenge via a wedged bronchoscope.
10 tly caused by a loose biopsy-port cap in the bronchoscopes.
11 rom the biopsy ports of the three implicated bronchoscopes.
12 s, and observed cleaning and disinfection of bronchoscopes.
13 s of M. tuberculosis, obtained from the same bronchoscope 2 days apart, that demonstrated unique mole
15 a greater percentage removed with the rigid bronchoscope (67%) than with the flexible bronchoscope (
16 Inadequate cleaning and disinfection of the bronchoscope after the procedure performed on Patient 5
18 e that residual DNA can remain in sterilized bronchoscopes and can be a source of false-positive PCR
19 tbreaks most commonly relate to contaminated bronchoscopes and endoscopic cleaning machines (M. absce
20 M. tuberculosis DNA could remain in sterile bronchoscopes and potentially be a cause of false-positi
21 ures that use the working channel of a rigid bronchoscope are better performed in the patient under g
22 iliarity with the use of flexible fiberoptic bronchoscope are key components while managing patients
24 h approach to use, 'blind' versus fiberoptic bronchoscope-assisted, is influenced by many factors.
31 sed by either hypocapnia (0% CO2 through the bronchoscope for 3 min) or by aerosolized acetylcholine
36 easurements made on the lower airway via the bronchoscope have been successful in adults, but have no
37 biopsy specimens obtained with the flexible bronchoscope have contributed extensively to our underst
38 Not only has clinical use of the flexible bronchoscope improved our evaluation and management of a
39 ecimens obtained with use of endoscopy-suite bronchoscopes increased from 10.4 percent at base line t
41 racts (500 microg) was instilled through the bronchoscope into the lungs of nonsmoking volunteers.
42 olony-forming units were instilled through a bronchoscope into the right lower and middle lung lobes
43 tracheobronchial anatomy with the fiberoptic bronchoscope is mandatory to increase the successful pla
45 We conclude that TBNA through the flexible bronchoscope is safe and effective in the diagnosis of i
47 debate continues as to whether a fiberoptic bronchoscope must be used to position a double-lumen tub
49 patterns of P. aeruginosa isolates from the bronchoscopes, patients, and two environmental samples w
50 choscopes were usually only available in the bronchoscope suite for the exclusive use of the pulmonar
52 of the peripheral airways, we used a wedged bronchoscope technique to study asthmatic and normal sub
57 s of Surfaxin were administered via a wedged bronchoscope to each of the 19 bronchopulmonary segments
60 of the catheter, pressure at the tip of the bronchoscope was measured with the subject breath-holdin
65 breathing, NO concentrations sampled with a bronchoscope were higher in the nasopharynx than at the
66 ifications, the biopsy-port caps on all four bronchoscopes were easily removable, and P. aeruginosa w
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