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13 protocols using um s20 20r

1

Flexible Bronchoscopic Ultrasound Aspiration

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All procedures were performed using an electronic flexible bronchoscope (Olympus 1T260 or Olympus 1TQ290, Olympus Medical Systems Co. Ltd, Tokyo, Japan), ultrasonic host (EV-ME1 universal ultrasonic endoscope image processing device, Olympus Medical Systems Co. Ltd., Tokyo, Japan), R-EBUS with a 1.7 mm diameter (UM-S20-20R, Olympus Medical Systems Co. Ltd., Tokyo, Japan), WANG™ transbronchial aspiration histology needles (MWF-319, ConMed Company, New York, USA), and a cell brush (Nanjing Micro-tech Medical Science and Technology Co., Ltd., Nanjing, China).
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2

EBUS-GS and CTBB Biopsy Techniques

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In EBUS-GS TBB, we used video bronchoscopes (BFp-260F, 4.0-mm outer diameter and BF1T-260, 5.9-mm outer diameter; Olympus, Tokyo, Japan) with an ultrasound scanner (EU-ME-1; Olympus) for the EBUS-GS biopsies. We used guide sheath kits with two sizes (K-201 and K-203 unit; Olympus). Each guide sheath kit consisted of a guide sheath, forceps, and a cytology brush. To detect the target lesion, we used radial endobronchial ultrasound probes (UM-S20-17S, 1.7-mm outer diameter and UM-S20-20R, 2.0-mm outer diameter; Olympus). In the CTBB group, we used several types of bronchoscopes for biopsy (BF260, BF6C260, BFp260F, and BF1T260; Olympus), disposable biopsy forceps (FB-231D; Olympus), and disposable cytology brushes (BC-202D-2010; Olympus).
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3

Flexible Bronchoscopy with EBUS and Cryo Biopsy

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The procedures used in this study were described previously [14 (link)]. A flexible fiber bronchoscope (BF-1TQ290; Olympus, Tokyo, Japan), 20-MHz radial EBUS probe (UM-S20-20R; Olympus), guide sheath (SG-201C; Olympus), brush (BC-202D-2010; Olympus), forceps (FB-231D; Olympus), and 1.9 mm cryo probe (CRYO2; ERBE, Tuebingen, Germany) were employed [14 (link)]. Thrombin (Liquid Thrombin MOCHIDA Softbottle 10,000; Mochida Pharmaceutical, Tokyo, Japan) and balloon catheter (B5-2C; Olympus) were prepared in case of mild or severe bleeding [14 (link)]. Local anesthesia with 1% lidocaine for nebulizing, 2% lidocaine bolus to the bronchus, intravenous injection of 2–2.5 mg of midazolam, and intra-muscular injection of 35 mg pethidine hydrochloride for conscious sedation were used during the procedures [9 (link), 14 (link)]. The blood pressure, oxygen saturation, pulse rate, and electrocardiography of all patients were monitored in this study [9 (link), 14 (link)].
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4

Flexible Bronchoscopy Approach for Peripheral Lung Lesions

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All examinations were performed using a flexible bronchoscope. The bronchoscope was inserted through the oral route under mild sedation following pharyngeal anesthesia. In cases of PPLs, virtual bronchoscopic navigation (Ziostation2; AMIN, Japan) was created prior to performing endobronchial ultrasound with a guide sheath (EBUS-GS). The radial EBUS probe (20 MHz mechanical radial type, UM-S20-20R or UM-S20-17S; Olympus, Japan) was inserted into the GS kit (K-201 or K-203; Olympus, Japan). After reaching the target lesion, TBB, brushing, and/or needle aspiration was performed under fluoroscopic guidance. In this study, bronchoscopically visible target lesions were defined as central lesions, whereas other lesions were classified as peripheral lesions.
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5

EBUS-GS for Lesion Identification

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In the group 3 (patients performed EBUS-GS), equipped with endoscopic ultrasound system (EU-M30S, Olympus, Tokyo, Japan), a 20 MHz radial small-diameter probe (UM-S20–20R Olympus) with guide sheath was inserted through the working channel of the bronchoscope. Once the precise location of the lesion was identified by EBUS, the probe was withdrawn, leaving the GS in place. Subsequently, the specimen were harvested through the brushing, forceps biopsy, and BALF for ROSE and pathologic diagnosis as other groups.
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6

EBUS-Guided Transbronchial Biopsy for Peripheral Pulmonary Lesions

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The procedure was performed by chest fellows under the supervision of experienced pulmonologists. Conventional bronchoscopy with a 2.0-mm working channel (BF-P260F bronchoscope; Olympus, Tokyo, Japan) was first conducted to inspect the bronchial trees, after local anaesthesia with 5 ml of 2% lidocaine sprayed or nebulized into the upper airway mucosa and intramuscular injection of meperidine 50 mg if not contraindicated.[14 (link), 15 (link)] Additional 1–2 ml of 2% lidocaine were instilled onto the larynx, carina and second carina following insertion of the bronchoscope. EBUS was then performed with an endoscopic ultrasound centre (EU-M30S; Olympus) and a 20-MHz radial-type ultrasonic probe (UM-S20-20R; Olympus). After locating the PPLs on the EBUS images, EBUS-guided TBB was performed as described previously.[16 (link)] The biopsy procedures were repeated until at least 2 adequate samples were retrieved. Bronchial washing or brushing was conducted after TBB, based on the judgment of the pulmonologists in charge. Other ancillary bronchoscopic techniques, including guiding sheath, ultrathin bronchoscopy, fluoroscopy, virtual bronchoscopic navigation, electromagnetic navigation, and rapid on-site evaluation, were not applied in this study.
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7

Transbronchial Lung Biopsy Protocol

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Bronchoscopy was carried out with a flexible bronchoscope (BF‐1T260; Olympus) under local anesthesia. For patients receiving EBUS‐TBLB, ultrasound analysis was carried out employing an EBUS system (processor EU‐ME2; Olympus), equipped with a 20 MHz mechanical radial miniprobe (UM‐S20‐20R; Olympus). A thorough examination of the target bronchus with the bronchoscope was performed. Once the target PPL was localized, we measured the distance between it and the outer orifice of the bronchoscope working channel for the purpose of performing TBLB at the same PPL site. Subsequently, the miniprobe was withdrawn, and biopsy forceps were inserted into the bronchoscope working channel to acquire five or more biopsy specimens in the same location and depth indicated by the minprobe.20 In addition, bronchial brushes were introduced routinely to acquire the cytological specimens. The final diagnosis of EBUS‐TBLB was based on the pathological and cytological specimens. All procedures were performed by experienced thoracic surgeons who possessed at least five years of experience in bronchoscopy.
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8

Endobronchial Ultrasound-Guided Navigational Biopsy

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All ENB procedures were performed using the SuperDimensionTM navigation system version 7.1 (Medtronic, Minneapolis, MN, USA). All additional procedural decisions, including choice of biopsy tools (forceps, needle, cytobrushes, bronchial lavage), order of biopsy tool use and use of fluoroscopy (confirmed with frontal images), were performed at the operator’s discretion. In all three centers, intravenous Midazolam and Fentanyl were used for sedation, and all procedures were performed using Olympus (190F) bronchoscopes, rEBUS probes were Olympus UMS20-20R and forceps were Olympus FB-231D.
The location of the lesions (central, middle, peripheral) were recorded based on the definition used in the NAVIGATE study [15 (link)], with peripheral lesions defined as lesions in the peripheral outer third of the lungs and the central lesions located in proximity to the hilum.
All operators used rEBUS as a standardized part of the ENB procedure whenever possible. There was no access to rapid onsite evaluation of cytological material (ROSE). All procedures were performed under conscious sedation and any adverse events related to the procedures were recorded. None of the pulmonologists had access to supervision by experienced ENB operators.
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9

Multimodal Examination of Lung Tumors

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Conventional bronchoscopy (BF-P260F or BF-P290; Olympus, Tokyo, Japan) was initially performed to examine the trachea and bronchi. R-EBUS was then performed using an endoscopic ultrasound center (EU-M30S; Olympus) and a 20-MHz radial ultrasonic probe (UM-S20-20R; Olympus). The R-EBUS probe position was recorded as within or adjacent to the target tumor. After a lesion was located, the radial probe was withdrawn from the working channel of the bronchoscope, and the R-EBUS procedure consisting of transbronchial biopsy, bronchial brushing, and bronchial washing was then performed.
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10

Comparison of EBUS-GS and CT-TTNA for Tissue Sampling

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EBUS-GS was performed using a dedicated endobronchial ultrasonography instrument [Xenon light source: CLV-260SL; endoscopic ultrasound system: EU-ME1; cavity ultrasound probe: UM-S20-17S; UM-S20-20R, Olympus (Olympus Sales Service Co., Ltd., Beijin, China)] after 8 h of fasting. Patients were routinely given glottic local anesthesia with 2% lidocaine.4 (link) General anesthesia was performed for patients who could not tolerate local anesthesia.5 (link) An endoscope was inserted through the nasal cavity or mouth. When lesions were detected, tissues were collected by negative pressure suction (the 20 ml volume negative pressure syringe tube was attached to the back end of the guide sheaths and tissues were collected by negative pressure). CT-TTNA was performed with a SIEMENS 64-slice spiral CT [SOMATOM Definition AS, Siemens Co., Ltd. (Beijing, China)]. Patients received a subcutaneous injection of 2% lidocaine as local anesthesia. After locating the lesions with CT, tissues were obtained via core needle biopsy under negative pressure. Patients in the CT-TTNA group were routinely biopsied with an 80 mm needle; if the lesion from the chest wall was >80 mm but ⩽100 mm, a 100 mm needle was used for biopsy operation.
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