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Cv 170

Manufactured by Olympus
Sourced in Japan

The CV-170 is a compact and versatile video processor designed for use in medical and surgical environments. It provides a high-quality video signal from endoscopic and other imaging devices, enabling clear visualization during procedures. The CV-170 offers a range of video output options and supports various image enhancement features to optimize image quality.

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6 protocols using cv 170

1

Assessing Laryngeal Obstruction During CPET

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CPET in the PDA-surgery group was performed with concomitant continuous transnasal flexible video-laryngoscopy (ENF TYPE V2, video processor CV-170, OLYMPUS, Tokyo, Japan) as described previously (22 (link)). LVCP was identified and later verified by laryngeal stroboscopy. The video recordings of the laryngeal inlet during treadmill running were assessed and rated for laryngeal obstruction according to a modified version of the classification described by Maat et al. (23 (link)). Because of laryngeal asymmetry in subjects with LVCP, a modified CLE-score (0–24 points) was developed, assessing the right and left glottic and supraglottic areas separately. The visually assessed medial rotation of the aryepiglottic folds and medialization of the vocal folds were scored ranging from normal (0 points) to maximal (3 points) at moderate (fast walking) and at maximal effort. The left and right sides were scored separately. The total modified CLE-score was the sum of the sub-scores at moderate and maximal exercise.
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2

Evaluating AI-Assisted Colonoscopy System

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We retrospectively reviewed colonoscopy reports and corresponding videos of our randomized controlled trial’s pilot phase data. Here, examiners with at least 10 years of experience in performing colonoscopies were asked to evaluate EndoMind before starting the randomized study phase (NCT05006092). Only complete video recordings were included. The evaluated video recordings originate from four different endoscopy processors (Olympus CV-170 and CV-190 (Olympus Europa SE & Co. KG, Hamburg, Germany), Pentax i7000 (Pentax Europe GmbH, Hamburg, Germany), and Storz TC301 (Karl Storz SE & Co. KG, Tuttlingen, Germany)). Centers included three outpatient gastroenterological practices and one community-based hospital.
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3

Continuous Laryngeal Evaluation During CPET

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Continuous laryngoscopy was performed during the CPET using a transnasal flexible video-laryngoscopy (ENF TYPE V2, video processor CV-170; OLYMPUS, Tokyo, Japan) as described previously [31 (link)]. Laryngeal obstruction during treadmill running was assessed and rated according to a modified version of the classification described by Maatet al. (Figure 1) [13 (link)]. Laryngeal obstruction on either glottic or supraglottic level at moderate and maximum exercise was rated from 0 to 3 at each level, giving a score ranging from 0 to 12 (CLE score). CLE test recordings were evaluated blinded in retrospect by two experienced reviewers (O.D. Røksund and H.H. Clemm), and disagreements were resolved by consensus.
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4

Transnasal Endoscopic Assessment of Laryngeal Lesions

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Our outpatient clinic is equipped with a video rhinolaryngoscope and built-in NBI technology (CV-170; Olympus Medical System, Tokyo, Japan). The endoscopic examination was performed by a single experienced otolaryngologist with the patient in supine position. During the exam, a button allowed switching from white light endoscopy (WLE) to NBI. Ecocain®, (Molteni Dental srl, Milan, Italy) Lidocaine, 10 g/mL; dose: 2 sprays was administered 15 min before the procedure. Transnasal endoscopic images were reproduced on a 1080 p monitor and all exams were recorded for remote replay and review by a second examiner. Lesions assessed in WLE were classified as benign (0), uncertain (1) or clearly malignant (2), depending on the opinion of each examiner. Using NBI, laryngeal lesions were categorized according to the classifications proposed by Ni et al. [6 (link)] as follows: (0) non-malignant (pattern type I and II); (1) suspected leucoplakia and high-grade dysplasia or carcinoma (pattern type III, IV and V). In case of concordance between diagnoses of the two examiners, the lesion was classified as described. In case of disagreement, both examiners reviewed the video of the endoscopy again and a joint diagnosis was expressed.
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5

Fiberoptic Endoscopic Evaluation of Swallowing

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All patients underwent FEES. Equipment consisted of a 3.9‐mm‐diameter (ENF‐VH, Olympus, Shinjuku, Japan) or 3.5‐mm‐diameter (Storz 11101 RP2, Karl Storz, Tuttlingen, Germany) flexible fiberoptic rhinolaryngoscope with a video processor (CV‐170, Olympus, Shinjuku, Japan), and processing software (rpSzene 10.7 g on Panel‐PC‐226/227, Rehder/Partner, Hamburg, Germany), or a 2.9‐mm‐diameter flexible fiberoptic rhinolaryngoscope (CMOS, Karl Storz, Tuttlingen, Germany) with a portable video processor (CMAC, Karl Storz, Tuttlingen, Germany) linked to a 19" flat screen monitor (9519NB, Karl Storz, Tuttlingen, Germany). FEES was performed as previously described.14
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6

Etomidate and Remazolam for Gastroenteroscopy

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All patients need regular fasting for 12 hours and drinking for 8 hours before examination. Lateral prone position is taken, oxygen is inhaled by nasal catheter at 3.0 L/min, and ECG and heart rate are monitored by DASH4000 multifunctional monitor (GE). In the single-drug group, 0.9% normal saline is injected, and etomidate (Jiangsu Hengrui Pharmaceutical Co., Ltd., Production lot no. 20171015) is injected 2 min later at a rate of 0.2 mg/(kg/min). On the basis of the single-drug group, anesthesia induction is performed with remazolam (Jiangsu Hengrui Pharmaceutical Co., Ltd., Batch No. 200725) at 12 mg/(kg/h), and anesthesia is maintained at 1.0-2.0 mg/(kg·h). After the patient's consciousness disappeared, gastroenteroscopy (Olympus, Japan, model: CV-170) is performed. According to the patient's physical reaction during the examination, 4–6 mg etomidate is added appropriately. After the gastroenteroscopy reached the ileocecal area, the administration is stopped.
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