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Logiq e9 ultrasound

Manufactured by GE Healthcare
Sourced in United Kingdom

The Logiq E9 is an ultrasound system designed for general diagnostic imaging. It provides high-resolution imaging capabilities for a variety of clinical applications.

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6 protocols using logiq e9 ultrasound

1

Partial Thermal Ablation of Tumors

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Rats were randomized to thermal ablation (N=6) or sham ablation (N=6). All ablation experiments were performed using an FDA-approved 980-nm laser generator (Visualase, Houston, TX) (26 (link),27 (link)). Under ultrasound-guidance (logiq E9 Ultrasound, GE Healthcare), a bare 400μm core optical laser fiber with a 1.0 cm diffusing tip was inserted at the tumor margin. For the ablation group, tumors were ablated at a power setting of 3 watts for 45 seconds under continuous US-monitoring in order to generate an intentional partial ablation. The laser was not activated for sham-ablated animals.
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2

Partial Laser Ablation of Orthotopic HCC in Rats

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All studies were approved by the institutional animal care and use committee (IACUC). The N1S1 orthotopic HCC model was developed as previously described (n = 8) [41 (link)]. Rats were randomized to ultrasound (US)-guided partial laser ablation (n = 5) or sham laser ablation (n = 3) using methods previously described [41 (link)]. Briefly, all ablation experiments were performed using an US Food and Drug Administration-approved 980-nm laser generator (Visualase, Houston, TX). Under ultrasound guidance with an L8-18i transducer (logiq E9 Ultrasound, GE Healthcare), a bare 400-μm core optical laser fiber with a 1.0-cm diffusing tip was percutaneously inserted through a 22-gauge introducer sheath at the tumor margin, and a 22-gauge needle with a 25-gauge wire thermocouple (Valleylab, Boulder, CO) was inserted 4–5 mm from the laser fiber tip within the tumor for intraprocedural temperature monitoring. For the ablation group, tumors were ablated at a power setting of 3 W under continuous US monitoring, and the ablation stopped when the thermocouple reached 45 °C in order to generate an intentional partial ablation. The laser was not turned on for sham-ablated animals. Rats were euthanized by CO2 inhalation 24 h after laser or sham ablation.
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3

Prostatic Calcifications: Ultrasound Assessment

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All patients underwent TRUS (Pro Focus 2202 Ultrasound System, BK-Medical, Herlev, Denmark; and LOGIQ E9 Ultrasound, GE healthcare, Tampa, FL, USA). Total prostate volume was calculated using the prolate ellipsoid formula (height × width × length × π/6).11 (link)
Prostatic calculi were viewed and scored in both axial and sagittal planes. Two investigators (DGL and SHY, each with ≥5 years of TRUS experience) independently assessed prostatic calculi. Disagreements between these two investigators were resolved by discussion with another investigator (SK), Senior Professor of Urology at Chonnam National University Hospital. In accordance with the definition of PUC suggested by Han et al.,9 (link) we defined PUC as prostatic calcification within 2 mm of the prostatic urethra on the midsagittal plane during TRUS. According to its location, PUC was categorized into one of the three types: proximal (proximal third of prostatic urethra), middle (middle third of prostatic urethra), and distal (distal third of prostatic urethra), as shown in Figure 1. PUC was also categorized into one of the four types according to its severity: none, mild (1–2), moderate (3–5), and severe (>5), as shown in Figure 2.
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4

Fetal Growth Restriction Doppler Assessment

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All pregnancies complicated by FGR underwent complete fetal sonographic assessment of both anatomy and Doppler evaluation as part of the study protocol on the same day as the MRI study using a LOGIQ E9 ultrasound scanner (GE Healthcare, WI). Abdominal circumference, head circumference, femur length and estimated fetal weight were measured and plotted according to gestational age GA (15 (link)). Fetal middle cerebral (MCA) and umbilical arterial (UA) flow velocities were measured using a pulse-wave Doppler, and pulsatility indices (PI) were calculated. The cerebroplacental ratio (CPR) was calculated by dividing the middle cerebral artery pulsatility index by the umbilical artery pulsatility index (27 (link)). Subjects were classified into the sub-group of abnormal Doppler studies if the CPR was less than 1 (28 (link)). All sonographic studies were reviewed by a single attending radiologist as per institutional protocol.
Healthy control pregnancies underwent complete fetal echocardiographic assessment using a Vivid 7 ultrasound scanner (GE Healthcare, Waukesha, WI) as part of an adjunct prospective study. Fetal middle cerebral and umbilical arterial flow velocities were measured using a pulse-wave Doppler; pulsatility indices, CPR and z-scores (derived from normal references) were calculated (28 (link)).
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5

In ovo Ultrasound Evaluation of Tumor

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On day 14 of incubation, after 240 s of cumulated CAP or sham treatment, in ovo ultrasonography was performed to assess tumor volume and vasculature as previously described by our working group [35 (link)]. The GE Healthcare Ultrasound LOGIQ E9 (GE Healthcare, Little Chalfont, UK) 15 MHz linear transducer was used in B-Mode (Gain 35) for ultrasonographical imaging. The space between the CAM and shell opening was filled with an average of 4 mL NaCl 0.9% (w/v) to allow transduction of ultrasound waves. Tumors were visualized in both longitudinal and transversal axes to enable a consistent assessment of the tumor tissue. The respective images were frozen using the “Freeze” function and sagittal, transversal, and coronar tumor diameters were documented. Tumor volume was calculated by using the triaxial ellipsoid formula:
Intratumoral hemorrhages, resembled by areas of low echogenicity in the tumor tissue, were evaluated. The NaCl solution was removed after each measurement using an electrical pipette (INTEGRA Biosciences GmbH, Biebertal, Germany) with a 10 mL sterile tube (Greiner CELLSTAR® serological pipette, Greiner AG, Bischofsheim, Germany).
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6

Tumor Growth Quantification using Ultrasound

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Starting from day 12 of incubation (5 days after tumor inoculation) the GE Healthcare Ultrasound LOGIQ E9 (GE Healthcare Little Chalfont, UK) 15 MHz linear transducer was used in the B-Mode (Gain 35) for ultrasonographic imaging (Fig. 1). Instead of ultrasound gel the space between the CAM and shell opening was lled with an average of 4 ml Sodium chloride (NaCl) 0.9% to allow transduction of ultrasound waves. Tumors were then visualized in both longitudinal and transversal axes to enable a three-dimensional quanti cation of the tumor size. The respective image was frozen using the "Freeze" function and the tumor length, width and thickness was measured and documented.
Color-duplex-sonography was carried out using the same methodology while the built-in Duplex mode enabled visualization of the vessels within the tumor. Video sequences were saved for o ine analysis.
For repetitive measurements, the same procedure was carried out on days 12, 13, and 14 respectively. The NaCl 0.9% solution was removed after each measurement using an electrical pipette (INTEGRA Biosciences GmbH, Biebertal, Germany) with a 10 ml sterile tube (Greiner CELLSTAR® serological pipette, Greiner AG, Bischofsheim, Germany)
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