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Logiq p6

Manufactured by GE Healthcare
Sourced in United States, United Kingdom

The LOGIQ P6 is a portable ultrasound system designed for general imaging applications. It offers high-quality imaging performance and a compact, lightweight design for easy mobility.

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24 protocols using logiq p6

1

Ultrasound Assessment of Vastus Lateralis

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A 7.5 MHz ultrasound probe (LOGIQ P6, General Electric Healthcare, Wauwatosa, WI, USA) was used to measure CSA, MT, FL, and PA of the vastus lateralis (VL). Measurements were taken in a standing position as described by Wagle et al. [49 (link)], as this position has been shown to correlate better with both isometric and dynamic performance. The tester identified and marked 50% of the distance between the greater trochanter and the lateral epicondyle of the right leg. Three MT images were then taken five centimeters anteromedial to the mid-femur mark. The best image from the three was selected for analysis, and the mean of three MT and PA measurements was taken from the first, second, and third portions of the image. Three CSA images were attained by using a panoramic image sweep perpendicular to the VL muscle at the mid-femur mark. CSA was then determined by selecting two out of the three images that best displayed the region of interest and using an image processing software (ImageJ 1.52a, National Institutes of Health, Bethesda, MD, USA) to trace the intermuscular area (Figure 3a). Lastly, FL was estimated by calculating MT∙sin(PA)−1 (Figure 3b). The US technician remained the same throughout all five testing sessions, and all images were analyzed by a single researcher on the same computer.
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2

Cross-Sectional Area Assessment of Lower Limb Muscles

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Prior to performing the warm-up and 1RM back squat protocol, CSA measurements of the participants’ right vastus lateralis (VL) and biceps femoris (BF) muscles were assessed using a linear probe scanning head with a 3.4–10.8 MHz bandwidth range (LOGIQ P6, GE Healthcare, Wauwatosa, WI, USA). The probe was coated with a water soluble transmission gel (Aquasonic 100 ultrasound transmission gel, Parker Laboratories, Inc., Fairfield, NJ, USA) and positioned on the surface of the skin to provide acoustic contact without depressing the dermal layer to collect an image. The CSA images for the VL and BF were obtained using a sweep of the muscle in the extended field of view mode with the gain set to 50 dB and an image depth to 5 cm. For the VL CSA measurements, participants laid on an athletic training table on their left side with their legs together and relaxed with 15° of knee flexion as measured by a manual goniometer [24 (link)]. For the BF CSA measurements, participants laid in a prone position with their feet hanging off the end of the athletic training table. The anatomical location for all CSA measurements was standardized for all participants. VL CSA was measured at 50% of the distance between the greater trochanter and the lateral condyle of the tibia. BF CSA was measured at 50% of the distance between the ischial tuberosity and the posterior aspect of the fibular head.
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3

Renal Cortical Perfusion Measurement

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We used the Logiq P6 (GE Healthcare, Seoul, Korea) ultrasound equipment with a 4 L (2–5 MHz) convex transducer to scan and record 3–5 s of color Doppler clips showing renal cortical blood flow, as it was described earlier [18 (link)]. Clips were assessed in the medical device (PixelFlux, Chameleon Software, Leipzig, Germany). Then the average intensity of arterial cortical blood flow as the renal cortical perfusion (RCP) [cm/s] and renal cortical arterial area (RCAA) [cm2] were estimated [19 (link),20 (link)].
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4

Renal Resistive Index Measurement Protocol

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First, the flow velocities in the aorta and renal arteries were evaluated to rule out morphological abnormality or renal artery stenosis. Second, the renal RI was determined in the interlobar arteries of both kidneys and expressed as the mean of these values. The digital diagnostic ultrasound systems used were the Aplio XG SSA-790A with a PVT-375BT convex array transducer (Toshiba Medical Systems, Otawara, Tochigi, Japan) operating at a frequency of 3.5 MHz, and the LOGIQ P6 with a 4C convex array transducer (GE Medical Systems, Milwaukee, WI, US) operating in the frequency range of 4.0 MHz to 5.5 MHz. The ultrasound examinations were performed by two well-trained technicians. Renal RI was calculated as follows (Figure 1):

Example of renal resistive index measurement. Pulsed Doppler ultrasonography was obtained in the intra-renal artery at the level of the corticomedullary junction. Renal resistive index is measured as {peak systolic velocity (a) - end diastolic velocity (b)} / peak systolic velocity (a).

RenalRI = (peak systolic velocity − end diastolic velocity)/peak systolic velocity [22 (link),23 (link)].
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5

Diaphragm Thickness in Myotonic Dystrophy

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The patients included to the study were diagnosed with DM1 based on molecular studies at the Neuromuscular Diseases outpatient clinic of Çukurova University Faculty of Medicine, Department of Neurology. Up-to-date information and previous test results of the patients received from the supervisor of Neuromuscular Diseases clinic. Age, sex, body mass index (BMI), age of onset (AO), and disease duration (DD) of the patients were recorded. Pulmonary function tests (PFT) were performed with CareFusion micro RPM device. Diaphragm thickness was measured in B-mode ultrasonography (USG) (GE, logiq P6) with a high frequency (8–12 mHz) using linear transducer at the end of the inspiration and expiration. The thickness was measured from the two echogenic lines (peritoneal line and pleural line).
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6

Carotid Intima-Media Thickness Measurement

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A single experienced vascular sonographer, who was blind to the clinical and laboratory data of the study subjects, performed all imaging studies. The images were obtained using a General Electric medical ultrasonographic machine (model: GE LOGIQ P6) equipped with a 7.5–10 MHz linear-array transducer. Imaging of the carotid arteries was performed at the radiology department at Abo el Rish Cairo University by a specialized pediatrics hospital, the subject resting in the supine position with his/her neck extended, and the head turned 45° toward the contralateral side. A transverse section of the common carotid artery was imaged first to screen for any atheromatous plaques and then a longitudinal section at the middle third of the common carotid artery was imaged to achieve a consistent site of measurement. Generally, images are recorded in the plane where the maximal CIMT can be visualized. Magnification of the vessel wall allows easy identification of the intima-medial complex, defined by the border between the echolucent vessel lumen and the echogenic intima and the border between the echolucent media and echogenic adventitia.
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7

Breast Tumor Ultrasound Imaging Protocol

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All the patients were examined using a GE machine LOGIQ P6 with a linear probe 3.42–13 MHz; the patient was in both supine and sitting position with the arm of the examined side put over the head to expose axilla. The examination was carried out both radially and anti-radially to cover all ducto-lobular components, the mass is further analyzed regarding the site, the longest diameter of the mass in cm, echogenicity, shadowing, calcification, and borders. If there is an echogenic halo surrounding the tumor (i.e., desmoplastic reaction), it will be included in the measurement. Then, color Doppler is used to assess the vascularity of the mass. In our study, the largest mass dimension is taken and compared with the largest size taken by the post-operative pathology report; the result of pathology is divided into pathological categories including invasive ductal carcinoma (IDC), ductal carcinoma in-situ (DCIS), invasive lobular carcinoma (ILC), and others (tumors had to be excised for some reason and proved to be fibrocystic disease, ductal hyperplasia, medullary carcinoma, hemorrhage, and fibroadenoma).
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8

Sonographic Grading of Salivary Glands

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SGUS was performed by the same investigator, an experienced radiologist, using a real-time scanner (Logiq P6; GE Healthcare, Waukesha, WI, USA) with a 12-MHz linear array transducer. Both the parotid and submandibular glands were scanned and echostructure of each gland was graded on a scale of 1 to 4. According to this scale, grade 1 = small hypoechogenic areas without echogenic bands, grade 2 = multiple hypoechogenic areas measuring < 2 mm with echogenic bands, grade 3 = multiple hypoechogenic areas measuring 2–6 mm with hyperechogenic bands, and grade 4 = multiple hypoechogenic areas measuring > 6 mm or multiple calcifications with echogenic bands [12 (link)]. Each patient received one score per gland and the highest score obtained was considered in the analysis.
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9

Ultrasound-Guided Adductor Canal Block

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The patients in the ACB group received an ultrasound-guided single-shot ACB, based on earlier studies.[18 (link),19 (link)] ACB was performed at mid-thigh (midpoint between the knee and the inguinal crease) by the lead author with ultrasound equipment (Logiq P6, GE Healthcare, Buckinghamshire, UK) using a 10 to 13 Hz high-frequency linear ultrasound transducer which was placed transverse to the longitudinal axis of the leg. Underneath the sartorius muscle, the saphenous nerve was identified in a short axis view as it descends lateral to the femoral artery in the adductor canal. The lead author injected 9 mL of 1% of lidocaine and 1 mL of 10 mg triamcinolone acetonide with a 23-gauge 6-cm long needle.
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10

Ultrasound-Guided Anesthetic Injection for Forearm Tendon Procedures

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We enrolled 8 consecutive patients who underwent tendon transfer or tendon graft surgery at the forearm in our department from February 2013 to April 2014. Three of the 8 patients underwent tendon graft or tendon transfer for flexor tendon injuries in zone 4 or 5, 3 underwent opponensplasty of the thumb for carpal tunnel syndrome, and 2 underwent tendon transfer according to Brand’s procedure for posterior interosseous nerve palsy. Each patient underwent ultrasound-guided anesthetic injection 1 hour before surgery. The peripheral nerves in the upper extremities were examined using an ultrasound unit (LOGIQ P6; General Electric, Fairfield, Conn.) with a 16-MHz linear matrix probe. A 23-gauge, 70-mm needle was used for injection. All cutaneous nerves were carefully blocked using the in-plane method of ultrasound guidance. We selected one of the several injection patterns depending on the operative procedure performed. The anesthetic method used for each procedure is described below.
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