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Logiq book xp

Manufactured by GE Healthcare
Sourced in United States, United Kingdom, Germany

The LOGIQ Book XP is a portable ultrasound system designed for general diagnostic imaging. It features a compact and lightweight design with a high-resolution display, enabling healthcare professionals to perform examinations in a variety of clinical settings.

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30 protocols using logiq book xp

1

Real-time Achilles Tendon Ultrasound Imaging

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Real-time ultrasound images (LOGIQ Book XP, General Electric, Bedford, UK) were recorded at 28 Hz using a wide-band linear probe (8L-RS, General Electric) with a 39 mm wide field of view and coupling gel (Ultrasound gel, Dahlhausen, Cologne, Germany) between the probe and skin was used to image the GM-Achilles MTJ (see Figure 2). The probe was positioned perpendicular to the skin with zinc-oxide adhesive tape to ensure consistent imaging of the MTJ during the trials. The distance between the MTJ and distal edge of the ultrasound image was manually digitized (LOGIQ Book XP, General Electric).
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2

Abdominal Ultrasound for Hepatobiliary Assessment

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Abdominal scans were performed using a mobile high-resolution ultrasound-imaging appliance (GE model LOGIQ Book XP), as described43 (link)73 (link). Hepatobiliary abnormalities including periductal fibrosis in liver parenchyma, gallbladder wall, gallbladder size, sludge, and suspected CCA (dilated intra or extrahepatic bile duct and/or liver mass) were graded and recorded34 (link)42 (link). Based on the ultrasonography, grading of periductal biliary fibrosis was assigned as follows: grade 0 = absence of periportal echo(s) from all segments of liver; grade 1 = presence of periportal echo(s) in one segment of liver; grade 2 = periportal echo(s) in two to three segments; grade 3 = periportal echo(s) in more than three segments. Status of infection with liver fluke or presence of species of Helicobacter was not known by the radiologist during the abdominal ultrasonography.
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3

Unilateral Lung Flooding Technique

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Just before USMB, the right lung was flooded by saline. Briefly, a 19G epidural catheter (Vygon, Écouen, France) was inserted between the trachea and the intratracheal tube. The rabbit was positioned on its right side and 9 ml of saline were instilled into the trachea through the catheter. The flooding (and so the condensation) of the right lung but also the absence of flooding of the left lung were verified using lung echography (Logiq Book XP, General Electric Healthcare).
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4

Carotid Intima-Media Thickness Measurement

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Experienced vascular technicians measured carotid intima media-thickness (CIMT) using a LOGIQ Book XP with a 10-MHz transducer (GE Healthcare, Milwaukee, WI, USA). Maximum values for the left and right common carotid arteries of the CIMT were calculated with automated digital edge-detection software (Intimascope; MediaCross, Tokyo, Japan) following a protocol that has been described in detail elsewhere [20 ]. The higher values of right and left CIMT not including plaque measurements were then calculated, and the maximum CIMT value was used for analysis. Since a previous study reported a CIMT value of < 1.1 mm as normal [21 (link)], we defined samples with a CIMT value of ≥ 1.1 mm as atherosclerotic.
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5

Ultrasonographic Assessment of Liver Fibrosis

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A detailed description of the ultrasonography methods used in this study can be found in the following references [8 (link)–10 (link)]. Briefly, a mobile, high-resolution ultrasound (US) machine (GE model LOGIQ Book XP) was used. Hepatobiliary abnormalities including portal vein radical echoes, echoes in liver parenchyma, indistinct gallbladder wall, gallbladder size, sludge and suspected CCA were graded and recorded. Individuals were classified as “Non-Advanced Periductal Fibrosis” (APF-) or “controls” if the US grade was 0 or 1, and “Advanced Periductal Fibrosis” (APF+) or “case” if the US grade was 2 or 3. Individuals with alcoholic liver disease, which is seen as fatty liver by US exam, were excluded from this study. Also, individuals with marked hepatic fibrosis not related to OV infection (e.g., cirrhosis from HBV or HCV) were also excluded from this study (see Fig 1).
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6

Ultrasound Evaluation of Periductal Fibrosis

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A detailed description of the ultrasonography methods used in this study can be found in previous publications (14 (link), 15 (link)). Using a mobile, high-resolution ultrasound (US) machine (GE model LOGIQ Book XP, GE healthcare, WI), hepatobiliary abnormalities including portal vein radical echoes, echoes in liver parenchyma, indistinct gallbladder wall, gallbladder size, sludge and suspected CCA were graded and recorded. Individuals were classified as having “non-advanced periductal fibrosis” or “APF−” if the US grade was 0 or 1, and “advanced periductal fibrosis” or “APF+” if the US grade was 2 or 3. Individuals with alcoholic liver disease, which is seen as fatty liver by US examination, were excluded. Individuals with marked hepatic fibrosis not related to O. viverrini infection (e.g., cirrhosis from HBV or HCV) were also excluded from this study.
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7

Comprehensive Thyroid Evaluation Protocol

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Trained interviewers obtained information on clinical characteristics. Body weight and height were measured with an automatic body composition analyzer (BF-220; Tanita, Tokyo, Japan) to calculate BMI (kg/m2). Systolic blood pressure (SBP) and diastolic blood pressure (DBP) were recorded at rest.
A fasting blood sample was collected. TSH, free T3, and free T4 levels were measured using a chemiluminescent immunoassay (CLIA) at the LSI Medience Corporation (Tokyo, Japan). Normal ranges for free T3 (2.1–4.1 pg/mL), free T4 (1.0–1.7 ng/dL), and TSH (0.39–4.01 μIU/mL) based on this method were reported [12 ]. Hemoglobin A1c (HbA1c), triglyceride (TG), high-density lipoprotein cholesterol (HDLc), and serum creatinine levels were measured using standard procedures at SRL, Inc. (Tokyo, Japan).
The presence of thyroid cysts was determined by experienced ultrasound technicians using a LOGIQ Book XP with a 10-MHz transducer (GE Healthcare, Milwaukee, WI, USA). For the present study, a thyroid cyst was defined as a structure with a maximum diameter of ≥ 2.0 mm and no solid components [5 (link), 8 (link), 9 (link)].
Spot urine dipstick was used to assess for the presence of proteinuria. Proteinuria was diagnosed as +1 or above.
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8

Thyroid Volume Measurement via Ultrasound

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Thyroid volumes were measured using a portable ultrasound instrument equipped with a 10 MHz linear transducer (LOGIQ BOOK XP, GE healthcare, Seoul, Republic of Korea). The examination was performed by a single experienced endocrinologist with two additional persons assisting and record-keeping. The subjects were in the supine position with the hyperextension of neck for examination. The volume of each lobe was calculated using the following formula [18 (link)]: width (cm) × length (cm) × depth (cm) × 0.479. The thyroid volume was then the sum of the volumes of both lobes. Isthmus volume was not taken into account.
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9

Carotid Intima-Media Thickness Measurement

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CIMT was measured by an experienced vascular technician based on ultrasonography of the left and right common carotid arteries using a LOGIQ Book XP with a 10-MHz transducer (GE Healthcare, Milwaukee, WI, USA). Mean values for the left and right CIMT were calculated with automated digital edge-detection software (Intimascope; MediaCross, Tokyo, Japan) according to a previously described protocol [26 (link)]. The values of right and left CIMT, not including plaque measurements, were then calculated, and the mean CIMT value was used for analysis.
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10

Carotid Intima-Media Thickness and Arterial Stiffness Measurement

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Measurements of common CIMT by ultrasonography of the right common carotid artery was carried out using an Ethiroli Tiny‐16a (Surabi Biomedical Instrumentation, Coimbatore, India) in APCAPS, and LOGIQ Book XP with a 10‐MHz transducer (GE Healthcare, Milwaukee, WI, USA) in NaIS. The protocol used has been described in detail elsewhere.13, 15 The mean CIMT was calculated as the mean of right CIMT measurements with carotid plaque excluded. Although AtheroEdge Software in the original APCAPS study and Intima Scope Software (Cross Media, Tokyo, Japan) were used to measure mean CIMT, we re‐evaluated the mean CIMT of APCAPS participants using Intima Scope to avoid the systematic difference of CIMT in the two different types of software.16 Arterial stiffness was evaluated as PWV by the Vicorder system (Skidmore Medical Limited, Bristol, UK) in APCAPS, and cardio‐ankle vascular index (CAVI) by the VaSera system (Fukuda Denshi, Tokyo, Japan) in NaIS.
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