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Sonosite m turbo

Manufactured by Fujifilm
Sourced in United States, Japan

The SonoSite M-Turbo is a compact and portable ultrasound system designed for a variety of medical applications. It features a high-resolution display, intuitive user interface, and advanced imaging capabilities to support clinical decision-making. The SonoSite M-Turbo is a versatile tool that can be used in various healthcare settings.

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54 protocols using sonosite m turbo

1

Lung Ultrasound Assessment of Atelectasis

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Lung ultrasound assessment will be performed by a blinded trained anesthesiologist. As shown in a previous study, ultrasound scanning will select a 5–12 MHz linear transducer (SonoSite M-Turbo) to parallelly scan all the intercostal space of 12 regions from right to left, anterior to posterior of patients’ chest in the supine position [25 (link)]. The six regions are divided by anterior midline, clavicular midline, anterior axillary line, posterior axillary line, and pectoral nipple line in each hemithorax. This anesthesiologist will complete the assessment according to the LUS criteria at the same time as scanning, and the significant images and videos will be recorded.
Atelectasis LUS criteria: 0 indicates normally ventilated areas with lung sliding sign: A-line, or isolated B-lines (< 3); 1 indicates a mild reduction in lung ventilation/moderate loss of lung tissue gasification; B lines (≥ 3) with clear boundary, regular distribution, and spacing ≥ 7 mm, or irregular, clear interval; 2 indicates a severe reduction in lung ventilation/severe lung tissue gasification: multiple coalescent B-lines spaced ≤ 3 mm and continuous fusion; 3 indicates atelectasis/pulmonary consolidation: tissue-like signs, fragment signs, and bronchial inflation signs.
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2

Evaluating Ultrasound Puzzle Phantoms in Medical Education

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We conducted a prospective evaluation of our ultrasound puzzle phantoms using pretests and posttests, obtained by scanning an assessment puzzle phantom, as well as student questionnaires. Data was linked by unique student-created, anonymous identifiers.
This study took place at the Stony Brook University School of Medicine in New York, USA, a suburban allopathic medical school. Medical students in the graduating classes of 2019 (Phase 1) and 2021 (Phase 2) participated.
During Phase 1, four ultrasound machines (Mindray M7, Mindray North America, Mahwah, NJ) were available during each class. Linear 7.5 MHz ultrasound transducers (Mindray 7L4s, Mindray North America, Mahwah, NJ) were used during the practice and assessment scans. During Phase 2, an additional ultrasound machine (SonoSite M Turbo, SonoSite, Inc., Bothell, WA), with linear probe (13-6 MHz, SonoSite, Inc., Bothell, WA) was available.
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3

Ultrasound-Guided Femoral Nerve Block Protocol

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CFNB was performed with patients in the supine position. After the skin was sterilized, a Sonosite M-Turbo (Sonosite, Bothell, WA, USA) 6-13 MHz linear high frequency US probe covered with a sterile vinyl cover and gel was placed at the level of the inguinal crease, and a short-axis US of the femoral nerve was obtained.
The skin was infiltrated with 2–3 ml 1% lidocaine at the puncture site, approximately 2–3 cm lateral to the probe, and an 18-G 10-cm insulated Tuohy needle (Contiplex B®, B. Braun, Melsungen, Germany) connected to the nerve stimulator (Stimuplex®, B. Braun, Melsungen, Germany) was inserted via an in-plane approach under US guidance.
The nerve stimulator was set to 0.5 mA, with a pulse duration of 0.1 ms and stimulation frequency of 2 Hz, and was used to check for contraction of the quadriceps femoris or sartorius muscle. The insertion point for the in-plane approach of the 18-G Tuohy needle was 2–3 cm lateral to the US probe at the level of the inguinal crease.
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4

Ultrasound-Guided Quadratus Lumborum Block

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All blocks were performed after induction of general anesthesia with the patient in the lateral decubitus position. After local sterilization with povidone iodine, a high-frequency (6–13 MHz) linear array ultrasound probe (Sonosite M-turbo, SonoSite, Inc., Bothell, WA, USA) covered with a sterile sheath was placed above the iliac crest and moved cranially until the three abdominal wall muscles were clearly identified. Then, it was slid medially until latissimus dorsi and quadratus lumborum muscles were confirmed within identical short-axis views. A 22-gauge, short-beveled stimulating needle (B. Braun Melsungen AG, Melsungen, Germany) was used for the single-injection block. The needle tip was inserted in-plane with an ultrasound beam targeting the posterior of the quadratus lumborum muscle. Accurate needle tip position was initially readjusted by injecting 1–2 mL of normal saline for hydrodissection image guidance, and 0.5 mL/kg of 0.375% bupivacaine was injected into the lumbar interfascial triangle behind the quadratus lumborum muscle under real-time ultrasound guidance.
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5

Ultrasound-Guided Thoracic Paravertebral Block

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Ultrasound-guided TPVB was performed by one experienced anesthetist with a low frequency (2 ~ 5 MHz) curved array transducer (SonoSite M-Turbo; SonoSite Inc., Bothell, WA, USA). Patients were placed in the lateral position with the side to be operated upwards. Using aseptic precautions, the T4 and T5 paravertebral space was located by counting from the 12th rib to the 4th rib. TPVB was performed at the T4 paravertebral space first. The transducer was placed at an oblique transverse position along the long axis of the rib and tilted until the transverse process, the internal intercostal membrane and the pleura were visualized. After infiltration with 2 ml of 1% lidocaine, a 22-gauge, 120-mm stimuplex needle (Stimuplex® D; B. Braun; Melsungen; Germany) was advanced from lateral to medial with in-plane technique under real-time ultrasound guidance. Once the needle passed through the internal intercostal membrane, 10 ml of 0.4% ropivacaine was injected. Using the same technique, another 10 ml of 0.4% ropivacaine was injected at the T5 paravertebral space.
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6

Echocardiography Analysis of Cardiac Function

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Two-dimensional M-mode echocardiograms were performed under isofluorane anesthesia 24 hours prior to surgery (pre-infarction baseline) and at 48 hours, 4, and 8 weeks after surgery (SonoSite® M-Turbo, Bothell, WA). Percent fractional shortening (FS) was calculated from left ventricular end-diastolic (LVEDD) and end-systolic (LVESD) dimensions as [(LVEDD-LVEDS)/LVEDD]×100.
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7

Ultrasound-Based Brachial Artery FMD Assessment

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Vasomotor endothelial function was assessed after 15 minutes of supine
rest in a 21°C room, using a standard clinical ultrasound-based method to
measure FMD18 (link). High-resolution
ultrasound of the right brachial artery was performed one cm distal to the
antecubital fossa with a 10 MHz linear array probe coupled to a GE Vivid 7
Imaging System and Sonosite M-turbo (FMD studies were performed only at UCSF).
To assess FMD, after recording baseline B-mode ultrasound images of the brachial
artery and spectral Doppler images of flow velocity, a forearm cuff was inflated
to 250 mmHg for five minutes to induce transient ischemia. Immediately after
deflation, Doppler images were obtained to measure reactive hyperemia.20 (link) Digital images for FMD were
analyzed by a blinded investigator with dedicated software (Information
Integrity Inc.; Iowa City, Iowa) and Doppler velocity signal with NIH ImageJ. To
minimize the variation in FMD during the ovarian cycle, menstruating women were
tested during the first 5 days of their menstrual period.21 (link)
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8

Ultrasound-Guided Erector Spinae Plane Block

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Standard technique for the ESPB was performed by the lead investigator. With the cadaver in prone position, a Sonosite M-Turbo (Sonosite Inc., Bothell, WA, USA) ultrasound machine with a high-frequency linear transducer (13–6 MHz) was used to longitudinally scan and identify the sacrum and then moved cephalad to identify the spinous process of L4. The transducer was then moved laterally until the transverse process of L4 with overlying erector spinae muscle plane was identified. A 9 cm, 21 G needle (Arrow StimuQuik ECHO Stimulating and Echogenic Peripheral Nerve Block Needle) was inserted in-plane in a caudocranial direction until it was visualized contacting the dorsal surface of the transverse process of L4. A solution consisting of 1 ml of methylene blue and 19 ml of 0.25% bupivacaine was used to more closely approximate injectate used during ESPBs. The 20 ml solution was slowly injected, over approximately 30 s, under direct ultrasound visualization to confirm spread deep to the erector spinae muscle fascial plane (Fig. 1). The procedure was then repeated on the contralateral side.

In-plane ultrasound-guided erector spinae plane block at the transverse process of L4 with highlighted area of injectate spread

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9

Evaluating Back Muscle Activation and Morphology

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Each participant underwent rest and maximum isometric contraction measurements of EMG signals of the DM using the sEMG system, and muscle thickness and cross-sectional area measurement using ultrasound (SonoSite M-Turbo, Seattle, USA). Participants underwent measurements in randomly-assigned order, and the assessment lasted approximately 40 mins. Participants were told to maintain back muscle contractions during the task, and each subject was familiarized with MVIC of the DM during Biering-Sorensen testing. A single practice was performed prior to measurements being recorded.
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10

Carotid Ultrasound for Intima-Media Thickness

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Carotid ultrasound for evaluation of IMT was performed using the SonoSite M-Turbo portable ultrasound device (SonoSite, Bothell, WA, USA) coupled to a 5- to 10-MHz multifrequency high-resolution linear transducer. SonoCalc software (SonoSite) was used for calculation of mean IMT values. The measurements were obtained with the subject lying down, with the head extended and slightly turned opposite to the examined carotid. Measurements were made of the common carotid artery after the examination of a longitudinal section of 10 mm at a distance of 1 cm from the bifurcation. The measurements were performed in the far wall in the lateral, anterior and posterior projections. The within- and between-observer CVs for mean IMT were 2.2 % and 5.9 %, respectively.
A standard deviation score (SDS) of IMT for each subject was calculated using height-specific IMT normative values published by Jourdan et al. [25 (link)].
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