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Voluson v730 expert

Manufactured by GE Healthcare
Sourced in Germany, United States

The Voluson-V730 Expert is a diagnostic ultrasound system designed for obstetric and gynecological examinations. It features advanced imaging technologies and a user-friendly interface to support clinical decision-making.

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4 protocols using voluson v730 expert

1

Transvaginal Ultrasound for Adnexal Mass Evaluation

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All transvaginal ultrasonography was performed in the same hospital by two trained ultrasonographers (MR, CR), using a microconvex endocavity probe (type RIC5-9, Voluson-V730 Expert; GE, Munich, Germany). The examinations were interpreted in real-time. Adnexal masses were evaluated and interpreted according to the IOTA group directions and were classified according to the simple rules for ovarian masses described by this group.6 (link)Level of risk assessed by transvaginal ultrasonography and tumor biomarker levels were compared between the three groups.
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2

Assessing Ovarian Sonographic Variables

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Sonographic variables for each ovary were assessed by an expert sonographer (CR), who was blinded to the treatment allocation, and assessments were performed within 30 days prior to surgery, and at 3 and 6 months after surgery. For AFC determination, the total number of antral follicles with a mean diameter of 2–9 mm was counted. Ovarian volume was calculated using the prolate ellipsoid formula (length × width × height × 0.523).
All transvaginal ultrasound examinations were carried out using a microconvex endocavity probe (type RIC5-9, Voluson-V730 Expert; GE Medical systems, Munich, Germany).
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3

Comprehensive Ultrasound Assessment of Adenomyosis and Endometriosis

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All patients underwent high resolution 2D-3D TVUS using an endovaginal probe (type RIC5-9, Voluson V730 Expert, GE Healthcare, Milwaukee, WI, USA) and received bowel preparation to improve DE identification and measurement, as previously described following the protocol of our center25 (link). The exam was performed by two expert sonographers (CR, MR), who were not aware of the patient’s participation in the study, and the diagnoses of AD and END were established following the Morphological Uterus Sonographic Assessment (MUSA) group consensus23 (link) for AD and the International Deep Endometriosis Analysis (IDEA) group consensus24 (link) for END. Regarding AD, one point was given for the presence of each of the 6 following MUSA criteria: intramyometrial cysts, hyperechoic islands, fan-shaped shadowing, asymmetrical thickening, translesional vascularity and interrupted junctional zone23 (link), requiring at least the presence of two criteria for establishing a diagnosis of AD23 (link),27 (link). The variables studied regarding END were the presence and size (mean of both maximum diameters, expressed in millimeters) of OE and rectosigmoid DE, uterosacral ligaments (USL) DE, torus, vaginal, ureteral, and vesical DE24 (link).
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4

Radiotracer Injection for Uterine Mapping

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As previously described, [99mTc] Tc-Nanocolloid (Nanocoll®; GE Healthcare, Saluggia, Italy) was injected into the myometrium guided by transvaginal ultrasound imaging 18 to 24 hours prior to surgery, with the patient awake after the application of local anesthesia [12 (link)]. The volume injected ranged from 4 to 8 mL, and the dose was of 3 to 6 MCi [14 ]. The Aspen (Siemens-Acuson Inc., Mountain View, CA, USA) or Voluson (Voluson v730Expert; General Electric, Frankfurt am Main, Germany) ultrasound imaging devices, equipped with a 4–9 MHz 2D vaginal probe with an attached needle guide, were used for the injection. In an anteverted uterus, a 20-gauge biopsy needle (Gallini Medical Devices, Mantova, Italy) crossed the anterior wall to inject half of the volume in the posterior wall. The remaining volume of radiotracer was injected into the anterior myometrial wall (Fig. 1). Once the radiotracer was administered, the needle was flushed with saline solution. In a retroverted uterus, the injection of radiotracer was first performed into the anterior uterine wall and secondly into the posterior uterine wall [12 (link)]. All the procedures were performed by experienced gynecological sonographers together with nuclear medicine physicians. Tolerance to the procedure was assessed using a visual analog scale (range 0–10; no pain to severe pain).
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