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Iplan cranial v3

Manufactured by Brainlab
Sourced in Germany

Iplan Cranial v3.0 is a software application developed by Brainlab for neurosurgical planning and visualization. It provides tools for analyzing medical images, creating 3D models of the patient's anatomy, and planning surgical procedures.

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2 protocols using iplan cranial v3

1

Retrospective Analysis of GBM Surgical Outcomes

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This retrospective observational study involved 64 patients diagnosed with GBM who underwent surgery at our institution between 1 January 2012 and 1 September 2021. Patients’ data collection included clinical data and all MRI images on pre- and post-operative tumor localization, volume in contrast-enhanced T1 sequences, area volume of FLAIR abnormalities, and the presence of edema. MRI images were acquired through a 3 T scanner (Siemens) 48 h after surgery, and tumor volumes were analyzed via a semiautomatic region of interest (ROI) analysis with Iplan Cranial v3.0 software (Brainlab, Feldkirchen, Germany). The study included patients who had a single surgically removable neoplastic lesion GBM on pre-operative MRI while excluding those with multicentric GBM, other primary neoplastic disorders, metastases, and infectious diseases.
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2

Preoperative and Postoperative MRI Assessment

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Magnetic resonance imaging (MR) with measurement of the pre-and postoperative tumor volumes was done. The lesion volume was measured by means of volumetric MRI acquired through a 3-T MRI scanner (Siemens, Munich, Germany) before surgery through a semiautomatic region of interest (ROI) analysis with Iplan Cranial v3.0 software (Brainlab, Feldkirchen, Germany). Contrast-enhanced T1 sequences and T2 sequences were used to define the preoperative enhancing tumor volume and the interface between normal brain and enhanced areas, respectively. Extent of resection (EOR) was measured on postoperative MRI performed within 48 hours after surgery; postoperative MRI was coregistered with the preoperative dataset. Postoperative diffusionweighted imaging (DWI) was also coregistered to rule out postoperative ischemic injury.
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