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Artis zeego and pheeno scanners

Manufactured by Siemens
Sourced in Germany

The ARTIS Zeego and Pheeno scanners are medical imaging systems manufactured by Siemens. The ARTIS Zeego is a multi-axis C-arm system designed for interventional radiology procedures, while the Pheeno is a mobile diagnostic imaging scanner. Both products are intended for use in healthcare settings, but their specific intended uses are not included in this factual, unbiased description.

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Lab products found in correlation

2 protocols using artis zeego and pheeno scanners

1

Intraoperative Radiation Exposure in Surgery

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Radiation dose, time from induction to incision, placement of T‐bar to incision, incision to closure, hospital stay, and complication rates were recorded. The total skin dose (expressed in mGy) was used as a measure of radiation exposure. Skin dose data were collected from the “‘Exam Protocol”’ of the ARTIS Zeego and Pheeno scanners (Siemens Healthineers, Germany). Comparison was performed with outcomes of the clinical phase I and II trial (NCT01847209). Statistical analyses were using performed using JMP Pro software (version 14, Cary, NC). Descriptive statistics are reported as median (range) for continuous data and as number (%) for categorical data. The Kruskal–Wallis test was used to compare the outcomes with those from the clinical trial. The Pearson correlation coefficient was used to investigate the association between the procedure time and the surgeon's experience. All P‐values were two‐tailed, with P < .05 being considered statistically significant.
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2

Radiation Exposure in Robotic Breast Surgery

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Radiation dose, time from induction to incision, placement of T-bar to incision, incision to closure, hospital stay, and complication rates were recorded. The total skin dose (expressed in mGy) was used as a measure of radiation exposure. Skin dose data were collected from the “‘Exam Protocol”‘ of the ARTIS Zeego and Pheeno scanners (Siemens Healthineers, Germany). Comparison was performed with outcomes of the clinical phase I and II trial (NCT01847209). Statistical analyses were using performed using JMP Pro software (version 14, Cary, NC). Descriptive statistics are reported as median (range) for continuous data and as number (%) for categorical data. The Kruskal–Wallis test was used to compare the outcomes with those from the clinical trial. The Pearson correlation coefficient was used to investigate the association between the procedure time and the surgeon’s experience. All P-values were two-tailed, with P < .05 being considered statistically significant.
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