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Summary of the telephone interviews.

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posted on 2023-11-08, 18:26 authored by Elisabeth Sartoretti, Selina Largiadèr, Thomas Sartoretti, Simin Laures, Martin Alexander Walter, Eva Monti, Ina Füchsel, Mira Dettling, Stephan Pfister, Peter Dubsky, Alexander Ort, Sabine Sartoretti-Schefer, Matthias Meissnitzer, Klaus Hergan, Rosemarie Forstner, Simon Matoori, Rasmus Bech- Hohenberger, John M. Froehlich, Tino Plümecke, Dorothee Harder, Dow Mu Koh, Andreas Gutzeit

Introduction

A trend towards less male radiologists specializing in breast ultrasound was observed. A common notion in the field of breast radiology is, that female patients feel more comfortable being treated by female radiologists. The aim of the study was to understand and report the needs of women undergoing breast ultrasound with regards to the sex of the radiologist performing the investigation.

Methods

Informed consent was obtained from all patients prior to inclusion in a prospective bi-center quality study. At center 1 (72 patients), the women were examined exclusively by female radiologists, at center 2 (100 patients) only by male radiologists. After the examination the patients were asked about their experiences and their wishes for the future.

Results

Overall, women made no distinction between female and male radiologists; 25% of them wanted a female radiologist and 1.2% wanted a male radiologist. The majority (74%) stated that it made no difference whether a female or male radiologist performed the examination. The majority of women in group 2, who were investigated exclusively by male radiologists, stated that they had no preferences with regard to the sex of the radiologist (93%); 5% of the women wished to be investigated solely by a female radiologist and 2% exclusively by a male radiologist.

Discussion

The majority of women undergoing breast ultrasound are unconcerned about the radiologist’s sex. It would appear that women examined by male radiologists are less selective about the sex of the examining radiologist.

Trial registration

Written informed consent was obtained from all patients. All patient data were anonymized. The physicians had no access to any further personal data. National regulations did not require dedicated ethics approval with anonymized lists or retrospective questionnaires.

History