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Communication Between Japanese Patients With Hereditary Breast and Ovarian Cancer and Healthcare Providers on Sexual Health After Risk-Reducing Bilateral Salpingo-Oophorectomy.

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第一作者： Manami,Matsukawa

第一单位： Department of Genetic Medicine and Service, National Cancer Center Hospital, Tokyo, Japan.;Department of Healthcare Ethics, Kyoto University School of Public Health, Kyoto, Japan.

作者： Manami,Matsukawa ^[1] ; Eri,Habano ^[2] ; Masako,Torishima ^[3] ; Makiko,Dazai ^[4] ; Makoto,Hirata ^[5] ; Shinji,Kosugi ^[6]

作者单位： Department of Genetic Medicine and Service, National Cancer Center Hospital, Tokyo, Japan.;Department of Healthcare Ethics, Kyoto University School of Public Health, Kyoto, Japan. ^[1] Department of Healthcare Ethics, Kyoto University School of Public Health, Kyoto, Japan.;Department of Clinical Genetics Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.;Division of Integrative Genomics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan. ^[2] Department of Genomic Medicine, Kyoto University School of Public Health, Kyoto, Japan.;Department of Clinical Genetics Units, Kyoto University Hospital, Kyoto, Japan. ^[3] Nonprofit Organization, Clavis Arcus, Association of Patients for Hereditary Breast and Ovarian Cancer Syndrome (HBOC), Tokyo, Japan.;Genetic Alliance JP, General Incorporated Association, Tokyo, Japan. ^[4] Department of Genetic Medicine and Service, National Cancer Center Hospital, Tokyo, Japan. ^[5] Department of Healthcare Ethics, Kyoto University School of Public Health, Kyoto, Japan.;Department of Genomic Medicine, Kyoto University School of Public Health, Kyoto, Japan.;Department of Clinical Genetics Units, Kyoto University Hospital, Kyoto, Japan. ^[6]

关键词 communication tool health communication hereditary breast and ovarian cancer risk‐reducing bilateral salpingo‐oophorectomy sexual health