Risk-reducing oophorectomy for women with no personal history of breast cancer
- risk-reducing bilateral oophorectomy is appropriate only for a small proportion of women who are from high-risk families and should be managed by a multidisciplinary team
 - women considering risk-reducing bilateral oophorectomy should be informed of possible psychosocial and sexual consequences of the procedure and have the opportunity to discuss these issues
 - women not at high risk who raise the possibility of risk-reducing bilateral oophorectomy should be offered appropriate information, and if seriously considering this option should be offered referral to the team that deals with women at high risk
 - women undergoing bilateral risk-reducing oophorectomy should have their fallopian tubes removed as well
 
Breast cancer risk category
 |  |  |  | 
Lifetime risk from age 20  |  | Greater than 17% but less than 30%  |  | 
Risk between ages 40 and 50  |  |  |  | 
*This group includes known BRCA1, BRCA2 and TP53 mutations and rare conditions that carry an increased risk of breast cancer such as Peutz-Jegher syndrome (STK11), Cowden (PTEN) and familial diffuse gastric cancer (E-Cadherin)
Notes:
- HRT for women with no personal history of breast cancer who have a bilateral salpingo-oophorectomy before the natural menopause 
- when women with no personal history of breast cancer have either a BRCA1 or BRCA2 mutation or a family history of breast cancer and they have had a bilateral salpingo-oophorectomy before their natural menopause, offer them: 
- combined HRT if they have a uterus
 - oestrogen-only HRT if they don't have a uterus
 - up until the time they would have expected natural menopause (average age for natural menopause is 51-52 years)
 
 - manage menopausal symptoms occurring when HRT is stopped in the same way as symptoms of natural menopause
 
 
Reference: