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Oophorectomy
View on Wikipedia| Oophorectomy | |
|---|---|
| ICD-10-PCS | 0UB00ZX - 0UB28ZZ |
| ICD-9-CM | 65.3-65.6 |
| MeSH | D010052 |
Oophorectomy or Oöphorectomy (/ˌoʊ.əfəˈrɛktəmi/; from Greek ᾠοφόρος, ōophóros, 'egg-bearing' and ἐκτομή, ektomḗ, 'a cutting out of'), historically also called ovariotomy, is the surgical removal of an ovary or ovaries.[1] The surgery is also called ovariectomy, but this term is mostly used in reference to non-human animals, e.g. the surgical removal of ovaries from laboratory animals. Removal of the ovaries of females is the biological equivalent of castration of males; the term castration is only occasionally used in the medical literature to refer to oophorectomy of women. In veterinary medicine, the removal of ovaries and uterus is called ovariohysterectomy (spaying) and is a form of sterilization.
The first reported successful human oophorectomy was carried out by Sir Sydney Jones at Sydney Infirmary, Australia, in 1870.[2]
Partial oophorectomy or ovariotomy is a term sometimes used to describe a variety of surgeries such as ovarian cyst removal, or resection of parts of the ovaries.[3] This kind of surgery is fertility-preserving, although ovarian failure may be relatively frequent. Most of the long-term risks and consequences of oophorectomy are not or only partially present with partial oophorectomy.
In humans, oophorectomy is most often performed because of diseases such as ovarian cysts or cancer; as prophylaxis to reduce the chances of developing ovarian cancer or breast cancer; or in conjunction with hysterectomy (removal of the uterus). In the 1890s people believed oophorectomies could cure menstrual cramps, back pain, headaches, and chronic coughing, although no evidence existed that the procedure impacted any of these ailments.[4]
The removal of an ovary together with the fallopian tube is called salpingo-oophorectomy or unilateral salpingo-oophorectomy (USO). When both ovaries and both fallopian tubes are removed, the term bilateral salpingo-oophorectomy (BSO) is used. Oophorectomy and salpingo-oophorectomy are not common forms of birth control in humans; more usual is tubal ligation, in which the fallopian tubes are blocked but the ovaries remain intact. In many cases, surgical removal of the ovaries is performed concurrently with a hysterectomy. The formal medical name for removal of a woman's entire reproductive system (ovaries, fallopian tubes, uterus) is "total abdominal hysterectomy with bilateral salpingo-oophorectomy" (TAH-BSO); the more casual term for such a surgery is "ovariohysterectomy". "Hysterectomy" is removal of the uterus (from the Greek ὑστέρα hystera "womb" and εκτομία ektomia "a cutting out of") without removal of the ovaries or fallopian tubes.
Oophorectomy is used as part of castration to punish some female sex offenders.[5]
Technique
[edit]Oophorectomy for benign causes is most often performed by abdominal laparoscopy. Abdominal laparotomy or robotic surgery is used in complicated cases[clarification needed] or when a malignancy is suspected.[citation needed]
Statistics
[edit]According to the Centers for Disease Control, 454,000 women in the United States underwent oophorectomy in 2004. The first successful operation of this type, account of which was published in the Eclectic Repertory and Analytic Review (Philadelphia) in 1817, was performed by Ephraim McDowell (1771–1830), a surgeon from Danville, Kentucky.[6] McDowell was dubbed as the "father of ovariotomy".[7][8] It later became known as Battey's Operation, after Robert Battey, a surgeon from Augusta, Georgia, who championed the procedure for a variety of conditions, most successfully for ovarian epilepsy.[9]
Indication
[edit]Most bilateral oophorectomies (63%) are performed without any medical indication, and most (87%) are performed together with a hysterectomy.[10] Conversely, unilateral oophorectomy is commonly performed for a medical indication (73%; cyst, endometriosis, benign tumor, inflammation, etc.) and less commonly in conjunction with hysterectomy (61%).[10]
Special indications include several groups of women with substantially increased risk of ovarian cancer, such as high-risk BRCA mutation carriers and women with endometriosis who also have frequent ovarian cysts.[citation needed]
Bilateral oophorectomy has been traditionally done in the belief that the benefit of preventing ovarian cancer would outweigh the risks associated with removal of ovaries. However, it is now clear that prophylactic oophorectomy without a reasonable medical indication decreases long-term survival rates substantially[11] and has deleterious long-term effects on health and well-being even in post-menopausal women.[12] The procedure has been postulated as a possible treatment method for female sex offenders.[13]
The procedure is sometimes performed at the same time as hysterectomy in transgender men and non-binary people. The long term effects of oophorectomy in this population are not well studied.[14]
Cancer prevention
[edit]Oophorectomy can significantly improve survival for women with high-risk BRCA mutations, for whom prophylactic oophorectomy around age 40 reduces the risk of ovarian and breast cancer and provides significant and substantial long-term survival advantage.[15] On average, earlier intervention does not provide any additional benefit but increases risks and adverse effects.
For women with high-risk BRCA2 mutations, oophorectomy around age 40 has a relatively modest benefit for survival; the positive effect of reduced breast and ovarian cancer risk is nearly balanced by adverse effects. The survival advantage is more substantial when oophorectomy is performed together with prophylactic mastectomy.[16][17]
The risks and benefits associated with oophorectomy in the BRCA1/2 mutation carrier population are different than those for the general population. Prophylactic risk-reducing salpingo-oophorectomy (RRSO) is an important option for the high-risk population to consider. Women with BRCA1/2 mutations who undergo salpingo-oophorectomy have lower all-cause mortality rates than women in the same population who do not undergo this procedure. In addition, RRSO has been shown to decrease mortality specific to breast cancer and ovarian cancer. Women who undergo RRSO are also at a lower risk for developing ovarian cancer and first occurrence breast cancer. Specifically, RRSO provides BRCA1 mutation carriers with no prior breast cancer a 70% reduction of ovarian cancer risk. BRCA1 mutation carriers with prior breast cancer can benefit from an 85% reduction. High-risk women who have not had prior breast cancer can benefit from a 37% (BRCA1 mutation) and 64% (BRCA2 mutation) reduction of breast cancer risk. These benefits are important to highlight, as they are unique to this BRCA1/2 mutation carrier population.[18]
Endometriosis
[edit]In rare cases, oophorectomy can be used to treat endometriosis by eliminating the menstrual cycle, which will reduce or eliminate the spread of existing endometriosis as well as reducing pain. Since endometriosis results from an overgrowth of the uterine lining, removal of the ovaries as a treatment for endometriosis is often done in conjunction with a hysterectomy to further reduce or eliminate recurrence.[citation needed]
Oophorectomy for endometriosis is used only as last resort, often in conjunction with a hysterectomy, as it has severe side effects for women of reproductive age. However, it has a higher success rate than retaining the ovaries.[19]
Partial oophorectomy (i.e., ovarian cyst removal not involving total oophorectomy) is often used to treat milder cases of endometriosis when non-surgical hormonal treatments fail to stop cyst formation. Removal of ovarian cysts through partial oophorectomy is also used to treat extreme pelvic pain from chronic hormonal-related pelvic problems.
Risks and adverse effects
[edit]Surgical risks
[edit]Oophorectomy is an intra-abdominal surgery and serious complications stemming directly from the surgery are rare. When performed together with hysterectomy, it has influence on choice of surgical technique as the combined surgery is much less likely to be performed by vaginal hysterectomy.[citation needed]
Laparotomic adnexal surgeries are associated with a high rate of adhesive small bowel obstructions (24%).[20]
An infrequent complication is injuring of the ureter at the level of the suspensory ligament of the ovary.[21]
Long-term effects
[edit]Oophorectomy has serious long-term consequences stemming mostly from the hormonal effects of the surgery and extending well beyond menopause. The reported risks and adverse effects include premature death,[22][23] cardiovascular disease, cognitive impairment or dementia,[24] parkinsonism,[25] osteoporosis and bone fractures, decline in psychological well-being,[26] and decline in sexual function. Hormone replacement therapy does not always reduce the adverse effects.[11]
Mortality
[edit]Oophorectomy is associated with significantly increased all-cause long-term mortality except when performed for cancer prevention in carriers of high-risk BRCA mutations. This effect is particularly pronounced for women who undergo oophorectomy before age 45.[23]
The effect is not limited to women who have oophorectomy performed before menopause; an impact on survival is expected even for surgeries performed up to the age of 65.[27] Surgery at age 50-54 reduces the probability of survival until age 80 by 8% (from 62% to 54% survival), surgery at age 55-59 by 4%. Most of this effect is due to excess cardiovascular risk and hip fractures.[27]
Removal of ovaries causes hormonal changes and symptoms similar to, but generally more severe than, menopause. Women who have had an oophorectomy are usually encouraged to take hormone replacement drugs to prevent other conditions often associated with menopause. Women younger than 45 who have had their ovaries removed with prophylactic bilateral oophorectomy face a mortality risk 170% higher than women who have retained their ovaries.[23] Retaining the ovaries when a hysterectomy is performed is associated with better long-term survival.[22] Hormone therapy for women with oophorectomies performed before age 45 improves the long-term outcome and all-cause mortality rates.[23][28]
Menopausal effects
[edit]Women who have had bilateral oophorectomy surgeries lose most of their ability to produce the hormones estrogen and progesterone, and lose about half of their ability to produce testosterone, and subsequently enter what is known as "surgical menopause" (as opposed to normal menopause, which occurs naturally in women as part of the aging process). In natural menopause the ovaries generally continue to produce low levels of hormones, especially androgens, long after menopause, which may explain why surgical menopause is generally accompanied by a more sudden and severe onset of symptoms than natural menopause, symptoms that may continue until the natural age of menopause.[29] These symptoms are commonly addressed through hormone therapy, utilizing various forms of estrogen, testosterone, progesterone, or a combination.[citation needed]
Cardiovascular risk
[edit]When the ovaries are removed, a woman is at a seven times greater risk of cardiovascular disease,[30][31][32] but the mechanisms are not precisely known. The hormone production of the ovaries currently cannot be sufficiently mimicked by drug therapy. The ovaries produce hormones a woman needs throughout her entire life, in the quantity they are needed, at the time they are needed, in response to and as part of the complex endocrine system.
Osteoporosis
[edit]Oophorectomy is associated with an increased risk of osteoporosis and bone fractures.[33][34][35][36][37] A potential risk for oophorectomy performed after menopause is not fully elucidated.[38][39] Reduced levels of testosterone in women is predictive of height loss, which may occur as a result of reduced bone density.[40] In women under the age of 50 who have undergone oophorectomy, hormone replacement therapy (HRT) is often used to offset the negative effects of sudden hormonal loss such as early-onset osteoporosis as well as menopausal problems like hot flashes that are usually more severe than those experienced by women undergoing natural menopause.
Adverse effect on sexuality
[edit]Oophorectomy substantially impairs sexuality.[41] Substantially more women who had both an oophorectomy and a hysterectomy reported libido loss, difficulty with sexual arousal, and vaginal dryness than those who had a less invasive procedure (either hysterectomy alone or an alternative procedure), and hormone replacement therapy was not found to improve these symptoms.[42] In addition, oophorectomy greatly reduces testosterone levels, which are associated with a greater sense of sexual desire in women.[43] However, at least one study has shown that psychological factors, such as relationship satisfaction, are still the best predictor of sexual activity following oophorectomy.[44] Sexual intercourse remains possible after oophorectomy and coitus can continue. Reconstructive surgery remains an option for women who have experienced benign and malignant conditions.[45] : 1020–1348
Effect on fertility
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Managing side effects of prophylactic oophorectomy
[edit]Non-hormonal treatments
[edit]The side effects of oophorectomy may be alleviated by medicines other than hormonal replacement. Non-hormonal biphosphonates (such as Fosamax and Actonel) increase bone strength and are available as once-a-week pills. Low-dose selective serotonin reuptake inhibitors such as Paxil and Prozac alleviate vasomotor menopausal symptoms, i.e., "hot flashes".[46]
Hormonal treatments
[edit]In general, hormone replacement therapy is somewhat controversial due to the known carcinogenic and thrombogenic properties of estrogen; however, many physicians and patients feel the benefits outweigh the risks in women who may face serious health and quality-of-life issues as a consequence of early surgical menopause. The ovarian hormones estrogen, progesterone, and testosterone are involved in the regulation of hundreds of bodily functions; it is believed by some doctors that hormone therapy programs mitigate surgical menopause side effects such as increased risk of cardiovascular disease,[47] and female sexual dysfunction.[48]
Short-term hormone replacement with estrogen has negligible effect on overall mortality for high-risk BRCA mutation carriers. Based on computer simulations, overall mortality appears to be marginally higher for short-term HRT after oophorectomy or marginally lower for short-term HRT after oophorectomy in combination with mastectomy.[49] This result can probably be generalized to other women at high risk in whom short-term (i.e., one- or two-year) treatment with estrogen for hot flashes may be acceptable.
See also
[edit]References
[edit]- ^ "About - Mayo Clinic". www.mayoclinic.org. Retrieved 2018-11-07.
- ^ John Garrett: "Jones, Sir Philip Sydney (1836–1918)", Australian Dictionary of Biography, 1972
- ^ "Definition of "ovariotomy" at Collins Dictionary". Retrieved 3 May 2013.
- ^ Bryson, Bill (2019). "In the Beginning: Conception and Birth". The Body (1st ed.). New York: Penguin Random House. p. 295. ISBN 9780385539302.
- ^ Nolan, Delaney. "What is the controversy behind Louisiana's new surgical castration law?". Al Jazeera. Retrieved 2025-01-24.
- ^ McDowell, Ephraim (1817). "Three cases of extirpation of diseased ovaries". Eclectic Repertory & Analytic Review. 7: 242–244.
- ^ Lewis S. Pilcher. Ephraim McDowell, Father of Ovariotomy and Founder of Abdominal Surgery, Annals of Surgery, 1922 (January), Volume 75 (1), p. 125–126.
- ^ The Biographical Dictionary of America, vol. 7, p. 147.
- ^ Thiery, Michel (1998). "Battey's operation: an exercise in surgical frustration". European Journal of Obstetrics & Gynecology and Reproductive Biology. 81 (2): 243–246. doi:10.1016/s0301-2115(98)00197-3. PMID 9989872.
- ^ a b Melton LJ 3rd, Bergstralh EJ, Malkasian GD, O'Fallon WM (Mar 1991). "Bilateral oophorectomy trends in Olmsted County, Minnesota, 1950-1987". Epidemiology. 2 (2): 149–52. doi:10.1097/00001648-199103000-00011. PMID 1932314.
- ^ a b Shuster LT, Gostout BS, Grossardt BR, Rocca WA (Sep 2008). "Prophylactic oophorectomy in premenopausal women and long-term health". Menopause Int. 14 (3): 111–6. doi:10.1258/mi.2008.008016. PMC 2585770. PMID 18714076.
- ^ Bhattacharya, S. M.; Jha, A. (2010). "A comparison of health-related quality of life (HRQOL) after natural and surgical menopause". Maturitas. 66 (4): 431–434. doi:10.1016/j.maturitas.2010.03.030. PMID 20434859.
- ^ "Alabama lawmaker proposes castration bill for sex offenders". salon.com. 7 March 2016. Retrieved 8 April 2018.
- ^ Kumar, Sahil; Mukherjee, Smita; O'Dwyer, Cormac; Wassersug, Richard; Bertin, Elise; Mehra, Neeraj; Dahl, Marshall; Genoway, Krista; Kavanagh, Alexander G. (2022). "Health Outcomes Associated With Having an Oophorectomy Versus Retaining One's Ovaries for Transmasculine and Gender Diverse Individuals Treated With Testosterone Therapy: A Systematic Review". Sexual Medicine Reviews. 10 (4): 636–647. doi:10.1016/j.sxmr.2022.03.003. PMID 35831234. S2CID 250435764.
- ^ Stan DL, Shuster LT (October 2013). "Challenging and Complex Decisions in the Management of the BRCA Mutation Carrier". Journal of Women's Health. 22 (10): 825–834. doi:10.1089/jwh.2013.4407. PMC 4047843. PMID 23987739.
- ^ Kurian, A.; Sigal, B.; Plevritis, S. (2010). "Survival analysis of cancer risk reduction strategies for BRCA1/2 mutation carriers". Journal of Clinical Oncology. 28 (2): 222–231. doi:10.1200/JCO.2009.22.7991. PMC 2815712. PMID 19996031.
- ^ Stadler, Z. K.; Kauff, N. D. (2009). "Weighing Options for Cancer Risk Reduction in Carriers of BRCA1 and BRCA2 Mutations". Journal of Clinical Oncology. 28 (2): 189–91. doi:10.1200/JCO.2009.25.6875. PMID 19996025.
- ^ Domchek SM, Friebel TM, Singer CF, Evans DG, Lynch HT, Isaacs C, et al. (September 2010). "Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality". JAMA. 304 (9): 967–75. doi:10.1001/jama.2010.1237. PMC 2948529. PMID 20810374.
- ^ Rizk B, Fischer AS, Lotfy HA, Turki R, Zahed HA, Malik R, Holliday CP, Glass A, Fishel H, Soliman MY, Herrera D (2014). "Recurrence of endometriosis after hysterectomy". Facts Views Vis Obgyn. 6 (4): 219–27. PMC 4286861. PMID 25593697.
- ^ Barmparas, G.; Branco, B. C.; Schnüriger, B.; Lam, L.; Inaba, K.; Demetriades, D. (2010). "The Incidence and Risk Factors of Post-Laparotomy Adhesive Small Bowel Obstruction". Journal of Gastrointestinal Surgery. 14 (10): 1619–1628. doi:10.1007/s11605-010-1189-8. PMID 20352368. S2CID 22720831.
- ^ "Oophorectomy with Transection of Ureter - Medical Illustration, Human Anatomy Drawing, Anatomy Illustration". graphicwitness.medicalillustration.com.
- ^ a b Parker WH, Broder MS, Liu Z, Shoupe D, Farquhar C, Berek JS (August 2005). "Ovarian conservation at the time of hysterectomy for benign disease". Obstet Gynecol. 106 (2): 219–26. doi:10.1097/01.AOG.0000167394.38215.56. PMID 16055568. S2CID 21266475.
- ^ a b c d Rocca WA, Grossardt BR, de Andrade M, Malkasian GD, Melton LJ 3rd (Oct 2006). "Survival patterns after oophorectomy in premenopausal women: a population-based cohort study". Lancet Oncol. 7 (10): 821–8. doi:10.1016/S1470-2045(06)70869-5. PMID 17012044.
- ^ Rocca WA, Bower JH, Maraganore DM, Ahlskog JE, Grossardt BR, de Andrade M, Melton LJ III (Sep 2007). "Increased risk of cognitive impairment or dementia in women who underwent oophorectomy before menopause". Neurology. 69 (11): 1074–83. doi:10.1212/01.wnl.0000276984.19542.e6. PMID 17761551. S2CID 73140117.
- ^ Rocca WA, Bower JH, Maraganore DM, Ahlskog JE, Grossardt BR, de Andrade M, Melton LJ 3rd (Jan 2008). "Increased risk of parkinsonism in women who underwent oophorectomy before menopause". Neurology. 70 (3): 200–9. doi:10.1212/01.wnl.0000280573.30975.6a. PMID 17761549. S2CID 21876656.
- ^ Rocca WA, Grossardt BR, Geda YE, Gostout BS, Bower JH, Maraganore DM, de Andrade M, Melton LJ 3rd (Nov–Dec 2008). "Long-term risk of depressive and anxiety symptoms after early bilateral oophorectomy". Menopause. 15 (6): 1050–9. doi:10.1097/gme.0b013e318174f155. PMID 18724263. S2CID 7146179.
- ^ a b Shoupe, D.; Parker, W. H.; Broder, M. S.; Liu, Z.; Farquhar, C.; Berek, J. S. (2007). "Elective oophorectomy for benign gynecological disorders". Menopause. 14 (Suppl. 1): 580–585. doi:10.1097/gme.0b013e31803c56a4. PMID 17476148. S2CID 37549821.
- ^ "News and views". Menopause Int. 12 (4): 133–7. December 2006. doi:10.1258/136218006779160472. S2CID 208272164. Archived from the original on 2011-07-15. Retrieved 2009-07-03.
Further evidence in favour of HRT in early menopause
- ^ "Medical Definition of Surgical menopause". Archived from the original on 2007-03-11. Retrieved 2007-01-13.
- ^ Parish HM, et al. (1967). "Time interval from castration in premenopausal women to development of excessive coronary atherosclerosis". Am. J. Obstet. Gynecol. 99 (2): 155–62. doi:10.1016/0002-9378(67)90314-6. PMID 6039061.
- ^ Colditz GA, Willett WC, Stampfer MJ, Rosner B, Speizer FE, Hennekens CH (April 1987). "Menopause and the risk of coronary heart disease in women". N. Engl. J. Med. 316 (18): 1105–10. doi:10.1056/NEJM198704303161801. PMID 3574358.
- ^ Rivera CM, Grossardt BR, Rhodes DJ, Brown RD Jr, Roger VL, Melton LJ III, Rocca WA (Jan–Feb 2009). "Increased cardiovascular mortality after early bilateral oophorectomy". Menopause. 16 (1): 15–23. doi:10.1097/gme.0b013e31818888f7. PMC 2755630. PMID 19034050.
- ^ Kelsey JL, Prill MM, Keegan TH, Quesenberry CP, Sidney S (November 2005). "Risk factors for pelvis fracture in older persons". Am. J. Epidemiol. 162 (9): 879–86. doi:10.1093/aje/kwi295. PMID 16221810.
- ^ van der Voort DJ, Geusens PP, Dinant GJ (2001). "Risk factors for osteoporosis related to their outcome: fractures". Osteoporos Int. 12 (8): 630–8. doi:10.1007/s001980170062. PMID 11580076. S2CID 9421669. Archived from the original on 2001-10-24. Retrieved 2009-07-03.
- ^ Hreshchyshyn MM, Hopkins A, Zylstra S, Anbar M (October 1988). "Effects of natural menopause, hysterectomy, and oophorectomy on lumbar spine and femoral neck bone densities". Obstet Gynecol. 72 (4): 631–8. PMID 3419740.
- ^ Levin RJ (October 2002). "The physiology of sexual arousal in the human female: a recreational and procreational synthesis" (PDF). Arch Sex Behav. 31 (5): 405–11. doi:10.1023/A:1019836007416. PMID 12238607. S2CID 24432594.
- ^ Masters, W.H., et al. The Uterus, Physiological and Clinical Considerations Human Sexual Response 1966 p.111-140
- ^ Melton, L. J.; Khosla, S.; Malkasian, G. D.; Achenbach, S. J.; Oberg, A. L.; Riggs, B. L. (2003). "Fracture Risk After Bilateral Oophorectomy in Elderly Women". Journal of Bone and Mineral Research. 18 (5): 900–905. doi:10.1359/jbmr.2003.18.5.900. PMID 12733730. S2CID 22363719.
- ^ Antoniucci DM, Sellmeyer DE, Cauley JA, Ensrud KE, Schneider JL, Vesco KK, Cummings SR, Melton LJ 3rd, Study of Osteoporotic Fractures Research Group (May 2005). "Postmenopausal bilateral oophorectomy is not associated with increased fracture risk in older women". J Bone Miner Res. 20 (5): 741–7. doi:10.1359/JBMR.041220. PMID 15824846. S2CID 10648925.
- ^ Jassal SK, Barrett-Connor E, Edelstein SL (April 1995). "Low bioavailable testosterone levels predict future height loss in postmenopausal women". J. Bone Miner. Res. 10 (4): 650–4. doi:10.1002/jbmr.5650100419. PMID 7610937. S2CID 30094806.
- ^ Castelo-Branco, C.; Palacios, S.; Combalia, J.; Ferrer, M.; Traveria, G. (2009). "Risk of hypoactive sexual desire disorder and associated factors in a cohort of oophorectomized women". Climacteric. 12 (6): 525–532. doi:10.3109/13697130903075345. PMID 19905904. S2CID 24700993.
- ^ McPherson K, Herbert A, Judge A, et al. (September 2005). "Psychosexual health 5 years after hysterectomy: population-based comparison with endometrial ablation for dysfunctional uterine bleeding". Health Expectations. 8 (3): 234–43. doi:10.1111/j.1369-7625.2005.00338.x. PMC 5060293. PMID 16098153.
- ^ Shifren, JL (2002). "Androgen deficiency in the oophorectomized woman". Fertility and Sterility. 77 (Suppl 4): S60–2. doi:10.1016/s0015-0282(02)02970-9. PMID 12007904..
- ^ Lorenz, T.; McGregor, B.; Swisher, E. (2014). "Relationship satisfaction predicts sexual activity following risk-reducing salpingo-oophorectomy". Journal of Psychosomatic Obstetrics & Gynecology. 35 (2): 62–8. doi:10.3109/0167482X.2014.899577. PMC 4117249. PMID 24693956.
- ^ Hoffman, Barbara (2012). Williams gynecology (2nd ed.). New York: McGraw-Hill Medical. p. 65. ISBN 978-0071716727.
- ^ "Menopause Symptoms, Treatments and Stages of Menopause". Brigham and Women's Hospital, Boston, Massachusetts. 2007-04-26. Archived from the original on 2006-01-27. Retrieved 2007-06-05.
- ^ Ben Hirschler, "Expert believes early HRT can have heart benefits" 21 December 2006; Reuters Health
- ^ Warnock JK, Bundren JC, Morris DW (1999). "Female hypoactive sexual disorder: case studies of physiologic androgen replacement". J Sex Marital Ther. 25 (3): 175–82. doi:10.1080/00926239908403992. PMID 10407790.
- ^ Armstrong K, Schwartz JS, Randall T, Rubin SC, Weber B (2004). "Hormone replacement therapy and life expectancy after prophylactic oophorectomy in women with BRCA1/2 mutations: a decision analysis". J. Clin. Oncol. 22 (6): 1045–54. doi:10.1200/JCO.2004.06.090. PMID 14981106.
External links
[edit]Oophorectomy
View on GrokipediaDefinition and Types
Definition
Oophorectomy is a surgical procedure to remove one (unilateral) or both (bilateral) ovaries from the female reproductive system.[2][11] The ovaries are paired, almond-shaped organs, each approximately 3-5 cm in length, located in the pelvic cavity on either side of the uterus and attached via the ovarian ligament and mesovarium.[2][1] These structures serve primary functions in gamete production—releasing mature ova during ovulation—and endocrine regulation, secreting hormones such as estrogen, progesterone, and androgens that influence reproductive cycles, secondary sexual characteristics, and bone health.[1] Unilateral oophorectomy preserves the remaining ovary's capacity for ovulation and hormone production, whereas bilateral oophorectomy eliminates ovarian tissue entirely, typically inducing immediate surgical menopause in premenopausal women due to abrupt cessation of ovarian hormone output.[1][12] The procedure may be performed via open laparotomy, laparoscopy, or robotic-assisted techniques, depending on clinical context, though specific procedural classifications are delineated separately.[2][1] Oophorectomy differs from salpingo-oophorectomy, which additionally excises the fallopian tubes, but the term alone refers strictly to ovarian removal.[11][1]Classification of Procedures
Oophorectomy procedures are primarily classified by the extent of ovarian tissue removed, distinguishing between unilateral oophorectomy, which involves excision of a single ovary, and bilateral oophorectomy, which entails removal of both ovaries.[1][2][12] Bilateral procedures induce immediate menopause due to complete loss of ovarian hormone production, whereas unilateral approaches preserve some endocrine function from the remaining ovary.[1] Procedures are further subclassified based on concurrent removal of adjacent structures, particularly the fallopian tubes, resulting in salpingo-oophorectomy when one ovary and its ipsilateral tube are excised (unilateral salpingo-oophorectomy) or both ovaries and tubes are removed (bilateral salpingo-oophorectomy, or BSO).[1][2][12] Simple oophorectomy without salpingectomy is less common in contemporary practice, as tubal removal reduces ovarian cancer risk by interrupting potential pathways for malignant transformation.[1] Surgical approaches classify oophorectomy by invasiveness and access method, with laparoscopy as the preferred minimally invasive technique involving small incisions, insufflation of the abdomen, and specialized instruments for dissection and specimen retrieval in a containment bag to minimize spillage risks.[1][2] Open laparotomy employs a larger abdominal incision for direct visualization and is reserved for cases with suspected malignancy or anatomical complexities precluding laparoscopy.[1][2][12] Vaginal approaches may be used selectively, often in conjunction with hysterectomy, offering reduced infection rates but limited applicability.[12] Robotic-assisted laparoscopy enhances precision in select centers but follows similar principles to standard laparoscopy.[2]Historical Development
Origins in the 19th Century
The surgical removal of ovaries, initially termed ovariotomy, originated with procedures targeting diseased ovaries, particularly large cystic tumors, in the early 19th century. On December 25, 1809, American surgeon Ephraim McDowell performed the first successful ovariotomy on Jane Todd Crawford in Danville, Kentucky, excising a 22.5-pound ovarian cyst without anesthesia or antisepsis; Crawford survived for over 30 years post-operation, demonstrating the feasibility of abdominal surgery despite prevailing fears of peritonitis and sepsis.[13] [14] This landmark case, conducted in a remote setting, challenged medical orthodoxy that deemed ovarian extirpation impossible due to inevitable infection, and McDowell's 1817 publication in the Eclectic Repertory and Analytical Review detailed the technique, encouraging subsequent attempts.[13] By the mid-19th century, ovariotomy gained traction in Britain and Europe for benign ovarian pathology, with mortality rates exceeding 50% initially due to hemorrhage, shock, and infection, though improvements in ligation techniques and patient selection reduced risks toward the century's end.[15] Pioneers like Charles Clay in Manchester (1842) and Thomas Spencer Wells in London (from 1858) refined the procedure, performing hundreds of cases for ovarian cysts and tumors, establishing it as a viable intervention for life-threatening masses.[15] A controversial expansion occurred in the 1870s with "normal ovariotomy," the removal of ostensibly healthy ovaries to treat non-malignant conditions such as hysteria, dysmenorrhea, neuralgia, and menstrual-related epilepsy, predicated on theories attributing psychiatric and neural symptoms to ovarian dysfunction.[15] [16] American gynecologist Robert Battey (1828–1895) performed the first documented such procedure on August 27, 1872, in Rome, Georgia, on a patient suffering severe neuralgia, coining the term to distinguish it from cystectomies and advocating it as a curative measure despite inducing surgical menopause and sterility.[17] [16] Battey's series of cases, publicized from 1872 to 1878, spurred adoption across the U.S. and Europe, with surgeons like Alfred Hegar in Germany performing similar excisions by 1872 for benign indications, though the practice faced sharp criticism for its experimental basis and complications, including high operative mortality (up to 20–30% in early reports) and induced menopausal symptoms.[18] [15]20th Century Evolution
In the early 20th century, surgical approaches to oophorectomy emphasized ovarian conservation due to growing recognition of the ovaries' endocrine functions, with physicians like Louise McIlroy advocating preservation unless the ovaries were severely diseased to avoid inducing premature menopause.[15] This conservatism contrasted with 19th-century practices but persisted amid high operative risks, even as anesthesia and antisepsis improved mortality rates from over 50% in the 1880s to under 5% by the 1920s. Indications remained focused on benign conditions such as cysts, tumors, and endometriosis, alongside oncologic needs, though prophylactic removal for non-malignant reasons was debated.[15] By the 1930s, concerns over ovarian cancer's poor prognosis—often diagnosed late with insidious onset—drove expanded prophylactic oophorectomy, particularly bilateral removal during hysterectomy in perimenopausal women to prevent malignancy in residual ovarian tissue.[15] This practice gained traction mid-century; for instance, by 1964, textbooks like Macleod and Howkins endorsed removal in women aged 45 or older, reflecting a risk-benefit calculus where lifetime ovarian cancer incidence (estimated at 1:3000–1:5000) justified intervention despite menopausal symptoms.[15] Concurrently, oophorectomy emerged as the first endocrine adjuvant therapy for premenopausal breast cancer, achieving tumor regression in approximately 30% of advanced cases by inducing estrogen withdrawal, a approach pioneered in the late 19th century but standardized through 20th-century trials showing survival benefits in hormone-responsive tumors.[19] Elective bilateral oophorectomy with hysterectomy became routine, with U.S. rates peaking in the latter half of the century, often exceeding 20% of procedures in women under 50.[20] Techniques remained predominantly open abdominal throughout most of the century, leveraging advances in surgical instrumentation and postoperative care, including antibiotics from the 1940s that reduced infection risks. The advent of hormone replacement therapy in the 1950s, such as diethylstilbestrol, further facilitated acceptance by mitigating vasomotor and skeletal effects of surgical menopause. Toward the late 20th century, operative laparoscopy revolutionized approaches; building on diagnostic laparoscopy from the 1950s, gynecologic procedures like laparoscopic oophorectomy became feasible by the 1980s–1990s, enabling minimally invasive removal with smaller incisions, reduced recovery time, and lower morbidity compared to laparotomy.[21] This shift marked a transition from radical excisions to more precise, fertility-sparing options in select cases, though open surgery dominated until widespread adoption post-1990.70374-4/abstract)Recent Advances (Post-2000)
Laparoscopic oophorectomy became more prevalent in the early 2000s as a standard minimally invasive approach, offering shorter hospital stays, reduced blood loss, and lower postoperative pain compared to open surgery, with adoption driven by technological improvements in instrumentation and imaging. Robotic-assisted oophorectomy emerged shortly thereafter, with the first gynecologic robotic procedure—a tubal anastomosis—performed in 2000, followed by the inaugural robot-assisted hysterectomy incorporating oophorectomy in 2002; these systems provided enhanced precision, three-dimensional visualization, and tremor filtration, particularly beneficial for complex cases involving adhesions or obesity.[22] [23] By the 2010s, robotic platforms had expanded to single-site techniques, further minimizing incisions while maintaining oncologic safety in salpingo-oophorectomy for malignancy.[24] Meta-analyses post-2010 confirm comparable outcomes to conventional laparoscopy in blood loss and complications for benign indications, though robotic approaches incur higher costs without consistent superiority in operative time or conversion rates.[25] Post-2000 epidemiological data revealed a marked decline in bilateral oophorectomy rates, especially premenopausal procedures concurrent with hysterectomy, attributed to growing evidence of adverse long-term effects like accelerated aging, increased cardiovascular mortality, and osteoporosis when performed before age 45 without estrogen replacement. In the United States, incidence peaked around 2000–2004 but decreased thereafter across age groups, prompting guidelines favoring ovarian conservation in benign cases unless oncologic risks outweigh benefits.[26] [27] This shift aligns with studies quantifying elevated all-cause mortality risks in women under 50 undergoing the procedure, influencing surgical decision-making toward unilateral or delayed bilateral approaches where feasible.[28] Advances in genetic screening post-2000, including widespread BRCA1/2 testing, refined prophylactic salpingo-oophorectomy protocols, reducing ovarian cancer incidence by approximately 80% in high-risk carriers while balancing menopausal sequelae. Updated National Comprehensive Cancer Network guidelines recommend risk-reducing salpingo-oophorectomy at ages 35–40 for BRCA1 carriers and 40–45 for BRCA2, often with opportunistic salpingectomy as an interim strategy to delay menopause.[29] [30] Concurrent pathologic protocols emphasize meticulous examination of fallopian tubes, as serous tubal intraepithelial carcinoma precursors predominate in BRCA-associated cases, informing more targeted resections.[31] Management of induced surgical menopause has evolved with evidence-based hormone therapy protocols, prioritizing systemic estrogen (with progestin if uterus retained) in women under 50 to counteract deficits in bone mineral density, cardiovascular protection, and cognitive function, though uptake remains suboptimal due to historical concerns over malignancy risks unsubstantiated in this context.[32] [33] Longitudinal data underscore the need for individualized counseling on vasomotor symptoms, sexual dysfunction, and metabolic changes, with non-hormonal adjuncts like SSRIs for mood disorders gaining traction in HRT-intolerant patients.[34]Epidemiology and Statistics
Global and Regional Prevalence
In the United States, bilateral oophorectomy prevalence among women aged 20-84 years is approximately 10%, based on self-reported data from the National Health and Nutrition Examination Survey (NHANES) cycles 2011-2018, with notable regional disparities: 12.3% in the South, 10.8% in the Midwest, 9.4% in the West, and 8.0% in the Northeast.[35] This prevalence rises sharply with age, from less than 1% among women aged 20-29 years to 29% among those aged 70-79 years.[36] Unilateral oophorectomy is less common, comprising about 40% of oophorectomy procedures in population-based studies from defined regions like Olmsted County, Minnesota, over 1950-2018, though bilateral procedures predominate overall.[27] Comprehensive global prevalence data for oophorectomy remain limited, as most epidemiological studies focus on high-income countries and often aggregate it with hysterectomy procedures, where concomitant oophorectomy occurs in 50-78% of benign cases historically but has declined since the early 2000s due to evidence of associated cardiovascular and mortality risks.[37] [38] Hysterectomy rates, a proxy for potential oophorectomy incidence, vary widely: approximately 255 per 100,000 women annually in Australia, higher than in many European nations like Denmark (around 351 per 100,000 but with trends toward ovarian conservation).[39] In Europe and Asia, overall rates appear lower than in the US, reflecting lower hysterectomy utilization and greater emphasis on preserving ovarian function in premenopausal women for benign indications.[40] In low- and middle-income regions such as parts of Africa and Asia, oophorectomy rates are substantially lower, driven by limited access to elective gynecologic surgery and lower incidence of procedures for non-oncologic reasons, though data gaps persist due to underreporting in national registries.[41] Prophylactic bilateral salpingo-oophorectomy in high-risk populations (e.g., BRCA mutation carriers) shows regional variation, with uptake rates exceeding 57% in some cohorts but higher in Northern European countries like Norway compared to others.[42] Across regions, procedures for oncologic indications remain steady, while benign and risk-reduction cases have trended downward in monitored populations since 2000.[43]Long-Term Outcomes and Mortality Data
Bilateral salpingo-oophorectomy (BSO) performed in premenopausal women for benign indications is associated with increased all-cause mortality compared to ovarian conservation, particularly when conducted before age 50 without subsequent estrogen therapy. In the Nurses' Health Study cohort of 30,398 women followed for 28 years, all-cause mortality was 16.8% among those undergoing hysterectomy with BSO versus 13.3% with ovarian conservation, yielding a hazard ratio (HR) of 1.17 (95% CI, 1.02-1.35).[44] This elevated risk persisted after adjustments for confounders and was driven by higher mortality from coronary heart disease (HR 1.28), lung cancer (HR 1.92), and colorectal cancer (HR 1.73).[45] Cardiovascular mortality shows a pronounced age-dependent increase following early BSO. A Mayo Clinic study of 1,273 women undergoing BSO before age 45 reported a 1.67-fold higher risk of cardiovascular death (95% CI, 1.04-2.70), with cardiac mortality specifically elevated at HR 1.89 (95% CI, 1.09-3.29), independent of estrogen use.[46] Meta-analyses confirm this pattern, associating premenopausal BSO with greater incidence of cardiovascular events, including heart failure (relative risk 1.45, 95% CI 1.09-1.92), though overall cardiovascular mortality effects vary by follow-up duration and hormone replacement therapy (HRT) adherence.[4] Cancer-specific outcomes reflect trade-offs: BSO reduces ovarian cancer risk but elevates others. A 2023 systematic review and meta-analysis of 66 studies found BSO decreased ovarian cancer incidence (HR 0.15) and breast cancer mortality but increased colorectal cancer mortality (HR 1.78, 95% CI 1.24-2.55), thyroid cancer, and renal cancer risks.[10] All-cause mortality rose in women aged 45-54 at BSO (10-year rate higher by statistical significance), though benefits emerge in high-risk populations; among BRCA1/2 carriers, BSO lowered all-cause mortality (HR 0.47, 95% CI 0.29-0.79) and breast cancer-specific death.[6][47] HRT mitigates some risks but not fully. In the Nurses' Health Study, estrogen therapy post-BSO reduced but did not eliminate excess mortality in women under 50 (HR 1.12 vs. 1.67 without therapy).[45] Long-term non-cancer outcomes include heightened osteoporosis and cognitive decline risks, with premenopausal BSO linked to dementia (adjusted OR 1.60, 95% CI 1.14-2.25 by age 50).[5] These data underscore causal links to ovarian hormone deprivation, with risks accruing over decades absent mitigation.[28]Indications
Oncologic Applications
Oophorectomy serves as a primary surgical intervention in the treatment of epithelial ovarian cancer, fallopian tube cancer, and primary peritoneal cancer, where bilateral salpingo-oophorectomy (BSO) is routinely combined with hysterectomy and comprehensive staging procedures to achieve maximal cytoreduction and assess disease extent.[48] In early-stage disease, this approach facilitates adjuvant chemotherapy decisions, with NCCN guidelines endorsing six cycles of intravenous chemotherapy for stage I high-grade serous carcinoma following such surgery.[49] For advanced stages, BSO contributes to debulking efforts, aiming for optimal residual disease less than 1 cm, which correlates with improved progression-free survival.[50] In endometrial cancer management, particularly for apparent early-stage disease, total hysterectomy with BSO represents the standard surgical treatment, enabling pathologic evaluation and reducing recurrence risk by addressing potential occult ovarian involvement.[51] This procedure is recommended for postmenopausal women, where ovarian preservation offers no survival benefit and may increase morbidity from metachronous ovarian neoplasms.[52] In premenopausal patients, ovarian conservation may be considered selectively if no extrauterine disease is evident, though evidence indicates comparable oncologic outcomes with BSO in low-risk cases.[53] Risk-reducing salpingo-oophorectomy (RRSO) is indicated for women with hereditary predispositions, such as BRCA1 or BRCA2 pathogenic variants, to mitigate ovarian cancer incidence by 80-96% and breast cancer risk by approximately 50%.[54] Guidelines recommend RRSO between ages 35-40 for BRCA1 carriers and 40-45 for BRCA2 carriers, prior to natural menopause, yielding reductions in all-cause mortality (hazard ratio 0.52) and breast cancer-specific mortality in long-term follow-up.[6] This intervention also lowers second primary cancer risks, though it necessitates counseling on associated endocrine consequences like cardiovascular and skeletal effects.[55] In colorectal cancer with ovarian metastases, palliative oophorectomy may extend survival in select cases, but its role remains adjunctive to systemic therapy.[56]Benign Gynecologic Conditions
Oophorectomy is indicated for benign gynecologic conditions when conservative treatments, such as watchful waiting, medical therapy, or cystectomy, fail to resolve persistent symptoms like severe pelvic pain, mass effect, or recurrent complications including torsion or rupture.[1] In premenopausal women, ovarian conservation is generally preferred to avoid iatrogenic surgical menopause and its associated risks, including cardiovascular disease and osteoporosis, unless the pathology compromises ovarian viability or poses ongoing threats.[1] [57] Guidelines from organizations like ACOG emphasize cystectomy over oophorectomy for isolated benign cysts to preserve fertility and endocrine function.[58] For benign ovarian cysts and neoplasms, such as functional cysts, dermoid cysts, or serous cystadenomas, unilateral oophorectomy may be performed if the lesion exceeds 5-10 cm, persists beyond 8-12 weeks despite observation, causes hemodynamic instability from rupture or torsion, or if imaging and tumor markers suggest a need for definitive histology despite benign features.[59] [60] In cases of adnexal torsion, oophorectomy is reserved for ovaries with irreversible ischemia, occurring in approximately 10-15% of detorsed cases where viability cannot be salvaged intraoperatively.[8] Severe endometriosis involving the ovaries, particularly large endometriomas (>4 cm) refractory to hormonal suppression or prior excisions, may warrant oophorectomy to alleviate chronic pain and reduce recurrence risk, which approaches 20-40% after cystectomy alone.[61] [62] Bilateral oophorectomy is considered in advanced disease with deep infiltrating lesions or when combined with hysterectomy for symptom control, though evidence shows higher postoperative pain relief but at the cost of ovarian reserve depletion.[8] [1] Tubo-ovarian abscesses secondary to pelvic inflammatory disease, unresponsive to broad-spectrum antibiotics and percutaneous drainage, often necessitate salpingo-oophorectomy to prevent sepsis, with surgical intervention required in up to 15-20% of severe cases.[62] [63] Ectopic pregnancies with ovarian involvement or rupture may also prompt oophorectomy if conservative salpingostomy risks persistent trophoblast or ovarian damage.[8] Across these indications, patient selection prioritizes those with completed family planning or perimenopausal status to mitigate long-term endocrine deficits.[1]Prophylactic and Risk-Reduction Scenarios
Prophylactic oophorectomy, typically performed as bilateral salpingo-oophorectomy (BSO), is recommended for women at substantially elevated risk of ovarian cancer due to hereditary genetic mutations, such as BRCA1 and BRCA2 pathogenic variants.[64][65] This procedure removes both ovaries and fallopian tubes to prevent high-grade serous carcinoma, which often originates in the fallopian tubes.[66] In BRCA1 carriers, the lifetime ovarian cancer risk approaches 40-60%, and in BRCA2 carriers, 10-30%, justifying risk-reduction surgery after completion of childbearing.[67] Guidelines from the American College of Obstetricians and Gynecologists (ACOG) and National Comprehensive Cancer Network (NCCN) endorse risk-reducing BSO (RRSO) for these high-risk groups, with timing advised at ages 35-40 for BRCA1 and 40-45 for BRCA2 mutation carriers to balance cancer prevention against premature menopause effects.[68][69] RRSO reduces ovarian cancer incidence by 80-95% and overall mortality by approximately 68-94% in these populations, based on prospective cohort studies and meta-analyses.[67][66] It also confers a 50% reduction in breast cancer risk, particularly if performed before age 40, due to elimination of ovarian hormone exposure, as evidenced by long-term follow-up data from BRCA cohorts.[70][71] In Lynch syndrome (hereditary nonpolyposis colorectal cancer), characterized by mismatch repair gene mutations (e.g., MLH1, MSH2), prophylactic hysterectomy with BSO is an effective strategy to mitigate elevated risks of endometrial (40-60% lifetime) and ovarian (8-14% lifetime) cancers.[72][73] A prospective study of 261 women with Lynch syndrome demonstrated near-complete prevention of gynecologic cancers following this surgery, with no cases observed post-procedure over extended follow-up.[73] NCCN guidelines suggest considering BSO alongside hysterectomy upon completion of childbearing or near menopause, though ovarian cancer risk in Lynch is lower than in BRCA, influencing individualized decision-making.[74] For carriers of other actionable deleterious mutations predisposing to ovarian cancer (e.g., RAD51C/D, BRIP1), ACOG recommends offering RRSO similar to BRCA protocols, though evidence is sparser and derived from smaller cohorts showing comparable risk elevations.[68] Shared decision-making is emphasized, weighing benefits against surgical menopause risks like osteoporosis and cardiovascular disease, with hormone replacement therapy often advised until natural menopause age for non-breast cancer risks.[64][75] Primary peritoneal carcinomatosis remains a rare residual risk (1-6%) post-RRSO across these syndromes.[66]Contraindications and Selection Criteria
Absolute and Relative Contraindications
No absolute contraindications exist for oophorectomy, as the procedure can technically be performed in nearly all scenarios when surgical risks are deemed manageable, though the ovaries' roles in hormone production and fertility necessitate individualized assessment.[1][76] Relative contraindications include scenarios where the potential harms—such as irreversible infertility, premature menopause, or exacerbation of comorbidities—may outweigh benefits absent a compelling indication like malignancy.[1] These encompass:- Desire for fertility preservation: Bilateral oophorectomy eliminates ovarian function and oocyte production, rendering natural conception impossible; unilateral procedures may preserve fertility if the contralateral ovary is functional, but this is weighed against disease risks.[1][76]
- Premenopausal status without oncologic imperative: In women under 45-50 years without high-risk genetic mutations (e.g., BRCA1/2) or confirmed pathology, removal induces surgical menopause, increasing risks of cardiovascular disease, osteoporosis, and cognitive decline by 1.5-2-fold compared to natural menopause, per cohort studies.[77] Guidelines advise conservation in low-risk benign cases to avoid these outcomes unless alternatives fail.[28]
- Prophylactic intent in very young women: For risk-reducing salpingo-oophorectomy in BRCA carriers, procedures before age 30-35 are relatively discouraged without family history of ovarian cancer, as lifetime risk reduction must balance against 20-30% heightened mortality from non-oncologic causes like heart disease.[78] National Comprehensive Cancer Network guidelines recommend delaying until completion of childbearing or age 35-40 for BRCA1, prioritizing surveillance alternatives.[79]
- Severe pelvic adhesions or adhesions: Extensive adhesive disease complicates access and raises intraoperative injury risk (e.g., bowel or ureteral damage in 1-2% of cases), favoring alternative approaches like staging or conservative management if feasible.[76]
- Uncontrolled comorbidities: Conditions like active pelvic infection, uncorrected coagulopathy, or decompensated cardiopulmonary disease elevate perioperative morbidity (e.g., thrombosis risk doubling in hypercoagulable states), rendering the procedure relatively inadvisable without optimization.[1]
