Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014:2014:191967.
doi: 10.1155/2014/191967. Epub 2014 Aug 7.

Medical treatments for endometriosis-associated pelvic pain

Affiliations
Review

Medical treatments for endometriosis-associated pelvic pain

Gabriella Zito et al. Biomed Res Int. 2014.

Abstract

The main sequelae of endometriosis are represented by infertility and chronic pelvic pain. Chronic pelvic pain causes disability and distress with a very high economic impact. In the last decades, an impressive amount of pharmacological agents have been tested for the treatment of endometriosis-associated pelvic pain. However, only a few of these have been introduced into clinical practice. Following the results of the controlled studies available, to date, the first-line treatment for endometriosis associated pain is still represented by oral contraceptives used continuously. Progestins represent an acceptable alternative. In women with rectovaginal lesions or colorectal endometriosis, norethisterone acetate at low dosage should be preferred. GnRH analogues may be used as second-line treatment, but significant side effects should be taken into account. Nonsteroidal anti-inflammatory drugs are widely used, but there is inconclusive evidence for their efficacy in relieving endometriosis-associated pelvic pain. Other agents such as GnRH antagonist, aromatase inhibitors, immunomodulators, selective progesterone receptor modulators, and histone deacetylase inhibitors seem to be very promising, but there is not enough evidence to support their introduction into routine clinical practice. Some other agents, such as peroxisome proliferator activated receptors-γ ligands, antiangiogenic agents, and melatonin have been proven to be efficacious in animal studies, but they have not yet been tested in clinical studies.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Giudice LC, Kao LC. Endometriosis. The Lancet. 2004;364(9447):1789–1799. - PubMed
    1. Guo S, Wang Y. The prevalence of endometriosis in women with chronic pelvic pain. Gynecologic and Obstetric Investigation. 2006;62(3):121–130. - PubMed
    1. Simoens S, Dunselman G, Dirksen C, et al. The burden of endometriosis: costs and quality of life of women with endometriosis and treated in referral centres. Human Reproduction. 2012;27(5):1292–1299. - PubMed
    1. Menakaya U, Infante F, Condous G. Consensus on current management of endometriosis. Human Reproduction. 2013;28:3162–3163. - PubMed
    1. Dunselman GA, Vermeulen N, Becker C, et al. ESHRE guideline: management of women with endometriosis. Human Reproduction. 2014;29:400–412. - PubMed

MeSH terms