Immediate and delayed add‐back hormonal replacement therapy during ultra long GnRH agonist treatment of chronic cyclical pelvic pain

Majedah Al‐Azemi, Georgina Jones, Füsun Sirkeci, Stephen J. Walters, M Houdmont, William J. Ledger
In: BJOG: An International Journal of Obstetrics & Gynaecology · 2009 · vol. 116(12) , pp. 1646–1656 · doi:10.1111/j.1471-0528.2009.02319.x · PMID:19735378 · W1865102798
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This randomized trial found that immediate add-back hormonal replacement therapy during GnRH agonist treatment for pelvic pain preserved bone mineral density and reduced symptoms compared to delayed HRT, although long-term outcomes were similar.

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Abstract

OBJECTIVE: To assess the safety and efficacy of long-term use of long-acting GnRH agonist in women with chronic cyclical pelvic pain using immediate versus delayed add-back hormonal replacement therapy (HRT). DESIGN: A prospective randomised trial. SETTING: Reproductive and Developmental Medicine, Academic Unit, University Teaching Hospital and NHS Hospitals. POPULATION: Thirty-eight premenopausal women with chronic cyclical pelvic pain were recruited. METHODS: Women were given Zoladex 10.8 mg over 18 months and randomised to receive HRT (tibolone 2.5 mg) either immediately or after 6 months. Follow up was 12-month post-treatment. MAIN OUTCOME MEASURES: Bone mineral density at 6 months, the end of treatment (18 months), and 12 months later, pain and quality of life. RESULTS: Women treated with immediate HRT add-back showed less bone mineral density loss at 6 months and less vasomotor symptoms compared with those who had delayed HRT add-back treatment. Long-term follow up showed both groups experienced equivalent bone mineral density loss. Pain and health-related quality-of-life assessment showed improvement in both groups but there was evidence of a return to baseline levels after ending treatment. CONCLUSION: Long-term use of GnRH agonist plus immediate add-back HRT is a safe and acceptable approach to intractable cyclical pelvic pain. Given the delay in reactivation of the hypothalamo-pituitary-ovarian axis after long-term suppression, an intermittent dose regime with GnRH agonist might warrant investigation.

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