Effect of catheter-directed ethanol sclerotherapy on ovarian reserve in patients with recurrent endometrioma: comparative analysis with primary endometriosis

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Catheter-directed ethanol sclerotherapy showed no significant difference in anti-Müllerian hormone levels for recurrent endometrioma compared to primary endometrioma.

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This retrospective, single-institution observational study evaluated changes in ovarian reserve, measured by anti-Müllerian hormone (AMH), in adults with recurrent ovarian endometrioma undergoing catheter-directed ethanol sclerotherapy (CDS), comparing them with patients with primary endometrioma. AMH and other baseline variables (including cyst diameter and CA-125) were assessed before CDS and at multiple follow-up times (1 month through 3 years), with outcomes analyzed both overall and stratified by laterality, baseline AMH, and initial cyst size. The study found no significant difference in AMH levels between primary and recurrent groups at baseline and no significant difference in the delta change in AMH at any follow-up time, with no recurrences reported in either group. The paper’s main limitation, as framed by its methods, is that it is retrospective and observational without randomization. This paper is centrally about endometriosis — it directly examines ovarian reserve changes after CDS specifically in recurrent versus primary endometrioma.

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Abstract

OBJECTIVE: Catheter-directed ethanol sclerotherapy (CDS) is known to less affect the ovarian function, with comparable efficacy. This study aims to investigate the change in ovarian reserve after catheter-directed ethanol sclerotherapy in patients with recurrent endometrioma, as compared to primary endometrioma. MATERIALS AND METHODS: Retrospective, observational study. Electronic medical records and images of patients with endometrioma who underwent CDS from August 2014 to April 2022 at a single institution were obtained. Patients aged > 18 years old and with anti-Müllerian hormone (AMH) level between 0.8 and 10.0 with regular menstruation were enrolled. Cyst diameter, laterality, AMH level, and CA-125 level before and after 1 month, 6 months, 1 year, 2 years, and 3 years of sclerotherapy were obtained. RESULTS: A total of 180 patients were fit for analysis. There was no statistical difference in age and cyst size between the two groups. Mean values of AMH in each group were 3.35 in the primary group and 3.00 in the recurrent group prior to the procedure (p = 0.347). There was no significant difference in delta value of AMH after sclerotherapy in both groups at each follow-up period. Also, this result was consistent when stratified by laterality, preprocedural AMH level, and initial size of endometrioma. No case of recurrence was reported in both groups. CONCLUSIONS: The effect of CDS on ovarian reserve is not inferior in recurrent endometrioma compared to primary endometrioma. Since sclerotherapy is known to less deteriorate the ovarian function than surgical removal of endometrioma, clinician could consider this as the first-line therapy in patients with recurrent endometrioma. CLINICAL RELEVANCE STATEMENT: Catheter-directed ethanol sclerotherapy for patients with recurrent endometrioma has similar effect on ovarian reserve compared to patients with primary endometrioma. KEY POINTS: • Secondary surgery for endometrioma has significant deleterious effect on ovarian function. • Catheter-directed sclerotherapy (CDS) for endometrioma had equally minimal adverse effect on ovarian reserve, represented as anti-Müllerian hormone (AMH), in both primary and recurrent groups. • Physicians should consider CDS for patients with recurrent endometrioma who desire to preserve ovarian function.
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Abstract

Objective Catheter-directed ethanol sclerotherapy (CDS) is known to less affect the ovarian function, with comparable efficacy. This study aims to investigate the change in ovarian reserve after catheter-directed ethanol sclerotherapy in patients with recurrent endometrioma, as compared to primary endometrioma.

Materials and methods

Retrospective, observational study. Electronic medical records and images of patients with endometrioma who underwent CDS from August 2014 to April 2022 at a single institution were obtained. Patients aged > 18 years old and with anti-Müllerian hormone (AMH) level between 0.8 and 10.0 with regular menstruation were enrolled. Cyst diameter, laterality, AMH level, and CA-125 level before and after 1 month, 6 months, 1 year, 2 years, and 3 years of sclerotherapy were obtained.

Results

A total of 180 patients were fit for analysis. There was no statistical difference in age and cyst size between the two groups. Mean values of AMH in each group were 3.35 in the primary group and 3.00 in the recurrent group prior to the procedure (p = 0.347). There was no significant difference in delta value of AMH after sclerotherapy in both groups at each follow-up period. Also, this result was consistent when stratified by laterality, preprocedural AMH level, and initial size of endometrioma. No case of recurrence was reported in both groups.

Conclusions

The effect of CDS on ovarian reserve is not inferior in recurrent endometrioma compared to primary endometrioma. Since sclerotherapy is known to less deteriorate the ovarian function than surgical removal of endometrioma, clinician could consider this as the first-line therapy in patients with recurrent endometrioma. Clinical relevance statement Catheter-directed ethanol sclerotherapy for patients with recurrent endometrioma has similar effect on ovarian reserve compared to patients with primary endometrioma. Key Points • Secondary surgery for endometrioma has significant deleterious effect on ovarian function. • Catheter-directed sclerotherapy (CDS) for endometrioma had equally minimal adverse effect on ovarian reserve, represented as anti-Müllerian hormone (AMH), in both primary and recurrent groups. • Physicians should consider CDS for patients with recurrent endometrioma who desire to preserve ovarian function. Similar content being viewed by others Abbreviations - AFC: - Antral follicle count - AMH: - Anti-Müllerian hormone - BMI: - Body mass index - CA-125: - Cancer antigen 125 - CDS: - Catheter-directed sclerotherapy - FSH: - Follicle-stimulating hormone - IQR: - Interquartile range - PCOS: - Polycystic ovarian syndrome - PSM: - Propensity score matching

References

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Eur Radiol 31(1):543–548 Ferrero S, Scala C, Racca A et al (2015) Second surgery for recurrent unilateral endometriomas and impact on ovarian reserve: a case-control study. Fertil Steril 103(5):1236–1243 Mol BWJ, Bayram N, Lijmer JG et al (1998) The performance of CA-125 measurement in the detection of endometriosis: a meta-analysis. Fertil Steril 70(6):1101–1108 May KE, Conduit-Hulbert SA, Villar J, Kirtley S, Kennedy SH, Becker CM (2010) Peripheral biomarkers of endometriosis: a systematic review. Hum Reprod Update 16(6):651–674 Chen Y, Pan M, Zuo Y, Yang B, Wang S (2022) Research progress of CA125 in endometriosis: teaching an old dog new tricks. Gynecol Obstet Clin Med 2(4):191–198 Hsieh C-L, Shiau C-S, Lo L-M, Hsieh T's-T'a, Chang M-Y (2009) Effectiveness of ultrasound-guided aspiration and sclerotherapy with 95% ethanol for treatment of recurrent ovarian endometriomas. Fertil Steril 91(6):2709–2713 Lee JK, Ahn SH, In Kim H et al (2022) Therapeutic efficacy of catheter-directed ethanol sclerotherapy and its impact on ovarian reserve in patients with ovarian endometrioma at risk of decreased ovarian reserve: a preliminary study. J Minim Invasive Gynecol 29(2):317–323 Younis JS, Shapso N, Fleming R, Ben-Shlomo I, Izhaki I (2019) Impact of unilateral versus bilateral ovarian endometriotic cystectomy on ovarian reserve: a systematic review and meta-analysis. Hum Reprod Update 25(3):375–391 Celik HG, Dogan E, Okyay E et al (2012) Effect of laparoscopic excision of endometriomas on ovarian reserve: serial changes in the serum antimüllerian hormone levels. Fertil Steril 97(6):1472–1478 Noma J, Yoshida N (2001) Efficacy of ethanol sclerotherapy for ovarian endometriomas. Int J Gynaecol Obstet 72(1):35–39 Ferraretti AP, La Marca A, Fauser BCJM et al (2011) ESHRE consensus on the definition of ‘poor response’ to ovarian stimulation for in vitro fertilization: the Bologna criteria. Hum Reprod 26(7):1616–1624 Song DK, Oh J-Y, Lee H, Sung Y-A (2017) Differentiation between polycystic ovary syndrome and polycystic ovarian morphology by means of an anti-Mullerian hormone cutoff value. Korean J Intern Med 32(4):690–698 Hart R, Doherty DA, Norman RJ et al (2010) Serum antimullerian hormone (AMH) levels are elevated in adolescent girls with polycystic ovaries and the polycystic ovarian syndrome (PCOS). Fertil Steril 94(3):1118–1121 Nardo LG, Yates AP, Roberts SA, Pemberton P, Laing I (2009) The relationships between AMH, androgens, insulin resistance and basal ovarian follicular status in non-obese subfertile women with and without polycystic ovary syndrome. Hum Reprod 24(11):2917–2923 Pigny P, Jonard S, Robert Y, Dewailly D (2006) Serum anti-Mullerian hormone as a surrogate for antral follicle count for definition of the polycystic ovary syndrome. J Clin Endocrinol Metab 91(3):941–945 Konishi S, Nishihama Y, Iida A, Yoshinaga J, Imai H (2014) Association of antimullerian hormone levels with menstrual-cycle type and dysmenorrhea in young asymptomatic women. Fertil Steril 102(5):1439–1443 Kostrzewa M, Wilczyński JR, Głowacka E, Żyła M, Szyłło K, Stachowiak G (2019) One-year follow-up of ovarian reserve by three methods in women after laparoscopic cystectomy for endometrioma and benign ovarian cysts. Int J Gynaecol Obstet 146(3):350–356 Kovacevic VM, Andelic LM, MitrovicJovanovic A (2018) Changes in serum antimullerian hormone levels in patients 6 and 12 months after endometrioma stripping surgery. Fertil Steril 110(6):1173–1180 Funding This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (NRF-2020R1C1C1013849). This study was also supported by a CMB-Yuhan research grant of Yonsei University College of Medicine (6–2018-0173). Author information Authors and Affiliations Corresponding authors Ethics declarations Guarantor The scientific guarantor of this publication is Seok Kyo Seo. Conflict of interest The authors of this manuscript declare no relationships with any companies, whose products or services may be related to the subject matter of the article. Statistics and biometry One of the authors has significant statistical expertise (Hae-Rim Kim). Informed consent Written informed consent was waived by the Institutional Review Board, owing to the retrospective nature of the study. Ethical approval Approval was obtained from the Institutional Review Board of the Severance Hospital, Yonsei University College of Medicine (approval no. 4–2021-1793). Study subjects or cohorts overlap Fifty-six of 180 patients who had undergone CDS have been previously reported [10]. The prior study was a study focused on patients at risk for decreased ovarian reserve, whereas in this manuscript, we compared effect of CDS on AMH between the primary group and recurrent group. Methodology • retrospective • observational • performed at one institution Additional information Publisher's note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Supplementary Information Below is the link to the electronic supplementary material. Rights and permissions Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. About this article Cite this article Lee, J.K., Han, K., Choi, E. et al. Effect of catheter-directed ethanol sclerotherapy on ovarian reserve in patients with recurrent endometrioma: comparative analysis with primary endometriosis. Eur Radiol 34, 3298–3308 (2024). https://doi.org/10.1007/s00330-023-10320-z Received: Revised: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1007/s00330-023-10320-z

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endometriosisendometrioma

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Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis

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