Long-term outcomes of catheter-directed sclerotherapy for ovarian endometrioma

The Seoul National University Bundang Hospital Institutional Review Board approved this retrospective study (decision no: B-2003-602-301; approved on: 05-10-2023) and waived the requirement for informed consent due to the study design. Data of patients who underwent CDS for ovarian endometrioma between January 2020 and February 2022 were obtained from the institution’s electronic medical record system (date of access to patient data: 01/20/2023). The inclusion criteria for the CDS procedure were: (a) age >18 years; (b) symptoms suggesting endometriosis (dyspareunia, dysmenorrhea, and lower abdominal or pelvic pain) (c) largest diameter of cyst ≥3 cm; (d) ultrasound features suggestive of endometrioma; (e) no evidence of malignancy on contrast-enhanced magnetic resonance or computed tomography images; and (f) serum cancer antigen 125 (CA-125) levels <200 U/mL. Patients who lacked baseline serum AMH levels or were lost to follow-up less than 6 months after CDS were excluded ( Figure 1 ). Following the CDS procedure, patients were required to continue taking dienogest or oral contraceptive pills for at least 2 years to prevent recurrence. 18 During the follow-up period, serum AMH and CA-125 levels were monitored, and the largest diameter and mean volume of the lesion were measured using transvaginal ultrasonography. One board-certified radiologist (J.H.L) with 10 years of experience in interventional radiology and pelvic imaging performed the CDS. The procedure was performed as previously described. 6 , 7 Preprocedural ultrasonography was performed 1–2 weeks prior to CDS to evaluate the lesion characteristics, lesion size/volume, and access route (transvaginal or transabdominal). For transvaginal access, the target lesion was punctured using an 18-G 20 cm needle (Chiba biopsy needle, Bloomington, Cook, USA), followed by the placement of a 0.035-inch hydrophilic guidewire (Radifocus, Terumo, Japan) and 8.5-F drainage catheter (Dawson-Mueller Drainage catheter; Cook). After drainage of the contents and irrigation with normal saline, 2–3 cc of contrast was infused into the lesion to evaluate any signs of leakage or rupture. 7 If there was no leakage or rupture, 99% ethanol was infused carefully at 25% of the drained volume, with a maximum dose of <100 mL. The patient’s position (clockwise rotation from supine to left decubitus, prone, and right decubitus) was then changed every 5 min. Finally, ethanol was aspirated and the catheter was removed. To rule out malignancy, the aspirated contents were sent to pathology for cytology evaluation. 6 , 7 All patients underwent the procedure on the day of admission and were discharged the following day. All patients underwent ultrasonography at 6 and 12 months after CDS to follow up on cyst size and any recurrence. To evaluate cyst size, the volume of the ovarian endometrioma was calculated using the formula for an ellipsoid, with the length and width of the lesion measured by ultrasound. Volume reduction was calculated by the percentage change in volume from pre-procedure to post-procedure measurements. Serum AMH levels were tested 6 and 12 months after CDS to evaluate the effect of CDS on ovarian reserve. Serum CA-125 levels, which reflect endometrioma burden, were assessed at the same time points. Complications related to the procedure were recorded for each instance. Data are presented as mean ± standard deviation. Changes in endometrioma volume and serum AMH and CA-125 levels before and after CDS were analyzed using the paired t-test or Wilcoxon signed-rank test, depending on the normality of the variable. The PASW 18.0 software (IBM, Armonk, NY, USA) was used for all statistical analyses. A P value of <0.050 was considered statistically significant. Recurrence was defined as the return of symptoms and/or newly developed detectable endometrioma on follow-up ultrasound.

In total, 33 of the 45 patients originally chosen were enrolled in this study; those without baseline serum AMH levels (n = 9) and those who were lost to follow-up less than 6 months after CDS (n = 3) were excluded. Table 1 summarizes the baseline characteristics of patients and lesions. The mean AMH level was 2.99 ± 2.16 ng/mL. The technical success rate of CDS was 100%. The hospitalization period for all patients was 2 days. One patient experienced moderate abdominal pain (visual analog scale score: 5), but it was resolved with conservative management. All cytological analyses of the aspirates were negative for malignant cells. The largest diameter and mean volume of the endometriomas continuously decreased for 1 year after CDS ( Table 2 ). The mean volume reduction percentage at 12 months after CDS was 98.99 ± 1.54%. The mean follow-up period was 12 months (range: 8.36–17.5 months), with data focusing primarily on the 12-month outcomes. No recurrences were observed during the follow-up period. The serum CA-125 level significantly decreased at 6 months and this was maintained at 1 year ( P = 0.010); however, there was no significant difference in the serum AMH levels before and 1 year after CDS ( P = 0.302) ( Figure 2 ).

This study aimed to evaluate the long-term efficacy and safety of CDS with 99% ethanol for the treatment of ovarian endometriomas. We found that the endometrioma volume rapidly decreased in the first 6 months, with a 99% reduction maintained over a year. The trends in serum CA-125 levels were consistent with the changes in endometrioma volume, reflecting a decrease in the burden of disease. These findings align with previous reports. 6 , 7 As the catheter is securely located, the risk of potential spillage of the contents is low, and patients can change their position to enhance the cyst wall exposure to ethanol. 6 , 7 , 10 Interestingly, the treated endometriomas had not recurred by the end of the follow-up period. No recurrence after CDS has been reported in the literature, including this study. 6 , 7 In a review article comparing 11 studies on recurrence rates after ablation or cystectomy, recurrence rates over 1 year ranged from 4.4% to 37.0%. 4 In previous articles on CDS, as well as in this study, patients were not prevented from continuing medication after the CDS treatment. Given the nature of ovarian endometriomas with frequent recurrence, CDS combined with hormonal treatment seems to suppress the recurrence of endometrioma effectively. In this study, serum AMH, which reflects the ovarian reserve, was well preserved after CDS. Although laparoscopic cystectomy is the current standard treatment, it has several disadvantages, including the risk of general anesthesia, perilesional adhesions, and decline in ovarian function. 1 , 7 , 15 In addition to the inevitable removal of ovarian follicles adjacent to the endometrioma, hemostatic cauterization may add collateral damage to the ovarian circulation and cause further follicular loss. 15 In CDS, catheters can be accurately placed in the lesion, and unintended injury to the adjacent healthy ovarian parenchyma can be minimized. Previous studies have demonstrated AMH changes up to 6 months after the procedure, whereas this study included results up to 12 months, providing the most extended follow-up data available. Furthermore, this study has the advantage of having one skilled expert performing all procedures, eliminating the possibility of variation among different operators. This study has several limitations. Due to its retrospective design, consistent and comparable data on intraprocedural and postprocedural pain were difficult to obtain. Nevertheless, medical records indicate that only one patient required additional analgesics for abdominal pain beyond conventional post-procedural management, suggesting the procedure was generally well-tolerated. Additionally, having a single operator perform all procedures and the absence of a control group limit the generalizability of the findings. Future prospective studies with standardized pain assessments and comparative analyses are needed. In conclusion, CDS for ovarian endometrioma showed favorable safety and long-term outcomes without recurrence. The ovarian reserve was well preserved during the follow-up period of 1 year.