Limited Added Value of Magnetic Resonance Imaging After Dynamic Transvaginal Ultrasound for Preoperative Staging of Endometriosis in Daily Practice: A Prospective Cohort Study

The characteristics of the 72 patients are summarized in Table 3 . All 72 patients underwent surgery; in 59, deep infiltrating endometriosis was confirmed; and 13 patients had a diagnosis of “low‐grade endometriosis.” With respect to the surgical location, all patients had peritoneal endometriosis; 34 patients had bowel endometriosis; 3 patients had bladder endometriosis; 3 patients had endometriosis around the ureter; and 26 patients had an ovarian endometrioma. Clinical Characteristics of the Patients (n = 72) The sensitivity, specificity, PPV. and NPV for each consecutive step in the diagnosis of pelvic endometriosis are given in Table 4 . Notably, the sensitivity after adding the results from the history, clinical examination, and dynamic TVUS was 93.7% ( P  < .001). When the MRI results were included, the sensitivity was 85.9% ( P  = .219). However, after including MRI, the specificity was less for dynamic TVUS only. Comparison of the Consecutive steps: History, Clinical Examination, Dynamic TVUS, and MRI in the Diagnosis of Endometriosis (n = 72) Significance was calculated by comparison of step 2 to 1, step 3 to 2, and step 4 to 3. The added value of MRI compared to step 2 was significant ( P   .05). In 59 of 72 patients, deep infiltrating endometriosis was confirmed by laparoscopy. In Table 5 , the sensitivity, specificity, PPV, and NPV for each consecutive step in the diagnosis of deep infiltrating endometriosis are given. The sensitivity for the history, clinical examination, and dynamic TVUS was 93.2% ( P  < .001), whereas after inclusion of MRI findings, the sensitivity dropped to 88.1% ( P  = .375). As a consequence of the observational design of our study and the selection criteria for surgery, only patients with deep infiltrating endometriosis or a visual analog score of less than 7 underwent surgery; this approach explains why the NPV and specificity were either 0 or could not be calculated. Comparison of the Consecutive Steps: History, Clinical Examination, Dynamic TVUS, and MRI in the Diagnosis of Deep Infiltrating Endometriosis (n = 59) Significance was calculated by comparison of step 2 to 1, step 3 to 2, and step 4 to 3. The added value of MRI compared to step 2 was significant ( P   .05). Results of proper staging of endometriosis after each consecutive step in the diagnostic routine are given in Table 6 . Correct staging after dynamic TVUS was 88.9% (64 of 72 patients); after MRI, it was 83.3%. Including dynamic TVUS findings only, underestimation by 1 stage performed better than after inclusion of MRI findings (5.6% versus 11.2%). Prediction of the Correct Stage of Endometriosis (Stage I–IV) According to the Revised AFS Classification of Each Diagnostic Step Compared to Laparoscopic Findings (n = 72)

A prospective observational study was conducted in our referral center for endometriosis between April 22, 2014, and May 1, 2015. Exclusion criteria comprised patients younger than age 18 years, patients for whom dynamic TVUS was not possible (eg, Virgo condition), and patients with claustrophobia or contraindications to MRI. A total of 363 patients with a clinical suspicion of endometriosis were included. The local Ethical Committee approved the study as exempt from review because this study had no impact on routine patient care. All patients underwent a history, clinical examination, and dynamic TVUS examination. After each step in the diagnostic pathway, the extent and severity of the endometriosis were determined. Most of the patients (n = 274) underwent conservative treatment according to the European Society of Human Reproduction and Embryology guidelines (Table 1 ). 18 Finally, 89 patients were selected for surgery, of whom 72 patients underwent the full diagnostic pathway: ie, history, clinical examination, dynamic TVUS, and MRI (Figure 1 ). Study flowchart. DIE indicates deep infiltrating endometriosis. Conservative Treatment in Patients With Signs of Endometriosis (n = 274) The history included symptoms of dyspareunia, dysmenorrhea, dysuria, dyschezia, and cyclic or chronic pelvic pain and subfertility. In addition, patients were questioned about the quality of their social life: ie, physical discomfort and depression (Table 2 ). History Checklist Physical examinations were performed by 2 examiners, both with more than 15 years of experience in endometriosis (M.S. and J.R.). Patients underwent a pelvic examination focusing on blue spots on the cervix, vaginal wall involvement, and the posterior vaginal fornix. Mobility of the uterus and ovaries, uterosacral ligaments, and nodules in the pouch of Douglas or anterior fornix was assessed by palpation. Suspected deep infiltrating endometriosis was noted separately. Based on the information obtained during the history and pelvic examination, a dynamic TVUS examination was performed by a single examiner with 5 years of specialization in US for endometriosis (J.P.B.) using a transvaginal transducer at a frequency of 5–9 MHz (Voluson E8; GE Healthcare, Buckinghamshire, England). No bowel preparations or vaginal contrast agents were used; the bladder needed to be partially filled. First, a standard evaluation of the uterus and ovaries was performed. Then, the dynamic part of the examination was conducted: the uterine sliding sign, tenderness‐guided US, and evaluation of hard and soft markers. The uterine sliding sign establishes whether the rectum moves freely across the posterior wall of the uterus, cervix, or both when pressed gently with the vaginal transducer. If the sign is negative (ie, the rectum or rectosigmoid does not slide freely across the uterus or cervix), the pouch of Douglas is considered obliterated. 14 , 15 Tenderness‐guided US exploits the fact that endometriotic nodules can evoke pain. Therefore, patients can indicate which points are painful during the examination. These sites are then examined with extra attention. 16 , 17 Hard markers are structural abnormalities: ie, hydrosalpinx or an endometrioma. Soft markers are loculated peritoneal fluid, ovarian mobility, and site‐specific tenderness. 18 Hypoechoic nodules were actively looked for in the bowel, bladder, sacral uterine ligaments, posterior vaginal fornix, and paraureteral area as described by Bazot et al 7 and noted separately. Magnetic resonance imaging was performed within 6 weeks after dynamic TVUS. The MRI examinations were performed on a 1.5‐T superconducting magnet (Magnetom Avantofit; Siemens AG, Erlangen, Germany) using an 18‐channel radiofrequency body coil. The MRI protocol consisted of multiplanar turbo spin echo T2‐weighted images (512 matrix; axial, sagittal, and coronal with a voxel size of 0.8 × 0.8 × 4.0 mm) and axial and sagittal T1‐weighted fat‐saturated breath hold sequences (320 matrix; voxel size of 1.3 × 1.3 × 6.0 mm. Twenty minutes before the MRI, patients were administrated 20 mg of butylscopolamine bromide intravenously (Buscopan; Sanofi‐Aventis, Paris, France) for bowel movement inhibition. No enema was administered; no vaginal distention was applied; and patients did not fast. No contrast agent was used. All MRI examinations were evaluated by a single radiologist with 10 years of experience in endometriosis. The radiologist was blinded to the results of the history, clinical examination, and dynamic TVUS. The diagnosis of deep infiltrating endometriosis was made essentially as described by Bazot et al 7 if one of the following criteria was met: hyperintense foci on the fat‐suppressed T1‐weighted images with corresponding hemorrhagic foci on T2‐weighted images, areas of fibrosis in the pelvic region, distortion of normal anatomy without any other explanation, and discontinuation of normal fatty tissue between organs. All patients included (n = 72) underwent laparoscopic resection of all endometriosis. Staging of endometriosis was determined by 2 gynecologists on visual inspection at laparoscopy according to the revised American Fertility Society (AFS) criteria; deep infiltrating endometriosis nodules were noted separately. 19 All visual diagnosis of endometriosis was confirmed by a histologic examination, as visual diagnosis does not correlate well with pathologic findings. 20 All analyses were performed with SPSS version 23 software (IBM Corporation, Armonk, NY). The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were calculated for each step in the diagnostic process. The nonparametric McNemar test was used for comparing between each step in the diagnostic algorithm. P  < .05 was considered statistically significant.

As endometriosis is a chronic and progressive disease, early diagnosis and proper staging are important for the patient and for the clinician to discuss and plan the required surgical procedures for treatment. 3 Preoperative staging, using common diagnostic tools, such as the clinical history, physical examination, dynamic TVUS, and MRI, is very well feasible in deep infiltrating endometriosis. In this study, we evaluated the added value of each step in the diagnostic pathway for the assessment of (deep infiltrating) endometriosis in outpatient settings. After the clinical history and pelvic examination, gynecologists were able to detect the correct stage of endometriosis according to the revised AFS classification in 47.2% of the patients. After the dynamic TVUS, this percentage increased to 88.9%. After MRI, this percentage decreased to 83.3%. This finding was due to the fact that MRI was not able to show (histologically confirmed) small rectal nodules in 7 of 72 patients: all between 1.5 and 2.5 cm. The advantage of dynamic TVUS is the ability to evaluate the mobility of the pelvic organs and site‐specific pain. 15 , 16 , 17 , 18 This ability provides the gynecologist with additional information, which contributes to the assessment of the correct stage of disease. This factor may, in our opinion, explain why after the dynamic TVUS, the correct stage was more frequently predicted than after MRI. Although MRI gives a better overview of the abdomen, most deep infiltrating endometriosis lies in the pelvis. 21 Different combinations of diagnostic tools have been evaluated recently. Marasinghe et al 22 compared the history, pelvic examination, and mobility of ovaries to detect pelvic adhesions. They found sensitivity of 91% and specificity of 60.9% for identifying fixed ovaries secondary to endometriosis. Hudelist et al 8 investigated the combination of clinical examination and TVUS for preoperative diagnosis of pelvic endometriosis and concluded that the combination of the physical examination accurately predicted the presence of endometriosis affecting the ovaries, vagina, rectum, uterosacral ligaments, rectovaginal septum, and pouch of Douglas in patients with suspected endometriosis. Abrao et al 9 compared clinical examination, TVUS, and MRI for the diagnosis of deep infiltrating endometriosis and found that TVUS had better sensitivity and specificity in cases of deep retrocervical and rectosigmoid endometriosis compared to MRI and physical examination. However, Abrao et al 9 focused on deep infiltrating endometriosis in the posterior compartment, and Hudelist et al 8 compared TVUS to clinical examination only and without comparison to MRI, whereas Marasinghe et al 22 only focused on pelvic adhesions. To our knowledge, our study is the first prospective study to evaluate the added value of MRI after dynamic TVUS for staging endometriosis preoperatively and to test its usefulness in routine clinical practice. The most important factor for planning a laparoscopic resection of endometriosis is to identify all nodules caused by deep infiltrating endometriosis, since this step may influence the planning of the procedure. 3 In an expert center, 88.9% of all patients with endometriosis can have the correct stage diagnosed at the first visit (Table 4 ), since TVUS is easily accessible in an outpatient setting. Also, TVUS and MRI are highly sensitive diagnostic tools for staging deep infiltrating endometriosis preoperatively. Although TVUS is less expensive and more accessible than MRI, our results were obtained by a single expert gynecologist for dynamic TVUS and a single radiologist for MRI. Ultrasound is much more operator dependent than MRI. Ultrasound is less sensitive for endometriosis beyond the field of view of the transvaginal transducer. 23 It is also likely less sensitive for anterior compartment endometriosis. 23 Routine MRI scans are therefore redundant and should only be performed when an extrapelvic location of deep infiltrating endometriosis is suspected or when a TVUS examination is not possible. This approach is in line with the findings of Turocy and Benacerraf. 24 Several limitations of our study need to be considered. First, different scoring systems are proposed to document US findings regarding deep infiltrating endometriosis. Both the Enzian score 25 and the scoring system used by Coccia and Rizello 26 are more detailed than the revised AFS classification, as is the classification system developed by Exacoustos et al. 27 However, these classification systems are still not widely used, so for the purpose of this study and comparison to the literature, classification by the revised AFS system was used, and deep infiltrating endometriosis nodules were noted separately. Second, similar to the findings of Bazot et al, 7 the prevalence of deep infiltrating endometriosis was particularly high, resulting in a particularly high rate of diagnosis by the clinical history and physical examination. This finding was inherent to the fact that the study was performed in a center with expertise in endometriosis. Another explanation for the high prevalence of deep infiltrating endometriosis in our study was that low‐grade endometriosis was treated conservatively. We conclude that routine MRI after dynamic TVUS has no added value based on the following lines of evidence: First, the results in Table 4 clearly show that for diagnosis of pelvic endometriosis, inclusion of dynamic TVUS alone performed as well as after MRI. Second, the same conclusion can be drawn from Table 5 for diagnosis of deep infiltrating endometriosis. Third, dynamic TVUS performed even better at predicting the correct stage in patients predominantly affected by deep infiltrating endometriosis. Our results clearly show that there is no substantial added value of routine MRI after dynamic TVUS for the preoperative staging of endometriosis. After the history and physical examination, dynamic TVUS and MRI both yield similar added value in preoperative staging of endometriosis with great overlap in clinical information. Both have their advantages and disadvantages, so choosing proper diagnostic imaging depends on the availability of an expert sonographer or MRI radiologist and on the anatomic site of interest based on the history and physical examination. Hopefully, this approach will eventually result in the reduction of costs for routine MRI scans, and more personalized preoperative counseling can be given to the patient.