Endometriosis/adenomyosis is associated with more typical cystoscopic findings of interstitial cystitis in patients with elevated PUF scores
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In this paper, we present our experience with cystoscopy and hydrodistension for the diagnosis of interstitial cystitis (IC) and association with endometriosis/adenomyosis. This is a retrospective study of 116 patients who have undergone cystoscopy and hydrodistension because of suspicion of interstitial cystitis as shown by elevated Pain Urgency and Frequency questionnaire (PUF) scores and, in some patients, positive potassium sensitivity test (PST) or anesthetic bladder challenge (ABC) tests as well. Cystoscopic findings were grouped into “no IC,” “atypical IC,” and “typical IC” groups. Chi-square analysis was used for comparing percentages. PUF questionnaire showed high sensitivity (98%) with ≥5 score but low specificity (0%). The best specificity was found with PST (30%). Among IC patients, 60 (60%) had adenomyosis or endometriosis with an increasing endometriosis/adenomyosis rate from “no IC” to “typical IC” groups (37.5% to 67.74%, P < 0.05). PST is the most specific of the screening tests for IC, and cystoscopy with hydrodistension is the only test that allows direct visualization and grading of bladder abnormalities as “typical”, “atypical”, and “no IC”. The presence of endometriosis has a stronger association with typical IC findings on cystoscopy including glomerulations, ulcers, and reduced bladder capacity.
KeywordsInterstitial cystitis Endometriosis Adenomyosis PUF PST ABC
Interstitial cystitis (IC) is thought to be underestimated especially in the younger female population [5, 6]. It manifests with the triad: pelvic pain, urinary urgency/frequency, and nocturia. These symptoms may overlap with those of other common gynecologic and urologic conditions and may annoy the patient for years before interstitial cystitis is diagnosed . According to literature, hysterectomy is performed more frequently in patients with undiagnosed interstitial cystitis than in patients with a confirmed IC diagnosis [2, 8]. Many patients continue to experience persistent pelvic pain despite having had their uterus removed until interstitial cystitis is diagnosed and treated [2, 8]. Careful history, physical examination, and the use of Pain Urgency and Frequency (PUF) questionnaire and potassium (KCl) sensitivity test (PST) help detect the majority of interstitial cystitis cases. As an alternative to the PST, a symptomatic patient can undergo anesthetic bladder challenge (ABC) . Direct visualization of typical interstitial cystitis lesions in the bladder can be achieved only through cystoscopy with hydrodistension. Laparoscopy is frequently required to exclude other sources of pelvic pain, mainly endometriosis and/or adnexal adhesions [1, 4].
In this paper, we present our experience with cystoscopy and hydrodistension for the diagnosis of IC and put forth a theory explaining the relationship between interstitial cystitis and endometriosis/adenomyosis.
Materials and methods
This is a retrospective study of 116 patients who have undergone cystoscopy with hydrodistension (distension of the bladder to 70 to 100 cm of water pressure for 2–5 minutes). Cystoscopy with hydrodistension was recommended by the National Institute for Diabetes and Digestive and Kidney Diseases (Bethesda, MD, 1987) as an objective test for the diagnosis of interstitial cystitis in research protocols . These patients had cystoscopy with hydrodistension alone for failed office management of presumed interstitial cystitis based on PUF ≥10 with either positive PST, ABC, or both (N=10) or at the time of certain gynecological procedures, including total laparoscopic hysterectomy (N=39), total laparoscopic hysterectomy with anterior and/or posterior repair (N=3), diagnostic or operative laparoscopy (N=42), anterior and/or posterior colporrhaphy with Prolift placement (N=14), midurethral sling procedures (N=7), and myomectomy (N=1). PUF questionnaires were filled by all patients except three. PST was performed in 68 patients and ABC in 31 patients. Age range was 15–77 years and body mass index 17–50 kg/m2.
We studied the percentage of patients with different cystoscopic findings characteristic of interstitial cystitis, the sensitivity and specificity of the three diagnostic tests—PUF, PST, and ABC—regarding interstitial cystitis, and the association between interstitial cystitis and endometriosis/adenomyosis. Regression analysis and graphing were performed using SPSS v15.
Sixty-two (53.4%) patients had typical IC findings with glomerulations and/or Hunner’s ulcers and bladder capacity ≤800 cc.
Thirteen (11.2%) had atypical findings with no glomerulations or less than anticipated, i.e., <10 per four separate cystoscopic fields and no Hunner's ulcers; however, bladder capacity was ≤800 cc.
Twenty-five (21.6%) had typical glomerulations or Hunner's ulcers, but a bladder capacity >800 cc or the capacity not documented (only three).
Four (3.4%) had less than four cystoscopic fields of view with ≥10 glomerulations and bladder capacity >800 cc. Some of these patients had positive PST and can be considered as painful bladder syndrome patients of uncertain long-term significance or may just be very early in the course of the disease (IC).
Twelve (10.3%) had bladder capacity >800 cc with no or few glomerulations and no Hunner's ulcers.
Pathology reports showed 49 patients had endometriosis. Adenomyosis was diagnosed by pathologists in 22 cases, by ultrasound in two cases, and by hysteroscopy in two cases. Among patients with interstitial cystitis, 60 (60%) patients had adenomyosis or endometriosis.
For the last 3 years, our practice has utilized the PUF questionnaire as a screening tool on all annual exams, new gynecological patient evaluations, and pelvic pain evaluations. For PUF scores ≥10, PST was recommended. If the patient had indications for gynecological surgery, concomitant cystoscopy with hydrodistension was performed to confirm the diagnosis, predict response to therapy based on bladder findings, and to induce temporary remission enough to give medical therapy time to work.
Our study is a retrospective case-series analysis based on known implemented criteria of routine PUF questionnaire screening with intent to do PST, ABC, and/or cystoscopy with hydrodistension in patients that needed gynecological surgery who were felt to have interstitial cystitis as suggested by an elevated PUF score, a tender trigone on physical exam, or complaints of nocturia, a strong marker for interstitial cystitis . Hence, with a known history of endometriosis or adenomyosis (intrauterine endometriosis), we erred on the side of further evaluation with cystoscopy and hydrodistension in patients with these findings as well.
The majority of these patients were undergoing other concomitant GYN procedures which made them available for confirmation of diagnosis and placement into diagnostic groups. Our observations allow us to postulate a strong primary correlation between interstitial cystitis and endometriosis/adenomyosis. These data were obtained from cystoscopy with hydrodistension, pathology, hysteroscopy, and preoperative ultrasound imaging reports. They are consistent with findings from other studies showing increasing incidence of coexistence of interstitial cystitis and endometriosis/adenomyosis [1, 4, 5]. We found a 60% association rate between interstitial cystitis and endometriosis/adenomyosis, but it is probably higher given the inability to diagnose endometriosis or adenomyosis in some types of procedures (e.g., Prolift procedure) or due to unavailiability of pathology reports from prior hysterectomy in some patients. Our study expands on previous reports by showing that the presence of endometriosis has a stronger association with typical IC findings on cystoscopy, including glomerulations, ulcers, and reduced bladder capacity.
The antiproliferative factor (APF) and the heparin-binding epidermal growth factor-like growth factor (HB-EPF) identified in bladders affected by interstitial cystitis seem to play a role in the relationship between interstitial cystitis and endometriosis/adenomyosis [12, 13]. Interstitial cystitis seems to occur as a result of misbalance in the concentrations of APF and HB-EPF with resultant inhibition of bladder epithelial repair [14, 15]. This would also explain the 8:1 incidence of interstitial cystitis in women compared with men [7, 16]. The fact that men may also develop interstitial cystitis suggests that other still-unknown initiators may shift the balance of APF and HB-EPF. The effect of the antipoliferative factor would also explain many of the symptoms associated with endometriosis like menorrhagia, metrorrhagia, and infertility. Similarly, many of the symptomatic bowel problems associated with endometriosis like diarrhea, bloating, and cyclic rectal bleeding (even when no colorectal endometriosis is found) could also be explained by the effect of the antipoliferative factor [12, 17]. This is further supported by the exacerbation of symptoms of interstitial cystitis in late luteal and menstrual phases when the inflammatory response to endometriosis/adenomyosis is most intense. This concept along with genetic stability of the AFP–HB-EPF homeostasis can explain the puzzling finding that some women with minimal endometriosis have severe IC symptoms while others with severe endometriosis have minimal or no IC symptoms.
One would theorize that, in a large number of patients who go into remission after hydrodistension, a positive balance in favor of endothelial proliferation factors occurs promoted by tissue injury at the time of hydrodistension overcoming the effect of endothelial antiproliferation factors. This way of viewing the pathologic process might also explain the effect of pentosan polysulfate sodium in putting patients into remission.
We believe the categorization of cystoscopic findings as set forth above is essential for prognosis of interstitial cystitis patients and assists in encouraging those with reduced bladder capacity to adhere to their dietary restrictions and medications while allowing less aggressive treatment of those with preserved bladder capacity who may represent women who have a less fulminant course that may be candidates for intermittent therapy.
In the USA, cystoscopy with hydrodistension is still considered optional in the evaluation of patients with symptoms suggestive of interstitial cystitis, including urinary urgency, frequency, nocturia, and/or pelvic pain [18, 19]. However, cystoscopy with hydrodistension is the only objective method allowing direct visualization of bladder mucosal abnormalities and thus has a diagnostic and a prognostic value . Cystoscopy with hydrodistension is the only objective means that allows direct visualization of bladder mucosal abnormalities and thus has a diagnostic and a prognostic value. It thus helps diagnose and categorize patients into those with a classic picture of IC including mucosal abnormalities and those without . Unfortunately, the diagnosis of IC is usually delayed because of lack of enthusiasm about cystoscopy with hydrodistension [7, 20]. A recent European study showed correlations between cystoscopic findings, maximal bladder capacity, and bladder histology and considered cystoscopy with hydrodistension and biopsy mandatory for further typing of patients with bladder painful syndrome . The questionnaire and supplementary tests may suffice if the patient responds to medical therapy and has exacerbations to known dietary indiscretions, in other words, running a typical course and responding to therapy. However, failing to proceed to performing cystoscopy and hydrodistension in nonresponding patients or those with risk factors for bladder cancer would be irresponsible [18, 20]. If we follow the logic of those that want to deemphasize the use of cystoscopy with hydrodistension to other organ systems, then why do we perform endoscopy in patients with persistent gastrointestinal complaints?
In addition, cystoscopy with hydrodistension has a therapeutic effect with more than half the patients reporting improvement in symptoms for an average of 2 months [20, 22]. This, by itself, is a very helpful diagnostic marker of interstitial cystitis. More than half of patients report improvement in symptoms after this procedure with a mean duration of 2 months .
Gynecologists should be trained in cystoscopy with hydrodistension and in the care and treatment of women with interstitial cystitis and the commonly associated syndrome of myofascial pelvic pain and spasm. We need to take the lead in dealing with this very debilitating and now understood to be fairly common condition (as many as 12.6% of the female population ) where delayed diagnosis continues to be habitual leading to untold and unnecessary human suffering.