Shedding Light on Male Pelvic Pain and Sexual Dysfunction

In Male Pelvic Pain by Stephanie Prendergast16 Comments

Guest blogger Dr. Jeannette Potts, of Vista Urology and Pelvic Pain Partners, has a great deal of experience treating male pelvic pain. In this post, she sheds some light on sexual dysfunction associated with male pelvic pain.

The continued misuse of the generic diagnosis, “prostatitis,” remains a disservice to the vast majority of patients suffering from pelvic and genital pain frequently associated with lower urinary tract symptoms and sexual dysfunction. Growing evidence over the past two decades shows that fewer than 10% of patients have an infectious cause for their symptoms and that end-organ or prostatocentric approaches are inadequate. Meanwhile, more comprehensive care, emphasizing  biopsychosocial  and neuromuscular  components of pain, have been shown to be more beneficial for men suffering with UCPPS. And indeed, the NIH-NIDDK conference of 1996 recognized the fact that the condition may not be a malady of the prostate to begin with!

Unfortunately, when UCPPS is associated with sexual dysfunction, i.e. painful ejaculation or post coital discomfort, patients are more likely to be diagnosed with prostatitis and, therefore, even more likely to endure weeks of unnecessary antibiotic therapy.

Sexual dysfunction in this setting can be manifest in many ways: Dysorgasmia (painful ejaculation), post ejaculatory or post coital aching or pain, painful arousal, and decreases in erectile function and libido secondary to the pain, fear and anxiety.

(It is important to reassure men about these secondary effects, as many believe they have a separate terrible disease.)

During my career, I’ve developed a theory regarding dysorgasmia and postcoital discomfort, within the context of pelvic neuromuscular floor dysfunction and myofascial trigger points. In patients suffering from these sexual symptoms, the pleasurable sensations and “spasms” of orgasm evolve into painful contractions and abnormal tightening of the pelvic floor. This is worsened and perpetuated by the anticipation of yet another unpleasurable or painful climax. (Imagine trying to enjoy sex while fearing the approach of orgasm as pain rather than rapture.)

As I first hypothesized about the neuromuscular influence on this condition, I made another observation: Many men with the condition also described a marked decrease or absence of semen during ejaculation, or, in some, a delayed dripping of the ejaculate. This certainly exacerbated their anxiety as many men justifiably wondered what was happening to the fluid and was it “backing up” into their already allegedly inflamed sex organs. But of course this was not the case.

Yet another clue emerged. And as any sensitive healthcare provider knows, our continuing medical education comes by way of our own patients as much as by a conference, these clues came from unrelated patients.

Several men in my practice practice martial arts and Taoism. To preserve their Chi (energy), they do not ejaculate during sex or climax. They’ve trained themselves to contract the pelvic floor muscles, thereby causing an intentional form of retrograde ejaculation. By squeezing the muscles that tighten the external sphincter muscle, just distal (just beyond the end of the prostate), the ejaculation entering the prostatic urethra no longer travels frontwards and out the tip of the penis. The path of least resistance is no longer outward, as the tightened sphincter now provokes the flow of semen backward and into the urinary bladder. This causes no physical harm and is excreted with the urine during urination. Men who try to do this intentionally require practice and many have experienced significant pain.

It now made sense to me that UCPPS patients with dysorgasmia were involuntarily performing similar techniques practiced by those persons intentionally trying to withhold their ejaculation. This, I’ve termed ejaculatory dyssynergia.

Although this remains just a theory, I am encouraged by yet another piece of the puzzle. As the symptoms of UCPPS in men improve and resolve through specialized pelvic floor PT and manual trigger point release, many patients describe as secondary improvements, increasing pleasure with sex and orgasm, as well as increase in the volume and force of ejaculation.

I believe that ejaculatory dyssynergia helps to better conceptualize this phenomenon as one of the most stressful and debilitating facets of UCPPS. This is especially true among those patients in whom we also observe dysfunctional defecation (tenesmus, puborectalis syndrome, etc) and those whose LUTS may be derived from similar acquired habits such as pseudo-DSD (Detrusor-sphincter-dyssynergia).

Jeannette M. Potts, MD

Vista Urology and Pelvic Pain Partners

www.drjeannettepotts.com

jeannetteAbout Jeannette M. Potts, MD:

During her 15 year tenure at the Cleveland Clinic’s Glickman Urological Institute Dr. Jeannette Potts developed her signature biopsychosocial approach to Urological Chronic Pelvic Pain Syndromes (UCPPS).

She is the editor of three urological textbooks, published by Humana and Springer Press as well as author of the book, Tango: Lesson for Life,  published by Cleveland Clinic Press. (www.doctortango.net)

She has been a passionate collaborator with the NIH and the IPCN, to advance research and care of patients suffering from UCPPS. She was co-investigator for the NIH clinical trial showing the benefits of specialized physical therapy for patients with UCPPS.

She has published numerous articles in urology and family medicine and has given over 100 lectures on UCPPS and related topics, as an invited speaker at medical and urological conferences worldwide. She has invited back to direct her course on UCPPS at the AUA.

I miss my long walks. Walking definitely seems to be making me flare. I have a desk job and the sitting makes me hurt too. All i want to do when I get home is sit my but on a heating pad and take medicine. Where do I begin to stop this pattern. Feel like a big blob and so tired.

 

Comments

  1. I read about Dr. Potts in an article on the web. I have been experience ing chronic pelvic pain for quite a few years. I had hoped she was still in the cleveland area. My problem started following a back surgery with resulting infection 10 plus years ago. I’ ‘ve been to one urologist with little help. Is there someone you could recommend in Cleve. Ohio area who understands CPP. Thank you sincerely Tom

    1. Author

      Hello Thomas,

      I’m sorry, but we do not have a recommendation for your area. Are you able to travel elsewhere?

      All my best,

      Rachel

      1. hi everyone . i feeling pain in pelvic area and while standing feeling dizzy and weakness with mild headache anyone can help me what u think about this kind of condition also have fever i see doctor but nothing found . anybody can help me what is reason about it ???

  2. Hello,

    I’ve been experiencing pudendal neuralgia and all of the associated symptoms, including ED, for at least three years now. over the course of the last year and a half of treatment with physical therapy and LLLT I have made immense strides.

    I was wondering if you’ve had any experience with PRP injections and if they help to induce increased or faster healing?

    thank you so much
    Sincerely,
    Christopher Lord

    1. Author

      Hello Christopher,

      There is evidence to support PRP may be a helpful adjunct to physical therapy in other areas of the body. To date, research has not yet been done on its usage for pelvic floor muscles or pelvic pain. With that said, my personal opinion on PRP is that it physiologically makes sense and is worth considering if it is available at a reasonable cost. Your physical therapist should be able to help you pinpoint the exact muscles that may benefit from the injection. I hope this helps.

      All my best,

      Stephanie

  3. I have searched years and years, been to dozens of Dr.’s and not one of them has been able to even respond to my plea’s for at least information about my Pelvic Floor Nerve Damage, caused by a Total Proctectomy in 2001. I have been in a horrible world of constant agonizing pain almost 14 years since the surgery. My wife of 30 years even left me 6 years after the surgery. Is there any help for me here? The main problem has always seemed to be, my rectum has been removed in the surgery, leaving no access for a Urologist, or Neurologist.etc. Please help me if you have any information about my condition. Thank You

    1. Author

      Hello Samuel,

      I’m sorry to hear about your situation. We can refer you to a pelvic physical therapist in your area that can evaluate you. Where are you located?

      All my best,

      Casie

  4. Hello, about 8 years ago I started to notice some pain in my lower back and hips during orgasim. At the same time I started have some mild to moderate ED and my semen turned clear and then stopped. I’m now 40 and the pain is still here. During orgasim it starts in my hips then move to my groin and lower back. As soon as the orgasim is over the pain stops. Still no semen. My PSA is .5. What do I need to do? I want my sex life back. Thank you.

    1. Hello Henry,

      There may be muscular impairments which are contributing to your symptoms. Please consult with a local pelvic floor therapist for an evaluation.

      Best,

      Liz

      1. Since my post my doctor put me on Wellbutrin for depression /anxiety. For some reason the pain stopped. I stopped taking Wellbutrin and the pain came back even worse. After a month I started taking Wellbutrin again and just like before. After 3 days no more pain during orgasm. Any thoughts on why this would happen?

        1. Author Stephanie Prendergast says:

          Welbutrin is a dopamine agonist which may have an effect orogasm. We suggest that you discuss this with the prescribing physician.

  5. Thank you for this excellent article. I believe I have ejaculatory dyssynergia from SSRI usage. Not from the SSRIs themselves, but from trying so hard physically to achieve orgasm while on the SSRIs. Then once I discontinued the SSRIs, the ejaculatory dyssynergia has continued over a year later.

    I’ve had my case and symptoms reviewed by several urologists and psychiatrist experts through a Medical Expert Service my company provided. Despite extensive case histories and symptoms description, I don’t believe any of them has quite hit the mark as well as your article seems to describe the symptoms.

    Can you please elaborate on what pelvic floor PT and manual trigger point release? Are there exercises I can work on at home or do I need to see a PT?

    Thank you.

  6. i experience lower back pains,painful ejaculation,poor erection and constipation.its now almost a year experiencing these.my pelvic muscles are painful and also the urethra.

Leave a Comment