Pages

Showing posts with label bladder. Show all posts
Showing posts with label bladder. Show all posts

Wednesday, 3 July 2013

June Roundup in July



Unfortunately I’ve been a bit behind this month, but I always keep my eye on what going on in the world of endo research.

So with that in mind let’s have a look at what’s been going on

Firstly, a study into surgical treatment for endometriosis of the bladder. This form of the disease isn’t particularly common, but it does add another layer of misery to the sufferer so knowing the optimal treatment is important. This study took sixty nine patients with bladder endometriosis and recorded what surgical procedures they had and how this affected their symptoms afterward. After follow up period of between 4 and 92 months, 92.7% of the women either had no symptoms, or a reduction in symptoms. What this study highlighted was the need for surgeons with specialist training in different types of endo (i.e. bladder, bowel etc) as they may require a different surgical approach.

Speaking of bladder and bowel surgery, up next is a report on the use of robotic assisted surgery for the treatment of just those conditions. This study included 19 cases of bowel surgery and 5 cases of bladder surgery, all of which occurred without complications. Now, robot-assisted surgery is a hot topic at the moment because it is a new and growing technique. But we are also stuck in a catch-22 situation with robotic surgery. You see, people are reluctant to support robotic surgery until there are more studies into its effectiveness, but you can’t have more studies until you support wider use of robotic surgery. Either way it looks like robotic surgery is here to stay and it is a safe and effective tool with a skilled surgeon at the helm.

Speaking of robot-assisted surgery, there are many different types of surgical procedure the robot can be utilised for in the treatment of endometriosis. In severe cases of the disease, doctors may opt for hysterectomy and our next study examines the safety and effectiveness of using the robot for such a procedure. In summary this study looked at 43 cases of women with severe endo (19 with stage III and 24 with stage IV). The results of which were -  operating times averaged at 145 minutes (with a variation of 67-325 mins); 41 out of 43 women only had a 1day hospital stay, with one woman needing to stay for 5days due to needing a laparotomy and one woman staying 3days because of a bowel obstruction that cleared. There were no reported complications during surgery though after surgery one woman had to be readmitted with a vaginal cuff abscess which was treated with antibiotics and drained. The authors of this study make some good points about the pros and cons of robotic surgery, namely – “The robotic platform improves the depth of perception and facilitates the resection of deep infiltrating lesions. In addition, the robotic system improves dexterity, filters the surgeon’s tremor, and improves intuitive movements”; however they also say “Robotic surgery has several disadvantages compared with traditional laparotomy. These include increased cost; the lack of tactile feedback to the surgeon [i.e the ‘feel’ of the toughness or resistance of tissues]; the presence of bulky robotic arms, as well as long and thick cords; the inability to move the surgical table once the robot arms are attached; and a limited range of motion with respect to operating in different quadrants in the same case”.

Sticking with a surgical theme is a study from the US looking at the effectiveness of surgical excision of endometriosis across five different medical centre’s. All the women included in this study were suffering endometriosis associated pain, of which 90 had operative information. Once these women were operated on, 65 were confirmed to have endometriosis and 25 had no confirmation of endo. Interestingly, of all the patients who had endometriosis confirmed at these centres, 84.6% had previously been given hormonal therapy or ablation (burning away of endo) surgery, indicating that these treatments are not very effective at reducing endo pain symptoms.  After their surgeries, all of the women in the different centres noticed a significant reduction in all but bowel symptoms (bowel symptoms were reduced though, but the amount of reduction wasn’t considered statistically significant). Interestingly the authors of this study found there was no significant difference in the pain and quality of life scores between women who were given hormonal therapy after excision surgery and those who weren’t. However, the post-operative information was collected 6 months after surgery, so long term effectiveness couldn’t be gauged. In any case this study shows that excision of endometriosis is still the preferred method of treatment for the disease where possible.

It is rapidly becoming apparent that endometriosis is a disease that begins to present itself in adolescence. This is extremely important to know because it means general practitioners need to be able to spot the signs of endometriosis in young girls and make sure they get treatment as soon as possible. But what are the major signs of endo? A new study looking at diagnosis of endo in adolescent girls found that 75% of girls with chronic pelvic pain (which is any pain in the pelvic area that lasts more than six months) that did not respond to medical treatment and 70% of girls with dysmenorrhoea (excessively painful/heavy periods) were later diagnosed with endometriosis. All doctors need to be aware of these ‘red flags’ and act on them quickly.

Next up is copper, which is great for electrical wiring and making cheap jewellery, but also may be important for endometriosis. Our bodies need miniscule amount of copper to function properly, but as with so very many things in this world, there is fine balance to be kept. In your body copper can float around by itself, but is also carried around by a protein called ceruplasmin and this latest study looked at the levels of both of these in the blood of women with advanced stage endometriosis compared to disease free women. What they found was that levels of copper and ceruplasmin were much higher in the blood of women with endo, but what does this mean? That’s a tricky question to answer because we’re still not sure what role copper might play in endo. Excess levels of copper are known to be a marker for oxidative stress and oxidative stress certainly seems to be elevated in women with endo. Oxidative stress, as the name suggests, is not something you want happening to excess in your body; prolonged exposure to oxidative stress can make you run down and generally feel like crap, in addition localised oxidative stress can actually promote the survival of endometriosis. Further study is needed to find out if copper is a cause or effect of oxidative stress, but as an interesting aside, elevated levels of copper in the blood could possibly be used as an indicator of advanced stage endometriosis.

Finally is a study from Denmark about the risk of endometriosis and fertility problems in the daughters of women with the disease. This was quite a large study, including information from 12,389 women with endometriosis and 52,371 without. Overall daughters of women with endometriosis were just over two times more likely to be diagnosed with endo. However, daughters of women with endo had no difference in the rate of deliveries, risk of miscarriage and ectopic pregnancy compared to the daughters of women without endo.  

Tuesday, 12 March 2013

Endometriosis Awareness Month 2013 – Part III




 Endometriosis awareness month continues to power forward and I think this year has already been a major success – the buzz on Twitter, Facebook and all over the internet is incredible. I think 2013 may turn out to be the best year for endometriosis awareness yet and the only way is up!

So without further ado, let’s have a look at a few more selected pieces of endometriosis research that’s been published recently.

First up is a review paper examining all the current evidence concerning the link between chronic pelvic pain and bladder pain syndrome (BPS). The term bladder pain syndrome is often used interchangeably with interstitial cystitis (which is different from bacterial cystitis) and is characterised by painful inflammation of the bladder leading to frequent need to urinate and painful urination.  The cause of BPS is often difficult to ascertain unknown (or requires trial and error investigation to find out).  The above review found that, out of 1016 patients with chronic pelvic pain, 61% had BPS and 70% had endometriosis. Interestingly, in those women with endometriosis, BPS was recorded in 48% of cases. This means that almost half of women with endometriosis may suffer from bladder pain. This raises some interesting questions, perhaps most obviously –what is causing such frequent bladder pain in women with endo? Women with endometriosis are known to suffer from recurrent urinary infections, but this can be distinguished from interstitial cystitis as a urinary tract infection will clear up with antibiotic treatment. Another obvious conclusion could be endometriosis of the bladder is causing BPS. The problem is, endometriosis of the bladder is considered uncommon, occurring in around 1% of patients according to reports. It may be that, because the bladder and places endometriosis is more commonly found are close together, chronic inflammation related to pelvic endometriosis irritates the bladder as well. In order to see whether this were true, it would be useful to conduct a study  following women with BPS and endo, who have had their endometriosis surgically removed and see if their BPS abates after surgery.

 Next up is a study, which you can read in full here, looking at the involvement of macrophages in endometriosis. A good place to start would be asking, what is a macrophage? Macrophages (literally translated meaning ‘big eater’) are one of the many different types of cell that make up your immune system. Macrophages are found in every tissue of the body and their primary job is to ‘consume’ and destroy diseased/cancerous cells or pathogens like bacteria, then send out chemical signals recruiting other immune cells.  Normally macrophages should recognise endometriotic cells as abnormal and destroy them however, as this study points out, in women with endometriosis their macrophages are somehow defective and treat endometriosis as a wound rather than diseased tissue. What this means is that macrophages actually promote the survival of endometriotic cells. As the authors of this review point out though, this opens up quite a novel avenue for the treatment of endometriosis i.e. restore the correct function of these macrophages and let your own body destroy the disease without the need for drugs or surgery. Of course how one would go about doing that, I have no idea and I’m not even sure if the ability to do so exists yet. Nevertheless it’s a fascinating prospect to consider.

Finally for this post is a study looking at whether there are any differences in the clinical characteristics of adolescent girls with endometriotic ovarian cysts (endometrioma). This study took 376 women who were undergoing surgical treatment for endometrioma and divided them into four groups according to age: Group 1 – under 20 years old, Group 2 – 21-30 years old, Group 3 – 31-40 years old, Group 4 – 41-45 years old. The clinical characteristics of these groups (e.g. menstrual history, symptoms etc) were then compared to see if there were any differences or similarities.
Here are some points of interest from the results:

  • Most of the Group 1 and Group 2 women sought treatment because of initial pain symptoms (77% and 72% respectively). Women in Group 3 and Group 4 also sought treatment for pain, but at a lower percentage (45% and 40%) with almost half their cases of endometrioma being discovered incidentally

  • The authors speculate that adolescents who develop endometrioma may do so because they have more ‘adult like’ menstrual cycles (i.e. regular in terms of duration and timing). Although the authors point out a comparison with disease-free adolescents is necessary to confirm this.

  • There was no significant difference seen in endometrioma size, position and stage between the four groups.

  • Another interesting finding was that none of the women, in any of the groups, were found to have deep endometriosis. Although it is speculative to say, this does hint that endometrioma and deep endometriosis may have different origins.


It is important that studies such as these are being undertaken. Endometriosis in adolescents has, and still is, a grossly under recognised problem. More studies characterising the disease in young girls means greater awareness and earlier intervention.

 Bonus Content!
The 4th annual scientific and surgical symposium on endometriosis has been held very recently by the wonderful Endometriosis Foundation of America. This conference brought together expert surgeons, scientists and women with endo from all over America and the world to talk about advances in our understanding of the disease.



If you couldn’t be there and missed the live broadcasts, don’t worry! You can watch all the talks and presentations as streaming videos via this link. They’re well worth a watch; I guarantee you’ll learn something you never knew about endo!