Good intentions
Forum Replies Created
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That’s a weird one. Two weeks and you’re measuring semen quantity? Seems early to worry…
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I would start here.
https://atriumhealth.org/for-providers/todd-heniford
atriumhealth.org
B. Todd Heniford, MD | Department of Surgery | Atrium Health
B. Todd Heniford, MD, is the founder and chief of the Division of Gastrointestinal and Minimally Invasive Surgery at Atrium Health.
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William, when you create a new Discussion you have to scroll down to the bottom of the page and choose a sub-forum. Even though there is only one choice. If you don’t the forum softwae will give an error message that does not indicate how to fix the problem. “<strong style=”font-family: inherit; font-size: inherit; color: var(–bb-body-text-color);”>ERROR: Forum ID is missing.”
Yes, the forum is still “clunky”, it has not changed much since the early correction of a few problems. I still get the endless “Updating” message on some days. When the News page does show up it often does not show new Discussion replies, that’s why I always add a “What’s on your mind” after I reply to a Discussion. The “News” updates scroll away in to oblivion pretty quickly, so they are kind of like Tweets, only seen for a very short time.
But it is still a good place to collect some thoughts and report some things like you just did. Who knows, it might eventually start working like a normal forum someday. Just keep hoping.
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Laparoscopy usually causes significant swelling in the first few days afterward. Very odd that your swelling was so minimal that you could still feel the original lump. Also strange that the surgeon diagnosed the femoral hernia by feel. My understanding is that femoral hernias are hard to diagnose that way.
You’ve only mentioned the lump. What about the pain from the hernia itself?
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Renowned means well-known. Might as well tell us who it was. Did they do the full official Shouldice Hospital procedure? Or one of the modified versions. Might be relevant.
Eight weeks is not very long since surgery.
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You probably meant Dr. Sbayi, not Sabayi. Did you actually talk to him or did you see his comment somewhere on the internet? A link would help a lot. Maybe you misunderstood the comment, it doesn’t really fit.
Ken had a friend from Mexico in a similar situation, seeking mesh removal. Ken seems to have disappeared from the forum though. Is there any reason that your friend couldn’t join the forum? Ken’s friend apparently did not speak English well. The “friend” questions are more likely to be not-quite-right.
Dr. Sbayi has been on Dr. Towfigh’s HerniaTalk Live YouTube channel. Good luck.
https://www.stonybrookmedicine.edu/patientcare/surgery/blog/hernia-talk-live
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I had been posting about changing my clothes to reduce all external pressure on the areas that were involved in my original hernia and mesh repair/removal. I ended up with suspenders. They have made a big difference. So much so that, as is common with a person who used to be very athletic, I have been trying to expand my physical range. More/harder exercise, longer walks/hikes/runs, etc. Now that the localized right side pain is reduced, I’ve worked up to a broader, lower level of soreness.
I feel much better, but I’ve realized that the areas that the mesh was in contact with, or the areas involved in the dissection process, to create the space for the mesh, were really ravaged by the whole implantation repair process, and will probably never really recover. My lower abodmen, from hip-bone to hip-bone, and navel to pubic bone, is really messed up. Sometimes I still wonder in amazement about how I got in to this situation. It really is incredible. It’s been almost ten years since I trusted my surgeon to “fix” me and let me get back to my very healthy and active life. Instead I feel like I’ve been in some sort of horrible accident.
Anyway, it’s a long road back and I can’t imagine that I will ever get back to where I was before. My gut is still distorted, my clothes still don’t fit right, and I still get sore after extended sessions of physical activity, although things are still getting better. But I’ll probably spend the rest of my life “taking care of” my gut.
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This report is pretty fascinating. The defendants (Bard) are trying to pin the blame for insufficient warning on the surgeon who implanted the PerFix plug. So now it is the community of surgeons being attacked directly by the mesh makers. How will this new development play out? They have been working hand-in-hand to promote these mesh products but now the truth is coming out.
They really need to get in to those “internal reports” that are used in the marketing brochures, and internal e-mails. Those will probably show that the mesh makers have known about these problems for many years.
The drama continues. This is the first big trial, the current Bard 3D Max trial should have much more incriminating evidence. I hope that they find it.
“February 1, 2024 Update
Judge Sargus denied a motion for a new trial in Stinson yesterday.
Bard made three real arguments and the judge rejected all three:
- Inadequacy of IFU: Defendants contended that the plaintiff failed to demonstrate that the IFU for the PerFix Plug was inadequate in warning about the device’s risks. They argued that the trial testimony of did not suffice to prove inadequacy in warning about the risks associated with the device. The court, however, noted that the defendants focused more on discrediting the witnesses’ conclusions rather than addressing the sufficiency of the evidence presented. The court maintained its stance from the summary judgment phase, emphasizing that it does not weigh evidence or make credibility determinations when ruling on a motion for judgment as a matter of law.
- Causation: Defendants argued that the plaintiff did not present sufficient evidence to show that any allegedly inadequate warning caused his injuries. They relied on the learned intermediary doctrine, asserting that their duty to warn was met since the implanting surgeon, Dr. Tan, was aware of the risks involved. Dr. Tan testified to warning the plaintiff about potential pain and nerve damage and acknowledged being aware of the risks of fibrosis, inflammation, and long-term pain. Defendants also referenced a patient education brochure warning about similar risks, suggesting Dr. Tan was informed about the risks pertinent to the case. However, the court pointed out that during the summary judgment phase, it was established that Dr. Tan expected the IFU to warn about risks specific to the PerFix Plug, like chronic pain and mesh contraction, indicating that there was a genuine issue regarding whether the warnings were adequate and whether they contributed to the plaintiff’s injuries.
- Failure to Warn and Negligence: The jury found for the plaintiff on the negligence claim based on failure to warn, not on design defect. Defendants tried to argue that if the plaintiff’s claims failed under a strict liability theory, they should also fail under a negligence theory. However, the court did not find this argument compelling enough to revisit its summary judgment ruling, indicating that the defendants did not present any new evidence or arguments that would lead the court to alter its previous decision.
…”
https://www.lawsuit-information-center.com/bard-hernia-mesh-lawsuits.html
lawsuit-information-center.com
Hernia Mesh Lawsuit Against C.R. Bard
C.R. Bard is defending over 18,000 hernia mesh lawsuits alleging that its mesh devices were defective, resulting in injuries and complications for thousands of hernia surgery patients. Our hernia ...
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100 more cases added in January. The Bard 3D Max case opens the door to all Bard polypropylene products since even the flat meshes fold and migrate and cause inflammation and chronic pain. I had Bard Soft Mesh, made of the same material as the Bard 3D Max. Pretty fascinating. The pipeline of lawsuits is still being fed, every day, and Medtronic appears to be fine with it. They’ll just raise their prices to cover the litigation costs, and those costs will be passed on to the insurance companies. The patients don’t seem to matter. High damages seem like the only viable way to drive change. For the patients.
“<strong style=”background-color: var(–bb-content-background-color); font-family: inherit; font-size: inherit; color: var(–bb-body-text-color);”>February 1, 2023: 100 More Cases Added to MDL
Nearly 100 new cases were added to the C.R. Bard hernia mesh class action in the month of January. That brings the total number of pending cases up to 21,169.
January 15, 2024: 20,973 Cases in Bard MDL
As we head into the new, the C.R. Bard hernia mesh class action MDL has 20,973 pending cases. It is still the largest of the hernia mesh MDLs.
January 4, 2024: Plaintiffs Push for More Trials
We need more hernia mesh trials to get these cases settled. It has been too long. This litigation began in 2018. We have to turn the page in 2024.
The plaintiff’s hernia mesh lawyers believe there is a path. They have submitted a detailed memorandum to support their request for a new Case Management Order. This order is intended to set a roadmap for what should be done to speed this process up.
Strategy for Case Remand
The plaintiff’s mesh attorneys are not looking for the chaos that would come with sending all of these lawsuits home to their local federal courts. Instead, they suggest a phased approach, dealing with cases in large batches. The initial phase would include about 1,500 cases, representing a fraction of the total. They also propose a plan for which hernia mesh lawsuits to push forward. The selection criteria for these cases would be based on the severity of injuries, the duration since filing, and involvement in previous bellwether trials.
Efficiency and Justice in Trial Management
The proposal advocates for multi-plaintiff trials, which would be more efficient and cost-effective, avoiding repetitive testimony and allowing for shared trial expenses. The unspoken part? Trials with multiple plaintiffs also put more pressure on Bard.
So, keeping some of the structure the MDL provides, they propose that case-specific discovery should be managed under the current Court’s supervision to ensure that the cases are nearly ready for trial upon transfer to the remand courts. This plan is presented as a way to accelerate the delivery of justice for plaintiffs, ensuring that their cases are resolved in a timely manner. The judge has ordered the defendants to respond on January 10th. We should get a ruling, hopefully, by the end of the month.
…”
https://www.millerandzois.com/products-liability/hernia-mesh-case-value/
millerandzois.com
Hernia Mesh Lawsuit Settlement Compensation Payouts
Our hernia mesh lawyers seek new clients suffering severe side effects from these defective products. Over 20,000 hernia mesh lawsuits have been filed. Three hernia mesh device lawsuits have gone ...
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Actual experiences will definitely be hard to find especially on this forum since traffic has dropped so dramatically. Beside the fact that there is so much chaos across all forms of hernia repair.
Don’t overlook that the Shouldice repair has been done with stainless steel sutures for decades.
It’s not clear what you’re trying to define. Looks like you might be looking for the perfect repair, taking you all the way back to undamaged tissue with no foreign material inside. That is a dream, I think.
I went through that large study paper again and see that they don’t really define why anyone would choose even a late absorbable suture over a permanent one. They seem to imply that a permanent suture “might” be more likely to allow a recurrence. But that doesn’t really make sense. They don’t talk about pain at all. So, why use absorbable at all? What is the potential benefit? They don’t say. They just did a study about recurrence rates by suture material, and reported what most people would expect. Permanent gives the lowest recurrence rate.
For some reason they also blended in Shouldice versus other non-mesh methods. Really, kind of an odd paper. “By the way, Shouldice is better…”
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Thanks for the reply Mark T. I did read through the last paper cited. I had written some comments about unintended bias by researchers trying to prove an opinion rather than finding or defining the truth of a situation. It is a big problem, especially in the medical field where many of the authors don’t seem to have real training in reearch methods. Many of them want to state a clear conclusion when the data just says “we can’t tell a difference”. Or the difference is real but it’s very small.
One thing that I haven’t seen described explicitly is how fixation via sutures or tacks affects the shrinkage of the mesh. Shrinkage is well-known, but nobody seems to ponder how the fixation points of the mesh are pulled by the shrinkage. It seems obvious when visualizing what must be happening. But it is not discussed. Does fixation stop shrinkage but create tension? Or does shrinkage happen anyway but pull the fixation material through the tissue it’s attached to?
Overall though, the one constant is the knitted mesh structure. All of the synthetic fiber meshes consist of an assembly of many tiny knots through which nerves, veins and new tissue form. It’s very cheap to make, it’s just aquarium fishnet material, and very profitable. I think that there are new ideas in the mesh maker companies but they are not supplying the funding to develop them. The lawsuits might drive them to do so in the future. It’s all the motivation that they have. The surgeons just keep going around in circles studying different ways to use bad materials. My standard soapbox proclamation.
By the way, if you “paste as plain text” all of the extra formatting garbage will get left behind.
Still a shame that people’s posts get sprinkled randomly through the threads instead of chronologically. Hard to understand. Even Dr. Towfigh must have trouble reading her own comments.
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The numbers that you just cited come from a paper in which the researchers thenselves concluded that permanent (non-absorbable) or “late absorbable” (long-lasting) sutures are both recommended. They don’t distinguish between the two, so, in other words permanent is just as good as late absorbable. As fas as reoperation is concerned.
If you read more about absorbable sutures you might find that they don’t react the same way in the people that they are used in. Why take a chance on an absorbable suture if a permanent suture gives the same results? That seems a reasonable cause for “fear”. Fear of the unknown.
It is interesting though that they don’t mention pain at all. The paper was published in 2003. The primary author did eventually get involved in pain studies though. Here’s one from 2020.
https://www.sciencedirect.com/science/article/abs/pii/S0039606019307676
“Discussion
This nationwide registry-based questionnaire study showed a high prevalence of chronic pain 1 y after open, anterior mesh repair of 14.8% for self-gripping mesh and of 15.7% for lightweight sutured mesh. We observed no difference regarding the prevalence of chronic pain and recurrence between the 2 types of mesh; however, the use of self-gripping mesh was associated with a markedly decreased operative time.
This study represents a large number of patients, and the high rate of chronic pain…”
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You are conflating mesh repair results with pure tissue results. And, as is common with many of these types of studies, the data set is small and the time frame is short. Many of these studies are essentially worthless. A simple question is posed, poor work is done, and the results are presented as fact. Look at the numbers reported and the margin of error. It’s nonsense.
“A comparative study of inguinal hernia using monofilament non-absorbable suture versus monofilament absorbable suture in Lichtenstein tension free hernia repair at tertiary care government hospital.”
“Results: Total 152 patients of unilateral or bilateral inguinal hernia were studied 76 in each group. Chronic groin pain mean visual analogue scale score at 3 months was higher in group with non-absorbable suture compared to monofilament absorbable group (1.3±0.9 v/s 0.95±0.8 p value <0.05).”
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In the videos he shows that he’s suturing three layers. The first seems to be to a ligament, not sure which one. Somebody that is versed in the various methods might recognize what name it falls under or if it is a variation. The vidoes are pretty short, about 2 – 4 minutes each, but he does spend time on the repair. The removal portion is the typical cauterise and peel method.
His page says that removal and repair takes 1 – 2 hours. He makes a pretty big incision. He seems to be going through the muscle wall, not the canal. Like TREPP but without mesh. I think that Dr. Meyers does his repairs that way. But maybe he only does that for removals. I did not watch any repair only videos. And I am not informed at all about the details of the various possible ways to do removals or repairs. I am probably way off.
He also mentions general anesthesia. So, another possible reason to go to Korea. But, he is close and seems to have a good reputation. Plus he plays some good club music while he’s working.
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The plaintiff attorneys are realizing that the defendant attorneys are using delay tactics and are suggesting ways to get some cases settled.
This is from the Miller & Zois site above. Meanwhile, every day, more of the same mesh products are being implanted. Nothing has changed.
p.s. remember to use the backward arrow in this post to reply. Not the big red Reply button to the right. The red button will place your post randomly in the thread where it makes no sense.
“January 4, 2024: Plaintiffs Push for More Trials
We need more hernia mesh trials to get these cases settled. It has been too long. This litigation began in 2018. We have to turn the page in 2024.
The plaintiff’s hernia mesh lawyers believe there is a path. They have submitted a detailed memorandum to support their request for a new Case Management Order. This order is intended to set a roadmap for what should be done to speed this process up.
Strategy for Case Remand
The plaintiff’s mesh attorneys are not looking for the chaos that would come with sending all of these lawsuits home to their local federal courts. Instead, they suggest a phased approach, dealing with cases in large batches. The initial phase would include about 1,500 cases, representing a fraction of the total. They also propose a plan for which hernia mesh lawsuits to push forward. The selection criteria for these cases would be based on the severity of injuries, the duration since filing, and involvement in previous bellwether trials.
Efficiency and Justice in Trial Management
The proposal advocates for multi-plaintiff trials, which would be more efficient and cost-effective, avoiding repetitive testimony and allowing for shared trial expenses. The unspoken part? Trials with multiple plaintiffs also put more pressure on Bard.
So, keeping some of the structure the MDL provides, they propose that case-specific discovery should be managed under the current Court’s supervision to ensure that the cases are nearly ready for trial upon transfer to the remand courts. This plan is presented as a way to accelerate the delivery of justice for plaintiffs, ensuring that their cases are resolved in a timely manner. The judge has ordered the defendants to respond on January 10th. We should get a ruling, hopefully, by the end of the month.
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Another publication about TREPP and maybe TIPP. Pre-peritoneal both. Dr. Reinhorn is the last author on the list.
These publications seem to have an inherent conflict between promoting the topic under study and objective reporting of results. Very strange that none of the authors see the mixed messaging.
The title states firmly that “Open preperitoneal inguinal hernia repair has superior 1-year patient-reported outcomes compared to Shouldice non-mesh repair.”
But the conclusion seems more reality based. “Conclusion
Our data suggest that OPP is associated with significantly better patient-reported QoL, in the first month after surgery and up to 1 year postoperatively, especially with respect to lesser pain, when compared to the Shouldice repair.”
Also, these authors are still blending superficial concerns in the ACHQC data reporting, aesthetics, with actual performance concerns. Pain and activity restriction. Just report the individual scores. The blending is a subjective choice and waters down what many patients are really concerned about. How can the size of the scar be anywhere near as important as the other two?
At least they are still looking for alternatives. If they could just stop trying to “win” and/or promote what they are doing. Just do the work, report the results, and suggest improvements.
Another pay-per-view article. “Suggest”, “may”, “encourage”. A lot of maybe here.
https://link.springer.com/article/10.1007/s10029-023-02936-3
Hernia
<b data-test=”article-title” data-article-title=””>Open preperitoneal inguinal hernia repair has superior 1-year patient-reported outcomes compared to Shouldice non-mesh repair
- Original Article
- Published: <time datetime=”2023-12-23″>23 December 2023</time>
“…
EuraHS scores were used to estimate QoL, and further analysis on the EuraHS domains of pain, aesthetics, and activity restriction were performed between the two cohorts.
…
<b data-test=”abstract-sub-heading” style=”background-color: var(–bb-content-background-color); font-family: inherit; font-size: inherit; color: var(–bb-body-text-color);”>Conclusion
Our data suggest that OPP is associated with significantly better patient-reported QoL, in the first month after surgery and up to 1 year postoperatively, especially with respect to lesser pain, when compared to the Shouldice repair. In specialized inguinal hernia practices, open posterior mesh repairs may lead to better outcomes than non-mesh repairs. We encourage more training in both repairs to facilitate larger prospective studies and evaluation of the generalizability of these results to all surgeons performing IHR.”
link.springer.com
Introduction The Shouldice method for inguinal hernia repair remains the gold standard for prosthesis-free repairs. Nonetheless, international guidelines have favored posterior mesh reinforcement as the standard of care for inguinal hernia repair due to lower risk of recurrence and chronic … Continue reading
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Just another followup. These new things I ‘ve been trying have made me realize that I have been trying to get my body to adapt to the still painful lump of mesh/cord/veins/nerves in my inguinal canal, to get back to my previously normal life. But daily life is better now, taking the odd steps of suspenders and belts and bands to reduce the soreness than in trying to suffer the constant mild irritation of tight pants and belts and normal clothes. I’ve been stuck at 90-95% for years but haven’t been able to work through it. It’s like I’ve been wearing shoes that were two sizes too small for years, hoping that my feet will shrink. It’s not going to happen.
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Hello @JohnParker Thanks for the reply. If you want your replies to make sense in a chronological fashion, don’t use the big red Reply button on the side. It will place your post in some random spot in the thread. Use the small Reply button with the backward arrow in the last post. That will place your post at the end of the thread.
Are you able to access the database, as a member of the ACHQC? Do you have the ability to sort the data so that you can see if there is a prevalence of certain types of mesh or procedures or device-makers that seem to give better or worse results? Of course, a proper look would show the rate per device usage level, but the work has to start somewhere.
There has been much talk over the years about registries and some online comments about devices like the plug but nobody is creating something that a patient could use to increase their chance of a good outcome. Much talk and supposed concern but no usable results to help the individual patient. Which is kind of ironic because it makes the overall field of hernia repair look worse. The bad products and methods are staining everybody involved.
Good luck with your efforts.
