tag:blogger.com,1999:blog-33960805.post116657638536355655..comments2023-10-30T02:03:47.513-07:00Comments on Clinical Psychology and Psychiatry: A Closer Look: A VNS DebateCL Psychhttp://www.blogger.com/profile/13990549972520745769noreply@blogger.comBlogger5125tag:blogger.com,1999:blog-33960805.post-1167539469100634012006-12-30T20:31:00.000-08:002006-12-30T20:31:00.000-08:00I’ve read comments from a few readers who disagree...I’ve read comments from a few readers who disagreed with my take on vagus nerve stimulation (VNS) therapy. One reader provided a link to the FDA’s site regarding VNS trials. It can be accessed <A HREF="http://www.fda.gov/cdrh/PDF/p970003s050b.pdf" REL="nofollow"> here</A>. I’ll quote from the FDA review on the site:<BR/><BR/>“The primary effectiveness endpoint for the randomized, sham-controlled study was an analysis of the percent responders (greater or equal to 50% decrease in HAM-D score from baseline to exit) between the 2 groups. In an evaluable patient population, 15.3% (17/111) of the active stimulation group were considered responders as compared to 10.0% of the sham group (11/110). The difference was <I> not </I> statistically significant (p=.238). [emphasis in original].” There were five other measures of depression and VNS was superior only one of them. So VNS batted one for six in its pivotal outcome study.<BR/><BR/>To put it in layman’s terms, VNS was no better than sham (fake) VNS therapy. Yet this was the main study upon which the evidence for its efficacy rests. Uncontrolled studies seem to yield results of about 20% relapse at 2-year follow-up. Since these studies are uncontrolled, there is simply no way of knowing about how much of the 20% is due to VNS or the passage of time or other factors. Given that the sham therapy produced pretty much equivalent results to VNS, I believe that something outside of VNS is likely producing much of the 20% remission rate. <BR/><BR/>I understand the desperation of patients who have not found success through a variety of treatments. Perhaps VNS should be made available for some patients, but should insurers and/or the government pick up the tab for an expensive procedure that has such weak evidence of efficacy? Should controlled research emerge indicating VNS works better than psychotherapy, medication, and other alternatives in the long run, then I’ll gladly eat my words. Until that point, I see no reason to get on the bandwagon.CL Psychhttps://www.blogger.com/profile/13990549972520745769noreply@blogger.comtag:blogger.com,1999:blog-33960805.post-1166737794543297532006-12-21T13:49:00.000-08:002006-12-21T13:49:00.000-08:00As a person who has suffered from Treatment Resist...As a person who has suffered from Treatment Resistant Depression for more than 30 years, with the usual hospitalizations; many meds and combination of meds; therapy; self-help books; hard work in research and personal growth; alternative treatments; and ECT, I was astonished to read that you "were not impressed" after a 2-year follow-up study showed some improvement or remission in (only) 22% of the patients who tried VNS Therapy. Do you have any idea what that improvement means to those people who have been helped? That, by the way, is a conservative estimate. Many people are in the process of the early months of treatment. Even if it is 'only 22%" at this point, that is an incredibly high percentage of people helped, when nothing.....do you understand.....nothing! offers hope by the time we get to the place of even learning about VNS Therapy. Hope is sometimes the only suicide prevention there is. And this offers hope. <BR/> I am an expert on Treatment Resistant Depression, suicidality, and loss of hope. I am appalled at this strange mixed message we have been given by your article. Do you know something we don't....is there anything that offers 22% or more remission after 2 years' treatment??? (Actually, as the process is refined, there is a greater possibility the results will be better, and the success stories.) Even at this time, the success of this treatment is better than your conservative estimate. <BR/>cdCDhttps://www.blogger.com/profile/08875993483624613554noreply@blogger.comtag:blogger.com,1999:blog-33960805.post-1166662701834564682006-12-20T16:58:00.000-08:002006-12-20T16:58:00.000-08:00Dear Doctor,I was a study subject in the D-02, dou...Dear Doctor,<BR/><BR/>I was a study subject in the D-02, double-blind, placebo-controlled investigational trial of vagus nerve stimulation for severe depression. I am now in the fifth year of "enjoying" the placebo effect of vagus nerve stimulation therapy.<BR/><BR/>One problem with pioneering investigational studies is that there it is difficult to design the perfect pioneering trial protocol.<BR/><BR/>After 25 years of depression, it was unreasonable to expect a clinically meaningful response after an eight week fixed dosage of VNS. Personally, I would much rather have a five year sustained response than an unsustained 8-week response.<BR/><BR/>As posted on the FDA's web site:<BR/><BR/>http://www.fda.gov/cdrh/PDF/p970003s050b.pdf<BR/><BR/>pages 13 and 14, fifty-percent of the study subjects had a clinically meaningful response. The facts man, nothing but the facts.<BR/><BR/>I don't know of any clinician who would say to a patient with a disease that has become incurable, life threatening and debilitating, " I won't recommend a safe, ninety-minute out patient operation, because it only has a 50% chance of improving your illness, is not 100% risk-free and works gradually over time".<BR/><BR/>Taking aspirin is now officially risky.<BR/><BR/><BR/>Full disclosure: I wrote, self-published, 100% financed a book-<BR/><BR/><I><B>Out of the Black Hole: The Patient's Guide to Vagus Nerve Stimulation and Depression</I></B> by Charles E. Donovan, III. Forwards by John M. Zajecka, M.D.( of Rush University Medical) and Nancy Williger, Ph.D. ( of Washington University-St. Louis)<BR/><BR/>Just my thoughts. My best wishes to all depression sufferers, their caretakers and loved ones.October1929https://www.blogger.com/profile/13980935104890679227noreply@blogger.comtag:blogger.com,1999:blog-33960805.post-1166658841948157182006-12-20T15:54:00.000-08:002006-12-20T15:54:00.000-08:00Dear Doc,As an addendum to my post earlier this mo...Dear Doc,<BR/><BR/>As an addendum to my post earlier this morning I wanted to share the following with you. My spouse and I had a scheduled appointment with her psychiatrist this afternoon. As usual, as part of the office visit her prosthesis is interrogated, my wife shares her thoughts and I in turn share my observations and thoughts too. In doing so I brought up our recent dialog and your comment:<BR/><BR/><BR/>“Among individuals who showed an initial response to VNS therapy, 22% had a remission of depressive symptoms at 2-year follow-up. I am not impressed.”<BR/><BR/><BR/>I then elaborated on my somewhat lengthy response to you earlier this morning.<BR/><BR/>His reply to me was simply, and I shall paraphrase, “Why didn’t you simply ask the good doctor what alternative would he suggest for his similar patients if 22% remission is unimpressive?”<BR/><BR/>Okay Doc, what would you do for your patients suffering under similar circumstances and often experiencing suicidal ideations?<BR/><BR/>We were also introduced to a young woman in the doctor’s waiting room who is one of his patients and who recently received the therapy option. She turned down ECT as she “didn’t want to fry my brain” and she was just about desperate to try anything. She’s responding and apparently has no regrets and much hope now.<BR/><BR/>I do look forward to your sharing your thoughts on the subject. I also hope to encourage some potential patients and patients to also come forth to share their thoughts on the subject too.<BR/><BR/>Warmly,<BR/>Herb Stein<BR/>VNSdepression.com<BR/><BR/><BR/>.Anonymousnoreply@blogger.comtag:blogger.com,1999:blog-33960805.post-1166628152336029362006-12-20T07:22:00.000-08:002006-12-20T07:22:00.000-08:00Dear Doc,Thank you, I shall take you up on your of...Dear Doc,<BR/><BR/>Thank you, I shall take you up on your offer to respectfully respond.<BR/><BR/>I would like to state that my intention was not to offend you by my remarks pertaining to the fact that you receive no drug funding as I understood your intentions but it was an attempt on my part to take your words as written to sensationalize or distort and/or make innuendos as I found in some of your commentary and that relating to the Dr. Nemeroff such as “pimp” and other sensationalistic news media reporting relating to the VNS Therapy for TRD that I come upon. If we’re going to discuss the therapy let’s stick to the therapy and not make innuendos or imply as you’ve also attempted relating to the finances, the management of the company and/or the researchers in order to taint the therapy.<BR/><BR/>I may differ with you upon your opinions on subject matter but “warmly” stands as my respectful salutation to you and others as individuals.<BR/><BR/><BR/>“…the most relevant marker of one’s expertise, as someone with a lesser education than I, with proper training and education, could certainly know as much or more than myself.”<BR/><BR/><BR/>I am in agreement with your statement. 43 years of empirical observations of my spouse’s illness and numerous therapies as well as my own research and collaborations with the experts in the field qualifies me, in my own mind, as a depression lay-expert to my wife. No one knows better than me what has or has not worked in terms of her treatments and therapies and the fact her illness’s origin is a genetic bio-neurochemical malfunctioning in her brain not caused by or affected by parental upbringing or situational or traumatic events in her life.<BR/><BR/>While I have only read your posts relating to the VNS Therapy I acknowledge your statement “I typically allude to research, not relying on my clinical experience” except for the fact it is often clinical experiences and/or empirical observations that in my opinion lead to discoveries and prompting research. It was the clinical observations of the neurologists and other physicians attending to their epilepsy patients that lead to the study of this therapy for depression.<BR/><BR/>Okay, we both agree that there is a need for sponsorship funding and improprieties do exist.<BR/><BR/>I disagree with you as to Drs. Lurie and Wolfe’s lack of training in this field is very relevant just as I would interpret and put little value in your ability to “interpret research findings” in techniques for brain surgery or the interpretation of the readings of MRI or other scans etc. The more I read the research data and opinions of the data from the professionals the more I see conflicting opinions taking place. I read one side supplying data that ECT is harmful and damaging to the brain and the other side reads the same data and presents their own findings that no such events take place and in fact I further read the research of Dr. Yvette Sheline indicating that ECT stimulates neurogenesis. Now I’m only a depression lay-expert to my spouse looking for answers from professionals like yourself and I find you professionals in conflict over the exact same information which leads me to the following points.<BR/><BR/><BR/>“Based on last observation carried forward analyses, HAM-D-28 response rates were 31% (18/59) after 3 months, 44% (26/59) after 1 year, and 42% (25/59) after 2 years of adjunctive VNS. Remission rates were 15% (9/59) at 3 months, 27% (16/59) at 1 year, and 22% (13/59) at 2 years. By 2 years, 2 deaths (unrelated to VNS) had occurred, 4 participants had withdrawn from the study, and 81% (48/59) were still receiving VNS. Longer-term VNS was generally well tolerated. CONCLUSION: These results suggest that patients with chronic or recurrent, treatment-resistant depression may show long-term benefit when treated with VNS.”<BR/><BR/><BR/>Here is a part of the same abstract we both read and yet, you the professional and I the depression lay-expert to my spouse strongly differ. Since I am not aware nor have you indicated the nature of the population of patients you attend to I’ll share with you that my spouse and those who attended our support groups and those who I currently collaborate with are what I would refer to as “the worst of the worst patients” suffering from treatment resistant depression. These are patients suffering the illness for 10, 20, and 30 or like my spouse, almost 40 years. These are patients with multiple yearly hospitalizations costing health insurance organizations and our government (Medicare) in the hundreds of thousands of dollars per patient each year. These are patients who have tried not one, two or three medications but have often been treated with 20 or more medications individually and/or in combination as well as other alternative and adjunctive therapies. These are patients who in desperation resort to ECT which has its own history of efficacy, side-effects and conflicts. These are patients who in many instances resort to the last resort to relieve their pain and anguish through single or multiple suicide attempts. So this is the unique population of severely ill and disenfranchised patients who cannot even advocate for oneself of whom I speak that have not obtained any efficacy let alone any thoughts of long-term remission.<BR/><BR/>So while you are “not impressed” with the data of “22% had a remission of depressive symptoms at 2-year follow” I’ll give you my interpretation and suggest you go back and read all of your colleagues comments and those who presented the “con” thoughts which I also unbiasedly included but you didn’t read.<BR/><BR/>Did you notice the response rate from 3 months to 1 year increasing and essentially holding at 2 years?<BR/><BR/>Did you know this response is unheard of for medications and most other therapies for this patient population?<BR/><BR/>Did you not notice the remission rates at 3 months to 1 year increasing and essentially holding at 2 years? <BR/><BR/>Did you know this remission is unheard of for medications and most other therapies for this patient population?<BR/><BR/>Are you not also aware this population of serious ill patients is excluded from drug studies?<BR/><BR/>The VNS Therapy for TRD study took “the worst of the worst” patient population.<BR/><BR/>May I also point out to you that a true double-blind study of this medical device cannot ethically be performed and if so the patients who are not the sham subjects would know almost immediately and be cognizant of the fact they are obtaining the therapy?<BR/><BR/>While you are “not impressed” I like many of those professionals commenting to CMS recognize the remarkable events and data being presented. A significant percentage of the most difficult patient population unresponsive to multiple treatments options over decades of trying are for the first time obtaining varying degrees of efficacious responses and more significantly as the therapy remains active 24/7/365 requiring no patient compliance (which is another serious issue in the treatment of patients) are obtaining and maintaining longer-term remissions, safely.<BR/><BR/>By the way something also not unheard of in medicine is the crossover use of medications for one illness to be used for another is essentially what is being done with this therapy.<BR/><BR/>What impresses me is the solid real-time efficacy being obtained by patients who otherwise would have just about given up.<BR/><BR/><BR/>“*You cite letters from doctors and (I think) an endorsement from the American Psychiatric Association. I’m not sure about how APA’s 36,000 members tie into this. I don’t believe APA officially endorsed the treatment.”<BR/><BR/><BR/>I cited my link for you to read the responses from some of the professionals. Included in that link and highlighted in yellow is the response of the APA and its 36,000 or so members unaffiliated with the sponsor. <BR/><BR/>The APA officially endorses the treatment contrary to your belief!<BR/><BR/>I would also like to offer up for you and your readership my screen capture of the entire response to CMS (Medicare – National) so that your readership may have an even clearer picture of this therapy option and in turn make their determination.<BR/><BR/>http://www.vnsdepression.com/pp10-804-articles_8-10-06-Medicare-Coverage-Database-5-07PM.htm<BR/><BR/>Let us not forget the field of Psychiatry as a whole. It is an art or practice trying to become a science. It is a field using a book, DSM IV, which in my mind is anything but scientific describing symptomology and assigning terminology without any diagnostic and/or quantitative means via blood tests, x-rays, MRI etc to establish the validity of any of the diagnosis that your profession assigns and/or labels patients and yet here we are debating the research data of illnesses not scientifically established. Lastly, many if not most of the research documents I read as it pertains to Psychiatric research are nothing more than theorizes. <BR/><BR/>Once again, I appreciate your thoughts and opinions and this opportunity to freely discuss what I personally think is another viable and safe treatment option to be considered through education by the patient and his/her support persons and then to make an informed and un-coerced medical decision in collaboration with one’s trusted, compassionate, knowledgeable and licensed health care professional.<BR/><BR/>Warmly,<BR/>Herb<BR/>VNSdepression.com<BR/><BR/><BR/>.Anonymousnoreply@blogger.com