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02-15-2013, 05:24 PM | #1 | ||
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Two questions, pertaining mostly to the early stage PD patient.
First, is there a clear crisp answer (or even a consensus) whether to try to delay levodopa as long as possible, especially whether even first exposure (“challenge” or diagnostic dose) starts the clock toward dyskinesias? The literature seems contradictive/unclear, even argumentative. Some say “proven” benefits especially if start in early UPDRS stages, maybe even neuroprotective, dyskinesias due to disease progression (increasing amount of levodopa needed) not an effect of levodopa itself. Others say “proven” it produces both motor, mental complications eventually, even challenge dose starts the clock, eventually decreases dopamine receptor sensitivity, worsens disease, don’t start until you really need it. Second, what about neurostimulation, both DBS and extradural motor cortex (EMCS). New articles appeared recently suggesting that EMCS is efficacious, safe, little if any downside. If so what if any reasons not to try it? Then on Valentine’s Day the NEJM article on the EARLYSTIM trial. If I read correctly, DBS improves motor symptoms and major secondary outcomes significantly better than medical therapy alone for earlier stage PD, no significant difference in serious adverse events, bottom line in favor for carefully chosen young patients. For patients with primarily motor symptoms the appeal of relief without starting the clock on levodopa is obvious, but I'm sure I'm ignorant of many things. All thoughts/recommendations welcome, including additional references. Thank you!! |
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02-15-2013, 06:34 PM | #2 | ||
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I'm in the same boat. On Azilect 1MG daily since Oct last year when I was diagnosed. I can already tell I will need to make a move to new medication soon. Would rather not start the levodopa route. If anyone has had DBS, EMCS early in the Disease please chime in and give us the scoop.
My hope is the Ceregene project pans out and this becomes a viable alternative soon. |
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02-15-2013, 07:56 PM | #3 | |||
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Definitely keep your eye on Ceregene. Neurotrophics are closest we may come to a cure, imho. The NIH and Genzyme are also conducting similar trials. Okay here is my lengthy reply to you both. I am sure you will get other opinions but I just set forth the facts and the important things to consider. Hope it helps! BTW, I can provide research to back everything I post, so just ask if you want it... Unfortunately, I was started on drugs day one of diagnosis after five years of being treated for Essential Tremor, so I never even questioned the meds, at that point I just wanted relief and normalcy. I was far too trusting. Looking back I wish I had started with amino acid replacement (levodopa precursors), mucuna pruriens (plant source of dopamine), and intense exercise. However it may not have been enough symptom control while still working, so who knows? You will find it is all largely trial and error. Whatever you choose you need to think first about how symptomatic you can tolerate being. If you don't have to hide your condition, you have more options. Likely the doctor will want to start you on agonists, but although they alone do not cause the dreaded "D" word, they do cause personality changes akin to Obsessive Compulsive and Bi-polar like disorders. There are things neurologists do not readily share about Mirapex or Sinemet. Agonists do not provide as good a symptom control as Levodopa, so most likely you will be on a high dose sooner than later. That commonly causes hallucinations. For me, starting Sinemet early was an easy decision because it totally alleviates my symptoms and on just that I felt most normal and my best. I also feel like Sinemet is the devil I know whereas the adverse effects of agonists are just now starting to reveal themselves. Lastly, the dyskinesia fear mongering is really over the top and the common belief that levodopa only works for five years is just false. Many people do fine with it long term. Dyskinesia is a temporary effect of having taken too much levodopa; it is not a constant state. In my PD circles, I have enountered maybe 5 people who had out of control dyskinesia and that is over a period of 7 years. However, I have met too many people who are worse after DBS. In my book 1 botched DBS wipes out like 20 successes. If it were a matter of improving vs. baseline then bring on the wires! It is far too risky. It is, in my opinion, a highly invasive way to make up for the addictive effects of Sinemet. It was also not even necessary in that an intestinal pump delivery system for levodopa already existed and Medtronic could easily have developed it, so right off the bat, I question the whole concept of DBS. Keep in mind there is a Duodopa pump system that we hope/think will be approve by the FDA this year. It seems a far superior treatment and has been available in Europe for like 15 years. After two years of trying at least 10 different PD meds in varying combos, my doctor is pushing DBS. I am in my 40's and have a child at home. I am applying to clinical trials either neurotrophic factors, or Pico Tesla Magnetic fields. DBS is a last resort; I will go on a drug holiday before I got that route. Be wary of the DBS promotion early on; there is a trend in promoting it in younger patients and many are doing it. It is scary; there is conflicting research on its neuroprotective potential; they cannot even figure out how it works let alone determine it slows progression. Plus, the few studies I have seen were totally biased with authors disclosing ties to Medtronic. I will leave you with this article: Management of Referred Deep Brain Stimulation Failures A Retrospective Analysis From 2 Movement Disorders Centers Laura |
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"Thanks for this!" says: | lab rat (02-16-2013), moondaughter (03-16-2013), NorCalGal (03-16-2013), rappleman (03-04-2013), Tupelo3 (03-20-2013), VICTORIALOU (02-16-2013) |
02-15-2013, 08:57 PM | #4 | ||
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Magnate
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i had a different experience, didn't have kids to raise, was self-employed, worked at home, not much of a social life so held off on drugs as long as i could. i tried a lot of alternative medicine including chelation, IV glutathione, 1200mg coq10 daily, b-12 injections, every supplement mentioned in research papers, LOW DOSE NALTREXONE, vigorous exercise mainly because i enjoyed it which involved playing 2-3 men's soccer games a week, running or swimming on the non-soccer days for 5 years, much more vigorous exercise than the forced exercise they are doing on the bikes. this was before exercise became such a hot topic. and here i am, 11 years after diagnosis, taking 800mg of sinemet daily and acting like a 90 year old man when off. now maybe i should have continued some of those alternative therapies longer but the day i took my first sinemet was a very happy day and i have no regrets. i have tried mucana, makes me naseous and doesn't help my parkinson's, i am planning on trying it again but toasting it first to inactivate enzymes - 225 F for 30minutes. as far as AA therapy, just haven't met anyone that has tried it. so i guess i'm saying i tried a lot of stuff and i still have advanced pd. of course everyone is different but i'm not regretting starting sinemet at all. |
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"Thanks for this!" says: | Conductor71 (02-16-2013), moondaughter (03-21-2013), rappleman (03-04-2013), VICTORIALOU (02-16-2013) |
02-16-2013, 01:37 PM | #5 | |||
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Laura and soccertese;
I very much appreciate and applaud your thorough and frank replies to these new forum posters. You both do a great job of laying out the options without biasing their decisions about the way forward for someone recently diagnosed. Keyboard work never has been a strong talent for me, so I allow myself to be somewhat lazy with responses. Robert |
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02-16-2013, 05:15 PM | #6 | ||
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You already received two thorough exceptional answers from two of the most knowledgeable people on this list. If I might add another couple of thoughts. First is a request to consider being part of the Michael J Fox PPMI research study. They are looking for people who are diagnosed with Parkinson's but have not started any medication. This does not mean that you don't get to start medication, just that when they are doing their baseline reports you have not had any yet. The person who is taking Azilect will not qualify for the Michael J Fox program. Second, it's important to understand, as the others have emphasized, that every person has their own personal journey with Parkinson's. My onset was later, after I was 62 years old, and has followed a different course than the others. A year after my diagnosis I began cycling and by doing that was able to decrease my dose of dopamine agonist and eliminate Azilect. You can read more about that on the Pedaling for Parkinson's thread. I have needed to try three different types of dopamine agonists and then I'm constantly monitoring myself to see where I am and what more I might need or what less I might need. The one constant is my ability to cycle and I need to keep on cycling. it will not work for everyone, but it is worth giving it a try.
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"Thanks for this!" says: | Conductor71 (02-16-2013), rappleman (03-04-2013) |
03-16-2013, 02:01 PM | #7 | ||
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Norcalgal |
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03-20-2013, 07:45 PM | #8 | ||
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I absolutely agree with you about Ceregene. As I am less than a year since my PD diagnosis, I don't have a lot of experience with the meds (I take Azilect and Amantadine). However, i've been doing extensive reading on new drugs in research, particularly those which are hopefully neuroprotctive. Cere-120 seems to have had the most impressive results to date. I hope they begin their Phase III studies soon. Gary |
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02-15-2013, 07:37 PM | #9 | ||
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Magnate
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as i alway do, i suggest you get a used copy of "THE PARKINSON'S DISEASE TREATMENT BOOK" and start from there. http://www.amazon.com/The-Parkinsons...treatment+book "Older guidelines for treating PD often suggest that the best drugs, especially l-dopa therapy, should be deferred until absolutely necessary. However, there is now increasing recognition that the slow progression of pd continues, regardless of whether we treat conservatively or aggressively early in the course. If we choose to suffer now, hoping to catch the best responses later, we may have done this for naught, we probably have lost an opportunity." Keep in mind that the intestinally delivered DUODOPA l-dopa is given in slightly higher dosages than oral L-DOPA and dyskinesias are greatly reduced, so it appears that it is the fluctuation in l-dopa levels that cause the dyskinesias, not the l-dopa directly, not absolutely certain on that, have also read that short acting apomorphine can cause dyskinesias. IMPAX labs is hopefully getting the improved extended release "sinemet" approved soon which supposedly reduces dysk. and there are other improved sinemts in the pipeline. My comment on DBS is it's a very personal decision for you and your caregivers - they'll have to take care of you if the are serious complications after the DBS, but if you qualify, have access to a center that has an excellent reputation, feel comfortable with the risk potential and can afford it, I'd say it's better than dealing with ON/OFF fluctuations and keep adding/changing drugs. Can't hurt to get a few opinions. You do have to dig into these studies and decide if the researchers were totally unbiased and was the population cherry picked. I'd at least wait until the CEREGENE and COGANE trial results are out since a DBS might preclude you from participating in a clinical trial and/or getting those treatments. Basically, if seems you have the dilemma of the risk of brain surgery complications and/or a DBS that could have some major side affects - affecting balance, voice, etc., when you could have just continued with very low risk medication. Personally, for peace of mind, knowing what I know now and now experiencing on/off if i miss a dose - but no dyskinesia - the honeymoon is over - I'd still have to have more bad than good times with sinemet before risking a DBS. but again, haven't researched DBS very much. |
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"Thanks for this!" says: | crimsoncrew (02-15-2013), lab rat (02-16-2013), moondaughter (03-21-2013), rappleman (03-04-2013), Tupelo3 (03-20-2013), VICTORIALOU (02-16-2013) |
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