Taking a Closer Look at DBS: By Dr. De Leon

Recently, there has been a spur of interest in the surgical treatment known as deep brain stimulation (DBS) among the Parkinson’s community. Although, this procedure is by no means a ‘novel’ or ‘new’ treatment being approved by FDA back in the late 1990’s for tremor and 2002 for PD has begun to reach general stream awareness due to postings in the media by concert master R. Frisch playing the “fiddle,” during brain procedure (DBS). Of course, who can forget the recent nationally televised event which took place at University Hospitals Case medical Center in Cleveland, OH on October 25th on a YOPD patient began another debate of when and who should be having this procedure done?

Despite some reservations which include non-disclosure of funding by Medtronic’s to hospital and surgeons performing operation as well as an increased risk of possible complications due to outside factors usually not-present in the operating room; I believe that educational broadcasts such as this one play a very crucial role in validating DBS as a viable and effective treatment while raising awareness and promoting its use.

Even though, DBS is the standard of care in the treatment of Parkinson’s disease, since its approval only roughly 5% of all PD patients have had this procedure done, according to Dr. Allison Willis, Assistant professor of Neurology & Biostatistics and Epidemiology at The University of Pennsylvania school of Medicine. This is a great travesty considering that nearly $100 billion were invested by Medtronic’s to bring this technology forth. However, the worst part in my opinion is the huge discrepancy seen in those implanted, at least here in this country, which tend to be white males (95%). Even when women and other minorities are seeing and being followed by the same specialist as the men implanted, these groups seldom even get the option of DBS as a potential treatment.

So how do we decrease these discrepancies?

First, by being aware of its existence and coverage by insurance including Medicare (other assistance programs available through Medtronic’s). Now we also have a new competitor on the market known as the Brio Neurostimulation System. This unlike the Medtronic constant voltage device- it has a “constant current” delivery system allowing it to react to brain wave changes over time, thus potentially decreasing number of reprogramming visits.

Second, knowing that there is a specific type of person that benefits most from this procedure as well as a time window for obtaining best results.

Third, although usually offered or reserved for those who have clear cut tremors, dyskinesias, or intolerability to medications due to side effects of the same in the presence of good and clear cut symptom control with levodopa; some physicians are opting to perform this procedure in YOPD patients early in the disease in hopes it might alter the disease process. This is not yet known. At present DBS is not a cure nor does it alter disease progression however, it does buy the individual with Parkinson’s time for other advances to occur as well as decrease both the doses and medication side effects.

The one reservation I have in performing the procedure too soon is knowing when is best time to do? Since we still don’t have a biomarker or blood test or other objective testing to say a person has PD unequivocally besides a brain biopsy, I worry that for those that have other slower progressive parkinsonian symptoms – an implant maybe done unnecessarily.  However, I will venture to say that at 10 years one should have a clear indication of disease and whether or not it conforms to typical PD progression and if a patient would be a good candidate.

As I find myself in the process of weighing in the benefits of having a DBS for the sole purpose of reversing medication intolerability; I am again revisiting the top reasons why a patient can or does poorly with this procedure.

TOP REASONS for Less than Optimal outcome once RIGHT candidate chosen.

1.Neurosurgeon technique– find one with experience- one that has done many- ask names of people that have had done.

  1. Programmer’s experience is the most crucial in my opinion!!!! Best if the programmer is the SAME MDS/neurologist adjusting your medications. As voltage goes up medications MUST come down! Second best option is seeing programmer at same time in same office as neurologist. Find out about the programmer you will be seeing beforehand…how good are they? Bedside manner? Patient satisfaction?
  2. Patient’s lack of support from inner circle of family and friends. This is crucial if care partners are not on board with procedure – it won’t be successful. Or frail elder caregivers.
  3. Patients sometimes fail to fully grasp their own disease stage as well as their own age in regards to having risk for other medical issues. Unfortunately, as we age not only might we develop other problems like high blood pressure, diabetes, etc. but PD will continue to progress so distance to programmer is very important. Think about fact that you will make several trips a year especially at the beginning of DBS to make adjustments; thus traveling 5 hours may not be such a big deal at first but can get old and more difficult to do as time passes. If this is a problem and still a good candidate consider pallidotomy surgery instead or hopefully in next couple of years Focused ultrasound. I have had several patients who have undergone procedure only to not benefit from it because they could no longer travel to centers where programming was being done. Fortunately, now we also have two choices of devices both by Medtronic’s and Brio which produce constant current.

Now that you are aware of this new technology my esteemed reader, I recommend that you bring up the topic with your physician yourself but do in a separate visit to discuss this thoroughly.

Questions to ask?  

  • Am I a candidate?
  • Who and where will the surgery be done?
  • Who will do programming?
  • How many steps are involved in procedure because it seems to me like every teaching institution has different protocols-ranging from bilateral implants as an outpatient with no general anesthesia or sedation other than the part when battery is implanted in the chest wall to a 5 step procedure as is being done at Vanderbilt in which I believe also like to have patients asleep during surgery. Other concerns although purely for vanity purposes but also one that might cause more or less possible skin infections in scalp is the manner in which patient is prepped –total head shave or only minimal plus will they be using titanium halo for stereotactic mapping or a lighter frame?
  • Most importantly how long will you have to be off medications for the procedure? Some people have such severe pain or dystonia’s off medication that will make procedure much more difficult.

Now we are ready to embark on a life changing journey with the knowledge at our finger tips to help us and our doctors make the right decision of whether DBS is right for us or not? For me the idea of taking much fewer meds is extremely appealing but having to drive 6 hours round trip to get adjusted every few months is somewhat of a draw back since I will have to do this on my own most of the time. keep you posted!

Good luck to all of us!

Sources:

https://www.facebook.com/parkinsonsdiseasefoundation/photos/a.442545474003.246436.34178524003/10153629275519004/?type=3&theater

http://blog.pdf.org/2015/10/23/dbs-in-primetime-natgeo-to-air-brain-surgery-live-this-sunday/

https://www.michaeljfox.org/foundation/news-detail.php?fda-approves-new-deep-brain-stimulation-device http://www.uphs.upenn.edu/news/News_Releases/2014/01/willis/
go to http://www.pdf.org for more information on topic

The Top 10 SPOOKY Things Living with PD which Can Send a Frightful Scream! : By Dr. De Leon

1. Getting PD Diagnosis– this can suddenly make your heart stop beating – feels like you have flat lined until a helpful friend comes along.

2. Losing control of your mind. I get off the car to check the mail only to see my car rolling down the hill because I just step out without putting brakes or turning engine off!

3. Losing control of your body– food is flying in every direction except into your mouth as you try to remain calm and poise while attempting to look dignified.

4.Losing control of your bowels. no matter the age, circumstances, or location – this is enough to send one howling and expelling such frightful wailings that causes a chill to run down anyone within ear range!

5.Bladder urgency/loss– if you have to find a bathroom one more time after having gone 20 times in the last 30 minutes you must just flush yourself down the drain as well.

6.Pills,Pills, Pills- all colors, sizes and shapes- how can anyone person take so many medications and not pass out? where do they all go? you think they would fill ,up my stomach and I would not need to eat!

7.Visual disturbances: see playing children all around that no one else can see but the car in front of us that everyone else sees we cannot see well.

8.Doctors, doctors, doctors: I have my own collection of specialists for everybody part even when I look at the mirror I see one staring right at me!

9.PAIN!! EVERYWHERE PAIN!!– what a pain it is to be in constant pain- irritable and shout-y, I have become. Sometimes, I scream just to let out the frustration of being  me with this disease.

10. People Judging: I can’t smile much so must be depressed; can’t talk loud must not have much too say/contribute; constant shaking and shuffling must be mentally challenged.

This Halloween I ask to NOT let your PARKINSON”S DISEASE SPOOK you and others-After all, “the only thing we have to fear is fear itself and perhaps a spider or two.”

Put an end to the fear by self -advocating and raising awareness for others that can’t do for themselves! 

Brain Storms

Making waves..I still have to read…but any book that brings hope and perspective to a disease still not fully understood is always welcomed in both the medical, scientific and Parkinson’s community..

Sharon Krischer's avatarTwitchy Woman: My Adventures with Parkinson's

I have been listening to books on Audible for a while now, usually when I am walking or driving. Few have kept my interest like Jon Palfreman’s new book Brain Storms, The Race to Unlock the Mysteries of Parkinson’s Disease. Unlike other audiobooks, I have rarely had to back track to find ut what I missed while distracted by something else. The book was engaging, informative and written in language that a reader with no medical background could understand.

Palferman was diagnosed with Parkinson’s at about the same time that I was and at about the same age. He also seems to have had a similar trajectory in the progress of the disease. He is a medical science journalist, and in that role, he oftened covered scientific discoveries leading to treatments and cures of chronic diseases. Thirty years ago he produced a documentary film for Nova,The Case of…

View original post 452 more words

Lighthouses: by Maria De Leon

Source: Lighthouses: by Maria De Leon

Something’s Missing: By Maria De Leon

Source: Something’s Missing: By Maria De Leon

Purpose: A Powerful Tool Against Hopelessness: By Dr. De Leon

In the last few weeks everyone has been talking more openly about depression in living with Parkinson’s from being the patient to being the care partner or care giver every one is impacted by this disease albeit in different ways. Finding ways to cope with the hopelessness that invariably arises in all of us is one of the biggest challenges we must face.
How do we do this?
To start, as I described in my book the ‘Parkinson’s Diva’ there are 4 main keys to finding and achieving happiness. The biggest determinant of a happy, full life with a good quality of life despite chronic illness is having a PURPOSE in life.
In a recent publication in ‘Practical Neurology,’ it revealed that there is a direct link between valuing life and post mortem changes found in the brain. Those that had a purpose while alive had a 50% reduction in macroscopic brain infarcts. This confirms what I discussed as my 3rd point to happiness is living for others. Life is NOT all about us!
John Gardner said it best when he quipped that “when people are serving, life is no longer meaningless.”  We are then less likely to be dragged down to the abyss when we are involved in the giving instead of receiving.
When you have a purpose although you may still have episodes of depression or sadness because life stressors never stop coming but if you learn to change your attitude and your mind towards the things that make you down even though the situation does not change you will be different and even sleep better.  We know that a lot of us with PD have sleep deficits which only serve to reinforce the exhaustion, fatigue and depression we feel. However, another study found that having a strong sense of purpose in life reduced sleep disturbances by 16% and lessen the risk of mortality by 57%. Some believe that this improvement in sleep is due to decreased stress that comes by achieving and setting small meaningful goals. So start small with what makes you happy!
This idea of purposeful therapy was also introduced by Dr. R.D. Dobkin, Associate Professor of Psychiatry at Rutgers -Robert Wood Johnson Medical School.
She recommends that we RETHINK the Big Picture!

This means:

Catch the negative thoughts & don’t dwell on them -feeding them

Press Pause

Rewind

&

RePlay

Then

Increase meaningful and social interactions to replace these thought- i.e. find PURPOSE

  • Do Volunteer work (become Pair advocate, join a research study, be a mentor)
  • Increase time with those that matter- your spouse, family, children, grandchildren
  • Get a Hobby/ find your Passion- painting, writing, photography, cooking, decorating, teaching, etc.
  • Find time for spiritual health- join a church, a bible study, a prayer group, etc.

Purpose can be a powerful therapy and tool which can clearly lead to much improvement in quality of life by lessening our daily burdens and struggles in living with Parkinson’s. Not only will it help us but others around us as well. The challenge remains in finding the one thing that fills our lives with joy and give us meaning and a reason to get out of bed every day.

For me my daughter and family are one important reason to continue fighting, another one is faith in God that everything happens for a reason so I know did not spend all these years in medical school and training learning about PD just to give up when the going gets tough. One approach is setting goals- short term, intermediate, and long-term goals. Each no matter how small or trivial will serve to boost your confidence and release natural occurring hormones like dopamine- which we need desperately- every time a goal is reached. The fun of life is enjoying small victories along the way!!!

Sources:

Fotuhi, M and Mehr S. (September 2015): “The science Behind the Powerful benefits of Having a Purpose.” Practical Neurology. 14(7).32-33.

Dobkin, R. “The psychological and Emotional landscape of Parkinson’s Disease.” power point presentation at Women & Parkinson’s Initiative, September 18, 2015.

De Leon, M. (June 2015) “Chapter15: Four keys to unlocking Happiness in the midst of PD.”  Parkinson’s Diva: A Woman’s Guide to Parkinson’s Disease.

Empower yourself through exercise

Important to exercise..I just stared water aerobics again myself …felt so good to get in the water and feel all my muscles begin to relax again …best when done in the deep end helps to strengthen core axial muscles and improve balance!! Plus if you have lots of sweating from medications ( amantadine is one of the worse culprits) the cool water can relieve the heat and be extremely soothing..plus getting out works on improving your inner chemical for happiness and well being ..it allows you do do something for yourself, stay healthy and socialize..not only are you decreasing need for meds especially pain medications plus it helps deter memory loss by boosting ball gnglia cells keeping them oxygenated and bathed in blood flow….keep moving…for your health and that of your family! #pwr # exercise # Parkinsonsdiva

mydancingintherain's avatarLiving Well with Parkinsons Disease

Aerobics - Step 10

By Sheryl Jedlinski

I was 10 years old when President John F. Kennedy called Americans’ “growing softness and increasing lack of physical fitness a menace to our security.” It was as if he had pointed his finger directly at me through our tv and called me an enemy of the state. I knew he didn’t really mean it, so I stayed my course, refusing to put down my Nancy Drew books and go outside to play.

It wasn’t until 34 years later, when diagnosed with Parkinson’s disease (PD), that I finally got up from my couch and adopted a healthier, more active lifestyle, thanks to my neurologist. She told me up front that if I wanted to forestall disability and maintain a good quality of life, daily exercise was imperative. It delivers better results than any medicine currently on the market, and has no negative side effects. “The proof is in…

View original post 305 more words

A Good Resource for all things Parkinson’s

Great resources for all to have at their disposal …happy weekend!

Sharon Krischer's avatarTwitchy Woman: My Adventures with Parkinson's

You can’t control the wind, but you can adjust your sails.

Yiddish proverb

I just saw this post on Parkinson’s Women Support about a site called Parkinson’s Patients Support Groups.  Although it is based in the Bay Area, there is a lot of good information about Parkinson’s organizations, the latest news on PD and clinical trials.  A similar sight with resources in the LA area is The NeuroCommunity Foundation  which has support groups and other services in the Valley and points north.

In addition, I was informed this morning that I have been featured in a testimonial on the Parkinson’s Disease Foundation website.  One of the goals of the Women & Parkinson’s Initiative conference that I attended is that participants will reach out to other women with Parkinson’s.  I will be planning an event in the spring for Women with PD living in in Los Angeles along with Jennifer…

View original post 97 more words

Go PINK & THINK BIG! : by Maria De Leon

Source: Go PINK & THINK BIG! : by Maria De Leon

Source: Go PINK & THINK BIG! : by Maria De Leon