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Steven Y. Park, MD
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  • New York, NY
  • United States
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Steven Y. Park, MD added 2 discussions
yesterday
There are a number of FDA phase I studies in progress using hypoglossal nerve stimulation paced to the muscles of respiration, kind of like a pacemaker. I wrote about this in one of my past blogs here.
yesterday
I'll be happy to distribute a head's up on this to the members of the Manhattan A.W.A.K.E. Support Group in the morning.
yesterday
I had a sleep study a while ago which was completely unremarkable, except for a few alpha intrusions. It was using nasal pressure monitors. I do agree that Asians are more susceptible to sleep-breathing problems since they have smaller jaws. This i…
March 11
I'm a bit biased (being an ENT), but I think everyone with sleep apnea should undergo an ENT evaluation. By definition, if you have sleep apnea, you'll also have nasal/sinus/ear issues or throat reflux issues. Once in a while I see patients that hav…
March 11
My feeling is that most cases of chronic insomnia is caused by or aggravated by an underlying sleep-breathing disorder, whether or not it's obstructive sleep apnea. Most people with insomnia have upper airway resistance syndrome, which is not usuall…
March 10
March 5
Not surprising. Did he give a reference? Numerous studies have shown multiple areas of brain damage or low neuron density in sleep apnea patients, particularly in the areas that control breathing, autonomic function, memory, and executive function.…
March 4

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Steven Y. Park, MD's Articles

Steven Y. Park, MD

Upper Airway Resistance Syndrome — A Primer

Note: This is an edited transcription of a podcast recording

Today, we are going to spend the next 30 minutes talking about upper airway resistance syndrome, or UARS. It’s a relatively new description of a condition that’s related to obstructive sleep apnea but as you’ll hear in this podcast, has enormous ramifications in regards to so many health conditions that we see, not only in our field, but in almost every other field in general. I have to say, however, that this is a condition that is n… Continue

Posted on February 8, 2009 at 8:00pm — 5 Comments

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At 8:59am on March 5, 2010, Renee said…
Hello Dr. Park,

I very much appreciate your many postings of advice and support on SG and I would like to ask for your thoughts on a particular issue, that is, lack of S-3 and REM.

I was diagnosed with OSA and have been using CPAP since 12-09 and I am now using CPAP 7 nights a week.

My pressure has been increased from 9 to 12 and my OSA is improving.
Recent 6 wks at pressure of 12 – Per Hr – AI - .8; HI – 3.0; AHI – 3.8
1st 5 wks at the pressure of 9 – Per Hr – AI – 1.5; HI – 4.3; AHI – 5.8

However, I also have alpha intrusion and very little S-3 and REM.

S-3 & REM – % Of Sleep
2nd Titration – 1st Titration – 1st Sleep Study

S-1 – 42.9% – 68.2% – 35.6%
S-2 – 50.2% – 18.6% – 35.9%
S-3 – 6.3% – 6.5% – 20.2%
REM – 0.6% – 6.7% – 8.4%

After a 3rd titration on 2-23, I asked the tech in the morning and found that I, again, did not have REM sleep. I expect to go soon for a consultation to go over my latest titration results. However, on the morning after the titration, the doctor asked me to begin taking Gabapentin (Neurontin) 100mg at bedtime and I have been doing that for the past 10 days. (Although 100mg is a very low dosage, I also take Topomax 25mg daily for benign intention tremor and so that also needs to be taken into account.)

I was hoping that once I found out I had sleep apnea and used CPAP that it would be the answer I needed and, although I had a really difficult time adjusting to CPAP, I have persisted. But, with alpha intrusion and lack of S-3 and REM, I am not getting restorative sleep and so I remain incapacitatingly tired. And so I thought to ask if you have any thoughts or suggestions re: info / testing / treatment – any ideas regarding lack of S-3 and REM and related alpha intrusion.

Thank you very much for considering this long message on an individual issue and for any / all thoughts, suggestions or recommendations that you might have – as well as for all your on-going support and advise to SG members.

Best Regards,
Renee
At 8:32pm on February 21, 2010, Mike said…
Wonder what you think of this new treatment in clinical trials: http://www.sleepguide.com/forum/topics/imthera-tongue-implant-sleep
At 4:33pm on November 10, 2009, susan mccord said…
Hi Steve!

Susan McCord :-)
At 10:57am on November 6, 2009, 99 said…
FYI mark beds is a salesman and not interested in apnea

i have withdrawn my friendship with him
At 9:32am on November 1, 2009, RD said…
Thanks for your response. I'll be talking to them soon about that.
At 4:52am on November 1, 2009, Beth Parascandolo said…
Dear Dr. Park,
Thank you for your response. My Dr. said he doesn't feel it is UARS from the study. He finds nothing abnormal and is thinking it might be narcolepsy. I have no symptoms of that except for the sleepiness. He said I need to change my Paxil for a different type of SSRI because he wants to do another study to r/o narcolepsy. He said he can't do it while I'm on Paxil and my Psychiatrist said no. I am frustrated and ready to just give up and keep napping everyday. I could just cry. What should I do? Throw in the towel?
At 9:42am on October 31, 2009, Maxine Driscoll said…
Thank you for the information about Iron for my RLS. I will mention it to my doctor. I first went to a neurologist for balance problems. He diagnosed Peripheral Neuropahy and ordered extensive laboratory tests. Everything was in the normal range. A lung function test and a fancy nuclear heart test showed no abnormalities. It was only when I mentioned that I get up frequently at night to urinate, that he sent me for tests for Sleep Apnea. Diagnosis: severe sleep apnea. I am in great shape for my age - 80. Normal blood pressure, etc. All of the neurological problems surfaced about two years ago. I am now taking Mirapex for the RLS. Not sure if it is helping as I wake up with severe leg pain, which goes away when I get up. Again, thank you for the information about Iron.
At 10:00am on October 13, 2009, RD said…
Good Morning Dr. Park,
I am on my 13th day of CPAP therapy. I'm using a Respironics Elite II with a Mirage Quattro full-face mask. For the last 3-4 days now I have woke up with bags under my eyes that look like blisters. It feels like I'm in the middle hay season. My eyes are pinkish, weepy and a little sticky. I don't have any of the "crustys" that I would associate with an allergy. Typically, it takes 2-3 hours to "normalize" my appearance but I still carry dark circles and some puffiness throughout the day.
Is this, in your opinion, a normal reaction to the equipment I'm using? Is there something I can do to mitigate waking up with my eyes swollen semi-shut?
At 12:23pm on September 24, 2009, susan mccord said…
Dr. Park--there's an active discussion going on re: CPAP/safety/monitoring as it relates to medical procedures, i.e., colonoscopy, endoscopy, etc. People, including me, are worried about being sedated without CPAP and proper monitoring of apnea during and after sedation.
When you have time, would you mind weighing in on this? It's a big concern...

Thanks!! Susan McCord :-)
At 10:52am on September 22, 2009, susan mccord said…
FYI--I deleted that original website I put up on Discussion. No sense confusing people unnecessarily.
I'm interested in hearing what you think about the chin strap thing though, at your convenience. Looks like your line's hoppin' today!!

Susan McCord
 
 

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