*UPDATE* 1.5 years on ASV with NO RELIEF
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Re: *UPDATE* 1.5 years on ASV with NO RELIEF
OAI = 91.4
CAI = 2.6
HI = 38.1
CAI = 2.6
HI = 38.1
Re: *UPDATE* 1.5 years on ASV with NO RELIEF
So the original diagnosis was severe OSA with an AHI = 132.1Coolsideofthepillow wrote:OAI = 91.4
CAI = 2.6
HI = 38.1
Now can you fill us in on how you wound up on the ASV? The usual path to that machine involves some serious problems with CAs showing up---either before CPAP (not your case) or after CPAP was started. And the path usually looks something like this:
- Initiate CPAP; if the pressure gets as high as 15cm OR if serious numbers of CAs start to happen once CPAP is started, consider switching to a bi-level titration.
Continue to titrate for a bi-level (BiPAP) and most likely start the person on a BiPAP that does NOT have the ST mode.
If CAs continue on treatment OR if symptoms are not resolved in spite of good compliance, move on to a BiPAP ST or a BIPAP ASV titration in order to determine all the settings.
And---are you using the ASV in ASV mode or straight BiPAP mode?
It's critical to get this answered because you stated: "My pressure is set for the max the machine can take per the scrip, any lower apparently causes centrals."
And we need to understand just how many central apneas you are talking about when you were on lower pressures. Because the particular difficulties of dealing with high pressure AND significant pressure swings in ASV mode when the machine is triggering inhalations is a particularly difficult set of problems to deal with. But as JohnBFisher indicates, there are a number of experienced ASV users who will be able to help you conquer that problem.
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Machine: DreamStation BiPAP® Auto Machine |
Mask: Swift™ FX Nasal Pillow CPAP Mask with Headgear |
Additional Comments: PR System DreamStation and Humidifier. Max IPAP = 9, Min EPAP=4, Rise time setting = 3, minPS = 3, maxPS=5 |
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Re: *UPDATE* 1.5 years on ASV with NO RELIEF
I remember during treatment that when the cpap was applied the pressure went too high and caused centrals. I believe the centrals got worse until they got up to the max pressure which I believe reduced them. I am going to have to sit down with my report and analyze it. It's been so long I need a refresher.
Also I believe it is in auto. I will have to read up on how to check.
Also I believe it is in auto. I will have to read up on how to check.
Re: *UPDATE* 1.5 years on ASV with NO RELIEF
I suspected from the first page that you do not have central sleep apnea. ASV machine was throwing me.Coolsideofthepillow wrote:OAI = 91.4
CAI = 2.6
HI = 38.1
What is the manufacturer name and the exact model number of your machine?
While you are figuring that out you need to be making an appointment with an ENT to get an opinion on those "huge" tonsils. It seems so obvious.
I am not a medical professional and I have no medical training.
- JohnBFisher
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Re: *UPDATE* 1.5 years on ASV with NO RELIEF
While technically correct, this patient may indeed need an ASV unit. He also notes:Therapist wrote:I suspected from the first page that you do not have central sleep apnea. ASV machine was throwing me. ...Coolsideofthepillow wrote:... OAI = 91.4, CAI = 2.6, HI = 38.1 ...
This would indicate Complex Sleep Apnea which includes a reaction of increased central sleep apnea in response to the increasing pressure.Coolsideofthepillow wrote:... I remember during treatment that when the cpap was applied the pressure went too high and caused centrals. I believe the centrals got worse until they got up to the max pressure which I believe reduced them. ...
Coolsideofthepillow, I have to agree. You need to register your equipment so we can be certain we are providing appropriate responses. To learn more about how to register your equipment, see the following link:Therapist wrote:... What is the manufacturer name and the exact model number of your machine? ...
wiki/index.php/Registering_Equipment_in_User_Profile
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Mask: Quattro™ FX Full Face CPAP Mask with Headgear |
Additional Comments: User of xPAP therapy for over 20 yrs. Resmed & Respironics ASV units with EEP=9cm-14cm H2O; PSmin=4cm H2O; PSmax=15cm H2O; Max=25cm H2O |
"I get up. I walk. I fall down. Meanwhile, I keep dancing” from Rabbi Hillel
"I wish to paint in such a manner as if I were photographing dreams." from Zdzisław Beksiński
"I wish to paint in such a manner as if I were photographing dreams." from Zdzisław Beksiński
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Re: *UPDATE* 1.5 years on ASV with NO RELIEF
Just took a glance at my machine. Model # 1040716 respironics. What is this in Lyman's terms??? I looked under equipment but cannot find anything that matches this.
Re: *UPDATE* 1.5 years on ASV with NO RELIEF
Is this it?Coolsideofthepillow wrote:Just took a glance at my machine. Model # 1040716 respironics. What is this in Lyman's terms??? I looked under equipment but cannot find anything that matches this.
http://1800cpap.com/respironics-bipap-a ... ifier.aspx
If so..look in the equipment drop down list for Remstar BiPap AutoSV machine.
Its in the grouping that begins with Remstar.
The humidifier would be Remstar Heated Humidifier (assuming yours is heated but there is a choice for Passover which is water in tank but no heat)
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Machine: AirCurve™ 10 VAuto BiLevel Machine with HumidAir™ Heated Humidifier |
Additional Comments: Mask Bleep Eclipse https://bleepsleep.com/the-eclipse/ |
I may have to RISE but I refuse to SHINE.
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Re: *UPDATE* 1.5 years on ASV with NO RELIEF
So far the best night has been 3 hours. I fitted the mask at max pressure while lying down. Then I set ramp and fell asleep. 3 hours later I awoke and took the mask off,for no apparent reason.
- JohnBFisher
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- Joined: Wed Oct 14, 2009 6:33 am
Re: *UPDATE* 1.5 years on ASV with NO RELIEF
Good for you!! That's the way to get going with it.
It's not unusual for people to remove their mask during the night .. and be totally unaware of it. Some people use things like a chin strap .. or the Pad-A-Cheek anti-leak strap. They help reduce leaks and make it a little harder to remove the mask.
Perhaps others have some ideas on how to handle removal of the mask while asleep ??
It's not unusual for people to remove their mask during the night .. and be totally unaware of it. Some people use things like a chin strap .. or the Pad-A-Cheek anti-leak strap. They help reduce leaks and make it a little harder to remove the mask.
Perhaps others have some ideas on how to handle removal of the mask while asleep ??
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Mask: Quattro™ FX Full Face CPAP Mask with Headgear |
Additional Comments: User of xPAP therapy for over 20 yrs. Resmed & Respironics ASV units with EEP=9cm-14cm H2O; PSmin=4cm H2O; PSmax=15cm H2O; Max=25cm H2O |
"I get up. I walk. I fall down. Meanwhile, I keep dancing” from Rabbi Hillel
"I wish to paint in such a manner as if I were photographing dreams." from Zdzisław Beksiński
"I wish to paint in such a manner as if I were photographing dreams." from Zdzisław Beksiński
Re: *UPDATE* 1.5 years on ASV with NO RELIEF
Coolsideofthepillow,Coolsideofthepillow wrote:So far the best night has been 3 hours. I fitted the mask at max pressure while lying down. Then I set ramp and fell asleep. 3 hours later I awoke and took the mask off,for no apparent reason.
Just keep putting that mask on every night at the beginning of the night.
And if you wake up in the middle of the night and you find you've taken the mask off, just put it back on and then try to get back to sleep.
Perseverance is the name of the game: The more you sleep with the mask on the easier it will become to sleep with the mask on. With a bit of luck, eventually you'll get to where you're keeping it on all night.
_________________
Machine: DreamStation BiPAP® Auto Machine |
Mask: Swift™ FX Nasal Pillow CPAP Mask with Headgear |
Additional Comments: PR System DreamStation and Humidifier. Max IPAP = 9, Min EPAP=4, Rise time setting = 3, minPS = 3, maxPS=5 |
- JohnBFisher
- Posts: 3821
- Joined: Wed Oct 14, 2009 6:33 am
Re: *UPDATE* 1.5 years on ASV with NO RELIEF
Let's face it, having a mask strapped to your face each and every night is NOT normal. But you will get used to it. I've been doing this for the past 22 or 23 years. I hardly notice it .. unless I'm having a bad leak night.
Here's hoping you stick with it. You will feel ever so much better by getting the rest you need.
Here's hoping you stick with it. You will feel ever so much better by getting the rest you need.
_________________
Mask: Quattro™ FX Full Face CPAP Mask with Headgear |
Additional Comments: User of xPAP therapy for over 20 yrs. Resmed & Respironics ASV units with EEP=9cm-14cm H2O; PSmin=4cm H2O; PSmax=15cm H2O; Max=25cm H2O |
"I get up. I walk. I fall down. Meanwhile, I keep dancing” from Rabbi Hillel
"I wish to paint in such a manner as if I were photographing dreams." from Zdzisław Beksiński
"I wish to paint in such a manner as if I were photographing dreams." from Zdzisław Beksiński
- NachtWürger
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Re: *UPDATE* 1.5 years on ASV with NO RELIEF
JohnBFisher wrote:Let's face it, having a mask strapped to your face each and every night is NOT normal.
"The New Normal"
Re: *UPDATE* 1.5 years on ASV with NO RELIEF
The mask keeps mother nature from solving apnea the natural way. i.e. early death.JohnBFisher wrote:Let's face it, having a mask strapped to your face each and every night is NOT normal.
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Mask: Swift™ FX Nasal Pillow CPAP Mask with Headgear |
Humidifier: S9™ Series H5i™ Heated Humidifier with Climate Control |
Additional Comments: Also SleepyHead, PRS1 Auto, Respironics Auto M series, Legacy Auto, and Legacy Plus |
Please enter your equipment in your profile so we can help you.
Click here for information on the most common alternative to CPAP.
If it's midnight and a DME tells you it's dark outside, go and check for yourself.
Useful Links.
Click here for information on the most common alternative to CPAP.
If it's midnight and a DME tells you it's dark outside, go and check for yourself.
Useful Links.
- DavidCarolina
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- Joined: Wed Feb 23, 2011 6:23 pm
Re: *UPDATE* 1.5 years on ASV with NO RELIEF
to cool side, do you have the help and support you need to find the right path to healthy weight loss? You cant do it alone, you need a system of some kind without feeling like youre on some rigid system that doesnt work for you.
Also, have you considered supplemental oxygen? I have a concentrator that I use when i awaken agitated. Better than pills, but have those too, Klonapin as needed.
You sound as if you have the same things working against you--former athlete, got heavier, narrow airway, large tongue?, heredity, and possibly deviated septum and positional sleeeping issues. Its a complicated web, but thats why were' all here, to help each other.
Also, have you considered supplemental oxygen? I have a concentrator that I use when i awaken agitated. Better than pills, but have those too, Klonapin as needed.
You sound as if you have the same things working against you--former athlete, got heavier, narrow airway, large tongue?, heredity, and possibly deviated septum and positional sleeeping issues. Its a complicated web, but thats why were' all here, to help each other.
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- Joined: Tue Jun 08, 2010 9:07 am
Re: *UPDATE* 1.5 years on ASV with NO RELIEF
I'm back. Since the last reply I have switched over to a Whisp. I tape my mouth shut ms wear a breath right and while not perfect it's much much better.
A few questions:
Pugsy,
The machine you linked above is the machine I have. As far as data collection I guess I am stuck with the respironics software and a card reader?
Is it possible that this machines pressure could be going to high????
A few questions:
Pugsy,
The machine you linked above is the machine I have. As far as data collection I guess I am stuck with the respironics software and a card reader?
Is it possible that this machines pressure could be going to high????