How do I help my Father with CPAP
Re: How do I help my Father with CPAP
BTW, just for info, you can always tack on new thoughts/notes to older ones just above them rather than always starting new ones... can make it easier for us to follow (and realize there's been more), by editing the earlier notes rather than starting new.
Re: How do I help my Father with CPAP
I'm not sure I completely follow?
I actually rather like the chronological threads that read through time rather than being expected to jump back to an original post to read updates? If that is not what you meant, then sorry please elaborate with an example.
Anyway, Today's news, we had a virtual visit with the Sleep Med Practitioner and she finally agreed that the CPAP was not working for him and he is doing everything he is supposed to be doing, the machine just can't do what he needs. She put in the order for the new titration study for an ASV machine even though he hasn't had the heart echo yet. This is good news since the heart echo isn't scheduled till November and he has had nights where the AHI was over 67.
_________________
Machine: Aircurve 11 asv |
Mask: Fisher & Paykel Vitera Full Face Mask with Headgear (S, M, or L Cushion) |
Additional Comments: Initial study 36 OA, 53 MA, 90 Central Apnea. AH! 34.1 |
Daughter Posting on behalf of my 81 year old Father with Parkinson's and Dementia (Dementia, I believe was brought on by the sleep disorder.)
Re: How do I help my Father with CPAP
It's about friggin time that someone would read the writing on the wall. It was in big neon letters.
He still needs to try to sort out the leak situation though. The ASV pressures needed to deal with the central apneas aren't going to be doing the leak situation any favors.
But....even with leaks he will get better therapy with the ASV than he is getting now without leaks.
Good luck and God Bless you for trying to do your best to care for your dad.
_________________
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.
Re: How do I help my Father with CPAP
I agree that he still has nights where the leaking gets out of control (I mean when you start pulling at the mask and struggling to take it off, it leaks,) However, he is also having nights like this. Though I realize that the minimal leak is because there is almost no pressure at this point.
I did finally get to give the sleep med practitioner the sleep hq link to his data as well as some screen shots from oscar. I now get the impression she has never seen sleep hq or oscar data from a resmed machine. The best she sees is the compliance report from the machine, not the minute by minute data. She has probably only seen minute by minute data from in lab sleep studies.
I did finally get to give the sleep med practitioner the sleep hq link to his data as well as some screen shots from oscar. I now get the impression she has never seen sleep hq or oscar data from a resmed machine. The best she sees is the compliance report from the machine, not the minute by minute data. She has probably only seen minute by minute data from in lab sleep studies.
_________________
Machine: Aircurve 11 asv |
Mask: Fisher & Paykel Vitera Full Face Mask with Headgear (S, M, or L Cushion) |
Additional Comments: Initial study 36 OA, 53 MA, 90 Central Apnea. AH! 34.1 |
Daughter Posting on behalf of my 81 year old Father with Parkinson's and Dementia (Dementia, I believe was brought on by the sleep disorder.)
Re: How do I help my Father with CPAP
Anyone Got any ASV Advise for us? Dad really needs a machine that can actively monitor his breathing and deliver a real breath when he has centrals. Also he seems to have cheyne stokes respiration several nights out of the week and there are even huge stretches that look like it to me but the machine isn't flagging all of it.
Anyway, we finally got the Sleep Dr to put in the order for a titration study for ASV since it is painfully obvious that the cpap isn't working and they already ruled out bi-level during the first titration study.
So is there anyone out there who can share any tips/tricks about how the ASV feels different or things to keep in mind or to know about ASV therapy vs regular cpap? We had a lot of issues with leaking at higher pressures on cpap, is that going to be a problem with the ASV? Or is it likely to just kinda blow by since it doesn't keep up the constant high pressure after delivering the breath?
Anyway, we finally got the Sleep Dr to put in the order for a titration study for ASV since it is painfully obvious that the cpap isn't working and they already ruled out bi-level during the first titration study.
So is there anyone out there who can share any tips/tricks about how the ASV feels different or things to keep in mind or to know about ASV therapy vs regular cpap? We had a lot of issues with leaking at higher pressures on cpap, is that going to be a problem with the ASV? Or is it likely to just kinda blow by since it doesn't keep up the constant high pressure after delivering the breath?
_________________
Machine: Aircurve 11 asv |
Mask: Fisher & Paykel Vitera Full Face Mask with Headgear (S, M, or L Cushion) |
Additional Comments: Initial study 36 OA, 53 MA, 90 Central Apnea. AH! 34.1 |
Daughter Posting on behalf of my 81 year old Father with Parkinson's and Dementia (Dementia, I believe was brought on by the sleep disorder.)
Re: How do I help my Father with CPAP
We really won't know much until we see what happens when he has the centrals and the machine kicks in with the rapid rise in PS to force breathing. One or two occasionally probably not going to be high levels of pressure but if he ends up having a LOT of centrals back to back then the pressure may stay elevated for a longer period of time.....or at least seem to stay elevated for longer durations.
Also depends on what baseline EPAP pressure is is going to be needed to deal with the obstructive stuff going on.
Also will depend on which mode is used...regular ASV mode or auto ASV mode.
With regular ASV mode the EPAP is fixed but PS auto adjust for the central apneas.
With auto ASV mode the EPAP will auto adjust as needed (within parameters set) and EPAP going up will make IPAP going up (even if PS doesn't go up) and that could maybe make for a prolonged period of time with EPAP/IPAP pressures a lot higher.
Two problems....central apnea and obstructive apnea and each has a different way it needs to be dealt with.
I have some experience with both ASV modes but I did it just to be doing it and not because I had a problem with centrals so not really a viable comparison to rely on. Meaning I tried ASV just to be trying to see what it was like and not because I need ASV. I also never used a full face mask with it to see what happens with leaking.
Contrary to what some people will say.....ASV doesn't mean you just HAVE to use a full face mask (old wives tale).
_________________
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.
- ChicagoGranny
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Re: How do I help my Father with CPAP
What you are doing is fine. Julie is a little bit duh at times.
"It's not the number of breaths we take, it's the number of moments that take our breath away."
Cuando cuentes cuentos, cuenta cuántas cuentos cuentas.
Cuando cuentes cuentos, cuenta cuántas cuentos cuentas.
Re: How do I help my Father with CPAP
I agree. What you are doing is fine.ChicagoGranny wrote: ↑Sat Sep 14, 2024 3:04 pmWhat you are doing is fine. [...]
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Mask: AirFit™ P10 Nasal Pillow CPAP Mask with Headgear |
Additional Comments: Machine: Resmed AirSense10 for Her with Climateline heated hose ; alternating masks. |
And now here is my secret, a very simple secret; it is only with the heart that one can see rightly, what is essential is invisible to the eye.
Antoine de Saint-Exupery
Good advice is compromised by missing data
Forum member Dog Slobber Nov. 2023
Antoine de Saint-Exupery
Good advice is compromised by missing data
Forum member Dog Slobber Nov. 2023
Re: How do I help my Father with CPAP
So today I'm trying to set up dad's old laptop computer with oscar and everything to monitor and check stuff so we can take it with us if we decide we need to go to the DME office since I want to show them what looks like the machine may be malfunctioning.
I don't actually want to have them replace this one because it obviously (even when working properly) can't actually help dad with his problems.
But I think I should also set it up with the bluestacks App Player so that I can put the pulse ox monitor on it since Dad's phone doesn't make it through the night keeping the dashboard open to get the pulse ox alerts since even plugged in, apparently the battery doesn't charge fast enough to keep from killing it in less than 11 hours.
Is it worth setting up with the sleep hq subscription to be able to import the pulse ox there? Or do I just continue with Oscar and doing that manually. It would be nice to be able to share the pulse ox stuff with the Dr easily along side the Cpap but I didn't think to test the pulse Ox with it until after the sleep hq pro trial ran out. We really don't need another monthly subscription.
Ok, in the process of setting up a computer just for sleep, pap and o2 monitoring. What are the primary things I should make sure to include?
I will set up bluestacks so I can include Android apps on it.
I will put;
Oscar
Link to Sleep HQ account
Camera app
ViHealth app
Any others?
I don't actually want to have them replace this one because it obviously (even when working properly) can't actually help dad with his problems.
But I think I should also set it up with the bluestacks App Player so that I can put the pulse ox monitor on it since Dad's phone doesn't make it through the night keeping the dashboard open to get the pulse ox alerts since even plugged in, apparently the battery doesn't charge fast enough to keep from killing it in less than 11 hours.
Is it worth setting up with the sleep hq subscription to be able to import the pulse ox there? Or do I just continue with Oscar and doing that manually. It would be nice to be able to share the pulse ox stuff with the Dr easily along side the Cpap but I didn't think to test the pulse Ox with it until after the sleep hq pro trial ran out. We really don't need another monthly subscription.
Ok, in the process of setting up a computer just for sleep, pap and o2 monitoring. What are the primary things I should make sure to include?
I will set up bluestacks so I can include Android apps on it.
I will put;
Oscar
Link to Sleep HQ account
Camera app
ViHealth app
Any others?
_________________
Machine: Aircurve 11 asv |
Mask: Fisher & Paykel Vitera Full Face Mask with Headgear (S, M, or L Cushion) |
Additional Comments: Initial study 36 OA, 53 MA, 90 Central Apnea. AH! 34.1 |
Daughter Posting on behalf of my 81 year old Father with Parkinson's and Dementia (Dementia, I believe was brought on by the sleep disorder.)
Re: How do I help my Father with CPAP
Not sure If I should start a new thread now or not.
We did finally get in for a sleep study (they finally relented and went ahead and ordered the study before getting the cardio echo done.)
Unfortunately, at the sleep study he really didn't sleep. He kept waking up. Probably a combination of weather since that was the night Helene was passing us and he didn't get his rivastigmine patch changed that evening which seems to mess up his sleep a bit too.
Since the sleep study while waiting to see what was going to happen, I finally gave up on making him use the CPAP since about all it was doing was making it hard for him to sleep. We have just been making him sleep on his side as much as possible and he has been doing fairly well for the past few weeks. Of course we don't have any real good way to monitor his sleep/breathing when he isn't wearing the machine other than the little O2 ring.
But even without getting a good titration, they went ahead and prescribed the ASV and we got it Monday.
But Since they didn't really get a titration, They basically just guessed on the settings.
He hasn't really been able to sleep with it much at all, I put the smaller mask to my face with it on and it is definitely way more aggressive than the cpap was.
Anyway, The Device is
the ResMed AirCurve Bi-Level AutoSV Advance E0471
the settings they entered are
Min EPAP 4
EPAP Max 8
PS Min 5
PS Max 10
So please some one help me understand the pressures, Does this mean he is feeling min pressure of 4 on exhale and then 5 on inhale for minimums? Or is it more like 4 on exhale and 9 on inhale for minimum?
He is complaining that it is exhausting him making him inhale too much.
What are the range of settings allowable on the ASV? Since we are working to make him sleep on his side, I don't really think we need much pressure support for the obstructive apnea. At least until he gets comfortable with the machine and isn't afraid of it anyway. If it is possible to have it basically run at a constant low pressure and monitor him and Only up the pressure if it detect a central apnea or other breathing instability. Even if it is basically doing nothing but monitoring with a gentle flow of air so we can get some readings for a few days.
We did finally get in for a sleep study (they finally relented and went ahead and ordered the study before getting the cardio echo done.)
Unfortunately, at the sleep study he really didn't sleep. He kept waking up. Probably a combination of weather since that was the night Helene was passing us and he didn't get his rivastigmine patch changed that evening which seems to mess up his sleep a bit too.
Since the sleep study while waiting to see what was going to happen, I finally gave up on making him use the CPAP since about all it was doing was making it hard for him to sleep. We have just been making him sleep on his side as much as possible and he has been doing fairly well for the past few weeks. Of course we don't have any real good way to monitor his sleep/breathing when he isn't wearing the machine other than the little O2 ring.
But even without getting a good titration, they went ahead and prescribed the ASV and we got it Monday.
But Since they didn't really get a titration, They basically just guessed on the settings.
He hasn't really been able to sleep with it much at all, I put the smaller mask to my face with it on and it is definitely way more aggressive than the cpap was.
Anyway, The Device is
the ResMed AirCurve Bi-Level AutoSV Advance E0471
the settings they entered are
Min EPAP 4
EPAP Max 8
PS Min 5
PS Max 10
So please some one help me understand the pressures, Does this mean he is feeling min pressure of 4 on exhale and then 5 on inhale for minimums? Or is it more like 4 on exhale and 9 on inhale for minimum?
He is complaining that it is exhausting him making him inhale too much.
What are the range of settings allowable on the ASV? Since we are working to make him sleep on his side, I don't really think we need much pressure support for the obstructive apnea. At least until he gets comfortable with the machine and isn't afraid of it anyway. If it is possible to have it basically run at a constant low pressure and monitor him and Only up the pressure if it detect a central apnea or other breathing instability. Even if it is basically doing nothing but monitoring with a gentle flow of air so we can get some readings for a few days.
_________________
Machine: Aircurve 11 asv |
Mask: Fisher & Paykel Vitera Full Face Mask with Headgear (S, M, or L Cushion) |
Additional Comments: Initial study 36 OA, 53 MA, 90 Central Apnea. AH! 34.1 |
Daughter Posting on behalf of my 81 year old Father with Parkinson's and Dementia (Dementia, I believe was brought on by the sleep disorder.)
Re: How do I help my Father with CPAP
This is what he is initially going to feel.
When you have PS in use then you have to add the PS to your EPAP to get IPAP (at least the starting EPAP/IPAP).
And yes....with the increase in PS to 5 he is going to feel the difference.
With current settings the PS can increase to 10 so that would add 10 cm more to that EPAP of 4....so that's an even bigger jump but the idea is when the machine does that jump it is in response to a central apnea because that's how you jump start breathing....give it a big rapid burst.
I am a bit concerned about the 10 PS limit though. It might not be enough to adequately deal with the centrals.
10 cm is generally considered a minimum amount of PS needed to force breathing when central apneas are present.
The machine won't do it all the time...just when it thinks centrals are happening.
BUT that 5 PS is going to be there all the time and a consideration might be to have minimum PS set to 3 (more along the lines of what EPR does and he is used to). Might be easier adjustment for your dad.
_________________
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.
Re: How do I help my Father with CPAP
So I think the goal should be (at least for this weekend) get a very gentle setting so that he can actually wear it and sleep and we can collect some breathing data. The way it is set right now, we are lucky to keep it on him for 3 hours and I don't think he is actually sleeping much at all with it on.
Once we get through the weekend, we look at the data and start adjusting the levels to handle the events. I'm hoping the sleep med practitioner is amenable to that Idea.
I realize that a certain amount of pressure may be needed to really do anything about a central apnea, however, I need to get a setting on him that will let him actually wear it AND sleep before it will have any chance of doing anything for a central apnea.
My question is, do we have to have so much pressure support all the time? Like is a min ipap of 5 required? What does the machine look at to decide what ipap and epap level to use?
Is the machine smart enough to tell when someone is sleeping? The Cpap machine had an auto ramp setting that I think was supposed to judge when they had fallen to sleep before going into the regular settings.
So anyway I just spoke to them about the settings and they seem ok with me changing it to epap 4-4 and PS 0-5 (yes I realize that this setting probably won't work for jump starting from a central event but it will maybe let me keep the mask on him for a night so I can get some data to look at and try to adjust from there.)
Once we get through the weekend, we look at the data and start adjusting the levels to handle the events. I'm hoping the sleep med practitioner is amenable to that Idea.
I realize that a certain amount of pressure may be needed to really do anything about a central apnea, however, I need to get a setting on him that will let him actually wear it AND sleep before it will have any chance of doing anything for a central apnea.
My question is, do we have to have so much pressure support all the time? Like is a min ipap of 5 required? What does the machine look at to decide what ipap and epap level to use?
Is the machine smart enough to tell when someone is sleeping? The Cpap machine had an auto ramp setting that I think was supposed to judge when they had fallen to sleep before going into the regular settings.
So anyway I just spoke to them about the settings and they seem ok with me changing it to epap 4-4 and PS 0-5 (yes I realize that this setting probably won't work for jump starting from a central event but it will maybe let me keep the mask on him for a night so I can get some data to look at and try to adjust from there.)
_________________
Machine: Aircurve 11 asv |
Mask: Fisher & Paykel Vitera Full Face Mask with Headgear (S, M, or L Cushion) |
Additional Comments: Initial study 36 OA, 53 MA, 90 Central Apnea. AH! 34.1 |
Daughter Posting on behalf of my 81 year old Father with Parkinson's and Dementia (Dementia, I believe was brought on by the sleep disorder.)
Re: How do I help my Father with CPAP
Not really.
That Auto Ramp thing is ONLY for ramp and it's an educated guess at best.
So while I do understand your thoughts on starting more gently with the pressure and have the idea to look at the data later and hopefully fine tune things a bit you have to realize that by allowing more apneas to happen because of sub optimal settings you run the risk of those apneas messing with his sleep and causing wake ups and the "data you wanted to get" might not be all that helpful if he doesn't sleep.TCLynx wrote: ↑Thu Oct 24, 2024 1:17 pmSo anyway I just spoke to them about the settings and they seem ok with me changing it to epap 4-4 and PS 0-5 (yes I realize that this setting probably won't work for jump starting from a central event but it will maybe let me keep the mask on him for a night so I can get some data to look at and try to adjust from there.)
_________________
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.