RERA Questions

General Discussion on any topic relating to CPAP and/or Sleep Apnea.
augustsilverbear
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RERA Questions

Post by augustsilverbear » Mon Mar 14, 2016 8:45 pm

I have been experiencing numerous RERAs for each of the last ten nights of therapy. Please provide some insight into these events. I have read the definition, but do not fully understand.
What are RERAs?
What impact do they have on sleep quality?
What health risks do they indicate?
What can be done to reduce their frequency?
Should I raise these issues with the sleep doc in my upcoming review appointment?

I have posted a screen shot of a cluster of RERAs from last night for reference. I left the pie chart to demonstrate the percentage of events that are RERAs.
Thanks for any help you can provide.
augustsilverbear


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Julie
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Re: RERA Questions

Post by Julie » Mon Mar 14, 2016 9:07 pm

You could Google "Respiratory Effort Related Arousals", or look it up under the lightbulb at the top of the main pg here... I don't know enough about them to otherwise advise you, but I also believe they are not indications of a serious problem.

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Re: RERA Questions

Post by lilly747 » Mon Mar 14, 2016 9:48 pm

It looks like a raise in min & max pressure would help.Looking at your data, I would say you are not resting much: too many RERA's. Hypo's, etc. Do you know how to raise your pressure??

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Re: RERA Questions

Post by Julie » Tue Mar 15, 2016 4:31 am

His pressure's already fairly high and I'd want to investigate further before raising it again.

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Re: RERA Questions

Post by LSAT » Tue Mar 15, 2016 8:05 am

Julie wrote:His pressure's already fairly high and I'd want to investigate further before raising it again.
Max 12 is not high enough...Should increase to 15 and see what happens after a few days. He is maxing out for most of the period shown.

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Re: RERA Questions

Post by augustsilverbear » Tue Mar 15, 2016 10:31 am

Thanks for your responses.

I have read about RERAs. Definition is fairly cryptic.
Respiratory Event Related Arousal... a sequence of breaths characterized by increasing respiratory effort leading to an arousal from sleep, but which does not meet criteria for an apnea or hypopnea.”

RERA Detection in the Respironics System One data..Respiratory effort-related arousal..defined as an arousal from sleep that follows a 10 second or longer sequence of breaths that are characterized by increasing respiratory effort, but which does not meet criteria for an apenea or hypopnea. Snoring, though usually associated with this condition need not be present. The RERA algorithm monitors for a sequence of breaths that exhibit both a subtle reduction in airflow and progressive flow limitation. If this breath sequence is terminated by a sudden increase in airflow along with the absence of flow limitation, and the event does not meet the conditions for an apnea or hypopnea, a RERA is indicated.


Other definitions I have read characterize RERAs as indications of events of increasing respiratory effort without an oxygen desaturation. So they are not like an obstructive apnea, nor like a hypopnea, but do cause arousals, change sleep levels, and sometimes cause awakenings.

My sleep is highly fragmented, due to having a RERA thirty+ times per night. Some of my arousals in conjunction with a RERA do result in an awakening. During my sleep study I had NO obstructive apneas, but did have 26 hypopneas. My recent pressure elevation (ordered by sleep doc) has lowered AHI from average of low teens to now around average of 4. Have only been at 8-12 pressure level since March 11; so a self initiated pressure change at this duration of a recent pressure increase would not be warranted. And, No, I do not know how to increase the pressure on my DreamStation device. I have a review appointment with sleep doc on March 23.

Can anyone advise if RERAs are indicative of some underlying condition about which I should be concerned?
Since the only suggested remedy was crank up the pressure; I have to ask how would that address the issue? By its definition, these events are not associated with a narrowing, nor an occlusion, of the airway. So what would more pressure do for an irregular "subtle reduction in airflow along with the absence of flow limitation?"

I believe the pressure increase prescribed for me on March 11 DID markedly lower my AHI; however, I am not experiencing a corresponding level of more restful and restorative sleep. My numbers of apneas is lower, but some are continuing to occur. My time in apnea has been around 11 minutes for a 7+ hours of sleep experience. Hypopnea are still higher than desired, and likely would be reduced further by more pressure. I will discuss pressure levels with the sleep doc next week, but believe he is likely to say give the new pressure level some time to work before he will change it again, given an 8 point drop overnight in AHI when the last increase was instituted.

I was just hopeful someone could answer the questions in my above post, and give me some insight into how I might achieve more restful and less fragmented sleep. Thanks for any assistance you can provide.
augustsilverbear

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Re: RERA Questions

Post by Julie » Tue Mar 15, 2016 10:46 am

It is not known to any useful degree what causes RERAs, but they do not seem to be associated with any particularly serious condition apart from the general ones surrounding apnea. I wouldn't worry so much about the cause at this time as just trying to lower the occurrences.

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Re: RERA Questions

Post by hpm08161947 » Tue Mar 15, 2016 10:48 am

I was just hopeful someone could answer the questions in my above post, and give me some insight into how I might achieve more restful and less fragmented sleep. Thanks for any assistance you can provide.
augustsilverbear
I can not speak to your particular situation, but I can tell you that my wife also has many RERAs and has been told by her physician that it is not related to her sleep apnea, but is directly related to her COPD. Hope that helps.

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Re: RERA Questions

Post by lilly747 » Tue Mar 15, 2016 12:12 pm

augustsilverbear wrote:I believe the pressure increase prescribed for me on March 11 DID markedly lower my AHI; however, I am not experiencing a corresponding level of more restful and restorative sleep. My numbers of apneas is lower, but some are continuing to occur. My time in apnea has been around 11 minutes for a 7+ hours of sleep experience. Hypopnea are still higher than desired, and likely would be reduced further by more pressure. I will discuss pressure levels with the sleep doc next week, but believe he is likely to say give the new pressure level some time to work before he will change it again, given an 8 point drop overnight in AHI when the last increase was instituted.

I was just hopeful someone could answer the questions in my above post, and give me some insight into how I might achieve more restful and less fragmented sleep. Thanks for any assistance you can provide.
augustsilverbear
I know it is flustrating when things don't go the way we hope or expect. I am sorry if I missed that your Pressure was change on the !!th, but I did not see that in your post. I suggest the Pressure change because of your FL and hypopneas and OA's and the fact your CA's look OK. Usually you up EPAP for OA's and up IPAP for FL and Hypopneas. I was hoping that upping your pressure and thus lowering the Hypopneas and FL and OA's would help you rest better thus MAYBE helping with the RERAs. Yes talk to your DR> Also PM some of our more experienced members. If you need a list of who they are you can PM me, or see if they come along. Sorry I was not more helpful

EDIT for spelling

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Re: RERA Questions

Post by robysue » Tue Mar 15, 2016 9:21 pm

augustsilverbear wrote:Thanks for your responses.

I have read about RERAs. Definition is fairly cryptic.
Respiratory Event Related Arousal... a sequence of breaths characterized by increasing respiratory effort leading to an arousal from sleep, but which does not meet criteria for an apnea or hypopnea.”

RERA Detection in the Respironics System One data..Respiratory effort-related arousal..defined as an arousal from sleep that follows a 10 second or longer sequence of breaths that are characterized by increasing respiratory effort, but which does not meet criteria for an apenea or hypopnea. Snoring, though usually associated with this condition need not be present. The RERA algorithm monitors for a sequence of breaths that exhibit both a subtle reduction in airflow and progressive flow limitation. If this breath sequence is terminated by a sudden increase in airflow along with the absence of flow limitation, and the event does not meet the conditions for an apnea or hypopnea, a RERA is indicated.


Other definitions I have read characterize RERAs as indications of events of increasing respiratory effort without an oxygen desaturation. So they are not like an obstructive apnea, nor like a hypopnea, but do cause arousals, change sleep levels, and sometimes cause awakenings.
Informally, it's easiest to think of RERAs as part of a continuum of sleep disordered breathing-type events. In a sleep lab, a RERA is scored under very particular circumstances, but it boils down to the airway is slightly compromised (so there is increasing respiratory effort), but the person has an EEG-detectable arousal and a return to normal sleep breathing before the breathing has deteriorated to the point where a hypopnea or an obstructive apnea can be scored.

In a RERA, the arousal may occur before the 10 seconds needed to score a hypopnea have passed. Or it could be that the reduction in airflow is less than the 30-50% needed to score a hypopnea. (How much the airflow must decrease depends on which rules are used to score the hypopnea.) Or both.

So it's reasonable to think of a RERA as a "hypopnea wannabe"---you arouse (or wake up) before the breathing deteriorates enough to be a hypopnea, but the breathing has started to deteriorate before you arouse just enough to get the airway fully opened back up.
My sleep is highly fragmented, due to having a RERA thirty+ times per night. Some of my arousals in conjunction with a RERA do result in an awakening. During my sleep study I had NO obstructive apneas, but did have 26 hypopneas.
Are we talking about RERAs scored on your PR DreamStation?
My recent pressure elevation (ordered by sleep doc) has lowered AHI from average of low teens to now around average of 4. Have only been at 8-12 pressure level since March 11; so a self initiated pressure change at this duration of a recent pressure increase would not be warranted. And, No, I do not know how to increase the pressure on my DreamStation device. I have a review appointment with sleep doc on March 23.
Personally, I can see why you want to wait for the review appointment. Yes, there are a lot of folks on this board who advocate self-treatment and changing your own pressures. But there is a lot to be said when you are new PAPer to be more patient and work with the doc when the doc is willing to work with you. If your pressures were changed on March 11 and you have an appointment on March 23 to review that data, it makes a lot of sense to just be patient until that March 23 meeting.

Can anyone advise if RERAs are indicative of some underlying condition about which I should be concerned?
Again, are you talking about RERAs scored by your PR DreamStation?

If so, my best guess is that the RERAs are just part of your overall sleep apnea. As some pressure is applied by the machine, the potential apneas often turn into hypopneas and the potential hypopneas turn into FL and RERAs. As more pressure is applied, the RERAs and FLs should start to disappear. In a "good" titration, the goal is to find a pressure level that is high enough to prevent the OAs, Hs, FLs, and RERAs, but low enough to not cause the patient any difficulty. (Too much pressure can lead to spontaneous arousals, problems with aerophagia, and in rare cases problems with pressure-induced centrals.)

Since the only suggested remedy was crank up the pressure; I have to ask how would that address the issue? By its definition, these events are not associated with a narrowing, nor an occlusion, of the airway. So what would more pressure do for an irregular "subtle reduction in airflow along with the absence of flow limitation?"
No, you've got a misunderstanding: RERAs are caused by a very subtle narrowing of the airway. The narrowing is not enough to cause the significant reduction in airflow that is required to score a hypopnea, but the narrowing is enough to cause additional respiratory effort: It takes more work to breathe during the flow limitation that precedes the arousal in a RERA. The arousal is caused by the increased respiratory effort, which is caused by the subtly narrowed airway.

There are some descriptions that describe the kind of increasing respiratory effort associated with a RERA as trying to breathe through a straw: The narrower the straw, the more you have to work on drawing the air in through the straw---even though the straw is not so narrow that you can't actually move enough air through the straw to stay properly oxygenated.

Additional pressure addresses the issue of RERAs by making it more difficult for the airway to become subtly compromised and slightly narrowed.
I believe the pressure increase prescribed for me on March 11 DID markedly lower my AHI; however, I am not experiencing a corresponding level of more restful and restorative sleep. My numbers of apneas is lower, but some are continuing to occur. My time in apnea has been around 11 minutes for a 7+ hours of sleep experience. Hypopnea are still higher than desired, and likely would be reduced further by more pressure. I will discuss pressure levels with the sleep doc next week, but believe he is likely to say give the new pressure level some time to work before he will change it again, given an 8 point drop overnight in AHI when the last increase was instituted.
First: For most CPAPers, the overnight AHI is seldom a 0.0 and there's not much point in chasing a 0.0 just for the sake of having a 0.0 AHI. The point of CPAP is to get the AHI low enough to allow you get normal, restful and restorative sleep. Which you're not yet getting. But CPAP is a process. It may take a few weeks to really settle in and learn how to sleep well with the machine. There's a lot of sensory stuff coming from the machine that we have to grow accustomed in order to sleep well with the machine. So yes, it is quite likely that your doc may suggest keeping the pressures at the new setting for a while longer when you talk to him/her on the 23rd.

Next, it's not clear to me that the total time in apnea will be something the doc will care about. The Encore software the doc is likely to use to analyze data from your machine does not compute that particular statistic. On the other hand, I don't want to suggest that it's not important at all. Its significance, however, may be more dependent on whether you are known to have serious O2 desats during apneas.
I was just hopeful someone could answer the questions in my above post, and give me some insight into how I might achieve more restful and less fragmented sleep. Thanks for any assistance you can provide.
augustsilverbear
1) Since you want to wait until you talk to the doc before possibly increasing the pressure, it's important to be a bit patient. And try hard to separate "how I feel?" each day from "how bad does the data look?" What I mean by this is don't automatically expect that you're going to feel awful if your RERA index is up a bit one day vs. another.

2) Prudent, watchful waiting is not a bad idea right now. Give yourself the time to really adjust to these settings before your appointment with the sleep doc.

3) Work on making sure that non-OSA, non-RERA causes of fragmented sleep are addressed. If you are waking fully awake several times each night for any reason, that can cause the sleep to feel less than restful and restorative. So work on encouraging high quality sleep through good sleep hygiene practices.

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Re: RERA Questions

Post by augustsilverbear » Wed Mar 16, 2016 4:00 pm

Thank you lilly747,
I did not wish to imply that your suggestion was not helpful. Forgive me if it appeared so. I appreciate all the responses I have gotten
to these concerns. Perhaps a pressure increase is the answer; I will discuss that with the sleep doc next week.

Thanks robysue, for again providing a detailed explanation to the issues I have raised. Yes, all the RERAs of which I speak have been reflected in data from the DreamStation over the past ten days or so. Numbers of RERAs consistently in the 30 per night range. During my sleep study there were 0 RERAs in both diagnostic and therapeutic phases. There was reported 22 Respiratory Disturbance Events (hypopneas) during the diagnostic phase of the test, and there was only one in the therapeutic phase, a central apnea. Oxygen saturation level during diagnostic portion of sleep study was:(REM) Mean:90.3%; Min:85%; Max: 96%; NREM Mean: 93.6%; Min:89%; Max: 96%. Oxygen stats for therapeutic portion were: (combined REN/NREM): Mean: 95%; Min:92%; Max:98%. So there was a showing of a therapeutic benefit from CPAP during the sleep study.

I have been somewhat bewildered by the increase in the DreamStation reporting of nightly events since starting home sleep therapy. (See previous post for which you provided explanation and guidance.) I am going to take your advice to quit obsessing (my terms, not yours) and try to concentrate more on perceived sleep improvement than MY perception of negative daily data. I will ask questions of the sleep doc, and inquire about an additional pressure increase when warranted after what is judged to be a sufficient observation period of data at this pressure level. I will also seek advice on lowering leak rates. (See previous post for which you gave additional insight and explanation.) It is noted that the leak rate during sleep study was reported to be in the 50-60 L/Min range for the Pico mask I wore. I am averaging about that Total Leak rate in the Amara View I an now wearing.

I am impatient by nature, and somewhat obsessive over the details; neither of which promote healthy response to therapy. I have recently improved my running regimen, as Spring has graced us with warmer temps. I am trying to commence sleep at the same time nightly, and rise after 7+ hours of therapy.

Thanks again for all your gracious explanations and suggestions.
augustsilverbear

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Re: RERA Questions

Post by PEF » Wed Mar 16, 2016 6:36 pm

I believe that RERA's are sometimes associated with a condition that I believe I have called UARS, Upper Airway Resistance Syndrome. The expert on this is a guy named Dr. Steven Park. His book is titled "Sleep Interrupted".

Robysue is very knowledgable and her explanation of RERA's is exactly right. Dr. Park thinks that people with UARS don't usually stop breathing when events occur. Their brain detects a flow limitation (caused by airway obstruction) and in response, tries to suck in the breath by building pressure in the chest. There is even a specialized sleep test for this condition where a catheter is placed in the person'r esophagus to test for pressure buildup and then release. UARS can often cause stomach contents to be sucked up into the respiratory system, causing LPR (a form of GERD). I began CPAP after years of waking up with sore throats after nighttime events that I could almost predict because they always happened during my deep sleep. The soreness in my throat, tingling ears, and taste of acid would wake me up and I would have to get up to get rid of my symptoms. CPAP therapy has kept these symptoms at bay, among other issues. However, I don't get AHI's at all, never did.

I believe and so does Dr. Park, that these events are a health hazard.

What I do not know and would be happy if someone could tell me, is how high the pressure should be to stop these events. I had to begin with low pressure, 4 to 6 because I had so many mask problems. If I use pillows, I really should tape my mouth or use a cervical collar. I am gradually raising the pressure. I know that CPAP is recommended for people with UARS, but I have never found anything about details of therapy.

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Re: RERA Questions

Post by robysue » Wed Mar 16, 2016 8:42 pm

PEF wrote:I
What I do not know and would be happy if someone could tell me, is how high the pressure should be to stop these events (RERAs).
The pressure to prevent RERAs varies from UARS patient to UARS patient just like the pressure needed to prevent the hyponeas and apneas in patients with OSA.
I had to begin with low pressure, ... I am gradually raising the pressure. I know that CPAP is recommended for people with UARS, but I have never found anything about details of therapy.
The usual recommendation by the sleep medicine community would be to do a titration study in a lab that is equipped to detect RERAs. In a sleep lab, the pressure would be titrated until a pressure is found where the RERAs are no longer happening. There's no real way to predict how much pressure a particular UARS patient might need.

Since it appears that you are self treating and attempting to self titrate, there are a few things to keep in mind.

1) The Resmed S9 AutoSet for Her machine you are using has an "Auto for Her" mode. I believe that in that mode (and only that mode) the machine will record RERAs. I don't know anything about the algorithm that Resmed uses for detecting RERAs. However, it has to be an approximation algorithm since there is no way the S9 AutoSet for Her can tell whether you've had a real arousal. The RERA detection algorith has to be based on looking at characteristics in the flow rate data that are commonly seen in RERAs identified in a sleep lab with lots of other channels of data. Nonetheless, approximate RERA data is better than no RERA data at all. So I would strongly suggest that you run your machine in the Auto for Her mode.

2) You could start by running the machine in Auto For Her mode (so you see the RERA data) with the pressure range set pretty wide. After a couple of weeks of gathering data, you can see what the 95% pressure level is. You should also look at how many RERAs are scored each night.

3) If you want to tighten the pressure range, once you know what the 95% pressure level is, you can set the min pressure 1-2 cm below the 95% level and the max pressure 1-2 cm above the 95%. And wath the data. As long as there are not a lot of RERAs and FL being scored, you can pretty much assume that the pressure is high enough to prevent most of the RERAs from happening.
4 to 6 because I had so many mask problems. If I use pillows, I really should tape my mouth or use a cervical collar.
If you are having a lot of serious leaks at 4-6cm of pressure, you're going to have to deal with the leaks before you can reasonably do a self titration.

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Re: RERA Questions

Post by PEF » Wed Mar 16, 2016 9:01 pm

Thanks so much, Robysue, for the great information! Yes, it all makes sense and I will get started.

I am only doing self help because we are living in Panama, retired here about 10 years ago. But a US doctor I saw on a visit back to the US gave me my prescription. He recommended an APAP because he did know that much about therapy for UARS. There is one place in Panama City that does work with CPAP but I wouldn't trust them. So I am on my own unless I go back to the US where I can use my Medicare. Maybe someday. It is funny because I also have an insurance plan here, but they will not cover CPAP. They probably have no idea what it is.

Thanks again!

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Re: RERA Questions

Post by PEF » Sat Mar 19, 2016 12:47 pm

I am not trying to hijack someone else's thread, but wanted to pick this up because I have been doing a lot of thinking about Robysue's advice to me, specifically on the issue of leaks. When I first started, I intended to use FFM, but none that I tried would fit my face, which is small with recessed chin. I finally did find one, the Amara View that fits and I bought 2, but have not worn them all night yet, for several reasons which I won't go into here. So I have been using only nasal masks. Since I believe that mouth breathing is responsible for some of my uncomfortable respiratory symptoms, I decided to teach myself to stop mouth breathing. So each night I use either a cervical collar or tape my mouth. When I first started, my pressure was set wide open 4 - 20. Of course, I did not know anything about CPAP at the time. After having a very difficult time falling asleep, I would wake up all night long with mouth leaks, chipmunk cheeks, etc. Mouth tape did not work, because it only stopped air from going out my mouth, not from coming into my mouth. Finally I lowered the pressure to 4-6 and then I was able to sleep mostly through the night. I waited 2 months and all was pretty good, but I thought I needed more pressure. I upped the max to 7 and the mouth leaks started again. I turned the max pressure back to 6 and all was well again. About 2 weeks later, I tried the max pressure at 7 again and this time it worked and I did not wake up with mouth leaks. I left the max pressure at 7 for about a month. Then upped the it to 8. This time, instead of chipmunk cheeks and hissing from air escaping the corners of my mouth, I got dry mouth. I think this still means that air is entering my mouth. I backed it off to 7, but am still getting dry mouth.

So I wanted to see if my machine thought there were a lot of leaks. The mask fit always gave the smiley face, so I started looking at the leak rate. Other than the last few days since upping the max pressure to 8, the leak rate has averaged 7L/min. But the last 3 nights, with max pressure set to 8, it jumped up to 20L/min. It would seem that whenever I up the max pressure, I get leaks for awhile, at least until my brain gets used to the added pressure. Can anyone tell me what this means? I am starting to wonder if the real problem is that any leaking at all is waking me up at night!

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