Entries in CPAP (4)


Wild Camping with CPAP


Wild Camping (also known as Dry Camping) is where you camp with a minimum of kit using what you can find around you: drinking stream water, eating plants, hunting, trapping and building shelters (think "Ray Mears" and you'll get the picture - living with nature), and it's something that I'm taking an interest in, so much so that I decided to spend a few nights "under the stars", of course my CPAP machine came with me...

Why did I decide to do to do this?

Well, after an overnight power cut at home I realised how dependent we were on technology and electricity for pretty much everything we do, and that made me feel pretty helpless, it's all very well having the kit to treat my sleep apnoea but it becomes useless without electricity. My computers became black mirrors, my freezer became a box full of water, the hot water wasn't hot... anyway you get the picture.

It's all well and good having spare masks and tubing for your CPAP, but it's another to not have any electricity!

Fortunately during the power cut we had a car jump-start battery pack to power my son's BiPAP, but at his prescribed pressures it only lasts little more than a night. I began wondering how we'd cope with more than a day without electricity.

Yes, I could charge the battery from the car and risk it flattening my car battery, or I could let him sleep in the car while I drove us to a relative's house that had electricity, but that didn't seem to be a complete solution.

Although it's unlikely that we'd be without power for more than a day, it's better to be safe than sorry. How much easier is it to change over to battery backup than to go on a midnight quest for electricity?

This made me wonder how I would cope with a minimum of kit in the wilderness. I'd camped before, even in a desert in the Middle East, but that was with a 4x4 crammed full of kit and I wasn't a CPAP user then, travelling light was the plan for this trip, and the CPAP and Jump-Start battery pack were going to be an awful lot of kit to drag along.

So I invested in a relatively lightweight dedicated battery and tested how long it would support my pressures at home.

The "Super CPAP Battery" sustained my Resmed S9 Autoset machine for at least 5 full nights, so I knew it would last for my short one night stay in a woodland in Wales.

The idea of Wild Camping is that you take a minimum of kit with you, and it felt like cheating to be taking something as high-tech as my CPAP along but to be honest, I really don't like being without it now, so I decided that it was coming along. It would be my Desert Island Discs Luxury Item.

To try to cure that cheating feeling I decided that if I could charge my battery before I left using Solar energy then I was still qualified to play the self-sufficiency game without cheating.













Charging either of the batteries using Solar Power was simple and relatively cheap. I used a 13W solar briefcase from Maplin Electronics.

Camping aside, being able to do this gave me a sense of security, especially considering that if we were without power for more than one night I'd need a way to charge my son's BiPAP battery pack at home.

Of course I had other options, rather than taking the CPAP along for me. I could have slept on my side, but I wasn't keen on that as I often wake up uncomfortable in the mornings after using a side-sleeping device and I wasn't sure how well that would work if I ended up sleeping in a hammock. I could have taken 5-HTP but to be honest, I liked the idea of making a campfire and sharing a couple of whiskies around it with my brother, so that would likely negate the positive effect of the 5-HTP, besides, I know that alcohol has a detrimental effect on nightly AHI and hence I'd need CPAP more than ever if I drank.

I also wasn't keen on taking my shiny S9 Autoset into the woods for a night. I did contemplate buying a cheaper APAP to travel with but unless I did so and used it at home for a while I wouldn't trust the machine to behave in the same way as the S9 Autoset. 

Maybe that is something that I'll do if camping becomes a regular thing for me.

After putting a few more bits of kit into my rucksack we headed for Wales with the "Super CPAP Battery" charged full of English sunshine (yes, we have some every now and then). The sunlight had travelled 96 million miles, I'm sure it wouldn't mind another couple of hundred.

This is probably the point to confess that I packed too much kit. In hindsight there is much that I would leave behind as I didn't use it, and some things that I should have taken that I didn't (a sleeping bag being the major thing that I was pining for in the night).

One of the items that I took but didn't use (although I would have done had our stay been longer) was a fantastic piece of kit called Powerfilm. This is a flexible solar panel.

The panels come in many sizes and power ratings depending on how much electricity you need. Mine was the R-15 1200 which has an output of 15.4V and is rated at 1.2A 20W. This is more than enough to recharge the CPAP battery pack even in fairly overcast conditions...








On arriving in Wales our first port of call was a shop where we were able to buy some, eggs, whisky and gloves as the weather was already worse than the forecast had indicated. Oddly this made me remember a lucid dream that I'd had about being in Wales and left me wondering what the next night would have in store for me. 



We set up our camp in drizzle, so I made a simple shelter with an inbuilt groundsheet that would keep me and my kit dry.

In hindsight I should have sheltered in it until the drizzle stopped and then built something that offered more protection from the cold.



We took the Sawyer Point Zero Two water purifier with us, this filters everything out of the water that is larger than 0.02 microns. That means that all bacteria and viruses were removed. I suppose that you could use this to provide water for a humidifier, but I am so used to boiling water at home for when I used a humidifier that I'd still boil it anyway, not least because it would help with preventing limescale buildup in the humidifier tray.

Once the filter was hung from a tree we built a fire and I unpacked my CPAP setup ready for the night.

Fortunately the CPAP battery was more reliable than our fire (which lasted about 3 hours into the nighttime rain). The CPAP battery lasted all night despite it being cold (which I feared would affect it).






After a cold night I woke to find that everything (including me, the battery pack and CPAP) was covered in a heavy layer of dew and a touch of frost but it was still working. 






The other thing that I noticed was that a great deal of my kit had been slimed by a slug or a snail!

This night proved to be a good test of the kit that I'd taken but it also showed me where I was going wrong. I can assure you that the massively lower than predicted 4ºC felt awful during the night without a sleeping bag! 

For the following night we headed a couple of hundred miles south-east to Stonehenge for a night of hotel survival.

On arrival at the hotel, after foraging for the room service menu and having a nice hot shower, I realised that I wasn't prepared for the night because I didn't have the mains power lead or an extension lead with me to power the CPAP but fortunately the battery pack had more than enough power to last the night, and it meant that it could sit on the bedside table under the S9 leaving the room cable-free. 

So while the power-pack discharged its battery I was able to recharge mine...



This just goes to show how important a good sleeping environment is!





Waking up in the night to turn the air-conditioning on for some cool air and white noise was a far cry from scavenging around for dry wood in the cold wet night although the white noise of the nearby river and stream at our camp the previous night was vastly more impressive than the hum of the hotel air-conditioning...

... and it is that sort of natural feature that made me want to do this again but this time be better prepared. It was all very well reading about this sort of thing but it's another to actually try it. I'd made the transition from "Armchair Wild Camper" to a real life Wild Camper and wasn't going to give up now. After making a reasonable attempt the first time I decided to give it another go and put in place some of the things that I'd learned the hard way from the first night. So re-energised I removed some kit that I didn't use and packed some other things that I thought would be useful (including a sleeping bag and Trangia stove) then on my own at a new location nearer home set up my shelter in a more enclosed way.

Remembering the slug / snail trail, it occurred to me that the CPAP and battery combination may need a sleeping bag / hammock of its own. If it did nothing more than keep them slime-free then it would be worth it but it may also help with the problem of them accumulating a layer of morning dew by keeping them off the cold groundsheet.

I was concerned that whatever method I used would still need to enable decent airflow to the CPAP so I put the battery, adapter and CPAP into a string "turtle" bag and suspended it from the ridge line using a caribina but this could also have been achieved using a decent knot (something that is a real test of how tight you are able to make the ridge line because although the S9 is light, the power brick and battery aren't). 

In this photo I've lowered the side of my shelter to make the bag easier to see...

The string bag worked well because it allowed a good airflow and I was able to feed the CPAP hose through one of the holes in the bag. The bag was able to be moved along the line so that it was in a good position for when I went to sleep (not directly above my head, and not too near the edge of the shelter).


The bag helped a fair bit with the dew problem, although to be fair the weather conditions and my shelter weren't the same.

It would also be possible to wrap the CPAP / Battery combo in a lightweight towel before putting it into the bag as long as you were careful not to obstruct the air-intake of the CPAP.

It's also worth mentioning that it would be prudent to leave the CPAP machine safely tucked away until the smoke from your fire has subsided, otherwise every breath you take will smell of campfire smoke! 

I'll definitely do this again. As far as my bushcraft skills go, I've got a lot to learn but as far as the CPAP is concerned I'm very happy with how things went and have proved to myself that being tethered to a machine at night shouldn't put a limitation on activities like this. 


CPAP - It's well worth taking the time to get it right

Previously I'd used CPAP for a few days to try to get an idea of how my son felt as he started to use it.

Initially I tried it in the hospital where it was prescribed. I used it whilst awake using a variety of masks and pressures to see what high pressures felt like and to see how it responded to me exhaling, holding my breath, trying to talk and opening my mouth etc. Then I used it for a few nights. I wanted to know what problems he could encounter because he isn't able to move to correct them for himself, so I thought that if I were familiar with some of the problems it'd at the very least give me a frame of reference for when he told me what issues he was having.

For practical reasons I purchased an additional CPAP (technically an APAP machine - Auto CPAP). I chose the Resmed S9 Autoset, which to its credit doesn't look like a piece of medical kit; it looks more like a modern bedside clock radio. Yes, the pressures should be set by a professional and you need a prescription to buy one but it looks like a piece of consumer electronics, which is a great thing because it doesn't make your bedroom look like a High Dependency Unit.


Resmed also make coloured "skins" for the device which would be helpful when trying to introduce it to children as part of their therapy.

The S9 has a coloured display screen which allows the user to adjust the comfort settings and climate control and to allow them to see an instant indication of whether the mask is fitted properly along with a morning readout of your AHI (Apnoea Hypopnea Index).

The S9 records overnight summary data and detailed data to an SD card, which via the ResScan software allows you to see the following data: 

  • Respiratory Events via flags on the timeline (Central Apnoeas, Obstructive Apnoeas and Hypopneas)
  • Pressures chosen by the machine at any given time
  • An indication of snoring level
  • Flow (allowing individual breathing waveforms to be seen)
  • Leak
  • Flow Limitation (an indicator of the degree of obstruction)
  • Compliance data (how long I used it for)

An example of the data from one of the nights that my son used it is shown below.

All of this is very useful to have access to because it lets you see a record of the choices that the machine makes which helped me to trust that the machine wasn't going to deliver a high pressure unless there was a good reason to. This is all recorded automatically while you sleep at home (or in the sleep lab). Compared to a one-night study in a sleep lab (especially a split night study) the data may be a more realistic representation of your sleep because you'll be sleeping in a familiar place and adhering to your usual routine.

The output that we collected from the ResScan software was viewed by my son's doctors during his initial trials with CPAP before changing over to Bi Level ventilation (BiPAP / VPAP / BPAP)



I chose Resmed's Swift FX Nasal pillows as they left a lot of my face free, they didn't feel trapping and are easy to remove if I really felt like it in the night.

My son uses them with Bi-Level PAP and prefers them over a wide range of masks that he's experimented with, although he can't move below his shoulders he has learned to remove the Swift FX pillows by a head movement, so he feels comfortable using them as he knows that he can take it off if needed.





The S9 has an "AutoSet" mode where it can alter the delivery pressures as it deems necessary. The machine can be forced to work within a range of pressures. I decided to let the machine have a free reign and didn't force it to choose between limits. 

I managed to keep the CPAP on for most of the night, but I remember waking frequently and moving the tubing and to keep checking the machine because... well to be honest... I was nervous. The machine is very quiet which was another reason to check it every time I stirred in the night in case I'd managed to turn it off in the same way that I snooze the alarm clock. 

Over the few days I was tired because, as I said above, I'd been awake due to my own anxiety and the strangeness of it all, also I managed to get caught up in the tubing one night! The following evening I arrived home from work and dived face down into bed without CPAP. Due to my sleep debt over the previous few nights I experienced sleep paralysis and a lucid dream, so it wasn't all bad.

...and that's where my trial with CPAP ended.

However, recently I've fallen in love with CPAP and in particular Resmed's S9 Autoset (the photo above is my S9 beside my bed), and here's how it happened...

There's a lot to get used to with strange tubes and masks on you and your bed plus a new machine on the bedside table - and that's without getting used to the pressures that the machine delivers... considering this, my experience wasn't really a fair trial for CPAP, especially since it is considered to be the "Gold Standard" in treating obstrucitve sleep apnoea.

In hindsight, I suspect it would have been better to begin by choosing a low pressure and just wearing it to get used to the mask and tubing - almost a dress rehearsal before the therapeutic pressures are used.

My CPAP experience was well over a year ago and before the time that I started this blog and before the time that I realised that I had mild to moderate obstructive sleep apnoea. Now that I have a better understanding of my own sleep and have found various ways to reduce my AHI without CPAP I decided to give it another go and compare the results, after all we now had my son's "old" (barely used) S9 Autoset sitting in a cupboard doing nothing because he actually needed Bi-Level PAP.

This time I paid a lot more attention to my own AHI.

I also decided to eliminate the uncertainty of whether the machine was going to wake me with a high pressure during the night, so I did a gradual titration over several nights using the "Straight CPAP" setting of my son's backup Respironics BiPAP S/T.

I found myself making slow deliberate breaths while I tried to sleep. This wasn't particularly helpful, because (even if you aren't wearing CPAP) when you think about your breathing you find yourself consciously taking over, and to be honest this is something that our bodies do better if we don't let consciousness interfere with it.

However, I found myself calmly waking up every now then wondering why I wasn't breathing and finding that I had to consciously take a breath, I listened to machine respond, then dropped back off to sleep. This happened maybe 5 or 6 times that I remember during the night and wasn't anything like waking with a snort or a choke, in fact it felt quite strange. 

In the mornings I took a look at the data (the BiPAP S/T also records data to an SD Card that is readable via the Respironics Encore Viewer or Encore Pro software. 

I found an explanation for the breathless awakenings...

Whilst the obstructive apnoeas were few and far between, the machine had detected "Central Apnoeas". These are when the airway is open yet no air flows. This can be from a variety of causes, but from my own baseline sleep studies I know that my apnoeas are usually obstructive in nature, so I knew that these new Central Apnoeas were because my chosen pressure was too high.

If breathing is too effective at clearing CO2 from the bloodstream then central apnoeas can occur because during normal breathing the brain sends a signal to breathe when CO2 in the bloodstream reaches a certain trigger level. We then breathe causing gas exchange, (taking oxygen in and exhaling CO2), after which our bodies produce more CO2 which reaches the trigger level and the cycle begins again.

If the CO2 level is too low then the brain doesn't need to clear it, so doesn't send a signal to breathe. Our oxygen levels then drop which wakes us up and allows us to consciously take a breath.

I adjusted the pressure down by 1 cmH2O the following night, but I still wanted more data. Were these really "centrals"? A night wearing the Black Shadow Sleep Monitor whilst on CPAP confirmed that they were.

I switched machines back to the Resmed S9 Autoset because it allows you to see a lot more data as opposed to the trend data given by the Respironics BiPAP S/T. It actually allows you to look at the data at a much higher resolution (you can see every breath taken) so I could then verify any detected apnoeas for myself.

Along with the lower pressure setting, I set the S9's EPR (Expiratory Pressure Relief) to full (3) which drops the pressure down by 3cmH2O (or 1 or 2 cmH2O, depending on your chosen setting) when it detects that you are exhaling. This is very helpful, even for psychological reasons as not only does it help you to exhale, but it provides a form of tactile feedback letting you know that the machine is "listening" to you and not trying to force a gale into your nostrils whether you like it or not.

One interesting thing that the S9's additional data allowed me to see was the moment that I stopped doing those forced breaths I that I mentioned above. This is the moment that I fell asleep. 

I fell asleep fairly quickly, and woke once when I turned onto my side and found that I needed to adjust the nasal-pillows slightly.

The following morning I checked the data and found that the central apnoeas had cleared and my AHI was a very respectable 0.4 which varied over the next few nights but still remained under 1.0.

One night I found that the S9 data showed that I'd been quietly snoring, it was also on this night that my AHI was the highest that I've had so far whilst on CPAP (0.9), although this is still a fantastically low AHI.

So the next night I crept the pressures up by 0.4 cmH2O, only to find that the snoring cleared but some central apnoeas returned, so I dropped the pressures again. It became obvious that finding a pressure that was perfect for every night was going to be a challenge.

Of course I realise that there is going to be some "natural variation" from night to night due to factors such as body position and time spent in each sleep stage but wouldn't it be good to be able to pin down what the other less obvious variables are?

My main factors are related to body position (apnoeas are more likely and frequent when I sleep supine) and REM sleep (when muscle tone is decreased in the airway), but I suspect that other factors during the day play a part.

This is where the S9 Autoset excels: In AutoSet mode it adjusts the pressure it delivers based on your need at the time, so where "Straight CPAP" is limited because it can only give me one pressure throughout the night meaning that 8cmH20 may be too much for me at some parts of the night (causing Central Apnoeas), yet not adequate for other parts of the night) where 10 or 11 cmH2O is more appropriate.

I set my S9 to "Autoset" mode and adjusted the settings so that the machine would work within fairly restrictive limits just to get me comfortable with the idea. In the morning I could see from the ResScan software that the machine had delivered the maximum permitted pressure at some points in the night, so I gradually extended the pressure range over a few nights until the machine didn't reach my ceiling limit and was able to deliver the necessary pressures.

The following graph of the pressure that the S9 delivered over one of the later nights illustrates how my requirement varies through the night. 

On the night above I woke myself up snoring after several hours (just before the red vertical line), so I raised the lower limit and went back to sleep, this is why the graph above shows the delivery of pressure that is lower than permitted minimum pressure at the start of the night.

Had I been prescribed straight CPAP based on the pressures titrated on this night then I would have had to have a constant pressure of between 10 and 11 cmH2O to eliminate all my obstructive apnoeas. However, the chances are that I would have then had more central apnoeas occurring. A compromise pressure of 9 cmH2O would have removed the majority of apnoeas but would have been inadequate when my obstructions were at their most severe. There could also have been central apnoeas occuring at this pressure for some of the night.

The textbook, "Sleep Medicine Pearls" by Richard Berry MD describes this well with a case study of a patient unable to tolerate the high pressures needed to treat his obstructive apnoea. If you have access to the book you can find the details under Patient #43. In fact the whole book is packed with case studies that provide a unique insight into treating sleep issues.

If high pressures can't be tolerated it may be preferable to have a lower than optimal pressure setting just to ensure that some benefit is obtained, although it is likely that these patients would benefit more from Bi-Level PAP which allows a much lower expiratory pressure.

In Autoset mode, the S9 allows low pressures but can deliver the higher pressures when necessary, giving you the flexibility (and comfort) of both in one setting. 

Some good news: my nose isn't as big as I thought...

I found that I woke up several times in the night and had to adjust the nasal pillows but each pack of Swift FX nasal pillows come with three sizes of pillows. I found that when I decreased the size of the nasal pillows to the medium size (although the large were comfortable and the leak minimal) the medium pillows were more comfortable and needed a lot less adjusting when I first put them on and hardly any throughout the night.  

I slept really well and took a look at the display screen on the S9 when I woke.

I was greeted by an AHI of 0.0 and a green smiling face telling me that the nasal pillows were a good fit and weren't excessively leaking.

The ResScan software also confirmed the Zero AHI


Now that I use the Autoset mode, my AHI is always under 1.0 regardless of what position I sleep in or even if I've had a glass of wine.

It actually feels good to sleep on my back again, I'd been using the Rematee side-sleeping belt for a while and found that I missed sleeping on my back. With CPAP I didn't ache when I woke up. CPAP was surprisingly unrestrictive and I soon learned a manoeuvre to clutch the hose and move it with me if I wanted to turn in the night.

To be fair I could have just let the S9 go on full unrestricted auto from day one and it would have delivered the same pressures, but from mine and my son's previous experience with Non-invasive Ventilation, a large factor in whether it is successful is down to whether the sleeper (patient) feels comfortable with it, yes the numbers are important (after all that is the whole point of the therapy), but the patient experience is also key as that alone will probably be the biggest factor in whether they are "compliant" with it (ie use it for 4 hours or more a night), after all many PAP machines don't allow the user to see their AHI data so they can only judge based on how it feels.  

Another part of the experience is the mask that is used. There is a wide choice of masks available, and it's important to find one that is right. Also humidification can help people feel more comfortable with PAP therapy, this is something else that should be available to them along with all manner of accesories such as hose holders - really anything that will prevent someone giving up. That said, CPAP therapy isn't right for everyone as my son's situation shows, so good communication with a committed Sleep Consultant is vital in order that the right treatment be offered. 

I think looking into things in this detail was necessary for me, although it was a rather involved way of getting used to CPAP and trusting it, it has been well worth it. I feel a lot more awake in the mornings (generally only sleeping for 7.5 hours now) and my AHI has been consistency the lowest it has been in probably 20 years.

I think the graph below speaks for itself.

CPAP is a clear winner and one that is likely going to be impossible to beat but that's not going to stop me trying out other apnoea remedies to see if they can come close.

CPAP has also made a huge difference to my snoring, the results of which I'll post in a few days. 

For the future: 

  • I'd like to see if the pressure requirement decreases if I take a dose of 5-HTP at bedtime.
  • Although I don't intend to change my nasal pillows, I would like to see what difference other masks make to the experience.


Useful Links

Michael F. Fitzpatrick, Christi E. D. Alloway, Tracy M. Wakeford, Alistair W. MacLean, Peter W. Munt and Andrew G. Day
Can Patients with Obstructive Sleep Apnea Titrate Their Own Continuous Positive Airway Pressure? 
(full text PDF available to non-subscribers via the link)

Gao W, Jin Y, Wang Y, Sun M, Chen B, Zhou N, Deng Y. 
Is automatic CPAP titration as effective as manual CPAP titration in OSAHS patients? A meta-analysis.




Sleep Onset Apnoeas / "Throat Closing"

One of the search terms that people find this blog with surprised me by how frequently people search for it, there are several variations but these two sum things up well:

  • Throat closes as I go to sleep
  • Choke as I fall asleep

I hadn't really considered this before but I really should have done because it happens to me, and one of my parents. Normally when I experience those throat-closing moments they are accompanied by the first snore / cluck / snort of the night, a flash of whatever broken dream images were going through my mind and the knowledge that I'll soon be asleep. I guess it's something that a lot of us experience but don't really talk about it because it sounds a little strange.

Polite and usual "sleep chat" is usually along the lines of "Did you sleep well?" and not much deeper than that which is a shame because it's such a fascinating subject that few of us speak about because many (wrongly) consider sleeping to be a waste of 8 hours and some even see it as a weakness ("Sleep is for wimps" etc etc).

I've been using CPAP for a month or so now and have been adjusting my own pressures based on the sleep study data that I record each night. When I reviewed each night's data, one of the things that stood out about breathing as we drop off to sleep was how it changes at sleep onset (the moment that a sleep lab would declare that we are now asleep).

This becomes more pronounced with CPAP (or at least for me as a relative newcomer to using CPAP for myself) because when I first switch the machine on at night I instantly become aware of my breathing and try to control it. Oddly, consciously controlling our breathing is something that we don't do very well and it is best left when our bodies do it for us automatically. Can you imagine the chaos that would result if we had to consciously take every breath or control every heartbeat?

The following is a few minutes of data representing my breathing as I was dropping off to sleep whilst wearing CPAP. It's taken from Resmed's ResScan software (click for a larger version).

The breathing on the left is when I was awake, it is clearly different to the smooth regular breaths on the right side of the graph. Falling asleep is what brought about the change as I "forgot" to consciously breathe and my body took over.

So far so good, but on several nights I noticed that the handover from from awake breathing to asleep breathing wasn't so smooth... 

Notice how there are gaps in my breathing? This is from a night where some apnoeas were still occuring; I remember that as I was falling asleep I experienced at least two of those "throat closing" moments. The apnoea briefly woke me as left me realising that a moment before I was asleep, which also seemed to shift the hypnagogia into my conscious mind and then into my memory because this night was also a night that I remembered a lot of it.

Several different images and phrases came and went as I drifted off to sleep. The Zeo recorded that I briefly entered REM as I fell asleep (possibly causing a loss in muscle tone resulting in apnoeas)...

This is something that I see on many nights when I look at my Zeo data, but in the interest of accuracy, Zeo do point out that if your sleep is generally healthy with 7-9 hours per night and no feelings of tiredness during the day that this brief period of REM could be wake being misinterpreted as REM. It could be that N1 sleep mixed with brief periods of wake (from my respiratory arousals) were interpreted as REM by the Zeo (as wake is so similar to REM). 

The following night my sleep looked very different and I achieved a lot more REM along with no apnoeas or hypopneas recorded at sleep onset, intriguingly the Zeo data doesn't show me passing through REM as I fell asleep. So this could actually be REM, although this could also be because there were no respiratory related arousals during the transition from wake to sleep.

With the Black Shadow Sleep Monitor I've seen that less significant respiratory events are linked with altered REM sleep, in my case a series of hypopneas leading to a Lucid Dream. This raises an interesting issue that may provide some insight into dream formation.

I used to be comfortable with those throat-closures before I knew I had Sleep Apnoea as they had become so familiar to me. I used to use them as a way of knowing that I'd soon be asleep. In a strange way I will be sad if they go because after each "cluck" or snort I'd briefly wake and commit the partial dream or hypnagogic image to memory and would be able to study sleep as I drifted off.

Famously people have used a technique that relies on waking from hypnagogia in order to remember it which involves napping in a chair whilst holding a metal spoon over a metal tray or plate. Once you drop off to sleep you automatically release the spoon, causing a clattering sound which then wakes you allowing you to recall what you saw and heard.

I see my sleep onset apnoeas as such a system, alebit a naturally occuring one. I think that during the times that I want the best of both worlds of having the apnoeas at sleep onset but sleeping safely for the remainder of the night that I will experiment with setting a RAMP on my CPAP which delays the maximum pressure by up to 45 minutes, giving me time to explore the hypnagogic world.

Knowing that I have obstructive sleep apnoea and that the first apnoeas of the night are usually at sleep onset, I would suggest that anyone who experiences these throat-closures at sleep onset should at the very least be aware that they could have Obstructive Sleep Apnoea and look out for other symptoms. The best thing to do it get it checked professionally as it could also be a sign of another condition such as Acid Reflux (GERD) or Laryngospasm.


Non-Invasive Ventilation 

I could rehash the many excellent write-ups of non-invasive ventilation (NIV) that already exist on the internet, but I thought it would be more personal for me to tell how my son came to use it, explaining NIV along the way...

Bear in mind that these events took place over a period of 10 years and involved many medical professionals from various hospitals and clinics, although it may read as if it took just a few nights. 

A person's breathing might not be enough to sustain them for various reasons including:

  • Illness (short term or long term)
  • Injury (critical phases)
  • Neuro-muscular issues

Sometimes a person will need respiratory support during these times. Sometimes it can be for a short while whilst in intensive-care or a high-dependency unit, other times it can be a life-long need, in which case they will likely have to have a tracheostomy tube fitted in order to leave their face free and unobstructed.

There are also people who only need respiratory support whilst they are asleep.

Due to changes in our respiratory drive and how our muscles respond during sleep our breathing undergoes many changes, this can even vary depending on the stage of sleep we are in. 

The following graphs contain information about how much air I was breathing per minute during the various stages of sleep (as scored by Zeo)...


I won't go into great detail about the why here, instead I want to concentrate on what can be done about the problems that these changes can cause.

At the time of writing, there is a good Wikipedia article about these changes entitled "Sleep & Breathing" 

When he was first paralysed, my son was on full time ventilation. This was considered to be a long-term and possibly a life-long situation and he was give a tracheostomy tube (a tube inserted through an opening in the neck and directly into the windpipe) to allow the ventilator to be connected to him.

10 years on, he is still paralysed but fortunately after several months of being in hospital the tracheostomy tube was able to be removed because the higher part of his spine had partially recovered. He had been slowly weaned off ventilation.

After the tube was removed his oxygen levels were continuously monitored and it was discovered that his oxygen saturations plummetted when he was asleep, but they always picked up again. We left hospital with a pulse-oximeter (a device that monitors pulse rate and blood oxygen saturations via a finger probe).

On some occasions his levels dropped as low as 65% (Generally speaking most people maintain a level of >92%). It was this that prompted me to buy the equipment to record his oxygen saturations so that I could show the relevant doctors involved in his care. Although, not a chart of the lowest that he dropped, this is a chart from early on (right) that is a good guide to what used to happen.

Each row is 4 hours of data (grey parts are when the machine was not monitoring due to him being awake).

Red = heart rate (bpm). Green = oxygen saturations (%) 











Left: How the chart should appear (taken from a fairly recent night when he was breathing oxygen via a mask)

 Right: His chart from a typical night


So why not just use oxygen, if it makes the graph all straight and pretty?

Well, oxygen is only one of the gasses involved in breathing, granted it's an important one, but Carbon Dioxide is also involved.

At school we were all taught that we breathe in air, use the oxygen then exhale carbon dioxide, but the carbon dioxide actually serves a purpose. It is used as a trigger to breathe. When the levels rise to a certain level, we breathe to remove the CO2.

If the "sense and control" mechanism in the brain is damaged, or if the muscles are not able to respond to its signal to breathe, then CO2 can build up in a condition known as hypercapnia.

That is what was going on while my son was using oxygen. We were able to see this by the use of a split cannula. It looks like a standard nasal cannula for oxygen delivery, but the tube to one nostril is used to deliver oxygen whilst the other is used to monitor the CO2 using an end-tidal CO2 monitor / Capnograph.

High CO2 can lead to other health issues, and it actually affects the Ph of your blood.

So my son was trialed on a type of ventilation known as Continuous Positive Airway Pressure (CPAP). This involves a constant pressure of air being delivered into your nose (or nose and mouth) via a mask. 

If you ask a child to blow a balloon up, then they will probably struggle, but if you "do the tricky bit" and start it off for them then they will probably be able to top up what you've started and finish inflating the balloon.

That's essentially the idea of CPAP. The airways are kept open by the pressure, leaving the user the task of inflating their lungs.

CPAP can be a great help when people suffer from Obstructive Sleep Apnoea. It can prevent the airway closing off, thus allowing the sleeper to breathe normally.

However, CPAP wasn't preventing my son's apnoeas.

This could have been because he needed much higher pressures, or because the apnoeas were "central" and not "obstructive" in nature.

A central apnoea is where the brain doesn't tell the sleeper to breathe.

Fortunately, the CPAP machine records the overnight data to an SD Card and can decide whether the apnoeas are obstructive (airway closed) or central (airway open but no flow).

It showed that he had mainly obstructive apnoeas with hypopneas, but also the odd central apneoa, along with many apnoeas tagged as "unknown".

The night above shows them towards the end of the night. This didn't fit with the pattern of oxygen desaturation that we saw begin around an hour after sleep onset, even whilst on CPAP, hence we weren't sure how much to trust the detected central apnoeas as they seemed few and far between. However, if someone has both obstructive and central apnoeas, CPAP can reveal those central ones after it has removed the clutter of obstructive apnoeas

The CPAP that he was prescribed was "Auto-titrating CPAP" this means that the machine decides which pressures are needed. You can see this in the graph above (the pressure line varies throughout the night). Intriguingly, the when the pressure is the highest there are no apnoeas, but he still desaturated.

The auto-pressure function can be set to choose between limits, or forced to give a constant set pressure. After many nights of alarms. We obtained a chart from a night at 6cmH20 (left) and a night at 15cmH20 (right) to see what was going on.









 6cmH20 had little effect. 15cmH20 was better, but still unacceptable and uncomfortable for him.

He would wake in the middle of the night and not be able to call out due to the mask over his nose and mouth. His heart rate would then increase and his alarm sound to alert me. I'd have to turn the CPAP off and it would have to be re-ramped again (start at a low pressure and build up over time, hoping that he was asleep before it delivered high pressure again). 

Because his blood-oxygen only dropped at certain times of the night rather than be low ALL night it was suspected that it had something to do with a particular stage of sleep. Below is a picture of a normal hypnogram (a graph detailing the stages of sleep, as shown on the Zeo entry of this blog) overlaid with a graph of his oxygen levels from one night.

Seeing this was a goosebump moment...

The pattern of his oxygen desaturations matched up really well with a standard hypnogram, so it was pretty certain that his condition was REM related. However, this wasn't a graph of his REM.  A way of working out and recording when he was in REM was needed.

New equipment was also needed...

Due to the possible presence of central apnoeas, it seemed unlikely that CPAP was going to be an effective solution, afterall there is little point in keeping the airway open if the brain isn't initiating a breath (or the muscles aren't able to respond to the signal to breathe). It was suspected that he would need Bi-level ventilation. Well known brand names for this are BiPAP and VPAP.

These are both Bi-level Positive Airway Pressure devices. Bi-level delivers two alternating pressures. The higher one is the IPAP (Inspiratory Positive Airway Pressure) and the lower one is the EPAP (Expiratory Positive Airway Pressure). The IPAP is essentially the breath, while the EPAP is the amount of pressure required in order to keep the airway open. Usually the breaths are triggered by the sleeper's breathing efforts, but to cover the possibility that he did indeed also have central apnoeas we used a BiPAP machine that could also be set to deliver "backup breaths" if my son didn't breathe a certain number of times a minute.

The CPAP / BiPAP was delivered via nasal pillows. These are fantastic as they allow the user to speak whilst using them. However, this left us with no way of being able to reliably monitor his CO2 using a capnograph.

CO2 monitoring is essential, without this it would be too easy to adjust the ventilator so that there were no oxygen desaturations, but actually be hyperventilating him, or worse causing trauma to his lungs and airways; so unless we could find a way to reliably monitor his CO2 we couldn't go any further. A different type of CO2 monitor was bought in...  A transcutaneous CO2 monitor.

The transcutaneous CO2 monitor gathers its data by way of a probe that is attached to the skin of the chest or arm. It then heats up the skin and evaluates the gasses given off. The probe needs to be removed after several hours and placed on a new site in order to reduce the risk of probe burns to the skin.

The titration process wasn't a one night affair, so we had the luxury of being able to record readings at home between appointments. However, at home we didn't have an EEG machine to record brainwave data, so we couldn't tell what stage of sleep he was in.

We needed to see when (and if) he achieved REM sleep while his settings were adjusted over the course of several nights. We also needed to make sure that the pressures weren't waking him up. Afterall, if he didn't have much REM (or his REM was disturbed) then his oxygen levels would look good and give the false impression that the settings were working. The Zeo was perfect for this.

This graph is from one of the first nights of BiPAP (when the settings were good but not optimal) and it shows a great correlation between his oxygen desaturations and Zeo's calculations of REM sleep. (The dips in the green oxygen line are a near perfect match for the green chunks of REM from Zeo), as are the rises in pulse rate and CO2.

This gave me a lot of confidence in the Zeo's decisions as REM is probably the hardest state to detect due to its similarity to being awake. In fact I'd even feel confident enough to say that the piece of missing data from the Zeo (headband was too loose) would have shown REM.

The result of a few nights adjustments during REM was that BiPAP at the correct pressures eliminated his oxygen desaturations completely and allowed him (and me) to sleep all through the night for the first time in a very long time.

It turned out that obtaining a machine that could provide additional "backup" breaths was a good investment... Pressures alone weren't enough to prevent his oxygen levels dropping, so a backup-rate was set of 13 breaths per minute.

This meant that if he didn't breathe 13 times a minute of his own accord, that the machine would make up the number of breaths. 









The graph on the left is with BiPAP pressures set to 18/10. This was fine for his oxygen requirements, but it still was uncomfortable for him (but tolerable). The high EPAP of 10cmH20 made it hard for him to exhale (remember that he has neuro-muscular issues).

The pressures were re-titrated but this time with a lower EPAP. This seems essential for him to be able to exhale effectively, and provides a more comfortable night.

These settings will be reviewed periodically by the medical professionals that have been involved in his care to see if they are still optimal.

He now loves the BiPAP machine and doesn't like sleeping without it, he doesn't sleep in until noon at the weekends, he doesn't fall asleep at school and can stay awake until long into the evening. He also has a ZQ of 137 which he likes to use to mock my awful average ZQ of 68.