Sunday, August 12, 2007

Oh, what a night.

Quent had dose 6 at 7.40pm and rigoured two hours later, as usual. Even allowing for the now routine SATS drop, around 4 hours after the interleukin 2 goes in, all was looking good for a reasonable night's sleep - and a "lie in" thanks to the new 12 hourly doses.

The SATS drop was not exactly routine, however. It started at 11.30pm. Exhausted, I did eventually get some sleep at 3.30pm. By that time the room was so full of doctors and equipment, my bed wouldn't fit, so they gave me a side room down the corridor. Not that I slept well, of course, as my mind was still with Quent... (although they were by then declaring him "comfortable").

To cut a long story short, Quent's SATS and blood pressure seemed to be quite low for a long time. The problem is this (in broad layman's - and undoubtedly medically inaccurate -terms ). When your SATS drop, your body focuses on the key organs and "shuts down" other bits - such as the extremities to which the probes are attached. This makes it hard to get reliable readings. In the end, they got round this by doing "blood gases", taken directly from an artery. It's a nasty procedure and one you can't be doing all the time. The results revealed Quent's SATS to be low (90%) but not as bad as some of the measurements had indicated.

By then the Registrar had been called in and the Critical Care anaesthetist had come up. Both felt that the alarming readings could not be reliable or Quent would be looking much worse / bluer. (They would not be compatible with life, was how Frances, my sister-doctor, put it this morning). The doctors manually checked his chest, heartrate, breathing etc. and seemed happy to leave him where he was. If anyone is looking for a business idea, I reckon there's a market for a reliable probe - you could sell it to the fretting relatives, even if the hospitals don't go for it.

Another way to check how the patient is? Ask the patient. Unfortunately, in Quent's case, this is even less reliable than the probe. Quent always says "great", "fine" or, in extreme cases "a bit tired". This morning he could remember very little of last night's episodes and visitors and admits he was away with the fairies.

So where do we stand now?

Quent is due to have another dose around 2pm, although it will be a lower dose on the advice of Prof NOS. (Quent's response, "low doses are for pussies" was thankfully rejected). Some results to do with his kidneys are quite high and there's something not quite right with his bloods. He couldn't pass urine for about 18 hours, although he then delivered a magnificent 820 ml (too much detail, I know, but we're amongst friends). He looks exhausted, old and very swollen - he has put on 10kg since Thursday afternoon - but so, so much better than in the middle of the night. It's amazing how quickly things change, yet how long it seems to last when they're bad.

Quent will probably only get, at most, 2 more doses due to the weight gain. They only let you put on 15% of your body mass (in 5 days) and Quent only has 2 kg more of his allowance to go. He has done extremely well, so I can't say I am disappointed. Our friend Philip-the-success-story, who is with us again, had 10 doses on his first visit and 6 on his second. He's cured and, although you can't draw conclusions on dose vs response, it's still a reassuring benchmark.

5 Comments:

Blogger Clive said...

Helen
It seems like you both know exactly what and who you are chasing this time! except instead of a nice policeman there is the full cast of ER to help.
Thinking of you both.
Love Clive

Sunday, August 12, 2007 7:13:00 pm  
Anonymous Anonymous said...

Hi H,

Back from the wilds of Herefordshire farms and can finally report the harvest has well and truly started.

Most if not all the flood water has gone and with the dry weather these last couple of weeks I think we've saved about 80% of the crop.

Whilst I was out there I thought of Quent and each morning as the sun came up I looked up at the sky and prayed to any god and all gods, to give Quent the spirit he always shows to keep taking the battle to this illness.

I know he'll win and with you and Oakley by his side every step of the way the result is in the bag.

Keep on posting, because it's inspirational and you're making a difference.

Next time you kiss him, give him a peck from me (on the cheek of course)

Love you lots, always thinking and praying for you guys.

Les, Sarah and Ellie
xx xx xx

Sunday, August 12, 2007 8:19:00 pm  
Blogger Catherine and Mark said...

Helen,
Just caught up with the most recent posts, and we are praying and thinking about you both so very much.
We've come back from a huge canoe polo tournament in Belgium, some of the boys (Ed & Andy, and Rob) did better than others (Jonny and Tom) but the true Batchworth spirit (and a lot more that I can't print here) was on show too.
Give Quent a huge hug from us; just hang on in there Helen, you're doing more than brilliantly yourself.

Love The Turners xx

Sunday, August 12, 2007 10:17:00 pm  
Anonymous Anonymous said...

Hi Helen,

Thanks for keeping everyone in the loop with all the latest. I just thought I'd check up on how things were before bed and as always its an inspiring upbeat read despite all the unpleasantness you're both going through. You're in our thoughts and prayers lots. We've been out dancing tonight and spent the last few hours lying on the garden table watching these meteors the beeb keeps going on about. (Well I say watching.. Picture Renee saying "Ooo look over there!", me turning round, going "Where?!" ..and then repeat. ;-) Please give Quent Big hugs from both of us!

Love Rob & Renee

Monday, August 13, 2007 12:54:00 am  
Blogger Sylvaine said...

If you had two doses to go at around 1pm yesterday with the first one going in at 2pm and the second one 12 hours later, and it's almost 9 am on Monday, I think you're done for this second round.
...Or do I need another coffee?.

I hope you can get some rest now.

Sylvaine

Monday, August 13, 2007 8:56:00 am  

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