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Re: Peak Flows

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Belinda, We have the exact same situation with Lucas. Our doc told us that it

is not based on age but size. I know that each time in the past that we have

used a good long course of steroids that Lucas had a significant increase in

peak flows like the inflammation had been reduced so that he had more

capacity. I also wonder if at times there is hyperinflation due to air

trapping. I have seen his chest get very hyperinflated especially if we have

a long period of frequent treatments. A peak flow is useful to see what

there normal are when they are not having problems. The question then becomes

what is there O2 saturation level. We go into the doc and do a pulse ox

reading as well as a PFT on the computer that we compare his large and small

airways to his usual readings. This is both reassuring or gives us an

indication that he needs more help. Hope this helps. By the way. Lucas will

be six tomorrow and his normal peak flows are 210-240 when he is well. When

he is not we are in the 170-180 range and below that we are on pred. He also

uses Servent 2 puff and Flovent 110 1 puff 2x day. when he is well and we

increase the flovent to up to 3 puffs 3x day depending on how he is doing.

We have tried singulair but he is allergic . We also do albuterol and

atrovent neb treatments increasingly as needed sometimes for weeks. I guess

what I am saying is that it is an ongoing process and low peak flows and

coughing is a symptom that may need more management but atleast needs to be

checked out. Hope this does not confuse you but is an example of what one doc

does for my son. BARBIE

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Belinda - We go by the personal bests. When Macey first started doing a peak

flow we had a book that came with it with

standards for age and height. But the one that would be for Macey was so far

off that I thought she was surely headed

for ICU. Mine wasn't even near what I do (when I occasionally have to). So, we

found a time when things were calm, and

we charted 5 days of personal bests, twice a day every day. And we use those to

go by. She's 6 1/2, 47 " and 55 lbs and

runs a personal best of 170.

Ursula Holleman

Macey's mom (6 yr. old with CVID, asthma, sinus disease, GERD, kidney reflux,

Sensory Integration Disorder, Diabetes

Insipidus,colonic inertia)

http://maceyh.home.att.net

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Barbie,

Happy Birthday to Lucas!!!!! Thanks for your response. This whole asthma

thing is about to drive me nuts. If you don't mind me asking: What does a

hyperinflated chest look like? Is it sticking out? I notice Cassie will

sometimes keep her shoulders higher (almost shrugged) when she is having

significant problems. And, if she cries, it gets a whole lot worse quickly.

We had a pretty bad attack at Piper Pizza because she started crying

that she did not get her way. It almost scared her too much to cry anymore.

Hope Lucas has a wonderful day tomorrow.

Belinda Rose,

Mom to Allyssa (9) and Cassie (7), igg immunodeficient, asthma, sinusitis,

IVIG for 5 years

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I've been wondering about age-related peak flows also. Autumn has just

started doing them in the past 2 weeks & she averages around 120-130. Her

personal best is 150. Since she's not sick right now, I'm guessing that

these #'s are ok for her??? I'd ask the ped but he's on vacation until

after Christmas.

Ray, mother to Tabitha (age 6), Autumn, age 3 (IgG Def., asthma,

chronic sinusitis, and allergies), and Duncan Avery, 7 months

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Autumn weighs 39 pounds (give or take).

Ray, mother to Tabitha (age 6), Autumn, age 3 (IgG Def., asthma,

chronic sinusitis, and allergies), and Duncan Avery, 7 months

> Ray,

> Another thing that factors into what the peak flow

threshold

> should be

> calculated against is the childs weight.

>

>

> ( mom to 9 yrs asthma, allergies, hyper IgE syndrome)

>

>

>

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  • 4 years later...
Guest guest

First off....I would like to thank and I

believe it was Addy for the wonderful glossary!! I

can SO relate to all of these terms.

On another note, I did my Peak Flow this morning (have

been using it religiously since going/staying on pred

since November 2005). I BLEW 450 THIS MORNING!!!

This was upon wakening, before bronchiodialators and

using no Ventolin during the night. I have NEVER

blown this number before! I can only assume it is

relation to Xolair (just had my 3rd shot last

Thursday...receiving 1 vial once month). Yeah for

Xolair and this wonderful group!

I use the Personal Best PF handheld meter...have had

it for about 10 years. It is square shaped. When I

went to the hospital last November they gave me a

round shaped one (and chastised me for not bringing my

PF meter in with me!). I do not like how it feels,

had a harder time blowing and as a result had lower PF

than using my other meter....hmm....don't know if this

is a good thing or a bad thing, but I think

consistency is the best. My normal BEST range is

375-400 after bronchiodialators and I would be happy

blowing anything over 325 prior to breathing

treatments.

bye for now

Pamela (who is down to 9mg evil candy and hoping to

get down to 8mg in a couple of days!)

Kingston, Ontario

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