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| Pediatric Tracheostomies For parents and caregivers of children with tracheostomies. Please limit discussion to seeking and sharing of information pertaining to tracheostomy care, medical issues, special needs, disabilities, networking and moral support. |

02-28-2011, 11:49 AM
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Junior Member
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Join Date: Apr 2010
Location: Indiana
Posts: 87
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Trach size?
I was wondering when (or if) you ever move up a size? Ezra has had a 3.5 (neo then peds) shiley since he was trached at a few weeks old, he is now a year old. I was just wondering because he was given a PMV at 9 months and we slowly work up to him being able to tolerate it for about 30 minutes at a time. He never was able to wear it any longer than that and suddenly would start to cough and gag when he wore it so we stopped using it all together. He had a bronch, scope etc.. recently in preparation for decan and they saw that the trach took up his entire airway. The pulmo commented that he had a "rather small airway" but then said nothing about it later.. I know I tend to over think things but does that seem normal? Not normal? FWIW we switched hospitals and this was the first time any of these doctors had seen him.
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02-28-2011, 12:28 PM
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Member
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Join Date: Apr 2010
Location: Canada
Posts: 261
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If you are working towards a decann then putting in a smaller trach would probably be the next step. It would allow him to pass air more easily past the trach and through his upper airway. It may also help with him wearing the PMV too.
We moved from a 3.5 Peds to a 3.0 when David was 8 months old and it has made a world of difference in the amount of sounds he can make.
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Jessica
Mom to David, Born Jan 1/2010, Trached Feb 11, 2010 for Bilateral Vocal Cord Paralysis and Laryngotracheobroncho malacia... Currently working on decann attempt #3
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02-28-2011, 04:27 PM
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Senior Member
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Join Date: Feb 2007
Location: Seattle WA
Posts: 6,484
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I think generally they don't upsize unless the child is having issues, working too hard to breathe with their current trach size. Upsizing will make PMV use more difficult. Downsizing, though it can help with PMV use means a 3.0 and a 3.0 trach plugs more easily. And having a 2.5 as an emergency back up trach can be a bit worrisome since a 2.5 is practically worthless. My ENT calls them "placecard holders".
Ainsley still wears a 3.5 and she is a large 4 year old.
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SUSAN - Mom to Ainsley (age 6 - DOB 10/18/06) + Evie (age 12) and Adrian (age 9). Adorable and Trached since 11/06 (scarred vocal cords & OSA) but capping with mixed success since 1/09, sagittal craniosynostosis (cranial reconstructions 1/07 & 7/07), MicKey G-tube 06/07, Nissen 10/08, unusual form of cerebellar hypoplasia, hip dysplasia (Surgery 11/07 & 4/10), ptosis(post-surgery).
Blog Link: http://ainsleyrae.blogspot.com/
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02-28-2011, 04:56 PM
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Join Date: Jan 2010
Location: CT
Posts: 161
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Sofia is 2.5 yrs old and is still wearing a NEO size trach. They are significantly shorter than the PED so you may want to ask the docs about going back.
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Sofia's Mom
born: 9/08 at 24wks 5days (1 of 2 surviving triplets). Home 4/09. Off the vent 1/10. Trach, mic-key button, strabismus, mild hearing loss. First LTR 4/10, Second LTR 7/11.
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02-28-2011, 10:48 PM
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Junior Member
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Join Date: Apr 2010
Location: Indiana
Posts: 87
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Thanks guys! I wondered why they didn't downsize him but we do have issues with his trach plugging so I'm glad they didn't!
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02-28-2011, 11:06 PM
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Join Date: Oct 2010
Location: Calgary, Alberta, Canada
Posts: 201
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I was told that the trach size had alot to do with the issues and why they have a trach in the first place. For example, Lauryn's issues are all upper airway, so it doesn't really matter if we move from a neo to a ped...the length doesn't make a difference to it's performance for her. If someone had more lower airway issues or softening of the trachea then it might be more important to have the trach be as close to the corina as possible.
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