Evidence map›Paper›PMID 40353737›Full record

ArticleThe Laryngoscope2025

Outcomes of Virtually Assisted Personalized Tracheostomy Tubes for Congenital Airway Anomalies.

Anna Christina Clements, Sean S Evans, Blair Mockler, Clare Richardson, Randall A Bly, Kaalan E Johnson, Seth D Friedman, John P Dahl, Sanjay R Parikh, Juliana Bonilla-Velez

Abstract read
In one paragraph

Article in The Laryngoscope, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Anna Christina ClementsDivision of Pediatric Otolaryngology, Seattle Children's Hospital, Seattle, Washington, DC, USA.ORCID 0000-0002-6869-3339
Sean S EvansDivision of Pediatric Otolaryngology, Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
Blair MocklerDivision of Pediatric Pulmonology, Seattle Children's Hospital, Seattle, Washington, DC, USA.
Clare RichardsonDivision of Pediatric Otolaryngology, Phoenix Children's Hospital, Phoenix, Arizona, USA.ORCID 0000-0002-1462-2957
Randall A BlyDivision of Pediatric Otolaryngology, Seattle Children's Hospital, Seattle, Washington, DC, USA.ORCID 0000-0001-5308-527X
Kaalan E JohnsonDivision of Pediatric Otolaryngology, Seattle Children's Hospital, Seattle, Washington, DC, USA.ORCID 0000-0002-2961-6058
Seth D FriedmanCenter for Respiratory Biology and Therapeutics, Seattle Children's Research Institute, Seattle, Washington, DC, USA.
John P DahlDivision of Pediatric Otolaryngology, Seattle Children's Hospital, Seattle, Washington, DC, USA.
Sanjay R ParikhDivision of Pediatric Otolaryngology, Seattle Children's Hospital, Seattle, Washington, DC, USA.
Juliana Bonilla-VelezDivision of Pediatric Otolaryngology, Seattle Children's Hospital, Seattle, Washington, DC, USA.ORCID 0000-0002-7174-7609

Funding

Clinician-Scientist Research Education and Training in OtolaryngologyR25DC021791 · NIDCD · UNIVERSITY OF WASHINGTON · PI Jay T. Rubinstein, Jennifer S. Stone · 2024 to 2026
$1.6M
Center for Clinical and Translational Research. Seattle Children's Research InstituteNIDCD NIH HHS R25 DC021791
6 · The paper itself

Abstract

OBJECTIVE(S): To measure clinical outcomes and respiratory trajectories after the placement of virtually assisted personalized tracheostomy tubes (vapTT) designed for patients with congenital airway anomalies (CAA).

methodsRetrospective review was performed of vapTT candidates, which included patients with CAA experiencing recurrent respiratory failure due to ongoing TT obstruction despite exhaustion of commercially available TT. VapTT design used a previously reported protocol for virtual modeling from CT images correlated with endoscopy findings. Outcomes obtained from medical records included the presence of TT-related granulation/ulceration, symptomatic tracheoscopy frequency, progression of inpatient care, ventilatory parameters, and serum bicarbonate levels.

resultsSix patients were included. CAA pathology included tracheal cartilaginous sleeve, tortuosity, and stenosis in the setting of conditions such as craniosynostosis syndromes, skeletal dysplasia, and long-gap esophageal atresia with scoliosis. Three patients were hospitalized for greater than 5 months at the time of vapTT implementation; all three demonstrated improvement in acute obstructive events, resolution of granulation on tracheoscopy, significant improvement in serum bicarbonate (p < 0.005), and progression of care to discharge. Of the three outpatients undergoing vapTT implementation, one patient experienced resolution of recurrent tracheitis and one had resolution of acutely symptomatic airway events. For the group, there was a significant decrease in compiled serum bicarbonate levels after vapTT implementation (3.6, 95% CI: 2.85-4.31, p < 0.001).

conclusionsVapTT is a feasible option when airway obstruction cannot be overcome with standard TTs in children with CAA. Our early experience with vapTT demonstrated improved respiratory function without significant adverse events. Future studies are required to investigate long-term outcomes of vapTT. LEVEL OF EVIDENCE: 4:

Indexed as

Airway ObstructionRespiratory System AbnormalitiesTracheaTracheostomyChildChild, PreschoolFemaleHumansInfantMaleRespiratory InsufficiencyRetrospective StudiesTomography, X-Ray ComputedTreatment Outcomecraniofacialpediatric airwaytracheotomy

Identifiers

PMID40353737
PMCPMC13330573

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.