Evidence map›Paper›PMID 26997148›Full record

ReviewSeminars in fetal & neonatal medicine2016

Craniofacial disorders associated with airway obstruction in the neonate.

Christopher M Cielo, Fernando M Montalva, Jesse A Taylor

Abstract readReview
In one paragraph

Review in Seminars in fetal & neonatal medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 7% of its field
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Virtually Assisted Personalized Tracheostomy Tube Design in Pediatric Complex Airway Anomalies.Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Neural crest-specific deletion ofDisease models & mechanisms · 2021
    Article
  8. [Progress of diagnosis and treatment of upper respiratory obstruction in patients with Treacher Collins syndrome].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2019
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. NOVELAACE clinical case reports
    Article
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

3 authors at 2 institutions in 2 countries.

Christopher M CieloPerelman School of Medicine at the University of Pennsylvania, Division of Pulmonary Medicine, The Children's Hospital of Philadelphia, Philadelphia, PA, USA. Electronic address: cieloc@email.chop.edu.
Fernando M MontalvaHospital Angeles Pedregal, Magdalena Contreras, Mexico City, Mexico.
Jesse A TaylorPerelman School of Medicine at the University of Pennsylvania, Division of Plastic and Reconstructive Surgery, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
University of Pennsylvania · USHospital Angeles Pedregal · MX

Funding

Institutional Clinical and Translational Science AwardKL2TR001879 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI MEAGHER, EMMA ANNE · 2016 to 2025
$13.7M
Institutional Clinical and Translational Science AwardKL2TR000139 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2012 to 2015
$3.9M
NCATS NIH HHS KL2 TR000139NCATS NIH HHS KL2 TR001879NHLBI NIH HHS L40 HL129939
6 · The paper itself

Abstract

In infants with craniofacial disorders, upper airway obstruction is one of the primary causes for morbidity and mortality in the neonatal period. Infants with craniofacial disorders, including Pierre Robin sequence, are at high risk for obstructive sleep apnea syndrome. Because of the complexity of their care, these neonates are usually followed by a multidisciplinary team to ensure timely evaluation and optimal treatment. In addition to history and physical examination, clinical evaluation may include genetic testing, imaging, endoscopy, and polysomnography. There are various treatment options, both surgical and non-surgical, that may be used depending on clinical assessment, underlying condition, and severity of disease. Recent advances have led to better assessment and treatment of these patients, but many questions remain. This review outlines the available literature pertaining to the evaluation and management of upper airway obstruction in the neonate with craniofacial conditions, with a particular focus on Pierre Robin sequence.

Indexed as

AchondroplasiaAirway ObstructionCleft LipCleft PalateCraniosynostosesDown SyndromeHumansInfantInfant, NewbornPierre Robin SyndromeApnea–hypopnea indexCraniosynostosisMicrognathiaObstructive sleep apneaPierre Robin sequenceTreacher Collins

Identifiers

PMID26997148
PMCPMC4967408
OpenAlexW2300265886

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.