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Author
- Andersen, Nick1
- Baird, Christopher W1
- Bryant, Roosevelt III1
- Chiswell, Karen1
- Dupont, Pierre E1
- Guleserian, Kristine J1
- Ha, Junhyoung1
- He, Jiankang1
- Hill, Kevin D1
- Huang, Lijun1
- Jacobs, Jeffrey P1
- Jacobs, Marshall L1
- Jennings, Russell W1
- Jo, Vickie Y1
- Kamran, Ali1
- Kaza, Aditya K1
- Labuz, Daniel F1
- Li, Xiaofei1
- Liu, Wenhao1
- Mondal, Abhijit1
- Morales, David LS1
- Riggs, Kyle W1
- Thibault, Dylan1
- Tweddell, James S1
- Wang, Lei1
Keyword
- tracheobronchomalacia2
- adjusted odds ratio1
- airway stent1
- aOR1
- bronchi1
- CHD1
- CI1
- CL1
- computed tomography1
- confidence interval1
- congenital cardiac1
- CT1
- EtOH1
- L11
- NiTi1
- R11
- SEM1
- SNC1
- Society of Thoracic Surgeons Congenital Heart Surgery Database1
- Society of Thoracic/European Association for Congenital Heart Surgery Mortality1
- STAT1
- STS-CHSD1
- SWC1
- TBM1
- UT1
Congenital - Trachea
4 Results
- Congenital: Trachea
Reoperation to correct unsuccessful vascular ring and vascular decompression surgery
The Journal of Thoracic and Cardiovascular SurgeryVol. 164Issue 1p199–207Published online: November 11, 2021- Daniel F. Labuz
- Ali Kamran
- Russell W. Jennings
- Christopher W. Baird
Cited in Scopus: 2Although most children do well after operations to relieve vascular compression of the esophagus and airway, many will have persistent/recurrent symptoms. We review our surgical experience using a customized approach to correct various etiologies of failure after vascular ring/decompression surgery. - Congenital: TracheaOpen Archive
Tracheal surgery for airway anomalies associated with increased mortality in pediatric patients undergoing heart surgery: Society of Thoracic Surgeons Database analysis
The Journal of Thoracic and Cardiovascular SurgeryVol. 161Issue 3p1112–1121.e7Published online: November 26, 2020- Kyle W. Riggs
- Farhan Zafar
- Marshall L. Jacobs
- Jeffrey P. Jacobs
- Dylan Thibault
- Kristine J. Guleserian
- and others
Cited in Scopus: 12Airway anomalies are common in children with cardiac disease but with an unquantified impact on outcomes. We sought to define the association between airway anomalies and tracheal surgery with cardiac surgery outcomes using the Society of Thoracic Surgery Congenital Heart Surgery Database. - Congenital: Trachea: Evolving TechnologyOpen Archive
Preclinical evaluation of a pediatric airway stent for tracheobronchomalacia
The Journal of Thoracic and Cardiovascular SurgeryVol. 161Issue 1e51–e60Published online: March 15, 2020- Abhijit Mondal
- Junhyoung Ha
- Vickie Y. Jo
- Fei-Yi Wu
- Aditya K. Kaza
- Pierre E. Dupont
Cited in Scopus: 6We sought to demonstrate in an animal model that helical stents made from a nickel titanium alloy called nitinol (NiTi) and designed for malacic airways could be delivered and removed without significant trauma while minimally impeding mucus clearance during the period of implantation. - Congenital: Trachea: Case ReportOpen Archive
Treatment of bronchomalacia using three-dimensional printed polycaprolactone scaffold in a pediatric patient
The Journal of Thoracic and Cardiovascular SurgeryVol. 157Issue 5e287–e290Published online: December 12, 2018- Lei Wang
- Wenhao Liu
- Jiankang He
- Xiaofei Li
- Lijun Huang
Cited in Scopus: 5Bronchomalacia, a weakness of the bronchus due to the reduction and/or atrophy of the longitudinal elastic fibers or impaired cartilage integrity, is a rare respiratory disease in children. Green and colleagues1,2 first used a 3-dimensional printed (3DP) polycaprolactone (PCL) scaffold to suspend the malacic bronchus and achieved excellent therapeutic results. However, few cases have been reported on the application of this technology or the clinical features of scaffold in vivo. Herein, a pediatric patient with left mainstem bronchomalacia was cured using the 3DP PCL scaffold technique.